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CVS Health

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FY2019 Annual Report · CVS Health
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Delivering health
when, where and
how people need it.

2019 Annual Report

Financial Highlights

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2019 

2018 

% change 

Total revenues 

$ 

256,776 

$ 

194,579  

32.0%

Operating income 

Net income (loss) 

Diluted EPS from continuing operations 

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Stock price at year-end 

Market capitalization at year-end 

$ 

$ 

$ 

$ 

$ 

$ 

11,987 

6,631  

5.08  

12,848 

$ 

$ 

$ 

$ 

4,021 

(596) 

(0.57) 

NM

NM

NM

8,865 

 44.9%

74.29 

 $ 

65.52 

13.4%

96,651 

$ 

84,843 

13.9%

Total revenues
in billions of dollars

Diluted EPS from  
continuing operations  
in dollars

Adjusted EPS*
in dollars per common share

153.3

177.5

184.8

194.6 256.8

4.62

4.91

6.45

(cid:62)(cid:94)(cid:17)(cid:99)(cid:101)(cid:63) 5.08

5.16

5.84

(cid:99)(cid:17)(cid:103)(cid:94) (cid:101)(cid:17)(cid:94)(cid:102)

7.08

   15 

16 

17 

18 

19

   15  

16 

17 

18 

19

   15 

16 

17 

18 

19

NM = not meaningful

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(cid:211)(cid:208)(cid:204)(cid:207)(cid:212)(cid:217)(cid:210)(cid:3)(cid:32)(cid:195)(cid:208)(cid:206)(cid:218)(cid:217)(cid:206)(cid:212)(cid:215)(cid:212)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:33)(cid:3)(cid:212)(cid:217)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:205)(cid:204)(cid:206)(cid:214)(cid:3)(cid:219)(cid:204)(cid:210)(cid:208)(cid:222)(cid:3)(cid:218)(cid:209)(cid:3)(cid:223)(cid:211)(cid:212)(cid:222)(cid:3)(cid:178)(cid:217)(cid:217)(cid:224)(cid:204)(cid:215)(cid:3)(cid:195)(cid:208)(cid:219)(cid:218)(cid:221)(cid:223)(cid:17)

 
  
  
Dear Fellow Stockholders:

This past year was a remarkable one for CVS Health. We completed our 
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with the progress we achieved in executing on our strategic priorities.  
We have set a clear and bold path for CVS Health to be the most 
consumer-centric health company. Powered by our unmatched 
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care is delivered in the United States. 

As consumers take a more active role 
in their health care decisions, we have 
the ability to deliver health care when, 
where and how consumers need it. That 
could happen in the community, right at 
home or in the palm of the hand through 
one of our digital products. We have 
CVS Pharmacy retail locations within 
three miles of nearly 70 percent of the 
U.S. population, and the frequency of 
our consumer interactions provides  
us the opportunity to introduce and 
expand our programs and services 
into consumers’ existing routines. 

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and services, including pharmacy 
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mail order and specialty pharmacy, and 
retail and long-term care pharmacy 
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(cid:205)(cid:208)(cid:217)(cid:208)(cid:242)(cid:223)(cid:222)(cid:3)(cid:219)(cid:221)(cid:218)(cid:207)(cid:224)(cid:206)(cid:223)(cid:222)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:222)(cid:208)(cid:221)(cid:225)(cid:212)(cid:206)(cid:208)(cid:222)(cid:19)(cid:3)(cid:180)(cid:218)(cid:221)(cid:204)(cid:216)(cid:92)(cid:3)
(cid:212)(cid:217)(cid:209)(cid:224)(cid:222)(cid:212)(cid:218)(cid:217)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:178)(cid:206)(cid:206)(cid:218)(cid:221)(cid:207)(cid:204)(cid:217)(cid:223)(cid:92)(cid:3)(cid:217)(cid:224)(cid:221)(cid:222)(cid:208)(cid:3)(cid:206)(cid:204)(cid:221)(cid:208)(cid:3)
management services. Taken together, 
these integrated assets allow us 
to engage with about one in three 
Americans every year. Additionally, we 
now use text messaging to engage with 
more than 80 million people who are 
enrolled in our text messaging program 
across our Enterprise.

(cid:179)(cid:208)(cid:209)(cid:218)(cid:221)(cid:208)(cid:3)(cid:186)(cid:3)(cid:207)(cid:208)(cid:215)(cid:225)(cid:208)(cid:3)(cid:216)(cid:218)(cid:221)(cid:208)(cid:3)(cid:207)(cid:208)(cid:208)(cid:219)(cid:215)(cid:228)(cid:3)(cid:212)(cid:217)(cid:223)(cid:218)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)
transformation and review the  
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(cid:186)(cid:3)(cid:226)(cid:204)(cid:217)(cid:223)(cid:3)(cid:223)(cid:218)(cid:3)(cid:224)(cid:219)(cid:207)(cid:204)(cid:223)(cid:208)(cid:3)(cid:228)(cid:218)(cid:224)(cid:3)(cid:218)(cid:217)(cid:3)(cid:222)(cid:218)(cid:216)(cid:208)(cid:3)(cid:218)(cid:209)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)

(cid:208)(cid:241)(cid:218)(cid:221)(cid:223)(cid:222)(cid:3)(cid:204)(cid:223)(cid:3)(cid:216)(cid:212)(cid:223)(cid:212)(cid:210)(cid:204)(cid:223)(cid:212)(cid:217)(cid:210)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:212)(cid:216)(cid:219)(cid:204)(cid:206)(cid:223)(cid:3)(cid:218)(cid:209)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)
(cid:180)(cid:218)(cid:221)(cid:218)(cid:217)(cid:204)(cid:225)(cid:212)(cid:221)(cid:224)(cid:222)(cid:3)(cid:40)(cid:180)(cid:192)(cid:199)(cid:186)(cid:181)(cid:35)(cid:95)(cid:103)(cid:41)(cid:3)(cid:219)(cid:204)(cid:217)(cid:207)(cid:208)(cid:216)(cid:212)(cid:206)(cid:17)(cid:3)

We quickly assembled CVS Health’s 
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unprecedented and uncertain time, 
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being and safety of our employees, 
consumers, members and the 
communities we serve. As part of a 
multi-faceted response, we waived the 
fees on home delivery of prescriptions 
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(cid:180)(cid:204)(cid:221)(cid:208)(cid:3)(cid:179)(cid:208)(cid:217)(cid:208)(cid:242)(cid:223)(cid:222)(cid:3)(cid:222)(cid:208)(cid:210)(cid:216)(cid:208)(cid:217)(cid:223)(cid:3)(cid:226)(cid:208)(cid:3)(cid:226)(cid:204)(cid:212)(cid:225)(cid:208)(cid:207)(cid:3)
co-pays for any telemedicine visits 
and eliminated out of pocket costs for 
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partnered with the U.S. government to 
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help facilitate increased frequency and 
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to visit CVSHealth.com as we continue 
to provide updates on our initiatives.

In 2019, CVS Health posted record 
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(cid:204)(cid:206)(cid:211)(cid:212)(cid:208)(cid:225)(cid:212)(cid:217)(cid:210)(cid:3)(cid:222)(cid:212)(cid:210)(cid:217)(cid:212)(cid:242)(cid:206)(cid:204)(cid:217)(cid:223)(cid:3)(cid:206)(cid:218)(cid:222)(cid:223)(cid:35)(cid:222)(cid:204)(cid:225)(cid:212)(cid:217)(cid:210)(cid:3)
(cid:212)(cid:217)(cid:223)(cid:208)(cid:210)(cid:221)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:3)(cid:222)(cid:228)(cid:217)(cid:208)(cid:221)(cid:210)(cid:212)(cid:208)(cid:222)(cid:3)(cid:209)(cid:221)(cid:218)(cid:216)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:178)(cid:208)(cid:223)(cid:217)(cid:204)(cid:3)
(cid:204)(cid:206)(cid:220)(cid:224)(cid:212)(cid:222)(cid:212)(cid:223)(cid:212)(cid:218)(cid:217)

(cid:81)   Total revenues for the year increased 
by 32.0 percent to a record $256.8 
billion, with operating income and 
adjusted operating income totaling 
(cid:114)(cid:95)(cid:96)(cid:17)(cid:94)(cid:3)(cid:205)(cid:212)(cid:215)(cid:215)(cid:212)(cid:218)(cid:217)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:114)(cid:95)(cid:99)(cid:17)(cid:97)(cid:3)(cid:205)(cid:212)(cid:215)(cid:215)(cid:212)(cid:218)(cid:217)(cid:19)(cid:23)(cid:3)
respectively.

(cid:23)(cid:3)(cid:3)(cid:178)(cid:207)(cid:213)(cid:224)(cid:222)(cid:223)(cid:208)(cid:207)(cid:3)(cid:218)(cid:219)(cid:208)(cid:221)(cid:204)(cid:223)(cid:212)(cid:217)(cid:210)(cid:3)(cid:212)(cid:217)(cid:206)(cid:218)(cid:216)(cid:208)(cid:3)(cid:212)(cid:222)(cid:3)(cid:204)(cid:3)(cid:217)(cid:218)(cid:217)(cid:35)(cid:184)(cid:178)(cid:178)(cid:193)(cid:3)(cid:242)(cid:217)(cid:204)(cid:217)(cid:206)(cid:212)(cid:204)(cid:215)(cid:3)(cid:216)(cid:208)(cid:204)(cid:222)(cid:224)(cid:221)(cid:208)(cid:17)(cid:3)(cid:178)(cid:3)(cid:221)(cid:208)(cid:206)(cid:218)(cid:217)(cid:206)(cid:212)(cid:215)(cid:212)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:3)(cid:218)(cid:209)(cid:3)(cid:218)(cid:219)(cid:208)(cid:221)(cid:204)(cid:223)(cid:212)(cid:217)(cid:210)(cid:3)(cid:212)(cid:217)(cid:206)(cid:218)(cid:216)(cid:208)(cid:3)(cid:223)(cid:218)(cid:3)(cid:204)(cid:207)(cid:213)(cid:224)(cid:222)(cid:223)(cid:208)(cid:207)(cid:3)

(cid:218)(cid:219)(cid:208)(cid:221)(cid:204)(cid:223)(cid:212)(cid:217)(cid:210)(cid:3)(cid:212)(cid:217)(cid:206)(cid:218)(cid:216)(cid:208)(cid:3)(cid:212)(cid:222)(cid:3)(cid:219)(cid:221)(cid:218)(cid:225)(cid:212)(cid:207)(cid:208)(cid:207)(cid:3)(cid:218)(cid:217)(cid:3)(cid:219)(cid:204)(cid:210)(cid:208)(cid:3)(cid:95)(cid:100)(cid:97)(cid:3)(cid:218)(cid:209)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:204)(cid:223)(cid:223)(cid:204)(cid:206)(cid:211)(cid:208)(cid:207)(cid:3)(cid:178)(cid:217)(cid:217)(cid:224)(cid:204)(cid:215)(cid:3)(cid:195)(cid:208)(cid:219)(cid:218)(cid:221)(cid:223)(cid:3)(cid:218)(cid:217)(cid:3)(cid:183)(cid:218)(cid:221)(cid:216)(cid:3)(cid:95)(cid:94)(cid:35)(cid:188)(cid:17)

(cid:96)(cid:94)(cid:95)(cid:103)(cid:3)(cid:178)(cid:217)(cid:217)(cid:224)(cid:204)(cid:215)(cid:3)(cid:195)(cid:208)(cid:219)(cid:218)(cid:221)(cid:223)

1

Larry J. Merlo
Larry J. Merlololo
(cid:193)(cid:221)(cid:208)(cid:222)(cid:212)(cid:207)(cid:208)(cid:217)(cid:223)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:180)(cid:211)(cid:212)(cid:208)(cid:209)(cid:3)(cid:182)(cid:227)(cid:208)(cid:206)(cid:206)(cid:206)(cid:206)(cid:206)(cid:206)(cid:224)(cid:223)(cid:212)(cid:225)(cid:208)(cid:3)(cid:192)(cid:244)(cid:206)(cid:208)(cid:221)
(cid:193)(cid:221)(cid:208)(cid:222)(cid:212)(cid:207)(cid:208)(cid:217)(cid:223)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:180)(cid:211)(cid:212)(cid:208)(cid:209)(cid:3)(cid:182)(cid:227)(cid:208)(cid:206)(cid:224)(cid:223)(cid:212)(cid:225)(cid:208)(cid:3)(cid:192)(cid:244)(cid:206)(cid:208)(cid:221)

(cid:179)(cid:208)(cid:3)(cid:215)(cid:218)(cid:206)(cid:204)(cid:215)
(cid:200)(cid:208)(cid:3)(cid:216)(cid:208)(cid:208)(cid:223)(cid:3)(cid:206)(cid:218)(cid:217)(cid:222)(cid:224)(cid:216)(cid:208)(cid:221)(cid:222)(cid:3)(cid:226)(cid:211)(cid:208)(cid:221)(cid:208)(cid:3)(cid:223)(cid:211)(cid:208)(cid:228)(cid:3)(cid:204)(cid:221)(cid:208)(cid:17)

(cid:180)(cid:199)(cid:196)(cid:3)(cid:185)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:30)(cid:222)(cid:3)(cid:221)(cid:208)(cid:204)(cid:206)(cid:211)(cid:3)(cid:208)(cid:217)(cid:204)(cid:205)(cid:215)(cid:208)(cid:222)(cid:3)(cid:224)(cid:222)(cid:3)(cid:223)(cid:218)(cid:3)(cid:218)(cid:241)(cid:208)(cid:221)(cid:3)(cid:206)(cid:204)(cid:221)(cid:208)(cid:3)(cid:226)(cid:211)(cid:208)(cid:221)(cid:208)(cid:19)(cid:3)(cid:226)(cid:211)(cid:208)(cid:217)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:211)(cid:218)(cid:226)(cid:3)(cid:219)(cid:204)(cid:223)(cid:212)(cid:208)(cid:217)(cid:223)(cid:222)(cid:3)(cid:217)(cid:208)(cid:208)(cid:207)(cid:3)(cid:212)(cid:223)(cid:39)(cid:212)(cid:217)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:215)(cid:218)(cid:206)(cid:204)(cid:215)(cid:3)(cid:206)(cid:218)(cid:216)(cid:216)(cid:224)(cid:217)(cid:212)(cid:223)(cid:228)(cid:19)(cid:3)(cid:212)(cid:217)(cid:3)
(cid:223)(cid:211)(cid:208)(cid:3)(cid:211)(cid:218)(cid:216)(cid:208)(cid:3)(cid:218)(cid:221)(cid:3)(cid:208)(cid:225)(cid:208)(cid:217)(cid:3)(cid:212)(cid:217)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:219)(cid:204)(cid:215)(cid:216)(cid:3)(cid:218)(cid:209)(cid:3)(cid:223)(cid:211)(cid:208)(cid:212)(cid:221)(cid:3)(cid:211)(cid:204)(cid:217)(cid:207)(cid:17)(cid:3)

(cid:192)(cid:224)(cid:221)(cid:3)(cid:222)(cid:223)(cid:218)(cid:221)(cid:208)(cid:222)(cid:3)(cid:204)(cid:221)(cid:208)(cid:3)(cid:212)(cid:217)(cid:3)(cid:223)(cid:211)(cid:208)(cid:212)(cid:221)(cid:3)
community 

~70% 

of U.S. population lives 
within three miles of  
a CVS Pharmacy

We are embedded 
in consumer’s digital 
lives, in their hands

>80M 

patients enrolled in 
text messaging

Consumers invite us  
into their homes

700K 

visits annually to 
homes or other 
community settings

 1  in 3

Americans interact 
with CVS Health 
annually

PATIE NT SNA PS HOT 
Susan
(cid:196)(cid:224)(cid:222)(cid:204)(cid:217)(cid:3)(cid:211)(cid:204)(cid:222)(cid:3)(cid:206)(cid:211)(cid:221)(cid:218)(cid:217)(cid:212)(cid:206)(cid:3)(cid:214)(cid:212)(cid:207)(cid:217)(cid:208)(cid:228)(cid:3)(cid:207)(cid:212)(cid:222)(cid:208)(cid:204)(cid:222)(cid:208)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)
(cid:207)(cid:212)(cid:244)(cid:206)(cid:224)(cid:215)(cid:223)(cid:35)(cid:223)(cid:218)(cid:35)(cid:206)(cid:218)(cid:217)(cid:223)(cid:221)(cid:218)(cid:215)(cid:3)(cid:211)(cid:212)(cid:210)(cid:211)(cid:3)(cid:205)(cid:215)(cid:218)(cid:218)(cid:207)(cid:3)(cid:219)(cid:221)(cid:208)(cid:222)(cid:222)(cid:224)(cid:221)(cid:208)(cid:17)(cid:3)
(cid:196)(cid:211)(cid:208)(cid:3)(cid:226)(cid:204)(cid:217)(cid:223)(cid:222)(cid:3)(cid:223)(cid:218)(cid:3)(cid:205)(cid:208)(cid:3)(cid:223)(cid:211)(cid:208)(cid:221)(cid:208)(cid:3)(cid:209)(cid:218)(cid:221)(cid:3)(cid:211)(cid:208)(cid:221)(cid:3)(cid:209)(cid:204)(cid:216)(cid:212)(cid:215)(cid:228)(cid:19)(cid:3)(cid:222)(cid:218)(cid:3)(cid:222)(cid:211)(cid:208)(cid:3)
(cid:217)(cid:208)(cid:208)(cid:207)(cid:222)(cid:3)(cid:204)(cid:3)(cid:211)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:3)(cid:219)(cid:221)(cid:218)(cid:210)(cid:221)(cid:204)(cid:216)(cid:3)(cid:223)(cid:211)(cid:204)(cid:223)(cid:3)(cid:226)(cid:212)(cid:215)(cid:215)(cid:3)(cid:205)(cid:208)(cid:3)(cid:243)(cid:208)(cid:227)(cid:212)(cid:205)(cid:215)(cid:208)(cid:3)
(cid:226)(cid:212)(cid:223)(cid:211)(cid:3)(cid:211)(cid:208)(cid:221)(cid:3)(cid:222)(cid:206)(cid:211)(cid:208)(cid:207)(cid:224)(cid:215)(cid:208)(cid:17)(cid:3)

(cid:181)(cid:208)(cid:225)(cid:212)(cid:206)(cid:208)(cid:222)(cid:3)(cid:224)(cid:222)(cid:208)(cid:207)(cid:18)(cid:3)Phone

(cid:193)(cid:221)(cid:208)(cid:209)(cid:208)(cid:221)(cid:208)(cid:217)(cid:206)(cid:208)(cid:222)(cid:18)(cid:3)(cid:178)(cid:219)(cid:219)(cid:221)(cid:208)(cid:206)(cid:212)(cid:204)(cid:223)(cid:208)(cid:222)(cid:3)(cid:219)(cid:221)(cid:218)(cid:204)(cid:206)(cid:223)(cid:212)(cid:225)(cid:208)(cid:3)(cid:218)(cid:224)(cid:223)(cid:221)(cid:208)(cid:204)(cid:206)(cid:211)(cid:3)
(cid:204)(cid:222)(cid:3)(cid:222)(cid:211)(cid:208)(cid:3)(cid:205)(cid:204)(cid:215)(cid:204)(cid:217)(cid:206)(cid:208)(cid:222)(cid:3)(cid:226)(cid:218)(cid:221)(cid:214)(cid:19)(cid:3)(cid:209)(cid:204)(cid:216)(cid:212)(cid:215)(cid:228)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:211)(cid:208)(cid:221)(cid:3)(cid:211)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)

(cid:193)(cid:221)(cid:218)(cid:210)(cid:221)(cid:204)(cid:216)(cid:18)(cid:3)(cid:180)(cid:211)(cid:221)(cid:218)(cid:217)(cid:212)(cid:206)(cid:3)(cid:188)(cid:212)(cid:207)(cid:217)(cid:208)(cid:228)(cid:3)(cid:181)(cid:212)(cid:222)(cid:208)(cid:204)(cid:222)(cid:208)(cid:3)(cid:180)(cid:204)(cid:221)(cid:208)(cid:3)
(cid:190)(cid:204)(cid:217)(cid:204)(cid:210)(cid:208)(cid:216)(cid:208)(cid:217)(cid:223)

SUS AN’S JOURNE Y 

(cid:32)(cid:3)(cid:190)(cid:228)(cid:3)(cid:206)(cid:204)(cid:221)(cid:208)(cid:3)(cid:226)(cid:204)(cid:222)(cid:3)(cid:219)(cid:208)(cid:221)(cid:222)(cid:218)(cid:217)(cid:35)
(cid:204)(cid:215)(cid:212)(cid:229)(cid:208)(cid:207)(cid:19)(cid:3)(cid:204)(cid:206)(cid:206)(cid:208)(cid:222)(cid:222)(cid:212)(cid:205)(cid:215)(cid:208)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)
(cid:186)(cid:3)(cid:226)(cid:204)(cid:222)(cid:3)(cid:208)(cid:225)(cid:208)(cid:217)(cid:3)(cid:204)(cid:205)(cid:215)(cid:208)(cid:3)(cid:223)(cid:218)(cid:3) 
(cid:210)(cid:208)(cid:223)(cid:3)(cid:211)(cid:208)(cid:215)(cid:219)(cid:3)(cid:212)(cid:217)(cid:3)(cid:216)(cid:228)(cid:3)(cid:218)(cid:226)(cid:217)(cid:3)
(cid:211)(cid:218)(cid:216)(cid:208)(cid:17)(cid:33)

(cid:180)(cid:199)(cid:196)(cid:3)(cid:188)(cid:212)(cid:207)(cid:217)(cid:208)(cid:228)(cid:3)(cid:180)(cid:204)(cid:221)(cid:208)(cid:3)
(cid:212)(cid:207)(cid:208)(cid:217)(cid:223)(cid:212)(cid:242)(cid:208)(cid:222)(cid:3)(cid:196)(cid:224)(cid:222)(cid:204)(cid:217)(cid:3)(cid:204)(cid:222)(cid:3)
(cid:211)(cid:204)(cid:225)(cid:212)(cid:217)(cid:210)(cid:3)(cid:206)(cid:211)(cid:221)(cid:218)(cid:217)(cid:212)(cid:206)(cid:3)(cid:214)(cid:212)(cid:207)(cid:217)(cid:208)(cid:228)(cid:3)
(cid:207)(cid:212)(cid:222)(cid:208)(cid:204)(cid:222)(cid:208)(cid:17)(cid:3)(cid:196)(cid:224)(cid:222)(cid:204)(cid:217)(cid:3)(cid:222)(cid:208)(cid:208)(cid:222)(cid:3)(cid:204)(cid:3)
(cid:217)(cid:208)(cid:219)(cid:211)(cid:221)(cid:218)(cid:215)(cid:218)(cid:210)(cid:212)(cid:222)(cid:223)(cid:17)

(cid:196)(cid:224)(cid:222)(cid:204)(cid:217)(cid:3)(cid:212)(cid:222)(cid:3)(cid:219)(cid:221)(cid:218)(cid:225)(cid:212)(cid:207)(cid:208)(cid:207)(cid:3)
(cid:212)(cid:217)(cid:209)(cid:218)(cid:221)(cid:216)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:3)(cid:223)(cid:218)(cid:3)(cid:211)(cid:208)(cid:215)(cid:219)(cid:3)(cid:207)(cid:208)(cid:215)(cid:204)(cid:228)(cid:3)
(cid:219)(cid:221)(cid:218)(cid:210)(cid:221)(cid:208)(cid:222)(cid:222)(cid:212)(cid:218)(cid:217)(cid:3)(cid:218)(cid:209)(cid:3)(cid:211)(cid:208)(cid:221)(cid:3)(cid:207)(cid:212)(cid:222)(cid:208)(cid:204)(cid:222)(cid:208)(cid:3)
(cid:204)(cid:217)(cid:207)(cid:3)(cid:218)(cid:219)(cid:223)(cid:212)(cid:218)(cid:217)(cid:222)(cid:3)(cid:209)(cid:218)(cid:221)(cid:3)(cid:209)(cid:224)(cid:223)(cid:224)(cid:221)(cid:208)(cid:3)
(cid:221)(cid:208)(cid:217)(cid:204)(cid:215)(cid:3)(cid:221)(cid:208)(cid:219)(cid:215)(cid:204)(cid:206)(cid:208)(cid:216)(cid:208)(cid:217)(cid:223)(cid:3)(cid:223)(cid:211)(cid:208)(cid:221)(cid:204)(cid:219)(cid:228)(cid:17)

Susan chooses  
(cid:204)(cid:223)(cid:35)(cid:211)(cid:218)(cid:216)(cid:208)(cid:3)(cid:211)(cid:208)(cid:216)(cid:218)(cid:207)(cid:212)(cid:204)(cid:215)(cid:228)(cid:222)(cid:212)(cid:222)(cid:3)
(cid:204)(cid:217)(cid:207)(cid:3)(cid:212)(cid:222)(cid:3)(cid:204)(cid:205)(cid:215)(cid:208)(cid:3)(cid:223)(cid:218)(cid:3)(cid:206)(cid:218)(cid:217)(cid:223)(cid:212)(cid:217)(cid:224)(cid:208)(cid:3)
(cid:226)(cid:218)(cid:221)(cid:214)(cid:212)(cid:217)(cid:210)(cid:17)

2

CVS Health

(cid:191)(cid:218)(cid:223)(cid:3)(cid:204)(cid:217)(cid:3)(cid:204)(cid:206)(cid:223)(cid:224)(cid:204)(cid:215)(cid:3)(cid:219)(cid:204)(cid:223)(cid:212)(cid:208)(cid:217)(cid:223)(cid:19)(cid:3)(cid:205)(cid:224)(cid:223)(cid:3)(cid:204)(cid:3)(cid:221)(cid:208)(cid:219)(cid:221)(cid:208)(cid:222)(cid:208)(cid:217)(cid:223)(cid:204)(cid:223)(cid:212)(cid:225)(cid:208)(cid:3)(cid:213)(cid:218)(cid:224)(cid:221)(cid:217)(cid:208)(cid:228)(cid:17)(cid:3)

(cid:81)   GAAP diluted earnings per share 

(cid:40)(cid:182)(cid:193)(cid:196)(cid:41)(cid:3)(cid:209)(cid:221)(cid:218)(cid:216)(cid:3)(cid:206)(cid:218)(cid:217)(cid:223)(cid:212)(cid:217)(cid:224)(cid:212)(cid:217)(cid:210)(cid:3)(cid:218)(cid:219)(cid:208)(cid:221)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:222)(cid:3)(cid:221)(cid:218)(cid:222)(cid:208)(cid:3)
(cid:223)(cid:218)(cid:3)(cid:114)(cid:99)(cid:17)(cid:94)(cid:102)(cid:19)(cid:3)(cid:226)(cid:212)(cid:223)(cid:211)(cid:3)(cid:178)(cid:207)(cid:213)(cid:224)(cid:222)(cid:223)(cid:208)(cid:207)(cid:3)(cid:182)(cid:193)(cid:196)(cid:3)(cid:204)(cid:223)(cid:3)(cid:114)(cid:101)(cid:17)(cid:94)(cid:102)(cid:17)(cid:23)(cid:3)

(cid:81)(cid:3)(cid:3)(cid:3)(cid:180)(cid:204)(cid:222)(cid:211)(cid:3)(cid:243)(cid:218)(cid:226)(cid:3)(cid:209)(cid:221)(cid:218)(cid:216)(cid:3)(cid:218)(cid:219)(cid:208)(cid:221)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:222)(cid:3)(cid:212)(cid:217)(cid:206)(cid:221)(cid:208)(cid:204)(cid:222)(cid:208)(cid:207)(cid:3)
(cid:205)(cid:228)(cid:3)(cid:98)(cid:98)(cid:17)(cid:103)(cid:3)(cid:219)(cid:208)(cid:221)(cid:206)(cid:208)(cid:217)(cid:223)(cid:3)(cid:223)(cid:218)(cid:3)(cid:114)(cid:95)(cid:96)(cid:17)(cid:102)(cid:3)(cid:205)(cid:212)(cid:215)(cid:215)(cid:212)(cid:218)(cid:217)(cid:19)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)
we continue to take steps to further 
strengthen our balance sheet by 
reducing debt and our leverage ratio. 

(cid:81)(cid:3)(cid:3)(cid:3)(cid:186)(cid:217)(cid:3)(cid:96)(cid:94)(cid:95)(cid:103)(cid:19)(cid:3)(cid:226)(cid:208)(cid:3)(cid:207)(cid:208)(cid:215)(cid:212)(cid:225)(cid:208)(cid:221)(cid:208)(cid:207)(cid:3)(cid:204)(cid:219)(cid:219)(cid:221)(cid:218)(cid:227)(cid:212)(cid:216)(cid:204)(cid:223)(cid:208)(cid:215)(cid:228)(cid:3)

$500 million of cost-saving 
integration synergies from the Aetna 
acquisition, ahead of our initial goal 
of $300 million–$350 million.

(cid:200)(cid:208)(cid:3)(cid:204)(cid:221)(cid:208)(cid:3)(cid:216)(cid:204)(cid:214)(cid:212)(cid:217)(cid:210)(cid:3)(cid:216)(cid:208)(cid:204)(cid:217)(cid:212)(cid:217)(cid:210)(cid:209)(cid:224)(cid:215)(cid:3)(cid:219)(cid:221)(cid:218)(cid:210)(cid:221)(cid:208)(cid:222)(cid:222)(cid:3)
(cid:204)(cid:206)(cid:221)(cid:218)(cid:222)(cid:222)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)(cid:209)(cid:218)(cid:224)(cid:221)(cid:3)(cid:182)(cid:217)(cid:223)(cid:208)(cid:221)(cid:219)(cid:221)(cid:212)(cid:222)(cid:208)(cid:35)(cid:226)(cid:212)(cid:207)(cid:208)(cid:3)
(cid:219)(cid:221)(cid:212)(cid:218)(cid:221)(cid:212)(cid:223)(cid:212)(cid:208)(cid:222)(cid:3)

The following four Enterprise-wide 
priorities guide our long-term growth 
strategy and support our vision for 
improving health care: 

(cid:81)(cid:3)(cid:3)(cid:3)(cid:184)(cid:221)(cid:218)(cid:226)(cid:212)(cid:217)(cid:210)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:207)(cid:212)(cid:241)(cid:208)(cid:221)(cid:208)(cid:217)(cid:223)(cid:212)(cid:204)(cid:223)(cid:212)(cid:217)(cid:210)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)

businesses;

(cid:81)(cid:3)(cid:3)(cid:3)(cid:181)(cid:208)(cid:215)(cid:212)(cid:225)(cid:208)(cid:221)(cid:212)(cid:217)(cid:210)(cid:3)(cid:223)(cid:221)(cid:204)(cid:217)(cid:222)(cid:209)(cid:218)(cid:221)(cid:216)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:204)(cid:215)(cid:3)(cid:219)(cid:221)(cid:218)(cid:207)(cid:224)(cid:206)(cid:223)(cid:222)(cid:3)

and services;

(cid:81)   Creating a consumer-centric  
technology infrastructure; and

(cid:81)(cid:3)(cid:3)(cid:3)(cid:190)(cid:218)(cid:207)(cid:208)(cid:221)(cid:217)(cid:212)(cid:229)(cid:212)(cid:217)(cid:210)(cid:3)(cid:182)(cid:217)(cid:223)(cid:208)(cid:221)(cid:219)(cid:221)(cid:212)(cid:222)(cid:208)(cid:3)(cid:209)(cid:224)(cid:217)(cid:206)(cid:223)(cid:212)(cid:218)(cid:217)(cid:222)(cid:3)

and capabilities.

(cid:182)(cid:227)(cid:219)(cid:208)(cid:206)(cid:223)

600 to 650

(cid:185)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:185)(cid:198)(cid:179)(cid:3)(cid:215)(cid:218)(cid:206)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:222)(cid:3) 
(cid:205)(cid:228)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:208)(cid:217)(cid:207)(cid:3)(cid:218)(cid:209)(cid:3)(cid:96)(cid:94)(cid:96)(cid:94)

(cid:186)(cid:3)(cid:223)(cid:218)(cid:224)(cid:206)(cid:211)(cid:208)(cid:207)(cid:3)(cid:205)(cid:221)(cid:212)(cid:208)(cid:243)(cid:228)(cid:3)(cid:212)(cid:217)(cid:3)(cid:215)(cid:204)(cid:222)(cid:223)(cid:3)(cid:228)(cid:208)(cid:204)(cid:221)(cid:30)(cid:222)(cid:3)(cid:215)(cid:208)(cid:223)(cid:223)(cid:208)(cid:221)(cid:3)(cid:218)(cid:217)(cid:3)
(cid:223)(cid:211)(cid:208)(cid:3)(cid:185)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:185)(cid:198)(cid:179)(cid:92)(cid:3)(cid:206)(cid:218)(cid:217)(cid:206)(cid:208)(cid:219)(cid:223)(cid:3)(cid:215)(cid:218)(cid:206)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:222)(cid:3)(cid:226)(cid:208)(cid:3)
had just begun rolling out in Houston. 
(cid:192)(cid:224)(cid:221)(cid:3)(cid:219)(cid:221)(cid:218)(cid:210)(cid:221)(cid:208)(cid:222)(cid:222)(cid:3)(cid:222)(cid:212)(cid:217)(cid:206)(cid:208)(cid:3)(cid:223)(cid:211)(cid:208)(cid:217)(cid:3)(cid:218)(cid:241)(cid:208)(cid:221)(cid:222)(cid:3)(cid:213)(cid:224)(cid:222)(cid:223)(cid:3)(cid:218)(cid:217)(cid:208)(cid:3)
(cid:208)(cid:227)(cid:204)(cid:216)(cid:219)(cid:215)(cid:208)(cid:3)(cid:218)(cid:209)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)(cid:222)(cid:224)(cid:206)(cid:206)(cid:208)(cid:222)(cid:222)(cid:209)(cid:224)(cid:215)(cid:3)(cid:208)(cid:241)(cid:218)(cid:221)(cid:223)(cid:222)(cid:3)(cid:204)(cid:223)(cid:3)
(cid:207)(cid:212)(cid:241)(cid:208)(cid:221)(cid:208)(cid:217)(cid:223)(cid:212)(cid:204)(cid:223)(cid:212)(cid:217)(cid:210)(cid:3)(cid:180)(cid:199)(cid:196)(cid:3)(cid:185)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:17)(cid:3)(cid:178)(cid:222)(cid:3)(cid:204)(cid:3)(cid:217)(cid:208)(cid:226)(cid:3)
(cid:221)(cid:208)(cid:223)(cid:204)(cid:212)(cid:215)(cid:3)(cid:208)(cid:217)(cid:210)(cid:204)(cid:210)(cid:208)(cid:216)(cid:208)(cid:217)(cid:223)(cid:3)(cid:216)(cid:218)(cid:207)(cid:208)(cid:215)(cid:19)(cid:3)(cid:185)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:185)(cid:198)(cid:179)(cid:3)
locations provide customers with a 

convenient and compelling destination 
to manage their overall health—from 
prevention and wellness to chronic 
disease management. They include 
care concierges, a curated selection 
of health and wellness products and 
(cid:217)(cid:208)(cid:226)(cid:3)(cid:190)(cid:212)(cid:217)(cid:224)(cid:223)(cid:208)(cid:180)(cid:215)(cid:212)(cid:217)(cid:212)(cid:206)(cid:92)(cid:3)(cid:222)(cid:208)(cid:221)(cid:225)(cid:212)(cid:206)(cid:208)(cid:222)(cid:3)(cid:222)(cid:224)(cid:206)(cid:211)(cid:3)(cid:204)(cid:222)(cid:3)
in-clinic blood draws and enhanced 
screenings.

(cid:186)(cid:217)(cid:3)(cid:96)(cid:94)(cid:95)(cid:103)(cid:19)(cid:3)(cid:226)(cid:208)(cid:3)(cid:206)(cid:221)(cid:208)(cid:204)(cid:223)(cid:208)(cid:207)(cid:3)(cid:216)(cid:218)(cid:221)(cid:208)(cid:3)(cid:223)(cid:211)(cid:204)(cid:217)(cid:3)(cid:99)(cid:94)(cid:3)
(cid:185)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:185)(cid:198)(cid:179)(cid:3)(cid:215)(cid:218)(cid:206)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:222)(cid:3)(cid:212)(cid:217)(cid:3)(cid:185)(cid:218)(cid:224)(cid:222)(cid:223)(cid:218)(cid:217)(cid:19)(cid:3)
Tampa, Atlanta and Philadelphia. We 
expect that number to rise to between 
600 and 650 by the end of 2020 and 
(cid:223)(cid:218)(cid:3)(cid:95)(cid:19)(cid:99)(cid:94)(cid:94)(cid:3)(cid:215)(cid:218)(cid:206)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:222)(cid:3)(cid:205)(cid:228)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:208)(cid:217)(cid:207)(cid:3)(cid:218)(cid:209)(cid:3)(cid:96)(cid:94)(cid:96)(cid:95)(cid:17)(cid:3)
(cid:197)(cid:218)(cid:3)(cid:207)(cid:204)(cid:223)(cid:208)(cid:19)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)(cid:185)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:185)(cid:198)(cid:179)(cid:3)(cid:215)(cid:218)(cid:206)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:222)(cid:3)(cid:211)(cid:204)(cid:225)(cid:208)(cid:3)
outperformed their control group 
with higher prescription volume and 
(cid:212)(cid:217)(cid:206)(cid:221)(cid:208)(cid:204)(cid:222)(cid:208)(cid:207)(cid:3)(cid:190)(cid:212)(cid:217)(cid:224)(cid:223)(cid:208)(cid:180)(cid:215)(cid:212)(cid:217)(cid:212)(cid:206)(cid:3)(cid:225)(cid:212)(cid:222)(cid:212)(cid:223)(cid:222)(cid:17)(cid:3)(cid:186)(cid:217)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)
(cid:185)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:185)(cid:198)(cid:179)(cid:3)(cid:215)(cid:218)(cid:206)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:222)(cid:19)(cid:3)(cid:209)(cid:221)(cid:218)(cid:217)(cid:223)(cid:3)(cid:222)(cid:223)(cid:218)(cid:221)(cid:208)(cid:3)(cid:222)(cid:204)(cid:215)(cid:208)(cid:222)(cid:3)
have been in line with our expecta-
tions, and we have seen increased 
(cid:224)(cid:223)(cid:212)(cid:215)(cid:212)(cid:229)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:3)(cid:218)(cid:209)(cid:3)(cid:211)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:35)(cid:221)(cid:208)(cid:215)(cid:204)(cid:223)(cid:208)(cid:207)(cid:3)(cid:222)(cid:208)(cid:221)(cid:225)(cid:212)(cid:206)(cid:208)(cid:222)(cid:17)(cid:3)
(cid:186)(cid:217)(cid:3)(cid:204)(cid:207)(cid:207)(cid:212)(cid:223)(cid:212)(cid:218)(cid:217)(cid:19)(cid:3)(cid:218)(cid:225)(cid:208)(cid:221)(cid:3)(cid:223)(cid:212)(cid:216)(cid:208)(cid:19)(cid:3)(cid:226)(cid:208)(cid:3)(cid:208)(cid:227)(cid:219)(cid:208)(cid:206)(cid:223)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)
(cid:185)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:3)(cid:180)(cid:204)(cid:221)(cid:208)(cid:3)(cid:179)(cid:208)(cid:217)(cid:208)(cid:242)(cid:223)(cid:222)(cid:3)(cid:216)(cid:208)(cid:207)(cid:212)(cid:206)(cid:204)(cid:215)(cid:3)(cid:206)(cid:218)(cid:222)(cid:223)(cid:222)(cid:3)(cid:223)(cid:218)(cid:3)
(cid:205)(cid:208)(cid:3)(cid:219)(cid:218)(cid:222)(cid:212)(cid:223)(cid:212)(cid:225)(cid:208)(cid:215)(cid:228)(cid:3)(cid:204)(cid:241)(cid:208)(cid:206)(cid:223)(cid:208)(cid:207)(cid:3)(cid:205)(cid:228)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)(cid:216)(cid:208)(cid:207)(cid:212)(cid:206)(cid:204)(cid:215)(cid:3)
members meeting their needs at 
(cid:185)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:185)(cid:198)(cid:179)(cid:3)(cid:215)(cid:218)(cid:206)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:222)(cid:17)

Among our transformational products 
and services, we continue to advance 
innovative pilot programs and intro-
(cid:207)(cid:224)(cid:206)(cid:208)(cid:3)(cid:217)(cid:208)(cid:226)(cid:3)(cid:218)(cid:241)(cid:208)(cid:221)(cid:212)(cid:217)(cid:210)(cid:222)(cid:17)(cid:3)(cid:183)(cid:218)(cid:221)(cid:3)(cid:208)(cid:227)(cid:204)(cid:216)(cid:219)(cid:215)(cid:208)(cid:19)(cid:3)(cid:226)(cid:208)(cid:3)
began rolling out Pharmacist Panels 
(cid:204)(cid:223)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)(cid:185)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:185)(cid:198)(cid:179)(cid:3)(cid:215)(cid:218)(cid:206)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:222)(cid:19)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:226)(cid:208)(cid:3)
see an opportunity to expand this pro-
gram to other retail locations. These 
panels provide a holistic, 360-degree 
view of a patient by combining phar-
(cid:216)(cid:204)(cid:206)(cid:228)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:216)(cid:208)(cid:207)(cid:212)(cid:206)(cid:204)(cid:215)(cid:3)(cid:207)(cid:204)(cid:223)(cid:204)(cid:17)(cid:3)(cid:179)(cid:228)(cid:3)(cid:211)(cid:204)(cid:225)(cid:212)(cid:217)(cid:210)(cid:3)
(cid:212)(cid:217)(cid:223)(cid:208)(cid:210)(cid:221)(cid:204)(cid:223)(cid:208)(cid:207)(cid:3)(cid:207)(cid:204)(cid:223)(cid:204)(cid:3)(cid:204)(cid:223)(cid:3)(cid:223)(cid:211)(cid:208)(cid:212)(cid:221)(cid:3)(cid:242)(cid:217)(cid:210)(cid:208)(cid:221)(cid:223)(cid:212)(cid:219)(cid:222)(cid:19)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)
pharmacists can improve medication 
(cid:204)(cid:207)(cid:211)(cid:208)(cid:221)(cid:208)(cid:217)(cid:206)(cid:208)(cid:19)(cid:3)(cid:218)(cid:219)(cid:223)(cid:212)(cid:216)(cid:212)(cid:229)(cid:208)(cid:3)(cid:216)(cid:208)(cid:207)(cid:212)(cid:206)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:3)
regimens, close gaps in care and 
connect patients to their health plan, 
(cid:204)(cid:3)(cid:190)(cid:212)(cid:217)(cid:224)(cid:223)(cid:208)(cid:180)(cid:215)(cid:212)(cid:217)(cid:212)(cid:206)(cid:3)(cid:218)(cid:221)(cid:3)(cid:218)(cid:223)(cid:211)(cid:208)(cid:221)(cid:3)(cid:204)(cid:219)(cid:219)(cid:221)(cid:218)(cid:219)(cid:221)(cid:212)(cid:204)(cid:223)(cid:208)(cid:3)
local resources. 

We are also excited about our 
(cid:197)(cid:221)(cid:204)(cid:217)(cid:222)(cid:209)(cid:218)(cid:221)(cid:216)(cid:3)(cid:192)(cid:217)(cid:206)(cid:218)(cid:215)(cid:218)(cid:210)(cid:228)(cid:3)(cid:180)(cid:204)(cid:221)(cid:208)(cid:92)(cid:3)(cid:219)(cid:221)(cid:218)(cid:210)(cid:221)(cid:204)(cid:216)(cid:19)(cid:3)
which includes a precision medicine 
approach that helps patients receive 
(cid:223)(cid:211)(cid:208)(cid:3)(cid:216)(cid:218)(cid:222)(cid:223)(cid:3)(cid:208)(cid:241)(cid:208)(cid:206)(cid:223)(cid:212)(cid:225)(cid:208)(cid:3)(cid:206)(cid:204)(cid:217)(cid:206)(cid:208)(cid:221)(cid:3)(cid:223)(cid:221)(cid:208)(cid:204)(cid:223)(cid:216)(cid:208)(cid:217)(cid:223)(cid:222)(cid:3)
and matches eligible patients to clinical 

trials when appropriate. The program 
(cid:212)(cid:222)(cid:3)(cid:217)(cid:218)(cid:226)(cid:3)(cid:204)(cid:225)(cid:204)(cid:212)(cid:215)(cid:204)(cid:205)(cid:215)(cid:208)(cid:3)(cid:212)(cid:217)(cid:3)(cid:95)(cid:98)(cid:3)(cid:222)(cid:223)(cid:204)(cid:223)(cid:208)(cid:222)(cid:17)(cid:3)(cid:197)(cid:221)(cid:204)(cid:217)(cid:222)(cid:209)(cid:218)(cid:221)(cid:216)(cid:3)
(cid:192)(cid:217)(cid:206)(cid:218)(cid:215)(cid:218)(cid:210)(cid:228)(cid:3)(cid:180)(cid:204)(cid:221)(cid:208)(cid:3)(cid:224)(cid:223)(cid:212)(cid:215)(cid:212)(cid:229)(cid:208)(cid:222)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)(cid:215)(cid:218)(cid:206)(cid:204)(cid:215)(cid:3)
footprint and unique assets to improve 
outcomes and lower overall costs at 
every point of the patient journey. 

(cid:197)(cid:221)(cid:204)(cid:217)(cid:222)(cid:209)(cid:218)(cid:221)(cid:216)(cid:3)(cid:192)(cid:217)(cid:206)(cid:218)(cid:215)(cid:218)(cid:210)(cid:228)(cid:3)(cid:180)(cid:204)(cid:221)(cid:208)(cid:3) 
(cid:212)(cid:222)(cid:3)(cid:204)(cid:225)(cid:204)(cid:212)(cid:215)(cid:204)(cid:205)(cid:215)(cid:208)(cid:3)(cid:212)(cid:217)(cid:3)

14 states

(cid:186)(cid:217)(cid:3)(cid:96)(cid:94)(cid:95)(cid:100)(cid:19)(cid:3)(cid:190)(cid:208)(cid:207)(cid:212)(cid:206)(cid:204)(cid:221)(cid:208)(cid:3)(cid:209)(cid:208)(cid:208)(cid:35)(cid:209)(cid:218)(cid:221)(cid:35)(cid:222)(cid:208)(cid:221)(cid:225)(cid:212)(cid:206)(cid:208)(cid:3)(cid:222)(cid:219)(cid:208)(cid:217)(cid:223)(cid:3)
(cid:204)(cid:219)(cid:219)(cid:221)(cid:218)(cid:227)(cid:212)(cid:216)(cid:204)(cid:223)(cid:208)(cid:215)(cid:228)(cid:3)(cid:114)(cid:95)(cid:95)(cid:98)(cid:3)(cid:205)(cid:212)(cid:215)(cid:215)(cid:212)(cid:218)(cid:217)(cid:3)(cid:223)(cid:218)(cid:3)(cid:206)(cid:218)(cid:225)(cid:208)(cid:221)(cid:3)
people with kidney disease, represent-
(cid:212)(cid:217)(cid:210)(cid:3)(cid:216)(cid:218)(cid:221)(cid:208)(cid:3)(cid:223)(cid:211)(cid:204)(cid:217)(cid:3)(cid:218)(cid:217)(cid:208)(cid:3)(cid:212)(cid:217)(cid:3)(cid:242)(cid:225)(cid:208)(cid:3)(cid:207)(cid:218)(cid:215)(cid:215)(cid:204)(cid:221)(cid:222)(cid:3)(cid:222)(cid:219)(cid:208)(cid:217)(cid:223)(cid:3)
(cid:205)(cid:228)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:223)(cid:221)(cid:204)(cid:207)(cid:212)(cid:223)(cid:212)(cid:218)(cid:217)(cid:204)(cid:215)(cid:3)(cid:190)(cid:208)(cid:207)(cid:212)(cid:206)(cid:204)(cid:221)(cid:208)(cid:3)(cid:219)(cid:221)(cid:218)(cid:210)(cid:221)(cid:204)(cid:216)(cid:17)†  
(cid:181)(cid:224)(cid:221)(cid:212)(cid:217)(cid:210)(cid:3)(cid:96)(cid:94)(cid:95)(cid:103)(cid:19)(cid:3)(cid:226)(cid:208)(cid:3)(cid:206)(cid:218)(cid:217)(cid:223)(cid:212)(cid:217)(cid:224)(cid:208)(cid:207)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)(cid:208)(cid:217)(cid:223)(cid:221)(cid:228)(cid:3)
into the kidney care space with the 
launch of our chronic kidney disease 
(cid:40)(cid:180)(cid:188)(cid:181)(cid:41)(cid:3)(cid:216)(cid:204)(cid:217)(cid:204)(cid:210)(cid:208)(cid:216)(cid:208)(cid:217)(cid:223)(cid:3)(cid:219)(cid:221)(cid:218)(cid:210)(cid:221)(cid:204)(cid:216)(cid:3)(cid:223)(cid:218)(cid:3) 
(cid:211)(cid:208)(cid:215)(cid:219)(cid:3)(cid:219)(cid:204)(cid:223)(cid:212)(cid:208)(cid:217)(cid:223)(cid:222)(cid:3)(cid:226)(cid:212)(cid:223)(cid:211)(cid:3)(cid:180)(cid:188)(cid:181)(cid:3)(cid:207)(cid:208)(cid:215)(cid:204)(cid:228)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3) 
progression of the disease. This 
program currently is available to 
approximately 3.5 million people across 
(cid:178)(cid:208)(cid:223)(cid:217)(cid:204)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:95)(cid:98)(cid:3)(cid:218)(cid:223)(cid:211)(cid:208)(cid:221)(cid:3)(cid:193)(cid:179)(cid:190)(cid:3)(cid:206)(cid:215)(cid:212)(cid:208)(cid:217)(cid:223)(cid:222)(cid:17)(cid:3)(cid:197)(cid:211)(cid:212)(cid:222)(cid:3)
program is one part of our portfolio of 
approaches to managing end-stage 
renal disease, one of the biggest 
burdens on the health care system. We 
are also making progress in the clinical 
trial of our home hemodialysis device.

(cid:192)(cid:224)(cid:221)(cid:3)(cid:180)(cid:204)(cid:221)(cid:208)(cid:193)(cid:204)(cid:222)(cid:222)(cid:92)(cid:3)(cid:222)(cid:224)(cid:205)(cid:222)(cid:206)(cid:221)(cid:212)(cid:219)(cid:223)(cid:212)(cid:218)(cid:217)(cid:3)(cid:222)(cid:208)(cid:221)(cid:225)(cid:212)(cid:206)(cid:208)(cid:3) 
is one example of our consumer- 
centric technology. CarePass went 
(cid:215)(cid:212)(cid:225)(cid:208)(cid:3)(cid:217)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:204)(cid:215)(cid:215)(cid:228)(cid:3)(cid:212)(cid:217)(cid:3)(cid:215)(cid:204)(cid:223)(cid:208)(cid:3)(cid:96)(cid:94)(cid:95)(cid:103)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:204)(cid:215)(cid:221)(cid:208)(cid:204)(cid:207)(cid:228)(cid:3)
(cid:211)(cid:204)(cid:207)(cid:3)(cid:208)(cid:217)(cid:221)(cid:218)(cid:215)(cid:215)(cid:208)(cid:207)(cid:3)(cid:95)(cid:17)(cid:100)(cid:3)(cid:216)(cid:212)(cid:215)(cid:215)(cid:212)(cid:218)(cid:217)(cid:3)(cid:216)(cid:208)(cid:216)(cid:205)(cid:208)(cid:221)(cid:222)(cid:3)(cid:204)(cid:222)(cid:3)(cid:218)(cid:209)(cid:3)
(cid:181)(cid:208)(cid:206)(cid:208)(cid:216)(cid:205)(cid:208)(cid:221)(cid:3)(cid:97)(cid:95)(cid:19)(cid:3)(cid:96)(cid:94)(cid:95)(cid:103)(cid:17)(cid:3)(cid:180)(cid:204)(cid:221)(cid:208)(cid:193)(cid:204)(cid:222)(cid:222)(cid:3)(cid:218)(cid:241)(cid:208)(cid:221)(cid:222)(cid:3)(cid:204)(cid:3)
variety of perks for a $5 monthly fee, 
including free prescription delivery, 
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(cid:182)(cid:227)(cid:223)(cid:221)(cid:204)(cid:179)(cid:224)(cid:206)(cid:214)(cid:222)(cid:92)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:96)(cid:94)(cid:3)(cid:219)(cid:208)(cid:221)(cid:206)(cid:208)(cid:217)(cid:223)(cid:3)(cid:218)(cid:241)(cid:3)(cid:180)(cid:199)(cid:196)(cid:3)
Health brands every day. 

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†(cid:3)(cid:3)(cid:178)(cid:207)(cid:225)(cid:204)(cid:217)(cid:206)(cid:212)(cid:217)(cid:210)(cid:3)(cid:178)(cid:216)(cid:208)(cid:221)(cid:212)(cid:206)(cid:204)(cid:217)(cid:3)(cid:188)(cid:212)(cid:207)(cid:217)(cid:208)(cid:228)(cid:3)(cid:185)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:19)(cid:3)(cid:198)(cid:17)(cid:196)(cid:17)(cid:3)(cid:181)(cid:208)(cid:219)(cid:204)(cid:221)(cid:223)(cid:216)(cid:208)(cid:217)(cid:223)(cid:3)(cid:218)(cid:209)(cid:3)(cid:185)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:185)(cid:224)(cid:216)(cid:204)(cid:217)(cid:3)(cid:196)(cid:208)(cid:221)(cid:225)(cid:212)(cid:206)(cid:208)(cid:222)(cid:19)(cid:3)(cid:219)(cid:204)(cid:210)(cid:208)(cid:3)(cid:97)(cid:3)(cid:40)(cid:96)(cid:94)(cid:95)(cid:103)(cid:41)(cid:17)

2019 Annual Report

3

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delivered strong performance in its 
Medicare and Medicaid products and 
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its book of business

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(cid:222)(cid:208)(cid:215)(cid:209)(cid:35)(cid:212)(cid:217)(cid:222)(cid:224)(cid:221)(cid:208)(cid:207)(cid:3)(cid:206)(cid:218)(cid:216)(cid:219)(cid:204)(cid:217)(cid:212)(cid:208)(cid:222)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:208)(cid:227)(cid:219)(cid:204)(cid:217)(cid:207)(cid:3)
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(cid:216)(cid:208)(cid:216)(cid:205)(cid:208)(cid:221)(cid:222)(cid:211)(cid:212)(cid:219)(cid:17)(cid:3)

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(cid:223)(cid:204)(cid:210)(cid:208)(cid:3)(cid:219)(cid:215)(cid:204)(cid:217)(cid:222)(cid:3)(cid:212)(cid:217)(cid:3)(cid:222)(cid:208)(cid:215)(cid:208)(cid:206)(cid:223)(cid:3)(cid:210)(cid:208)(cid:218)(cid:210)(cid:221)(cid:204)(cid:219)(cid:211)(cid:212)(cid:208)(cid:222)(cid:3)(cid:209)(cid:218)(cid:221)(cid:3)
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(cid:216)(cid:208)(cid:217)(cid:223)(cid:3)(cid:219)(cid:221)(cid:218)(cid:210)(cid:221)(cid:204)(cid:216)(cid:3)(cid:204)(cid:212)(cid:216)(cid:208)(cid:207)(cid:3)(cid:204)(cid:223)(cid:3)(cid:204)(cid:207)(cid:207)(cid:221)(cid:208)(cid:222)(cid:222)(cid:212)(cid:217)(cid:210)(cid:3)
(cid:223)(cid:211)(cid:208)(cid:3)(cid:222)(cid:218)(cid:206)(cid:212)(cid:204)(cid:215)(cid:3)(cid:207)(cid:208)(cid:223)(cid:208)(cid:221)(cid:216)(cid:212)(cid:217)(cid:204)(cid:217)(cid:223)(cid:222)(cid:3)(cid:218)(cid:209)(cid:3)(cid:211)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:17)(cid:3)(cid:200)(cid:208)(cid:3)
(cid:215)(cid:204)(cid:224)(cid:217)(cid:206)(cid:211)(cid:208)(cid:207)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:219)(cid:221)(cid:218)(cid:210)(cid:221)(cid:204)(cid:216)(cid:3)(cid:212)(cid:217)(cid:3)(cid:209)(cid:218)(cid:224)(cid:221)(cid:3)(cid:222)(cid:208)(cid:221)(cid:225)(cid:212)(cid:206)(cid:208)(cid:3)
(cid:204)(cid:221)(cid:208)(cid:204)(cid:222)(cid:3)(cid:204)(cid:206)(cid:221)(cid:218)(cid:222)(cid:222)(cid:3)(cid:223)(cid:211)(cid:221)(cid:208)(cid:208)(cid:3)(cid:222)(cid:223)(cid:204)(cid:223)(cid:208)(cid:222)(cid:3)(cid:212)(cid:217)(cid:3)(cid:96)(cid:94)(cid:95)(cid:103)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)
expect to scale nationally across our 
(cid:190)(cid:208)(cid:207)(cid:212)(cid:206)(cid:204)(cid:221)(cid:208)(cid:3)(cid:178)(cid:207)(cid:225)(cid:204)(cid:217)(cid:223)(cid:204)(cid:210)(cid:208)(cid:3)(cid:209)(cid:218)(cid:218)(cid:223)(cid:219)(cid:221)(cid:212)(cid:217)(cid:223)(cid:3)(cid:212)(cid:217)(cid:3)(cid:96)(cid:94)(cid:96)(cid:94)(cid:17)

83% 

of Medicare Advantage plan 
members enrolled in plans 
with 2020 star ratings of at 
least 4.0 stars

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(cid:221)(cid:208)(cid:206)(cid:208)(cid:217)(cid:223)(cid:215)(cid:228)(cid:3)(cid:204)(cid:226)(cid:204)(cid:221)(cid:207)(cid:208)(cid:207)(cid:3)(cid:217)(cid:208)(cid:226)(cid:3)(cid:216)(cid:208)(cid:216)(cid:205)(cid:208)(cid:221)(cid:222)(cid:3)(cid:212)(cid:217)(cid:3)
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(cid:222)(cid:223)(cid:221)(cid:208)(cid:217)(cid:210)(cid:223)(cid:211)(cid:3)(cid:218)(cid:209)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)(cid:222)(cid:208)(cid:221)(cid:225)(cid:212)(cid:206)(cid:208)(cid:222)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:206)(cid:204)(cid:219)(cid:204)-
(cid:205)(cid:212)(cid:215)(cid:212)(cid:223)(cid:212)(cid:208)(cid:222)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:211)(cid:204)(cid:225)(cid:208)(cid:3)(cid:204)(cid:215)(cid:215)(cid:218)(cid:226)(cid:208)(cid:207)(cid:3)(cid:224)(cid:222)(cid:3)(cid:223)(cid:218)(cid:3)(cid:205)(cid:224)(cid:212)(cid:215)(cid:207)(cid:3)
(cid:224)(cid:219)(cid:218)(cid:217)(cid:3)(cid:208)(cid:227)(cid:212)(cid:222)(cid:223)(cid:212)(cid:217)(cid:210)(cid:3)(cid:221)(cid:208)(cid:215)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:222)(cid:211)(cid:212)(cid:219)(cid:222)(cid:3)(cid:226)(cid:212)(cid:223)(cid:211)(cid:3)(cid:223)(cid:226)(cid:218)(cid:3)
(cid:212)(cid:216)(cid:219)(cid:218)(cid:221)(cid:223)(cid:204)(cid:217)(cid:223)(cid:3)(cid:222)(cid:223)(cid:204)(cid:223)(cid:208)(cid:3)(cid:219)(cid:204)(cid:221)(cid:223)(cid:217)(cid:208)(cid:221)(cid:222)(cid:17)

Lastly, we continue to make progress 
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(cid:204)(cid:217)(cid:207)(cid:3)(cid:206)(cid:204)(cid:219)(cid:204)(cid:205)(cid:212)(cid:215)(cid:212)(cid:223)(cid:212)(cid:208)(cid:222)(cid:3)(cid:204)(cid:206)(cid:221)(cid:218)(cid:222)(cid:222)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:182)(cid:217)(cid:223)(cid:208)(cid:221)(cid:219)(cid:221)(cid:212)(cid:222)(cid:208)(cid:17)(cid:3)
(cid:200)(cid:208)(cid:3)(cid:208)(cid:227)(cid:219)(cid:208)(cid:206)(cid:223)(cid:3)(cid:223)(cid:218)(cid:3)(cid:221)(cid:208)(cid:204)(cid:219)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:212)(cid:217)(cid:212)(cid:223)(cid:212)(cid:204)(cid:215)(cid:3)(cid:205)(cid:208)(cid:217)(cid:208)(cid:242)(cid:223)(cid:222)(cid:3)
(cid:218)(cid:209)(cid:3)(cid:182)(cid:217)(cid:223)(cid:208)(cid:221)(cid:219)(cid:221)(cid:212)(cid:222)(cid:208)(cid:3)(cid:190)(cid:218)(cid:207)(cid:208)(cid:221)(cid:217)(cid:212)(cid:229)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:3)(cid:212)(cid:217)(cid:3)(cid:96)(cid:94)(cid:96)(cid:94)(cid:17)(cid:3)
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(cid:222)(cid:212)(cid:216)(cid:219)(cid:215)(cid:212)(cid:209)(cid:228)(cid:212)(cid:217)(cid:210)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)(cid:222)(cid:208)(cid:221)(cid:225)(cid:212)(cid:206)(cid:208)(cid:3)(cid:218)(cid:219)(cid:208)(cid:221)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:222)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)
(cid:211)(cid:204)(cid:225)(cid:208)(cid:3)(cid:208)(cid:216)(cid:205)(cid:208)(cid:207)(cid:207)(cid:208)(cid:207)(cid:3)(cid:212)(cid:217)(cid:223)(cid:208)(cid:215)(cid:215)(cid:212)(cid:210)(cid:208)(cid:217)(cid:223)(cid:3)(cid:204)(cid:224)(cid:223)(cid:218)(cid:216)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:3)
(cid:223)(cid:218)(cid:3)(cid:222)(cid:223)(cid:221)(cid:208)(cid:204)(cid:216)(cid:215)(cid:212)(cid:217)(cid:208)(cid:3)(cid:221)(cid:218)(cid:224)(cid:223)(cid:212)(cid:217)(cid:208)(cid:3)(cid:219)(cid:221)(cid:218)(cid:206)(cid:208)(cid:222)(cid:222)(cid:208)(cid:222)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)
(cid:209)(cid:224)(cid:221)(cid:223)(cid:211)(cid:208)(cid:221)(cid:3)(cid:204)(cid:207)(cid:225)(cid:204)(cid:217)(cid:206)(cid:208)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)(cid:207)(cid:212)(cid:210)(cid:212)(cid:223)(cid:204)(cid:215)(cid:3)(cid:209)(cid:218)(cid:218)(cid:223)(cid:219)(cid:221)(cid:212)(cid:217)(cid:223)(cid:17)(cid:3)
(cid:200)(cid:208)(cid:3)(cid:205)(cid:208)(cid:215)(cid:212)(cid:208)(cid:225)(cid:208)(cid:3)(cid:226)(cid:208)(cid:3)(cid:221)(cid:208)(cid:216)(cid:204)(cid:212)(cid:217)(cid:3)(cid:218)(cid:217)(cid:3)(cid:206)(cid:218)(cid:224)(cid:221)(cid:222)(cid:208)(cid:3)(cid:223)(cid:218)(cid:3)
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(cid:221)(cid:204)(cid:223)(cid:208)(cid:3)(cid:217)(cid:208)(cid:223)(cid:3)(cid:222)(cid:204)(cid:225)(cid:212)(cid:217)(cid:210)(cid:222)(cid:3)(cid:212)(cid:217)(cid:3)(cid:96)(cid:94)(cid:96)(cid:96)(cid:17)(cid:3)(cid:197)(cid:211)(cid:208)(cid:3)(cid:205)(cid:208)(cid:217)(cid:208)(cid:242)(cid:223)(cid:222)(cid:3)
(cid:226)(cid:208)(cid:3)(cid:208)(cid:227)(cid:219)(cid:208)(cid:206)(cid:223)(cid:3)(cid:209)(cid:221)(cid:218)(cid:216)(cid:3)(cid:182)(cid:217)(cid:223)(cid:208)(cid:221)(cid:219)(cid:221)(cid:212)(cid:222)(cid:208)(cid:3)(cid:190)(cid:218)(cid:207)(cid:208)(cid:221)(cid:217)(cid:212)(cid:229)(cid:204)-
(cid:223)(cid:212)(cid:218)(cid:217)(cid:3)(cid:204)(cid:221)(cid:208)(cid:3)(cid:212)(cid:217)(cid:3)(cid:204)(cid:207)(cid:207)(cid:212)(cid:223)(cid:212)(cid:218)(cid:217)(cid:3)(cid:223)(cid:218)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:212)(cid:217)(cid:223)(cid:208)(cid:210)(cid:221)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:3)
(cid:222)(cid:228)(cid:217)(cid:208)(cid:221)(cid:210)(cid:212)(cid:208)(cid:222)(cid:3)(cid:209)(cid:221)(cid:218)(cid:216)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:178)(cid:208)(cid:223)(cid:217)(cid:204)(cid:3)(cid:204)(cid:206)(cid:220)(cid:224)(cid:212)(cid:222)(cid:212)(cid:223)(cid:212)(cid:218)(cid:217)(cid:3) 
(cid:186)(cid:3)(cid:216)(cid:208)(cid:217)(cid:223)(cid:212)(cid:218)(cid:217)(cid:208)(cid:207)(cid:3)(cid:208)(cid:204)(cid:221)(cid:215)(cid:212)(cid:208)(cid:221)(cid:17)

$0 

out-of-pocket program 
for diabetes care 
launched this year

Pharmacy Services segment revenues 
and operating income continued to 
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solutions for plan members

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(cid:221)(cid:208)(cid:225)(cid:208)(cid:217)(cid:224)(cid:208)(cid:222)(cid:3)(cid:221)(cid:218)(cid:222)(cid:208)(cid:3)(cid:99)(cid:17)(cid:94)(cid:3)(cid:219)(cid:208)(cid:221)(cid:206)(cid:208)(cid:217)(cid:223)(cid:3)(cid:223)(cid:218)(cid:3)(cid:114)(cid:95)(cid:98)(cid:95)(cid:17)(cid:99)(cid:3)
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(cid:114)(cid:98)(cid:17)(cid:101)(cid:3)(cid:205)(cid:212)(cid:215)(cid:215)(cid:212)(cid:218)(cid:217)(cid:17)(cid:3)(cid:178)(cid:3)(cid:214)(cid:208)(cid:228)(cid:3)(cid:221)(cid:208)(cid:225)(cid:208)(cid:217)(cid:224)(cid:208)(cid:3)(cid:207)(cid:221)(cid:212)(cid:225)(cid:208)(cid:221)(cid:3)
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(cid:206)(cid:208)(cid:217)(cid:223)(cid:3)(cid:212)(cid:217)(cid:206)(cid:221)(cid:208)(cid:204)(cid:222)(cid:208)(cid:3)(cid:212)(cid:217)(cid:3)(cid:219)(cid:211)(cid:204)(cid:221)(cid:216)(cid:204)(cid:206)(cid:228)(cid:3)(cid:206)(cid:215)(cid:204)(cid:212)(cid:216)(cid:222)(cid:3)
(cid:219)(cid:221)(cid:218)(cid:206)(cid:208)(cid:222)(cid:222)(cid:208)(cid:207)(cid:17)(cid:3)(cid:192)(cid:224)(cid:221)(cid:3)(cid:218)(cid:219)(cid:208)(cid:221)(cid:204)(cid:223)(cid:212)(cid:217)(cid:210)(cid:3)(cid:212)(cid:217)(cid:206)(cid:218)(cid:216)(cid:208)(cid:3)(cid:205)(cid:208)(cid:217)-
(cid:208)(cid:242)(cid:223)(cid:208)(cid:207)(cid:3)(cid:209)(cid:221)(cid:218)(cid:216)(cid:3)(cid:212)(cid:217)(cid:206)(cid:221)(cid:208)(cid:204)(cid:222)(cid:208)(cid:207)(cid:3)(cid:206)(cid:215)(cid:204)(cid:212)(cid:216)(cid:3)(cid:225)(cid:218)(cid:215)(cid:224)(cid:216)(cid:208)(cid:19)(cid:3)
(cid:223)(cid:211)(cid:208)(cid:3)(cid:204)(cid:207)(cid:207)(cid:212)(cid:223)(cid:212)(cid:218)(cid:217)(cid:3)(cid:218)(cid:209)(cid:3)(cid:178)(cid:208)(cid:223)(cid:217)(cid:204)(cid:30)(cid:222)(cid:3)(cid:216)(cid:204)(cid:212)(cid:215)(cid:3)(cid:218)(cid:221)(cid:207)(cid:208)(cid:221)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)
(cid:222)(cid:219)(cid:208)(cid:206)(cid:212)(cid:204)(cid:215)(cid:223)(cid:228)(cid:3)(cid:219)(cid:211)(cid:204)(cid:221)(cid:216)(cid:204)(cid:206)(cid:228)(cid:3)(cid:218)(cid:219)(cid:208)(cid:221)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:222)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)
(cid:212)(cid:216)(cid:219)(cid:221)(cid:218)(cid:225)(cid:208)(cid:207)(cid:3)(cid:219)(cid:224)(cid:221)(cid:206)(cid:211)(cid:204)(cid:222)(cid:212)(cid:217)(cid:210)(cid:3)(cid:208)(cid:206)(cid:218)(cid:217)(cid:218)(cid:216)(cid:212)(cid:206)(cid:222)(cid:17)(cid:3)

(cid:200)(cid:208)(cid:3)(cid:222)(cid:204)(cid:226)(cid:3)(cid:204)(cid:217)(cid:3)(cid:212)(cid:216)(cid:219)(cid:221)(cid:218)(cid:225)(cid:208)(cid:216)(cid:208)(cid:217)(cid:223)(cid:3)(cid:212)(cid:217)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:96)(cid:94)(cid:96)(cid:94)(cid:3)
(cid:222)(cid:208)(cid:215)(cid:215)(cid:212)(cid:217)(cid:210)(cid:3)(cid:222)(cid:208)(cid:204)(cid:222)(cid:218)(cid:217)(cid:3)(cid:221)(cid:208)(cid:222)(cid:224)(cid:215)(cid:223)(cid:222)(cid:3)(cid:218)(cid:225)(cid:208)(cid:221)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:206)(cid:218)(cid:224)(cid:221)(cid:222)(cid:208)(cid:3)
(cid:218)(cid:209)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:228)(cid:208)(cid:204)(cid:221)(cid:3)(cid:226)(cid:212)(cid:223)(cid:211)(cid:3)(cid:210)(cid:221)(cid:218)(cid:222)(cid:222)(cid:3)(cid:217)(cid:208)(cid:226)(cid:3)(cid:226)(cid:212)(cid:217)(cid:222)(cid:3)
(cid:223)(cid:218)(cid:223)(cid:204)(cid:215)(cid:212)(cid:217)(cid:210)(cid:3)(cid:114)(cid:99)(cid:17)(cid:95)(cid:3)(cid:205)(cid:212)(cid:215)(cid:215)(cid:212)(cid:218)(cid:217)(cid:19)(cid:3)(cid:226)(cid:211)(cid:212)(cid:206)(cid:211)(cid:3)(cid:212)(cid:217)(cid:206)(cid:215)(cid:224)(cid:207)(cid:208)(cid:207)(cid:3)
(cid:223)(cid:211)(cid:208)(cid:3)(cid:208)(cid:227)(cid:223)(cid:208)(cid:217)(cid:222)(cid:212)(cid:218)(cid:217)(cid:3)(cid:218)(cid:209)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)(cid:180)(cid:208)(cid:217)(cid:223)(cid:208)(cid:217)(cid:208)(cid:3)(cid:206)(cid:218)(cid:217)(cid:223)(cid:221)(cid:204)(cid:206)(cid:223)(cid:3)

4

(cid:180)(cid:199)(cid:196)(cid:3)(cid:185)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)

(cid:190)(cid:204)(cid:214)(cid:208)(cid:3)(cid:212)(cid:223)(cid:3)(cid:222)(cid:212)(cid:216)(cid:219)(cid:215)(cid:208)
(cid:193)(cid:204)(cid:223)(cid:212)(cid:208)(cid:217)(cid:223)(cid:3)(cid:206)(cid:204)(cid:221)(cid:208)(cid:3)(cid:211)(cid:204)(cid:222)(cid:3)(cid:217)(cid:208)(cid:225)(cid:208)(cid:221)(cid:3)(cid:205)(cid:208)(cid:208)(cid:217)(cid:3)(cid:208)(cid:204)(cid:222)(cid:212)(cid:208)(cid:221)(cid:19)(cid:3)(cid:209)(cid:218)(cid:221)(cid:3)(cid:204)(cid:215)(cid:215)(cid:17)(cid:3)
(cid:197)(cid:211)(cid:221)(cid:218)(cid:224)(cid:210)(cid:211)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)(cid:212)(cid:217)(cid:223)(cid:208)(cid:210)(cid:221)(cid:204)(cid:223)(cid:208)(cid:207)(cid:3)(cid:204)(cid:222)(cid:222)(cid:208)(cid:223)(cid:222)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:206)(cid:218)(cid:215)(cid:215)(cid:204)(cid:205)(cid:218)(cid:221)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:222)(cid:3)(cid:226)(cid:208)(cid:3)(cid:204)(cid:221)(cid:208)(cid:3)(cid:216)(cid:204)(cid:214)(cid:212)(cid:217)(cid:210)(cid:3)(cid:212)(cid:223)(cid:3)(cid:208)(cid:204)(cid:222)(cid:212)(cid:208)(cid:221)(cid:3)(cid:209)(cid:218)(cid:221)(cid:3)(cid:219)(cid:204)(cid:223)(cid:212)(cid:208)(cid:217)(cid:223)(cid:222)(cid:3)(cid:223)(cid:218)(cid:3)(cid:221)(cid:208)(cid:206)(cid:208)(cid:212)(cid:225)(cid:208)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:221)(cid:212)(cid:210)(cid:211)(cid:223)(cid:3)(cid:206)(cid:204)(cid:221)(cid:208)(cid:3)
(cid:212)(cid:217)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:219)(cid:221)(cid:218)(cid:219)(cid:208)(cid:221)(cid:3)(cid:222)(cid:208)(cid:223)(cid:223)(cid:212)(cid:217)(cid:210)(cid:17)

Easy access to health care 
(cid:190)(cid:212)(cid:217)(cid:224)(cid:223)(cid:208)(cid:180)(cid:215)(cid:212)(cid:217)(cid:212)(cid:206)(cid:3)(cid:206)(cid:204)(cid:217)(cid:3)(cid:223)(cid:221)(cid:208)(cid:204)(cid:223)(cid:3) 
(cid:102)(cid:94)(cid:173)(cid:3)(cid:218)(cid:209)(cid:3)(cid:226)(cid:211)(cid:204)(cid:223)(cid:3)(cid:204)(cid:3)(cid:223)(cid:228)(cid:219)(cid:212)(cid:206)(cid:204)(cid:215)(cid:3)(cid:219)(cid:221)(cid:212)(cid:216)(cid:204)(cid:221)(cid:228)(cid:3)
(cid:206)(cid:204)(cid:221)(cid:208)(cid:3)(cid:219)(cid:221)(cid:204)(cid:206)(cid:223)(cid:212)(cid:206)(cid:208)(cid:3)(cid:206)(cid:204)(cid:217)(cid:3)(cid:223)(cid:221)(cid:208)(cid:204)(cid:223)

360° view of consumer 
(cid:180)(cid:218)(cid:217)(cid:223)(cid:212)(cid:217)(cid:224)(cid:204)(cid:215)(cid:215)(cid:228)(cid:3)(cid:224)(cid:219)(cid:207)(cid:204)(cid:223)(cid:208)(cid:207)(cid:3)(cid:223)(cid:218)(cid:3)
(cid:219)(cid:208)(cid:221)(cid:222)(cid:218)(cid:217)(cid:204)(cid:215)(cid:212)(cid:229)(cid:208)(cid:3)(cid:217)(cid:208)(cid:227)(cid:223)(cid:3)(cid:205)(cid:208)(cid:222)(cid:223)(cid:3)
(cid:204)(cid:206)(cid:223)(cid:212)(cid:218)(cid:217)(cid:222)(cid:3)(cid:209)(cid:218)(cid:221)(cid:3)(cid:212)(cid:216)(cid:219)(cid:221)(cid:218)(cid:225)(cid:212)(cid:217)(cid:210)(cid:3)(cid:211)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)

Health monitoring 
(cid:181)(cid:212)(cid:210)(cid:212)(cid:223)(cid:204)(cid:215)(cid:3)(cid:223)(cid:218)(cid:218)(cid:215)(cid:222)(cid:3)(cid:216)(cid:204)(cid:214)(cid:208)(cid:3)(cid:212)(cid:223)(cid:3) 
(cid:222)(cid:212)(cid:216)(cid:219)(cid:215)(cid:208)(cid:221)(cid:3)(cid:223)(cid:218)(cid:3)(cid:221)(cid:208)(cid:216)(cid:204)(cid:212)(cid:217)(cid:3) 
(cid:204)(cid:207)(cid:211)(cid:208)(cid:221)(cid:208)(cid:217)(cid:223)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:216)(cid:204)(cid:217)(cid:204)(cid:210)(cid:208)(cid:3)(cid:206)(cid:204)(cid:221)(cid:208) 

Collaborating for success
(cid:180)(cid:199)(cid:196)(cid:3)(cid:211)(cid:204)(cid:222)(cid:3)(cid:95)(cid:94)(cid:94)(cid:3)(cid:211)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:3)(cid:222)(cid:228)(cid:222)(cid:223)(cid:208)(cid:216)(cid:3)
(cid:204)(cid:215)(cid:215)(cid:212)(cid:204)(cid:217)(cid:206)(cid:208)(cid:222)(cid:3)(cid:226)(cid:212)(cid:223)(cid:211)(cid:3)(cid:211)(cid:218)(cid:222)(cid:219)(cid:212)(cid:223)(cid:204)(cid:215)(cid:222)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)
(cid:216)(cid:208)(cid:207)(cid:212)(cid:206)(cid:204)(cid:215)(cid:3)(cid:219)(cid:221)(cid:218)(cid:209)(cid:208)(cid:222)(cid:222)(cid:212)(cid:218)(cid:217)(cid:204)(cid:215)(cid:222)

Convenient services
(cid:190)(cid:224)(cid:215)(cid:223)(cid:212)(cid:207)(cid:218)(cid:222)(cid:208)(cid:3)(cid:219)(cid:204)(cid:206)(cid:214)(cid:204)(cid:210)(cid:212)(cid:217)(cid:210)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:3)
(cid:222)(cid:204)(cid:216)(cid:208)(cid:35)(cid:207)(cid:204)(cid:228)(cid:19)(cid:3)(cid:217)(cid:208)(cid:227)(cid:223)(cid:35)(cid:207)(cid:204)(cid:228)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)
(cid:218)(cid:217)(cid:35)(cid:207)(cid:208)(cid:216)(cid:204)(cid:217)(cid:207)(cid:3)(cid:207)(cid:208)(cid:215)(cid:212)(cid:225)(cid:208)(cid:221)(cid:228)

Proactive outreach
(cid:180)(cid:218)(cid:217)(cid:222)(cid:224)(cid:216)(cid:208)(cid:221)(cid:35)(cid:209)(cid:218)(cid:206)(cid:224)(cid:222)(cid:208)(cid:207)(cid:3)(cid:204)(cid:219)(cid:219)(cid:221)(cid:218)(cid:204)(cid:206)(cid:211)(cid:3)
(cid:223)(cid:218)(cid:3)(cid:206)(cid:218)(cid:216)(cid:216)(cid:224)(cid:217)(cid:212)(cid:206)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:19)(cid:3)(cid:226)(cid:211)(cid:208)(cid:217)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)
(cid:218)(cid:226)(cid:3)(cid:219)(cid:208)(cid:218)(cid:219)(cid:215)(cid:208)(cid:3)(cid:219)(cid:221)(cid:208)(cid:209)(cid:208)(cid:221)
(cid:211)(cid:218)(cid:226)(cid:3)(cid:219)(cid:208)(cid:218)(cid:219)(cid:215)(cid:208)(cid:3)(cid:219)(cid:221)(cid:208)(cid:209)(cid:208)(cid:221)

PAT IENT SNAPSHOT 
Joseph
(cid:187)(cid:218)(cid:222)(cid:208)(cid:219)(cid:211)(cid:3)(cid:212)(cid:222)(cid:3)(cid:204)(cid:223)(cid:3)(cid:221)(cid:212)(cid:222)(cid:214)(cid:3)(cid:209)(cid:218)(cid:221)(cid:3)(cid:206)(cid:218)(cid:216)(cid:219)(cid:215)(cid:212)(cid:206)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:222)(cid:3)(cid:209)(cid:221)(cid:218)(cid:216)(cid:3)(cid:223)(cid:228)(cid:219)(cid:208)(cid:3)
(cid:96)(cid:3)(cid:207)(cid:212)(cid:204)(cid:205)(cid:208)(cid:223)(cid:208)(cid:222)(cid:17)(cid:3)(cid:185)(cid:212)(cid:222)(cid:3)(cid:207)(cid:208)(cid:216)(cid:204)(cid:217)(cid:207)(cid:212)(cid:217)(cid:210)(cid:3)(cid:213)(cid:218)(cid:205)(cid:3)(cid:211)(cid:204)(cid:222)(cid:3)(cid:216)(cid:204)(cid:207)(cid:208)(cid:3)(cid:212)(cid:223)(cid:3)
(cid:207)(cid:212)(cid:244)(cid:206)(cid:224)(cid:215)(cid:223)(cid:3)(cid:223)(cid:218)(cid:3)(cid:222)(cid:208)(cid:208)(cid:3)(cid:211)(cid:212)(cid:222)(cid:3)(cid:207)(cid:218)(cid:206)(cid:223)(cid:218)(cid:221)(cid:3)(cid:221)(cid:208)(cid:210)(cid:224)(cid:215)(cid:204)(cid:221)(cid:215)(cid:228)(cid:17)(cid:3)(cid:187)(cid:218)(cid:222)(cid:208)(cid:219)(cid:211)(cid:3)
(cid:217)(cid:208)(cid:208)(cid:207)(cid:222)(cid:3)(cid:222)(cid:212)(cid:216)(cid:219)(cid:215)(cid:208)(cid:3)(cid:222)(cid:223)(cid:208)(cid:219)(cid:222)(cid:3)(cid:223)(cid:218)(cid:3)(cid:211)(cid:208)(cid:215)(cid:219)(cid:3)(cid:211)(cid:212)(cid:216)(cid:3)(cid:210)(cid:208)(cid:223)(cid:3)(cid:211)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:228)(cid:17)(cid:3)

(cid:181)(cid:208)(cid:225)(cid:212)(cid:206)(cid:208)(cid:222)(cid:3)(cid:224)(cid:222)(cid:208)(cid:207)(cid:18)(cid:3)(cid:190)(cid:218)(cid:205)(cid:212)(cid:215)(cid:208)(cid:3)(cid:204)(cid:219)(cid:219)(cid:19)(cid:3)(cid:223)(cid:204)(cid:205)(cid:215)(cid:208)(cid:223)

(cid:193)(cid:221)(cid:208)(cid:209)(cid:208)(cid:221)(cid:208)(cid:217)(cid:206)(cid:208)(cid:222)(cid:18)(cid:3)(cid:200)(cid:204)(cid:217)(cid:223)(cid:222)(cid:3)(cid:208)(cid:204)(cid:222)(cid:228)(cid:35)(cid:223)(cid:218)(cid:35)(cid:210)(cid:208)(cid:223)(cid:3)(cid:204)(cid:207)(cid:225)(cid:212)(cid:206)(cid:208)(cid:3)(cid:223)(cid:218)(cid:3)
(cid:211)(cid:208)(cid:215)(cid:219)(cid:3)(cid:216)(cid:212)(cid:217)(cid:212)(cid:216)(cid:212)(cid:229)(cid:208)(cid:3)(cid:204)(cid:219)(cid:219)(cid:218)(cid:212)(cid:217)(cid:223)(cid:216)(cid:208)(cid:217)(cid:223)(cid:222)(cid:3)

(cid:193)(cid:221)(cid:218)(cid:210)(cid:221)(cid:204)(cid:216)(cid:18)(cid:3)(cid:197)(cid:221)(cid:204)(cid:217)(cid:222)(cid:209)(cid:218)(cid:221)(cid:216)(cid:3)(cid:181)(cid:212)(cid:204)(cid:205)(cid:208)(cid:223)(cid:208)(cid:222)(cid:3)(cid:180)(cid:204)(cid:221)(cid:208)

J OS EPH’S JOURNEY 

(cid:32)(cid:3)(cid:196)(cid:212)(cid:216)(cid:219)(cid:215)(cid:212)(cid:209)(cid:228)(cid:212)(cid:217)(cid:210)(cid:3)(cid:216)(cid:228)(cid:3)(cid:223)(cid:221)(cid:208)(cid:204)(cid:223)(cid:35)
(cid:216)(cid:208)(cid:217)(cid:223)(cid:3)(cid:226)(cid:204)(cid:222)(cid:3)(cid:204)(cid:3)(cid:223)(cid:218)(cid:219)(cid:3)(cid:219)(cid:221)(cid:212)(cid:218)(cid:221)(cid:212)(cid:223)(cid:228)(cid:3)
(cid:222)(cid:212)(cid:217)(cid:206)(cid:208)(cid:3)(cid:215)(cid:208)(cid:204)(cid:221)(cid:217)(cid:212)(cid:217)(cid:210)(cid:3)(cid:186)(cid:30)(cid:216)(cid:3)(cid:204)(cid:223)(cid:3)
(cid:221)(cid:212)(cid:222)(cid:214)(cid:3)(cid:209)(cid:218)(cid:221)(cid:3)(cid:206)(cid:218)(cid:216)(cid:219)(cid:215)(cid:212)(cid:206)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:222)(cid:3)
(cid:204)(cid:222)(cid:222)(cid:218)(cid:206)(cid:212)(cid:204)(cid:223)(cid:208)(cid:207)(cid:3)(cid:226)(cid:212)(cid:223)(cid:211)(cid:3)(cid:216)(cid:228)(cid:3)
(cid:207)(cid:212)(cid:204)(cid:205)(cid:208)(cid:223)(cid:208)(cid:222)(cid:17)(cid:33)

(cid:186)(cid:207)(cid:208)(cid:217)(cid:223)(cid:212)(cid:242)(cid:208)(cid:207)(cid:3)(cid:204)(cid:222)(cid:3)(cid:217)(cid:208)(cid:208)(cid:207)(cid:212)(cid:217)(cid:210)
(cid:204)(cid:217)(cid:3)(cid:204)(cid:217)(cid:217)(cid:224)(cid:204)(cid:215)(cid:3)(cid:207)(cid:212)(cid:204)(cid:205)(cid:208)(cid:223)(cid:208)(cid:222)
(cid:208)(cid:227)(cid:204)(cid:216)(cid:19)(cid:3)(cid:187)(cid:218)(cid:222)(cid:208)(cid:219)(cid:211)(cid:3)(cid:212)(cid:222)
(cid:206)(cid:218)(cid:224)(cid:217)(cid:222)(cid:208)(cid:215)(cid:208)(cid:207)(cid:3)(cid:226)(cid:211)(cid:212)(cid:215)(cid:208)(cid:3)(cid:242)(cid:215)(cid:215)(cid:212)(cid:217)(cid:210)
(cid:211)(cid:212)(cid:222)(cid:3)(cid:219)(cid:221)(cid:208)(cid:222)(cid:206)(cid:221)(cid:212)(cid:219)(cid:223)(cid:212)(cid:218)(cid:217)(cid:17)

(cid:190)(cid:212)(cid:217)(cid:224)(cid:223)(cid:208)(cid:180)(cid:215)(cid:212)(cid:217)(cid:212)(cid:206)
(cid:204)(cid:207)(cid:216)(cid:212)(cid:217)(cid:212)(cid:222)(cid:223)(cid:208)(cid:221)(cid:222)(cid:3)(cid:204)(cid:217)(cid:217)(cid:224)(cid:204)(cid:215)
(cid:207)(cid:212)(cid:204)(cid:205)(cid:208)(cid:223)(cid:208)(cid:222)(cid:3)(cid:208)(cid:227)(cid:204)(cid:216)(cid:17)(cid:3) 
(cid:191)(cid:208)(cid:208)(cid:207)(cid:3)(cid:209)(cid:218)(cid:221)(cid:3)(cid:204)(cid:207)(cid:207)(cid:212)(cid:223)(cid:212)(cid:218)(cid:217)(cid:204)(cid:215)(cid:3)
(cid:222)(cid:224)(cid:219)(cid:219)(cid:218)(cid:221)(cid:223)(cid:3)(cid:212)(cid:207)(cid:208)(cid:217)(cid:223)(cid:212)(cid:242)(cid:208)(cid:207)(cid:17)

(cid:180)(cid:204)(cid:221)(cid:208)(cid:3)(cid:216)(cid:204)(cid:217)(cid:204)(cid:210)(cid:208)(cid:221)
(cid:225)(cid:212)(cid:222)(cid:212)(cid:223)(cid:222)(cid:3)(cid:187)(cid:218)(cid:222)(cid:208)(cid:219)(cid:211)(cid:3)(cid:204)(cid:223)
(cid:211)(cid:218)(cid:216)(cid:208)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:206)(cid:221)(cid:208)(cid:204)(cid:223)(cid:208)(cid:222)
(cid:204)(cid:3)(cid:206)(cid:204)(cid:221)(cid:208)(cid:3)(cid:219)(cid:215)(cid:204)(cid:217)(cid:3)(cid:223)(cid:218)
(cid:214)(cid:208)(cid:208)(cid:219)(cid:3)(cid:211)(cid:212)(cid:216)(cid:3)(cid:218)(cid:217)(cid:3)(cid:223)(cid:221)(cid:204)(cid:206)(cid:214)(cid:17)

(cid:191)(cid:218)(cid:223)(cid:3)(cid:204)(cid:217)(cid:3)(cid:204)(cid:206)(cid:223)(cid:224)(cid:204)(cid:215)(cid:3)(cid:219)(cid:204)(cid:223)(cid:212)(cid:208)(cid:217)(cid:223)(cid:19)(cid:3)(cid:205)(cid:224)(cid:223)(cid:3)(cid:204)(cid:3)(cid:221)(cid:208)(cid:219)(cid:221)(cid:208)(cid:222)(cid:208)(cid:217)(cid:223)(cid:204)(cid:223)(cid:212)(cid:225)(cid:208)(cid:3)(cid:213)(cid:218)(cid:224)(cid:221)(cid:217)(cid:208)(cid:228)(cid:17)(cid:3)

(cid:96)(cid:94)(cid:95)(cid:103)(cid:3)(cid:178)(cid:217)(cid:217)(cid:224)(cid:204)(cid:215)(cid:3)(cid:195)(cid:208)(cid:219)(cid:218)(cid:221)(cid:223)

5

(cid:186)(cid:216)(cid:219)(cid:221)(cid:218)(cid:225)(cid:208)(cid:3)(cid:211)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)
(cid:200)(cid:208)(cid:3)(cid:219)(cid:221)(cid:218)(cid:225)(cid:212)(cid:207)(cid:208)(cid:3)(cid:206)(cid:204)(cid:221)(cid:208)(cid:19)(cid:3)(cid:209)(cid:221)(cid:218)(cid:216)(cid:3)(cid:222)(cid:212)(cid:216)(cid:219)(cid:215)(cid:208)(cid:3)(cid:223)(cid:218)(cid:3)(cid:206)(cid:218)(cid:216)(cid:219)(cid:215)(cid:208)(cid:227)(cid:17)

(cid:200)(cid:211)(cid:208)(cid:223)(cid:211)(cid:208)(cid:221)(cid:3)(cid:226)(cid:208)(cid:30)(cid:221)(cid:208)(cid:3)(cid:209)(cid:218)(cid:206)(cid:224)(cid:222)(cid:212)(cid:217)(cid:210)(cid:3)(cid:218)(cid:217)(cid:3)(cid:219)(cid:221)(cid:208)(cid:225)(cid:208)(cid:217)(cid:223)(cid:212)(cid:218)(cid:217)(cid:3)(cid:218)(cid:221)(cid:3)(cid:223)(cid:221)(cid:208)(cid:204)(cid:223)(cid:212)(cid:217)(cid:210)(cid:3)(cid:219)(cid:204)(cid:223)(cid:212)(cid:208)(cid:217)(cid:223)(cid:222)(cid:3)(cid:226)(cid:212)(cid:223)(cid:211)(cid:3)(cid:206)(cid:218)(cid:216)(cid:219)(cid:215)(cid:208)(cid:227)(cid:3)(cid:206)(cid:211)(cid:221)(cid:218)(cid:217)(cid:212)(cid:206)(cid:3)(cid:206)(cid:218)(cid:217)(cid:207)(cid:212)(cid:223)(cid:212)(cid:218)(cid:217)(cid:222)(cid:19)(cid:3)(cid:226)(cid:208)(cid:30)(cid:221)(cid:208)(cid:3)(cid:224)(cid:223)(cid:212)(cid:215)(cid:212)(cid:229)(cid:212)(cid:217)(cid:210)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)
(cid:212)(cid:217)(cid:223)(cid:208)(cid:210)(cid:221)(cid:204)(cid:223)(cid:208)(cid:207)(cid:3)(cid:206)(cid:204)(cid:219)(cid:204)(cid:205)(cid:212)(cid:215)(cid:212)(cid:223)(cid:212)(cid:208)(cid:222)(cid:3)(cid:223)(cid:218)(cid:3)(cid:205)(cid:221)(cid:212)(cid:217)(cid:210)(cid:3)(cid:211)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:3)(cid:206)(cid:204)(cid:221)(cid:208)(cid:3)(cid:223)(cid:218)(cid:3)(cid:204)(cid:217)(cid:218)(cid:223)(cid:211)(cid:208)(cid:221)(cid:3)(cid:215)(cid:208)(cid:225)(cid:208)(cid:215)(cid:17)

(cid:188)(cid:208)(cid:208)(cid:219)(cid:212)(cid:217)(cid:210)(cid:3)(cid:211)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:228)(cid:3)
patients healthy

(cid:186)(cid:217)(cid:223)(cid:208)(cid:221)(cid:225)(cid:208)(cid:217)(cid:223)(cid:212)(cid:218)(cid:217)(cid:222)(cid:3)(cid:223)(cid:218)(cid:3)
address health 

Leading disease 
management

(cid:190)(cid:204)(cid:217)(cid:204)(cid:210)(cid:212)(cid:217)(cid:210)(cid:3)(cid:206)(cid:211)(cid:221)(cid:218)(cid:217)(cid:212)(cid:206)(cid:3)
conditions

Treating advanced 
illnesses 

H E A LT H Y

S TA B L E

(cid:178)(cid:197) (cid:3) (cid:195) (cid:186) (cid:196) (cid:188)

C O M P L E X   C H R O N I C

C R I T I C A L   I L L N E S S

Thousands of health 
products available  
in store, by home 
delivery or by mail, 
and convenient ways 
(cid:223)(cid:218)(cid:3)(cid:221)(cid:208)(cid:242)(cid:215)(cid:215)(cid:3)(cid:219)(cid:221)(cid:208)(cid:222)(cid:206)(cid:221)(cid:212)(cid:219)(cid:223)(cid:212)(cid:218)(cid:217)(cid:222)

(cid:219)

(cid:219)

 CVS Health 
electronically 
connects with 
doctors to close 
gaps in care

 CVS Health has 
industry-leading 
programs for 
diabetes and  
kidney care

(cid:185)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:185)(cid:198)(cid:179)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)
(cid:190)(cid:212)(cid:217)(cid:224)(cid:223)(cid:208)(cid:180)(cid:215)(cid:212)(cid:217)(cid:212)(cid:206)(cid:3)(cid:215)(cid:218)(cid:206)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:222)(cid:3)
(cid:218)(cid:241)(cid:208)(cid:221)(cid:3)(cid:206)(cid:218)(cid:216)(cid:219)(cid:215)(cid:208)(cid:216)(cid:208)(cid:217)(cid:223)(cid:204)(cid:221)(cid:228)(cid:3)
disease management 
services

800 nurses 
dedicated to  
in-home visits 

PATIE NT SNA PS HOT 
(cid:178)(cid:217)(cid:217)(cid:204)
(cid:178)(cid:217)(cid:217)(cid:204)(cid:3)(cid:221)(cid:208)(cid:206)(cid:208)(cid:217)(cid:223)(cid:215)(cid:228)(cid:3)(cid:215)(cid:208)(cid:204)(cid:221)(cid:217)(cid:208)(cid:207)(cid:3)(cid:222)(cid:211)(cid:208)(cid:3)(cid:211)(cid:204)(cid:222)(cid:3)(cid:205)(cid:221)(cid:208)(cid:204)(cid:222)(cid:223)(cid:3)
(cid:206)(cid:204)(cid:217)(cid:206)(cid:208)(cid:221)(cid:17)(cid:3)(cid:196)(cid:211)(cid:208)(cid:3)(cid:226)(cid:204)(cid:217)(cid:223)(cid:222)(cid:3)(cid:223)(cid:218)(cid:3)(cid:207)(cid:218)(cid:3)(cid:204)(cid:215)(cid:215)(cid:3)(cid:222)(cid:211)(cid:208)(cid:3)(cid:206)(cid:204)(cid:217)(cid:3)(cid:223)(cid:218)(cid:3)
(cid:216)(cid:204)(cid:212)(cid:217)(cid:223)(cid:204)(cid:212)(cid:217)(cid:3)(cid:220)(cid:224)(cid:204)(cid:215)(cid:212)(cid:223)(cid:228)(cid:3)(cid:218)(cid:209)(cid:3)(cid:215)(cid:212)(cid:209)(cid:208)(cid:3)(cid:226)(cid:211)(cid:212)(cid:215)(cid:208)(cid:3)(cid:212)(cid:217)(cid:3)(cid:223)(cid:221)(cid:208)(cid:204)(cid:223)(cid:216)(cid:208)(cid:217)(cid:223)(cid:3)
(cid:204)(cid:217)(cid:207)(cid:3)(cid:242)(cid:217)(cid:207)(cid:3)(cid:226)(cid:204)(cid:228)(cid:222)(cid:3)(cid:223)(cid:218)(cid:3)(cid:212)(cid:216)(cid:219)(cid:221)(cid:218)(cid:225)(cid:208)(cid:3)(cid:211)(cid:208)(cid:221)(cid:3)(cid:211)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:17)(cid:3)

(cid:181)(cid:208)(cid:225)(cid:212)(cid:206)(cid:208)(cid:222)(cid:3)(cid:224)(cid:222)(cid:208)(cid:207)(cid:18)(cid:3)(cid:193)(cid:211)(cid:218)(cid:217)(cid:208)(cid:19)(cid:3)(cid:216)(cid:218)(cid:205)(cid:212)(cid:215)(cid:208)(cid:3)(cid:204)(cid:219)(cid:219)

(cid:193)(cid:221)(cid:208)(cid:209)(cid:208)(cid:221)(cid:208)(cid:217)(cid:206)(cid:208)(cid:222)(cid:18)(cid:3)(cid:200)(cid:204)(cid:217)(cid:223)(cid:222)(cid:3)(cid:218)(cid:217)(cid:35)(cid:206)(cid:204)(cid:215)(cid:215)(cid:3)(cid:211)(cid:208)(cid:215)(cid:219)(cid:3)(cid:222)(cid:218)(cid:3)(cid:222)(cid:211)(cid:208)(cid:3)
(cid:206)(cid:204)(cid:217)(cid:3)(cid:214)(cid:208)(cid:208)(cid:219)(cid:3)(cid:224)(cid:219)(cid:3)(cid:226)(cid:212)(cid:223)(cid:211)(cid:3)(cid:211)(cid:208)(cid:221)(cid:3)(cid:215)(cid:212)(cid:209)(cid:208)

(cid:193)(cid:221)(cid:218)(cid:210)(cid:221)(cid:204)(cid:216)(cid:18)(cid:3)(cid:197)(cid:221)(cid:204)(cid:217)(cid:222)(cid:209)(cid:218)(cid:221)(cid:216)(cid:3)(cid:192)(cid:217)(cid:206)(cid:218)(cid:215)(cid:218)(cid:210)(cid:228)(cid:3)(cid:180)(cid:204)(cid:221)(cid:208)(cid:3)

ANNA’S JOU RNE Y 

(cid:32)(cid:3)(cid:190)(cid:228)(cid:3)(cid:223)(cid:208)(cid:204)(cid:216)(cid:3)(cid:226)(cid:204)(cid:222)(cid:3) 
(cid:204)(cid:215)(cid:226)(cid:204)(cid:228)(cid:222)(cid:3)(cid:223)(cid:211)(cid:208)(cid:221)(cid:208)(cid:19)(cid:3)(cid:207)(cid:204)(cid:228)(cid:3)(cid:218)(cid:221)(cid:3)
(cid:217)(cid:212)(cid:210)(cid:211)(cid:223)(cid:19)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:211)(cid:208)(cid:215)(cid:219)(cid:208)(cid:207)(cid:3)
(cid:216)(cid:208)(cid:3)(cid:216)(cid:204)(cid:217)(cid:204)(cid:210)(cid:208)(cid:3)(cid:216)(cid:228)(cid:3)
(cid:223)(cid:221)(cid:208)(cid:204)(cid:223)(cid:216)(cid:208)(cid:217)(cid:223)(cid:17)(cid:33)

(cid:178)(cid:223)(cid:3)(cid:206)(cid:204)(cid:217)(cid:206)(cid:208)(cid:221)(cid:3)(cid:207)(cid:212)(cid:204)(cid:210)(cid:217)(cid:218)(cid:222)(cid:212)(cid:222)(cid:19)(cid:3)
(cid:178)(cid:217)(cid:217)(cid:204)(cid:30)(cid:222)(cid:3)(cid:178)(cid:206)(cid:206)(cid:218)(cid:221)(cid:207)(cid:204)(cid:217)(cid:223)(cid:3)(cid:217)(cid:224)(cid:221)(cid:222)(cid:208)(cid:3)
(cid:221)(cid:208)(cid:204)(cid:206)(cid:211)(cid:208)(cid:222)(cid:3)(cid:218)(cid:224)(cid:223)(cid:3)(cid:223)(cid:218)(cid:3)(cid:218)(cid:241)(cid:208)(cid:221)(cid:3)(cid:206)(cid:204)(cid:221)(cid:208)(cid:3)
(cid:216)(cid:204)(cid:217)(cid:204)(cid:210)(cid:208)(cid:216)(cid:208)(cid:217)(cid:223)(cid:3)(cid:222)(cid:224)(cid:219)(cid:219)(cid:218)(cid:221)(cid:223)(cid:17)

(cid:178)(cid:217)(cid:3)(cid:178)(cid:206)(cid:206)(cid:218)(cid:221)(cid:207)(cid:204)(cid:217)(cid:223)(cid:3)(cid:217)(cid:224)(cid:221)(cid:222)(cid:208)(cid:3)
(cid:219)(cid:221)(cid:218)(cid:225)(cid:212)(cid:207)(cid:208)(cid:222)(cid:3)(cid:178)(cid:217)(cid:217)(cid:204)(cid:3)(cid:226)(cid:212)(cid:223)(cid:211)(cid:3)
(cid:218)(cid:217)(cid:210)(cid:218)(cid:212)(cid:217)(cid:210)(cid:3)(cid:206)(cid:204)(cid:217)(cid:206)(cid:208)(cid:221)(cid:35)(cid:222)(cid:219)(cid:208)(cid:206)(cid:212)(cid:242)(cid:206)(cid:3)
(cid:206)(cid:204)(cid:221)(cid:208)(cid:3)(cid:216)(cid:204)(cid:217)(cid:204)(cid:210)(cid:208)(cid:216)(cid:208)(cid:217)(cid:223)(cid:3)
(cid:222)(cid:224)(cid:219)(cid:219)(cid:218)(cid:221)(cid:223)(cid:17)

(cid:178)(cid:217)(cid:217)(cid:204)(cid:3)(cid:212)(cid:222)(cid:3)(cid:206)(cid:218)(cid:217)(cid:217)(cid:208)(cid:206)(cid:223)(cid:208)(cid:207)(cid:3)(cid:226)(cid:212)(cid:223)(cid:211)(cid:3)
(cid:204)(cid:3)(cid:219)(cid:204)(cid:223)(cid:212)(cid:208)(cid:217)(cid:223)(cid:3)(cid:204)(cid:207)(cid:225)(cid:218)(cid:206)(cid:204)(cid:223)(cid:208)(cid:3)(cid:209)(cid:218)(cid:221)(cid:3)
(cid:217)(cid:218)(cid:217)(cid:35)(cid:206)(cid:215)(cid:212)(cid:217)(cid:212)(cid:206)(cid:204)(cid:215)(cid:3)(cid:221)(cid:208)(cid:222)(cid:218)(cid:224)(cid:221)(cid:206)(cid:208)(cid:222)(cid:19)(cid:3)
(cid:215)(cid:212)(cid:214)(cid:208)(cid:3)(cid:242)(cid:217)(cid:204)(cid:217)(cid:206)(cid:212)(cid:204)(cid:215)(cid:3)(cid:204)(cid:222)(cid:222)(cid:212)(cid:222)(cid:223)(cid:204)(cid:217)(cid:206)(cid:208)(cid:3)
(cid:204)(cid:217)(cid:207)(cid:3)(cid:211)(cid:218)(cid:216)(cid:208)(cid:3)(cid:206)(cid:215)(cid:208)(cid:204)(cid:217)(cid:212)(cid:217)(cid:210)(cid:3)
(cid:222)(cid:208)(cid:221)(cid:225)(cid:212)(cid:206)(cid:208)(cid:222)(cid:17)

6

CVS Health

(cid:191)(cid:218)(cid:223)(cid:3)(cid:204)(cid:217)(cid:3)(cid:204)(cid:206)(cid:223)(cid:224)(cid:204)(cid:215)(cid:3)(cid:219)(cid:204)(cid:223)(cid:212)(cid:208)(cid:217)(cid:223)(cid:19)(cid:3)(cid:205)(cid:224)(cid:223)(cid:3)(cid:204)(cid:3)(cid:221)(cid:208)(cid:219)(cid:221)(cid:208)(cid:222)(cid:208)(cid:217)(cid:223)(cid:204)(cid:223)(cid:212)(cid:225)(cid:208)(cid:3)(cid:213)(cid:218)(cid:224)(cid:221)(cid:217)(cid:208)(cid:228)(cid:17)(cid:3)

In 2019, we also applied our proprietary 
NovoLogix® technology across our 
(cid:185)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:3)(cid:180)(cid:204)(cid:221)(cid:208)(cid:3)(cid:179)(cid:208)(cid:217)(cid:208)(cid:242)(cid:223)(cid:222)(cid:3)(cid:205)(cid:218)(cid:218)(cid:214)(cid:3)(cid:218)(cid:209)(cid:3)(cid:205)(cid:224)(cid:222)(cid:212)(cid:217)(cid:208)(cid:222)(cid:222)(cid:19)(cid:3)
which should drive cost savings and 
(cid:208)(cid:244)(cid:206)(cid:212)(cid:208)(cid:217)(cid:206)(cid:212)(cid:208)(cid:222)(cid:3)(cid:209)(cid:218)(cid:221)(cid:3)(cid:206)(cid:215)(cid:212)(cid:208)(cid:217)(cid:223)(cid:222)(cid:17)(cid:3)(cid:191)(cid:218)(cid:225)(cid:218)(cid:189)(cid:218)(cid:210)(cid:212)(cid:227)(cid:3)(cid:211)(cid:208)(cid:215)(cid:219)(cid:222)(cid:3)
our clients manage the specialty phar-
macy claims that are typically covered 
(cid:205)(cid:228)(cid:3)(cid:211)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:3)(cid:219)(cid:215)(cid:204)(cid:217)(cid:3)(cid:205)(cid:208)(cid:217)(cid:208)(cid:242)(cid:223)(cid:222)(cid:3)(cid:221)(cid:204)(cid:223)(cid:211)(cid:208)(cid:221)(cid:3)(cid:223)(cid:211)(cid:204)(cid:217)(cid:3)
(cid:219)(cid:211)(cid:204)(cid:221)(cid:216)(cid:204)(cid:206)(cid:228)(cid:3)(cid:205)(cid:208)(cid:217)(cid:208)(cid:242)(cid:223)(cid:222)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:211)(cid:204)(cid:222)(cid:3)(cid:211)(cid:208)(cid:215)(cid:219)(cid:208)(cid:207)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)
PBM clients generate approximately 
$42 million in annual savings  per 
(cid:216)(cid:212)(cid:215)(cid:215)(cid:212)(cid:218)(cid:217)(cid:3)(cid:215)(cid:212)(cid:225)(cid:208)(cid:222)(cid:3)(cid:208)(cid:217)(cid:221)(cid:218)(cid:215)(cid:215)(cid:208)(cid:207)(cid:17)

Turning to our Medicare Part D 
products, SilverScript® remains 
the nation’s leading standalone 
(cid:219)(cid:221)(cid:208)(cid:222)(cid:206)(cid:221)(cid:212)(cid:219)(cid:223)(cid:212)(cid:218)(cid:217)(cid:3)(cid:207)(cid:221)(cid:224)(cid:210)(cid:3)(cid:219)(cid:215)(cid:204)(cid:217)(cid:3)(cid:40)(cid:193)(cid:181)(cid:193)(cid:41)(cid:17)(cid:3)(cid:178)(cid:222)(cid:3)(cid:226)(cid:208)(cid:3)
(cid:215)(cid:218)(cid:218)(cid:214)(cid:3)(cid:204)(cid:211)(cid:208)(cid:204)(cid:207)(cid:19)(cid:3)(cid:226)(cid:208)(cid:3)(cid:205)(cid:208)(cid:215)(cid:212)(cid:208)(cid:225)(cid:208)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)(cid:196)(cid:212)(cid:215)(cid:225)(cid:208)(cid:221)(cid:196)(cid:206)(cid:221)(cid:212)(cid:219)(cid:223)(cid:3)
(cid:193)(cid:181)(cid:193)(cid:3)(cid:216)(cid:208)(cid:216)(cid:205)(cid:208)(cid:221)(cid:222)(cid:3)(cid:226)(cid:212)(cid:215)(cid:215)(cid:3)(cid:205)(cid:208)(cid:3)(cid:204)(cid:217)(cid:3)(cid:212)(cid:216)(cid:219)(cid:218)(cid:221)(cid:223)(cid:204)(cid:217)(cid:223)(cid:3)
(cid:222)(cid:218)(cid:224)(cid:221)(cid:206)(cid:208)(cid:3)(cid:218)(cid:209)(cid:3)(cid:216)(cid:208)(cid:216)(cid:205)(cid:208)(cid:221)(cid:222)(cid:211)(cid:212)(cid:219)(cid:3)(cid:212)(cid:217)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)(cid:190)(cid:208)(cid:207)(cid:212)(cid:206)(cid:204)(cid:221)(cid:208)(cid:3)
(cid:178)(cid:207)(cid:225)(cid:204)(cid:217)(cid:223)(cid:204)(cid:210)(cid:208)(cid:3)(cid:219)(cid:215)(cid:204)(cid:217)(cid:222)(cid:17)

80% 

of the scope of a typical 
primary care practice 
can be addressed by 
MinuteClinic

Patient care solutions drove strong 
performance in our Retail/LTC 
segment 

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(cid:223)(cid:218)(cid:3)(cid:114)(cid:102)(cid:100)(cid:17)(cid:100)(cid:3)(cid:205)(cid:212)(cid:215)(cid:215)(cid:212)(cid:218)(cid:217)(cid:3)(cid:212)(cid:217)(cid:3)(cid:96)(cid:94)(cid:95)(cid:103)(cid:3)(cid:212)(cid:217)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)(cid:195)(cid:208)(cid:223)(cid:204)(cid:212)(cid:215)(cid:42)
(cid:189)(cid:218)(cid:217)(cid:210)(cid:35)(cid:197)(cid:208)(cid:221)(cid:216)(cid:3)(cid:180)(cid:204)(cid:221)(cid:208)(cid:3)(cid:222)(cid:208)(cid:210)(cid:216)(cid:208)(cid:217)(cid:223)(cid:17)(cid:3)(cid:181)(cid:208)(cid:222)(cid:219)(cid:212)(cid:223)(cid:208)(cid:3)
(cid:206)(cid:218)(cid:217)(cid:223)(cid:212)(cid:217)(cid:224)(cid:208)(cid:207)(cid:3)(cid:221)(cid:208)(cid:212)(cid:216)(cid:205)(cid:224)(cid:221)(cid:222)(cid:208)(cid:216)(cid:208)(cid:217)(cid:223)(cid:3)(cid:219)(cid:221)(cid:208)(cid:222)(cid:222)(cid:224)(cid:221)(cid:208)(cid:222)(cid:19)(cid:3)
(cid:223)(cid:211)(cid:212)(cid:222)(cid:3)(cid:205)(cid:224)(cid:222)(cid:212)(cid:217)(cid:208)(cid:222)(cid:222)(cid:3)(cid:205)(cid:208)(cid:217)(cid:208)(cid:242)(cid:223)(cid:208)(cid:207)(cid:3)(cid:209)(cid:221)(cid:218)(cid:216)(cid:3)(cid:212)(cid:217)(cid:206)(cid:221)(cid:208)(cid:204)(cid:222)(cid:208)(cid:207)(cid:3)
(cid:219)(cid:221)(cid:208)(cid:222)(cid:206)(cid:221)(cid:212)(cid:219)(cid:223)(cid:212)(cid:218)(cid:217)(cid:3)(cid:225)(cid:218)(cid:215)(cid:224)(cid:216)(cid:208)(cid:17)(cid:3)(cid:197)(cid:218)(cid:223)(cid:204)(cid:215)(cid:3)(cid:219)(cid:221)(cid:208)(cid:222)(cid:206)(cid:221)(cid:212)(cid:219)(cid:223)(cid:212)(cid:218)(cid:217)(cid:3)
(cid:225)(cid:218)(cid:215)(cid:224)(cid:216)(cid:208)(cid:3)(cid:210)(cid:221)(cid:208)(cid:226)(cid:3)(cid:205)(cid:228)(cid:3)(cid:99)(cid:17)(cid:102)(cid:3)(cid:219)(cid:208)(cid:221)(cid:206)(cid:208)(cid:217)(cid:223)(cid:3)(cid:218)(cid:217)(cid:3)(cid:204)(cid:3)
(cid:97)(cid:94)(cid:35)(cid:207)(cid:204)(cid:228)(cid:3)(cid:208)(cid:220)(cid:224)(cid:212)(cid:225)(cid:204)(cid:215)(cid:208)(cid:217)(cid:223)(cid:3)(cid:205)(cid:204)(cid:222)(cid:212)(cid:222)(cid:3)(cid:206)(cid:218)(cid:216)(cid:219)(cid:204)(cid:221)(cid:208)(cid:207)(cid:3)(cid:223)(cid:218)(cid:3)
(cid:96)(cid:94)(cid:95)(cid:102)(cid:17)(cid:3)(cid:186)(cid:217)(cid:3)(cid:209)(cid:204)(cid:206)(cid:223)(cid:19)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)(cid:219)(cid:221)(cid:208)(cid:222)(cid:206)(cid:221)(cid:212)(cid:219)(cid:223)(cid:212)(cid:218)(cid:217)(cid:3)(cid:210)(cid:221)(cid:218)(cid:226)(cid:223)(cid:211)(cid:3)
(cid:222)(cid:212)(cid:210)(cid:217)(cid:212)(cid:242)(cid:206)(cid:204)(cid:217)(cid:223)(cid:215)(cid:228)(cid:3)(cid:218)(cid:224)(cid:223)(cid:219)(cid:208)(cid:221)(cid:209)(cid:218)(cid:221)(cid:216)(cid:208)(cid:207)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:212)(cid:217)(cid:207)(cid:224)(cid:222)(cid:223)(cid:221)(cid:228)(cid:3)
(cid:204)(cid:225)(cid:208)(cid:221)(cid:204)(cid:210)(cid:208)(cid:3)(cid:212)(cid:217)(cid:3)(cid:96)(cid:94)(cid:95)(cid:103)(cid:17)(cid:3)(cid:200)(cid:208)(cid:3)(cid:207)(cid:212)(cid:222)(cid:219)(cid:208)(cid:217)(cid:222)(cid:208)(cid:207)(cid:3)
(cid:204)(cid:219)(cid:219)(cid:221)(cid:218)(cid:227)(cid:212)(cid:216)(cid:204)(cid:223)(cid:208)(cid:215)(cid:228)(cid:3)(cid:96)(cid:100)(cid:17)(cid:100)(cid:3)(cid:219)(cid:208)(cid:221)(cid:206)(cid:208)(cid:217)(cid:223)(cid:3)(cid:218)(cid:209)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:221)(cid:208)(cid:223)(cid:204)(cid:212)(cid:215)(cid:3)
(cid:219)(cid:221)(cid:208)(cid:222)(cid:206)(cid:221)(cid:212)(cid:219)(cid:223)(cid:212)(cid:218)(cid:217)(cid:222)(cid:3)(cid:212)(cid:217)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:198)(cid:217)(cid:212)(cid:223)(cid:208)(cid:207)(cid:3)(cid:196)(cid:223)(cid:204)(cid:223)(cid:208)(cid:222)(cid:3)(cid:209)(cid:218)(cid:221)(cid:3)
(cid:223)(cid:211)(cid:208)(cid:3)(cid:228)(cid:208)(cid:204)(cid:221)(cid:3)(cid:218)(cid:217)(cid:3)(cid:204)(cid:3)(cid:97)(cid:94)(cid:35)(cid:207)(cid:204)(cid:228)(cid:3)(cid:208)(cid:220)(cid:224)(cid:212)(cid:225)(cid:204)(cid:215)(cid:208)(cid:217)(cid:223)(cid:3)(cid:205)(cid:204)(cid:222)(cid:212)(cid:222)(cid:17)(cid:3)

Our approximately 1,100 MinuteClinic 
locations continued to expand their 
(cid:218)(cid:241)(cid:208)(cid:221)(cid:212)(cid:217)(cid:210)(cid:222)(cid:3)(cid:212)(cid:217)(cid:3)(cid:96)(cid:94)(cid:95)(cid:103)(cid:17)(cid:3)(cid:186)(cid:217)(cid:3)(cid:209)(cid:204)(cid:206)(cid:223)(cid:19)(cid:3)(cid:190)(cid:212)(cid:217)(cid:224)(cid:223)(cid:208)(cid:180)(cid:215)(cid:212)(cid:217)(cid:212)(cid:206)(cid:3)
(cid:206)(cid:204)(cid:217)(cid:3)(cid:217)(cid:218)(cid:226)(cid:3)(cid:204)(cid:207)(cid:207)(cid:221)(cid:208)(cid:222)(cid:222)(cid:3)(cid:204)(cid:205)(cid:218)(cid:224)(cid:223)(cid:3)(cid:102)(cid:94)(cid:3)(cid:219)(cid:208)(cid:221)(cid:206)(cid:208)(cid:217)(cid:223)(cid:3)
(cid:218)(cid:209)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:222)(cid:206)(cid:218)(cid:219)(cid:208)(cid:3)(cid:218)(cid:209)(cid:3)(cid:204)(cid:3)(cid:223)(cid:228)(cid:219)(cid:212)(cid:206)(cid:204)(cid:215)(cid:3)(cid:219)(cid:221)(cid:212)(cid:216)(cid:204)(cid:221)(cid:228)(cid:3)(cid:206)(cid:204)(cid:221)(cid:208)(cid:3)
(cid:219)(cid:221)(cid:204)(cid:206)(cid:223)(cid:212)(cid:206)(cid:208)(cid:17)(cid:3)(cid:200)(cid:211)(cid:208)(cid:217)(cid:3)(cid:204)(cid:3)(cid:207)(cid:218)(cid:206)(cid:223)(cid:218)(cid:221)(cid:3)(cid:212)(cid:222)(cid:3)(cid:217)(cid:208)(cid:208)(cid:207)(cid:208)(cid:207)(cid:19)(cid:3)
(cid:190)(cid:212)(cid:217)(cid:224)(cid:223)(cid:208)(cid:180)(cid:215)(cid:212)(cid:217)(cid:212)(cid:206)(cid:3)(cid:215)(cid:218)(cid:206)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:222)(cid:3)(cid:218)(cid:241)(cid:208)(cid:221)(cid:3)(cid:199)(cid:212)(cid:207)(cid:208)(cid:218)(cid:3) 
(cid:199)(cid:212)(cid:222)(cid:212)(cid:223)(cid:222)(cid:3)(cid:212)(cid:217)(cid:3)(cid:206)(cid:218)(cid:215)(cid:215)(cid:204)(cid:205)(cid:218)(cid:221)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:3)(cid:226)(cid:212)(cid:223)(cid:211)(cid:3)(cid:197)(cid:208)(cid:215)(cid:204)(cid:207)(cid:218)(cid:206)(cid:3) 
(cid:212)(cid:217)(cid:3)(cid:98)(cid:94)(cid:3)(cid:222)(cid:223)(cid:204)(cid:223)(cid:208)(cid:222)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:200)(cid:204)(cid:222)(cid:211)(cid:212)(cid:217)(cid:210)(cid:223)(cid:218)(cid:217)(cid:19)(cid:3)(cid:181)(cid:17)(cid:180)(cid:17)(cid:3)

I am also proud to note that the health 
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MinuteClinic locations have earned 
a Pathway to Excellence designation 
(cid:209)(cid:221)(cid:218)(cid:216)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:178)(cid:216)(cid:208)(cid:221)(cid:212)(cid:206)(cid:204)(cid:217)(cid:3)(cid:191)(cid:224)(cid:221)(cid:222)(cid:208)(cid:222)(cid:3)(cid:180)(cid:221)(cid:208)(cid:207)(cid:208)(cid:217)(cid:223)(cid:212)(cid:204)(cid:215)-
(cid:212)(cid:217)(cid:210)(cid:3)(cid:180)(cid:208)(cid:217)(cid:223)(cid:208)(cid:221)(cid:3)(cid:209)(cid:218)(cid:221)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:220)(cid:224)(cid:204)(cid:215)(cid:212)(cid:223)(cid:228)(cid:3)(cid:222)(cid:208)(cid:221)(cid:225)(cid:212)(cid:206)(cid:208)(cid:222)(cid:3) 
(cid:223)(cid:211)(cid:208)(cid:228)(cid:3)(cid:219)(cid:221)(cid:218)(cid:225)(cid:212)(cid:207)(cid:208)(cid:17)(cid:3)(cid:190)(cid:212)(cid:217)(cid:224)(cid:223)(cid:208)(cid:180)(cid:215)(cid:212)(cid:217)(cid:212)(cid:206)(cid:3)(cid:212)(cid:222)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:242)(cid:221)(cid:222)(cid:223)(cid:3)
and only retail clinic to receive this  
(cid:208)(cid:215)(cid:212)(cid:223)(cid:208)(cid:3)(cid:207)(cid:208)(cid:222)(cid:212)(cid:210)(cid:217)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:17)(cid:3)

(cid:195)(cid:208)(cid:223)(cid:204)(cid:212)(cid:215)(cid:3)(cid:209)(cid:221)(cid:218)(cid:217)(cid:223)(cid:3)(cid:222)(cid:223)(cid:218)(cid:221)(cid:208)(cid:3)(cid:221)(cid:208)(cid:225)(cid:208)(cid:217)(cid:224)(cid:208)(cid:222)(cid:3)(cid:221)(cid:218)(cid:222)(cid:208)(cid:3)(cid:205)(cid:228)(cid:3)(cid:95)(cid:17)(cid:103)(cid:3)
percent and gross margins expanded 
primarily due to increases in health and 
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(cid:218)(cid:209)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)(cid:219)(cid:208)(cid:221)(cid:222)(cid:218)(cid:217)(cid:204)(cid:215)(cid:212)(cid:229)(cid:204)(cid:223)(cid:212)(cid:218)(cid:217)(cid:3)(cid:222)(cid:223)(cid:221)(cid:204)(cid:223)(cid:208)(cid:210)(cid:212)(cid:208)(cid:222)(cid:17)(cid:3)(cid:197)(cid:211)(cid:208)(cid:3)
ExtraCare® loyalty program continues 
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helping us understand and anticipate 
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(cid:204)(cid:217)(cid:207)(cid:3)(cid:208)(cid:217)(cid:204)(cid:205)(cid:215)(cid:212)(cid:217)(cid:210)(cid:3)(cid:224)(cid:222)(cid:3)(cid:223)(cid:218)(cid:3)(cid:219)(cid:208)(cid:221)(cid:222)(cid:218)(cid:217)(cid:204)(cid:215)(cid:212)(cid:229)(cid:208)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)
(cid:218)(cid:224)(cid:223)(cid:221)(cid:208)(cid:204)(cid:206)(cid:211)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:222)(cid:204)(cid:225)(cid:212)(cid:217)(cid:210)(cid:222)(cid:3)(cid:218)(cid:219)(cid:219)(cid:218)(cid:221)(cid:223)(cid:224)(cid:217)(cid:212)(cid:223)(cid:212)(cid:208)(cid:222)(cid:17)

Dow Jones and CDP acknowledge our 
corporate social responsibility (CSR) 
performance in key industry rankings

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(cid:212)(cid:217)(cid:3)(cid:206)(cid:218)(cid:221)(cid:219)(cid:218)(cid:221)(cid:204)(cid:223)(cid:208)(cid:3)(cid:222)(cid:218)(cid:206)(cid:212)(cid:204)(cid:215)(cid:3)(cid:221)(cid:208)(cid:222)(cid:219)(cid:218)(cid:217)(cid:222)(cid:212)(cid:205)(cid:212)(cid:215)(cid:212)(cid:223)(cid:228)(cid:17)(cid:3)(cid:186)(cid:217)(cid:3)
2019, we earned a place on the Dow 
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seventh consecutive year, as well as 
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(cid:186)(cid:217)(cid:207)(cid:208)(cid:227)(cid:3)(cid:209)(cid:218)(cid:221)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:242)(cid:221)(cid:222)(cid:223)(cid:3)(cid:223)(cid:212)(cid:216)(cid:208)(cid:17)(cid:3)(cid:197)(cid:211)(cid:212)(cid:222)(cid:3)(cid:208)(cid:227)(cid:206)(cid:215)(cid:224)(cid:222)(cid:212)(cid:225)(cid:208)(cid:3)
(cid:215)(cid:212)(cid:222)(cid:223)(cid:3)(cid:212)(cid:217)(cid:206)(cid:215)(cid:224)(cid:207)(cid:208)(cid:222)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:223)(cid:218)(cid:219)(cid:3)(cid:95)(cid:94)(cid:3)(cid:219)(cid:208)(cid:221)(cid:206)(cid:208)(cid:217)(cid:223)(cid:3)(cid:218)(cid:209)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)
(cid:215)(cid:204)(cid:221)(cid:210)(cid:208)(cid:222)(cid:223)(cid:3)(cid:96)(cid:19)(cid:99)(cid:94)(cid:94)(cid:3)(cid:206)(cid:218)(cid:216)(cid:219)(cid:204)(cid:217)(cid:212)(cid:208)(cid:222)(cid:3)(cid:212)(cid:217)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:196)(cid:25)(cid:193)(cid:3)
(cid:184)(cid:215)(cid:218)(cid:205)(cid:204)(cid:215)(cid:3)(cid:179)(cid:221)(cid:218)(cid:204)(cid:207)(cid:3)(cid:190)(cid:204)(cid:221)(cid:214)(cid:208)(cid:223)(cid:3)(cid:186)(cid:217)(cid:207)(cid:208)(cid:227)(cid:3)(cid:205)(cid:204)(cid:222)(cid:208)(cid:207)(cid:3)(cid:218)(cid:217)(cid:3)
economic, environmental and social 
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(cid:204)(cid:206)(cid:223)(cid:212)(cid:225)(cid:212)(cid:223)(cid:212)(cid:208)(cid:222)(cid:3)(cid:218)(cid:225)(cid:208)(cid:221)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:217)(cid:208)(cid:227)(cid:223)(cid:3)(cid:207)(cid:208)(cid:206)(cid:204)(cid:207)(cid:208)(cid:17)(cid:3)(cid:186)(cid:3)(cid:204)(cid:215)(cid:222)(cid:218)(cid:3)
encourage you to read the CVS Health 
2019 Corporate Social Responsibility 
Report(cid:19)(cid:3)(cid:226)(cid:211)(cid:212)(cid:206)(cid:211)(cid:3)(cid:212)(cid:222)(cid:3)(cid:204)(cid:225)(cid:204)(cid:212)(cid:215)(cid:204)(cid:205)(cid:215)(cid:208)(cid:3)(cid:218)(cid:217)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)
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 “A” score 

on the CDP Climate 
Change Survey

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(cid:200)(cid:208)(cid:3)(cid:205)(cid:208)(cid:215)(cid:212)(cid:208)(cid:225)(cid:208)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)(cid:204)(cid:205)(cid:212)(cid:215)(cid:212)(cid:223)(cid:228)(cid:3)(cid:223)(cid:218)(cid:3)(cid:207)(cid:221)(cid:212)(cid:225)(cid:208)(cid:3)(cid:211)(cid:212)(cid:210)(cid:211)(cid:208)(cid:221)(cid:3)
engagement, reduce costs and create 
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accelerate our revenue and earnings 
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(cid:207)(cid:208)(cid:215)(cid:212)(cid:225)(cid:208)(cid:221)(cid:208)(cid:207)(cid:3)(cid:223)(cid:218)(cid:3)(cid:216)(cid:212)(cid:215)(cid:215)(cid:212)(cid:218)(cid:217)(cid:222)(cid:3)(cid:218)(cid:209)(cid:3)(cid:178)(cid:216)(cid:208)(cid:221)(cid:212)(cid:206)(cid:204)(cid:217)(cid:222)(cid:3)(cid:207)(cid:204)(cid:212)(cid:215)(cid:228)(cid:17)

Sincerely,
Sincerely,

(cid:189)(cid:204)(cid:221)(cid:221)(cid:228)(cid:3)(cid:187)(cid:17)(cid:3)(cid:190)(cid:208)(cid:221)(cid:215)(cid:218) 
(cid:193)(cid:221)(cid:208)(cid:222)(cid:212)(cid:207)(cid:208)(cid:217)(cid:223)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:180)(cid:211)(cid:212)(cid:208)(cid:209)(cid:3)(cid:182)(cid:227)(cid:208)(cid:206)(cid:224)(cid:223)(cid:212)(cid:225)(cid:208)(cid:3)(cid:192)(cid:244)(cid:206)(cid:208)(cid:221)

(cid:178)(cid:219)(cid:221)(cid:212)(cid:215)(cid:3)(cid:97)(cid:19)(cid:3)(cid:96)(cid:94)(cid:96)(cid:94)

(cid:96)(cid:94)(cid:95)(cid:103)(cid:3)(cid:178)(cid:217)(cid:217)(cid:224)(cid:204)(cid:215)(cid:3)(cid:195)(cid:208)(cid:219)(cid:218)(cid:221)(cid:223)

7

 
 
 
 
 
Transform Health 2030
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(cid:223)(cid:204)(cid:214)(cid:208)(cid:217)(cid:3)(cid:222)(cid:223)(cid:208)(cid:219)(cid:222)(cid:3)(cid:223)(cid:218)(cid:3)(cid:221)(cid:208)(cid:242)(cid:217)(cid:208)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:208)(cid:227)(cid:223)(cid:208)(cid:217)(cid:207)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)(cid:180)(cid:196)(cid:195)(cid:3)(cid:222)(cid:223)(cid:221)(cid:204)(cid:223)(cid:208)(cid:210)(cid:228)(cid:3)(cid:218)(cid:225)(cid:208)(cid:221)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:217)(cid:208)(cid:227)(cid:223)(cid:3)(cid:207)(cid:208)(cid:206)(cid:204)(cid:207)(cid:208)(cid:17)(cid:3)

(cid:192)(cid:224)(cid:221)(cid:3)(cid:217)(cid:208)(cid:226)(cid:3)(cid:180)(cid:196)(cid:195)(cid:3)(cid:222)(cid:223)(cid:221)(cid:204)(cid:223)(cid:208)(cid:210)(cid:228)(cid:19)(cid:3)(cid:197)(cid:221)(cid:204)(cid:217)(cid:222)(cid:209)(cid:218)(cid:221)(cid:216)(cid:3)(cid:185)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:3)(cid:96)(cid:94)(cid:97)(cid:94)(cid:19)(cid:3)(cid:212)(cid:222)(cid:3)(cid:210)(cid:221)(cid:218)(cid:224)(cid:217)(cid:207)(cid:208)(cid:207)(cid:3)(cid:212)(cid:217)(cid:3)(cid:209)(cid:218)(cid:224)(cid:221)(cid:3)(cid:219)(cid:212)(cid:215)(cid:215)(cid:204)(cid:221)(cid:222)(cid:18)(cid:3)(cid:185)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:228)(cid:3)(cid:193)(cid:208)(cid:218)(cid:219)(cid:215)(cid:208)(cid:19)(cid:3)(cid:185)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:228)(cid:3)(cid:179)(cid:224)(cid:222)(cid:212)(cid:217)(cid:208)(cid:222)(cid:222)(cid:19)(cid:3)
(cid:185)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:228)(cid:3)(cid:180)(cid:218)(cid:216)(cid:216)(cid:224)(cid:217)(cid:212)(cid:223)(cid:228)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:185)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:228)(cid:3)(cid:193)(cid:215)(cid:204)(cid:217)(cid:208)(cid:223)(cid:17)(cid:3)(cid:186)(cid:223)(cid:3)(cid:206)(cid:218)(cid:217)(cid:225)(cid:208)(cid:228)(cid:222)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)(cid:216)(cid:212)(cid:222)(cid:222)(cid:212)(cid:218)(cid:217)(cid:3)(cid:223)(cid:218)(cid:3)(cid:224)(cid:222)(cid:208)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)(cid:222)(cid:206)(cid:204)(cid:215)(cid:208)(cid:19)(cid:3)(cid:208)(cid:227)(cid:219)(cid:208)(cid:221)(cid:223)(cid:212)(cid:222)(cid:208)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:212)(cid:217)(cid:217)(cid:218)(cid:225)(cid:204)(cid:223)(cid:212)(cid:225)(cid:208)(cid:3) 
(cid:222)(cid:219)(cid:212)(cid:221)(cid:212)(cid:223)(cid:3)(cid:223)(cid:218)(cid:3)(cid:223)(cid:221)(cid:204)(cid:217)(cid:222)(cid:209)(cid:218)(cid:221)(cid:216)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:211)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:3)(cid:206)(cid:204)(cid:221)(cid:208)(cid:3)(cid:208)(cid:227)(cid:219)(cid:208)(cid:221)(cid:212)(cid:208)(cid:217)(cid:206)(cid:208)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:212)(cid:217)(cid:225)(cid:208)(cid:222)(cid:223)(cid:3)(cid:212)(cid:217)(cid:3)(cid:206)(cid:218)(cid:216)(cid:216)(cid:224)(cid:217)(cid:212)(cid:223)(cid:228)(cid:3)(cid:211)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:3)(cid:204)(cid:223)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:215)(cid:218)(cid:206)(cid:204)(cid:215)(cid:3)(cid:215)(cid:208)(cid:225)(cid:208)(cid:215)(cid:17)(cid:3)(cid:189)(cid:208)(cid:204)(cid:221)(cid:217)(cid:3)(cid:216)(cid:218)(cid:221)(cid:208)(cid:3)(cid:204)(cid:223)(cid:3)
(cid:180)(cid:199)(cid:196)(cid:185)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:17)(cid:206)(cid:218)(cid:216)(cid:42)(cid:180)(cid:196)(cid:195)(cid:3)(cid:204)(cid:217)(cid:207)(cid:3)(cid:205)(cid:228)(cid:3)(cid:207)(cid:218)(cid:226)(cid:217)(cid:215)(cid:218)(cid:204)(cid:207)(cid:212)(cid:217)(cid:210)(cid:3)(cid:218)(cid:224)(cid:221)(cid:3)(cid:180)(cid:199)(cid:196)(cid:3)(cid:185)(cid:208)(cid:204)(cid:215)(cid:223)(cid:211)(cid:3)(cid:96)(cid:94)(cid:95)(cid:103)(cid:3)(cid:180)(cid:218)(cid:221)(cid:219)(cid:218)(cid:221)(cid:204)(cid:223)(cid:208)(cid:3)(cid:196)(cid:218)(cid:206)(cid:212)(cid:204)(cid:215)(cid:3)(cid:195)(cid:208)(cid:222)(cid:219)(cid:218)(cid:217)(cid:222)(cid:212)(cid:205)(cid:212)(cid:215)(cid:212)(cid:223)(cid:228)(cid:3)(cid:195)(cid:208)(cid:219)(cid:218)(cid:221)(cid:223)(cid:17)

(cid:190)(cid:218)(cid:221)(cid:208)(cid:3)(cid:223)(cid:211)(cid:204)(cid:217)(cid:3)
(cid:97)(cid:94)(cid:19)(cid:94)(cid:94)(cid:94)(cid:3)

(cid:190)(cid:212)(cid:217)(cid:224)(cid:223)(cid:208)(cid:180)(cid:215)(cid:212)(cid:217)(cid:212)(cid:206)(cid:3)(cid:199)(cid:212)(cid:221)(cid:223)(cid:224)(cid:204)(cid:215)(cid:3)
Care health visits

Nearly 
(cid:97)(cid:19)(cid:94)(cid:94)(cid:94)(cid:3)

safe medication 
disposal sites in 
communities across 
the country

(cid:190)(cid:218)(cid:221)(cid:208)(cid:3)(cid:223)(cid:211)(cid:204)(cid:217)(cid:3)
(cid:96)(cid:97)(cid:19)(cid:94)(cid:94)(cid:94)(cid:3)

colleagues in 
colleague resource 
(cid:210)(cid:221)(cid:218)(cid:224)(cid:219)(cid:222)(cid:3)(cid:40)(cid:180)(cid:195)(cid:184)(cid:222)(cid:41)(cid:3)

Approximately 
$5.6 billion 

in economic impact 
from our Supplier 
(cid:181)(cid:212)(cid:225)(cid:208)(cid:221)(cid:222)(cid:212)(cid:223)(cid:228)(cid:3)(cid:219)(cid:221)(cid:218)(cid:210)(cid:221)(cid:204)(cid:216)

Healthy  
People

Healthy  
Business

Transform
Health

Healthy  
Planet

Healthy 
Community

Nearly 
(cid:96)(cid:99)(cid:19)(cid:94)(cid:94)(cid:94)(cid:3)

military members, 
veterans and  
their spouses hired  
(cid:222)(cid:212)(cid:217)(cid:206)(cid:208)(cid:3)(cid:96)(cid:94)(cid:95)(cid:99)

(cid:190)(cid:218)(cid:221)(cid:208)(cid:3)(cid:223)(cid:211)(cid:204)(cid:217)(cid:3)
$150 million

donated through cash, 
philanthropic and 
in-kind investments 
and colleague 
volunteerism

Named to 
CDP (cid:178)(cid:3)(cid:189)(cid:212)(cid:222)(cid:223)(cid:19)(cid:3)

one of only 34 U.S.-
based companies to 
be honored with this 
recognition for climate 
change leadership 

(cid:190)(cid:218)(cid:221)(cid:208)(cid:3)(cid:223)(cid:211)(cid:204)(cid:217)(cid:3)
$12 million

worth of colleague 
volunteer time  
across the Enterprise

Approximately 
$6.4 million 

of free medical 
services provided  
by Project Health

$50 million 

(cid:212)(cid:217)(cid:225)(cid:208)(cid:222)(cid:223)(cid:208)(cid:207)(cid:3)(cid:212)(cid:217)(cid:3)(cid:204)(cid:241)(cid:218)(cid:221)(cid:207)(cid:204)(cid:205)(cid:215)(cid:208)(cid:3)
housing to support 
at-risk populations 
through our work 
to address social 
determinants of health

7th 

consecutive year 
(cid:218)(cid:217)(cid:3)(cid:223)(cid:211)(cid:208)(cid:3)(cid:181)(cid:218)(cid:226)(cid:3)(cid:187)(cid:218)(cid:217)(cid:208)(cid:222)(cid:3)
(cid:196)(cid:224)(cid:222)(cid:223)(cid:204)(cid:212)(cid:217)(cid:204)(cid:205)(cid:212)(cid:215)(cid:212)(cid:223)(cid:228)(cid:3)(cid:186)(cid:217)(cid:207)(cid:208)(cid:227)(cid:3)
and debuted on the 
(cid:200)(cid:218)(cid:221)(cid:215)(cid:207)(cid:3)(cid:186)(cid:217)(cid:207)(cid:208)(cid:227)(cid:3)(cid:212)(cid:217)(cid:3)(cid:96)(cid:94)(cid:95)(cid:103)(cid:3)

(cid:190)(cid:218)(cid:221)(cid:208)(cid:3)(cid:223)(cid:211)(cid:204)(cid:217)(cid:3)
1.6 million 

empty miles saved 
(cid:212)(cid:217)(cid:3)(cid:96)(cid:94)(cid:95)(cid:103)(cid:3)(cid:223)(cid:211)(cid:221)(cid:218)(cid:224)(cid:210)(cid:211)(cid:3)
backhaul program 

8

CVS Health

UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 10-K 

(Mark One)

ANNUAL REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the fiscal year ended December 31, 2019 
or

TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the transition period from _________ to_________
Commission file number: 001-01011 

CVS HEALTH CORPORATION 
(Exact name of registrant as specified in its charter)

Delaware
(State or other jurisdiction of incorporation or organization)

05-0494040
(I.R.S. Employer Identification No.)

One CVS Drive, Woonsocket, Rhode Island
(Address of principal executive offices)

Registrant’s telephone number, including area code:

Securities registered pursuant to Section 12(b) of the Act:

02895
(Zip Code)

(401) 765-1500

Title of each class

Trading Symbol(s)

Name of each exchange on which registered

Common Stock, par value $0.01 per share

CVS

New York Stock Exchange

Securities registered pursuant to Section 12(g) of the Act:

None

Indicate by check mark if the registrant is a well-known seasoned issuer, as defined in Rule 405 of the Securities Act.

Indicate by check mark if the registrant is not required to file reports pursuant to Section 13 or Section 15(d) of the Act.

Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the
Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to
file such reports), and (2) has been subject to such filing requirements for the past 90 days.

Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted
pursuant to Rule 405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorter period
that the registrant was required to submit such files).

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller
reporting company, or an emerging growth company.  See the definitions of “large accelerated filer,” “accelerated filer,”
“smaller reporting company,” and “emerging growth company” in Rule 12b-2 of the Exchange Act.

Yes

Yes

No

No

Yes

No

Yes

No

Large accelerated filer
Non-accelerated filer

Accelerated filer

Smaller reporting company

Emerging growth company
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying
with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.

Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Act).

Yes

No

The aggregate market value of the registrant’s common stock held by non-affiliates was approximately $70,617,679,934 as of June 28, 2019, based 
on the closing price of the common stock on the New York Stock Exchange. For purposes of this calculation, only executive officers and directors 
are deemed to be affiliates of the registrant.

As of February 12, 2020, the registrant had 1,304,159,680 shares of common stock outstanding.

DOCUMENTS INCORPORATED BY REFERENCE

The following materials are incorporated by reference into this Form 10-K:

Information contained in the definitive proxy statement for CVS Health Corporation’s 2020 Annual Meeting of Stockholders, to be filed with 
the Securities and Exchange Commission within 120 days after the end of the fiscal year ended December 31, 2019 (the “Proxy Statement”), 
is incorporated by reference in Parts III and IV to the extent described therein.

TABLE OF CONTENTS

Part I

Item 1:

Business

Item 1A:

Risk Factors

Item 1B:

Unresolved Staff Comments

Item 2:

Item 3:

Item 4:

Part II

Item 5:

Item 6:

Item 7:

Properties

Legal Proceedings

Mine Safety Disclosures

Information about our Executive Officers

Market for Registrant’s Common Equity, Related Stockholder Matters and Issuer Purchases of Equity 
Securities
Selected Financial Data

Management’s Discussion and Analysis of Financial Condition and Results of Operations

Item 7A:

Quantitative and Qualitative Disclosures About Market Risk

Item 8:

Item 9:

Financial Statements and Supplementary Data

Changes in and Disagreements With Accountants on Accounting and Financial Disclosure

Item 9A:

Controls and Procedures

Item 9B:

Other Information

Part III

Item 10:

Item 11:

Item 12:

Item 13:

Item 14:

Part IV

Item 15:

Item 16:

Directors, Executive Officers and Corporate Governance

Executive Compensation

Security Ownership of Certain Beneficial Owners and Management and Related Stockholder Matters

Certain Relationships and Related Transactions, and Director Independence

Principal Accountant Fees and Services

Exhibits and Financial Statement Schedules

Form 10-K Summary

Signatures

Page

2

29

52

52

52

53

54

55

57

58

87

90

170

170

171

171

171

171

172

172

173

177

178

Unless the context otherwise requires, references to the terms “we,” “our” or “us” used throughout this Annual Report on Form 
10-K (this “10-K”) refer to CVS Health Corporation (a Delaware corporation) (“CVS Health”) and its subsidiaries (collectively,
the “Company”). References to competitors and other companies throughout this 10-K, including the information incorporated
herein by reference, are for illustrative or comparison purposes only and do not indicate that these companies are the
Company’s or any segment’s only competitors or closest competitors.

CAUTIONARY STATEMENT CONCERNING FORWARD-LOOKING STATEMENTS

The Private Securities Litigation Reform Act of 1995 (the “Reform Act”) provides a “safe harbor” for forward-looking 
statements, so long as (1) those statements are identified as forward-looking, and (2) the statements are accompanied by 
meaningful cautionary statements that identify important factors that could cause actual results to differ materially from those 
discussed in the statement. We want to take advantage of these safe harbor provisions.

Certain information contained in this 10-K is forward-looking within the meaning of the Reform Act or SEC rules. This 
information includes, but is not limited to: “Outlook for 2020” of Management’s Discussion and Analysis of Financial 
Condition and Results of Operations (“MD&A”) included in Item 7, “Quantitative and Qualitative Disclosures About Market 
Risk” included in Item 7A, “Government Regulation” included in Item 1, and “Risk Factors” included in Item 1A. In addition, 
throughout this 10-K and our other reports and communications, we use the following words or variations or negatives of these 
words and similar expressions when we intend to identify forward-looking statements:

· Anticipates
· Estimates
· Guidance
· Outlook
· Projects

· Believes
· Evaluate
· Intends
· Plans
· Seeks

· Can
· Expects
· Likely
· Potential
· Should

· Continue
· Explore
· May
· Predict
· View

· Could
· Forecast
· Might
· Probable
· Will

All statements addressing the future operating performance of CVS Health or any segment or any subsidiary and/or future 
events or developments, including statements relating to corporate strategy; revenue or adjusted revenue; operating income or 
adjusted operating income; earnings per share or adjusted earnings per share; Pharmacy Services segment business, sales 
results and/or trends and/or operations; Retail/LTC segment business, sales results and/or trends and/or operations; Health 
Care Benefits segment business, sales results and/or trends, medical cost trends, medical membership, Medicare Part D 
membership, medical benefit ratios and/or operations; incremental investment spending; interest expense; effective tax rate; 
weighted-average share count; cash flow from operations; net capital expenditures; cash available for debt repayment; 
integration synergies; net synergies; integration costs; enterprise modernization; transformation; leverage ratio; cash 
available for enhancing shareholder value; inventory reduction, turn rate and/or loss rate; debt ratings; the Company’s ability 
to attract or retain customers and clients; store development and/or relocations; new product development; and the impact of 
industry and regulatory developments, as well as statements expressing optimism or pessimism about future operating results or 
events, are forward-looking statements within the meaning of the Reform Act.

Forward-looking statements rely on a number of estimates, assumptions and projections concerning future events, and are 
subject to a number of significant risks and uncertainties and other factors that could cause actual results to differ materially 
from those statements. Many of these risks and uncertainties and other factors are outside our control. Certain of these risks 
and uncertainties and other factors are described under “Risk Factors” included in Item 1A of this 10-K; these are not the only 
risks and uncertainties we face. There can be no assurance that the Company has identified all the risks that affect it. 
Additional risks and uncertainties not presently known to the Company or that the Company currently believes to be immaterial 
also may adversely affect the Company’s businesses. If any of those risks or uncertainties develops into actual events, these 
events or circumstances could have a material adverse effect on the Company’s businesses, operating results, cash flows, 
financial condition and/or stock price, among other effects. 

You should not put undue reliance on forward-looking statements. Any forward-looking statement speaks only as of the date of 
this 10-K, and we disclaim any intention or obligation to update or revise forward-looking statements, whether as a result of 
new information, future events, uncertainties or otherwise.

1

Item 1.  Business.

Overview

PART I

CVS Health Corporation (“CVS Health”), together with its subsidiaries (collectively, the “Company,” “we,” “our” or “us”), is 
the nation’s premier health innovation company helping people on their path to better health. Whether in one of its pharmacies 
or through its health services and plans, CVS Health is pioneering a bold new approach to total health by making quality care 
more affordable, accessible, simple and seamless. CVS Health is community-based and locally focused, engaging consumers 
with the care they need when and where they need it. The Company has approximately 9,900 retail locations, approximately 
1,100 walk-in medical clinics, a leading pharmacy benefits manager with approximately 105 million plan members, a dedicated 
senior pharmacy care business serving more than one million patients per year and expanding specialty pharmacy services. 
CVS Health also serves an estimated 37 million people through traditional, voluntary and consumer-directed health insurance 
products and related services, including expanding Medicare Advantage offerings and a leading standalone Medicare Part D 
prescription drug plan (“PDP”). The Company believes its innovative health care model increases access to quality care, 
delivers better health outcomes and lowers overall health care costs.

On November 28, 2018 (the “Aetna Acquisition Date”), the Company acquired Aetna Inc. (“Aetna”) for a combination of cash 
and CVS Health stock (the “Aetna Acquisition”). The Company acquired Aetna to help improve the consumer health care 
experience by combining Aetna’s health care benefits products and services with CVS Health’s retail locations, walk-in medical 
clinics and integrated pharmacy capabilities with the goal of becoming the new, trusted front door to health care. Under the 
terms of the merger agreement, Aetna shareholders received $145.00 in cash and 0.8378 CVS Health shares for each Aetna 
share. The transaction valued Aetna at approximately $212 per share or approximately $70 billion. Including the assumption of 
Aetna’s debt, the total value of the transaction was approximately $78 billion. The Company financed the cash portion of the 
purchase price through a combination of cash on hand and by issuing approximately $45 billion of new debt, including senior 
notes and term loans. For additional information, see Note 2 ‘‘Acquisitions and Divestitures’’ included in Item 8 of this 10-K.

On October 10, 2018, the Company and Aetna entered into a consent decree with the U.S. Department of Justice (the “DOJ”) 
that allowed the Company’s proposed acquisition of Aetna to proceed, provided Aetna agreed to sell its individual standalone 
PDPs. As part of the agreement reached with the DOJ, Aetna entered into a purchase agreement with a subsidiary of WellCare 
Health Plans, Inc. (“WellCare”) for the divestiture of Aetna’s standalone PDPs effective December 31, 2018. On November 30, 
2018, the Company completed the sale of Aetna’s standalone PDPs. The Company provided administrative services to, and 
retained the financial results of, the divested plans through 2019. Subsequent to 2019, the Company will no longer retain the 
financial results of the divested plans. Aetna’s standalone PDPs had an aggregate of 2.5 million members as of December 31, 
2019.  

As a result of the Aetna Acquisition, the Company added the Health Care Benefits segment. Certain aspects of Aetna’s 
operations, including products for which the Company no longer solicits or accepts new customers, such as large case pensions 
and long-term care insurance products, are included in the Company’s Corporate/Other segment. 

Effective for the first quarter of 2019, the Company realigned the composition of its segments to correspond with changes to its 
operating model and reflect how its Chief Operating Decision Maker reviews information and manages the business. As a result 
of this realignment, the Company’s SilverScript® PDP moved from the Pharmacy Services segment to the Health Care Benefits 
segment. In addition, the Company moved Aetna’s mail order and specialty pharmacy operations from the Health Care Benefits 
segment to the Pharmacy Services segment. Segment financial information has been retrospectively adjusted to reflect these 
changes. See Note 17 ‘‘Segment Reporting’’ included in Item 8 of this 10-K for segment financial information.

The Company has four reportable segments: Pharmacy Services, Retail/LTC, Health Care Benefits and Corporate/Other.

Business Strategy

CVS Health’s purpose of helping people on their path to better health guides the Company’s approach to transforming the 
consumer health experience. The Company is working to create the most consumer-centric health company by being consumer 
obsessed and pursuing its three strategic goals: be local, make it simple and improve health. These goals are embedded in the 
Company’s four Enterprise priorities: growing and differentiating our businesses, delivering transformational products and 
services, creating a consumer-centric technology infrastructure and modernizing Enterprise functions and capabilities. The 

2

Company believes its strategy of putting the consumer at the center of care will drive long-term sustainable value and place the 
Company at the forefront of the evolution of health care.

Pharmacy Services Segment

The Pharmacy Services segment provides a full range of pharmacy benefit management (“PBM”) solutions, including plan 
design offerings and administration, formulary management, retail pharmacy network management services, mail order 
pharmacy, specialty pharmacy and infusion services, clinical services, disease management services and medical spend 
management. The Pharmacy Services segment’s clients are primarily employers, insurance companies, unions, government 
employee groups, health plans, PDPs, Medicaid managed care (“Managed Medicaid”) plans, plans offered on public health 
insurance exchanges (“Public Exchanges”) and private health insurance exchanges (“Private Exchanges” and together with 
Public Exchanges, “Insurance Exchanges”), other sponsors of health benefit plans and individuals throughout the U.S. The 
Pharmacy Services segment includes retail specialty pharmacy stores, specialty mail order pharmacies, mail order dispensing 
pharmacies, compounding pharmacies and branches for infusion and enteral nutrition services. During the year ended 
December 31, 2019, the Company’s PBM filled or managed 2.0 billion prescriptions on a 30-day equivalent basis.

PBM Services 

The Company dispenses prescription drugs directly through its mail order dispensing and specialty mail order pharmacies and 
through pharmacies in its retail network. All prescriptions processed by the Company are analyzed, processed and documented 
by the Company’s proprietary prescription management systems. These systems provide essential features and functionality to 
allow plan members to utilize their prescription drug benefits. These systems also streamline the process by which prescriptions 
are processed by staff and network pharmacists by enhancing review of various items through automation, including plan 
eligibility, early refills, duplicate dispensing, appropriateness of dosage, drug interactions or allergies, over-utilization and 
potential fraud.

Plan Design Offerings and Administration
The Company administers pharmacy benefit plans for clients who contract with it to facilitate prescription drug coverage and 
claims processing for their eligible plan members. The Company assists its PBM clients in designing pharmacy benefit plans 
that help improve health outcomes while minimizing the costs to the client. The Company also assists PBM clients in 
monitoring the effectiveness of their plans through frequent, informal communications, the use of proprietary software, as well 
as through formal annual, quarterly and sometimes monthly performance reviews.

The Company makes recommendations to help PBM clients design benefit plans that promote the use of lower cost, clinically 
appropriate drugs and helps its PBM clients control costs by recommending plan designs that encourage the use of generic 
equivalents of brand name drugs when such equivalents are available. Clients also have the option, through plan design, to 
further lower their pharmacy benefit plan costs by setting different member payment levels for different products on their drug 
lists or “formularies,” which helps guide members to choose lower cost alternatives through appropriate financial incentives.

Formulary Management
The Company utilizes an independent panel of doctors, pharmacists and other medical experts, referred to as the CVS 
Caremark National Pharmacy and Therapeutics Committee, to review and approve the selection of drugs that meet the 
Company’s standards of safety and efficacy for inclusion on one of the Company’s template formularies. The Company’s 
formularies provide recommended products in numerous drug classes to help ensure member access to clinically appropriate 
drugs with alternatives within a class under the client’s pharmacy benefit plan, while helping to drive the lowest net cost for 
clients that select one of the Company’s formularies. To help improve clinical outcomes for members and clients, the Company 
conducts ongoing, independent reviews of all drugs, including those appearing on the formularies and generic equivalent 
products. Many of the Company’s clients choose to adopt a template formulary offering as part of their plan design. Beginning 
in 2018, PBM clients were given new capabilities to offer real time benefits information for a member’s specific plan design, 
provided digitally at the point of prescribing, at the pharmacy and directly to members.

Retail Pharmacy Network Management Services
The Company maintains a national network of more than 68,000 retail pharmacies, consisting of approximately 41,000 chain 
pharmacies (which includes CVS Pharmacy locations) and approximately 27,000 independent pharmacies, in the United States, 
including Puerto Rico, the District of Columbia, Guam and the U.S. Virgin Islands. When a customer fills a prescription in a 
retail pharmacy, the pharmacy sends prescription data electronically to the Company from the point-of-sale. This data interfaces 
with the Company’s proprietary prescription management systems, which verify relevant plan member data and eligibility, 
while also performing a drug utilization review to help evaluate clinical appropriateness and safety and confirming that the 

3

pharmacy will receive payment for the prescription. The Company also offers a Performance program for non-Medicare 
customers. The Performance program may be applied to any network. It can be implemented with either the Company’s broad, 
national network or with a managed network (as allowed by applicable laws and regulations). Under the program, high 
performing pharmacies are eligible to receive an incremental positive performance payment. The program aligns with key 
Healthcare Effectiveness Data Information Set measures and is funded by client fees.  

Mail Order Pharmacy Services
The Pharmacy Services segment operates mail order dispensing pharmacies in the United States. Plan members or their 
prescribers submit prescriptions or refill requests, primarily for maintenance medications, to these pharmacies, and staff 
pharmacists review these prescriptions and refill requests with the assistance of the Company’s prescription management 
systems. This review may involve communications with the prescriber and, with the prescriber’s approval when required, can 
result in generic substitution, therapeutic interchange or other actions designed to help reduce cost and/or improve quality of 
treatment. The Company’s mail order dispensing pharmacies have been awarded Mail Service Pharmacy accreditation from 
URAC, a health care accrediting organization that establishes quality standards for the health care industry.

Specialty Pharmacy and Infusion Services
The Pharmacy Services segment operates specialty mail order pharmacies, retail specialty pharmacy stores and branches for 
infusion and enteral nutrition services in the United States. These specialty mail order pharmacies are used for delivery of 
advanced medications to individuals with chronic or genetic diseases and disorders. The Company’s specialty mail order 
pharmacies also have been awarded Specialty Pharmacy accreditation from URAC. Substantially all of the Company’s 
specialty mail order pharmacies also have been accredited by the Joint Commission, which is an independent, not-for-profit 
organization that accredits and certifies health care programs and organizations in the United States. 

Clinical Services
The Company offers multiple clinical programs and services to help clients manage overall pharmacy and health care costs in a 
clinically appropriate manner. These programs are primarily designed to promote better health outcomes and to help target 
inappropriate medication utilization and non-adherence to medication, each of which may result in adverse medical events that 
negatively affect member health and client pharmacy and medical spend. These programs include utilization management 
(“UM”), medication management, quality assurance, adherence and counseling programs to complement the client’s plan 
design and clinical strategies. To help address prescription opioid abuse and misuse, the Company introduced an industry-
leading UM approach that limits to seven days the supply of opioids dispensed for certain acute prescriptions for patients who 
are new to therapy, limits the daily dosage of opioids dispensed based on the strength of the opioid and requires the use of 
immediate-release formulations of opioids before extended-release opioids are dispensed. The Company’s Pharmacy Advisor® 
program facilitates pharmacist counseling, both face-to-face and over the telephone, to help participating plan members with 
certain chronic diseases, such as diabetes and cardiovascular conditions, to identify gaps in care, adhere to their prescribed 
medications and manage their health conditions. The Company also has digital connectivity that helps to lower drug costs for 
patients by providing expanded visibility to lower cost alternatives through enhanced analytics and data sharing. 

Disease Management Programs
The Company’s clinical programs and services utilize advanced protocols and offer clients convenience in working with health 
care providers (“providers”) and other third parties. The Company’s utilization management program covers diseases such as 
rheumatoid arthritis, Parkinson’s disease, seizure disorders and multiple sclerosis and is accredited by the National Committee 
for Quality Assurance (“NCQA”), a private, not-for-profit organization that evaluates, accredits and certifies a wide range of 
health care organizations. 

Medical Benefit Management 
The Company’s NovoLogix® online preauthorization tool helps identify and capture cost savings opportunities for specialty 
drugs billed under the medical benefit by identifying outliers to appropriate dosages and costs, and helps to ensure clinically 
appropriate use of specialty drugs.

Pharmacy Services Information Systems

The majority of the Pharmacy Services segment’s clients have migrated to a single claim adjudication platform. This platform 
incorporates architecture that centralizes the data generated from filling mail order prescriptions, adjudicating retail pharmacy 
claims and delivering other solutions to PBM clients. The Health Engagement Engine® technology and proprietary clinical 
algorithms help connect the various parts of the Enterprise and serve an essential role in cost management and health 
improvement. This capability transforms pharmacy data into actionable interventions at key points of care, such as mail and 
specialty pharmacists, to help provide quality care.

4

Pharmacy Services Clients

The Company’s Pharmacy Services clients are primarily employers, insurance companies, unions, government employee 
groups, health plans, Medicare Part D plans, Managed Medicaid plans and plans offered on Insurance Exchanges, other 
sponsors of health benefit plans and individuals located throughout the United States. Pharmaceuticals are provided to eligible 
members in benefit plans maintained by clients and utilize the Company’s information systems, among other things, to help 
perform safety checks, drug interaction screening and identify opportunities for generic substitution. Substantially all of the 
Pharmacy Services segment’s revenues are generated from dispensing and managing prescription drugs to eligible members in 
benefit plans maintained by clients. In 2018 and 2017, revenues from Aetna accounted for approximately 9.8% and 12.3%, 
respectively, of the Company’s consolidated total revenues. On the Aetna Acquisition Date, Aetna became a wholly-owned 
subsidiary of CVS Health. Subsequent to the Aetna Acquisition Date, revenues from Aetna continue to be reported in the 
Pharmacy Services segment; however, these revenues are eliminated in the consolidated financial statements. 

Pharmacy Services Seasonality

The majority of Pharmacy Services segment revenues are not seasonal in nature. 

Pharmacy Services Competition

The Company believes the primary competitive factors in the pharmacy services industry include: (i) the ability to negotiate 
favorable discounts from drug manufacturers as well as to negotiate favorable discounts from, and access to, retail pharmacy 
networks; (ii) the ability to identify and apply effective cost management programs utilizing clinical strategies, including the 
development and utilization of preferred formularies; (iii) the ability to market PBM products and services; (iv) the 
commitment to provide flexible, clinically-oriented services to clients and be responsive to clients’ needs; (v) the quality, scope 
and costs of products and services offered to clients and their members; and (vi) operational excellence in delivering services. 
The Pharmacy Services segment has a significant number of competitors (e.g., the Express Scripts business of Cigna 
Corporation, OptumRx, Prime Therapeutics, MedImpact, Humana and PillPack), offering PBM services, including large, 
national PBM companies, PBMs owned by large national health plans and smaller standalone PBMs. 

Retail/LTC Segment

The Retail/LTC segment sells prescription drugs and a wide assortment of general merchandise, including over-the-counter 
drugs, beauty products, cosmetics and personal care products, provides health care services through its MinuteClinic® walk-in 
medical clinics and conducts long-term care pharmacy (“LTC”) operations, which distribute prescription drugs and provide 
related pharmacy consulting and other ancillary services to chronic care facilities and other care settings. As of December 31, 
2019, the Retail/LTC segment operated approximately 9,900 retail locations, approximately 1,100 MinuteClinic locations as 
well as online retail pharmacy websites, LTC pharmacies and onsite pharmacies. During the year ended December 31, 2019, the 
Retail/LTC segment filled 1.4 billion prescriptions on a 30-day equivalent basis. For the year ended December 31, 2019, the 
Company dispensed approximately 26.6% of the total retail pharmacy prescriptions in the United States.

Retail/LTC Products and Services

A typical retail store sells prescription drugs and a wide assortment of high-quality, nationally advertised brand name and 
proprietary brand merchandise. Front store categories include over-the-counter drugs, beauty products, cosmetics and personal 
care products. LTC operations include distribution of prescription drugs and related consulting and ancillary services. The 
Company purchases merchandise from numerous manufacturers and distributors. The Company believes that competitive 
sources are readily available for substantially all of the products carried in its retail stores and the loss of any one supplier 
would not likely have a material effect on the Retail/LTC segment. The Company’s MinuteClinic locations offer a variety of 
health care services.

5

Retail/LTC revenues by major product group are as follows:

Pharmacy (1)
Front store and other (2)

_____________________________________________

(1)  Pharmacy includes LTC sales and sales in pharmacies within Target Corporation stores.
(2)  “Other” represents less than 5% of the “Front store and other” revenue category.

Percentage of Revenues

2019

2018

2017

76.7%

23.3%

76.4%

23.6%

75.0%

25.0%

100.0%

100.0%

100.0%

Pharmacy 
Pharmacy revenues represented approximately three-fourths of Retail/LTC segment revenues in each of 2019, 2018 and 2017. 
The Company believes that retail pharmacy operations will continue to represent a critical part of the Company’s business due 
to industry demographics, e.g., an aging American population consuming a greater number of prescription drugs, prescription 
drugs being used more often as the first line of defense for managing illness, the introduction of new pharmaceutical products, 
and Medicare Part D growth. The Company believes the retail pharmacy business benefits from investment in both people and 
technology, as well as innovative collaborations with health plans, PBMs and providers. Given the nature of prescriptions, 
consumers want their prescriptions filled accurately by professional pharmacists using the latest tools and technology, and ready 
when promised. Consumers also need medication management programs and better information to help them get the most out 
of their health care dollars. To assist consumers with these needs, the Company has introduced integrated pharmacy health care 
services that provide an earlier, easier and more effective approach to engaging consumers in behaviors that can help lower 
costs, improve health and save lives. 

Front Store
Front store revenues reflect the Company’s strategy of innovating with new and unique products and services, using innovative 
personalized marketing and adjusting the mix of merchandise to match customers’ needs and preferences. A key component of 
the front store strategy is the ExtraCare® card program, which is one of the largest and most successful retail loyalty programs 
in the United States. The ExtraCare program allows the Company to balance marketing efforts so it can reward its best 
customers by providing them with automatic sale prices, customized coupons, ExtraBucks® rewards and other benefits. The 
Company also offers a subscription-based membership program, CarePass®, under which members are entitled to a suite of 
benefits delivered over the course of the subscription period, as well as a promotional reward that can be redeemed for future 
goods and services. The Company continues to launch and enhance new and exclusive brands to create unmatched offerings in 
beauty products and deliver other unique product offerings, including a full range of high-quality CVS Health and other 
proprietary brand products that are only available through CVS stores. The Company currently carries approximately 7,000 
CVS Health and proprietary brand products, which accounted for approximately 22% of front store revenues during 2019. 

MinuteClinic
As of December 31, 2019, the Company operated approximately 1,100 MinuteClinic locations in the United States. The clinics 
are staffed by nurse practitioners and physician assistants who utilize nationally established guidelines to deliver a variety of 
health care services. Payors value these clinics because they provide convenient, high-quality, cost-effective care, in many cases 
offering an attractive alternative to more expensive sites of care. Visits paid for by employers, health insurers or other third 
parties accounted for approximately 92% of MinuteClinic’s total revenues in 2019. MinuteClinic is collaborating with the 
Pharmacy Services and Health Care Benefits segments to help meet the needs of CVS Caremark’s client plan members and the 
Company’s health plan members by offering programs that can improve member health and lower costs. MinuteClinic is now 
affiliated with more than 90 major health systems and continues to build a platform that supports primary care. 

Long-term Care Pharmacy Operations
The Retail/LTC segment provides LTC pharmacy services through the Omnicare® business. Omnicare’s customers consist of 
skilled nursing facilities, assisted living facilities, independent living communities, hospitals, correctional facilities, and other 
health care service providers. The Company provides pharmacy consulting, including monthly patient drug therapy evaluations, 
to assist in compliance with state and federal regulations and provide proprietary clinical and health management programs. It 
also provides pharmaceutical case management services for retirees, employees and dependents who have drug benefits under 
corporate-sponsored health care programs.

Onsite Pharmacies
The Company also operates a limited number of pharmacies located at client sites, which provide certain health plan members 
and customers with a convenient alternative for filling their prescriptions.

6

Retail Store Development

The addition of new retail locations has played, and will continue to play, a key role in the Company’s continued growth and 
success. The Company’s store development program focuses on three areas: entering new service areas, adding stores within 
existing service areas and relocating stores to more convenient sites. During 2019, the Company opened approximately 100 
new retail locations, relocated approximately 25 stores, converted approximately 50 stores into HealthHUB® locations and 
closed approximately 130 locations. HealthHUBs are stores with a redesigned format that provide enhanced services, offer a 
care concierge and focus on health and wellness products. HealthHUBs are designed to meet consumer needs and improve the 
customer experience by providing care that complements physician practices and hospital systems, enabling improved health 
outcomes and reducing overall health care costs. The Company expects to continue HealthHUB conversions through 2021. 
During the last five years, the Company opened approximately 790 new and relocated locations, and acquired approximately 
1,810 locations, including the pharmacies acquired from Target Corporation (“Target”) in 2015. The Company believes that 
continuing to assess the appropriateness of its store base and locate retail stores in more accessible locations are essential 
components of competing effectively in the current health care environment. As a result, the Company believes that its store 
development program is an integral part of its ability to meet the needs of customers and maintain its leadership position in the 
retail pharmacy marketplace given the changing health care landscape. 

Retail/LTC Information Systems

The Company has continued to invest in information systems to enable it to deliver exceptional customer service, enhance 
safety and quality, and expand patient care services while lowering operating costs. The proprietary WeCARE Workflow 
supports pharmacy teams by prioritizing work to meet customer expectations, facilitating prescriber outreach, and seamlessly 
integrating clinical programs. This solution delivers improved efficiency and enhances the customer experience, as well as 
providing a framework to accommodate the evolution of pharmacy practice and the expansion of clinical programs. The Health 
Engagement Engine technology and proprietary clinical algorithms enable the Company to help identify opportunities for 
pharmacists to deliver face-to-face counseling regarding patient health and safety matters, including medication adherence 
issues, gaps in care and management of certain chronic health conditions. The Company’s digital strategy is to empower the 
consumer to navigate their pharmacy experience and manage their condition through integrated online and mobile solutions that 
offer utility and convenience. The Company’s LTC digital technology suite, Omniview®, improves the efficiency of customers’ 
operations with tools that include executive dashboards, pre-admission pricing, electronic ordering of prescription refills, proof-
of-delivery tracking, access to patient profiles, receipt and management of facility bills, and real-time validation of Medicare 
Part D coverage, among other capabilities.

Retail/LTC Customers 

The success of the Retail/LTC segment’s businesses is dependent upon the Company’s ability to establish and maintain 
contractual relationships with pharmacy benefit managers and other payors on acceptable terms. Substantially all of the Retail/
LTC segment’s pharmacy revenues are derived from pharmacy benefit managers, managed care organizations, government 
funded health care programs, commercial employers and other third party payors. No single Retail/LTC payor accounted for 
10% or more of the Company’s consolidated total revenues in 2019, 2018 or 2017.

Retail/LTC Seasonality

The majority of Retail/LTC segment revenues, particularly pharmacy revenues, generally are not seasonal in nature. However, 
front store revenues tend to be higher during the December holiday season. In addition, both pharmacy and front store revenues 
are affected by the timing and severity of the cough, cold and flu season. Uncharacteristic or extreme weather conditions also 
can adversely affect consumer shopping patterns and Retail/LTC revenues, expenses and operating results.

Retail/LTC Competition

The retail pharmacy business is highly competitive. The Company believes that it competes principally on the basis of: (i) store 
location and convenience, (ii) customer service and satisfaction, (iii) product selection and variety, and (iv) price. In the areas it 
serves, the Company competes with other drugstore chains (e.g., Walgreens and Rite Aid), supermarkets, discount retailers 
(e.g., Wal-Mart), independent pharmacies, restrictive pharmacy networks, membership clubs, internet companies, and retail 
health clinics (including urgent care centers), as well as mail order dispensing pharmacies. 

LTC pharmacy services are highly regional or local in nature, and within a given geographic area of operation, highly 
competitive. The Company’s largest LTC pharmacy competitor nationally is PharMerica. The Company also competes with 

7

numerous local and regional institutional pharmacies, pharmacies owned by long-term care facilities and local retail 
pharmacies. Some states have enacted “freedom of choice” or “any willing provider” requirements as part of their state 
Medicaid programs or in separate legislation, which may increase the competition that the Company faces in providing services 
to long-term care facility residents in these states.

Health Care Benefits Segment

The Health Care Benefits segment is one of the nation’s leading diversified health care benefits providers, serving an estimated 
37 million people as of December 31, 2019. The Health Care Benefits segment has the information and resources to help 
members, in consultation with their health care professionals, make more informed decisions about their health care. The Health 
Care Benefits segment offers a broad range of traditional, voluntary and consumer-directed health insurance products and 
related services, including medical, pharmacy, dental and behavioral health plans, medical management capabilities, Medicare 
Advantage and Medicare Supplement plans, PDPs, Medicaid health care management services, workers’ compensation 
administrative services and health information technology (“HIT”) products and services. The Health Care Benefits segment’s 
customers include employer groups, individuals, college students, part-time and hourly workers, health plans, health care 
providers, governmental units, government-sponsored plans, labor groups and expatriates. For periods prior to November 28, 
2018 (the Aetna Acquisition Date), the Health Care Benefits segment was comprised of the Company’s SilverScript PDP 
business. 

Health Care Benefits Products and Services 

The Company refers to insurance products (where it assumes all or a majority of the risk for medical and dental care costs) as 
“Insured” and administrative services contract products (where the plan sponsor assumes all or a majority of the risk of medical 
and dental care costs) as “ASC.” Health Care Benefits products and services consist of the following:

•  Commercial Medical: The Health Care Benefits segment offers point-of-service (“POS”), preferred provider organization 
(“PPO”), health maintenance organization (“HMO”) and indemnity benefit (“Indemnity”) plans. Commercial medical 
products also include health savings accounts (“HSAs”) and consumer-directed health plans that combine traditional POS 
or PPO and/or dental coverage, subject to a deductible, with an accumulating benefit account (which may be funded by the 
plan sponsor and/or the member in the case of HSAs). Principal products and services are targeted specifically to large 
multi-site national, mid-sized and small employers, individual insureds and expatriates. The Company offers medical stop 
loss insurance coverage for certain employers who elect to self-insure their health benefits. Under medical stop loss 
insurance products, the Company assumes risk for costs associated with large individual claims and/or aggregate loss 
experience within an employer’s plan above a pre-set annual threshold.

•  Government Medical: In select geographies, the Health Care Benefits segment offers Medicare Advantage plans, Medicare 
Supplement plans and prescription drug coverage for Medicare beneficiaries; participates in Medicaid and subsidized 
Children’s Health Insurance Programs (“CHIP”); and participates in demonstration projects for members who are eligible 
for both Medicare and Medicaid (“Duals”). These Government Medical products are further described below:

•  Medicare Advantage: Through annual contracts with the U.S. Centers for Medicare & Medicaid Services 

(“CMS”), the Company offers HMO and PPO products for eligible individuals in certain geographic areas through 
the Medicare Advantage program. Members typically receive enhanced benefits over traditional fee-for-service 
Medicare coverage (“Original Medicare”), including reduced cost-sharing for preventive care, vision and other 
services. The Company offered network-based HMO and/or PPO plans in 1,416 counties in 45 states and 
Washington, D.C. in 2019. The Company has expanded to 1,680 counties in 45 states and Washington, D.C. for 
2020. For certain qualifying employer groups, the Company offers Medicare PPO products nationally. When 
combined with the Company’s PDP product, these national PPO plans form an integrated national Insured 
Medicare product for employers that provides medical and pharmacy benefits.

•  Medicare PDP: The Company is a national provider of drug benefits under the Medicare Part D prescription drug 
program. All Medicare eligible individuals are eligible to participate in this voluntary prescription drug plan. 
Members typically receive coverage for certain prescription drugs, usually subject to a deductible, co-insurance 
and/or co-payment. On November 30, 2018, the Company completed the sale of Aetna’s standalone PDPs to 
WellCare effective December 31, 2018. The Company provided administrative services to, and retained the 
financial results of, the divested plans through 2019. Subsequent to 2019, the Company will no longer retain the 
financial results of the divested plans. 

•  Medicare Supplement: For certain Medicare eligible members, the Company offers supplemental coverage for 
certain health care costs not covered by Original Medicare. The products included in the Medicare Supplement 
portfolio help to cover some of the gaps in Original Medicare, and include coverage for Medicare deductibles and 

8

coinsurance amounts. The Company offered a wide selection of Medicare Supplement products in 49 states and 
Washington, D.C. in 2019.

•  Medicaid and CHIP: The Company offers health care management services to individuals eligible for Medicaid 
and CHIP under multi-year contracts with government agencies in various states that are subject to annual 
appropriations. CHIP are state-subsidized insurance programs that provide benefits for families with uninsured 
children. The Company offered these services on an Insured or ASC basis in 16 states in 2019.

•  Duals: The Company provides health coverage to beneficiaries who are dually eligible for both Medicare and 

Medicaid coverage. These members must meet certain income and resource requirements in order to qualify for 
this coverage. The Company coordinates 100% of the care for these members and may provide them with 
additional services in order to manage their health care costs. 

• 

• 

Specialty: The Health Care Benefits segment has a portfolio of additional health products and services that complement its 
medical products such as dental plans, behavioral health and employee assistance products, provider network access and 
vision products and workers’ compensation administrative services. 
Transformative Products and Services: The Company has a portfolio of transformative products and services aimed at 
creating a holistic and integrated approach to individual health and wellness. These products and services complement the 
Commercial Medical and Government Medical products and aim to provide innovative solutions, create integrated 
experience offerings and enable enhanced care delivery to customers.

Health Care Benefits Provider Networks 

The Company contracts with physicians, hospitals and other providers for services they provide to the Company’s members. 
The Company uses a variety of techniques designed to help encourage appropriate utilization of medical services (“utilization”) 
and maintain affordability of quality coverage. In addition to contracts with providers for negotiated rates of reimbursement, 
these techniques include creating risk sharing arrangements that align economic incentives with providers, the development and 
implementation of guidelines for the appropriate utilization of medical services and the provision of data to providers to enable 
them to improve health care quality. At December 31, 2019, the Company’s underlying nationwide provider network had 
approximately 1.3 million participating providers, including over 706,000 primary care and specialist physicians and 
approximately 5,900 hospitals. Other providers in the Company’s provider networks also include laboratory, imaging, urgent 
care and other freestanding health facilities.

Health Care Benefits Quality Assessment

CMS uses a 5-star rating system to monitor Medicare health care and drug plans and ensure that they meet CMS’s quality 
standards. CMS uses this rating system to provide Medicare beneficiaries with a tool that they can use to compare the overall 
quality of care and level of customer service of companies that provide Medicare health care and drug plans. The rating system 
considers a variety of measures adopted by CMS, including quality of preventative services, chronic illness management and 
overall customer satisfaction. See “Health Care Benefits Pricing” below in this Item 1 for further discussion of star ratings. The 
Company seeks Health Plan accreditation for Aetna HMO plans from the NCQA. Health care plans seeking accreditation must 
pass a rigorous, comprehensive review and must annually report on their performance.

Aetna Life Insurance Company (“ALIC”), a wholly-owned subsidiary of the Company, has received nationwide NCQA PPO 
Health Plan accreditation. As of December 31, 2019, all of the Company’s Commercial HMO and all of ALIC’s PPO members 
who were eligible participated in HMOs or PPOs that are accredited by the NCQA.

The Company’s provider selection and credentialing/re-credentialing policies and procedures are consistent with NCQA and 
URAC, as well as state and federal, requirements. In addition, the Company is certified under the NCQA Credentials 
Verification Organization (“CVO”) certification program for all certification options and has URAC CVO accreditation. 

Quality assessment programs for contracted providers who participate in the Company’s networks begin with the initial review 
of health care practitioners. Practitioners’ licenses and education are verified, and their work history is collected by the 
Company or in some cases by the practitioner’s affiliated group or organization. The Company generally requires participating 
hospitals to be certified by CMS or accredited by the Joint Commission, the American Osteopathic Association, or Det Norske 
Veritas Healthcare.

The Company also offers quality and outcome measurement programs, quality improvement programs, and health care data 
analysis systems to providers and purchasers of health care services.

9

Health Care Benefits Information Systems

The Health Care Benefits segment currently operates and supports an end-to-end suite of information technology platforms to 
support member engagement, enrollment, health benefit administration, care management, service operations, financial 
reporting and analytics. The multiple platforms are supported by an integration layer to facilitate the transfer of real-time 
data. There is continued focus and investment in digital products to offer innovative solutions and a seamless experience to the 
Company’s members through mobile and web channels. The Company is making concerted investments in emerging 
technology capabilities such as voice, artificial intelligence and robotics to further automate and improve the experience for all 
of its constituents. The Health Care Benefits segment is integrating with the Retail/LTC and Pharmacy Services segments to 
build Enterprise technology assets that will help guide our members through their health care journey, provide them a high level 
of service, enable healthier outcomes and encourage them to take next best actions to lead healthier lives.

Health Care Benefits Customers

Medical membership is dispersed throughout the United States, and the Company also serves medical members in certain 
countries outside the United States. The Company offers a broad range of traditional, voluntary and consumer-directed health 
insurance products and related services, many of which are available nationwide. Depending on the product, the Company 
markets to a range of customers including employer groups, individuals, college students, part-time and hourly workers, health 
plans, providers, governmental units, government-sponsored plans, labor groups and expatriates.

For additional information on medical membership, see “Health Care Benefits Segment” in the Management’s Discussion and 
Analysis of Financial Condition and Results of Operations (the “MD&A”) included in Item 7 of this 10-K. 

The Company markets both Commercial Insured and ASC products and services primarily to employers that sponsor the 
Company’s products for the benefit of their employees and their employees’ dependents. Frequently, larger employers offer 
employees a choice among coverage options, from which the employee makes his or her selection during a designated annual 
open enrollment period. Typically, employers pay all of the monthly premiums to the Company and, through payroll 
deductions, obtain reimbursement from employees for a percentage of the premiums that is determined by each employer. 
Some Health Care Benefits products are sold directly to employees of employer groups on a fully employee-funded basis. In 
some cases, the Company bills the covered individual directly. 

The Company offers Insured Medicare coverage on an individual basis as well as through employer groups to their retirees. 
Medicaid and CHIP members are enrolled on an individual basis. The Company also offers Insured health care coverage to 
members who are dually-eligible for both Medicare and Medicaid. 

Health Care Benefits products are sold through the Company’s sales personnel; through independent brokers, agents and 
consultants who assist in the production and servicing of business; and through Private Exchanges. For large plan sponsors, 
independent consultants and brokers are frequently involved in employer health plan selection decisions and sales. In some 
instances, the Company may pay commissions, fees and other amounts to brokers, agents, consultants and sales 
representatives who place business with the Company. In certain cases, the customer pays the broker for services rendered, 
and the Company may facilitate that arrangement by collecting the funds from the customer and transmitting them to the 
broker. The Company supports marketing and sales efforts with an advertising program that may include television, radio, 
billboards, print media and social media, supplemented by market research and direct marketing efforts.

The U.S. federal government is a significant customer of the Health Care Benefits segment through contracts with CMS for 
coverage of Medicare-eligible individuals and federal employee-related benefit programs. Other than the contracts with CMS, 
the Health Care Benefits segment is not dependent upon a single customer or a few customers the loss of which would have a 
significant effect on the earnings of the segment. The loss of business from any one, or a few, independent brokers or agents 
would not have a material adverse effect on the earnings of the Health Care Benefits segment. In 2019, Health Care Benefits 
segment revenues from the federal government accounted for approximately 13% of the Company’s consolidated total 
revenues. Contracts with CMS for coverage of Medicare-eligible individuals accounted for approximately 95% of the 
Company’s revenues from the federal government in 2019. No single Health Care Benefits customer accounted for 10% or 
more of the Company’s consolidated total revenues in 2018 or 2017.

10

Health Care Benefits Pricing

For Commercial Insured plans, contracts containing the pricing and other terms of the relationship are generally established in 
advance of the policy period and typically have a duration of one year. Fees under ASC plans are generally fixed for a period 
of one year.

Generally, a fixed premium rate is determined at the beginning of the policy period for Commercial Insured plans. The 
Company typically cannot recover unanticipated increases in health care and other benefit costs in the current policy period; 
however, it may consider prior experience for a product in the aggregate or for a specific customer, among other factors, in 
determining premium rates for future policy periods. Where required by state laws, premium rates are filed and approved by 
state regulators prior to contract inception. Future operating results could be adversely affected if the premium rates requested 
are not approved or are adjusted downward or their approval is delayed by state or federal regulators. 

The Company has Medicare Advantage and PDP contracts with CMS to provide HMO, PPO and prescription drug coverage to 
Medicare beneficiaries in certain geographic areas. Under these annual contracts, CMS pays the Company a fixed per member 
(or “capitation”) payment and/or a portion of the premium, both of which are based on membership and adjusted for 
demographic and health risk factors. CMS also considers inflation, changes in utilization patterns and average per capita fee-
for-service Medicare costs in the calculation of the fixed capitation payment or premium. PDP contracts also provide a risk-
sharing arrangement with CMS to limit the Company’s exposure to unfavorable expenses or benefit from favorable expenses. 
Amounts payable to the Company under the Medicare arrangements are subject to annual revision by CMS, and the Company 
elects to participate in each Medicare service area or region on an annual basis. Premiums paid to the Company for Medicare 
products are subject to federal government reviews and audits, which can result, and have resulted, in retroactive and 
prospective premium adjustments and refunds to the government and/or members. In addition to payments received from CMS, 
some of Medicare Advantage products and all PDP products require a supplemental premium to be paid by the member or 
sponsoring employer. In some cases these supplemental premiums are adjusted based on the member’s income and asset levels. 
Compared to Commercial Medical products, Medicare contracts generate higher per member per month revenues and higher 
health care and other benefit costs. 

The Patient Protection and Affordable Care Act and the Health Care and Education Reconciliation Act of 2010 (collectively, the 
“ACA”) ties a portion of each Medicare Advantage plan’s reimbursement to the plan’s “star ratings.” Plans must have a star 
rating of four or higher (out of five) to qualify for bonus payments. CMS released the Company’s 2020 star ratings in October 
2019. The Company’s 2020 star ratings will be used to determine which of the Company’s Medicare Advantage plans have 
ratings of four stars or higher and qualify for bonus payments in 2021. Based on the Company’s membership at December 31, 
2019, 83% of the Company’s Medicare Advantage members were in plans with 2020 star ratings of at least 4.0 stars, compared 
to 79% of the Company’s Medicare Advantage members being in plans with 2019 star ratings of at least 4.0 stars based on the 
Company’s membership at December 31, 2018.

Rates for Medicare Supplement products are regulated at the state level and vary by state and plan.

Under Insured Medicaid contracts, state government agencies pay the Company fixed monthly rates per member that vary by 
state, line of business and demographics; and the Company arranges, pays for and manages the health care services provided 
to Medicaid beneficiaries. These rates are subject to change by each state, and, in some instances, provide for adjustment for 
health risk factors. CMS requires these rates to be actuarially sound. The Company also receives fees from customers where it 
provides services under ASC Medicaid contracts. ASC Medicaid contracts generally are for periods of more than one year, 
and certain of them contain performance incentives and limited financial risk sharing with respect to certain medical, financial 
and operational metrics. Under these arrangements, performance is evaluated annually, with associated financial incentive 
opportunities, and financial risk share obligations are typically limited to a percentage of the fees otherwise payable to the 
Company. Payments to the Company under Medicaid contracts are subject to the annual appropriation process in the 
applicable state.

Under Duals contracts, the rate setting process is generally established by CMS in partnership with the state government 
agency participating in the demonstration project. Both CMS and the state government agency may seek premium and other 
refunds under certain circumstances, including if the Company fails to comply with CMS regulations or other contractual 
requirements.

The Company offers HMO and consumer-directed medical and dental plans to federal employees under the Federal Employees 
Health Benefits (“FEHB”) Program and the Federal Employees Dental and Vision Insurance Program. Premium rates and fees 

11

for those plans are subject to federal government review and audit, which can result, and have resulted, in retroactive and 
prospective premium and fee adjustments and refunds to the government and/or members. 

Beginning in 2014, the ACA imposed significant new industry-wide fees, assessments and taxes, including an annual levy 
known as the Health Insurer Fee (the “HIF”). The HIF applies for 2020 and was temporarily suspended for 2019 and 2017. In 
December 2019, the HIF was repealed for calendar years after 2020. For additional information on the ACA fees, assessments 
and taxes, see Note 1 ‘‘Significant Accounting Policies’’ included in Item 8 of this 10-K. The Company’s goal is to collect in 
premiums and fees where possible, or solve for, all of the ACA-related fees, assessments and taxes.

Health Care Benefits Seasonality

For periods prior to the Aetna Acquisition Date, the Health Care Benefits segment was comprised of the Company’s 
SilverScript PDP business. The quarterly earnings and operating cash flows of the PDP business are impacted by the Medicare 
Part D benefit design and changes in the composition of PDP membership. The Medicare Part D standard benefit design results 
in coverage that varies with a member’s cumulative annual out-of-pocket costs. The benefit design generally results in 
employers or other entities that sponsor the Company’s products (“plan sponsors”) sharing a greater portion of the 
responsibility for total prescription drug costs in the early part of the year. As a result, the PDP pay percentage or benefit ratio 
generally decreases and operating income generally increases as the year progresses. For periods subsequent to the Aetna 
Acquisition, the Health Care Benefits segment’s quarterly operating income progression is also impacted by (i) the seasonality 
of benefit costs which generally increase during the year as Insured members progress through their annual deductibles and out-
of-pocket expense limits and (ii) the seasonality of operating expenses which are generally the highest during the fourth quarter 
due primarily to spending to support readiness for the start of the upcoming Medicare plan year and marketing associated with 
Medicare annual enrollment. 

Health Care Benefits Competition

The health care benefits industry is highly competitive, primarily due to a large number of for-profit and not-for-profit 
competitors, competitors’ marketing and pricing and a proliferation of competing products, including new products that are 
continually being introduced into the marketplace. New entrants into the marketplace, as well as consolidation within the 
industry, have contributed to and are expected to intensify the competitive environment. In addition, the rapid pace of change as 
the industry evolves towards a consumer-focused retail marketplace, including Insurance Exchanges, and the increased use of 
technology to interact with members, providers and customers, increase the risks the Company currently faces from new 
entrants and disruptive actions by existing competitors compared to prior periods.

The Company believes that the significant factors that distinguish competing health plans include the perceived overall 
quality (including accreditation status), quality of service, comprehensiveness of coverage, cost (including premium rates, 
provider discounts and member out-of-pocket costs), product design, financial stability and ratings, breadth and quality of 
provider networks, ability to offer different provider network options, providers available in such networks, and quality of 
member support and care management programs. The Company believes that it is competitive on each of these factors. The 
Company’s ability to increase the number of persons covered by its health plans or to increase Health Care Benefits segment 
revenues is affected by its ability to differentiate itself from its competitors on these factors. Competition may also affect the 
availability of services from health care providers, including primary care physicians, specialists and hospitals.

Insured products compete with local and regional health care benefits plans, health care benefits and other plans sponsored by 
other large commercial health care benefit insurance companies, health system owned health plans, new entrants into the 
marketplace and numerous for-profit and not-for-profit organizations operating under licenses from the Blue Cross and Blue 
Shield Association. The largest competitor in Medicare products is Original Medicare. Additional Health Care Benefits 
segment competitors include other types of medical and dental provider organizations, various specialty service providers 
(including PBM services providers), health care consultants, financial services companies, integrated health care delivery 
organizations (networks of providers who also coordinate administrative services for and assume insurance risk of their 
members), third party administrators (“TPAs”), HIT companies and, for certain plans, programs sponsored by the federal or 
state governments. Emerging competitors include start up health care benefits plans, technology companies, provider-owned 
health plans, new joint ventures (including not-for-profit joint ventures among firms from multiple industries), technology 
firms, financial services firms that are distributing competing products on their proprietary Private Exchanges, and consulting 
firms that are distributing competing products on their proprietary Private Exchanges, as well as non-traditional distributors 
such as retail companies. The Company’s ability to increase the number of persons enrolled in Insured Commercial Medical 
products also is affected by the desire and ability of employers to self-fund their health coverage.

12

The Health Care Benefits segment’s ASC plans compete primarily with other large commercial health care benefit companies, 
numerous for-profit and not-for-profit organizations operating under licenses from the Blue Cross and Blue Shield 
Association and TPAs.

The Health Care Benefits segment’s international products compete with local, global and U.S.-based health plans and 
commercial health care benefit insurance companies, many of whom are licensed in more geographies and have a longer 
operating history, better brand recognition and greater marketplace presence in one or more geographies.

The provider solutions and HIT marketplaces and products are evolving rapidly. The Company competes for provider 
solutions and HIT business with other large health plans and commercial health care benefit insurance companies as well as 
information technology companies and companies that specialize in provider solutions and HIT. Many information 
technology product competitors have longer operating histories, better brand recognition, greater marketplace presence and 
more experience in developing innovative products. 

In addition to competitive pressures affecting the Company’s ability to obtain new customers or retain existing customers, the 
Health Care Benefits segment’s medical membership has been and may continue to be adversely affected by adverse and/or 
uncertain economic conditions and reductions in workforce by existing customers due to adverse and/or uncertain general 
economic conditions, especially in the United States and industries where such membership is concentrated.

Health Care Benefits Reinsurance

The Company currently has several reinsurance agreements with non-affiliated insurers that relate to Health Care Benefits 
insurance policies. The Company entered into these contracts to reduce the risk of catastrophic losses which in turn reduces 
capital and surplus requirements. The Company frequently evaluates reinsurance opportunities and refines its reinsurance and 
risk management strategies on a regular basis.

Corporate/Other Segment

The Company presents the remainder of its financial results in the Corporate/Other segment, which consists of:

•  Management and administrative expenses to support the overall operations of the Company, which include certain aspects 
of executive management and the corporate relations, legal, compliance, human resources, information technology and 
finance departments, expenses associated with the Company’s investments in its transformation and Enterprise 
modernization programs and acquisition-related transaction and integration costs; and
Products for which the Company no longer solicits or accepts new customers such as large case pensions and long-term 
care insurance products.

• 

Generic Sourcing Venture

The Company and Cardinal Health, Inc. (“Cardinal”) each have a 50% ownership in Red Oak Sourcing, LLC (“Red Oak”), a 
generic pharmaceutical sourcing entity. Under this arrangement, the Company and Cardinal contributed their sourcing and 
supply chain expertise to Red Oak and agreed to source and negotiate generic pharmaceutical supply contracts for both 
companies through Red Oak. Red Oak does not own or hold inventory on behalf of either company.

Working Capital Practices

The Company funds the growth of its businesses through a combination of cash flow from operations, commercial paper and 
other short-term borrowings, proceeds from sale-leaseback transactions and long-term borrowings. For additional information 
on the Company’s working capital practices, see “Liquidity and Capital Resources” in the MD&A included in Item 7 of this 10-
K. The majority of the Retail/LTC segment non-pharmacy revenues are paid in cash, or with debit or credit cards. Managed care 
organizations, pharmacy benefit managers, government funded health care programs, commercial employers and other third 
party insurance programs, which represent the vast majority of the Company’s consolidated pharmacy revenues, typically settle 
in less than 30 days. The remainder of the Company’s consolidated pharmacy revenues are paid in cash, or with debit or credit 
cards. Employer groups, individuals, college students, part-time and hourly workers, health plans, providers, governmental 
units, government-sponsored plans (with the exception of Medicare Part D services, which are described below), labor groups 
and expatriates, which represent the vast majority of Health Care Benefits segment revenues, typically settle in less than 30 
days. As a provider of Medicare Part D services, the Company contracts annually with CMS. Utilization of services each plan 

13

year results in the accumulation of either a receivable from or a payable to CMS. The timing of settlement of the receivable or 
payable with CMS takes several quarters, which impacts working capital from year to year.

Colleague Development

As of December 31, 2019, the Company employed approximately 290,000 colleagues in all 50 states, the District of Columbia, 
Puerto Rico and a number of countries outside the United States. To deliver the highest levels of service to customers, the 
Company devotes considerable time and attention to its people and service standards. The Company emphasizes attracting and 
training knowledgeable, friendly and helpful associates to work in the organization.

Intellectual Property

The Company has registered and/or applied to register a variety of trademarks and service marks used throughout its 
businesses, as well as domain names, and relies on a combination of copyright, patent, trademark and trade secret laws, in 
addition to contractual restrictions, to establish and protect the Company’s proprietary rights. The Company regards its 
intellectual property as having significant value in the Pharmacy Services, Retail/LTC and Health Care Benefits segments. The 
Company is not aware of any facts that could materially impact the continuing use of any of its intellectual property.

Government Regulation

Overview

The Company’s operations are subject to comprehensive federal, state and local laws and regulations and comparable multiple 
levels of international regulation in the jurisdictions in which it does business. There also continues to be a heightened level of 
review and/or audit by federal, state and international regulators of the health and related benefits industry’s business and 
reporting practices. In addition, many of the Company’s PBM clients and the Company’s payors in the Retail/LTC segment, 
including insurers, Medicare Part D plans, Managed Medicaid plans and managed care organizations (“MCOs”), are themselves 
subject to extensive regulations that affect the design and implementation of prescription drug benefit plans that they sponsor. 
Similarly, the Company’s LTC clients, such as skilled nursing facilities, are subject to government regulations, including many 
of the same government regulations to which the Company is subject. 

The laws and rules governing the Company’s businesses and interpretations of those laws and rules continue to expand and 
become more restrictive each year and are subject to frequent change. The application of these complex legal and regulatory 
requirements to the detailed operation of the Company’s businesses creates areas of uncertainty. Further, there are numerous 
proposed health care, financial services and other laws and regulations at the federal, state and international levels, some of 
which could adversely affect the Company’s businesses if they are enacted. The Company cannot predict whether pending or 
future federal or state legislation or court proceedings, including fundamental changes to the dynamics of one or more of the 
industries in which it competes, such as the federal or one or more state governments fundamentally restructuring the 
Commercial, Medicare or Medicaid marketplace or reducing payments to the Company under or financing for Medicare, 
Medicaid, dual eligible or special needs programs, increasing its involvement in drug reimbursement, pricing, purchasing, and/
or importation or changing the laws governing PBMs, will change various aspects of the industries in which it competes or the 
health care industry generally or the impact those changes will have on the Company’s businesses, operating results, cash flows 
and/or stock price, but the effects could be materially adverse. Any failure or alleged failure to comply with applicable laws and 
regulations summarized below, or any adverse applications or interpretations of, or changes in, the laws and regulations 
affecting the Company and/or its businesses, could have a material adverse effect on the Company’s operating results, financial 
condition, cash flows and/or stock price. See Item 3 of this 10-K, “Legal Proceedings,” for further information.

The Company can give no assurance that its businesses, financial condition, operating results and/or cash flows will not be 
materially adversely affected, or that the Company will not be required to materially change its business practices, based on: (i) 
future enactment of new health care or other laws or regulations; (ii) the interpretation or application of existing laws or 
regulations, including the laws and regulations described in this Government Regulation section, as they may relate to one or 
more of the Company’s businesses, one or more of the industries in which the Company competes and/or the health care 
industry generally; (iii) pending or future federal or state governmental investigations of one or more of the Company’s 
businesses, one or more of the industries in which the Company competes and/or the health care industry generally; (iv) 
pending or future government audits, investigations or enforcement actions against the Company; (v) adverse developments in 
any pending qui tam lawsuit against the Company, whether sealed or unsealed, or in any future qui tam lawsuit that may be 
filed against the Company; or (vi) adverse developments in pending or future legal proceedings against the Company or 
affecting one or more of the industries in which the Company competes and/or the health care industry generally.

14

Laws and Regulations Related to Multiple Segments of the Company’s Business

Laws Related to Reimbursement by Government Programs - The Company is subject to various federal and state laws 
concerning its submission of claims and other information to Medicare, Medicaid and other federal and state government-
sponsored health care programs. Potential sanctions for violating these laws include recoupment or reduction of government 
reimbursement amounts, civil penalties, treble damages, and exclusion from participation in government health care programs. 
Such laws include the federal False Claims Act (the “False Claims Act”), the federal anti-kickback statute, state false claims 
acts and anti-kickback statutes in most states, the federal “Stark Law” and related state laws. In particular, the False Claims Act 
prohibits intentionally submitting, conspiring to submit, or causing to be submitted, false claims, records, or statements to the 
federal government, or intentionally failing to return overpayments, in connection with reimbursement by federal government 
programs. In addition, any claim for government reimbursement also violates the False Claims Act where it results from a 
violation of the federal anti-kickback statute. 

Both federal and state false claims laws permit private individuals to file qui tam or “whistleblower” lawsuits on behalf of the 
federal or state government. Participants in the health and related benefits industry, including the Company, frequently are 
subject to actions under the False Claims Act or similar state laws. The federal Stark Law generally prohibits physicians from 
referring Medicare or Medicaid beneficiaries for certain services, including outpatient prescription drugs, to any entity with 
which the physician, or an immediate family member of the physician, has a financial relationship. The Stark Law further 
prohibits the entity receiving a prohibited referral from presenting a claim for reimbursement by Medicare or Medicaid for 
services furnished pursuant to the prohibited referral. Various states have enacted similar laws.

The ACA - The ACA made broad-based changes to the U.S. health care system. While the Company anticipates continued 
efforts in 2020 and beyond to invalidate, modify, repeal or replace the ACA, the Company expects aspects of the ACA to 
continue to significantly impact its business operations and operating results, including pricing, medical benefit ratios 
(“MBRs”) and the geographies in which the Company’s products are available.

While most of the significant aspects of the ACA became effective during or prior to 2014, parts of the ACA continue to evolve 
through the promulgation of executive orders, legislation, regulations and guidance as well as ongoing litigation. Additional 
changes to the ACA and those regulations and guidance at the federal and/or state level are likely, and those changes are likely 
to be significant. Growing federal and state budgetary pressures make it more likely that any changes, including changes at the 
state level in response to changes to, or invalidation, repeal or replacement of, the ACA and/or changes in the funding levels 
and/or payment mechanisms of federally supported benefit programs, will be adverse to us. For example, if any elements of the 
ACA are invalidated or repealed at the federal level, the Company expects that some states would seek to enact similar 
requirements, such as prohibiting pre-existing condition exclusions, prohibiting rescission of insurance coverage, requiring 
coverage for dependents up to age 26, requiring guaranteed renewability of insurance coverage and prohibiting lifetime limits 
on insurance coverage.

The expansion of health care coverage contemplated by the ACA is being funded in part by reductions to the reimbursements 
the Company and other health plans are paid by the federal government for Medicare members, among other sources. While not 
all-inclusive, the following are some of the key funding changes related to the ACA (assuming it continues to be implemented 
in its current form) that become effective on or after January 1, 2020. The Company continues to evaluate these provisions and 
the related regulations and regulatory guidance to determine the impact that they will have on its business operations and 
operating results:

•  The repeal of the annual non-tax deductible industry-wide HIF for calendar years after 2020. The HIF was $14.3 billion for 

2018 and suspended for 2019. As currently enacted, the HIF will be $15.5 billion for 2020.

•  The repeal of the non-tax deductible 40% excise tax on employer-sponsored health care benefits above a certain threshold 

that was scheduled to begin in 2022.

•  Reduced funding for Medicaid expansion, which began in 2017.

The ACA also specifies minimum medical loss ratios (“MLRs”) for Commercial and Medicare Insured products, specifies 
features required to be included in Commercial benefit designs, limits Commercial individual and small group rating and 
pricing practices, encourages additional competition (including potential incentives for new participants to enter the 
marketplace) and significantly increases federal and state oversight of health plans, including regulations and processes that 
could delay or limit the Company’s ability to appropriately increase its health plan premium rates. This in turn could adversely 
affect the Company’s ability to continue to participate in certain product lines and/or geographies that it serves today.

15

Potential repeal of the ACA, ongoing legislative, regulatory and administrative policy changes to the ACA, the results of federal 
and state level elections, pending litigation challenging the constitutionality of the ACA or funding for the law and federal 
budget negotiations continue to create uncertainty about the ultimate impact of the ACA. The time frame for conclusion and 
final outcome and ultimate impact of this litigation are uncertain. Given the inherent difficulty of foreseeing the nature and 
scope of future changes to the ACA and how states, businesses and individuals will respond to those changes, the Company 
cannot predict the impact on it of future changes to the ACA. It is reasonably possible that invalidation, repeal or replacement 
of or other changes to the ACA and/or states’ responses to such changes, in the aggregate, could have a significant adverse 
effect on the Company’s businesses, operating results and cash flows.

Medicare Regulation - The Company’s Medicare Advantage products compete directly with Original Medicare and Medicare 
Advantage products offered by other Medicare Advantage organizations and Medicare Supplement products offered by other 
insurers. The Company’s Medicare PDP and Medicare Supplement products are products that Medicare beneficiaries who are 
enrolled in Original Medicare purchase to enhance their Original Medicare coverage.

The Company continues to expand the number of counties in which it offers Medicare products. The Company expects to 
further expand its Medicare service area and products in 2020 and is seeking to substantially grow its Medicare membership, 
revenue and operating results over the next several years, including through growth in Medicare Supplement products. The 
anticipated organic expansion of the Medicare service area and Medicare products offered and the Medicare-related provisions 
of the ACA significantly increase the Company’s exposure to funding and regulation of, and changes in government policy with 
respect to and/or funding or regulation of, the various Medicare programs in which the Company participates, including 
changes in the amounts payable to us under those programs and/or new reforms or surcharges on existing programs. For 
example, the ACA requires minimum MLRs for Medicare Advantage and Medicare Part D plans of 85%. If a Medicare 
Advantage or Medicare Part D contract pays minimum MLR rebates for three consecutive years, it will become ineligible to 
enroll new members. If a Medicare Advantage or Medicare Part D contract pays such rebates for five consecutive years, it will 
be terminated by CMS.

The Company’s Medicare Advantage and PDP products are heavily regulated by CMS. The regulations and contractual 
requirements applicable to the Company and other private participants in Medicare programs are complex, expensive to comply 
with and subject to change. For example, in the second quarter of 2014, CMS issued a final rule implementing the ACA 
requirements that Medicare Advantage and PDP plans report and refund to CMS overpayments that those plans receive from 
CMS. The precise interpretation, impact and legality of this rule are not clear and are subject to pending litigation. Payments the 
Company receives from CMS for its Medicare Advantage and Part D businesses also are subject to risk adjustment based on the 
health status of the individuals enrolled. Elements of that risk adjustment mechanism continue to be challenged by the DOJ, the 
Office of the Inspector General of the U.S. Department of Health and Human Services (the “OIG”) and CMS itself. Substantial 
changes in the risk adjustment mechanism, including changes that result from enforcement or audit actions, could materially 
affect the amount of the Company’s Medicare reimbursement, require the Company to raise prices or reduce the benefits 
offered to Medicare beneficiaries, and potentially limit the Company’s (and the industry’s) participation in the Medicare 
program.

The Company has invested significant resources to comply with Medicare standards, and its Medicare compliance efforts will 
continue to require significant resources. CMS may seek premium and other refunds, prohibit the Company from continuing to 
market and/or enroll members in or refuse to passively enroll members in one or more of the Company’s Medicare or 
Medicare-Medicaid demonstration (historically known as “dual eligible”) plans, exclude us from participating in one or more 
Medicare, dual eligible or dual eligible special needs plan programs and/or institute other sanctions and/or civil monetary 
penalties against the Company if it fails to comply with CMS regulations or its Medicare contractual requirements. The 
Company’s Medicare Supplement products are regulated at the state level and subject to similar significant compliance 
requirements and risks.

CMS regularly audits the Company’s performance to determine its compliance with CMS’s regulations and its contracts with 
CMS and to assess the quality of services it provides to Medicare Advantage and PDP beneficiaries. For example, CMS 
conducts risk adjustment data validation (“RADV”) audits of a subset of Medicare Advantage contracts for each contract year. 
Since 2013, CMS has selected certain of the Company’s Medicare Advantage contracts for various years for RADV audit, and 
the number of RADV audits continues to increase. The OIG also is auditing the Company’s risk adjustment data and that of 
other companies, and the Company expects CMS and the OIG to continue auditing risk adjustment data. The Company also has 
received Civil Investigative Demands (“CIDs”) from, and provided documents and information to, the Civil Division of the 
DOJ in connection with a current investigation of its patient chart review processes in connection with risk adjustment data 
submissions under Parts C and D of the Medicare program. 

16

On October 26, 2018, CMS issued proposed rules related to, among other things, changes to the RADV audit methodology 
established by CMS in 2012. CMS projects that the changes to the RADV audit methodology would increase its recoveries 
from Medicare Advantage plans as a result of RADV audits. CMS has requested comments on the proposed rules, including 
whether the proposed RADV rule change should apply retroactively to audits of Medicare Advantage plans for contract year 
2011 and forward. The Company is evaluating the potential adverse effect, which could be material, on the Company’s 
operating results, financial condition, and cash flows if the proposed RADV rule change were adopted as proposed. CMS also 
has announced that its goal is to subject all Medicare Advantage contracts to either a comprehensive or a targeted RADV audit 
for each contract year.

A portion of each Medicare Advantage plan’s reimbursement is tied to the plan’s “star ratings.” The star rating system considers 
a variety of measures adopted by CMS, including quality of preventative services, chronic illness management, compliance and 
overall customer satisfaction. Only Medicare Advantage plans with an overall star rating of four or more stars (out of five stars) 
are eligible for a quality bonus in their basic premium rates. As a result, the Company’s Medicare Advantage plans’ operating 
results in 2020 and going forward will be significantly affected by their star ratings. The Company’s star ratings and past 
performance scores are adversely affected by the compliance issues that arise each year in its Medicare operations. CMS 
released the Company’s 2020 star ratings in October 2019. The Company’s 2020 star ratings will be used to determine which of 
its Medicare Advantage plans have ratings of four stars or higher and qualify for bonus payments in 2021. Based on the 
Company’s membership at December 31, 2019, 83% of the Company’s Medicare Advantage members were in plans with 2020 
star ratings of at least 4.0 stars. CMS will release updated stars ratings in October 2020 that will be used to determine which 
Medicare Advantage plans have ratings of four stars or higher and qualify for bonus payments in 2022. CMS also gives PDPs 
star ratings which affect PDP’s enrollment. Medicare Advantage and PDP plans that are rated less than three stars for three 
consecutive years are subject to contract termination by CMS. CMS continues to revise its star ratings system to make it harder 
to achieve four stars or more. Despite the Company’s success in achieving high 2020 star ratings and other quality measures 
and the continuation of its improvement efforts, there can be no assurances that it will be successful in maintaining or 
improving its star ratings in future years. Accordingly, the Company’s Medicare Advantage plans may not be eligible for full 
level quality bonuses, which could adversely affect the benefits such plans can offer, reduce membership and/or reduce profit 
margins.

Overall, the Company projects the benchmark payment rates in CMS’s April 2019 final notice detailing final Medicare 
Advantage benchmark payment rates for 2020 (the “Final Notice”) will increase funding for the Company’s Medicare 
Advantage business, excluding the impact of the HIF, by approximately 2.0% in 2020 compared to 2019. This 2020 rate 
increase only partially offsets the challenge the Company faces from the impact of the increasing cost of medical care 
(including prescription medications) and CMS local and national coverage decisions that require the Company to pay for 
services and supplies that are not factored into the Company’s bids. The federal government may seek to impose restrictions on 
the configuration of pharmacy or other provider networks for Medicare Advantage and/or PDP plans, or otherwise restrict the 
ability of these plans to alter benefits, negotiate prices or establish other terms to improve affordability or maintain viability of 
products. The Company currently believes that the payments it has received and will receive in the near term are adequate to 
justify the Company’s continued participation in the Medicare Advantage and PDP programs, although there are economic and 
political pressures to continue to reduce spending on the program, and this outlook could change.

Going forward, the Company expects CMS, the OIG, the DOJ, other federal agencies and the U.S. Congress to continue to 
scrutinize closely each component of the Medicare program (including Medicare Advantage, PDP, demonstration projects such 
as Medicare-Medicaid plans and provider network access and adequacy), modify the terms and requirements of the program 
and possibly seek to recast or limit private insurers’ role. It is not possible to predict the outcome of this Congressional or 
regulatory activity, any of which could materially and adversely affect the Company.

Anti-Remuneration Laws - Federal law prohibits, among other things, an entity from knowingly and willfully offering, 
paying, soliciting or receiving, subject to certain exceptions and “safe harbors,” any remuneration to induce the referral of 
individuals or the purchase, lease or order of items or services for which payment may be made under Medicare, Medicaid or 
certain other federal and state health care programs. A number of states have similar laws, some of which are not limited to 
services paid for with government funds. Sanctions for violating these federal and state anti-remuneration laws may include 
imprisonment, criminal and civil fines, and exclusion from participation in Medicare, Medicaid and other federal and state 
government-sponsored health care programs. Companies involved in public health care programs such as Medicare and/or 
Medicaid are required to maintain compliance programs to detect and deter fraud, waste and abuse, and are often the subject of 
fraud, waste and abuse investigations and audits. The Company has invested significant resources to comply with Medicare and 
Medicaid program standards. Ongoing vigorous law enforcement and the highly technical regulatory scheme mean that the 
Company’s compliance efforts in this area will continue to require significant resources.

17

Antitrust and Unfair Competition - The U.S. Federal Trade Commission (“FTC”) investigates and prosecutes practices that 
are “unfair trade practices” or “unfair methods of competition.” Numerous lawsuits have been filed throughout the United 
States against pharmaceutical manufacturers, retail pharmacies and/or PBMs under various federal and state antitrust and unfair 
competition laws challenging, among other things: (i) brand name drug pricing and rebate practices of pharmaceutical 
manufacturers, (ii) the maintenance of retail or specialty pharmacy networks by PBMs, and (iii) various other business practices 
of PBMs and retail pharmacies. To the extent that the Company appears to have actual or potential market power in a relevant 
market or CVS Pharmacy, CVS Specialty or MinuteClinic plays a unique or expanded role in a PBM or Health Care Benefits 
segment product offering, the Company’s business arrangements and uses of confidential information may be subject to 
heightened scrutiny from an anti-competitive perspective and possible challenge by state and/or federal regulators and/or 
private parties.

Privacy and Confidentiality Requirements - Many of the Company’s activities involve the receipt, use and disclosure by the 
Company of personally identifiable information (“PII”) as permitted in accordance with applicable federal and state privacy and 
data security laws, which require organizations to provide appropriate privacy and security safeguards for such information. In 
addition to PII, the Company uses and discloses de-identified data for analytical and other purposes when permitted. 
Additionally, there are industry standards for handling credit card data known as the Payment Card Industry Data Security 
Standard, which are a set of requirements designed to help ensure that entities that process, store or transmit credit card 
information maintain a secure environment. Certain states have incorporated these requirements into state laws or enacted other 
requirements relating to the use and/or disclosure of PII.

The federal Health Insurance Portability and Accountability Act of 1996 and the regulations issued thereunder (collectively, 
“HIPAA”), as further modified by the American Recovery and Reinvestment Act of 2009 (“ARRA”) impose extensive 
requirements on the way in which health plans, health care providers, health care clearinghouses (known as “covered entities”) 
and their business associates use, disclose and safeguard protected health information (“PHI”). Further, ARRA requires the 
Company and other covered entities to report any breaches of PHI to impacted individuals and to the U.S. Department of 
Health and Human Services (“HHS”) and to notify the media in any states where 500 or more people are impacted by the 
unauthorized release or use of or access to PHI. Criminal penalties and civil sanctions may be imposed for failing to comply 
with HIPAA standards. The Health Information Technology for Economic and Clinical Health Act (the “HITECH Act”), 
enacted as part of ARRA, amended HIPAA to impose additional restrictions on third-party funded communications using PHI 
and the receipt of remuneration in exchange for PHI. The HITECH Act also extended HIPAA privacy and security requirements 
and penalties directly to business associates. HHS has begun to audit health plans, providers and other parties to enforce HIPAA 
compliance, including with respect to data security. 

In addition to HIPAA, state health privacy laws apply to the extent they are more protective of individual privacy than is 
HIPAA, including laws that place stricter controls on the release of information relating to specific diseases or conditions and 
requirements to notify members of unauthorized release or use of or access to PHI. States also have adopted regulations to 
implement provisions of the Financial Modernization Act of 1999 (also known as the Gramm-Leach-Bliley Act (“GLBA”)) 
which generally require insurers, including health insurers, to provide customers with notice regarding how their non-public 
personal health and financial information is used and the opportunity to “opt out” of certain disclosures before the insurer 
shares such information with a non-affiliated third party. Like HIPAA, GLBA sets a “floor” standard, allowing states to adopt 
more stringent requirements governing privacy protection. Complying with additional state requirements requires us to make 
additional investments beyond those the Company has made to comply with HIPAA and GLBA.

The Cybersecurity Information Sharing Act of 2015 encourages organizations to share cyber threat indicators with the federal 
government and, among other things, directs HHS to develop a set of voluntary cybersecurity best practices for organizations in 
the health care industry. In addition, states have begun to enact more comprehensive privacy laws and regulations addressing 
consumer rights to data access, deletion, protection or transparency, such as the California Consumer Privacy Act (“CCPA”). 
States also are starting to issue regulations and proposed regulations specifically related to cybersecurity, such as the regulations 
issued by the New York Department of Financial Services. Complying with conflicting cybersecurity regulations, which may 
differ from state to state, requires significant resources. In addition, differing approaches to state privacy and/or cyber-security 
regulation and varying enforcement philosophies may materially and adversely affect the Company’s ability to standardize its 
products and services across state lines. Widely-reported large scale commercial data breaches in the United States and abroad 
increase the likelihood that additional data security legislation will be considered by additional states. These legislative and 
regulatory developments will impact the design and operation of the Company’s businesses, its privacy and security strategy 
and its web-based and mobile assets.

Finally, each Public Exchange is required to adhere to privacy and security standards with respect to PII, and to impose privacy 
and security standards that are at least as protective of PII as those the Public Exchange has implemented for itself or non-

18

Public Exchange entities, which include insurers offering plans through the Public Exchange and their designated downstream 
entities, including PBMs and other business associates. These standards may differ from, and be more stringent than, HIPAA.

Consumer Protection Laws - The federal government has many consumer protection laws, such as the Federal Trade 
Commission Act, the Federal Postal Service Act, the Consumer Product Safety Act and the FTC’s Telemarketing Sales Rule. 
Most states also have similar consumer protection laws. In addition, the federal government and most states have adopted laws 
and/or regulations requiring places of public accommodation, health care services and other goods and services to be accessible 
to people with disabilities. These consumer protection and accessibility laws and regulations have been the basis for 
investigations, lawsuits and multistate settlements relating to, among other matters, the marketing of loyalty programs, and 
health care products and services, pricing accuracy, expired front store products, financial incentives provided by drug 
manufacturers to pharmacies in connection with therapeutic interchange programs, disclosures related to how personal data is 
used and protected and the accessibility of goods and services to people with disabilities. As a result of the Company’s direct-
to-consumer activities, including mobile and web-based solutions offered to members and to other consumers, the Company 
also is subject to federal and state regulations applicable to electronic communications and to other general consumer protection 
laws and regulations. For example, the CCPA became effective in 2020, and additional federal and state regulation of consumer 
privacy protection may be proposed or enacted in 2020. The Company expects these new laws and regulations to impact the 
design of its products and services and the management and operation of its businesses and to increase its compliance costs.

Telemarketing and Other Outbound Contacts - Certain federal and state laws, such as the Telephone Consumer Protection 
Act, give the FTC, the Federal Communications Commission and state attorneys general the ability to regulate, and bring 
enforcement actions relating to, telemarketing practices and certain automated outbound contacts such as phone calls, texts or 
emails. Under certain circumstances, these laws provide consumers with a private right of action. Violations of these laws could 
result in substantial statutory penalties and other sanctions.

Pharmacy and Professional Licensure and Regulation - The Company is subject to a variety of intersecting federal and state 
statutes and regulations that govern the wholesale distribution of drugs; operation of retail, specialty, infusion, LTC and mail 
order pharmacies; licensure of facilities and professionals, including pharmacists, technicians, nurses and other health care 
professionals; registration of facilities with the U.S. Drug Enforcement Administration (the “DEA”) and analogous state 
agencies that regulate controlled substances; packaging, storing, shipping and tracking of pharmaceuticals; repackaging of drug 
products; labeling, medication guides and other consumer disclosures; interactions with prescribers and health care 
professionals; compounding of prescription medications; dispensing of controlled and non-controlled substances; counseling of 
patients; transfers of prescriptions; advertisement of prescription products and pharmacy services; security; inventory control; 
recordkeeping; reporting to Boards of Pharmacy, the U.S. Food and Drug Administration (the “FDA”), the U.S. Consumer 
Product Safety Commission, the DEA and related state agencies; and other elements of pharmacy practice. Pharmacies are 
highly regulated and have contact with a wide variety of federal, state and local agencies with various powers to investigate, 
inspect, audit or solicit information, including Boards of Pharmacy and Nursing, the DEA, the FDA, the DOJ, HHS and others. 
Many of these agencies have broad enforcement powers, conduct audits on a regular basis, can impose substantial fines and 
penalties, and may revoke the license, registration or program enrollment of a facility or professional. 

State Insurance, HMO and Insurance Holding Company Regulation - A number of states regulate affiliated groups of 
insurers and HMOs such as the Company under holding company statutes. These laws may, among other things, require prior 
regulatory approval of dividends and material intercompany transfers of assets and transactions between the regulated 
companies and their affiliates, including their parent holding companies. The Company expects the states in which its insurance 
and HMO subsidiaries are licensed to continue to expand their regulation of the corporate governance and internal control 
activities of its insurance companies and HMOs. Changes to state insurance, HMO and/or insurance holding company laws or 
regulations or changes to the interpretation of those laws or regulations, including due to regulators’ increasing concerns 
regarding insurance company and/or HMO solvency due, among other things, to past and expected payor insolvencies, could 
negatively affect the Company’s businesses in various ways, including through increases in solvency fund assessments, 
requirements that the Company hold greater levels of capital and/or delays in approving dividends from regulated subsidiaries.

PBM offerings of prescription drug coverage under certain risk arrangements may be subject to laws and regulations in various 
states. Such laws may require that the party at risk become licensed as an insurer, establish reserves or otherwise demonstrate 
financial viability. Laws that may apply in such cases include insurance laws and laws governing MCOs and limited prepaid 
health service plans.

The states of domicile of the Company’s regulated subsidiaries have statutory risk-based capital, or “RBC”, requirements for 
health and other insurance companies and HMOs based on the National Association of Insurance Commissioners’ Risk-Based 
Capital (RBC) for Insurers Model Act (the “RBC Model Act”). These RBC requirements are intended to assess the capital 

19

adequacy of life and health insurers and HMOs, taking into account the risk characteristics of a company’s investments and 
products. The RBC Model Act sets forth the formula for calculating RBC requirements, which are designed to take into account 
asset risks, insurance risks, interest rate risks and other relevant risks with respect to an individual company’s business. In 
general, under these laws, an insurance company or HMO must submit a report of its RBC level to the insurance department or 
insurance commissioner of its state of domicile for each calendar year. At December 31, 2019, the RBC level of each of the 
Company’s insurance and HMO subsidiaries was above the level that would require regulatory action.

For information regarding restrictions on certain payments of dividends or other distributions by the Company’s HMO and 
insurance company subsidiaries, see Note 12 ‘‘Shareholders’ Equity’’ included in Item 8 of this 10-K.

The holding company laws for the states of domicile of certain of the Company’s subsidiaries also restrict the ability of any 
person to obtain control of an insurance company or HMO without prior regulatory approval. Under those statutes, without 
such approval (or an exemption), no person may acquire any voting security of an insurance holding company (such as the 
Company’s ultimate parent company, CVS Health) that controls an insurance company or HMO, or merge with such a holding 
company, if as a result of such transaction such person would control the insurance holding company. Control is generally 
defined as the direct or indirect power to direct or cause the direction of the management and policies of a person and is 
presumed to exist if a person directly or indirectly owns or controls 10% or more of the voting securities of another person.

Certain states have laws that prohibit submitting a false claim or making a false record or statement in order to secure 
reimbursement from an insurance company. These state laws vary, and violation of them may lead to the imposition of civil or 
criminal penalties.

Government Agreements and Mandates - The Company and/or its various affiliates are subject to certain consent decrees, 
settlement and other agreements, corrective action plans and corporate integrity agreements with various federal, state and local 
authorities relating to such matters as privacy practices, controlled substances, PDPs, expired products, environmental and 
safety matters, marketing and advertising practices, PBM, LTC and other pharmacy operations and various other business 
practices. Certain of these agreements contain ongoing reporting, monitoring and/or other compliance requirements for the 
Company. Failure to meet the Company’s obligations under these agreements could result in civil or criminal remedies, 
financial penalties, administrative remedies, and/or exclusion from participation in federal health care programs.

Environmental and Safety Regulation - The Company’s businesses are subject to various federal, state and local laws, 
regulations and other requirements pertaining to protection of the environment, public health and employee safety, including, 
for example, regulations governing the management of hazardous substances, the cleaning up of contaminated sites, and the 
maintenance of safe working conditions in the Company’s stores, distribution centers and other facilities. Governmental 
agencies at the federal, state and local levels continue to focus on the retail and health care sectors’ compliance with such laws 
and regulations, and have at times pursued enforcement activities. Any failure to comply with these regulations could result in 
fines or other sanctions by government authorities.

ERISA Regulation - The Employee Retirement Income Security Act of 1974 (“ERISA”), provides for comprehensive federal 
regulation of certain employee pension and benefit plans, including private employer and union sponsored health plans and 
certain other plans that contract with us to provide PBM services. In general, the Company assists plan sponsors in the 
administration of their health benefit plans, including the prescription drug benefit portion of those plans, in accordance with 
the plan designs adopted by the plan sponsors. In addition, the Company may have fiduciary duties where it has specifically 
contracted with a plan sponsor to accept limited fiduciary responsibility, such as for the adjudication of initial prescription drug 
benefit claims and/or the appeals of denied claims under a plan. In addition to its fiduciary provisions, ERISA imposes civil and 
criminal liability on service providers to health plans and certain other persons if certain forms of illegal remuneration are made 
or received. These provisions of ERISA are broadly written and their application to specific business practices is often 
uncertain.

Some of the Company’s health and related benefits and large case pensions products and services and related fees also are 
subject to potential issues raised by judicial interpretations relating to ERISA. Under those interpretations, together with U.S. 
Department of Labor (“DOL”) regulations, the Company may have ERISA fiduciary duties with respect to PBM members and/
or certain general account assets held under contracts that are not guaranteed benefit policies. As a result, certain transactions 
related to those general account assets are subject to conflict of interest and other restrictions, and the Company must provide 
certain disclosures to policyholders annually. The Company must comply with these restrictions or face substantial penalties. 

In addition, ERISA generally preempts all state and local laws that relate to employee benefit plans, but the extent of the pre-
emption continues to be reviewed by courts, including the U.S. Supreme Court.

20

Other Legislative Initiatives and Regulatory Initiatives - The U.S. federal and state governments, as well as governments in 
other countries where the Company does business, continue to enact and seriously consider many broad-based legislative and 
regulatory proposals that have had a material impact on or could materially impact various aspects of the health care and related 
benefits system and the Company’s businesses, operating results and/or cash flows. For example:

•  Under the Budget Control Act of 2011 and the American Taxpayer Relief Act of 2012 significant, automatic across-the-

board budget cuts (known as sequestration) began in March 2013, including Medicare spending cuts of not more than 2% 
of total program costs per year through 2024. Significant uncertainty remains as to whether and how the U.S. Congress will 
proceed with actions that create additional federal revenue and/or with entitlement reform. The Company cannot predict 
future federal Medicare or federal or state Medicaid funding levels or the impact that future federal or state budget actions 
or entitlement program reform, if it occurs, will have on the Company’s businesses, operations or operating results, but the 
effects could be materially adverse, particularly on the Company’s Medicare and/or Medicaid revenues, MBRs and 
operating results.

•  The European Union’s (“EU’s”) General Data Protection Regulation (“GDPR”) began to apply across the EU during 2018.

•  Other significant legislative and/or regulatory measures which are or recently have been under consideration include the 

following:

•  Elimination of the payment of manufacturer’s rebates on prescription drugs to PBMs, PDPs and Managed 

Medicaid organizations in connection with federally funded health care programs. 

• 

Imposing requirements and restrictions on the design and/or administration of pharmacy benefit plans offered by 
the Company’s and its clients’ health plans and/or its PBM clients and/or the services the Company provides to 
those clients, including prohibiting “differential” or “spread” pricing in PBM contracts; restricting or eliminating 
the use of formularies for prescription drugs; restricting the Company’s ability to require members to obtain drugs 
through a home delivery or specialty pharmacy; restricting the Company’s ability to place certain specialty or 
other drugs in the higher cost tiers of its pharmacy formularies; restricting the Company’s ability to make changes 
to drug formularies and/or clinical programs; limiting or eliminating rebates on pharmaceuticals; requiring the use 
of up front purchase price discounts on pharmaceuticals in lieu of rebates; restricting the Company’s ability to 
configure its health plan and retail pharmacy provider networks; and restricting or eliminating the use of certain 
drug pricing methodologies.

• 

Increased federal or state government regulation of, or involvement in, the pricing and/or purchasing of drugs.

•  Restricting the Company’s ability to limit providers’ participation in its networks and/or remove providers from its 
networks by imposing network adequacy requirements or otherwise (including in its Medicare and Commercial 
Health Care Benefits products).

• 

Imposing assessments on (or to be collected by) health plans or health carriers that may or may not be passed 
through to their customers. These assessments may include assessments for insolvency, the uninsured, 
uncompensated care, Medicaid funding or defraying health care provider medical malpractice insurance costs.

•  Mandating coverage by the Company’s and its clients’ health plans for additional conditions and/or specified 
procedures, drugs or devices (for example, high cost pharmaceuticals, experimental pharmaceuticals and oral 
chemotherapy regimens).

•  Regulating electronic connectivity.

•  Mandating or regulating the disclosure of provider fee schedules, manufacturer’s rebates and other data about the 
Company’s payments to providers and/or payments the Company receives from pharmaceutical manufacturers.

•  Mandating or regulating disclosure of provider outcome and/or efficiency information.

• 

• 

Prescribing or limiting members’ financial responsibility for health care or other covered services they utilize, 
including restricting “surprise” bills by providers and by specifying procedures for resolving “surprise” bills.

Prescribing payment levels for health care and other covered services rendered to the Company’s members by 
providers who do not have contracts with the Company.

•  Assessing the medical device status of HIT products and/or solutions, mobile consumer wellness tools and clinical 

decision support tools, which may require compliance with FDA requirements in relation to some of these 
products, solutions and/or tools.

•  Restricting the ability of employers and/or health plans to establish or impose member financial responsibility.

•  Amending or supplementing ERISA to impose greater requirements on PBMs or the administration of employer-
funded benefit plans or limit the scope of current ERISA pre-emption, which would among other things expose 
the Company and other health plans to expanded liability for punitive and other extra-contractual damages and 
additional state regulation.

21

It is uncertain whether the Company can counter the potential adverse effects of such potential legislation or regulation on its 
operating results or cash flows, including whether it can recoup, through higher premium rates, expanded membership or other 
measures, the increased costs of mandated coverage or benefits, assessments, fees, taxes or other increased costs, including the 
cost of modifying its systems to implement any enacted legislation or regulations.

The Company’s businesses also may be affected by other legislation and regulations. The Dodd-Frank Wall Street Reform and 
Consumer Protection Act (the “Financial Reform Act”) creates incentives for whistleblowers to speak directly to the 
government rather than utilizing internal compliance programs and reduces the burden of proof under the Foreign Corrupt 
Practices Act of 1977 (the “FCPA”). There also are laws and regulations that set standards for the escheatment of funds to 
states.

Health savings accounts, health reimbursement arrangements and flexible spending accounts and certain of the tax, fee and 
subsidy provisions of the ACA also are regulated by the U.S. Department of the Treasury and the Internal Revenue Service.

The Company also may be adversely affected by court and regulatory decisions that expand or revise the interpretations of 
existing statutes and regulations or impose medical malpractice or bad faith liability. Federal and state courts, including the U.S. 
Supreme Court, continue to consider cases, and federal and state regulators continue to issue regulations and interpretations, 
addressing bad faith liability for denial of medical claims, the scope of ERISA’s fiduciary duty requirements, the scope of the 
False Claims Act and the pre-emptive effect of ERISA on state laws.

Contract Audits - The Company is subject to audits of many of its contracts, including its PBM client contracts, its PBM 
rebate contracts, its PBM network contracts, its contracts relating to Medicare Advantage and/or Medicare Part D, the 
agreements the Company’s pharmacies enter into with other payors, its Medicaid contracts and its customer contracts. Because 
some of the Company’s contracts are with state or federal governments or with entities contracted with state or federal agencies, 
audits of these contracts are often regulated by the federal or state agencies responsible for administering federal or state 
benefits programs, including those which operate Medicaid fee for service plans, Managed Medicaid plans, Medicare Part D 
plans or Medicare Advantage organizations.

Federal Employee Health Benefits Program - The Company’s subsidiaries contract with the Office of Personnel Management 
(the “OPM”) to provide managed health care services under the FEHB program in their service areas. These contracts with the 
OPM and applicable government regulations establish premium rating arrangements for this program. OPM regulations require 
that community-rated FEHB plans meet a FEHB program-specific minimum MLR by plan code and market. Managing to these 
rules is complicated by the simultaneous application of the minimum MLR standards and associated premium rebate 
requirements of the ACA. The Company also has a contractual arrangement with carriers for the FEHB program, such as the 
BlueCross BlueShield Association, to provide pharmacy services to federal employees, postal workers, annuitants, and their 
dependents under the Government-wide Service Benefit Plan, as authorized by the FEHB Act and as part of the FEHB program. 
Additionally, the Company manages certain FEHB plans on a “cost-plus” basis. These arrangements subject the Company to 
certain aspects of FEHB Act, and other federal regulations, such as the FEHB Acquisition Regulation, that otherwise would not 
be applicable to the Company. The OPM also is auditing the Company and its other contractors to, among other things, verify 
that plans meet their applicable FEHB program-specific MLR and the premiums established under the OPM’s Insured contracts 
and costs allocated pursuant to the OPM’s cost-based contracts are in compliance with the requirements of the applicable FEHB 
program. The OPM may seek premium refunds or institute other sanctions against the Company if it fails to comply with the 
FEHB program requirements.

Clinical Services Regulation - The Company provides clinical services to health plan and PBM plan members for complex 
and common medical conditions, including arranging for those members to participate in disease management programs. State 
laws regulate the practice of medicine, the practice of pharmacy, the practice of nursing and certain other clinical activities. 
Clinicians engaged in a professional practice in connection with the provision of clinical services must satisfy applicable state 
licensing requirements and must act within their scope of practice.

Third Party Administration and Other State Licensure Laws - Many states have licensure or registration laws governing 
certain types of administrative organizations, such as PPOs, TPAs and companies that provide utilization review services. 
Several states also have licensure or registration laws governing the organizations that provide or administer consumer card 
programs (also known as cash card or discount card programs).

International Regulation - The Company has insurance licenses in several foreign jurisdictions and does business directly or 
through local affiliations in numerous countries around the world. The Company has taken steps to be able to continue to serve 

22

customers in the European Economic Area following the United Kingdom’s exit from the EU (“Brexit”). However, the impact 
of Brexit on the Company’s international business and operating results is uncertain. 

The Company’s international operations are subject to different, and sometimes more stringent, legal and regulatory 
requirements, which vary widely by jurisdiction, including anti-corruption laws; economic sanctions laws; various privacy, 
insurance, tax, tariff and trade laws and regulations; corporate governance, privacy, data protection (including the EU’s General 
Data Protection Regulation which began to apply across the EU during 2018), data mining, data transfer, labor and 
employment, intellectual property, consumer protection and investment laws and regulations; discriminatory licensing 
procedures; compulsory cessions of reinsurance; required localization of records and funds; higher premium and income taxes; 
limitations on dividends and repatriation of capital; and requirements for local participation in an insurer’s ownership. In 
addition, the expansion of the Company’s operations into foreign countries increases the Company’s exposure to the anti-
bribery, anti-corruption and anti-money laundering provisions of U.S. law, including the FCPA, and corresponding foreign laws, 
including the U.K. Bribery Act 2010 (the “UK Bribery Act”). 

Anti-Corruption Laws - The FCPA prohibits offering, promising or authorizing others to give anything of value to a foreign 
government official to obtain or retain business or otherwise secure a business advantage. The Company also is subject to 
applicable anti-corruption laws of the jurisdictions in which it operates. In many countries outside the United States, health care 
professionals are employed by the government. Therefore, the Company’s dealings with them are subject to regulation under 
the FCPA. Violations of the FCPA and other anti-corruption laws may result in severe criminal and civil sanctions as well as 
other penalties, and there continues to be a heightened level of FCPA enforcement activity by the U.S. Securities and Exchange 
Commission (the “SEC”) and the DOJ. The UK Bribery Act is an anti-corruption law that is broader in scope than the FCPA 
and applies to all companies with a nexus to the United Kingdom. Disclosures of FCPA violations may be shared with the UK 
authorities, thus potentially exposing companies to liability and potential penalties in multiple jurisdictions. The Company has 
internal control policies and procedures and conducts training and compliance programs for its employees to deter prohibited 
practices. However, if the Company’s employees or agents fail to comply with applicable laws governing its international or 
other operations, it may face investigations, prosecutions and other legal proceedings and actions which could result in civil 
penalties, administrative remedies and criminal sanctions.

Anti-Money Laundering Regulations - Certain lines of the Company’s businesses are subject to Treasury anti-money 
laundering regulations. Those lines of business have implemented anti-money laundering policies designed to ensure their 
compliance with the regulations. The Company also is subject to anti-money laundering laws in non-U.S. jurisdictions where it 
operates.

Office of Foreign Assets Control - The Company also is subject to regulation by OFAC. OFAC administers and enforces 
economic and trade sanctions based on U.S. foreign policy and national security goals against targeted foreign countries and 
regimes, terrorists, international narcotics traffickers, those engaged in activities related to the proliferation of weapons of mass 
destruction, and other threats to the national security, foreign policy or economy of the United States. In addition, the Company 
is subject to similar regulations in the non-U.S. jurisdictions in which it operates.

FDA Regulation - The FDA regulates the Company’s compounding pharmacy and clinical research operations. The FDA also 
generally has authority to, among other things, regulate the manufacture, distribution, sale and labeling of medical devices 
(including hemodialysis devices such as the device the Company is developing and mobile medical devices) and many products 
sold through retail pharmacies, including prescription drugs, over-the-counter medications, cosmetics, dietary supplements and 
certain food items. In addition, the FDA regulates the Company’s activities as a distributor of store brand products.

Laws and Regulations Related to the Pharmacy Services Segment

In addition to the laws and regulations discussed above that may affect multiple segments of the Company’s business, the 
Company is subject to federal, state and local statutes and regulations governing the operation of its Pharmacy Services 
segment specifically. Among these are the following:

PBM Laws and Regulation - Legislation and/or regulations seeking to regulate PBM activities in a comprehensive manner 
have been proposed or enacted in a number of states. This legislation could adversely affect the Company’s ability to conduct 
business on commercially reasonable terms in states where the legislation is in effect and the Company’s ability to standardize 
its PBM products and services across state lines. In addition, certain quasi-regulatory organizations, including the National 
Association of Boards of Pharmacy and the National Association of Insurance Commissioners (“NAIC”) and the National 
Council of Insurance Legislators, have issued model regulations or may propose future regulations concerning PBMs and/or 
PBM activities. Similarly, credentialing organizations such as NCQA and URAC may establish voluntary standards regarding 

23

PBM, mail order pharmacy and/or specialty pharmacy activities. While the actions of these quasi-regulatory or standard-setting 
organizations do not have the force of law, they may influence states to adopt their requirements or recommendations and 
influence client requirements for PBM, mail order pharmacy and/or specialty pharmacy services. Moreover, any standards 
established by these organizations could also impact the Company’s health plan clients and/or the services provided to those 
clients and/or the Company’s health plans.

The Company’s PBM activities also are regulated directly and indirectly at the federal and state levels, including being subject 
to the False Claims Act and state false claims acts and federal and state anti-kickback laws. These laws and regulations govern, 
and proposed legislation and regulations may govern and/or further restrict, critical PBM practices, including disclosure, receipt 
and retention of rebates and other payments received from pharmaceutical manufacturers; use of, administration of and/or 
changes to drug formularies, maximum allowable cost (“MAC”) list pricing, average wholesale prices (“AWPs”) and/or clinical 
programs; the offering to plan sponsors of pricing that includes retail network “differential” or “spread” (i.e., a difference 
between the drug price charged to the plan sponsor by a PBM and the price paid by the PBM to the dispensing provider); 
disclosure of data to third parties; drug utilization management practices; the level of duty a PBM owes its customers; 
configuration of pharmacy networks; the operations of the Company’s pharmacies (including audits of its pharmacies); 
disclosure of negotiated provider reimbursement rates; disclosure of fees associated with administrative service agreements and 
patient care programs that are attributable to members’ drug utilization; and registration or licensing of PBMs. Failure by the 
Company or one of its PBM services suppliers to comply with these laws or regulations could result in material fines and/or 
sanctions and could have a material adverse effect on the Company’s operating results and/or cash flows.

The Company’s PBM service contracts, including those in which the Company assumes certain risks under performance 
guarantees or similar arrangements, are generally not subject to insurance regulation by the states. However, state departments 
of insurance are increasing their oversight of PBM activities due to legislation passing in a number of states requiring PBMs to 
register or obtain a license with the department. Rulemaking is either underway or has already taken place in a number of states 
with the areas of focus on licensure requirements, pharmacy reimbursement for generics (MAC reimbursement) and pharmacy 
audits - most of which fall under the state insurance code.

Pharmacy Network Access Legislation - Medicare Part D and a majority of states now have some form of legislation 
affecting the Company’s (and its health plans’ and its health plan clients’) ability to limit access to a pharmacy provider network 
or remove pharmacy network providers. For example, certain “any willing provider” legislation may require the Company or its 
clients to admit a nonparticipating pharmacy if such pharmacy is willing and able to meet the plan’s price and other applicable 
terms and conditions for network participation. These laws could negatively affect the services and economic benefits 
achievable through a limited pharmacy provider network. Also, a majority of states now have some form of legislation affecting 
the Company’s ability (and the Company’s and its client health plans’ ability) to conduct audits of network pharmacies 
regarding claims submitted to the Company for payment. These laws could negatively affect the Company’s ability to recover 
overpayments of claims submitted by network pharmacies that the Company identifies through pharmacy audits. 

Pharmacy Pricing Legislation - A number of states have passed legislation regulating the Company’s ability to manage and 
establish MACs for generic prescription drugs. MAC methodology is a common cost management practice used by private and 
public payors (including CMS) to pay pharmacies for dispensing generic prescription drugs. MAC prices specify the allowable 
reimbursement by a PBM for a particular strength and dosage of a generic drug that is available from multiple manufacturers 
but sold at different prices. State legislation can regulate the disclosure of MAC prices and MAC price methodologies, the kinds 
of drugs that a PBM can pay for at a MAC price, and the rights of pharmacies to appeal a MAC price established by a PBM. 
These laws could negatively affect the Company’s ability to establish MAC prices for generic drugs.

Formulary and Plan Design Regulation - A number of government entities regulate the administration of prescription drug 
benefits. HHS regulates how Medicare Part D formularies are developed and administered, including requiring the inclusion of 
all drugs in certain classes and categories, subject to limited exceptions. Under the ACA, CMS imposes drug coverage 
requirements for health plans required to cover essential health benefits, including plans offered through federal or state Public 
Exchanges. Additionally, the NAIC and health care accreditation agencies like NCQA and URAC have developed model acts 
and standards for formulary development that are often incorporated into government requirements. Many states regulate the 
scope of prescription drug coverage, as well as the delivery channels to receive prescriptions, for insurers, MCOs and Medicaid 
managed care plans. The increasing government regulation of formularies could significantly affect the Company’s ability to 
develop and administer formularies, pharmacy networks and other plan design features on behalf of its insurer, MCO and other 
clients. Similarly, some states prohibit health plan sponsors from implementing certain restrictive pharmacy benefit plan design 
features. This regulation could limit or preclude (i) limited networks, (ii) a requirement to use particular providers, (iii) 
copayment differentials among providers and (iv) formulary tiering practices. 

24

Laws and Regulations Related to the Retail/LTC Segment

In addition to the laws and regulations discussed above that may affect multiple segments of the Company’s business, the 
Company is subject to federal, state and local statutes and regulations governing the operation of its Retail/LTC segment 
specifically. Among these are the following:

Retail Medical Clinics - States regulate retail medical clinics operated by nurse practitioners or physician assistants through 
physician oversight, clinic and lab licensure requirements and the prohibition of the corporate practice of medicine. A number 
of states have implemented or proposed laws or regulations that impact certain components of retail medical clinic operations 
such as physician oversight, signage, third party contracting requirements, bathroom facilities, and scope of services. These 
laws and regulations may affect the operation and expansion of the Company’s owned and managed retail medical clinics.

Other Laws - Other federal, state and local laws and regulations also impact the Company’s retail operations, including laws 
and regulations governing the practice of optometry, the practice of audiology, the provision of dietician services and the sale of 
durable medical equipment, contact lenses, eyeglasses, hearing aids and alcohol.

Laws and Regulations Related to the Health Care Benefits Segment

In addition to the laws and regulations discussed above that may affect multiple segments of the Company’s business, the 
Company is subject to federal, state, local and international statutes and regulations governing its Health Care Benefits segment 
specifically. 

Overview - Differing approaches to state insurance regulation and varying enforcement philosophies may materially and 
adversely affect the Company’s ability to standardize its Health Care Benefits products and services across state lines. These 
laws and regulations, including the ACA, restrict how the Company conducts its business and result in additional burdens and 
costs to the Company. Significant areas of governmental regulation include premium rates and rating methodologies, 
underwriting rules and procedures, required benefits, sales and marketing activities, provider rates of payment, restrictions on 
health plans’ ability to limit providers’ participation in their networks and/or remove providers from their networks and 
financial condition (including reserves and minimum capital or risk based capital requirements). These laws and regulations are 
different in each jurisdiction and vary from product to product.

Each health insurer and HMO must file periodic financial and operating reports with the states in which it does business. In 
addition, health insurers and HMOs are subject to state examination and periodic license renewal. Applicable laws also restrict 
the ability of the Company’s regulated subsidiaries to pay dividends, and certain dividends require prior regulatory approval. In 
addition, some of the Company’s businesses and related activities may be subject to PPO, managed care organization, 
utilization review or TPA-related licensure requirements and regulations. These licensure requirements and regulations differ 
from state to state, but may contain provider network, contracting, product and rate, financial and reporting requirements. There 
also are laws and regulations that set specific standards for the Company’s delivery of services, payment of claims, fraud 
prevention, protection of consumer health information, and payment for covered benefits and services.

Required Regulatory Approvals - The Company must obtain and maintain regulatory approvals to price, market and 
administer many of its Health Care Benefits products. Supervisory agencies, including CMS, the Center for Consumer 
Information and Insurance Oversight and the DOL, as well as state health, insurance, managed care and Medicaid agencies, 
have broad authority to take one or more of the following actions:

•  Grant, suspend and revoke the Company’s licenses to transact business;

• 

• 

Suspend or exclude the Company from participation in government programs;

Suspend or limit the Company’s authority to market products;

•  Regulate many aspects of the products and services the Company offers, including the pricing and underwriting of many of 

its products and services;

•  Assess damages, fines and/or penalties;

•  Terminate the Company’s contract with the government agency and/or withhold payments from the government agency to 

the Company;

• 

Impose retroactive adjustments to premiums and require the Company to pay refunds to the government, customers and/or 
members;

•  Restrict the Company’s ability to conduct acquisitions or dispositions;

25

•  Require the Company to maintain minimum capital levels in its subsidiaries and monitor its solvency and reserve 

adequacy;

•  Regulate the Company’s investment activities on the basis of quality, diversification and other quantitative criteria; and/or

•  Exclude the Company’s plans from participating in Public Exchanges if they are deemed to have a history of 
“unreasonable” premium rate increases or fail to meet other criteria set by HHS or the applicable state.

The Company’s operations, current and past business practices, current and past contracts, and accounts and other books and 
records are subject to routine, regular and special investigations, audits, examinations and reviews by, and from time to time the 
Company receives subpoenas and other requests for information from, federal, state and international supervisory and 
enforcement agencies, attorneys general and other state, federal and international governmental authorities and legislators. 

Commercial Product Pricing and Underwriting Restrictions - Pricing and underwriting regulation by states limits the 
Company’s underwriting and rating practices and those of other health insurers, particularly for small employer groups, and 
varies by state. In general, these limitations apply to certain customer segments and limit the Company’s ability to set prices for 
new or renewing groups, or both, based on specific characteristics of the group or the group’s prior claim experience. In some 
states, these laws and regulations restrict the Company’s ability to price for the risk it assumes and/or reflect reasonable costs in 
the Company’s pricing.

The ACA expanded the premium rate review process by, among other things, requiring the Company’s Commercial Insured 
rates to be reviewed for “reasonableness” at either the state or the federal level. HHS established a federal premium rate review 
process that generally applies to proposed premium rate increases equal to or exceeding a federally (or lower state) specified 
threshold. HHS’s rate review process imposes additional public disclosure requirements as well as additional review on filings 
requesting premium rate increases equal to or exceeding this “reasonableness” threshold. These combined state and federal 
review requirements may prevent, further delay or otherwise affect the Company’s ability to price for the risk it assumes, which 
could adversely affect its MBRs and operating results, particularly during periods of increased utilization of medical services 
and/or medical cost trend or when such utilization and/or trend exceeds the Company’s projections.

The ACA also specifies minimum MLRs of 85% for large group Commercial products and 80% for individual and small group 
Commercial products. Because the ACA minimum MLRs are structured as “floors” for many of their requirements, states have 
the latitude to enact more stringent rules governing these restrictions. For Commercial products, states have and may adopt 
higher minimum MLR requirements, use more stringent definitions of “medical loss ratio,” incorporate minimum MLR 
requirements into prospective premium rate filings, require prior approval of premium rates or impose other requirements 
related to minimum MLR. Minimum MLR requirements and similar actions further limit the level of margin the Company can 
earn in its Insured Commercial products while leaving the Company exposed to medical costs that are higher than those 
reflected in its pricing. The Company also may be subject to significant fines, penalties, premium refunds and litigation if it 
fails to comply with minimum MLR laws and regulations. 

In addition, the Company requested significant increases in its premium rates in its Commercial Health Care Benefits business 
for 2020 (including as a result of the reinstatement of the HIF for 2020 following the temporary suspension of the HIF for 
2019) and expects to continue to request increases in those rates for 2021 and beyond in order to adequately price for projected 
medical cost trends, required expansions of coverage and rating limits, and significant assessments, fees and taxes imposed by 
the federal and state governments, including as a result of the ACA. The Company’s rates also must be adequate to reflect 
adverse selection in its products, particularly in small group Commercial products, which the Company expects to continue and 
potentially worsen in 2020. These rate increases may be significant and thus heighten the risks of adverse publicity, adverse 
regulatory action and adverse selection and the likelihood that the Company’s requested premium rate increases will be denied, 
reduced or delayed, which could lead to operating margin compression.

Many of the laws and regulations governing the Company’s pricing and underwriting practices also limit the differentials in 
premium rates insurers and other carriers may charge between new and renewal business, and/or between groups based on 
differing characteristics. They may also require that carriers disclose to customers the basis on which the carrier establishes new 
business and renewal premium rates and limit the ability of a carrier to terminate customers’ coverage. 

Medicaid Regulation - The Company is seeking to substantially grow its Medicaid, dual eligible and dual eligible special 
needs plan businesses over the next several years. As a result, the Company also is increasing its exposure to changes in 
government policy with respect to and/or regulation of the various Medicaid, dual eligible and dual eligible special needs plan 
programs in which the Company participates, including changes in the amounts payable to the Company under those programs.

26

Since 2017, Managed Medicaid products, including those the Company offers, are subject to a minimum federal MLR of 85%. 
A Medicaid managed care quality rating system and provider network adequacy requirements also apply to Medicaid products. 
Because the federal minimum MLR is structured as a “floor,” states have the latitude to enact more stringent rules governing 
these restrictions. For Managed Medicaid products, states may adopt higher minimum MLR requirements, use more stringent 
definitions of “medical loss ratio” or impose other requirements related to minimum MLR. Minimum MLR requirements and 
similar actions further limit the level of margin the Company can earn in its Insured Medicaid products while leaving the 
Company exposed to medical costs that are higher than those reflected in its pricing. The Company also may be subject to 
significant fines, penalties, premium refunds and litigation if it fails to comply with minimum MLR laws and regulations.

The impact of Medicaid expansion under the ACA is uncertain. The future of the ACA is uncertain, and states may opt out of 
the elements of the ACA requiring expansion of Medicaid coverage without losing their current federal Medicaid funding. To 
date, a number of states and the District of Columbia have expanded Medicaid coverage to the higher eligibility levels 
contemplated by the ACA. In addition, the election of new governors and/or state legislatures may impact states’ previous 
decisions regarding Medicaid expansion. Proposals for substantial changes to federal funding of state Medicaid programs are 
likely to be considered in 2020 and beyond, including the possibility of converting federal Medicaid support to block grants 
(such as the block grant option outlined by CMS on January 30, 2020) and per capita caps on federal funding. Uncertainty 
regarding federal funding is causing and will continue to cause states to re-evaluate their Medicaid expansions and consider 
new assessments, fees and/or taxes on health plans. That re-evaluation and any changes to federal funding of state Medicaid 
programs may adversely affect Medicaid payment rates, the Company’s revenues and its Medicaid membership.

The economic aspects of the Medicaid, dual eligible and dual eligible special needs plan business vary from state to state and 
are subject to frequent change. Medicaid premiums are paid by each state and differ from state to state. The federal government 
and certain states also are considering proposals and legislation for Medicaid and dual eligible program reforms or redesigns, 
including restrictions on the collection of manufacturer’s rebates on pharmaceuticals by Medicaid MCOs and their contracted 
PBMs, further program, population and/or geographic expansions of risk-based managed care, increasing beneficiary cost-
sharing or payment levels, and changes to benefits, reimbursement, eligibility criteria, provider network adequacy requirements 
(including requiring the inclusion of specified high cost providers in the Company’s networks) and program structure. In some 
states, current Medicaid and dual eligible funding and premium revenue may not be adequate for the Company to continue 
program participation. The Company’s Medicaid and dual eligible contracts with states (or sponsors of Medicaid managed care 
plans) are subject to cancellation by the state (or the sponsors of the managed care plans) after a short notice period without 
cause (for example, when a state discontinues a managed care program) or in the event of insufficient state funding.

The Company’s Medicaid, dual eligible and dual eligible special needs plan products also are heavily regulated by CMS and 
state Medicaid agencies, which have the right to audit the Company’s performance to determine compliance with CMS 
contracts and regulations. The Company’s Medicaid products, dual eligible products and CHIP contracts also are subject to 
complex federal and state regulations and oversight by state Medicaid agencies regarding the services provided to Medicaid 
enrollees, payment for those services, network requirements (including mandatory inclusion of specified high-cost providers), 
and other aspects of these programs, and by external review organizations which audit Medicaid plans on behalf of state 
Medicaid agencies. The laws, regulations and contractual requirements applicable to the Company and other participants in 
Medicaid and dual eligible programs, including requirements that the Company submit encounter data to the applicable state 
agency, are extensive, complex and subject to change. The Company has invested significant resources to comply with these 
standards, and its Medicaid and dual eligible program compliance efforts will continue to require significant resources. CMS 
and/or state Medicaid agencies may fine the Company, withhold payments to the Company, seek premium and other refunds, 
terminate the Company’s existing contracts, elect not to award the Company new contracts or not to renew the Company’s 
existing contracts, prohibit the Company from continuing to market and/or enroll members in or refuse to automatically assign 
members to one or more of the Company’s Medicaid or dual eligible products, exclude the Company from participating in one 
or more Medicaid or dual eligible programs and/or institute other sanctions and/or civil monetary penalties against the 
Company if it fails to comply with CMS or state regulations or contractual requirements.

The Company cannot predict whether pending or future federal or state legislation or court proceedings will change various 
aspects of the Medicaid program, nor can it predict the impact those changes will have on its business operations or operating 
results, but the effects could be materially adverse.

State Workers’ Compensation Laws - The Company’s workers’ compensation business includes the comparison of medical 
claims data against the applicable state’s fee schedule pricing, including applicable regulations and clinical guidelines. State fee 
schedules, which typically represent the maximum reimbursement for medical services provided to the injured worker, differ by 
state and change as state laws and regulations are passed and/or amended. The Company’s workers’ compensation business also 
includes PBM and care management services, both of which are regulated at the state level. The Company’s workers’ 

27

compensation customers include insurance carriers and TPAs who also are regulated at the state level. The laws and regulations 
applicable to the Company and other participants in the workers’ compensation business are extensive, complex and subject to 
change. The Company has invested significant resources to comply with these standards, and its workers’ compensation 
compliance efforts will continue to require significant resources. The Company may be subject to significant fines, penalties 
and litigation if it fails to comply with those laws and regulations.

Federal and State Reporting - The Company is subject to extensive financial and business reporting requirements, including 
penalties for inaccuracies and/or omissions, at both the federal and state level. The Company’s ability to comply with certain of 
these requirements depends on receipt of information from third parties that may not be readily available or reliably provided in 
all instances. The Company is and will continue to be required to modify its information systems, dedicate significant resources 
and incur significant expenses to comply with these requirements. However, the Company cannot eliminate the risks of 
unavailability of or errors in its reports.

Product Design and Administration and Sales Practices - State and/or federal regulatory scrutiny of health care benefit 
product design and administration and marketing and advertising practices, including the filing of insurance policy forms, the 
adequacy of provider networks, the accuracy of provider directories, and the adequacy of disclosure regarding products and 
their administration, is increasing as are the penalties being imposed for inappropriate practices. Medicare, Medicaid and dual 
eligible products and products offering more limited benefits in particular continue to attract increased regulatory scrutiny.

Guaranty Fund Assessments/Solvency Protection - Under guaranty fund laws existing in all states, insurers doing business in 
those states can be assessed (in most states up to prescribed limits) for certain obligations of insolvent insurance companies to 
policyholders and claimants. The life and health insurance guaranty associations in which the Company participates that operate 
under these laws respond to insolvencies of long-term care insurers as well as health insurers. The Company’s assessments 
generally are based on a formula relating to the Company’s health care premiums in the state compared to the premiums of 
other insurers. Certain states allow assessments to be recovered over time as offsets to premium taxes. Some states have similar 
laws relating to HMOs and/or other payors such as not-for-profit consumer governed health plans established under the ACA. 
While historically the Company has ultimately recovered more than half of guaranty fund assessments through statutorily 
permitted premium tax offsets, significant increases in assessments could lead to legislative and/or regulatory actions that limit 
future offsets.

Available Information

CVS Health Corporation was incorporated in Delaware in 1996. The corporate office is located at One CVS Drive, 
Woonsocket, Rhode Island 02895, telephone (401) 765-1500. CVS Health’s common stock is listed on the New York Stock 
Exchange under the trading symbol “CVS.” General information about CVS Health is available through the Company’s website 
at http://www.cvshealth.com. The Company’s financial press releases and filings with the SEC are available free of charge 
within the Investors section of the Company’s website at http://investors.cvshealth.com. In addition, the SEC maintains an 
internet site that contains reports, proxy and information statements and other information regarding issuers, such as the 
Company, that file electronically with the SEC. The address of that website is http://www.sec.gov. The information on or linked 
to the Company’s website is neither a part of nor incorporated by reference in this 10-K or any of the Company’s other SEC 
filings. 

In accordance with guidance provided by the SEC regarding use by a company of its websites and social media channels as a 
means to disclose material information to investors and to comply with its disclosure obligations under SEC Regulation FD, 
CVS Health Corporation (the “Registrant”) hereby notifies investors, the media and other interested parties that it intends to 
continue to use its media and investor relations website (http://investors.cvshealth.com/) and its Twitter feed (@CVSHealthIR) 
to publish important information about the Registrant, including information that may be deemed material to investors. The list 
of social media channels that the Registrant uses may be updated on its media and investor relations website from time to time. 
The Registrant encourages investors, the media, and other interested parties to review the information the Registrant posts on its 
website and social media channels as described above, in addition to information announced by the Registrant through its SEC 
filings, press releases and public conference calls and webcasts. 

28

Item 1A.  Risk Factors.

You should carefully consider each of the following risks and uncertainties and all of the other information set forth in this 
Form 10-K. These risks and uncertainties and other factors may affect forward-looking statements, including those we make in 
this Form 10-K or elsewhere, such as in news releases or investor or analyst calls, meetings or presentations, on our websites or 
through our social media channels. The risks and uncertainties described below are not the only ones we face. There can be no 
assurance that we have identified all the risks that affect us. Additional risks and uncertainties not presently known to us or that 
we currently believe to be immaterial also may adversely affect our businesses. Any of these risks or uncertainties could cause 
our actual results to differ materially from our expectations and the expected results discussed in our forward-looking 
statements. You should not consider past results to be an indication of future performance.

If any of the following risks or uncertainties develops into actual events or if the circumstances described in the risks or 
uncertainties occur or continue to occur, those events or circumstances could have a material adverse effect on our businesses, 
operating results, cash flows, financial condition and/or stock price, among other effects on us. You should read the following 
section in conjunction with the MD&A, included in Item 7 of this Form 10-K, our consolidated financial statements and the 
related notes, included in Item 8 of this 10-K, and our “Cautionary Statement Concerning Forward-Looking Statements” in this 
10-K.

Risks Relating to Our Businesses

Each of our segments operates in a highly competitive and evolving business environment; and gross margins in the 
industries in which we compete may decline.

Each of our segments, Pharmacy Services, which includes our pharmacy benefit management (“PBM”) business, Retail/LTC, 
and Health Care Benefits, operates in a highly competitive and evolving business environment. Specifically:

•  As competition increases in the geographies in which we operate, including competition from new entrants, a significant 
increase in price compression and/or reimbursement pressures could occur, and this could require us to reevaluate our 
pricing structures to remain competitive.

•  The competitive success of our Pharmacy Services segment is dependent on our ability to establish and maintain 

contractual relationships with network pharmacies as PBM clients evaluate adopting narrow or restricted retail pharmacy 
networks. 

•  The competitive success of our Retail/LTC segment and our specialty pharmacy operations is dependent on our ability to 
establish and maintain contractual relationships with PBMs and other payors on acceptable terms as the payors’ clients 
evaluate adopting narrow or restricted retail pharmacy networks. 

• 

In our PBM business, we maintain contractual relationships with brand name drug manufacturers that provide for purchase 
discounts and/or rebates on drugs dispensed by pharmacies in our retail network and by our specialty and mail order 
pharmacies (all or a portion of which may be passed on to clients). Manufacturer’s rebates often depend on a PBM’s ability 
to meet contractual requirements, including the placement of a manufacturer’s products on the PBM’s formularies. If we 
lose our relationship with one or more drug manufacturers, or if the discounts or rebates provided by drug manufacturers 
decline, our operating results, cash flows and/or prospects could be adversely affected. 

•  The PBM industry has been experiencing price compression as a result of competitive pressures and increased client 

demands for lower prices, increased revenue sharing, including sharing in a larger portion of rebates received from drug 
manufacturers, enhanced service offerings and/or higher service levels. Marketplace dynamics and regulatory changes also 
have adversely affected our ability to offer plan sponsors pricing that includes the use of retail “differential” or “spread,” 
which could adversely affect our future profitability, and we expect these trends to continue.

•  Our retail pharmacy, specialty pharmacy and LTC pharmacy operations have been affected by reimbursement pressure 

caused by competition, including client demands for lower prices, generic drug pricing, earlier than expected generic drug 
introductions and network reimbursement pressure. If we are unable to increase our prices to reflect, or otherwise mitigate 
the impact of, increasing costs, our profitability will be adversely affected. If we are unable to limit our price increases, we 
may lose customers to competitors with more favorable pricing, adversely affecting our revenues and operating results.

•  A shift in the mix of our pharmacy prescription volume towards programs offering lower reimbursement rates as a result of 
competition or otherwise could adversely affect our margins, including the ongoing shift in pharmacy mix towards 90-day 
prescriptions at retail and the ongoing shift in pharmacy mix towards Medicare Part D prescriptions.

• 

PBM client contracts often are for a period of approximately three years. However, PBM clients may require early or 
periodic re-negotiation of pricing prior to contract expiration. PBM clients are generally well informed, can move between 
us and our competitors and often seek competing bids prior to expiration of their contracts. We are therefore under pressure 

29

to contain price increases despite being faced with increasing drug costs and increasing operating costs. If we are unable to 
increase our prices to reflect, or otherwise mitigate the impact of, increasing costs, our profitability will be adversely 
affected. If we are unable to limit our price increases, we may lose customers to competitors with more favorable pricing, 
adversely affecting our revenues and operating results.

•  The operating results and margins of our LTC business are further affected by the increased efforts of health care payors to 
negotiate reduced or capitated pricing arrangements and by the financial health of, and purchases and sales of, our LTC 
customers.

• 

In our Health Care Benefits segment we are seeking to substantially grow our Medicaid, dual eligible and dual eligible 
special needs plan membership over the next several years. In many instances, to acquire and retain our government 
customers’ business, we must bid against our competitors in a highly competitive environment. Winning bids often are 
challenged successfully by unsuccessful bidders.

•  Customer contracts in our Health Care Benefits segment are generally for a period of one year, and our customers have 
considerable flexibility in moving between us and our competitors. One of the key factors on which we compete for 
customers, especially in uncertain economic environments, is overall cost. We are therefore under pressure to contain 
premium price increases despite being faced with increasing health care and other benefit costs and increasing operating 
costs. If we are unable to increase our prices to reflect, or otherwise mitigate the impact of, increasing costs, our 
profitability will be adversely affected. If we are unable to limit our price increases, we may lose members to competitors 
with more favorable pricing, adversely affecting our revenues and operating results. In response to rising prices, our 
customers may elect to self-insure or to reduce benefits in order to limit increases in their benefit costs. Alternatively, our 
customers may purchase different types of products from us that are less profitable. Such elections may result in reduced 
membership in our more profitable Insured products and/or lower premiums for our Insured products, which may adversely 
affect our revenues and operating results, although such elections also may reduce our health care and other benefit costs. 
In addition, our Medicare, Medicaid and CHIP products are subject to termination without cause, periodic re-bid, rate 
adjustment and program redesign, as customers seek to contain their benefit costs, particularly in an uncertain economy, 
and our exposure to this risk is increasing as we grow our Government products membership. These actions may adversely 
affect our membership, revenues and operating results. 

•  We requested significant increases in our premium rates in our Commercial Health Care Benefits business for 2020 

(including as a result of the reinstatement for 2020 of the Health Insurer Fee (the “HIF”) imposed by the Patient Protection 
and Affordable Care Act and the Health Care and Education Reconciliation Act of 2010 (collectively, the “ACA”) 
following the temporary suspension of the HIF for 2019) and expect to continue to request increases in those rates for 2021 
and beyond in order to adequately price for projected medical cost trends, required expansions of coverage and rating 
limits, and significant assessments, fees and taxes imposed by the federal and state governments, including as a result of 
the ACA. Our rates also must be adequate to reflect the risk that our products will be selected by people with a higher risk 
profile or utilization rate than the pool of participants we anticipated when we established pricing for the applicable 
products (also known as “adverse selection”), particularly in small group Commercial products, which we expect to 
continue and potentially worsen in 2020. These rate increases may be significant and thus heighten the risks of adverse 
publicity, adverse regulatory action and adverse selection and the likelihood that our requested premium rate increases will 
be denied, reduced or delayed, which could lead to operating margin compression.

In addition, competitors in each of our businesses may offer services and pricing terms that we may not be willing or able to 
offer. Competition also may come from new entrants and other sources in the future. Unless we can demonstrate enhanced 
value to our clients through innovative product and service offerings in the rapidly changing health care industry, we may be 
unable to remain competitive.

Disruptive innovation by existing or new competitors could alter the competitive landscape in the future and require us to 
accurately identify and assess such alterations and make timely and effective changes to our strategies and business model to 
compete effectively. For example, decisions to buy our Pharmacy Services and Health Care Benefits products and services 
increasingly are made or influenced by consumers, either through direct purchasing (for example, Medicare Advantage plans 
and PDPs) or through public health insurance exchanges (“Public Exchanges”) and private health insurance exchanges 
(together with Public Exchanges, collectively, “Insurance Exchanges”) that allow individual choice. Consumers also are 
increasingly seeking to access consumer goods and health care products and services locally and through other direct channels 
such as mobile devices and websites. To compete effectively in the consumer-driven marketplace, we will be required to 
develop or acquire new capabilities, attract new talent and develop new service and distribution relationships that respond to 
consumer needs and preferences.

30

Changes in marketplace dynamics or the actions of competitors or manufacturers, including industry consolidation, the 
emergence of new competitors and strategic alliances, and decisions to exclude us from new narrow or restricted retail 
pharmacy networks could materially and adversely affect our businesses, operating results, cash flows and/or prospects. 

A change in our Health Care Benefits product mix may adversely affect our profit margins.

Our Insured Health Care Benefits products that involve greater potential risk generally tend to be more profitable than our ASC 
products. Historically, smaller employer groups have been more likely to purchase Insured Health Care Benefits products 
because such purchasers are generally unable or unwilling to bear greater liability for health care expenditures, although over 
the last several years even relatively small employers have moved to ASC products. We also serve, and expect to grow our 
business with, government-sponsored programs, including Medicare and Medicaid, that are subject to competitive bids and 
have lower profit margins than our Commercial Insured Health Care Benefits products. A shift of enrollees from more 
profitable products to less profitable products could have a material adverse effect on the Health Care Benefits segment’s 
operating results.

Negative public perception of the industries in which we operate, or of our industries’ or our practices, can adversely affect 
our businesses, operating results, cash flows and prospects.

Our brand and reputation are two of our most important assets, and the industries in which we operate have been and are 
negatively perceived by the public from time to time. Negative publicity may come as a result of adverse media coverage, 
litigation against us and other industry participants, the ongoing public debates over drug pricing, PBMs, government 
involvement in drug pricing and purchasing, the future of the ACA, “surprise” medical bills, governmental hearings and/or 
investigations, actual or perceived shortfalls regarding our industries’ or our own products and/or business practices (including 
PBM operations, drug pricing and insurance coverage determinations) and social media and other media relations activities.  
Negative publicity also may come from a failure to meet customer expectations for consistent, high quality and accessible care. 
This risk may increase as we continue to offer products and services that make greater use of data and as our business model 
becomes more focused on delivering health care to consumers. 

Negative public perception and/or publicity of our industries in general, or of us or our key vendors, brokers or product 
distribution networks in particular, can further increase our costs of doing business and adversely affect our operating results 
and our stock price by:

• 

• 

• 

• 

• 

adversely affecting our brand and reputation;

adversely affecting our ability to market and sell our products and/or services and/or retain our existing customers and 
members;

requiring us to change our products and/or services; 

reducing or restricting the revenue we can receive for our products and/or services; and/or

increasing or significantly changing the regulatory and legislative requirements with which we must comply.

We must maintain and improve our relationships with our retail and specialty pharmacy customers and increase the demand 
for our products and services, including proprietary brands.

The success of our businesses depends in part on customer loyalty, superior customer service and our ability to persuade 
customers to frequent our retail stores and online sites and to purchase products in additional categories and our proprietary 
brands. Failure to timely identify or effectively respond to changing consumer preferences and spending patterns, and evolving 
demographic mixes in the communities we serve, an inability to expand the products being purchased by our clients and 
customers, or the failure or inability to obtain or offer particular categories of products could adversely affect our relationship 
with our customers and clients and the demand for our products and services and could result in excess inventories of products.

We offer our retail customers proprietary brand products that are available exclusively at our retail stores and through our online 
retail sites. The sale of proprietary products subjects us to unique risks including potential product liability risks, mandatory or 
voluntary product recalls, potential supply chain and distribution chain disruptions for raw materials and finished products, our 
ability to successfully protect our intellectual property rights and the rights of applicable third parties, and other risks generally 
encountered by entities that source, market and sell private-label products. We also face similar risks for the other products we 
sell in our retail operations, including supply chain and distribution chain disruption risk. Any failure to adequately address 
some or all of these risks could have an adverse effect on our retail business, operating results, cash flows and/or financial 
condition. Additionally, an increase in the sales of our proprietary brands may adversely affect our sales of products owned by 

31

our suppliers and adversely impact certain of our supplier relationships. Our ability to locate qualified, economically stable 
suppliers who satisfy our requirements, and to acquire sufficient products in a timely and effective manner, is critical to 
ensuring, among other things, that customer confidence is not diminished. Any failure to develop sourcing relationships with a 
broad and deep supplier base could adversely affect our operating results and erode customer loyalty.

We also could be adversely affected if we fail to identify or effectively respond to changes in marketplace dynamics. For 
example, specialty pharmacy represents a significant and growing proportion of prescription drug spending in the U.S., a 
significant portion of which is dispensed outside of traditional retail pharmacies. Because our specialty pharmacy business 
focuses on complex and high-cost medications, many of which are made available by manufacturers to a limited number of 
pharmacies (so-called limited distribution drugs) that serve a relatively limited universe of patients, the future growth of our 
specialty pharmacy business depends largely upon expanding our access to key drugs and penetration in certain treatment 
categories. Any contraction of our base of patients or reduction in demand for the prescriptions we currently dispense could 
have an adverse effect on our specialty pharmacy business, operating results and cash flows.

We face risks relating to the availability, pricing and safety profiles of prescription drugs that we purchase and sell.

The profitability of our Retail/LTC and Pharmacy Services segments is dependent upon the utilization of prescription drug 
products. We dispense significant volumes of brand name and generic drugs from our retail, LTC, specialty and mail order 
pharmacies, and the retail pharmacies in our PBM’s network also dispense significant volumes of brand name and generic 
drugs. Our revenues, operating results and cash flows may decline if physicians cease writing prescriptions for drugs or the 
utilization of drugs is reduced due to:

• 

increased safety risk profiles or regulatory restrictions;

•  manufacturing or other supply issues;

• 

• 

• 

• 

certain products being withdrawn by their manufacturers or transitioned to over-the-counter products; 

future FDA rulings restricting the supply or increasing the cost of products;

the introduction of new and successful prescription drugs or lower-priced generic alternatives to existing brand name 
products; or 

inflation in the price of brand name drugs. 

In addition, increased utilization of generic drugs (which normally yield a higher gross profit rate than equivalent brand name 
drugs) has resulted in pressure to decrease reimbursement payments to retail, mail order, specialty and LTC pharmacies for 
generic drugs, causing a reduction in our margins on sales of generic drugs. Consolidation within the generic drug 
manufacturing industry and other external factors may enhance the ability of manufacturers to sustain or increase pricing of 
generic drugs and diminish our ability to negotiate reduced generic drug acquisition costs. Any inability to offset increased 
brand name or generic prescription drug acquisition costs or to modify our activities to lessen the financial impact of such 
increased costs could have a significant adverse effect on our operating results.

A number of factors, many of which are beyond our control, contribute to rising health care and other benefit costs. We may 
not be able to accurately forecast health care and other benefit costs, which could adversely affect our Health Care Benefits 
segment’s operating results.

Premiums for our Insured Health Care Benefits products, which comprised 91% of our Health Care Benefits revenues for 2019, 
are priced in advance based on our forecasts of health care and other benefit costs during a fixed premium period, which is 
generally one year. These forecasts are typically developed several months before the fixed premium period begins, are 
influenced by historical data (and recent historical data in particular), are dependent on our ability to anticipate and detect 
medical cost trends and changes in our members’ behavior and health care utilization patterns and require a significant degree 
of judgment. For example, our revenue on Medicare policies is based on bids submitted in June of the year before the contract 
year. Cost increases in excess of our projections cannot be recovered in the fixed premium period through higher premiums. As 
a result, our profits are particularly sensitive to the accuracy of our forecasts and our ability to anticipate and detect medical 
cost trends. Even relatively small differences between predicted and actual health care and other benefit costs as a percentage of 
premium revenues can result in significant adverse changes in our operating results.

A number of factors contribute to rising health care and other benefit costs, including previously uninsured members entering 
the health care system, changes in members’ behavior and health care utilization patterns, turnover in our membership, 
additional government mandated benefits or other regulatory changes, changes in the health status of our members, the aging of 
the population and other changing demographic characteristics, advances in medical technology, increases in the number and 

32

cost of prescription drugs (including specialty pharmacy drugs and ultra-high cost drugs and therapies), direct-to-consumer 
marketing by drug manufacturers, the increasing influence of social media on our members’ health care utilization and other 
behaviors, changes in health care practices and general economic conditions (such as inflation and employment levels). In 
addition, government-imposed limitations on Medicare and Medicaid reimbursements to health plans and providers have 
caused the private sector to bear a greater share of increasing health care and other benefits costs over time, and future 
amendments or repeal or replacement of the ACA that increase the uninsured population may exacerbate this problem. Other 
factors that affect our health care and other benefit costs include changes as a result of the ACA, changes to the ACA and other 
changes in the regulatory environment, the evolution toward a consumer driven business model, new technologies, influenza 
related health care costs (which may be substantial and higher than we project), clusters of high-cost cases, epidemics or 
pandemics, health care provider and member fraud, and numerous other factors that are or may be beyond our control. For 
example, the 2019-2020 influenza season had an earlier than average start and has a higher incidence of influenza than the 
2018-2019 influenza season; and influenza related health care costs were higher than Aetna projected in 2017-2018. 

Our Health Care Benefits segment’s operating results and competitiveness depend in large part on our ability to appropriately 
manage future health care and other benefit costs through underwriting criteria, product design, provider network configuration, 
negotiation of favorable provider contracts and medical management programs. Our medical cost management programs may 
not be successful and may have a smaller impact on health care and benefit costs than we expect. The factors described above 
may adversely affect our ability to predict and manage health care and other benefit costs, which can adversely affect our 
competitiveness and operating results.

The reserves we hold for expected claims in our Insured Health Care Benefits products are based on estimates that involve 
an extensive degree of judgment and are inherently variable. Any reserve, including a premium deficiency reserve, may be 
insufficient. If actual claims exceed our estimates, our operating results could be materially adversely affected, and our 
ability to take timely corrective actions to limit future costs may be limited.

A large portion of health care claims are not submitted to us until after the end of the quarter in which services are rendered by 
providers to our members. Our reported health care costs payable for any particular period reflect our estimates of the ultimate 
cost of such claims as well as claims that have been reported to us but not yet paid. We also must estimate the amount of rebates 
payable under the ACA’s, the U.S. Centers for Medicare & Medicaid Services’ (“CMS’s”) and the federal Office of Personnel 
Management’s (“OPM’s”) minimum medical loss ratio (“MLR”) rules and the amounts payable by us to, and receivable by us 
from, the United States federal government under the ACA’s remaining premium stabilization program.

Our estimates of health care costs payable are based on a number of factors, including those derived from historical claim 
experience, but this estimation process also makes use of extensive judgment. Considerable variability is inherent in such 
estimates, and the accuracy of the estimates is highly sensitive to changes in medical claims submission and processing patterns 
and/or procedures, turnover and other changes in membership, changes in product mix, changes in the utilization of medical 
and/or other covered services, including prescription drugs, changes in medical cost trends, changes in our medical 
management practices and the introduction of new benefits and products. We estimate health care costs payable periodically, 
and any resulting adjustments, including premium deficiency reserves, are reflected in current-period operating results within 
benefit costs. For example, as of December 31, 2019 and 2018, we established a premium deficiency reserve of $4 million and 
$16 million, respectively, related to Medicaid products in the Health Care Benefits segment. A worsening (or improvement) of 
health care cost trend rates or changes in claim payment patterns from those that we assumed in estimating health care costs 
payable as of December 31, 2019 would cause these estimates to change in the near term, and such a change could be material.

Furthermore, if we are not able to accurately and promptly anticipate and detect medical cost trends or accurately estimate the 
cost of incurred but not yet reported claims or reported claims that have not been paid, our ability to take timely corrective 
actions to limit future health care costs and reflect our current benefit cost experience in our pricing process may be limited, 
which would further exacerbate the extent of any adverse impact on our operating results. These risks are particularly acute 
during and following periods when utilization of medical and/or other covered services and/or medical cost trends are below 
recent historical levels and in products where there is significant turnover in our membership each year, and such risks are 
further magnified by the ACA and other legislation and regulations that limit our ability to price for our projected and/or 
experienced increases in utilization and/or medical cost trends.

Our operating results are affected by the health of the economy in general and in the geographies we serve.

Our businesses are affected by the U.S. economy and consumer confidence in general and in the geographies we serve, 
including various economic factors, including inflation and changes in consumer purchasing power, preferences and/or 
spending patterns. An unfavorable, uncertain or volatile economic environment could cause a decline in drug utilization, an 

33

increase in health care utilization and dampen demand for PBM services as well as consumer demand for products sold in our 
retail stores. 

If our customers’ operating and financial performance deteriorates, or they are unable to make scheduled payments or obtain 
adequate financing, our customers may not be able to pay timely, or may delay payment of, amounts owed to us. Any inability 
of our customers to pay us for our products and services may adversely affect our businesses, operating results and cash flows. 
In addition, both state and federal government sponsored payers, as a result of budget deficits or spending reductions, may 
suspend payments or seek to reduce their health care expenditures resulting in our customers delaying payments to us or 
renegotiating their contracts with us. 

Further, economic conditions including interest rate fluctuations, changes in capital market conditions and regulatory changes 
may affect our ability to obtain necessary financing on acceptable terms, our ability to secure suitable store locations under 
acceptable terms, our ability to execute sale-leaseback transactions under acceptable terms and the value of our investment 
portfolio. Adverse changes in the U.S. economy, consumer confidence and economic conditions could have an adverse effect on 
our businesses and financial results. This adverse effect could be further exacerbated by the increasing prevalence of high 
deductible health plans and health plan designs favoring co-insurance over co-payments as members and other consumers may 
decide to postpone, or not to seek, medical treatment which may lead them to incur more expensive medical treatment in the 
future and/or decrease our prescription volumes.

In addition, our Health Care Benefits membership remains concentrated in certain U.S. geographies and in certain industries. 
Unfavorable changes in health care or other benefit costs or reimbursement rates or increased competition in those geographic 
areas where our membership is concentrated could therefore have a disproportionately adverse effect on our Health Care 
Benefits segment’s operating results. Our Health Care Benefits membership has been and may continue to be affected by 
workforce reductions by our customers due to adverse and/or uncertain general economic conditions, especially in the U.S. 
geographies and industries where our membership is concentrated. As a result, we may not be able to profitably grow and 
diversify our Health Care Benefits membership geographically, by product type or by customer industry, and our revenues and 
operating results may be disproportionately affected by adverse changes affecting our customers.

We are exposed to risks relating to the solvency of other insurers.

We are subject to assessments under guaranty fund laws existing in all states for obligations of insolvent insurance companies 
(including long-term care insurers), HMOs, ACA co-ops and other payors to policyholders and claimants. For example, in the 
first quarter of 2017, Aetna recorded a discounted estimated liability expense of $231 million pretax for our estimated share of 
future assessments for long-term care insurer Penn Treaty Network America Insurance Company and one of its subsidiaries. 
Guaranty funds are maintained by state insurance commissioners to protect policyholders and claimants in the event that an 
insurer, HMO, ACA co-op and/or other payor becomes insolvent or is unable to meet its financial obligations. These funds are 
usually financed by assessments against insurers regulated by a state. Future assessments may have an adverse effect on our 
operating results and cash flows.

Extreme events, or the threat of extreme events, could materially increase our health care (including behavioral health) 
costs.

Nuclear, biological or other attacks, whether as a result of war or terrorism, other man-made disasters, natural disasters, 
epidemics, pandemics and other extreme events can affect the U.S. economy in general, our industries and us specifically. In 
particular, such extreme events or the threat of such extreme events could result in significant health care (including behavioral 
health) costs, which also would be affected by the government’s actions and the responsiveness of public health agencies and 
other insurers. Such extreme events or the threat of such extreme events also could disrupt our supply chains and/or our 
distribution chains for the products we sell. In addition, our employees and those of our vendors are concentrated in certain 
large, metropolitan areas which may be particularly exposed to these events. Such events could adversely affect our businesses, 
operating results and cash flows, and, in the event of extreme circumstances, our financial condition or viability, particularly if 
our responses to such events are less adequate than those of our competitors.

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Risks From Changes in Public Policy and Other Legal and Regulatory Risks

We are subject to potential changes in public policy, laws and regulations, including reform of the U.S. health care system, 
which can adversely affect our businesses. Entitlement program reform, if it occurs, could have a material adverse effect on 
our businesses, operations and/or operating results.

The political environment in which we operate remains uncertain. It is reasonably possible that our business operations and 
operating results could be materially adversely affected by legislative, regulatory and public policy changes at the federal or 
state level, increased government involvement in drug reimbursement, pricing, purchasing and/or importation and/or increased 
regulation of PBMs, including: changes to the Medicare or Medicaid programs (including the block grant option outlined by 
CMS on January 30, 2020) or the regulatory environment for health care and related benefits, including the ACA; changes to 
laws or regulations governing drug reimbursement and/or pricing; changes to the laws and regulations governing PBMs’, PDPs’ 
and/or Managed Medicaid organizations’ interactions with government funded health care programs; changes to laws and/or 
regulations governing drug manufacturers’ rebates; changes to laws and/or regulations governing reimbursements paid to 
pharmacists by and/or reporting required by PBMs; changes to immigration policies and/or other public policy initiatives. It is 
not possible to predict whether or when any such changes will occur or what form any such changes may take (including 
through the use of U.S. Presidential Executive Orders). Other significant changes to health care and related benefits system 
legislation or regulation as well as changes with respect to tax and trade policies, tariffs and other government regulations 
affecting trade between the United States and other countries also are possible and could adversely affect our businesses. If we 
fail to respond adequately to such changes, including by implementing strategic and operational initiatives, or do not respond as 
effectively as our competitors, our businesses, operations and operating results may be materially adversely affected.

In addition to efforts to amend, repeal or replace the ACA and related regulations, we expect the federal and state governments 
to continue to enact and seriously consider many broad-based legislative and regulatory proposals that will or could materially 
impact various aspects of the health care and related benefits system and our businesses. Potential modification to the ACA, 
including changes in enforcement and/or funding that further destabilize the Public Exchanges, as well as significant changes to 
Medicaid funding (including the block grant option outlined by CMS on January 30, 2020) could impact the number of 
Americans with health insurance and, consequently, prescription drug coverage. Further changes to federal health care and 
related benefits laws, including the ACA, drug reimbursement and pricing laws, laws governing PBMs and/or laws governing 
PBMs’, PDPs’ and/or Managed Medicaid organizations’ interactions with government funded health care programs, are 
probable. We cannot predict the effect, if any, that new health care and related benefits legislation, future changes to the ACA or 
the implementation of or failure to implement the outstanding provisions of ACA, may have on our Pharmacy Services, retail 
pharmacy, LTC pharmacy and/or Health Care Benefits operations and/or operating results. The federal and many state 
governments also are considering changes in the interpretation, enforcement and/or application of existing programs, laws and 
regulations, including changes to payments under and funding of Medicare and Medicaid programs and increased regulation of 
PBMs.

Further, changes in existing federal or state laws or regulations or the adoption of new laws or regulations relating to additional 
regulation of PBMs (including formulary management or other PBM services), drug pricing or purchasing, patent term 
extensions and/or purchase discount and/or rebate arrangements with drug manufacturers also could reduce the discounts or 
rebates we receive. Changes in existing federal or state laws or regulations or the adoption of new laws or regulations relating 
to claims processing and billing, including our ability to use MAC lists and collect transmission fees, also could adversely 
affect our profitability.

We cannot predict the enactment or content of new legislation or regulations or changes to existing laws or regulations or their 
enforcement, interpretation or application, or the effect they will have on our business operations or operating results, which 
could be materially adverse. Even if we could predict such matters, it is not possible to eliminate the adverse impact of public 
policy changes that would fundamentally change the dynamics of one or more of the industries in which we compete. Examples 
of such changes include: the federal or one or more state governments fundamentally restructuring or reducing the funding 
available for Medicare, Medicaid, dual eligible or dual eligible special needs plan programs, increasing its involvement in drug 
reimbursement, pricing, purchasing and/or importation, changing the laws and regulations governing PBMs’, PDPs’ and/or 
Managed Medicaid organizations’ interactions with government funded health care programs, changing the tax treatment of 
health or related benefits, or repealing or otherwise significantly altering the ACA. The likelihood of adverse changes remains 
high due to state and federal budgetary pressures, and our businesses and operating results could be materially and adversely 
affected by such changes, even if we correctly predict their occurrence. 

For more information on these matters, see “Government Regulation” included in Item 1 of this Form 10-K.

35

If we fail to comply with applicable laws and regulations, many of which are highly complex, we could be subject to 
significant adverse regulatory actions or suffer brand and reputational harm.

Our businesses are subject to extensive regulation and oversight by state, federal and international governmental authorities. 
The laws and regulations governing our operations and interpretations of those laws and regulations are increasing in number 
and complexity, change frequently and can be inconsistent or conflict with one another. In general, these laws and regulations 
are designed to benefit and protect customers, members and providers rather than us or our investors. In addition, the 
governmental authorities that regulate our businesses have broad latitude to make, interpret and enforce the laws and 
regulations that govern us and continue to interpret and enforce those laws and regulations more strictly and more aggressively 
each year. We also must follow various restrictions on certain of our businesses and the payment of dividends by certain of our 
subsidiaries put in place by certain state regulators.

Certain of our Pharmacy Services and Retail/LTC operations, products and services are subject to:

• 

• 

• 

• 

the clinical quality, patient safety and other risks inherent in the dispensing, packaging and distribution of drugs and other 
health care products and services, including claims related to purported dispensing and other operational errors (any failure 
by our Pharmacy Services and/or Retail/LTC operations to adhere to the laws and regulations applicable to the dispensing 
of drugs could subject us to civil and criminal penalties);

federal and state anti-kickback and other laws that govern our relationship with drug manufacturers, customers and 
consumers;

compliance requirements under the Employee Retirement Income Security Act of 1974 (“ERISA”), including fiduciary 
obligations in connection with the development and implementation of items such as drug formularies and preferred drug 
listings; and

federal and state legislative proposals and/or regulatory activity that could adversely affect pharmacy benefit industry 
practices.

Our Health Care Benefits products are highly regulated, particularly those that serve Medicare, Medicaid, dual eligible, dual 
eligible special needs and small group Commercial customers and members. The laws and regulations governing participation 
in Medicare Advantage, Medicare Part D, Medicaid, dual eligible and dual eligible special needs plan programs are complex, 
are subject to interpretation and can expose us to penalties for non-compliance. 

The scope of the practices and activities that are prohibited by federal and state false claims acts is the subject of pending 
litigation. Claims under federal and state false claims acts can be brought by the government or by private individuals on behalf 
of the government through a qui tam or “whistleblower” suit, and we are a defendant in a number of such proceedings. If we are 
convicted of fraud or other criminal conduct in the performance of a government program or if there is an adverse decision 
against us under the federal False Claims Act (the “False Claims Act”), we may be temporarily or permanently suspended from 
participating in government health care programs, including Medicare Advantage, Medicare Part D, Medicaid, dual eligible and 
dual eligible special needs plan programs, and we also may be required to pay significant fines and/or other monetary penalties. 
Whistleblower suits have resulted in significant settlements between governmental agencies and health care companies. The 
significant incentives and protections provided to whistleblowers under applicable law increase the risk of whistleblower suits.

If we fail to comply with laws and regulations that apply to government programs, we could be subject to criminal fines, civil 
penalties, premium refunds, prohibitions on marketing or active or passive enrollment of members, corrective actions, 
termination of our contracts or other sanctions which could have a material adverse effect on our ability to participate in 
Medicare Advantage, Medicare Part D, Medicaid, dual eligible, dual eligible special needs plan and other programs and on our 
operating results, cash flows and financial condition.

Our businesses, profitability and growth also may be adversely affected by (i) judicial and regulatory decisions that change and/
or expand the interpretations of existing statutes and regulations, impose medical or bad faith liability, increase our 
responsibilities under ERISA or the remedies available under ERISA, or reduce the scope of ERISA pre-emption of state law 
claims (including Rutledge v. Pharm. Care Mgmt. Assoc., which is currently pending before the U.S. Supreme Court) or (ii) 
other legislation and regulations.

36

If our compliance or other systems and processes fail or are deemed inadequate, we may suffer brand and reputational 
harm and become subject to regulatory actions and/or litigation.

In addition to being subject to extensive and complex regulations, many of our contracts with customers include detailed 
requirements. In order to be eligible to offer certain products or bid on certain contracts, we must demonstrate that we have 
robust systems and processes in place that are designed to maintain compliance with all applicable legal, regulatory and 
contractual requirements. These systems and processes frequently are reviewed and audited by our customers and regulators. If 
our systems and processes designed to maintain compliance with applicable legal and contractual requirements, and to prevent 
and detect instances of, or the potential for, non-compliance fail or are deemed inadequate, we may suffer brand and 
reputational harm and be subject to regulatory actions, litigation and other proceedings which may result in damages, fines, 
suspension or loss of licensure, suspension or exclusion from participation in government programs and/or other penalties, any 
of which could adversely affect our businesses, operating results, cash flows and/or financial condition.

We routinely are subject to litigation and other adverse legal proceedings, including class actions and qui tam actions. Many 
of these proceedings seek substantial damages which may not be covered by insurance. These proceedings are costly to 
defend, may result in changes in our business practices, harm our brand and reputation and adversely affect our businesses 
and operating results.

PBM, retail pharmacy, mail order pharmacy, specialty pharmacy, LTC pharmacy and health care and related benefits are highly 
regulated industries whose participants frequently are subject to litigation and other adverse legal proceedings. We are currently 
subject to various litigation and arbitration matters, investigations, regulatory audits, inspections, government inquiries, and 
regulatory and other legal proceedings, both inside and outside the U.S. Outside the U.S., contractual rights, tax positions and 
applicable regulations may be subject to interpretation or uncertainty to a greater degree than in the U.S. Litigation related to 
our provision of professional services in our medical clinics, pharmacies and LTC operations is increasing as we expand our 
services along the continuum of health care.

Litigation, and particularly securities, derivative, collective or class action and qui tam litigation, is often expensive and 
disruptive. Many of the legal proceedings against us seek substantial damages (including non-economic or punitive damages 
and treble damages), and certain of these proceedings also seek changes in our business practices. While we currently have 
insurance coverage for some potential liabilities, other potential liabilities may not be covered by insurance, insurers may 
dispute coverage and/or the amount of our insurance may not be enough to cover the damages awarded or costs incurred. In 
addition, some types of damages, like punitive damages, may not be covered by insurance, and in some jurisdictions the 
coverage of punitive damages is prohibited. Insurance coverage for all or some forms of liability also may become unavailable 
or prohibitively expensive in the future.

The outcome of litigation and other adverse legal proceedings is always uncertain, and outcomes that are not justifiable by the 
evidence or existing law or regulation can and do occur, and the costs incurred frequently are substantial regardless of the 
outcome. Litigation and other adverse legal proceedings could materially adversely affect our businesses, operating results and/
or cash flows because of brand and reputational harm to us caused by such proceedings, the cost of defending such proceedings, 
the cost of settlement or judgments against us, or the changes in our operations that could result from such proceedings. See 
Item 3 of this Form 10-K for additional information.

We frequently are subject to regular and special governmental audits, investigations and reviews that could result in 
changes to our business practices and also could result in material refunds, fines, penalties, civil liabilities, criminal 
liabilities and other sanctions.

As one of the largest national retail, mail order, specialty and LTC pharmacy, PBM and health care and related benefits 
providers, we frequently are subject to regular and special governmental market conduct and other audits, investigations and 
reviews by, and we receive subpoenas and other requests for information from, various federal and state agencies, regulatory 
authorities, attorneys general, committees, subcommittees and members of the U.S. Congress and other state, federal and 
international governmental authorities. For example, we have received civil investigative demands (“CIDs”) from, and provided 
documents and information to, the Civil Division of the DOJ in connection with a current investigation of our patient chart 
review processes in connection with risk adjustment data submissions under Parts C and D of the Medicare program. CMS and 
the Office of the Inspector General of the U.S. Department of Health and Human Services (the “OIG”) also are auditing the risk 
adjustment-related data of certain of our Medicare Advantage plans, and the number of such audits continues to increase. 
Several such audits, investigations and reviews by governmental authorities currently are pending, some of which may be 
resolved in 2020, the results of which may be adverse to us.

37

Federal and state governments have made investigating and prosecuting health care and other insurance fraud, waste and abuse 
a priority. Fraud, waste and abuse prohibitions encompass a wide range of activities, including kickbacks for referral of 
members, billing for unnecessary medical and/or other covered services, improper marketing and violations of patient privacy 
rights. The regulations and contractual requirements applicable to us and other industry participants are complex and subject to 
change, making it necessary for us to invest significant resources in complying with our regulatory and contractual 
requirements. Ongoing vigorous law enforcement and the highly technical regulatory scheme mean that our compliance efforts 
in this area will continue to require significant resources. In addition, our medical costs and the medical expenses of our Health 
Care Benefits ASC customers may be adversely affected if we do not prevent or detect fraudulent activity by providers and/or 
members.

Regular and special governmental audits, investigations and reviews by federal, state and international regulators could result in 
changes to our business practices, and also could result in significant or material premium refunds, fines, penalties, civil 
liabilities, criminal liabilities or other sanctions, including suspension or exclusion from participation in government programs 
and suspension or loss of licensure. Any of these audits, investigations or reviews could have a material adverse effect on our 
businesses, operating results, cash flows and/or financial condition or result in significant liabilities and negative publicity for 
us. 

See “Legal and Regulatory Proceedings” in Note 16 “Commitments and Contingencies” included in Item 8 of this 10-K for 
additional information.

Our litigation and regulatory risk profile are changing as we offer new products and services and expand in business areas 
beyond our historical core businesses of Pharmacy Services, Retail/LTC and Health Care Benefits.

Historically, we focused primarily on providing Pharmacy Services, Retail/LTC and Health Care Benefits products and 
services. As a result of our transformation program and other innovation initiatives, we are expanding our presence in the health 
care space and plan to offer new products and services (such as the home hemodialysis device we are developing) which 
present a different litigation and regulatory risk profile than the products and services that we historically have offered. 

The increased volume of business in areas beyond our historical core businesses and new products and services subject us to 
litigation and regulatory risks that are different from the risks of providing Pharmacy Services, Retail/LTC and Health Care 
Benefits products and services and increase significantly our exposure to other risks.

We face unique regulatory and other challenges in our Medicare and Medicaid businesses.

We are seeking to substantially grow the Medicare and Medicaid membership in our Health Care Benefits segment in 2020 and 
over the next several years. We face unique regulatory and other challenges that may inhibit the growth and profitability of 
those businesses.

• 

In April 2019, CMS issued a final notice detailing final Medicare Advantage benchmark payment rates for 2020 (the “Final 
Notice”). Overall, we project the benchmark rates in the Final Notice will increase funding for our Medicare Advantage 
business, excluding the impact of the HIF, by approximately 2.0 percent in 2020 compared to 2019. This 2020 rate increase 
only partially offsets the challenge we face from the impact of the increasing cost of medical care (including prescription 
medications) and CMS local and national coverage decisions that require us to pay for services and supplies that are not 
factored into our bids and creates continued pressure on our Medicare Advantage operating results. We cannot predict 
future Medicare funding levels, the impact of future federal budget actions or ensure that such changes or actions will not 
have an adverse effect on our Medicare operating results.

•  The organic expansion of our Medicare Advantage and Medicare Part D service area is subject to the ability of CMS to 
process our requests for service area expansions and our ability to build cost competitive provider networks in the 
expanded service areas that meet applicable network adequacy requirements. CMS’ decisions on our requests for service 
area expansions also may be affected adversely by compliance issues that arise each year in our Medicare operations. 

•  CMS regularly audits our performance to determine our compliance with CMS’s regulations and our contracts with CMS 
and to assess the quality of the services we provide to our Medicare members. As a result of these audits, we may be 
subject to significant or material retroactive adjustments to and/or withholding of certain premiums and fees, fines, 
criminal liability, civil monetary penalties, CMS imposed sanctions (including suspension or exclusion from participation 
in government programs) or other restrictions on our Medicare, Medicaid and other businesses, including suspension or 
loss of licensure. 

38

• 

• 

“Star ratings” from CMS for our Medicare Advantage plans will continue to have a significant effect on our plans’ 
operating results. Since 2015, only Medicare Advantage plans with a star rating of four or higher (out of five) are eligible 
for a quality bonus in their basic premium rates. CMS continues to change its rating system to make achieving and 
maintaining a four or higher star rating more difficult. Our star ratings and past performance scores are adversely affected 
by the compliance issues that arise each year in our Medicare operations. If our star ratings fall below 4 for a significant 
portion of our Medicare Advantage membership or do not match the performance of our competitors or the star rating 
quality bonuses are reduced or eliminated, our revenues, operating results and cash flows may be significantly adversely 
affected.

Payments we receive from CMS for our Medicare Advantage and Part D businesses also are subject to risk adjustment 
based on the health status of the individuals we enroll. Elements of that risk adjustment mechanism continue to be 
challenged by the DOJ, the OIG and CMS itself. Substantial changes in the risk adjustment mechanism, including changes 
that result from enforcement or audit actions, could materially affect the amount of our Medicare reimbursement, require us 
to raise prices or reduce the benefits we offer to Medicare beneficiaries, and potentially limit our (and the industry’s) 
participation in the Medicare program.

•  Medicare Part D has resulted in increased utilization of prescription medications and puts pressure on our pharmacy gross 
margin rates due to regulatory and competitive pressures. Further, as a result of the ACA and changes to the retiree drug 
subsidy rules, clients of our PBM business could decide to discontinue providing prescription drug benefits to their 
Medicare-eligible members. To the extent this phenomenon occurs, the adverse effects of increasing customer migration 
into Medicare Part D may outweigh the benefits we realize from growth of our Medicare Part D products. 

•  Our Medicare Part D operating results and our ability to expand our Medicare Part D business could be adversely affected 

if: the cost and complexity of Medicare Part D exceed management’s expectations or prevent effective program 
implementation or administration; changes to the regulations regarding how drug costs are reported for Medicare Part D 
are implemented in a manner that adversely affects the profitability of our Medicare Part D business; changes to the 
applicable regulations impact our ability to retain fees from third parties including network pharmacies; the government 
alters Medicare Part D program requirements or reduces funding because of the higher-than-anticipated cost to taxpayers of 
Medicare Part D or for other reasons; the government mandates the use of point-of-sale manufacturer’s rebates or up front 
drug pricing discounts, makes drug manufacturer’s rebates illegal, or makes changes to how pharmacy pay-for-
performance is calculated; or reinsurance thresholds are reduced below their current levels.

•  We have experienced challenges in obtaining complete and accurate encounter data for our Medicaid products due to 

difficulties with providers and third-party vendors submitting claims in a timely fashion in the proper format, and with state 
agencies in coordinating such submissions. As states increase their reliance on encounter data, these difficulties could 
affect the Medicaid premium rates we receive and how Medicaid membership is assigned to us, which could have a 
material adverse effect on our Medicaid operating results and cash flows and/or our ability to bid for, and continue to 
participate in, certain Medicaid programs.

• 

• 

• 

Federal funding for expanded Medicaid coverage began to decrease in 2017. This reduction is causing states to re-evaluate 
funding for their Medicaid expansions. That re-evaluation may adversely affect Medicaid payment rates, our Medicaid 
membership in those states, our revenues, our MLRs and our operating results.

If we fail to report and correct errors discovered through our own auditing procedures or during a CMS audit or otherwise 
fail to comply with the applicable laws and regulations, we could be subject to fines, civil monetary penalties or other 
sanctions, including fines and penalties under the False Claims Act, which could have a material adverse effect on our 
ability to participate in Medicare Advantage, Part D or other government programs, and on our operating results, cash 
flows and financial condition. 

In the second quarter of 2014, CMS issued a final rule implementing ACA requirements that Medicare Advantage and PDP 
plans report and refund to CMS overpayments that those plans receive from CMS. However, CMS’s statements in 
formalized guidance regarding “overpayments” to Medicare Advantage plans appear to be inconsistent with CMS’s prior 
risk adjustment data validation (“RADV”) audit guidance. These statements appear to equate each Medicare Advantage 
risk adjustment data error with an “overpayment” without reconciliation to the principles underlying the fee for service 
adjustment comparison contemplated by CMS’s RADV audit methodology. The precise interpretation, impact and legality 
of the final rule are not clear and are subject to pending litigation. If Medicare Advantage plans were not paid based on 
payment model principles that align with the requirements of the Social Security Act or such payments were not 
implemented correctly, it could have a material adverse effect on our operating results, cash flows and/or financial 
condition.

•  Certain of our Medicaid contracts require the submission of complete and correct encounter data. The accurate and timely 
reporting of encounter data is increasingly important to the success of our Medicaid programs because more states are 
using encounter data to determine compliance with performance standards and, in part, to set premium rates. We have 
expended and may continue to expend additional effort and incur significant additional costs to collect accurate, or to 

39

correct inaccurate or incomplete, encounter data and have been and could be exposed to premium withholding, operating 
sanctions and financial fines and penalties for noncompliance. We have experienced challenges in obtaining complete and 
accurate encounter data due to difficulties with providers and third-party vendors submitting claims in a timely fashion in 
the proper format, and with state agencies in coordinating such submissions. As states increase their reliance on encounter 
data, these difficulties could affect the Medicaid premium rates we receive and how Medicaid membership is assigned to 
us, which could have a material adverse effect on our Medicaid operating results and cash flows and/or our ability to bid 
for, and continue to participate in, certain Medicaid programs.

•  Our businesses that dispense drugs also face challenges in the Medicaid space. The ACA made several significant changes 

to Medicaid rebates and to reimbursement rates. One of these changes was to revise the definition of the Average 
Manufacturer Price, a pricing element common to most payment formulas, and the reimbursement formula for generic 
drugs. This change has adversely affected the reimbursements we receive when we dispense prescription drugs to Medicaid 
recipients.

Programs funded in whole or in part by the U.S. federal government account for a significant portion of our revenues, and 
we expect that percentage to increase.

Programs funded in whole or in part by the U.S. federal government account for a significant portion of our revenues, and we 
expect that percentage to increase. As our government funded businesses grow, our exposure to changes in federal and state 
government policy with respect to and/or regulation of the various government funded programs in which we participate also 
increases. 

Our revenues from government funded programs, including in Health Care Benefits’ Medicare, Medicaid, dual eligible and dual 
eligible special needs plan businesses and from government customers in its Commercial business, are dependent on annual 
funding by the federal government and/or applicable state or local governments. Federal, state and local governments have the 
right to cancel or not to renew their contracts with us on short notice without cause or if funds are not available. Funding for 
these programs is dependent on many factors outside our control, including general economic conditions, continuing 
government efforts to contain health care costs and budgetary constraints at the federal or applicable state or local level and 
general political issues and priorities. 

The U.S. federal government and our other government customers also may reduce funding for health care or other programs, 
cancel or decline to renew contracts with us, or make changes that adversely affect the number of persons eligible for certain 
programs, the services provided to enrollees in such programs, our premiums and our administrative and health care and other 
benefit costs, any of which could have a material adverse effect on our businesses, operating results and cash flows. When 
federal funding is delayed, suspended or curtailed, we continue to receive, and we remain liable for and are required to fund, 
claims from providers for providing services to beneficiaries of federally funded health benefits programs in which we 
participate. An extended federal government shutdown or a delay by Congress in raising the federal government’s debt ceiling 
also could lead to a delay, reduction, suspension or cancellation of federal government spending and a significant increase in 
interest rates that could, in turn, have a material adverse effect on the value of our investment portfolio, our ability to access the 
capital markets and our businesses, operating results, cash flows and liquidity.

Possible changes in industry pricing benchmarks and drug pricing generally can adversely affect our PBM and Retail/LTC 
businesses.

It is possible that the pharmaceutical industry or regulators may evaluate and/or develop an alternative pricing reference to 
replace Average Wholesale Price (“AWP”) or Wholesale Acquisition Cost (“WAC”), which are the pricing references used for 
many of our PBM and LTC client contracts, drug purchase agreements, retail network contracts, specialty payor agreements and 
other contracts with third party payors in connection with the reimbursement of drug payments. In addition, many state 
Medicaid fee-for-service programs (“FFS Medicaid”) have established pharmacy network payments on the basis of Actual 
Acquisition Cost (“AAC”). The use of an AAC basis in FFS Medicaid could have an impact on reimbursement practices in 
Health Care Benefits’ Commercial and other Government products. 

Future changes to the use of AWP, WAC or to other published pricing benchmarks used to establish drug pricing, including 
changes in the basis for calculating reimbursement by federal and state health care programs and/or other payors, could impact 
the reimbursement we receive from Medicare and Medicaid programs, the reimbursement we receive from our PBM clients and 
other payors and/or our ability to negotiate rebates and/or discounts with drug manufacturers, wholesalers, PBMs and retail 
pharmacies. A failure or inability to fully offset any increased prices or costs or to modify our operations to mitigate the impact 
of such increases could have a material adverse effect on our operating results. Additionally, any future changes in drug prices 
could be significantly different than our projections. We cannot predict the effect of these possible changes on our businesses.

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We may not be able to obtain adequate premium rate increases in our Insured Health Care Benefits products, which would 
have an adverse effect on our revenues, MBRs and operating results and could magnify the adverse impact of increases in 
health care and other benefit costs and of ACA assessments, fees and taxes.

Premium rates for our Insured Health Care Benefits products generally must be filed with state insurance regulators and are 
subject to their approval, which creates risk for us in the current political and regulatory environment. The ACA generally 
requires a review by HHS in conjunction with state regulators of premium rate increases that exceed a federally specified 
threshold (or lower state-specific thresholds set by states determined by HHS to have adequate processes). Rate reviews can 
magnify the adverse impact on our operating margins, medical benefit ratios (“MBRs”) and operating results of increases in 
health care and other benefit costs, increased utilization of covered services, and ACA assessments, fees and taxes, by 
restricting our ability to reflect these increases and/or these assessments, fees and taxes in our pricing. Further, our ability to 
reflect ACA assessments, fees and taxes in our Medicare, Medicaid and CHIP premium rates is limited.

Since 2013, HHS has issued determinations to health plans that their premium rate increases were “unreasonable,” and we 
continue to experience challenges to appropriate premium rate increases in certain states. Regulators or legislatures in several 
states have implemented or are considering limits on premium rate increases, either by enforcing existing legal requirements 
more stringently or proposing different regulatory standards. Regulators or legislatures in several states also have conducted 
hearings on proposed premium rate increases, which can result, and in some instances have resulted, in substantial delays in 
implementing proposed rate increases even if they ultimately are approved. Our plans can be excluded from participating in 
small group Public Exchanges if they are deemed to have a history of “unreasonable” rate increases. Any significant rate 
increases we may request heighten the risks of adverse publicity, adverse regulatory action and adverse selection and the 
likelihood that our requested premium rate increases will be denied, reduced or delayed, which could adversely affect our 
MBRs and lead to operating margin compression.

We anticipate continued regulatory and legislative action to increase regulation of premium rates in our Insured Health Care 
Benefits products. We may not be able to obtain rates that are actuarially justified or that are sufficient to make our policies 
profitable in one or more product lines or geographies. If we are unable to obtain adequate premium rates and/or premium rate 
increases, it could materially and adversely affect our operating margins and MBRs and our ability to earn adequate returns on 
Insured Health Care Benefits products in one or more states or cause us to withdraw from certain geographies and/or products.

Minimum MLR rebate requirements limit the level of margin we can earn in our Insured Health Care Benefits products 
while leaving us exposed to higher than expected medical costs. Challenges to our minimum MLR rebate methodology and/
or reports could adversely affect our operating results.

The ACA’s minimum MLR rebate requirements limit the level of margin we can earn in Health Care Benefits’ Commercial 
Insured and Medicare Insured businesses. CMS minimum MLR rebate regulations limit the level of margin we can earn in our 
Medicaid Insured business. Certain portions of our Health Care Benefits Medicaid and Federal Employees Health Benefits 
(“FEHB”) program business also are subject to minimum MLR rebate requirements in addition to but separate from those 
imposed by the ACA. Minimum MLR rebate requirements leave us exposed to medical costs that are higher than those 
reflected in our pricing. The process supporting the management and determination of the amount of MLR rebates payable is 
complex and requires judgment, and the minimum MLR reporting requirements are detailed. Federal and state auditors are 
challenging our Commercial Health Care Benefits business’ compliance with the ACA’s minimum MLR requirements as well 
as our FEHB plans’ compliance with OPM’s FEHB program-specific minimum MLR requirements. Our Medicare and 
Medicaid contracts also are subject to minimum MLR audits. If a Medicare Advantage or Medicare Part D contract pays 
minimum MLR rebates for three consecutive years, it will become ineligible to enroll new members. If a Medicare Advantage 
or Medicare Part D contract pays such rebates for five consecutive years, it will be terminated by CMS. Additional challenges 
to our methodology and/or reports relating to minimum MLR and related rebates by federal and state regulators and private 
litigants are reasonably possible. The outcome of these audits and additional challenges could adversely affect our operating 
results.

Our operating results may be adversely affected by changes in laws and policies governing employers and by union 
organizing activity.

The federal and certain state legislatures continue to consider and pass legislation that increases our costs of doing business, 
including increased minimum wages and requiring employers to provide paid sick leave or paid family leave. In addition, our 
employee-related operating costs may be increased by union organizing activity. If we are unable to reflect these increased 
expenses in our pricing or otherwise modify our operations to mitigate the effects of such increases, our operating results will 
be adversely affected.

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We face international political, legal and compliance, operational, regulatory, economic and other risks that may be more 
significant than in our domestic operations.

We significantly expanded our international operations as a result of the Aetna Acquisition. As a result of our expanded 
international operations, we face political, legal, compliance, operational, regulatory, economic and other risks that we do not 
face or that are more significant than in our domestic operations. These risks vary widely by country and include varying 
regional and geopolitical business conditions and demands, government intervention and censorship, discriminatory regulation, 
nationalization or expropriation of assets and pricing constraints. Our international products need to meet country-specific 
customer and member preferences as well as country-specific legal requirements, including those related to licensing, data 
privacy, data storage and data protection.

Our international operations increase our exposure to, and require us to devote significant management resources to implement 
controls and systems to comply with, the privacy and data protection laws of non-U.S. jurisdictions, such as the European 
Union’s (“EU’s”) General Data Protection Regulation (“GDPR”), and the anti-bribery, anti-corruption and anti-money 
laundering laws of the United States (including the FCPA) and the United Kingdom (including the UK Bribery Act) and similar 
laws in other jurisdictions. Implementing our compliance policies, internal controls and other systems upon our expansion into 
new countries and geographies may require the investment of considerable management time and financial and other resources 
over several years before any significant revenues or profits are generated. Violations of these laws and regulations could result 
in fines, criminal sanctions against us, our officers or employees, restrictions or outright prohibitions on the conduct of our 
business, and significant brand and reputational harm. We must regularly reassess the size, capability and location of our global 
infrastructure and make appropriate changes, and must have effective change management processes and internal controls in 
place to address changes in our businesses and operations. Our success depends, in part, on our ability to anticipate these risks 
and manage these difficulties, and the failure to do so could have a material adverse effect on our brand, reputation, businesses, 
operating results and/or financial condition.

Our international operations require us to overcome logistical and other challenges based on differing languages, cultures, legal 
and regulatory schemes and time zones. Our international operations encounter labor laws, standards and customs that can be 
difficult and make employee relationships less flexible than in our domestic operations and expensive to modify or terminate. In 
some countries we are required to, or choose to, operate with local business associates, which requires us to manage our 
relationships with these third parties and may reduce our operational flexibility and ability to quickly respond to business 
challenges.

In some countries we may be exposed to currency exchange controls or other restrictions that prevent us from transferring funds 
internationally or converting local currencies into U.S. dollars or other currencies. Fluctuations in foreign currency exchange 
rates may adversely affect our revenues, operating results and cash flows from our international operations. Some of our 
operations are, and are increasingly likely to be, in emerging markets where these risks are heightened. Any measures we may 
implement to reduce the effect of volatile currencies and other risks on our international operations may not be effective.

Risks Associated with Mergers, Acquisitions, and Divestitures 

Risks Relating to Our Acquisition of Aetna

We expect to continue to incur significant non-recurring costs associated with combining the operations of CVS Health and 
Aetna. We may not achieve the net benefit that we project of such expenditures associated with the elimination of duplicative 
costs, the realization of other efficiencies that we project related to the integration of our businesses or the realization of the 
growth opportunities that we project from the Aetna Acquisition in the near term, or at all. In addition, the post-closing 
integration of the operations of CVS Health and Aetna and related matters may require substantial commitments of 
management and other resources and management time which could otherwise have been devoted to our ongoing businesses 
and operations and/or to other opportunities that may have been beneficial to us.

Parties with which we do business may experience uncertainty associated with the Aetna Acquisition and/or the post-closing 
integration process, including with respect to current or future business relationships with the combined business. Our business 
relationships (including business relationships of our Health Care Benefits segment) may be subject to disruption as customers, 
members, manufacturers, providers, vendors and others may attempt to negotiate changes in existing business relationships or 
consider entering into business relationships with parties other than the combined business. 

42

We may be unable to successfully integrate companies we acquire.

Upon the closing of any acquisition we complete, we will need to successfully integrate the products, services and related 
assets, as well as internal controls into our business operations. If an acquisition is consummated, the integration of the acquired 
business, its products, services and related assets into our company also may be complex and time-consuming and, if the 
integration is not fully successful, we may not achieve the anticipated benefits, operating and cost synergies and/or growth 
opportunities of an acquisition. Potential difficulties that may be encountered in the integration process include the following:

• 

Integrating personnel, operations and systems (including internal control environments and compliance policies), while 
maintaining focus on producing and delivering consistent, high quality products and services;

•  Coordinating geographically dispersed organizations;

•  Disrupting management’s attention from our ongoing business operations;

•  Retaining existing customers and attracting new customers; and

•  Managing inefficiencies associated with integrating our operations.

An inability to realize the full extent of the anticipated benefits, operating and cost synergies, innovations and operations 
efficiencies or growth opportunities of an acquisition, as well as any delays or additional expenses encountered in the 
integration process, could have a material adverse effect on our businesses and operating results. Furthermore, acquisitions, 
even if successfully integrated, may fail to further our business strategy as anticipated, expose us to increased competition or 
challenges with respect to our products, services or service areas, and expose us to additional liabilities associated with an 
acquired business including risks and liabilities associated with litigation involving the acquired business. Any one of these 
challenges or risks could impair our ability to realize any benefit from our acquisitions after we have expended resources on 
them.

We expect to continue to pursue acquisitions, joint ventures, strategic alliances and other inorganic growth opportunities, 
which may be unsuccessful, cause us to assume unanticipated liabilities, disrupt our existing businesses, be dilutive or lead 
us to assume significant debt, among other things.

We expect to continue to pursue acquisitions, joint ventures, strategic alliances and other inorganic growth opportunities as part 
of our growth strategy. In addition to the integration risks noted above, some other risks we face with respect to acquisitions and 
other inorganic growth strategies include:

•  we frequently compete with other firms, some of which may have greater financial and other resources and a greater 

• 

• 

tolerance for risk, to acquire attractive companies;

the acquired, alliance and/or joint venture businesses may not perform as projected;

the goodwill or other intangible assets established as a result of our acquisitions may be incorrectly valued or may become 
impaired; for example, in 2018 we took $6.1 billion of goodwill impairment charges related to our LTC reporting unit 
within the Retail/LTC segment;

•  we may assume unanticipated liabilities, including those that were not disclosed to us or which we underestimated;

• 

• 

• 

the acquired businesses, or the pursuit of other inorganic growth strategies, could disrupt or compete with our existing 
businesses, distract management, result in the loss of key employees, divert resources, result in tax costs or inefficiencies 
and make it difficult to maintain our current business standards, controls, information technology systems, policies, 
procedures and performance;

as we did in the Aetna Acquisition, we may finance future acquisitions and other inorganic growth strategies by issuing 
common stock for some or all of the purchase price, which would dilute the ownership interests of our stockholders;

as we did in the Aetna Acquisition, we may incur significant debt in connection with acquisitions (whether to finance 
acquisitions or by assuming debt from the businesses we acquire);

•  we may not have the expertise to manage and profitably grow the businesses we acquire, and we may need to rely on the 

retention of key personnel and other suppliers of businesses we acquire, which may be difficult or impossible to 
accomplish;

•  we may enter into merger or purchase agreements but, due to reasons within or outside our control, fail to complete the 
related transactions, which could result in termination fees or other penalties that could be material, cause material 
disruptions to our businesses and operations and adversely affect our brand and reputation;

• 

in order to complete a proposed acquisition, we may be required to divest certain portions of our business, for which we 
may not be able to obtain favorable pricing;

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• 

• 

as is the case with the Aetna Acquisition and our acquisition of Omnicare, Inc., we may be involved in litigation related to 
mergers or acquisitions, including for matters that occurred prior to the applicable closing, which may be costly to defend 
and may result in adverse rulings against us that could be material; and

the integration into our businesses of the businesses and entities we acquire may affect the way in which existing laws and 
regulations apply to us, including subjecting us to laws and regulations that did not previously apply to us.

In addition, joint ventures present risks that are different from acquisitions, including selection of appropriate joint venture 
parties, initial and ongoing governance of the joint venture, joint venture compliance activities (including compliance with 
applicable CMS requirements), growing the joint venture’s business in a manner acceptable to all the parties, including other 
providers in the networks that include joint ventures, maintaining positive relationships among the joint venture parties and the 
joint venture’s customers, and member and business disruption that may occur upon joint venture termination.

Risks Related to Our Operations

Failure to meet customer expectations may harm our brand and reputation, our ability to retain and grow our customer base 
and membership and our operating results and cash flows.

Our ability to attract and retain customers and members is dependent upon providing cost effective, quality customer service 
operations (such as call center operations, PBM functions, retail pharmacy and LTC services, retail, mail order and specialty 
pharmacy prescription delivery, claims processing, customer case installation and online access and tools) that meet or exceed 
our customers’ and members’ expectations, either directly or through vendors. As we seek to reduce general and administrative 
expenses, we must balance the potential impact of cost-saving measures on our customer and other service and performance. If 
we misjudge the effects of such measures, customer and other service may be adversely affected. We depend on third parties for 
certain of our customer service, PBM and prescription delivery operations. If we or our vendors fail to provide service that 
meets our customers’ and members’ expectations, we may have difficulty retaining or profitably growing our customer base 
and/or membership, which could adversely affect our operating results. For example, noncompliance with any privacy or 
security laws or regulations or any security breach involving us or one of our third-party vendors could have a material adverse 
effect on our businesses, operating results, brand and reputation.

We and our vendors have experienced and continue to experience cyber attacks. We can provide no assurance that we or our 
vendors will be able to detect, prevent or contain the effects of such attacks or other information security (including 
cybersecurity) risks or threats in the future.

We and our vendors have experienced and continue to experience a variety of cyber attacks, and we and our vendors expect to 
continue to experience cyber attacks going forward. Among other things, we and our vendors have experienced automated 
attempts to gain access to public facing networks, brute force, SYN flood and distributed denial of service attacks, attempted 
malware infections, vulnerability scanning, ransomware attacks, spear-phishing campaigns, mass reconnaissance attempts, 
injection attempts, phishing, PHP injection and cross-site scripting. We also have seen an increase in attacks designed to obtain 
access to consumers’ accounts using illegally obtained demographic information. Although the impact of such attacks has not 
been material to our operations or operating results through December 31, 2019, we can provide no assurance that we or our 
vendors will be able to detect, prevent or contain the effects of such attacks or other information security (including 
cybersecurity) risks or threats in the future. As we expand our consumer-oriented products and services, increase the amount 
and types of data we acquire, generate and use, increase the amount of information we make available to members, consumers 
and providers on mobile devices, expand our use of vendors, expand internationally and expand our use of social media, our 
exposure to these data security and related cybersecurity risks, including the risk of undetected attacks, damage, loss or 
unauthorized disclosure or access to and/or disruption of our systems and the customer, member, provider, employee, 
accountable care organization (“ACO”), joint venture, vendor and other third party information they contain, increases, and the 
cost of attempting to protect against these risks also increases.

Although we deploy a layered approach to address information security (including cybersecurity) threats and vulnerabilities that 
is designed to protect confidential information against data security breaches, a compromise of our information security 
controls or of those businesses with whom we interact, which results in confidential information being accessed, obtained, 
damaged, or used by unauthorized or improper persons, could harm our reputation and expose us to regulatory actions and 
claims from customers and clients, financial institutions, payment card associations and other persons, any of which could 
adversely affect our businesses, operating results and financial condition. Because the techniques used to obtain unauthorized 
access, disable or degrade service, or sabotage systems change frequently and may not immediately produce signs of intrusion, 
we may be unable to anticipate these techniques or to implement adequate preventative measures. Moreover, a data security 
breach could require that we expend significant resources related to our information systems and infrastructure, and could 

44

distract management and other key personnel from performing their primary operational duties. We also could be adversely 
affected by any significant disruption in the systems of third parties we interact with, including key payors and vendors.

The costs of attempting to protect against the foregoing risks and the costs of responding to a cyber-incident are significant. 
Large scale data breaches at other entities increase the challenge we and our vendors face in maintaining the security of our 
information technology systems and proprietary information and of our customers’, members’ and other constituents’ sensitive 
information. Following a cyber-incident, our and/or our vendors’ remediation efforts may not be successful, and a cyber-
incident could result in interruptions, delays or cessation of service, and loss of existing or potential customers and members. In 
addition, breaches of our and/or our vendors’ security measures and the unauthorized dissemination of sensitive personal 
information or proprietary information or confidential information about us, our customers, our members or other third-parties, 
could expose our customers’, members’ and other constituents’ private information and our customers, members and other 
constituents to the risk of financial or medical identity theft, or expose us or other third parties to a risk of loss or misuse of this 
information, and result in investigations, regulatory enforcement actions, material fines and penalties, loss of customers, 
litigation or other actions which could have a material adverse effect on our brand, reputation, businesses, operating results and 
cash flows.

Data governance failures can adversely affect our reputation, businesses and prospects. Our use and disclosure of 
members’, customers’ and other constituents’ sensitive information is subject to complex regulations at multiple levels. We 
would be adversely affected if we or our business associates or other vendors fail to adequately protect members’, customers’ 
or other constituents’ sensitive information.

Our information systems are critical to the operation of our businesses. We collect, process, maintain, retain, evaluate, utilize 
and distribute large amounts of personal health and financial information and other confidential and sensitive data about our 
customers, members and other constituents in the ordinary course of our businesses. Some of our information systems rely upon 
third party systems to accomplish these tasks. The use and disclosure of such information is regulated at the federal, state and 
international levels, and these laws, rules and regulations are subject to change and increased enforcement activity, such as the 
California Consumer Privacy Act which went into effect January 1, 2020, the EU’s GDPR which began to apply across the EU 
during 2018 and the audit program implemented by HHS under HIPAA. In some cases, such laws, rules and regulations also 
apply to our vendors and/or may hold us liable for any violations by our vendors. International laws, rules and regulations 
governing the use and disclosure of such information are generally more stringent than U.S. laws and regulations, and they vary 
from jurisdiction to jurisdiction. Noncompliance with any privacy or security laws or regulations, or any security breach, cyber-
attack or cybersecurity breach, and any incident involving the theft, misappropriation, loss or other unauthorized disclosure of, 
or access to, sensitive or confidential customer, member or other constituent information, whether by us, by one of our business 
associates or vendors or by another third party, could require us to expend significant resources to remediate any damage, could 
interrupt our operations and could adversely affect our brand and reputation, membership and operating results and also could 
expose and/or has exposed us to mandatory disclosure to the media, litigation (including class action litigation), governmental 
investigations and enforcement proceedings, material fines, penalties and/or remediation costs, and compensatory, special, 
punitive and statutory damages, consent orders, adverse actions against our licenses to do business and/or injunctive relief, any 
of which could adversely affect our businesses, operating results, cash flows or financial condition.

Our businesses depend on our customers’, members’ and other constituents’ willingness to entrust us with their health related 
and other sensitive personal information. Events that adversely affect that trust, including inadequate disclosure to our members 
or customers of our uses of their information, failing to keep our information technology systems and our customers’, members’ 
and other constituents’ sensitive information secure from significant attack, theft, damage, loss or unauthorized disclosure or 
access, whether as a result of our action or inaction (including human error) or that of our business associates, vendors or other 
third parties, could adversely affect our brand and reputation, membership and operating results and also could expose and/or 
has exposed us to mandatory disclosure to the media, litigation (including class action litigation), governmental investigations 
and enforcement proceedings, material fines, penalties and/or remediation costs, and compensatory, special, punitive and 
statutory damages, consent orders, adverse actions against our licenses to do business and/or injunctive relief, any of which 
could adversely affect our businesses, operating results, cash flows or financial condition. Large scale data breaches at other 
entities increase the challenge we and our vendors face in maintaining the security of our information technology systems and 
proprietary information and of our customers’, members’ and other constituents’ sensitive information. There can be no 
assurance that additional such failures will not occur, or if any do occur, that we will detect them or that they can be sufficiently 
remediated.

45

Product liability, product recall or personal injury issues could damage our reputation and have a significant adverse effect 
on our businesses, operating results, cash flows and/or financial condition.

The products that we sell could become subject to contamination, product tampering, mislabeling, recall or other damage. In 
addition, errors in the dispensing and packaging of drugs and consuming drugs in a manner that is not prescribed could lead to 
serious injury or death. Product liability or personal injury claims may be asserted against us with respect to any of the drugs or 
other products we sell or services we provide. For example, we are a defendant in hundreds of litigation proceedings relating to 
opioids and the sale of products containing talc. Our businesses involve the provision of professional services, including by 
pharmacists, physician assistants, nurses and nurse practitioners, which exposes us to professional liability claims. Should a 
product or other liability issue arise, the coverage available under our insurance programs and the indemnification amounts 
available to us from third parties may not be adequate to protect us against the financial impact of the related claims. We also 
may not be able to maintain our existing levels of insurance on acceptable terms in the future. A product liability or personal 
injury issue or judgment against us or a product recall could damage our reputation and have a significant adverse effect on our 
businesses, operating results and/or financial condition.

We face significant competition in attracting and retaining talented employees. Further, managing succession for, and 
retention of, key executives is critical to our success, and our failure to do so could adversely affect our businesses, 
operating results and/or future performance.

Our ability to attract and retain qualified and experienced employees is essential to meet our current and future goals and 
objectives. There is no guarantee we will be able to attract and retain such employees or that competition among potential 
employers will not result in increased compensation and/or benefits costs. If we are unable to retain existing employees or 
attract additional employees, or we experience an unexpected loss of leadership, we could experience a material adverse effect 
on our businesses, operating results and/or future performance.

In addition, our failure to adequately plan for succession of senior management and other key management roles or the failure 
of key employees to successfully transition into new roles could have a material adverse effect on our businesses, operating 
results and/or future performance. The succession plans we have in place and our employment arrangements with certain key 
executives do not guarantee the services of these executives will continue to be available to us.

Sales of our products and services are dependent on our ability to attract and motivate internal sales personnel and 
independent third-party brokers, consultants and agents. New distribution channels create new disintermediation risk. We 
may be subject to penalties or other regulatory actions as a result of the marketing practices of brokers and agents selling 
our products.

Our products are sold primarily through our sales personnel, who frequently work with independent brokers, consultants and 
agents who assist in the production and servicing of business. The independent brokers, consultants and agents generally are not 
dedicated to us exclusively and may frequently recommend and/or market health care benefits products of our competitors. 
Accordingly, we must compete intensely for their services and allegiance. Our sales could be adversely affected if we are 
unable to attract, retain or motivate sales personnel and third-party brokers, consultants and agents, or if we do not adequately 
provide support, training and education to this sales network regarding our complex product portfolio, or if our sales strategy is 
not appropriately aligned across distribution channels. This risk is heightened as we develop, operate and expand our consumer-
oriented products and services and we expand in the health care space and our business model evolves to include a greater focus 
on consumers and direct-to-consumer sales, such as competing for sales on Insurance Exchanges.

New distribution channels for our products and services continue to emerge, including Private Exchanges operated by health 
care consultants and technology companies. These channels may make it more difficult for us to directly engage consumers and 
other customers in the selection and management of their health care benefits, in health care utilization and in the effective 
navigation of the health care system. We also may be challenged by new technologies and marketplace entrants that could 
interfere with our existing relationships with customers and health plan members in these areas.

In addition, there have been several investigations regarding the marketing practices of brokers and agents selling health care 
and other insurance products and the payments they receive. These investigations have resulted in enforcement actions against 
companies in our industry and brokers and agents marketing and selling those companies’ products. For example, CMS and 
state departments of insurance have increased their scrutiny of the marketing practices of brokers and agents who market 
Medicare products. These investigations and enforcement actions could result in penalties and the imposition of corrective 
action plans and/or changes to industry practices, which could adversely affect our ability to market our products.

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Failure of our businesses to effectively collaborate could prevent us from maximizing our operating results.

To maximize our overall Enterprise value, our various businesses need to collaborate effectively. Our businesses need to be 
aligned in order to prioritize goals and coordinate the design of new products intended to utilize the offerings of multiple 
businesses, including our transformation and Enterprise modernization programs. In addition, misaligned incentives, 
information siloes, ineffective product development and failure of our corporate governance policies or procedures, for example 
significant financial decisions being made at an inappropriate level in our organization, also could prevent us from maximizing 
our operating results and/or achieving our financial and other projections. 

The failure or disruption of our information technology systems or the failure of our information technology infrastructure 
to support our businesses could adversely affect our reputation, businesses, operating results and cash flows.

Our information systems are subject to damage or interruption from power outages, facility damage, computer and 
telecommunications failures, computer viruses, security breaches (including credit card or personally identifiable information 
breaches), cyber-attacks, vandalism, catastrophic events and human error. If our information systems are damaged, fail to work 
properly or otherwise become unavailable, we may incur substantial costs to repair or replace them, and may experience 
reputational damage, loss of critical information, customer disruption and interruptions or delays in our ability to perform 
essential functions and implement new and innovative services. In addition, compliance with changes in U.S. and foreign laws 
and regulations, including privacy and information security laws and standards, may cause us to incur significant expense due 
to increased investment in technology and the development of new operational processes.

Our business success and operating results depend in part on effective information technology systems and on continuing to 
develop and implement improvements in technology. Pursuing multiple initiatives simultaneously could make this continued 
development and implementation significantly more challenging.

Many aspects of our operations are dependent on our information systems and the information collected, processed, stored, and 
handled by these systems. We rely heavily on our computer systems to manage our ordering, pricing, point-of-sale, pharmacy 
fulfillment, inventory replenishment, claims processing, customer loyalty and subscription programs, finance and other 
processes. Throughout our operations, we collect, process, maintain, retain, evaluate, utilize and distribute large amounts of 
confidential and sensitive data and information, including personally identifiable information and protected health information, 
that our customers, members and other constituents provide to purchase products or services, enroll in programs or services, 
register on our websites, interact with our personnel, or otherwise communicate with us. In addition, for these operations, we 
depend in part on the secure transmission of confidential information over public networks.

We have many different information and other technology systems supporting our businesses (including as a result of our 
acquisitions). Our businesses depend in large part on these systems to adequately price our products and services; accurately 
establish reserves, process claims and report operating results; and interact with providers, employer plan sponsors, customers, 
members, consumers and vendors in an efficient and uninterrupted fashion. In addition, recent trends toward greater consumer 
engagement in health care require new and enhanced technologies, including more sophisticated applications for mobile 
devices. Certain of our technology systems (including software) are older, legacy systems that are less flexible, less efficient 
and require a significant ongoing commitment of capital and human resources to maintain, protect and enhance them and to 
integrate them with our other systems. We must re-engineer and reduce the number of these systems to meet changing 
consumer and vendor preferences and needs, improve our productivity and reduce our operating expenses. We also need to 
develop or acquire new technology systems, contract with new vendors or modify certain of our existing systems to support the 
consumer-oriented and transformation products and services we are developing, operating and expanding and/or to meet current 
and developing industry and regulatory standards, including to keep pace with continuing changes in information processing 
technology and emerging cybersecurity risks and threats. If we fail to achieve these objectives, our ability to profitably grow 
our business and/or our operating results may be adversely affected.

In addition, information technology and other technology and process improvement projects, including our transformation and 
Enterprise modernization programs, frequently are long-term in nature and may take longer to complete and cost more than we 
expect and may not deliver the benefits we project once they are complete. If we do not effectively and efficiently secure, 
manage, integrate and enhance our technology portfolio (including vendor sourced systems), we could, among other things, 
have problems determining health care and other benefit cost estimates and/or establishing appropriate pricing, meeting the 
needs of customers, consumers, providers, members and vendors, developing and expanding our consumer-oriented products 
and services or keeping pace with industry and regulatory standards, and our operating results may be adversely affected.

47

We are subject to payment-related risks that could increase our operating costs, expose us to fraud or theft, subject us to 
potential liability and disrupt our business operations.

We accept payments using a variety of methods, including cash, checks, credit cards, debit cards, gift cards, mobile payments 
and potentially other technologies in the future. Acceptance of these payment methods subjects us to rules, regulations, 
contractual obligations and compliance requirements, including payment network rules and operating guidelines, data security 
standards and certification requirements, and rules governing electronic funds transfers. These requirements may change in the 
future, which could make compliance more difficult or costly. For certain payment options, including credit and debit cards, we 
pay interchange and other fees, which could increase periodically thereby raising our operating costs. We rely on third parties to 
provide payment processing services, including the processing of credit cards, debit cards, and various other forms of electronic 
payment. If these vendors are unable to provide these services to us, or if their systems are compromised, our operations could 
be disrupted. The payment methods that we offer also expose us to potential fraud and theft by persons seeking to obtain 
unauthorized access to, or exploit any weaknesses in, the payment systems we use. If we fail to abide by applicable rules or 
requirements, or if data relating to our payment systems is compromised due to a breach or misuse, we may be responsible for 
any costs incurred by payment card issuing banks and other third parties or subject to fines and higher transaction fees. In 
addition, our reputation and ability to accept certain types of payments could each be harmed resulting in reduced sales and 
adverse effects on our operating results.

Both our and our vendors’ operations are subject to a variety of business continuity hazards and risks, any of which could 
interrupt our operations or otherwise adversely affect our performance and operating results.

We and our vendors are subject to business continuity hazards and other risks, including natural disasters, utility and other 
mechanical failures, acts of war or terrorism, disruption of communications, data security and preservation, disruption of supply 
or distribution, safety regulation and labor difficulties. The occurrence of any of these or other events to us or our vendors 
might disrupt or shut down our operations or otherwise adversely affect our operations. We also may be subject to certain 
liability claims in the event of an injury or loss of life, or damage to property, resulting from such events. Although we have 
developed procedures for crisis management and disaster recovery and business continuity plans and maintain insurance 
policies that we believe are customary and adequate for our size and industry, our insurance policies include limits and 
exclusions and, as a result, our coverage may be insufficient to protect against all potential hazards and risks incident to our 
businesses. In addition, our crisis management and disaster recovery procedures and business continuity plans may not be 
effective. Should any such hazards or risks occur, or should our insurance coverage be inadequate or unavailable, our 
businesses, operating results, cash flows and financial condition could be adversely affected.

Financial Risks

We would be adversely affected if we do not effectively deploy our capital. Downgrades or potential downgrades in our credit 
ratings, should they occur, could adversely affect our brand and reputation, businesses, operating results, cash flows and 
financial condition.

Our operations generate significant capital, and we have the ability to raise additional capital. The manner in which we deploy 
our capital, including investments in our businesses, our operations (such as information technology and other strategic and 
capital projects), dividends, acquisitions, share and/or debt repurchases, repayment of debt, reinsurance or other capital uses, 
impacts our financial strength, claims paying ability and credit ratings issued by nationally-recognized statistical rating 
organizations. Credit ratings issued by nationally-recognized statistical rating organizations are broadly distributed and 
generally used throughout our industries. Our ratings reflect each rating organization’s opinion of our financial strength, 
operating performance and ability to meet our debt obligations or obligations to our insureds. We believe our credit ratings and 
the financial strength and claims paying ability of our principal insurance and HMO subsidiaries are important factors in 
marketing our Health Care Benefits products to certain of our customers.

Each of the ratings organizations reviews our ratings periodically, and there can be no assurance that our current ratings will be 
maintained in the future. In connection with the completion of the Aetna Acquisition, each of Standard & Poor’s, Moody’s and 
Fitch downgraded certain of our debt, financial strength and/or other credit ratings. Downgrades in our ratings could adversely 
affect our businesses, operating results, cash flows and financial condition.

Goodwill and other intangible assets could, in the future, become impaired.

As of December 31, 2019, we had $112.9 billion of goodwill and other intangible assets. During the year ended December 31, 
2018, we took $6.1 billion of goodwill impairment charges related to our LTC reporting unit within the Retail/LTC segment. 

48

Goodwill and indefinitely-lived intangible assets are subject to annual impairment reviews, or more frequent reviews if events 
or circumstances indicate that the carrying value may not be recoverable. When evaluating goodwill for potential impairment, 
we compare the fair value of our reporting units to their respective carrying amounts. We estimate the fair value of our reporting 
units using a combination of a discounted cash flow method and a market multiple method. If the carrying amount of a 
reporting unit exceeds its estimated fair value, a goodwill impairment loss is recognized in an amount equal to the excess to the 
extent of the goodwill balance. Estimated fair values could change if, for example, there are changes in the business climate, 
industry-wide changes, changes in the competitive environment, adverse legal or regulatory actions or developments, changes 
in capital structure, cost of debt, interest rates, capital expenditure levels, operating cash flows or market capitalization. Because 
of the significance of our goodwill and intangible assets, any future impairment of these assets could require material noncash 
charges to our operating results, which also could have a material adverse effect on our financial condition.

Adverse conditions in the U.S. and global capital markets can significantly and adversely affect the value of our investments 
in debt and equity securities, mortgage loans, alternative investments and other investments, and our operating results and/
or our financial condition.

The global capital markets, including credit markets, continue to experience volatility and uncertainty. As an insurer, we have a 
substantial investment portfolio that supports our policy liabilities and surplus and is comprised largely of debt securities of 
issuers located in the U.S. As a result, the income we earn from our investment portfolio is largely driven by the level of interest 
rates in the U.S., and to a lesser extent the international financial markets; and volatility, uncertainty and/or disruptions in the 
global capital markets, particularly the U.S. credit markets, and governments’ monetary policy, particularly U.S. monetary 
policy, can significantly and adversely affect the value of our investment portfolio, our operating results and/or our financial 
condition by:

• 

• 

• 

• 

significantly reducing the value and/or liquidity of the debt securities we hold in our investment portfolio and creating 
realized capital losses that reduce our operating results and/or unrealized capital losses that reduce our shareholders’ equity;

keeping interest rates low on high-quality short-term or medium-term debt securities (such as we have experienced during 
recent years) and thereby materially reducing our net investment income and operating results as the proceeds from 
securities in our investment portfolio that mature or are otherwise disposed of continue to be reinvested in lower yielding 
securities;

reducing the fair values of our investments if interest rates rise;

causing non-performance of or defaults on their obligations to us by third parties, including customers, issuers of securities 
in our investment portfolio, mortgage borrowers and/or reinsurance and/or derivatives counterparties;

•  making it more difficult to value certain of our investment securities, for example if trading becomes less frequent, which 

could lead to significant period-to-period changes in our estimates of the fair values of those securities and cause period-to-
period volatility in our net income and shareholders’ equity;

• 

• 

reducing our ability to issue short-term debt securities at attractive interest rates, thereby increasing our interest expense 
and decreasing our operating results; and

reducing our ability to issue other securities.

Although we seek, within guidelines we deem appropriate, to match the duration of our assets and liabilities and to manage our 
credit and counterparty exposures, a failure adequately to do so could adversely affect our net income and our financial 
condition and, in extreme circumstances, our cash flows.

We have incurred and assumed significant indebtedness which has increased our consolidated interest expense and could 
adversely affect our business flexibility and increase our borrowing costs.

In order to complete the Aetna Acquisition, we incurred acquisition-related debt financing of approximately $45.0 billion and 
assumed Aetna’s existing indebtedness with a fair value of approximately $8.1 billion. Our substantial indebtedness and 
elevated debt-to-equity ratio have the effect, among other things, of reducing our flexibility to respond to changing business and 
economic conditions and increasing our interest expense compared to pre-Aetna Acquisition periods. In addition, the amount of 
cash required to service our increased indebtedness levels and thus the demands on our cash resources are greater than the 
amount of cash flows required to service our indebtedness prior to the Aetna Acquisition. We have suspended share repurchases 
until we reach our desired debt-to-equity ratio. The increased levels of indebtedness also could reduce funds available to engage 
in investments in product development, capital expenditures, dividend payments and other activities and may create competitive 
disadvantages for us relative to other companies with lower debt levels.

49

Risks Related to Our Relationships with Manufacturers, Providers, Suppliers and Vendors

We face risks relating to the market availability, pricing, suppliers and safety profiles of prescription drugs and other 
products that we purchase and sell.

Our Retail/LTC segment and our mail order and specialty pharmacy operations generate revenues in significant part by 
dispensing prescription drugs. Our PBM business generates revenues primarily by contracting with clients to provide 
prescription drugs and related health care services to plan members. As a result, we are dependent on our relationships with 
prescription drug manufacturers and suppliers. We acquire a substantial amount of our mail order and specialty pharmacies’ 
prescription drug supply from a limited number of suppliers. Certain of our agreements with such suppliers are short-term and 
cancelable by either party without cause. In addition, these agreements may allow the supplier to distribute through channels 
other than us. Certain of these agreements also allow pricing and other terms to be adjusted periodically for changing market 
conditions or required service levels. A termination or modification to any of these relationships could adversely affect our 
prescription drug supply and have a material adverse effect on our businesses, operating results and financial condition. 
Moreover, many products distributed by our pharmacies are manufactured with ingredients that are susceptible to supply 
shortages. In some cases, we depend upon a single source of supply. Any such supply shortages or loss of any such single 
source of supply could adversely affect our operating results and cash flows.

Much of the branded and generic drug product that we sell in our pharmacies, and much of the other merchandise we sell, is 
manufactured in whole or in substantial part outside of the United States. In most cases, the products or merchandise are 
imported by others and sold to us. As a result, significant changes in tax or trade policies, tariffs or trade relations between the 
United States and other countries, such as the imposition of unilateral tariffs on imported products, could result in significant 
increases in our costs, restrict our access to suppliers, depress economic activity, and have a material adverse effect on our 
businesses, operating results and cash flows. In addition, other countries may change their business and trade policies and such 
changes, as well as any negative sentiments towards the United States in response to increased import tariffs and other changes 
in U.S. trade regulations, could adversely affect our businesses.

Our suppliers are independent entities subject to their own operational and financial risks that are outside our control. If our 
current suppliers were to stop selling prescription drugs to us or delay delivery, including as a result of supply shortages, 
supplier production disruptions, supplier quality issues, closing or bankruptcies of our suppliers, or for other reasons, we may 
be unable to procure alternatives from other suppliers in a timely and efficient manner and on acceptable terms, or at all. 

Our operating results may be adversely affected if we are unable to contract with providers on competitive terms and develop 
and maintain attractive networks with high quality providers.

We are seeking to enhance our health care provider networks by entering into joint ventures and other collaborative risk-sharing 
arrangements with health care providers. Providers’ willingness to enter these arrangements with us depends upon, among other 
things, our ability to provide them with up to date quality of care data to support these value-based contracts. These 
arrangements are designed to give providers incentives to engage in population health management and optimize delivery of 
health care to our members. These arrangements also may allow us to expand into new geographies, target new customer 
groups, increase membership and reduce medical costs and, if we provide technology or other services to the relevant health 
system or provider organization, may contribute to our revenue and earnings from alternative sources. If such arrangements do 
not result in the lower medical costs that we project or if we fail to attract health care providers to such arrangements, or are less 
successful at implementing such arrangements than our competitors, our medical costs may not be competitive and may be 
higher than we project, our attractiveness to customers may be reduced, we may lose or be unable to grow medical membership, 
and our ability to profitably grow our business and/or our operating results may be adversely affected.

While we believe joint ventures, ACOs and other non-traditional health care provider organizational structures present 
opportunities for us, the implementation of our joint ventures and other non-traditional structure strategies may not achieve the 
intended results, which could adversely affect our operating results and cash flows. Among other things, joint ventures require 
us to maintain collaborative relationships with our counterparties, continue to gain access to provider rates that make the joint 
ventures economically sustainable and devote significant management time to the operation and management of the joint 
ventures. We may not be able to achieve these objectives in one or more of our joint ventures, which could adversely affect our 
operating results and cash flows.

50

If our service providers fail to meet their contractual obligations to us or to comply with applicable laws or regulations, we 
may be exposed to brand and reputational harm, litigation and/or regulatory action. This risk is particularly high in our 
Medicare, Medicaid, dual eligible and dual eligible special needs plan programs.

We contract with various third parties to perform certain functions and services and provide us with certain information 
technology systems. Our arrangements with these third parties may expose us to public scrutiny, adversely affect our brand and 
reputation, expose us to litigation or regulatory action, and otherwise make our operations vulnerable if we fail to adequately 
oversee, monitor and regulate their performance or if they fail to meet their contractual obligations to us or to comply with 
applicable laws or regulations. For example, certain of our vendors have been responsible for releases of sensitive information 
of our members and employees, which has caused us to incur additional expenses and given rise to regulatory actions and 
litigation against us.

These risks are particularly high in our Medicare, Medicaid, dual eligible and dual eligible special needs plan programs, where 
third parties perform PBM, medical management and other member related services for us. Any failure of our or these third 
parties’ prevention, detection or control systems related to regulatory compliance, compliance with our internal policies, data 
security and/or cybersecurity or any incident involving the theft, misappropriation, loss or other unauthorized disclosure of, or 
access to, members’, customers’ or other constituents’ sensitive information could require us to expend significant resources to 
remediate any damage, interrupt our operations and adversely affect our brand and reputation and also expose us to 
whistleblower, class action and other litigation, other proceedings, prohibitions on marketing or active or passive enrollment of 
members, corrective actions, fines, sanctions and/or penalties, any of which could adversely affect our businesses, operating 
results, cash flows and/or financial condition.

We may experience increased medical and other benefit costs, litigation risk and customer and member dissatisfaction when 
providers that do not have contracts with us render services to our Health Care Benefits members.

Some providers that render services to our Health Care Benefits members do not have contracts with us. In those cases, we do 
not have a pre-established understanding with these providers as to the amount of compensation that is due to them for services 
rendered to our members. In some states, the amount of compensation due to these nonparticipating providers is defined by law 
or regulation, but in most instances it is either not defined or it is established by a standard that is not clearly translatable into 
dollar terms. In such instances providers may believe that they are underpaid for their services and may either litigate or 
arbitrate their dispute with us or try to recover the difference between what we have paid them and the amount they charged us 
from our members, which may result in customer and member dissatisfaction. For example, in October 2018, an arbitrator 
awarded certain claimant hospitals approximately $150 million in a proceeding relating to Aetna’s out-of-network benefit 
payment and administration practices, and in March 2019 that award was reduced to approximately $86 million. Such disputes 
may cause us to pay higher medical or other benefit costs than we projected.

Continuing consolidation and integration among providers and other suppliers may increase our medical and other covered 
benefits costs, make it difficult for us to compete in certain geographies and create new competitors.

Hospitals and other providers and health systems continue to consolidate across the health care industry. While this 
consolidation could increase efficiency and has the potential to improve the delivery of health care services, it also reduces 
competition and the number of potential contracting parties in certain geographies. These health systems also are increasingly 
forming and considering forming health plans to directly offer health insurance in competition with us, a process that has been 
accelerated by the ACA. In addition, ACOs (including Commercial and Medicaid-only ACOs developed as a result of state 
Medicaid laws), practice management companies, consolidation among and by integrated health systems and other changes in 
the organizational structures that physicians, hospitals and other health care providers adopt continues to change the way these 
providers interact with us and the competitive landscape in which we operate. These changes may increase our medical and 
other covered benefits costs, may affect the way we price our products and services and estimate our medical and other covered 
benefits costs and may require us to change our operations, including by withdrawing from certain geographies where we do 
not have a significant presence across our businesses or are unable to collaborate or contract with providers on acceptable 
terms. Each of these changes may adversely affect our businesses and operating results.

51

Item 1B.  Unresolved Staff Comments.

There are no unresolved SEC Staff Comments.

Item 2.  Properties.

The Company’s principal office is an owned building complex located in Woonsocket, Rhode Island, which totals 
approximately one million square feet. The Company also leases office space in other locations in the United States. 

Pharmacy Services Segment

The Pharmacy Services segment includes owned or leased mail service dispensing pharmacies, call centers, on-site pharmacy 
stores, retail specialty pharmacy stores, specialty mail service pharmacies and branches for infusion and enteral services 
throughout the United States.

Retail/LTC Segment

As of December 31, 2019, the Retail/LTC segment operated the following properties:

•  Approximately 8,170 retail stores, of which approximately 5% were owned. Net selling space for retail stores was 

approximately 80.3 million square feet as of December 31, 2019. Approximately 45% of the store base was opened or 
significantly remodeled within the last five years;

•  Approximately 1,725 retail pharmacies and approximately 80 clinics in Target stores;

•  Owned distribution centers and leased distribution facilities throughout the U.S. totaling approximately 10.5 million square 

feet; and

•  Owned and leased LTC pharmacies throughout the U.S. and an owned LTC repackaging facility.

In connection with certain business dispositions completed between 1995 and 1997, the Company continues to guarantee lease 
obligations for 79 former stores. The Company is indemnified for these guarantee obligations by the respective initial 
purchasers. These guarantees generally remain in effect for the initial lease term and any extension thereof pursuant to a 
renewal option provided for in the lease prior to the time of the disposition. For additional information on these guarantees, see 
“Lease Guarantees” in Note 16 ‘‘Commitments and Contingencies’’ included in Item 8 of this 10-K.

Health Care Benefits Segment

The Health Care Benefits segment’s principal office is an owned building complex located in Hartford, Connecticut, which 
totals approximately 1.7 million square feet. The Health Care Benefits segment also owns or leases office space in other 
locations in the United States and several other countries. 

Management believes that the Company’s owned and leased facilities are suitable and adequate to meet the Company’s 
anticipated needs. At the end of the existing lease terms, management believes the leases can be renewed or replaced by 
alternative space. For additional information on the amount of right-of-use assets and lease liabilities for the Company’s leases, 
see Note 6 ‘‘Leases’’ included in Item 8 of this 10-K.

Item 3.  Legal Proceedings.

I.  Legal Proceedings

The information contained in Note 16 ‘‘Commitments and Contingencies’’ included in Item 8 of this 10-K is incorporated 
herein by reference.

II.  Environmental Matters

Item 103 of SEC Regulation S-K requires disclosure of environmental legal proceedings with a governmental authority if 
management reasonably believes that the proceedings involve potential monetary sanctions of $100,000 or more. The Company 
is in the process of negotiating with the New York State Department of Environmental Conservation to resolve claims of 

52

alleged historical noncompliance with hazardous waste regulations in connection with LTC pharmacies in the State of New 
York. These proceedings are not material to the Company’s business or financial condition.

Item 4.  Mine Safety Disclosures.

Not applicable.

53

Information about our Executive Officers 

The following sets forth the name, age and biographical information for each of the Registrant’s executive officers as of 
February 18, 2020. In each case the officer’s term of office extends to the date of the meeting of the CVS Health Board of 
Directors (the “Board”) following the next annual meeting of stockholders of CVS Health. Previous positions and 
responsibilities held by each of the executive officers over the past five years or more are indicated below:

Lisa G. Bisaccia, age 63, Executive Vice President of CVS Health Corporation since March 2016 and Chief Human 

Resources Officer of CVS Health Corporation since January 2010; Senior Vice President of CVS Health Corporation from 
January 2010 through February 2016. Ms. Bisaccia is also a member of the board of directors of Aramark, a leading global 
provider of food, facilities and uniform services.

Eva C. Boratto, age 53, Executive Vice President and Chief Financial Officer of CVS Health Corporation since 

November 2018; Executive Vice President - Controller and Chief Accounting Officer of CVS Health Corporation from March 
2017 through November 2018; Senior Vice President - Controller and Chief Accounting Officer of CVS Health Corporation 
from July 2013 through February 2017.

Troyen A. Brennan, M.D., age 65, Executive Vice President and Chief Medical Officer of CVS Health Corporation 

since November 2008; Executive Vice President and Chief Medical Officer of Aetna Inc. from February 2006 through 
November 2008.

James D. Clark, age 55, Senior Vice President - Controller and Chief Accounting Officer of CVS Health Corporation 
since November 2018; Vice President - Finance and Accounting of CVS Pharmacy, Inc. from September 2009 through October 
2018. 

Joshua M. Flum, age 50, Executive Vice President, Enterprise Strategy and Digital of CVS Health Corporation since 
November 2018; Executive Vice President, Corporate Strategy and Business Development of CVS Pharmacy, Inc. from June 
2016 through October 2018; Executive Vice President - Pharmacy Services of CVS Pharmacy, Inc. from March 2015 through 
May 2016; Senior Vice President of Retail Pharmacy of CVS Pharmacy, Inc. from December 2010 through February 2015. Mr. 
Flum is a member of the board of directors of CreditRiskMonitor.com, Inc., a company that facilitates the analysis of corporate 
financial risk, mostly in the context of the extension of trade credit from one business to another.

Alan M. Lotvin, M.D., age 58, served as Executive Vice President - Transformation of CVS Health Corporation from 

June 2018 through February 2020, and will serve as Executive Vice President of CVS Health Corporation and President of CVS 
Caremark following the departure of Mr. Rice. Dr. Lotvin served as Executive Vice President - Specialty Pharmacy, CVS 
Caremark from November 2012 through May 2018.

Karen S. Lynch, age 57, Executive Vice President of CVS Health Corporation since November 2018; President of 
Aetna since January 2015; Executive Vice President, Local and Regional Businesses of Aetna from February 2013 through 
December 2014. Ms. Lynch is a member of the board of directors of U.S. Bancorp, a banking and financial services company.

Larry J. Merlo, age 64, President and Chief Executive Officer of CVS Health Corporation since March 2011; and a 

director of CVS Health Corporation since May 2010.

Thomas M. Moriarty, age 56, Executive Vice President and General Counsel of CVS Health Corporation since 

October 2012; Chief Policy and External Affairs Officer since March 2017; Chief Strategy Officer from March 2014 through 
February 2017.

Derica W. Rice, age 54, Executive Vice President of CVS Health Corporation and President of CVS Caremark since 

March 2018; Executive Vice President of Global Services and Chief Financial Officer of Eli Lilly & Company from May 2006 
through December 2017. Mr. Rice is a director of The Walt Disney Company since March 2019 and was a director of Target 
Corporation from September 2007 until January 2018. Mr. Rice will be leaving the Company effective March 1, 2020. 

Jonathan C. Roberts, age 64, Executive Vice President and Chief Operating Officer of CVS Health Corporation since 
March 2017 and Interim President of CVS Pharmacy since January 2020; Executive Vice President of CVS Health Corporation 
and President of CVS Caremark from September 2012 through February 2017.

54

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
PART II

Item 5.  Market for Registrant’s Common Equity, Related Stockholder Matters and Issuer Purchases of Equity 
Securities.

On February 3, 2020, the Company announced that Richard J. Swift, Richard M. Bracken and Mark T. Bertolini would not 
stand for re-election at the Company’s upcoming Annual Meeting of Stockholders (the “2020 Annual Meeting”). On February 
7, 2020, Mr. Bertolini informed the Company of his decision to resign from the Board, effective immediately. On February 10, 
2020, the Board reduced the size of the Board from 16 to 15 members effective immediately and further reduced the size of the 
Board to 13 members effective at the time of the 2020 Annual Meeting. 

Market information

CVS Health’s common stock is listed on the New York Stock Exchange under the symbol “CVS.” 

Dividends 

CVS Health has paid cash dividends every quarter since becoming a public company. Future dividends will depend on the 
Company’s earnings, capital requirements, financial condition and other factors considered relevant by CVS Health’s Board of 
Directors. 

See Note 12 ‘‘Shareholders’ Equity’’ included in Item 8 of this 10-K for information regarding CVS Health’s dividends.

Holders of common stock

As of February 12, 2020, there were 26,656 registered holders of the registrant’s common stock according to the records 
maintained by the registrant’s transfer agent.

Issuer purchases of equity securities 

The following share repurchase programs have been authorized by the Board:

In billions
Authorization Date
November 2, 2016 (“2016 Repurchase Program”)

December 15, 2014 (“2014 Repurchase Program”)

    Remaining as of

Authorized December 31, 2019
13.9
$

15.0

$

10.0

—

Each of the share Repurchase Programs was effective immediately. The 2014 Repurchase Program has been completed. The 
2016 Repurchase Program permits the Company to effect repurchases from time to time through a combination of open market 
repurchases, privately negotiated transactions, accelerated share repurchase transactions, and/or other derivative transactions. 
The 2016 Repurchase Program can be modified or terminated by the Board at any time. During the three months ended 
December 31, 2019, the Company did not repurchase any shares of common stock. 

See Note 12 ‘‘Shareholders’ Equity’’ included in Item 8 of this 10-K for additional information regarding the Company’s share 
repurchases.

55

Stock Performance Graph

The following graph compares the cumulative total shareholder return on CVS Health’s common stock (assuming reinvestment 
of dividends) with the cumulative total return on the S&P 500 Index, the S&P 500 Food and Staples Retailing Industry Group 
Index and the S&P 500 Healthcare Sector Group Index from December 31, 2014 through December 31, 2019. The graph 
assumes a $100 investment in shares of CVS Health’s common stock on December 31, 2014.

December 31,

2014

2015

2016

2017

2018

2019

$

100
100

100

100

$

103
101

98

107

$

85
113

98

104

$

80
138

111

127

$

74
132

112

135

87
174

143

163

CVS Health Corporation
S&P 500 (1)
S&P 500 Food & Staples Retail Group Index (2)
S&P 500 Health Care Group Index (1) (3)
_____________________________________________

$

(1) 
(2) 
(3) 

Includes CVS Health.
Includes 5 companies (COST, KR, SYY, WBA, WMT).
Includes 61 companies.

The year-ended values of each investment shown in the preceding graph are based on share price appreciation plus dividends, 
with the dividends reinvested as of the last business day of the month during which such dividends were ex-dividend. The 
calculations exclude trading commissions and taxes. Total shareholder returns from each investment can be calculated from the 
year-end investment values shown beneath the graph. 

56

Item 6.  Selected Financial Data.

The selected consolidated financial data of CVS Health Corporation as of and for the periods indicated in the five-year period 
ended December 31, 2019, has been derived from the consolidated financial statements of CVS Health Corporation. The 
selected consolidated financial data should be read in conjunction with the MD&A included in Item 7 of this 10-K and the 
audited consolidated financial statements and related notes included in Item 8 of this 10-K.

In millions, except per share amounts

Statement of operations data:

Total revenues

Operating income

Income (loss) from continuing operations

Net income (loss) attributable to CVS Health

Per common share data:

Basic earnings (loss) per common share:

Income (loss) from continuing operations
attributable to CVS Health

Income (loss) from discontinued operations
attributable to CVS Health

Net income (loss) attributable to CVS Health

Diluted earnings (loss) per common share:

Income (loss) from continuing operations
attributable to CVS Health

Income (loss) from discontinued operations
attributable to CVS Health

Net income (loss) attributable to CVS Health

Dividends per common share

Balance sheet and other data:

Total assets

Long-term debt, less current portion

Total shareholders’ equity

Number of stores (at end of year)
_____________________________________________

2019

2018 (1)

2017

2016

2015

$

256,776

$

194,579

$

184,786

$

177,546

$

153,311

11,987

6,631

6,634

4,021
(596)
(594)

9,538

6,631

6,622

10,386

5,320

5,317

9,496

5,230

5,237

$

$

$

$

$

$

$

$

$

$

5.10

$

(0.57) $

6.48

$

4.93

$

— $

5.10

$

— $
(0.57) $

(0.01) $
$
6.47

— $

4.93

$

5.08

$

(0.57) $

6.45

$

4.91

$

— $

$

$

$

$

$

5.08

2.00

222,449

64,699

64,170

9,941

— $
(0.57) $
$
2.00

$

$

$

196,456

71,444

58,543

9,967

(0.01) $
$
6.44

$

$

$

$

2.00

95,131

22,181

37,695

9,846

— $

$

$

$

$

$

4.90

1.70

94,462

25,615

36,834

9,750

4.65

0.01

4.66

4.62

0.01

4.63

1.40

92,437

26,267

37,203

9,681

(1)  On November 28, 2018, the Company acquired Aetna. Aetna’s operations are included in the Company’s consolidated financial statements subsequent to 

the Aetna Acquisition Date. See Note 2 ‘‘Acquisitions and Divestitures’’ included in Item 8 of this 10-K for additional information. 

57

Item 7.  Management’s Discussion and Analysis of Financial Condition and Results of Operations. (“MD&A”) 

The following discussion and analysis should be read in conjunction with the audited consolidated financial statements and 
related notes included in Item 8 of this 10-K, “Risk Factors” included in Item 1A of this 10-K and the “Cautionary Statement 
Concerning Forward Looking Statements” in this 10-K.

Overview of Business

CVS Health Corporation (“CVS Health”), together with its subsidiaries (collectively, the “Company,” “we,” “our” or “us”), is 
the nation’s premier health innovation company helping people on their path to better health. Whether in one of its pharmacies 
or through its health services and plans, CVS Health is pioneering a bold new approach to total health by making quality care 
more affordable, accessible, simple and seamless. CVS Health is community-based and locally focused, engaging consumers 
with the care they need when and where they need it. The Company has approximately 9,900 retail locations, approximately 
1,100 walk-in medical clinics, a leading pharmacy benefits manager with approximately 105 million plan members, a dedicated 
senior pharmacy care business serving more than one million patients per year and expanding specialty pharmacy services. 
CVS Health also serves an estimated 37 million people through traditional, voluntary and consumer-directed health insurance 
products and related services, including expanding Medicare Advantage offerings and a leading standalone Medicare Part D 
prescription drug plan (“PDP”). The Company believes its innovative health care model increases access to quality care, 
delivers better health outcomes and lowers overall health care costs.

On November 28, 2018 (the “Aetna Acquisition Date”), the Company acquired Aetna Inc. (“Aetna”) for a combination of cash 
and CVS Health stock (the “Aetna Acquisition”). The Company acquired Aetna to help improve the consumer health care 
experience by combining Aetna’s health care benefits products and services with CVS Health’s retail locations, walk-in medical 
clinics and integrated pharmacy capabilities with the goal of becoming the new, trusted front door to health care. Under the 
terms of the merger agreement, Aetna shareholders received $145.00 in cash and 0.8378 CVS Health shares for each Aetna 
share. The transaction valued Aetna at approximately $212 per share or approximately $70 billion. Including the assumption of 
Aetna’s debt, the total value of the transaction was approximately $78 billion. The Company financed the cash portion of the 
purchase price through a combination of cash on hand and by issuing approximately $45 billion of new debt, including senior 
notes and term loans (see “Liquidity and Capital Resources” later in this MD&A). The consolidated financial statements reflect 
Aetna’s results subsequent to the Aetna Acquisition Date.

On October 10, 2018, the Company and Aetna entered into a consent decree with the U.S. Department of Justice (the “DOJ”) 
that allowed the Company’s proposed acquisition of Aetna to proceed, provided Aetna agreed to sell its individual standalone 
PDPs. As part of the agreement reached with the DOJ, Aetna entered into a purchase agreement with a subsidiary of WellCare 
Health Plans, Inc. (“WellCare”) for the divestiture of Aetna’s standalone PDPs effective December 31, 2018. On November 30, 
2018, the Company completed the sale of Aetna’s standalone PDPs. The Company provided administrative services to, and 
retained the financial results of, the divested plans through 2019. Subsequent to 2019, the Company will no longer retain the 
financial results of the divested plans. Aetna’s standalone PDPs had an aggregate of 2.5 million members as of December 31, 
2019.  

As a result of the Aetna Acquisition, the Company added the Health Care Benefits segment. Certain aspects of Aetna’s 
operations, including products for which the Company no longer solicits or accepts new customers, such as large case pensions 
and long-term care insurance products, are included in the Company’s Corporate/Other segment. 

Effective for the first quarter of 2019, the Company realigned the composition of its segments to correspond with changes to its 
operating model and reflect how its Chief Operating Decision Maker (the “CODM”) reviews information and manages the 
business. As a result of this realignment, the Company’s SilverScript® PDP moved from the Pharmacy Services segment to the 
Health Care Benefits segment. In addition, the Company moved Aetna’s mail order and specialty pharmacy operations from the 
Health Care Benefits segment to the Pharmacy Services segment. Segment financial information has been retrospectively 
adjusted to reflect these changes. See Note 17 ‘‘Segment Reporting’’ included in Item 8 of this 10-K for segment financial 
information.

The Company has four reportable segments: Pharmacy Services, Retail/LTC, Health Care Benefits and Corporate/Other, which 
are described below.

58

Overview of the Pharmacy Services Segment

The Pharmacy Services segment provides a full range of pharmacy benefit management (“PBM”) solutions, including plan 
design offerings and administration, formulary management, retail pharmacy network management services, mail order 
pharmacy, specialty pharmacy and infusion services, clinical services, disease management services and medical spend 
management. The Pharmacy Services segment’s clients are primarily employers, insurance companies, unions, government 
employee groups, health plans, PDPs, Medicaid managed care plans, plans offered on public health insurance exchanges and 
private health insurance exchanges, other sponsors of health benefit plans and individuals throughout the United States. The 
Pharmacy Services segment operates retail specialty pharmacy stores, specialty mail order pharmacies, mail order dispensing 
pharmacies, compounding pharmacies and branches for infusion and enteral nutrition services. During the year ended 
December 31, 2019, the Company’s PBM filled or managed 2.0 billion prescriptions on a 30-day equivalent basis.

Overview of the Retail/LTC Segment

The Retail/LTC segment sells prescription drugs and a wide assortment of general merchandise, including over-the-counter 
drugs, beauty products, cosmetics and personal care products, provides health care services through its MinuteClinic® walk-in 
medical clinics and conducts long-term care pharmacy (“LTC”) operations, which distribute prescription drugs and provide 
related pharmacy consulting and other ancillary services to chronic care facilities and other care settings. As of December 31, 
2019, the Retail/LTC segment operated approximately 9,900 retail locations, approximately 1,100 MinuteClinic® locations as 
well as online retail pharmacy websites, LTC pharmacies and onsite pharmacies. During the year ended December 31, 2019, the 
Retail/LTC segment filled 1.4 billion prescriptions on a 30-day equivalent basis. For the year ended December 31, 2019, the 
Company dispensed approximately 26.6% of the total retail pharmacy prescriptions in the United States.

Overview of the Health Care Benefits Segment

The Health Care Benefits segment is one of the nation’s leading diversified health care benefits providers, serving an estimated 
37 million people as of December 31, 2019. The Health Care Benefits segment has the information and resources to help 
members, in consultation with their health care professionals, make more informed decisions about their health care. The Health 
Care Benefits segment offers a broad range of traditional, voluntary and consumer-directed health insurance products and 
related services, including medical, pharmacy, dental and behavioral health plans, medical management capabilities, Medicare 
Advantage and Medicare Supplement plans, PDPs, Medicaid health care management services, workers’ compensation 
administrative services and health information technology products and services. The Health Care Benefits segment’s 
customers include employer groups, individuals, college students, part-time and hourly workers, health plans, health care 
providers (“providers”), governmental units, government-sponsored plans, labor groups and expatriates. The Company refers to 
insurance products (where it assumes all or a majority of the risk for medical and dental care costs) as “Insured” and 
administrative services contract products (where the plan sponsor assumes all or a majority of the risk for medical and dental 
care costs) as “ASC.” For periods prior to November 28, 2018 (the Aetna Acquisition Date), the Health Care Benefits segment 
was comprised of the Company’s SilverScript PDP business.

Overview of the Corporate/Other Segment

The Company presents the remainder of its financial results in the Corporate/Other segment, which consists of:

•  Management and administrative expenses to support the overall operations of the Company, which include certain aspects 
of executive management and the corporate relations, legal, compliance, human resources, information technology and 
finance departments, expenses associated with the Company’s investments in its transformation and Enterprise 
modernization programs and acquisition-related transaction and integration costs; and 

• 

Products for which the Company no longer solicits or accepts new customers such as large case pensions and long-term 
care insurance products.

59

Results of Operations

The following information summarizes the Company’s results of operations for 2019 compared to 2018. For discussion of the 
Company’s results of operations for 2018 compared to 2017, see “Management’s Discussion and Analysis of Financial 
Condition and Results of Operations with Retrospective Application of Segments” for the year ended December 31, 2018, 
which was revised to reflect the Company’s segment realignment and is included in Exhibit 99.2 to the Company’s Current 
Report on Form 8-K filed with the U.S. Securities and Exchange Commission (the “SEC”) on August 8, 2019.

Summary of Consolidated Financial Results

In millions
Revenues:
Products
Premiums
Services
Net investment income

Total revenues
Operating costs:

Cost of products sold
Benefit costs
Goodwill impairments
Operating expenses
Total operating costs
Operating income
Interest expense
Loss on early extinguishment of debt
Other expense (income)
Income before income tax provision
Income tax provision
Income (loss) from continuing operations
Loss from discontinued operations, net of
tax
Net income (loss)
Net (income) loss attributable to
noncontrolling interests

Net income (loss) attributable to CVS
Health

Commentary - 2019 compared to 2018

Year Ended December 31, 

2019 vs. 2018

2019

     2018

     2017

$

%

2018 vs. 2017

$

%

Change

$185,236
63,122
7,407
1,011
256,776

$183,910
8,184
1,825
660
194,579

$180,063
3,558
1,144
21
184,786

$ 1,326
54,938
5,582
351
62,197

0.7 % $ 3,847
4,626
681
639
9,793

671.3 %
305.9 %
53.2 %
32.0 %

158,719
52,529
—
33,541
244,789
11,987
3,035
79
(124)
8,997
2,366
6,631

156,447
6,594
6,149
21,368
190,558
4,021
2,619
—
(4)
1,406
2,002
(596)

153,448
2,810
181
18,809
175,248
9,538
1,062
—
208
8,268
1,637
6,631

2,272
45,935
(6,149)
12,173
54,231
7,966
416
79
(120)
7,591
364
7,227

2,999
1.5 %
3,784
696.6 %
5,968
(100.0)%
57.0 %
2,559
28.5 % 15,310
(5,517)
1,557
—
(212)
(6,862)
365
(7,227)

198.1 %
15.9 %
100.0 %
(3,000.0)%
539.9 %
18.2 %
1,212.6 %

2.1 %
130.0 %
59.5 %
3,042.9 %
5.3 %

2.0 %
134.7 %
3,297.2 %
13.6 %
8.7 %
(57.8)%
146.6 %
— %
(101.9)%
(83.0)%
22.3 %
(109.0)%

—
6,631

—
(596)

(8)
6,623

—
7,227

— %
1,212.6 %

8
(7,219)

100.0 %
(109.0)%

3

2

(1)

1

50.0 %

3

300.0 %

$

6,634

$

(594) $

6,622

$ 7,228

1,216.8 % $ (7,216)

(109.0)%

Revenues
•  Total revenues increased $62.2 billion or 32.0% in 2019 compared to 2018. The increase in total revenues was primarily 

due to the impact of the Aetna Acquisition (primarily reflected in the Health Care Benefits segment) which occurred in 
November 2018, a 5.0% increase in Pharmacy Services segment revenue and a 3.1% increase in Retail/LTC segment 
revenue.

• 

Please see “Segment Analysis” later in this MD&A for additional information about the revenues of the Company’s 
segments.

Operating expenses
•  Operating expenses increased $12.2 billion or 57.0% in 2019 compared to 2018. Operating expenses as a percentage of 

total revenues were 13.1% in 2019, an increase of 210 basis points compared to 2018. The increase in operating expenses 
was primarily due to the impact of the Aetna Acquisition (including intangible asset amortization) and higher operating 

60

expenses in the Retail/LTC segment, including $231 million of store rationalization charges and the $205 million pre-
tax loss on the sale of the Company’s Brazilian subsidiary, Drogaria Onofre Ltda. (“Onofre”), both recorded in the year 
ended December 31, 2019. 

• 

Please see “Segment Analysis” later in this MD&A for additional information about the operating expenses of the 
Company’s segments.

Operating income 
•  Operating income increased $8.0 billion in 2019 compared to 2018. The increase was primarily due to (i) the absence of 
the $6.1 billion of pre-tax goodwill impairment charges related to the LTC reporting unit recorded within the Retail/LTC 
segment in 2018, (ii) the impact of the Aetna Acquisition and (iii) increased prescription volume and improved purchasing 
economics in the Pharmacy Services and Retail/LTC segments. The increase was partially offset by:
•  Continued reimbursement pressure in the Retail/LTC segment;
•  Continued price compression in the Pharmacy Services segment;
•  An increase in intangible asset amortization primarily related to the Aetna Acquisition;
•  Higher operating expenses in the Retail/LTC segment, including $231 million of store rationalization charges and the 

$205 million pre-tax loss on the sale of Onofre; and

•  The absence of $536 million in interest income on the proceeds from the financing for the Aetna Acquisition recorded 

in the year ended December 31, 2018.

• 

Please see “Segment Analysis” later in this MD&A for additional information about the operating income of the 
Company’s segments.

Interest expense
• 

Interest expense increased $416 million in 2019 compared to 2018, primarily due to financing activity associated with the 
Aetna Acquisition and the assumption of Aetna’s debt as of the Aetna Acquisition Date. See Note 8 ‘‘Borrowings and 
Credit Agreements’’ included in Item 8 of this 10-K for additional information.

Loss on early extinguishment of debt
•  During 2019, the loss on early extinguishment of debt relates to the Company’s repayment of $4.0 billion of its outstanding 

senior notes pursuant to its tender offers for such senior notes in August 2019, which resulted in a loss on early 
extinguishment of debt of $79 million. See Note 8 ‘‘Borrowings and Credit Agreements’’ included in Item 8 of this 10-K 
for additional information. 

Other income
•  Other income increased $120 million in 2019 compared to 2018. Other income represents pension plan asset returns in 
excess of interest cost on pension plan obligations. The increase in other income in 2019 was primarily due to 2019 
including a full year of income associated with the Aetna pension plan, as compared to 2018 which only included the Aetna 
pension plan income for the period subsequent to the Aetna Acquisition Date. 

Income tax provision
•  The Company’s effective income tax rate was 26.3% in 2019 compared to 142.4% in 2018. The decrease in the effective 
income tax rate was primarily due to the absence of the $6.1 billion of pre-tax goodwill impairment charges recorded 
during 2018, the majority of which were not deductible for income tax purposes.

Loss from discontinued operations
• 

In connection with certain business dispositions completed between 1995 and 1997, the Company retained guarantees on 
store lease obligations for a number of former subsidiaries, including Linens ‘n Things, which filed for bankruptcy in 2008, 
and Bob’s Stores, which filed for bankruptcy in 2016. The Company’s loss from discontinued operations primarily includes 
lease-related costs required to satisfy its Linens ‘n Things and Bob’s Stores lease guarantees. 

• 

See “Discontinued Operations” in Note 1 ‘‘Significant Accounting Policies’’ and “Lease Guarantees” in Note 16 
‘‘Commitments and Contingencies’’ included in Item 8 of this 10-K for additional information about the Company’s 
discontinued operations and the Company’s lease guarantees, respectively. 

61

Outlook for 2020  

With respect to 2020, the Company believes you should consider the following important information:

•  The Pharmacy Services segment is expected to benefit from continued improvements in purchasing economics and 
Enterprise modernization, partially offset by net selling season losses during 2020 and continued price compression.

•  The Retail/LTC segment is expected to benefit from projected adjusted script growth driven by the continued successful 

execution of patient care programs, partially offset by continued reimbursement pressure.

•  The Health Care Benefits segment is expected to benefit from Government Services membership growth including 

projected above-industry growth in its Medicare Advantage products and new Medicaid contract wins, as well as 
integration synergies that will continue to disproportionately benefit the Health Care Benefits segment. 

•  The Patient Protection and Affordable Care Act and the Health Care and Education Reconciliation Act of 2010 

(collectively, the “ACA”) imposes a significant industry-wide fee known as the Health Insurer Fee (the “HIF”). The HIF is 
non-deductible for federal income tax purposes and is allocated to insurers based on the ratio of the amount of an insurer’s 
net premium revenues written during the preceding calendar year to the amount of health insurance premium for all U.S. 
health risk for certain lines of business during the preceding calendar year. The HIF was suspended for 2019, will be $15.5 
billion for 2020 and has been repealed for calendar years after 2020. While the Company expects the reintroduction of the 
HIF to result in a lower medical benefit ratio (“MBR”) in 2020 compared to 2019, all else being equal, the Company 
expects its 2020 consolidated net income will be negatively impacted due to an increase in its effective income tax rate in 
2020 compared to 2019 as a result of the non-deductibility of the HIF.

•  The Company believes that it is on track to achieve its 2020 target of $800-900 million of synergies from the Aetna 

Acquisition.

•  The Company expects changes to its business environment to continue for the next several years as elected and other 

government officials at the national and state levels continue to propose and enact significant modifications to public policy 
and existing laws and regulations that govern the Company’s businesses.

The Company’s current expectations described above are forward-looking statements. Please see “Risk Factors” in Item 1A of 
this 10-K for information regarding important factors that may cause the Company’s actual results to differ from those currently 
projected and/or otherwise materially affect the Company.

62

Segment Analysis

The following discussion of segment operating results is presented based on the Company’s reportable segments in accordance 
with the accounting guidance for segment reporting and is consistent with the segment disclosure in Note 17 ‘‘Segment 
Reporting’’ included in Item 8 of this 10-K.

The Company has three operating segments, Pharmacy Services, Retail/LTC and Health Care Benefits, as well as a Corporate/
Other segment. The Company’s segments maintain separate financial information, and the CODM evaluates the segments’ 
operating results on a regular basis in deciding how to allocate resources among the segments and in assessing segment 
performance. The CODM evaluates the performance of the Company’s segments based on adjusted operating income. Effective 
for the first quarter of 2019, adjusted operating income is defined as operating income (GAAP measure) excluding the impact 
of amortization of intangible assets and other items, if any, that neither relate to the ordinary course of the Company’s business 
nor reflect the Company’s underlying business performance. Segment financial information has been retrospectively adjusted to 
conform with the current period presentation. See the reconciliations of operating income (GAAP measure) to adjusted 
operating income below for further context regarding the items excluded from operating income in determining adjusted 
operating income. The Company uses adjusted operating income as its principal measure of segment performance as it 
enhances the Company’s ability to compare past financial performance with current performance and analyze underlying 
business performance and trends. Non-GAAP financial measures the Company discloses, such as consolidated adjusted 
operating income, should not be considered a substitute for, or superior to, financial measures determined or calculated in 
accordance with GAAP.

Effective for the first quarter of 2019, the Company realigned the composition of its segments to correspond with changes to its 
operating model and reflect how the CODM reviews information and manages the business. See Note 1 ‘‘Significant 
Accounting Policies’’ included in Item 8 of this 10-K for further discussion of this realignment. Segment financial information 
has been retrospectively adjusted to reflect these changes. 

The following is a reconciliation of financial measures of the Company’s segments to the consolidated totals:

In millions
2019

Pharmacy
Services (1)

Retail/
LTC

Health Care
Benefits

Corporate/
Other

Intersegment
Eliminations (2)

Consolidated
Totals

Total revenues

$ 141,491

$

86,608

$

69,604

$

Adjusted operating income (loss)

5,129

6,705

5,202

$

512
(1,000)

(41,439) $
(697)

256,776

15,339

2018

Total revenues

Adjusted operating income (loss)

2017

Total revenues

Adjusted operating income (loss)
_____________________________________________

134,736

4,955

130,822

4,628

83,989

7,403

79,398

7,475

8,962

528

3,587

359

606
(856)

16
(896)

(33,714)
(769)

(29,037)
(741)

194,579

11,261

184,786

10,825

(1)  Total revenues of the Pharmacy Services segment include approximately $11.5 billion, $11.4 billion and $10.8 billion of retail co-payments for 2019, 2018 

and 2017, respectively. See Note 1 ‘‘Significant Accounting Policies’’ included in Item 8 of this 10-K for additional information about retail co-payments.

(2)  Intersegment eliminations relate to intersegment revenue generating activities that occur between the Pharmacy Services segment, the Retail/LTC segment 

and/or the Health Care Benefits segment.  

63

The following is a reconciliation of operating income to adjusted operating income for the years ended December 31, 2019, 
2018 and 2017:

Adjusted operating income (loss)

$

5,129

$

6,705

$

5,202

$

In millions

Operating income (loss) (GAAP
measure)

Non-GAAP adjustments:

Amortization of intangible assets (1)
Acquisition-related integration costs (2)
Store rationalization charges (3)
Loss on divestiture of subsidiary (4)

In millions

Operating income (loss) (GAAP
measure)

Non-GAAP adjustments:

Amortization of intangible assets (1)
Acquisition-related transaction and 
integration costs (2)
Loss on divestiture of subsidiary (4)
Goodwill impairments (5)
Impairment of long-lived assets (6)
Interest income on financing for the 
Aetna Acquisition (7)

Year Ended December 31, 2019

Pharmacy 
Services

Retail/
LTC

Health Care
Benefits

Corporate/
Other

Intersegment
Eliminations

Consolidated
Totals

$

4,735

$

5,793

$

3,639

$

(1,483) $

(697) $

11,987

394

—

—

—

476

—

231

205

1,563

—

—

—

3

480

—

—

—

—

—
(1,000) $

—
(697) $

2,436

480

231

205

15,339

Year Ended December 31, 2018

Pharmacy 
Services

Retail/
LTC

Health Care
Benefits

Corporate/
Other

Intersegment
Eliminations

Consolidated
Totals

$

4,607

$

620

$

368

$

(805) $

(769) $

4,021

348

—

—

—

—

—

498

7

86

6,149

43

—

160

—

—

—

—

—

—

485

—

—

—

—

—

—

—

—

1,006

492

86

6,149

43

(536)
(856) $

—
(769) $

(536)
11,261

Adjusted operating income (loss)

$

4,955

$

7,403

$

528

$

64

In millions

Operating income (loss) (GAAP
measure)

Non-GAAP adjustments:

Amortization of intangible assets (1)
Acquisition-related transaction and 
integration costs (2)
Store rationalization charges (3)
Loss on divestiture of subsidiary (4)
Goodwill impairments (5)

Adjusted operating income (loss)
_____________________________________________

Year Ended December 31, 2017

Pharmacy 
Services

Retail/
LTC

Health Care
Benefits

Corporate/
Other

Intersegment
Eliminations

Consolidated
Totals

$

4,300

$

6,558

$

357

$

(936) $

(741) $

9,538

328

—

—

—

—

487

34

215

—

181

2

—

—

—

—

$

4,628

$

7,475

$

359

$

—

31

—

9

—

—

—

—

—
(896) $

—
(741) $

817

65

215

9

181

10,825

(1)  The Company’s acquisition activities have resulted in the recognition of intangible assets as required under the acquisition method of accounting which 

consist primarily of trademarks, customer contracts/relationships, covenants not to compete, technology, provider networks and value of business acquired. 
Definite-lived intangible assets are amortized over their estimated useful lives and are tested for impairment when events indicate that the carrying value 
may not be recoverable. The amortization of intangible assets is reflected in the Company’s statements of operations in operating expenses within each 
segment. Although intangible assets contribute to the Company’s revenue generation, the amortization of intangible assets does not directly relate to the 
underwriting of the Company’s insurance products, the services performed for the Company’s customers or the sale of the Company’s products or services. 
Additionally, intangible asset amortization expense typically fluctuates based on the size and timing of the Company’s acquisition activity. Accordingly, the 
Company believes excluding the amortization of intangible assets enhances the Company’s and investors’ ability to compare the Company’s past financial 
performance with its current performance and to analyze underlying business performance and trends. Intangible asset amortization excluded from the 
related non-GAAP financial measure represents the entire amount recorded within the Company’s GAAP financial statements, and the revenue generated 
by the associated intangible assets has not been excluded from the related non-GAAP financial measure. Intangible asset amortization is excluded from the 
related non-GAAP financial measure because the amortization, unlike the related revenue, is not affected by operations of any particular period unless an 
intangible asset becomes impaired or the estimated useful life of an intangible asset is revised.  

(2)  In 2019, 2018 and 2017, acquisition-related transaction and integration costs relate to the Aetna Acquisition. In 2018 and 2017, acquisition-related 

transaction and integration costs also relate to the acquisition of Omnicare, Inc. (“Omnicare”). The acquisition-related transaction and integration costs are 
reflected in the Company’s consolidated statements of operations in operating expenses within the Corporate/Other segment and the Retail/LTC segment.    
(3)  In 2019, the store rationalization charges relate to the planned closure of 46 underperforming retail pharmacy stores during the second quarter of 2019 and 
the planned closure of 22 underperforming retail pharmacy stores during the first quarter of 2020. In 2019, the store rationalization charges primarily relate 
to operating lease right-of-use asset impairment charges and are reflected in the Company’s consolidated statements of operations in operating expenses 
within the Retail/LTC segment. In 2017, the store rationalization charges related to the Company’s enterprise streamlining initiative and are reflected in the 
Company’s consolidated statements of operations in operating expenses within the Retail/LTC segment.      

(4)  In 2019, the loss on divestiture of subsidiary represents the pre-tax loss on the sale of Onofre, which occurred on July 1, 2019. The loss on divestiture 

primarily relates to the elimination of the cumulative translation adjustment from accumulated other comprehensive income. In 2018, the loss on divestiture 
of subsidiary represents the pre-tax loss on the sale of the Company’s RxCrossroads subsidiary for $725 million on January 2, 2018. In 2017, the loss on 
divestiture of subsidiary represents transaction costs associated with the sale of RxCrossroads. The loss on divestiture of subsidiary costs are reflected in the 
Company’s consolidated statements of operations in operating expenses within the Retail/LTC segment and Corporate/Other segment.  

(5)  In 2018, the goodwill impairments relate to the LTC reporting unit within the Retail/LTC segment. In 2017, the goodwill impairments relate to the 

RxCrossroads reporting unit within the Retail/LTC segment. 

(6)  In 2018, impairment of long-lived assets primarily relates to the impairment of property and equipment within the Retail/LTC segment and is reflected in 

operating expenses in the Company’s consolidated statements of operations. 

(7)  In 2018, the Company recorded interest income of $536 million on the proceeds of the $40 billion of unsecured senior notes it issued in March 2018 to 

partially fund the Aetna Acquisition. All amounts are for the periods prior to the close of the Aetna Acquisition, which occurred on November 28, 2018, and 
were recorded within the Corporate/Other segment.

65

Pharmacy Services Segment

The following table summarizes the Pharmacy Services segment’s performance for the respective periods:

In millions, except percentages

2019

2018

2017

$

%

Year Ended December 31,

2019 vs. 2018

Change

2018 vs. 2017

$

%

Revenues:

Products

Services

Total revenues

Cost of products sold

Operating expenses

$ 140,946

$ 134,285

$ 130,578

$ 6,661

5.0% $ 3,707

545

141,491

135,245

1,511

451

134,736

128,777

1,352

244

130,822

125,273

1,249

94

6,755

6,468

159

20.8%

5.0%

5.0%

11.8%

207

3,914

3,504

103

2.8%

84.8%

3.0%

2.8%

8.2%

Operating expenses as a % of total
revenues

1.1%

1.0%

1.0%

Operating income

$

4,735

$

4,607

$

4,300

Operating income as a % of total
revenues

3.3%

3.4%

3.3%

Adjusted operating income (1)

$

5,129

$

4,955

$

4,628

$

$

128

2.8% $

307

7.1%

174

3.5% $

327

7.1%

Adjusted operating income as a %
of total revenues

Revenues (by distribution channel): 

Pharmacy network (2) (3)
Mail choice (3) (4)
Other

Pharmacy claims processed: (5)

Total
Pharmacy network (2)
Mail choice (4)

Generic dispensing rate: (5)

Total
Pharmacy network (2)
Mail choice (4)

Mail choice penetration rate (4) (5)
_____________________________________________

3.6%

3.7%

3.5%

$ 88,755
52,141

$ 87,167
47,049

$ 84,677
45,731

$ 1,588
5,092

1.8% $ 2,490
1,318
10.8%

595

520

414

75

14.4%

106

2,014.2
1,704.0

310.2

1,889.8
1,601.4

288.4

1,781.9
1,516.7

265.2

124.4
102.6

21.8

6.6%
6.4%

7.6%

107.9

84.7

23.2

2.9%

2.9%

25.6%

6.1%

5.6%

8.7%

88.2%
88.7%

85.1%

15.4%

87.3%

87.9%

83.9%

15.3%

87.0%

87.7%

83.1%

14.9%

(1)  See “Segment Analysis” above in this MD&A for a reconciliation of operating income (GAAP measure) to adjusted operating income for the Pharmacy 

Services segment.

(2)  Pharmacy network revenues, pharmacy claims processed and generic dispensing rate do not include Maintenance Choice® activity, which is included within 
the mail choice category. Pharmacy network is defined as claims filled at retail and specialty retail pharmacies, including the Company’s retail pharmacies 
and LTC pharmacies, but excluding Maintenance Choice activity, which is included within the mail choice category. Maintenance choice permits eligible 
client plan members to fill their maintenance prescriptions through mail order delivery or at a CVS pharmacy retail store for the same price as mail order.

(3)  Certain prior year amounts have been reclassified for consistency with the current period presentation. 
(4)  Mail choice is defined as claims filled at a Pharmacy Services mail order facility, which includes specialty mail claims inclusive of Specialty Connect® 
claims picked up at a retail pharmacy, as well as prescriptions filled at the Company’s retail pharmacies under the Maintenance Choice program.
(5)  Includes an adjustment to convert 90-day prescriptions to the equivalent of three 30-day prescriptions. This adjustment reflects the fact that these 

prescriptions include approximately three times the amount of product days supplied compared to a normal prescription.

66

Commentary - 2019 compared to 2018

Revenues
•  Total revenues increased $6.8 billion, or 5.0%, to $141.5 billion in 2019 compared to 2018. The increase was primarily due 
to brand inflation as well as increased total pharmacy claims volume, partially offset by continued price compression and 
an increased generic dispensing rate.

•  As you review the Pharmacy Services segment’s performance in this area, you should consider the following important 

information about the business:

•  The Company’s mail choice claims processed, on a 30-day equivalent basis, increased 7.6% to 310.2 million claims in 
2019 compared to 288.4 million claims in 2018. The increase in mail choice claims was primarily driven by the 
continued adoption of Maintenance Choice offerings.

•  During 2019, the average revenue per mail choice claim, on a 30-day equivalent basis, increased by 3.0% compared to 

2018 primarily due to growth in specialty pharmacy claims processed.

•  The Company’s pharmacy network claims processed, on a 30-day equivalent basis, increased 6.4% to 1.7 billion 
claims in 2019 compared to 1.6 billion claims in 2018. The increase in the pharmacy network claim volume was 
primarily due to net new business, including the onboarding of Anthem, Inc.’s (“Anthem’s”) PBM, IngenioRx, during 
2019.

•  During 2019, the average revenue per pharmacy network claim processed, on a 30-day equivalent basis, decreased 

4.2% compared to 2018 as a result of continued price compression.

•  The segment’s total generic dispensing rate increased to 88.2% in 2019 compared to 87.3% in 2018. The continued 
increase in the segment’s generic dispensing rate was primarily due to the impact of new generic drug introductions 
and the Company’s ongoing efforts to encourage plan members to use generic drugs when they are available and 
clinically appropriate. The Company believes its generic dispensing rate will continue to increase in future periods, 
albeit at a slower pace. This increase will be affected by, among other things, the number of new brand and generic 
drug introductions and the Company’s success at encouraging plan members to utilize generic drugs when they are 
available and clinically appropriate.

Operating expenses

•  Operating expenses in the Pharmacy Services segment include selling, general and administrative expenses; 

depreciation and amortization related to selling, general and administrative activities; and expenses related to specialty 
retail pharmacies, which include store and administrative payroll, employee benefits and occupancy costs.

•  Operating expenses increased $159 million, or 11.8%, in 2019 compared to 2018. The increase in operating expenses 
was primarily due to growth in the business, including operating expenses associated with Aetna’s mail order and 
specialty pharmacy operations (including intangible asset amortization) and investments related to the Company’s 
agreement with Anthem’s PBM, IngenioRx, during 2019.

•  Operating expenses as a percentage of total revenues remained relatively consistent at 1.1% and 1.0% in 2019 and 

2018, respectively. 

Operating income and adjusted operating income
•  Operating income increased $128 million, or 2.8%, and adjusted operating income increased $174 million, or 3.5%, in 
2019 compared to 2018. The increase in both operating income and adjusted operating income was primarily driven by 
increased claims volume, the addition of Aetna’s mail order and specialty pharmacy operations and improved purchasing 
economics, partially offset by continued price compression. The increase in operating income also was partially offset by 
increased intangible asset amortization related to Aetna’s mail order and specialty pharmacy operations.

•  As you review the Pharmacy Services segment’s performance in this area, you should consider the following important 

information about the business:

•  The Company’s efforts to (i) retain existing clients, (ii) obtain new business and (iii) maintain or improve the rebates 

and/or discounts the Company receives from manufacturers, wholesalers and retail pharmacies continue to have an 
impact on operating income and adjusted operating income. In particular, competitive pressures in the PBM industry 
have caused the Company and other PBMs to continue to share with clients a larger portion of rebates and/or discounts 
received from pharmaceutical manufacturers. In addition, marketplace dynamics and regulatory changes have limited 
the Company’s ability to offer plan sponsors pricing that includes retail network “differential” or “spread,” and the 
Company expects these trends to continue. The “differential” or “spread” is any difference between the drug price 
charged to plan sponsors, including Medicare Part D plan sponsors, by a PBM and the price paid for the drug by the 
PBM to the dispensing provider. 

67

Retail/LTC Segment

The following table summarizes the Retail/LTC segment’s performance for the respective periods:

In millions, except percentages

2019

2018

2017

$

%

$

%

Year Ended December 31,

2019 vs. 2018

2018 vs. 2017

Change

Revenues:

Products

Services

Total revenues

Cost of products sold

Goodwill impairments

Operating expenses

$ 85,729

$83,175

$78,522

$ 2,554

879

86,608

62,688

—

18,127

814

83,989

59,906

6,149

17,314

876

79,398

56,066

181

16,593

65

2,619

2,782
(6,149)
813

3.1 % $ 4,653
(62)
3.1 % 4,591

8.0 %

4.6 % 3,840

5.9 %

(7.1)%

5.8 %

6.8 %

(100.0)% 5,968

3,297.2 %

4.7 %

721

4.3 %

Operating expenses as a % of total
revenues

20.9%

20.6%

20.9 %

Operating income

$

5,793

$

620

$ 6,558

$ 5,173

834.4 % $(5,938)

(90.5)%

Operating income as a % of total
revenues

Adjusted operating income (1)

Adjusted operating income as a % of
total revenues

Revenues (by major goods/service lines):

Pharmacy

Front Store

Other

Prescriptions filled (2)
Revenues increase (decrease):

Total

Pharmacy

Front Store

Total prescription volume increase (2)
Same store sales increase (decrease): (3)

Total
Pharmacy

Front Store
Prescription volume (2)
Generic dispensing rate (2)
_____________________________________________

6.7%

0.7%

8.3 %

$

6,705

$ 7,403

$ 7,475

$ (698)

(9.4)% $

(72)

(1.0)%

7.8 %

1.5 %

(31.4)%

8.8 %

7.7%

8.8%

9.4 %

$ 66,442

$64,179

$59,528

$ 2,263

3.5 % $ 4,651

(1.5)%

1.9 %

286
(346)
5.8 % 108.6

19,422

19,055

744

755

18,769

1,101

1,417.2

1,339.1

1,230.5

367
(11)
78.1

3.1%

3.5%

1.9%
5.8%

3.7%
4.5%

1.1%

7.2%

5.8%

7.8%

1.5%
8.8%

6.0%

7.9%

0.5%

9.1%

(2.1)%

(2.2)%

(1.9)%
0.6 %

(2.6)%

(2.6)%

(2.6)%

0.4 %

88.3%

87.5%

87.3 %

(1) 

(2) 

(3) 

See “Segment Analysis” above in this MD&A for a reconciliation of operating income (GAAP measure) to adjusted operating income for the Retail/LTC 
segment.
Includes an adjustment to convert 90 day prescriptions to the equivalent of three 30 day prescriptions. This adjustment reflects the fact that these 
prescriptions include approximately three times the amount of product days supplied compared to a normal prescription.
Same store sales and prescription volume exclude revenues from MinuteClinic, and revenue and prescriptions from stores in Brazil and LTC operations.

Commentary - 2019 compared to 2018

Revenues 
•  Total revenues increased approximately $2.6 billion, or 3.1%, to $86.6 billion in 2019 compared to 2018. The increase was 

primarily driven by increased prescription volume and brand inflation, partially offset by continued reimbursement 
pressure and an increased generic dispensing rate.

68

 
•  As you review the Retail/LTC segment’s performance in this area, you should consider the following important information 

about the business:

• 

• 

• 

• 

• 

Front store same store sales increased 1.1% in 2019 compared to 2018. The increase in front store sales in 2019 
was primarily driven by increases in health and beauty product sales.

Pharmacy same store sales increased 4.5% in 2019 compared to 2018. The increase was primarily driven by the 
7.2% increase in pharmacy same store prescription volumes on a 30-day equivalent basis driven mainly by (i) 
continued adoption of patient care programs, (ii) collaborations with PBMs and (iii) the Company’s preferred 
status in a number of Medicare Part D networks.

Pharmacy revenue growth continues to be adversely affected by reimbursement pressure. Pharmacy revenue 
growth also continues to be adversely affected by the conversion of brand name drugs to equivalent generic drugs, 
which typically have a lower selling price. The segment’s generic dispensing rate grew to 88.3% in 2019 
compared to 87.5% in 2018. 

Pharmacy revenue growth also continues to be adversely affected by industry challenges in the LTC business, 
such as continuing lower occupancy rates at skilled nursing facilities, as well as the deteriorating financial health 
of many skilled nursing facilities. 

Pharmacy revenue in 2019 continued to benefit from the Company’s ability to attract and retain managed care 
customers and the increased use of pharmaceuticals by an aging population as the first line of defense for health 
care.

Operating expenses
•  Operating expenses in the Retail/LTC segment include store payroll, store employee benefits, store occupancy costs, 
selling expenses, advertising expenses, depreciation and amortization expense and certain administrative expenses.

•  Operating expenses increased $813 million, or 4.7%, in 2019 compared to 2018, primarily due to the following:

• 

Store rationalization charges of $231 million recorded in 2019 primarily related to operating lease right-of-use 
asset impairment charges in connection with the planned closure of underperforming retail pharmacy stores during 
the second quarter of 2019 and the first quarter of 2020;

•  The $205 million pre-tax loss on the sale of Onofre, which occurred on July 1, 2019;

•  The increased prescription volume described above; and

•  The investment of a portion of the savings from the Tax Cuts and Jobs Act (the “TCJA”) in wages and benefits.

•  Operating expenses as a percentage of total revenues were 20.9% in 2019 compared to 20.6% in 2018. The increase in 

operating expenses as a percentage of total revenues was primarily driven by the increases in operating expenses described 
above.

Operating income and adjusted operating income
•  Operating income increased $5.2 billion in 2019 compared to 2018. The increase in operating income was primarily due to 
the absence of the $6.1 billion of pre-tax goodwill impairment charges related to the LTC reporting unit recorded in the 
year ended December 31, 2018, partially offset by the decrease in adjusted operating income described below, as well as 
the $231 million of store rationalization charges and the $205 million pre-tax loss on the sale of Onofre, both recorded in 
2019. 

•  Adjusted operating income decreased $698 million, or 9.4%, in 2019 compared to 2018. The decrease in adjusted operating 
income was primarily due to continued reimbursement pressure and increased operating expenses primarily driven by the 
investment of a portion of the savings from the TCJA in wages and benefits. The decrease was partially offset by increased 
prescription volume, an increased generic dispensing rate and improved purchasing economics.

•  As you review the Retail/LTC segment’s performance in this area, you should consider the following important information 

about the business:

•  The segment’s pharmacy operating income and adjusted operating income has been adversely affected by the 

efforts of managed care organizations, PBMs and governmental and other third-party payors to reduce their 
prescription drug costs, including the use of restrictive networks, as well as changes in the mix of business within 
the pharmacy portion of the Retail/LTC segment. If the reimbursement pressure accelerates, the segment may not 
be able grow revenues, and its operating income and adjusted operating income could be adversely affected.

•  The increased use of generic drugs has positively impacted the segment’s operating income and adjusted operating 
income but has resulted in third-party payors augmenting their efforts to reduce reimbursement payments to retail 
pharmacies for prescriptions. This trend, which the Company expects to continue, reduces the benefit the segment 
realizes from brand to generic drug conversions.

69

Health Care Benefits Segment 

For periods prior to November 28, 2018 (the Aetna Acquisition Date), the Health Care Benefits segment was comprised of the 
Company’s SilverScript PDP business. The following table summarizes the Health Care Benefits segment’s performance for the 
respective periods:

In millions, except percentages

2019

2018

2017

$

%

Year Ended December 31,

2019 vs. 2018

Change

2018 vs. 2017

$

%

Revenues:

Products

Premiums

Services

Net investment income

Total revenues

Cost of products sold

Benefit costs

$ — $

164

$ — $

63,031

5,974

599

69,604

—

53,092

8,180

3,558

560

58

8,962

147

6,678

24

5

3,587

—

2,810

(164)
54,851

5,414

541

60,642
(147)
46,414

(100.0)% $

164

670.6 %

966.8 %

932.8 %

676.7 %

(100.0)%

695.0 %

4,622

536

53

5,375

147

3,868

100.0%

129.9%

2,233.3%

1,060.0%

149.8%

100.0%

137.7%

MBR (Benefit costs as a % of premium 
revenues) (1) 

84.2%

NM

NM

Operating expenses

$12,873

$ 1,769

$

420

$ 11,104

627.7 % $ 1,349

321.2%

Operating expenses as a % of total
revenues

18.5%

19.7%

11.7%

Operating income

$ 3,639

Operating income as a % of total revenues

5.2%

Adjusted operating income (2)

$ 5,202

$

$

368

4.1%

528

$

$

357

$ 3,271

888.9 % $

11

3.1%

10.0%

359

$ 4,674

885.2 % $

169

47.1%

Adjusted operating income as a % of total
revenues

_____________________________________________

7.5%

5.9%

10.0%

(1) 

(2) 

For periods prior to the Aetna Acquisition Date, the Health Care Benefits segment was comprised of the Company’s SilverScript PDP business. 
Accordingly, the MBR for the years ended December 31, 2018 and 2017 are not meaningful (“NM”) and are not directly comparable to the MBRs for 
the year ended December 31, 2019.
See “Segment Analysis” above in this MD&A for a reconciliation of operating income (GAAP measure) to adjusted operating income for the Health 
Care Benefits segment.

Commentary - 2019 compared to 2018

Revenues 
•  Total revenues increased $60.6 billion in 2019 compared to 2018 primarily due to the Aetna Acquisition.

Operating expenses
•  Operating expenses in the Health Care Benefits segment include selling, general and administrative expenses and 

depreciation and amortization expenses.

•  Operating expenses increased $11.1 billion in 2019 compared to 2018 primarily due to the Aetna Acquisition (including the 

amortization of intangible assets).

Operating income and adjusted operating income
•  Operating income increased $3.3 billion and adjusted operating income increased $4.7 billion in 2019 compared to 2018. 
The increases were primarily due to the Aetna Acquisition. The increase in operating income was partially offset by 
increased intangible asset amortization related to the Aetna Acquisition.

70

The following table summarizes the Health Care Benefits segment’s medical membership as of December 31, 2019 and 2018:

In thousands
Medical membership:

Commercial

Medicare Advantage

Medicare Supplement

Medicaid

Total medical membership

Insured

3,591

2,321

881

1,398

8,191

2019
ASC 

14,159

—

—

558

14,717

Supplemental membership information:

Medicare Prescription Drug Plan (standalone) (1)

_____________________________________________

Total

Insured

2018

ASC

Total

17,750

2,321

881

1,956

22,908

5,994

3,871

1,758

793

1,128

7,550

13,888

—

—

663

14,551

17,759

1,758

793

1,791

22,101

6,134

(1)  Represents the Company’s SilverScript PDP membership only. Excludes 2.5 million and 2.3 million members as of December 31, 2019 and 2018, 

respectively, related to Aetna’s standalone PDPs that were sold effective December 31, 2018. The Company retained the financial results of the divested 
plans through 2019 through a reinsurance agreement. Subsequent to 2019, the Company will no longer retain the financial results of the divested plans.

Medical Membership
Medical membership as of December 31, 2019 increased compared with December 31, 2018, reflecting increases in Medicare, 
Commercial ASC and Medicaid products, partially offset by declines in Commercial Insured products.

Medicare Update
On April 1, 2019, the U.S. Centers for Medicare & Medicaid Services (“CMS”) issued its final notice detailing final 2020 
Medicare Advantage benchmark payment rates (the “Final Notice”). Overall the Company projects the benchmark rates in the 
Final Notice will increase funding for its Medicare Advantage business, excluding the impact of the health insurer fee, by 
approximately 2.0% in 2020 compared to 2019.

The ACA ties a portion of each Medicare Advantage plan’s reimbursement to the plan’s “star ratings.” Plans must have a star 
rating of four or higher (out of five) to qualify for bonus payments. CMS released the Company’s 2020 star ratings in October 
2019. The Company’s 2020 star ratings will be used to determine which of the Company’s Medicare Advantage plans have 
ratings of four stars or higher and qualify for bonus payments in 2021. Based on the Company’s membership at December 31, 
2019, 83% of the Company’s Medicare Advantage members were in plans with 2020 star ratings of at least 4.0 stars, compared 
to 79% of the Company’s Medicare Advantage members being in plans with 2019 star ratings of at least 4.0 stars based on the 
Company’s membership at December 31, 2018.

Corporate/Other Segment

Commentary - 2019 compared to 2018

Revenues
•  Total revenues decreased $94 million in 2019 compared to 2018. 

• 

In 2019, revenues relate to products for which the Company no longer solicits or accepts new customers, such as large case 
pensions and long-term care insurance products, that were acquired in the Aetna Acquisition. Revenues in 2019 include 
$104 million of net realized capital gains, primarily related to the sale of debt securities and other invested assets that 
support these insurance products. In 2018, revenues relate to interest income on the proceeds from the financing of the 
Aetna Acquisition.

Operating expenses
•  Operating expenses within the Corporate/Other segment include certain aspects of costs related to executive management 

and the corporate relations, legal, compliance, human resources, information technology and finance departments, expenses 
associated with the Company’s investments in its transformation and Enterprise modernization programs and acquisition-
related transaction and integration costs. After the Aetna Acquisition Date, such operating expenses also include operating 
costs to support the large case pensions and long-term care insurance products acquired in the Aetna Acquisition.

71

•  Operating expenses increased $321 million in 2019 compared to 2018. The increase was primarily driven by growth in the 
business, incremental operating expenses associated with the Company’s investments in transformation and Enterprise 
modernization, legal costs and a $30 million charitable contribution to the CVS Health Foundation in 2019.

Liquidity and Capital Resources

Cash Flows

The Company maintains a level of liquidity sufficient to allow it to meet its cash needs in the short-term. Over the long term, 
the Company manages its cash and capital structure to maximize shareholder return, maintain its financial condition and 
maintain flexibility for future strategic initiatives. The Company continuously assesses its regulatory capital requirements, 
working capital needs, debt and leverage levels, debt maturity schedule, capital expenditure requirements, dividend payouts, 
potential share repurchases and future investments or acquisitions. The Company believes its operating cash flows, commercial 
paper program, credit facilities, sale-leaseback program, as well as any potential future borrowings, will be sufficient to fund 
these future payments and long-term initiatives. As of December 31, 2019, the Company had approximately $5.7 billion in cash 
and cash equivalents, approximately $1.7 billion of which was held by the parent company or nonrestricted subsidiaries.

The net change in cash, cash equivalents and restricted cash for the years ended December 31, 2019, 2018 and 2017 is as 
follows:

In millions

2019

2018

2017

$

%

$

%

Year Ended December 31,

2019 vs. 2018

2018 vs. 2017

Change

Net cash provided by operating activities

Net cash used in investing activities

Net cash provided by (used in) financing
activities

Effect of exchange rate changes on cash, cash
equivalents and restricted cash

Net increase (decrease) in cash, cash
equivalents and restricted cash

Commentary - 2019 compared to 2018

$ 12,848

(3,339)

$ 8,865
(43,285)

$ 8,007
(2,877)

$ 3,983

39,946

44.9 % $
10.7 %
858
(92.3)% (40,408) 1,404.5 %

(7,850)

36,819

(6,751)

(44,669)

(121.3)% 43,570

(645.4)%

—

(4)

1

4

(100.0)%

(5)

(500.0)%

$ 1,659

$ 2,395

$ (1,620) $

(736)

(30.7)% $ 4,015

(247.8)%

•  Net cash provided by operating activities increased by $4.0 billion in 2019 compared to 2018 due primarily to the Aetna 

Acquisition as well as improvements in working capital, including the timing of certain payables and receipts. 
•  Net cash used in investing activities decreased by $39.9 billion in 2019 compared to 2018 largely due to the Aetna 

Acquisition in November 2018. The decrease was partially offset by the absence of the $725 million in proceeds from the 
sale of RxCrossroads in 2018 and net purchases of investments in 2019 compared to net sales of investments in 2018. 
•  Net cash used in financing activities was $7.9 billion in 2019 compared to net cash provided by financing activities of 
$36.8 billion in 2018. The decrease in cash provided by financing activities primarily related to long-term borrowings 
during 2018 to partially fund the Aetna Acquisition, as well as debt repayments during 2019 including (i) the repayment of 
$4.0 billion of outstanding senior notes pursuant to tender offers for such outstanding senior notes, (ii) the repayment of the 
remaining $3.0 billion of the term loan used to partially fund the Aetna Acquisition and (iii) the repayment of $1.2 billion 
aggregate principal amount of senior notes upon maturity. The decrease was partially offset by the issuance of $3.5 billion 
of senior notes in 2019.

72

Included in net cash used in investing activities for the years ended December 31, 2019, 2018 and 2017 was the following store 
development activity: (1)

Total stores (beginning of year)
New and acquired stores (2)
Closed stores (2)
Total stores (end of year)
Relocated stores (2)
_____________________________________________

2019

2018

2017

9,967  

102  
(128)  
9,941  

23  

9,846  

148  
(27)  
9,967  

34  

9,750

179
(83)
9,846

30

Includes retail drugstores, certain onsite pharmacy stores, retail specialty pharmacy stores and pharmacies within Target stores.

(1) 
(2)  Relocated stores are not included in new and acquired stores or closed stores totals.

Short-term Borrowings

Commercial Paper and Back-up Credit Facilities
The Company did not have any commercial paper outstanding as of December 31, 2019. The Company had $720 million of 
commercial paper outstanding at a weighted average interest rate of 2.8% as of December 31, 2018. In connection with its 
commercial paper program, the Company maintains a $1.0 billion 364-day unsecured back-up revolving credit facility, which 
expires on May 14, 2020, a $1.0 billion, five-year unsecured back-up revolving credit facility, which expires on May 18, 2022, 
a $2.0 billion, five-year unsecured back-up revolving credit facility, which expires on May 17, 2023 and a $2.0 billion, five-
year unsecured back-up revolving credit facility, which expires on May 16, 2024. The credit facilities allow for borrowings at 
various rates that are dependent, in part, on the Company’s public debt ratings and require the Company to pay a weighted 
average quarterly facility fee of approximately .03%, regardless of usage. As of December 31, 2019 and 2018, there were no 
borrowings outstanding under any of the Company’s back-up credit facilities.

Bridge Loan Facility
On December 3, 2017, in connection with the Aetna Acquisition, the Company entered into a $49.0 billion unsecured bridge 
loan facility commitment. The Company paid $221 million in fees upon entering into the agreement. The fees were capitalized 
in other current assets and were amortized as interest expense over the period the bridge loan facility commitment was 
outstanding. The bridge loan facility commitment was reduced to $44.0 billion on December 15, 2017 upon the Company 
entering into a $5.0 billion term loan agreement. The Company recorded $56 million of amortization of the bridge loan facility 
fees during the year ended December 31, 2017, which was recorded in interest expense in the consolidated statement of 
operations.

On March 9, 2018, the Company issued senior notes with an aggregate principal amount of $40.0 billion (see “Long-term 
Borrowings - 2018 Notes” below). At that time, the bridge loan facility commitment was reduced to $4.0 billion, and the 
Company paid $8 million in fees to retain the bridge loan facility commitment through the Aetna Acquisition Date. Those fees 
were capitalized in other current assets and were amortized as interest expense over the period the bridge loan facility 
commitment was outstanding. The Company recorded $173 million of amortization of the bridge loan facility commitment fees 
during the year ended December 31, 2018, which was recorded in interest expense in the consolidated statement of operations. 
On October 26, 2018, the Company entered into a $4.0 billion unsecured 364-day bridge term loan agreement to formalize the 
bridge loan facility discussed above. On November 28, 2018, in connection with the Aetna Acquisition, the $4.0 billion 
unsecured 364-day bridge term loan agreement terminated.

Federal Home Loan Bank of Boston
Since the Aetna Acquisition Date, a subsidiary of the Company is a member of the Federal Home Loan Bank of Boston (the 
“FHLBB”). As a member, the subsidiary has the ability to obtain cash advances, subject to certain minimum collateral 
requirements. The maximum borrowing capacity available from the FHLBB as of December 31, 2019 was approximately $850 
million. At both December 31, 2019 and 2018, there were no outstanding advances from the FHLBB.

Long-term Borrowings

2019 Notes
On August 15, 2019, the Company issued $1.0 billion aggregate principal amount of 2.625% unsecured senior notes due August 
15, 2024, $750 million aggregate principal amount of 3% unsecured senior notes due August 15, 2026 and $1.75 billion 
aggregate principal amount of 3.25% unsecured senior notes due August 15, 2029 (collectively, the “2019 Notes”) for total 

73

proceeds of approximately $3.5 billion, net of discounts and underwriting fees. The net proceeds of the 2019 Notes were used 
to repay certain of the Company’s outstanding debt.

Beginning in July 2019, the Company entered into several interest rate swap and treasury lock transactions to manage interest 
rate risk. These agreements were designated as cash flow hedges and were used to hedge the exposure to variability in future 
cash flows resulting from changes in interest rates related to the anticipated issuance of the 2019 Notes. In connection with the 
issuance of the 2019 Notes, the Company terminated all outstanding cash flow hedges. The Company paid a net amount of $25 
million to the hedge counterparties upon termination, which was recorded as a loss, net of tax, of $18 million in accumulated 
other comprehensive income and will be reclassified as interest expense over the life of the 2019 Notes. See Note 13 ‘‘Other 
Comprehensive Income’’ included in Item 8 of this 10-K for additional information. 

Early Extinguishment of Debt
In August 2019, the Company purchased $4.0 billion of its outstanding senior notes through cash tender offers. The senior notes 
purchased included the following: $1.3 billion of its 3.125% senior notes due 2020, $723 million of its floating rate notes due 
2020, $328 million of its 4.125% senior notes due 2021, $297 million of 4.125% senior notes due 2021 issued by Aetna, $413 
million of 5.45% senior notes due 2021 issued by Coventry Health Care, Inc., a wholly-owned subsidiary of Aetna, and $962 
million of its 3.35% senior notes due 2021. In connection with the purchase of such senior notes, the Company paid a premium 
of $76 million in excess of the aggregate principal amount of the senior notes that were purchased, incurred $8 million in fees 
and recognized a net gain of $5 million on the write-off of net unamortized deferred financing premiums, for a net loss on early 
extinguishment of debt of $79 million. 

2018 Notes
On March 9, 2018, the Company issued an aggregate of $40.0 billion in principal amount of unsecured floating rate notes and 
unsecured fixed rate senior notes (collectively the “2018 Notes”) for total proceeds of approximately $39.4 billion, net of 
discounts and underwriting fees. The net proceeds of the 2018 Notes were used to fund a portion of the Aetna Acquisition. The 
2018 Notes consisted of the following at the time of issuance:

In millions

3.125% senior notes due March 2020

Floating rate notes due March 2020

3.35% senior notes due March 2021

Floating rate notes due March 2021

3.7% senior notes due March 2023

4.1% senior notes due March 2025

4.3% senior notes due March 2028

4.78% senior notes due March 2038

5.05% senior notes due March 2048

Total debt principal

$

2,000

1,000

3,000

1,000

6,000

5,000

9,000

5,000

8,000

$

40,000

From December 2017 through March 2018, the Company entered into several interest rate swap and treasury lock transactions 
to manage interest rate risk. These agreements were designated as cash flow hedges and were used to hedge the exposure to 
variability in future cash flows resulting from changes in interest rates related to the anticipated issuance of long-term debt to 
fund the Aetna Acquisition. 

In connection with the issuance of the 2018 Notes, the Company terminated all outstanding cash flow hedges. In connection 
with the hedge transactions, the Company received a net amount of $446 million from the hedge counterparties upon 
termination, which was recorded as a gain, net of tax, of $331 million in accumulated other comprehensive income and will be 
reclassified as a reduction of interest expense over the life of the 2018 Notes. See Note 13 ‘‘Other Comprehensive Income’’ 
included in Item 8 of this 10-K for additional information. 

Term Loan Agreement
On December 15, 2017, in connection with the Aetna Acquisition, the Company entered into a $5.0 billion term loan 
agreement. The term loan agreement allowed for borrowings at various rates that were dependent, in part, on the Company’s 
debt ratings. In connection with the Aetna Acquisition, the Company borrowed $5.0 billion (a $3.0 billion three-year tranche 
and a $2.0 billion five-year tranche) under the term loan agreement in November 2018. The Company terminated the $2.0 
billion five-year tranche in December 2018 with the repayment of the borrowing. The Company made principal payments of 

74

$500 million in March 2019, $1.0 billion in May 2019 and $1.5 billion in July 2019 on the three-year tranche, and terminated 
the three-year tranche and the term loan agreement with the final repayment of the borrowing in July 2019, at which time the 
Company had repaid all term loans. 

Aetna Related Debt
Upon the closing of the Aetna Acquisition, the Company assumed long-term debt with a fair value of $8.1 billion, with stated 
interest rates ranging from 2.2% to 6.75%. 

See Note 8 ‘‘Borrowings and Credit Agreements’’ and Note 12 ‘‘Shareholders’ Equity’’ included in Item 8 of this 10-K for 
additional information about debt issuances, debt repayments, share repurchases and dividend payments. 

Derivative Financial Instruments

The Company uses derivative financial instruments in order to manage interest rate and foreign exchange risk and credit 
exposure. The Company’s use of these derivatives is generally limited to hedging risk and has principally consisted of using 
interest rate swaps, treasury rate locks, forward contracts, futures contracts, warrants, put options and credit default swaps. 

Debt Covenants

The Company’s back-up revolving credit facilities, unsecured senior notes and unsecured floating rate notes (see Note 8 
‘‘Borrowings and Credit Agreements’’ included in Item 8 of this 10-K) contain customary restrictive financial and operating 
covenants. These covenants do not include an acceleration of the Company’s debt maturities in the event of a downgrade in the 
Company’s credit ratings. The Company does not believe the restrictions contained in these covenants materially affect its 
financial or operating flexibility. As of December 31, 2019, the Company was in compliance with all of its debt covenants.

Debt Ratings 

As of December 31, 2019, the Company’s long-term debt was rated “Baa2” by Moody’s Investors Service, Inc. (“Moody’s) and 
“BBB” by Standard & Poor’s Financial Services LLC (“S&P”), and its commercial paper program was rated “P-2” by Moody’s 
and “A-2” by S&P. In December 2017, subsequent to the announcement of the proposed acquisition of Aetna, Moody’s changed 
the outlook on the Company’s long-term debt to “Under Review” from “Stable.” Similarly, S&P placed the Company’s long-
term debt outlook on “Watch Negative” from “Stable.” Upon the issuance of the 2018 Notes on March 9, 2018, S&P lowered 
its corporate credit rating on the Company’s long-term debt to “BBB” from “BBB+” and changed the outlook from “Watch 
Negative” to “Stable.” On November 27, 2018, S&P lowered its rating on the long-term debt of Aetna to “BBB” from “A.” On 
November 28, 2018, upon the completion of the Aetna Acquisition, Moody’s lowered its rating on CVS Health Corporation’s 
long-term debt to “Baa2” from “Baa1.” Additionally, Moody’s changed the outlook on CVS Health Corporation’s long-term 
debt to “Negative” from “Under Review” and changed the outlook on the long-term debt of Aetna to “Negative” from “Stable.” 
In assessing the Company’s credit strength, the Company believes that both Moody’s and S&P considered, among other things, 
the Company’s capital structure and financial policies as well as its consolidated balance sheet, its historical acquisition activity 
and other financial information. Although the Company currently believes its long-term debt ratings will remain investment 
grade, it cannot guarantee the future actions of Moody’s and/or S&P. The Company’s debt ratings have a direct impact on its 
future borrowing costs, access to capital markets and new store operating lease costs. 

Share Repurchase Programs

During the years ended December 31, 2019 and 2018, the Company did not repurchase any shares of common stock. See Note 
12 ‘‘Shareholders’ Equity’’ included in Item 8 of this 10-K for information about share repurchases for the year ended 
December 31, 2017. 

Quarterly Cash Dividend

In December 2016, CVS Health’s Board of Directors (the “Board”) authorized an 18% increase in CVS Health’s quarterly 
common stock cash dividend to $0.50 per share effective in 2017. This increase equated to an annual dividend rate of $2.00 per 
share. During 2019 and 2018, CVS Health maintained its quarterly dividend of $0.50 per share. CVS Health has paid cash 
dividends every quarter since becoming a public company and expects to maintain its quarterly dividend of $0.50 per share 
throughout 2020. Future dividends will depend on the Company’s earnings, capital requirements, financial condition and other 
factors considered relevant by the Board. 

75

Off-Balance Sheet Arrangements

Between 1995 and 1997, the Company sold or spun off a number of subsidiaries, including Bob’s Stores and Linens ‘n Things, 
each of which subsequently filed for bankruptcy, and Marshalls. In many cases, when a former subsidiary leased a store, the 
Company provided a guarantee of the former subsidiary’s lease obligations for the initial lease term and any extension thereof 
pursuant to a renewal option provided for in the lease prior to the time of the disposition. When the subsidiaries were disposed 
of and accounted for as discontinued operations, the Company’s guarantees remained in place, although each initial purchaser 
agreed to indemnify the Company for any lease obligations the Company was required to satisfy. If any of the purchasers or any 
of the former subsidiaries fail to make the required payments under a store lease, the Company could be required to satisfy 
those obligations.

As of December 31, 2019, the Company guaranteed 79 such store leases (excluding the lease guarantees related to Linens ‘n 
Things, which have been recorded as a liability on the consolidated balance sheets), with the maximum remaining lease term 
extending through 2030. Management believes the ultimate disposition of any of the remaining lease guarantees will not have a 
material adverse effect on the Company’s consolidated financial condition or future cash flows. See “Lease Guarantees” in Note 
16 ‘‘Commitments and Contingencies’’ included in Item 8 of this 10-K for further information regarding the Company’s 
guarantees of lease obligations.

Contractual Obligations

The following table summarizes certain estimated future obligations by period under the Company’s various contractual 
obligations at December 31, 2019. The table below does not include future payments of claims to health care providers or 
pharmacies because certain terms of these payments are not determinable at December 31, 2019 (for example, the timing and 
volume of future services provided under fee-for-service arrangements and future membership levels for capitated 
arrangements). 

Payments Due by Period

In millions
Operating lease liabilities
Finance lease liabilities
Contractual lease obligations with Target (1)
Lease obligations for discontinued operations
Long-term debt
Interest payments on long-term debt (2)
Other long-term liabilities on the consolidated balance 
sheets (3) 

Total
$ 27,833
1,454
2,218
8
68,438
35,343

     2020
$

2,699
84
—
4
3,754
2,751

$

$

2021 to 2022     2023 to 2024     Thereafter
15,654
$
1,056
2,218
—
43,869
23,217

4,438
153
—
—
11,258
4,299

5,042
161
—
4
9,557
5,076

Future policy benefits (4) 
Unpaid claims (4) 
Policyholders’ funds (4) (5)
Other liabilities

Total
_____________________________________________

6,127
2,522
1,156
1,540
$146,639

508
705
553
426
$ 11,484

$

937
514
137
801
22,229

$

809
346
85
89
21,477

$

3,873
957
381
224
91,449

(1)  The Company leases pharmacy and clinic space from Target Corporation (“Target”). See Note 6 ‘‘Leases’’ included in Item 8 of this 10-K for additional 
information regarding the lease arrangements with Target. Amounts related to such operating and finance leases are reflected within the operating lease 
liabilities and finance lease liabilities in the table above. Pharmacy lease amounts due in excess of the remaining estimated economic life of the buildings 
are reflected in the table above assuming equivalent stores continue to operate through the term of the arrangements.
Interest payments on long-term debt are calculated using outstanding balances and interest rates in effect on December 31, 2019.

(2) 
(3)  Payments of other long-term liabilities exclude Separate Accounts liabilities of approximately $4.5 billion because these liabilities are supported by assets 

that are legally segregated and are not subject to claims that arise out of the Company’s business.

(4)  Total payments of future policy benefits, unpaid claims and policyholders’ funds include $807 million, $2.5 billion and $291 million, respectively, of 
reserves for contracts subject to reinsurance. The Company expects the assuming reinsurance carrier to fund these obligations and has reflected these 
amounts as reinsurance recoverable assets on the consolidated balance sheets.

(5)  Customer funds associated with group life and health contracts of approximately $2.4 billion have been excluded from the table above because such funds 
may be used primarily at the customer’s discretion to offset future premiums and/or for refunds, and the timing of the related cash flows cannot be 
determined. Additionally, net unrealized capital gains on debt securities supporting experience-rated products of $83 million, before tax, have been 
excluded from the table above.

76

Restrictions on Certain Payments

In addition to general state law restrictions on payments of dividends and other distributions to stockholders applicable to all 
corporations, health maintenance organizations (“HMOs”) and insurance companies are subject to further regulations that, 
among other things, may require those companies to maintain certain levels of equity (referred to as surplus) and restrict the 
amount of dividends and other distributions that may be paid to their equity holders. These regulations are not directly 
applicable to CVS Health as a holding company, since CVS Health is not an HMO or an insurance company. In addition, in 
connection with the Aetna Acquisition, the Company made certain undertakings that require prior regulatory approval of 
dividends by certain of its HMOs and insurance companies. The additional regulations and undertakings applicable to the 
Company’s HMO and insurance company subsidiaries are not expected to affect the Company’s ability to service the 
Company’s debt, meet other financing obligations or pay dividends, or the ability of any of the Company’s subsidiaries to 
service their debt or other financing obligations. Under applicable regulatory requirements and undertakings, at December 31, 
2019, the maximum amount of dividends that may be paid by the Company’s insurance and HMO subsidiaries without prior 
approval by regulatory authorities was $366 million in the aggregate. 

The Company maintains capital levels in its operating subsidiaries at or above targeted and/or required capital levels and 
dividends amounts in excess of these levels to meet liquidity requirements, including the payment of interest on debt and 
stockholder dividends. In addition, at the Company’s discretion, it uses these funds for other purposes such as funding share and 
debt repurchase programs, investments in new businesses and other purposes considered advisable. 

At December 31, 2019 and 2018, the Company held investments of $537 million and $531 million, respectively, that are not 
accounted for as Separate Accounts assets but are legally segregated and are not subject to claims that arise out of the 
Company’s business. See Note 3 ‘‘Investments’’ included in Item 8 of this 10-K for additional information on investments 
related to the 2012 conversion of an existing group annuity contract from a participating to a non-participating contract.

Solvency Regulation

The National Association of Insurance Commissioners (the “NAIC”) utilizes risk-based capital (“RBC”) standards for 
insurance companies that are designed to identify weakly-capitalized companies by comparing each company’s adjusted surplus 
to its required surplus (the “RBC Ratio”). The RBC Ratio is designed to reflect the risk profile of insurance companies. Within 
certain ratio ranges, regulators have increasing authority to take action as the RBC Ratio decreases. There are four levels of 
regulatory action, ranging from requiring an insurer to submit a comprehensive financial plan for increasing its RBC to the state 
insurance commissioner to requiring the state insurance commissioner to place the insurer under regulatory control. At 
December 31, 2019, the RBC Ratio of each of the Company’s primary insurance subsidiaries was above the level that would 
require regulatory action. The RBC framework described above for insurers has been extended by the NAIC to health 
organizations, including HMOs. Although not all states had adopted these rules at December 31, 2019, at that date, each of the 
Company’s active HMOs had a surplus that exceeded either the applicable state net worth requirements or, where adopted, the 
levels that would require regulatory action under the NAIC’s RBC rules. External rating agencies use their own capital models 
and/or RBC standards when they determine a company’s rating.

77

Critical Accounting Policies

The Company prepares the consolidated financial statements in conformity with generally accepted accounting principles, 
which require management to make certain estimates and apply judgment. Estimates and judgments are based on historical 
experience, current trends and other factors that management believes to be important at the time the consolidated financial 
statements are prepared. On a regular basis, the Company reviews its accounting policies and how they are applied and 
disclosed in the consolidated financial statements. While the Company believes the historical experience, current trends and 
other factors considered by management support the preparation of the consolidated financial statements in conformity with 
generally accepted accounting principles, actual results could differ from estimates, and such differences could be material.

Significant accounting policies are discussed in Note 1 ‘‘Significant Accounting Policies’’ included in Item 8 of this 10-K. 
Management believes the following accounting policies include a higher degree of judgment and/or complexity and, thus, are 
considered to be critical accounting policies. The Company has discussed the development and selection of these critical 
accounting policies with the Audit Committee of the Board (the “Audit Committee”), and the Audit Committee has reviewed 
the disclosures relating to them.

Revenue Recognition

Pharmacy Services Segment
The Pharmacy Services segment sells prescription drugs directly through its mail service dispensing pharmacies and indirectly 
through the Company’s retail pharmacy network. The Company’s pharmacy benefit arrangements are accounted for in a manner 
consistent with a master supply arrangement as there are no contractual minimum volumes and each prescription is considered 
a separate purchasing decision and distinct performance obligation transferred at a point in time. PBM services performed in 
connection with each prescription claim are considered part of a single performance obligation which culminates in the 
dispensing of prescription drugs.

The Company recognizes revenue using the gross method at the contract price negotiated with its clients when the Company 
has concluded it controls the prescription drug before it is transferred to the client plan members. The Company controls 
prescriptions dispensed indirectly through its retail pharmacy network because it has separate contractual arrangements with 
those pharmacies, has discretion in setting the price for the transaction and assumes primary responsibility for fulfilling the 
promise to provide prescription drugs to its client plan members while also performing the related PBM services.

Revenues include (i) the portion of the price the client pays directly to the Company, net of any discounts earned on brand name 
drugs or other discounts and refunds paid back to the client (see “Drug Discounts” and “Guarantees” below), (ii) the price paid 
to the Company by client plan members for mail order prescriptions and the price paid to retail network pharmacies by client 
plan members for retail prescriptions (“retail co-payments”), and (iii) claims based administrative fees for retail pharmacy 
network contracts. Sales taxes are not included in revenues. 

The Company recognizes revenue when control of the prescription drugs is transferred to customers, in an amount that reflects 
the consideration the Company expects to be entitled to receive in exchange for those prescription drugs. The Company has 
established the following revenue recognition policies for the Pharmacy Services segment:

•  Revenues generated from prescription drugs sold by mail service dispensing pharmacies are recognized when the 

prescription drug is delivered to the client plan member. At the time of delivery, the Company has performed substantially 
all of its performance obligations under its client contracts and does not experience a significant level of returns or 
reshipments.

•  Revenues generated from prescription drugs sold by third party pharmacies in the Company’s retail pharmacy network and 
associated administrative fees are recognized at the Company’s point-of-sale, which is when the claim is adjudicated by the 
Company’s online claims processing system and the Company has transferred control of the prescription drug and 
performed all of its performance obligations.

For contracts under which the Company acts as an agent or does not control the prescription drugs prior to transfer to the client 
plan member, revenue is recognized using the net method.

Drug Discounts
The Company records revenue net of manufacturers’ rebates earned by its clients based on their plan members’ utilization of 
brand-name formulary drugs. The Company estimates these rebates at period-end based on actual and estimated claims data and 
its estimates of the manufacturers’ rebates earned by its clients. The estimates are based on the best available data at period-end 

78

and recent history for the various factors that can affect the amount of rebates due to the client. The Company adjusts its rebates 
payable to clients to the actual amounts paid when these rebates are paid or as significant events occur. Any cumulative effect of 
these adjustments is recorded against revenues at the time it is identified. Adjustments generally result from contract changes 
with clients or manufacturers that have retroactive rebate adjustments, differences between the estimated and actual product 
mix subject to rebates, or whether the brand name drug was included in the applicable formulary. The effect of adjustments 
between estimated and actual manufacturers’ rebate amounts has not been material to the Company’s operating results or 
financial condition.

Guarantees
The Company also adjusts revenues for refunds owed to clients resulting from pricing guarantees and performance against 
defined service and performance metrics. The inputs to these estimates are not subject to a high degree of subjectivity or 
volatility. The effect of adjustments between estimated and actual pricing and performance refund amounts has not been 
material to the Company’s operating results or financial condition.

Retail/LTC Segment
Retail Pharmacy
The Company’s retail drugstores recognize revenue at the time the customer takes possession of the merchandise. For pharmacy 
sales, each prescription claim is its own arrangement with the customer and is a performance obligation, separate and distinct 
from other prescription claims under other retail network arrangements. Revenues are adjusted for refunds owed to third party 
payers resulting from pricing guarantees and performance against defined value-based service and performance metrics. The 
inputs to these estimates are not subject to a high degree of subjectivity or volatility. The effect of adjustments between 
estimated and actual pricing and performance refund amounts has not been material to the Company’s operating results or 
financial condition.

Revenue from Company gift cards purchased by customers is deferred as a contract liability until goods or services are 
transferred. Any amounts not expected to be redeemed by customers (i.e., breakage) are recognized based on historical 
redemption patterns.

Customer returns are not material to the Company’s operating results or financial condition. Sales taxes are not included in 
revenues.

Loyalty and Other Programs
The Company’s customer loyalty program, ExtraCare®, consists of two components, ExtraSavingsTM and ExtraBucks® 
Rewards. ExtraSavings are coupons that are recorded as a reduction of revenue when redeemed as the Company concluded that 
they do not represent a promise to the customer to deliver additional goods or services at the time of issuance because they are 
not tied to a specific transaction or spending level. 

ExtraBucks Rewards are accumulated by customers based on their historical spending levels. Thus, the Company has 
determined that there is an additional performance obligation to those customers at the time of the initial transaction. The 
Company allocates the transaction price to the initial transaction and the ExtraBucks Rewards transaction based upon the 
relative standalone selling price, which considers historical redemption patterns for the rewards. Revenue allocated to 
ExtraBucks Rewards is recognized as those rewards are redeemed. At the end of each period, unredeemed ExtraBucks Rewards 
are reflected as a contract liability.

The Company also offers a subscription-based membership program, CarePass®, under which members are entitled to a suite of 
benefits delivered over the course of the subscription period, as well as a promotional reward that can be redeemed for future 
goods and services. Subscriptions are paid for on a monthly or annual basis at the time of or in advance of the Company 
delivering the goods and services. Revenue from these arrangements is recognized as the performance obligations are satisfied. 

Long-term Care
Revenue is recognized when control of the promised goods or services is transferred to customers in an amount that reflects the 
consideration the Company expects to be entitled to receive in exchange for those goods or services. Each prescription claim 
represents a separate performance obligation of the Company, separate and distinct from other prescription claims under 
customer arrangements. A significant portion of Long-term Care revenue from sales of pharmaceutical and medical products is 
reimbursed by the federal Medicare Part D program and, to a lesser extent, state Medicaid programs. The Company monitors its 
revenues and receivables from these reimbursement sources, as well as long-term care facilities and other third party insurance 
payors, and reduces revenue at the revenue recognition date to properly account for the variable consideration due to anticipated 

79

differences between billed and reimbursed amounts. Accordingly, the total revenues and receivables reported in the Company’s 
consolidated financial statements are recorded at the amount expected to be ultimately received from these payors. 

Patient co-payments associated with Medicare Part D, certain state Medicaid programs, Medicare Part B and certain third party 
payors typically are not collected at the time products are delivered or services are rendered, but are billed to the individuals as 
part of normal billing procedures and subject to normal accounts receivable collections procedures.

Walk-In Medical Clinics
For services provided by the Company’s walk-in medical clinics, revenue recognition occurs for completed services provided to 
patients, with adjustments taken for third party payor contractual obligations and patient direct bill historical collection rates.

Health Care Benefits Segment
Health Care Benefits revenue is principally derived from insurance premiums and fees billed to customers. Revenue is 
recognized based on customer billings, which reflect contracted rates per employee and the number of covered employees 
recorded in the Company’s records at the time the billings are prepared. Billings are generally sent monthly for coverage during 
the following month. 

The Company’s billings may be subsequently adjusted to reflect enrollment changes due to member terminations or other 
factors. These adjustments are known as retroactivity adjustments. In each period, the Company estimates the amount of future 
retroactivity and adjusts the recorded revenue accordingly. As information regarding actual retroactivity amounts becomes 
known, the Company refines its estimates and records any required adjustments to revenues in the period in which they arise. A 
significant difference in the actual level of retroactivity compared to estimated levels would have a significant effect on the 
Company’s operating results.

Premium Revenue
Premiums are recognized as revenue in the month in which the enrollee is entitled to receive health care services. Premiums are 
reported net of an allowance for estimated terminations and uncollectible amounts. Additionally, premium revenue subject to 
the ACA’s minimum medical loss ratio (“MLR”) rebate requirements is recorded net of the estimated minimum MLR rebates 
for the current calendar year. Premiums related to unexpired contractual coverage periods (unearned premiums) are reported as 
other insurance liabilities on the consolidated balance sheets and recognized as revenue when earned.

Some of the Company’s contracts allow for premiums to be adjusted to reflect actual experience or the relative health status of 
Insured members. Such adjustments are reasonably estimable at the outset of the contract, and adjustments to those estimates 
are made based on actual experience of the customer emerging under the contract and the terms of the underlying contract.

Services Revenue
Services revenue relates to contracts that can include various combinations of services or series of services which generally are 
capable of being distinct and accounted for as separate performance obligations. The Health Care Benefits segment’s services 
revenue primarily consists of the following components:

•  ASC fees are received in exchange for performing certain claim processing and member services for ASC members. ASC 

fee revenue is recognized over the period the service is provided. Some of the Company’s administrative services contracts 
include guarantees with respect to certain functions, such as customer service response time, claim processing accuracy and 
claim processing turnaround time, as well as certain guarantees that a plan sponsor’s benefit claim experience will fall 
within a certain range. With any of these guarantees, the Company is financially at risk if the conditions of the 
arrangements are not met, although the maximum amount at risk typically is limited to a percentage of the fees otherwise 
payable to the Company by the customer involved. Each period the Company estimates its obligations under the terms of 
these guarantees and records its estimate as an offset to services revenues.

•  Workers’ compensation administrative services consist of fee-based managed care services. Workers’ compensation 

administrative services revenue is recognized once the service is provided.

Accounting for Medicare Part D 
Revenues include insurance premiums earned by the Company’s PDPs, which are determined based on the PDP’s annual bid 
and related contractual arrangements with CMS. The insurance premiums include a beneficiary premium, which is the 
responsibility of the PDP member, and can be subsidized by CMS in the case of low-income members, and a direct premium 
paid by CMS. Premiums collected in advance are initially recorded within other insurance liabilities and are then recognized 
ratably as revenue over the period in which members are entitled to receive benefits.

80

Revenues also include a risk-sharing feature of the Medicare Part D program design referred to as the risk corridor. The 
Company estimates variable consideration in the form of amounts payable to, or receivable from, CMS under the risk corridor, 
and adjusts revenue based on calculations of additional subsidies to be received from or owed to CMS at the end of the 
reporting year.

In addition to Medicare Part D premiums, the Company receives additional payments each month from CMS related to 
catastrophic reinsurance, low-income cost sharing subsidies and coverage gap benefits. If the subsidies received differ from the 
amounts earned from actual prescriptions transferred, the difference is recorded in either accounts receivable, net or accrued 
expenses.

Other-Than-Temporary Impairments of Debt Securities

The Company regularly reviews its debt securities to determine whether a decline in fair value below the cost basis or carrying 
value is other-than-temporary. If a decline in the fair value of a debt security is considered other-than-temporary, the cost basis 
or carrying value of the debt security is written down. The write-down is then bifurcated into its credit and non-credit related 
components. The amount of the credit-related component is included in the Company’s net income (loss), and the amount of the 
non-credit related component is included in other comprehensive income (loss), unless the Company intends to sell the debt 
security or it is more likely than not that the Company will be required to sell the debt security prior to its anticipated recovery 
of the debt security’s amortized cost basis. The Company analyzes all facts and circumstances believed to be relevant for each 
investment when performing this analysis, in accordance with applicable accounting guidance.

Among the factors considered in evaluating whether a decline in fair value is other-than-temporary are whether the decline 
results from a change in the quality of the debt security itself, whether the decline results from a downward movement in the 
market as a whole, and the prospects for realizing the carrying value of the debt security based on the investment’s current and 
short-term prospects for recovery. For unrealized losses determined to be the result of market conditions (for example, 
increasing interest rates and volatility due to conditions in the overall market) or industry-related events, the Company 
determines whether it intends to sell the debt security or if it is more likely than not that the Company will be required to sell 
the debt security prior to its anticipated recovery of the debt security’s amortized cost basis. If either case is true, the Company 
recognizes an other-than-temporary impairment, and the cost basis/carrying amount of the debt security is written down to fair 
value. 

The risks inherent in assessing the impairment of a debt security include the risk that market factors may differ from projections 
and the risk that the facts and circumstances factored into the Company’s assessment may change with the passage of time. 
Unexpected changes to market factors and circumstances that were not present in past reporting periods are among the factors 
that may result in a current period decision to sell debt securities that were not impaired in prior reporting periods.

Vendor Allowances and Purchase Discounts

Pharmacy Services Segment
The Pharmacy Services segment receives purchase discounts on products purchased. Contractual arrangements with vendors, 
including manufacturers, wholesalers and retail pharmacies, normally provide for the Pharmacy Services segment to receive 
purchase discounts from established list prices in one, or a combination, of the following forms: (i) a direct discount at the time 
of purchase, (ii) a discount for the prompt payment of invoices or (iii) when products are purchased indirectly from a 
manufacturer (e.g., through a wholesaler or retail pharmacy), a discount (or rebate) paid subsequent to dispensing. These 
rebates are recognized when prescriptions are dispensed and are generally calculated and billed to manufacturers within 30 days 
of the end of each completed quarter. Historically, the effect of adjustments resulting from the reconciliation of rebates 
recognized to the amounts billed and collected has not been material to the Company’s operating results or financial condition. 
The Company accounts for the effect of any such differences as a change in accounting estimate in the period the reconciliation 
is completed. The Pharmacy Services segment also receives additional discounts under its wholesaler contracts if it exceeds 
contractually defined purchase volumes. In addition, the Pharmacy Services segment receives fees from pharmaceutical 
manufacturers for administrative services. Purchase discounts and administrative service fees are recorded as a reduction of cost 
of products sold.

Retail/LTC Segment
Vendor allowances received by the Retail/LTC segment reduce the carrying cost of inventory and are recognized in cost of 
products sold when the related inventory is sold, unless they are specifically identified as a reimbursement of incremental costs 
for promotional programs and/or other services provided. Amounts that are directly linked to advertising commitments are 
recognized as a reduction of advertising expense (included in operating expenses) when the related advertising commitment is 

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satisfied. Any such allowances received in excess of the actual cost incurred also reduce the carrying cost of inventory. The total 
value of any upfront payments received from vendors that are linked to purchase commitments is initially deferred. The 
deferred amounts are then amortized to reduce cost of products sold over the life of the contract based upon purchase volume. 
The total value of any upfront payments received from vendors that are not linked to purchase commitments is also initially 
deferred. The deferred amounts are then amortized to reduce cost of products sold on a straight-line basis over the life of the 
related contract.

There have not been any material changes in the way the Company accounts for vendor allowances or purchase discounts 
during the past three years.

Inventory

Inventories are valued at the lower of cost or net realizable value using the weighted average cost method.

The value of ending inventory is reduced for estimated inventory losses that have occurred during the interim period between 
physical inventory counts. Physical inventory counts are taken on a regular basis in each retail store and LTC pharmacy, and a 
continuous cycle count process is the primary procedure used to validate the inventory balances on hand in each distribution 
center and mail facility to ensure that the amounts reflected in the consolidated financial statements are properly stated. The 
Company’s accounting for inventory contains uncertainty since management must use judgment to estimate the inventory losses 
that have occurred during the interim period between physical inventory counts. When estimating these losses, a number of 
factors are considered which include historical physical inventory results on a location-by-location basis and current physical 
inventory loss trends.

The total reserve for estimated inventory losses covered by this critical accounting policy was $401 million as of December 31, 
2019. Although management believes there is sufficient current and historical information available to record reasonable 
estimates for estimated inventory losses, it is possible that actual results could differ. In order to help investors assess the 
aggregate risk, if any, associated with the inventory-related uncertainties discussed above, a ten percent (10%) pre-tax change in 
estimated inventory losses, which is a reasonably likely change, would increase or decrease the total reserve for estimated 
inventory losses by approximately $40 million as of December 31, 2019.

Although management believes that the estimates discussed above are reasonable and the related calculations conform to 
generally accepted accounting principles, actual results could differ from such estimates, and such differences could be 
material.

Right-of-Use Assets and Lease Liabilities

The Company determines if an arrangement contains a lease at the inception of a contract. Right-of-use assets represent the 
Company’s right to use an underlying asset for the lease term and lease liabilities represent the Company’s obligation to make 
lease payments arising from the lease. Right-of-use assets and lease liabilities are recognized at the commencement date of the 
lease, renewal date of the lease or significant remodeling of the lease space based on the present value of the remaining future 
minimum lease payments. As the interest rate implicit in the Company’s leases is not readily determinable, the Company 
utilizes its incremental borrowing rate, determined by class of underlying asset, to discount the lease payments. The operating 
lease right-of-use assets also include lease payments made before commencement and are reduced by lease incentives. 

The Company’s real estate leases typically contain options that permit renewals for additional periods of up to five years each. 
For real estate leases, the options to extend are not considered reasonably certain at lease commencement because the Company 
reevaluates each lease on a regular basis to consider the economic and strategic incentives of exercising the renewal options and 
regularly opens or closes stores to align with its operating strategy. Generally, the renewal option periods are not included 
within the lease term and the associated payments are not included in the measurement of the right-of-use asset and lease 
liability. Similarly, renewal options are not included in the lease term for non-real estate leases because they are not considered 
reasonably certain of being exercised at lease commencement. Leases with an initial term of 12 months or less are not recorded 
on the balance sheets, and lease expense is recognized on a straight-line basis over the term of the short-term lease.

For real estate leases, the Company accounts for lease components and nonlease components as a single lease component.  
Certain real estate leases require additional payments based on sales volume, as well as reimbursement for real estate taxes, 
common area maintenance and insurance, which are expensed as incurred as variable lease costs. Other real estate leases 
contain one fixed lease payment that includes real estate taxes, common area maintenance and insurance. These fixed payments 
are considered part of the lease payment and included in the right-of-use assets and lease liabilities.

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Long-Lived Asset Impairment

Recoverability of Definite-Lived Assets
The Company evaluates the recoverability of long-lived assets, excluding goodwill and indefinite-lived intangible assets, which 
are tested for impairment using separate tests described below, whenever events or changes in circumstances indicate that the 
carrying value of such an asset may not be recoverable. The Company groups and evaluates these long-lived assets for 
impairment at the lowest level at which individual cash flows can be identified. If indicators of impairment are present, the 
Company first compares the carrying amount of the asset group to the estimated future cash flows associated with the asset 
group (undiscounted and without interest charges). If the estimated future cash flows used in this analysis are less than the 
carrying amount of the asset group, an impairment loss calculation is prepared. The impairment loss calculation compares the 
carrying amount of the asset group to the asset group’s estimated future cash flows (discounted and with interest charges). If 
required, an impairment loss is recorded for the portion of the asset group’s carrying value that exceeds the asset group’s 
estimated future cash flows (discounted and with interest charges).

The long-lived asset impairment loss calculation contains uncertainty since management must use judgment to estimate each 
asset group’s future sales, profitability and cash flows. When preparing these estimates, the Company considers historical 
results and current operating trends and consolidated sales, profitability and cash flow results and forecasts. These estimates can 
be affected by a number of factors including general economic and regulatory conditions, efforts of third party organizations to 
reduce their prescription drug costs and/or increased member co-payments, the continued efforts of competitors to gain market 
share and consumer spending patterns.

During the year ended December 31, 2019, the Company recorded store rationalization charges of $231 million, primarily 
related to operating lease right-of-use asset impairment charges. During the year ended December 31, 2018, the Company 
recognized a $43 million long-lived asset impairment charge, primarily related to the impairment of property and equipment. 
There were no material impairment charges recognized on long-lived assets in the year ended December 31, 2017. 

Recoverability of Goodwill
Goodwill represents the excess of amounts paid for acquisitions over the fair value of the net identifiable assets acquired. 
Goodwill is subject to annual impairment reviews, or more frequent reviews if events or circumstances indicate that the 
carrying value may not be recoverable. Goodwill is tested for impairment on a reporting unit basis. The impairment test is 
performed by comparing the reporting unit’s fair value with its net book value (or carrying amount), including goodwill. The 
fair value of the reporting units is estimated using a combination of a discounted cash flow method and a market multiple 
method. If the net book value (carrying amount) of the reporting unit exceeds its fair value, the reporting unit’s goodwill is 
considered to be impaired, and an impairment is recognized in an amount equal to the excess.

The determination of the fair value of the reporting units requires the Company to make significant assumptions and estimates. 
These assumptions and estimates primarily include the selection of appropriate peer group companies; control premiums and 
valuation multiples appropriate for acquisitions in the industries in which the Company competes; discount rates; terminal 
growth rates; and forecasts of revenue, operating income, depreciation and amortization, income taxes, capital expenditures and 
future working capital requirements. When determining these assumptions and preparing these estimates, the Company 
considers each reporting unit’s historical results and current operating trends; consolidated revenues, profitability and cash flow 
results and forecasts; and industry trends. The Company’s estimates can be affected by a number of factors, including general 
economic and regulatory conditions; the risk-free interest rate environment; the Company’s market capitalization; efforts of 
customers and payers to reduce costs, including their prescription drug costs, and/or increase member co-payments; the 
continued efforts of competitors to gain market share and consumer spending patterns. 

2019 Goodwill Impairment Test
During the third quarter of 2019, the Company performed its required annual impairment test of goodwill. The results of this 
impairment test indicated that there was no impairment of goodwill as of the testing date. The goodwill impairment test resulted 
in the fair values of all of the Company’s reporting units exceeding their carrying values by significant margins, with the 
exception of the Commercial Business and LTC reporting units, which exceeded their carrying values by approximately 4% and 
9%, respectively.

As of the Aetna Acquisition Date, the Company added the Health Care Benefits segment which included the Commercial 
Business reporting unit. The transaction was accounted for using the acquisition method of accounting which requires, among 
other things, the assets acquired and liabilities assumed to be recognized at their fair values at the date of acquisition. As a 
result, at the time of the acquisition the fair value of the Commercial Business reporting unit was equal to its carrying value. 
Given the close proximity of the Aetna Acquisition Date to the 2019 annual impairment test of goodwill, as expected, the fair 

83

value of the Commercial Business reporting unit remained relatively in line with the carrying value of the reporting unit. In 
addition, this fair value estimate is sensitive to significant assumptions including changes in the revenue growth rate, operating 
income and the discount rate.

Although the Company believes the financial projections used to determine the fair value of the LTC reporting unit in the third 
quarter of 2019 were reasonable and achievable, the LTC reporting unit may continue to face challenges that may affect the 
Company’s ability to grow the LTC reporting unit’s business at the rate estimated when such goodwill impairment test was 
performed. These challenges and some of the key assumptions included in the Company’s financial projections to determine the 
estimated fair value of the LTC reporting unit include client retention rates; occupancy rates in skilled nursing facilities; the 
financial health of skilled nursing facility customers; facility reimbursement pressures; the Company’s ability to execute its 
senior living initiative; the Company’s ability to make acquisitions and integrate those businesses into its LTC operations in an 
orderly manner; and the Company’s ability to extract cost savings from labor productivity and other initiatives. The fair value 
of the LTC reporting unit also is dependent on market multiples of peer group companies and the risk-free interest rate 
environment, which impacts the discount rate used in the discounted cash flow valuation method. If the Company does not 
achieve its forecasts, it is reasonably possible in the near term that the goodwill of the LTC reporting unit could be deemed to be 
impaired by a material amount. As of December 31, 2019, the remaining goodwill balance in the LTC reporting unit was $431 
million. 

2018 Goodwill Impairment Tests
As discussed in Note 5 ‘‘Goodwill and Other Intangibles’’ included in Item 8 of this 10-K, during 2018, the LTC reporting unit 
continued to experience industry-wide challenges that impacted management’s ability to grow the business at the rate that was 
originally estimated when the Company acquired Omnicare and when the 2017 annual goodwill impairment test was 
performed. Those challenges included lower client retention rates, lower occupancy rates in skilled nursing facilities, the 
deteriorating financial health of numerous skilled nursing facility customers which resulted in a number of customer 
bankruptcies in 2018, and continued facility reimbursement pressures. In June 2018, LTC management submitted its initial 
budget for 2019 and updated the 2018 annual forecast which showed a deterioration in the projected financial results for the 
remainder of 2018 and in 2019, which also caused management to update its long-term forecast beyond 2019. Based on these 
updated projections, management determined that there were indicators that the LTC reporting unit’s goodwill may be impaired 
and, accordingly, management performed an interim goodwill impairment test as of June 30, 2018. The results of that interim 
impairment test showed that the fair value of the LTC reporting unit was lower than the carrying value, resulting in a $3.9 
billion pre-tax goodwill impairment charge in the second quarter of 2018. 

During the third quarter of 2018, the Company performed its required annual impairment tests of goodwill and concluded there 
was no impairment of goodwill. The goodwill impairment tests showed that the fair values of the Pharmacy Services and Retail 
Pharmacy reporting units exceeded their carrying values by significant margins and the fair value of the LTC reporting unit 
exceeded its carrying value by approximately 2%. 

During the fourth quarter of 2018, the LTC reporting unit missed its forecast primarily due to operational issues and customer 
liquidity issues, including one significant customer bankruptcy. Additionally, LTC management submitted an updated final 
budget for 2019 which showed significant additional deterioration in the projected financial results for 2019 compared to the 
analyses performed in the second and third quarters of 2018 primarily due to continued industry and operational challenges, 
which also caused management to make further updates to its long-term forecast beyond 2019. Based on these updated 
projections, management determined that there were indicators that the LTC reporting unit’s goodwill may be further impaired 
and, accordingly, management performed an interim goodwill impairment test during the fourth quarter of 2018. The results of 
that interim impairment test showed that the fair value of the LTC reporting unit was lower than the carrying value, resulting in 
an additional $2.2 billion pre-tax goodwill impairment charge in the fourth quarter of 2018. 

In 2018, the fair value of the LTC reporting unit was determined using a combination of a discounted cash flow method and a 
market multiple method. In addition to the lower financial projections, changes in risk-free interest rates and lower market 
multiples of peer group companies also contributed to the amount of the 2018 goodwill impairment charges. 

2017 Goodwill Impairment Tests
The Company recorded $181 million in goodwill impairment charges in 2017 related to the RxCrossroads reporting unit. 
During the third quarter of 2017, the Company performed its required annual impairment test of goodwill. The goodwill 
impairment test showed that the fair values of the Pharmacy Services and Retail Pharmacy reporting units exceeded their 
carrying values by significant margins and the fair values of the LTC and RxCrossroads reporting units exceeded their carrying 
values by approximately 1% and 6%, respectively. On January 2, 2018, the Company sold its RxCrossroads reporting unit to 
McKesson Corporation for $725 million.

84

Recoverability of Indefinite-Lived Intangible Assets
Indefinite-lived intangible assets are subject to annual impairment reviews, or more frequent reviews if events or circumstances 
indicate that their carrying value may not be recoverable. Indefinite-lived intangible assets are tested by comparing the 
estimated fair value of the asset to its carrying value. If the carrying value of the asset exceeds its estimated fair value, an 
impairment loss is recognized, and the asset is written down to its estimated fair value.

The indefinite-lived intangible asset impairment loss calculation contains uncertainty since management must use judgment to 
estimate fair value based on the assumption that, in lieu of ownership of an intangible asset, the Company would be willing to 
pay a royalty in order to utilize the benefits of the asset. Fair value is estimated by discounting the hypothetical royalty 
payments to their present value over the estimated economic life of the asset. These estimates can be affected by a number of 
factors including general economic conditions, availability of market information and the profitability of the Company. There 
were no impairment losses recognized on indefinite-lived intangible assets in any of the years ended December 31, 2019, 2018 
or 2017.

Health Care Costs Payable

At December 31, 2019 and 2018, 73% and 67% respectively, of health care costs payable are estimates of the ultimate cost of 
(i) services rendered to the Company’s Insured members but not yet reported to the Company and (ii) claims which have been 
reported to the Company but not yet paid (collectively, “IBNR”). Health care costs payable also include an estimate of the cost 
of services that will continue to be rendered after the financial statement date if the Company is obligated to pay for such 
services in accordance with contractual or regulatory requirements. The remainder of health care costs payable is primarily 
comprised of pharmacy and capitation payables, other amounts due to providers pursuant to risk sharing agreements and 
accruals for state assessments. The Company develops its estimate of IBNR using actuarial principles and assumptions that 
consider numerous factors. See Note 1 ‘‘Significant Accounting Policies’’ included in Item 8 of this 10-K for additional 
information on the Company’s reserving methodology.

During 2019, the Company observed an increase in completion factors relative to those assumed at the prior year end. After 
considering the claims paid in 2019 with dates of service prior to the fourth quarter of the previous year, the Company observed 
assumed incurred claim weighted average completion factors that were 27 basis points higher than previously estimated, 
resulting in a decrease of $240 million in 2019, in health care costs payable that related to the prior year. The Company has 
considered the pattern of changes in its completion factors when determining the completion factors used in its estimates of 
IBNR as of December 31, 2019. However, based on historical claim experience, it is reasonably possible that the Company’s 
estimated weighted average completion factors may vary by plus or minus 19 basis points from the Company’s assumed rates, 
which could impact health care costs payable by approximately plus or minus $227 million pretax.

Also during 2019, the Company observed that health care costs for claims with claim incurred dates of three months or less 
before the financial statement date were lower than previously estimated. Specifically, after considering the claims paid in 2019 
with claim incurred dates for the fourth quarter of the previous year, the Company observed health care costs that were 
approximately 3.2% lower than previously estimated during the fourth quarter of 2018, resulting in a reduction of $284 million 
in 2019 in health care costs payable that related to prior year.

Management considers historical health care cost trend rates together with its knowledge of recent events that may impact 
current trends when developing estimates of current health care cost trend rates. When establishing reserves as of December 31, 
2019, the Company increased its assumed health care cost trend rates for the most recent three months by 3.4% from health care 
cost trend rates recently observed. However, based on historical claim experience, it is reasonably possible that the Company’s 
estimated health care cost trend rates may vary by plus or minus 3.5% from the assumed rates, which could impact health care 
costs payable by plus or minus $349 million pretax.

Income Taxes

The Company accounts for income taxes using the asset and liability method. Deferred tax assets and liabilities are established 
for any temporary differences between financial and tax reporting bases and are adjusted as needed to reflect changes in the 
enacted tax rates expected to be in effect when the temporary differences reverse. Such adjustments are recorded in the period 
in which changes in tax laws are enacted, regardless of when they are effective. Deferred tax assets are reduced, if necessary, by 
a valuation allowance to the extent future realization of those losses, deductions or other tax benefits is sufficiently uncertain.
Significant judgment is required in determining the provision for income taxes and the related taxes payable and deferred tax 
assets and liabilities since, in the ordinary course of business, there are transactions and calculations where the ultimate tax 
outcome is uncertain. Additionally, the Company’s tax returns are subject to audit by various domestic and foreign tax 

85

authorities that could result in material adjustments based on differing interpretations of the tax laws. Although management 
believes that its estimates are reasonable and are based on the best available information at the time the provision is prepared, 
actual results could differ from these estimates resulting in a final tax outcome that may be materially different from that which 
is reflected in the consolidated financial statements.

The tax benefit from an uncertain tax position is recognized only if it is more likely than not that the tax position will be 
sustained on examination by the taxing authorities, based on the technical merits of the position. The tax benefits recognized in 
the consolidated financial statements from such positions are then measured based on the largest benefit that has a greater than 
50% likelihood of being realized upon settlement with the related tax authority. Interest and/or penalties related to uncertain tax 
positions are recognized in the income tax provision. Significant judgment is required in determining uncertain tax positions. 
The Company has established accruals for uncertain tax positions using its judgment and adjusts these accruals, as warranted, 
due to changing facts and circumstances.

New Accounting Pronouncements

See Note 1 ‘‘Significant Accounting Policies’’ included in Item 8 of this 10-K for a description of new accounting 
pronouncements applicable to the Company.

86

Item 7A.  Quantitative and Qualitative Disclosures About Market Risk.

The Company’s earnings and financial condition are exposed to interest rate risk, credit quality risk, market valuation risk, 
foreign currency risk, commodity risk and operational risk. 

Evaluation of Interest Rate and Credit Quality Risk

The Company manages interest rate risk by seeking to maintain a tight match between the durations of assets and liabilities 
when appropriate. The Company manages credit quality risk by seeking to maintain high average credit quality ratings and 
diversified sector exposure within its debt securities portfolio. In connection with its investment and risk management 
objectives, the Company also uses derivative financial instruments whose market value is at least partially determined by, 
among other things, levels of or changes in interest rates (short-term or long-term), duration, prepayment rates, equity markets 
or credit ratings/spreads. The Company’s use of these derivatives is generally limited to hedging risk and has principally 
consisted of using interest rate swaps, treasury rate locks, forward contracts, futures contracts, warrants, put options and credit 
default swaps. These instruments, viewed separately, subject the Company to varying degrees of interest rate, equity price and 
credit risk. However, when used for hedging, the Company expects these instruments to reduce overall risk.

Investments

The Company’s investment portfolio supported the following products at December 31, 2019 and 2018:

In millions

Experience-rated products

Remaining products

Total investments

2019

2018

$

$

1,100

18,587

19,687

$

$

1,063

17,191

18,254

Investment risks associated with experience-rated products generally do not impact the Company’s operating results. The risks 
associated with investments supporting experience-rated pension and annuity products in the large case pensions business in the 
Company’s Corporate/Other segment are assumed by the contract holders and not by the Company (subject to, among other 
things, certain minimum guarantees). Assets supporting experience-rated products may be subject to contract holder or 
participant withdrawals. 

The debt securities in the Company’s investment portfolio had an average credit quality rating of A at both December 31, 2019 
and 2018 with approximately $4.4 billion and $3.9 billion rated AAA at December 31, 2019 and 2018, respectively.  The debt 
securities that were rated below investment grade (that is, having a credit quality rating below BBB-/Baa3) were $1.2 billion 
and $1.1 billion at December 31, 2019 and 2018, respectively (of which 4% and 6% at December 31, 2019 and 2018, 
respectively, supported experience-rated products).

At December 31, 2019 and 2018, the Company held $333 million and $373 million, respectively, of municipal debt securities 
that were guaranteed by third parties, representing 2% of total investments at both December 31, 2019 and 2018. These 
securities had an average credit quality rating of AA and AA- at December 31, 2019 and 2018, respectively, with the guarantee. 
These securities had an average credit quality rating of A+ and A- at December 31, 2019 and 2018, respectively, without the 
guarantee. The Company does not have any significant concentration of investments with third party guarantors (either direct or 
indirect).

The Company generally classifies debt securities as available for sale, and carries them at fair value on the consolidated balance 
sheets. At both December 31, 2019 and 2018, less than 1% of debt securities were valued using inputs that reflect the 
Company’s assumptions (categorized as Level 3 inputs in accordance with accounting principles generally accepted in the 
United States of America). See Note 4 ‘‘Fair Value’’ included in Item 8 of this 10-K, for additional information on the 
methodologies and key assumptions used to determine the fair value of investments. For additional information related to 
investments, see Note 3 ‘‘Investments’’ included in Item 8 of this 10-K.

The Company regularly reviews debt securities in its portfolio to determine whether a decline in fair value below the cost basis 
or carrying value is other-than-temporary. When a debt security is in an unrealized capital loss position, the Company monitors 
the duration and severity of the loss to determine if sufficient market recovery can occur within a reasonable period of time. If a 
decline in fair value is considered other-than-temporary, the cost basis or carrying value of the debt security is written down. 
The write down is then bifurcated into its credit and non-credit related components. The amount of the credit-related component 

87

is included in net income, and the amount of the non-credit related component is included in other comprehensive income 
(loss), unless the Company intends to sell the debt security or it is more likely than not that the Company will be required to sell 
the debt security prior to its anticipated recovery of the debt security’s amortized cost basis. Accounting for other-than-
temporary impairment (“OTTI”) of debt securities is considered a critical accounting policy. See “Critical Accounting Policies - 
Other-Than-Temporary Impairment of Debt Securities” in the MD&A included in Item 7 of this 10-K for additional 
information. 

Evaluation of Market Valuation Risks

The Company regularly evaluates its risk from market-sensitive instruments by examining, among other things, levels of or 
changes in interest rates (short-term or long-term), duration, prepayment rates, equity markets and/or credit ratings/spreads. The 
Company also regularly evaluates the appropriateness of investments relative to management-approved investment guidelines 
(and operates within those guidelines) and the business objectives of its portfolios.

On a quarterly basis, the Company reviews the impact of hypothetical net losses in its investment portfolio on the Company’s 
consolidated near-term financial condition, operating results and cash flows assuming the occurrence of certain reasonably 
possible changes in near-term market rates and prices. Interest rate changes (whether resulting from changes in treasury yields 
or credit spreads or other factors) represent the most material risk exposure category for the Company. The Company has 
estimated the impact on the fair value of market sensitive instruments based on the net present value of cash flows using a 
representative set of likely future interest rate scenarios. The assumptions used were as follows: an immediate increase of 100 
basis points in interest rates (which the Company believes represents a moderately adverse scenario and is approximately equal 
to the historical annual volatility of interest rate movements for intermediate-term available-for-sale debt securities) and an 
immediate decrease of 15% in prices for domestic equity securities.

Assuming an immediate increase of 100 basis points in interest rates and an immediate decrease of 15% in the prices for 
domestic equity securities, the theoretical decline in the fair values of market sensitive instruments at December 31, 2019 is as 
follows:

•  The fair value of long-term debt would decline by approximately $4.5 billion ($5.7 billion pretax). Changes in the fair 

value of long-term debt do not impact the Company’s operating results or financial condition. 

•  The theoretical reduction in the fair value of investment securities partially offset by the theoretical reduction in the fair 
value of interest rate sensitive liabilities would result in a net decline in fair value of approximately $420 million ($530 
million pretax) related to continuing non-experience-rated products. Reductions in the fair value of investment securities 
would be reflected as an unrealized loss in equity, as the Company classifies these securities as available for sale. The 
Company does not record liabilities at fair value.

Based on overall exposure to interest rate risk and equity price risk, the Company believes that these changes in market rates 
and prices would not materially affect consolidated near-term financial condition, operating results or cash flows as of 
December 31, 2019.

Evaluation of Foreign Currency and Commodity Risk

As of each of December 31, 2019 and 2018, the Company did not have any material foreign currency exchange rate or 
commodity derivative instruments in place and believes its exposure to foreign currency exchange rate risk and commodity 
price risk is not material.

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Evaluation of Operational Risks

The Company also faces certain operational risks, including risks related to information security, including cybersecurity. The 
Company and its vendors have experienced and continue to experience a variety of cyber attacks, and the Company and its 
vendors expect to continue to experience cyber attacks going forward. Among other things, the Company and its vendors have 
experienced automated attempts to gain access to public facing networks, brute force, SYN flood and distributed denial of 
service attacks, attempted malware infections, vulnerability scanning, ransomware attacks, spear-phishing campaigns, mass 
reconnaissance attempts, injection attempts, phishing, PHP injection and cross-site scripting. The Company also has seen an 
increase in attacks designed to obtain access to consumers’ accounts using illegally obtained demographic information. The 
Company is dedicating and will continue to dedicate significant resources and incur significant expenses to maintain and update 
on an ongoing basis the systems and processes that are designed to mitigate the information security risks it faces and protect 
the security of its computer systems, software, networks and other technology assets against attempts by unauthorized parties to 
obtain access to confidential information, destroy data, disrupt or degrade service, sabotage systems or cause other damage. The 
impact of cyber attacks has not been material to the Company’s operations or operating results through December 31, 2019. The 
Board and its Audit Committee (the “Audit Committee”) and Nominating and Corporate Governance Committee are regularly 
informed regarding the Company’s information security policies, practices and status.

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Item 8.  Financial Statements and Supplementary Data.

Index to Consolidated Financial Statements

Consolidated Statements of Operations for the years ended December 31, 2019, 2018 and 2017

Consolidated Statements of Comprehensive Income (Loss) for the years ended December 31, 2019, 2018 and 2017

Consolidated Balance Sheets as of December 31, 2019 and 2018

Consolidated Statements of Cash Flows for the years ended December 31, 2019, 2018 and 2017

Consolidated Statements of Shareholders’ Equity for the years ended December 31, 2019, 2018 and 2017

Notes to Consolidated Financial Statements

Reports of Independent Registered Public Accounting Firm

Quarterly Financial Information (Unaudited)

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96

97

164

168

90

Consolidated Statements of Operations

For the Years Ended December 31,

2019

2018

2017

$

185,236

$

183,910

$

180,063

63,122

7,407
1,011

8,184

1,825

660

3,558

1,144

21

256,776

194,579

184,786

158,719

52,529

—

33,541

244,789

11,987
3,035

79
(124)
8,997

2,366

6,631

—

6,631

3

6,634

$

5.10

$

— $

5.10

$

1,301

5.08

$

— $

5.08

1,305

2.00

$

$

$

$

$

$

$

$

$

$

156,447

153,448

6,594

6,149

21,368

190,558

2,810

181

18,809

175,248

4,021

2,619

—
(4)
1,406

2,002
(596)
—
(596)
2
(594) $

(0.57) $
— $
(0.57) $
1,044

(0.57) $
— $
(0.57) $
1,044

2.00

$

9,538

1,062

—

208

8,268

1,637

6,631
(8)
6,623
(1)
6,622

6.48
(0.01)
6.47

1,020

6.45
(0.01)
6.44

1,024

2.00

In millions, except per share amounts

Revenues:

Products

Premiums

Services

Net investment income

Total revenues

Operating costs:

Cost of products sold

Benefit costs

Goodwill impairments

Operating expenses

Total operating costs

Operating income
Interest expense

Loss on early extinguishment of debt

Other expense (income)

Income before income tax provision

Income tax provision

Income (loss) from continuing operations

Loss from discontinued operations, net of tax

Net income (loss)

Net (income) loss attributable to noncontrolling interests

Net income (loss) attributable to CVS Health

Basic earnings (loss) per share:

Income (loss) from continuing operations attributable to CVS Health

Loss from discontinued operations attributable to CVS Health

Net income (loss) attributable to CVS Health

Weighted average basic shares outstanding

Diluted earnings (loss) per share:

Income (loss) from continuing operations attributable to CVS Health

Loss from discontinued operations attributable to CVS Health

Net income (loss) attributable to CVS Health

Weighted average diluted shares outstanding

Dividends declared per share

See accompanying notes to consolidated financial statements.

91

 
 
 
Consolidated Statements of Comprehensive Income (Loss)

In millions

Net income (loss)

Other comprehensive income (loss), net of tax:

Net unrealized investment gains

Foreign currency translation adjustments

Net cash flow hedges

Pension and other postretirement benefits

Other comprehensive income

Comprehensive income (loss)

Comprehensive (income) loss attributable to noncontrolling interests

For the Years Ended December 31,

2019

2018

2017

$

6,631

$

(596) $

6,623

677

162
(33)
111

917

7,548

3

97
(29)
330
(124)
274
(322)
2
(320) $

—
(2)
(10)
152

140

6,763
(1)
6,762

Comprehensive income (loss) attributable to CVS Health

$

7,551

$

See accompanying notes to consolidated financial statements.

92

Consolidated Balance Sheets

In millions, except per share amounts
Assets:

Cash and cash equivalents
Investments
Accounts receivable, net
Inventories
Other current assets
Total current assets
Long-term investments
Property and equipment, net
Operating lease right-of-use assets
Goodwill
Intangible assets, net
Separate accounts assets
Other assets

Total assets

Liabilities:

Accounts payable
Pharmacy claims and discounts payable
Health care costs payable
Policyholders’ funds
Accrued expenses
Other insurance liabilities
Current portion of operating lease liabilities
Short-term debt
Current portion of long-term debt

Total current liabilities

Long-term operating lease liabilities
Long-term debt
Deferred income taxes
Separate accounts liabilities
Other long-term insurance liabilities
Other long-term liabilities

Total liabilities
Commitments and contingencies (Note 16)

Shareholders’ equity:

Preferred stock, par value $0.01: 0.1 shares authorized; none issued or outstanding
Common stock, par value $0.01: 3,200 shares authorized; 1,727 shares issued and 1,302
shares outstanding at December 31, 2019 and 1,720 shares issued and 1,295 shares
outstanding at December 31, 2018 and capital surplus

Treasury stock, at cost: 425 shares at both December 31, 2019 and 2018
Retained earnings
Accumulated other comprehensive income
Total CVS Health shareholders’ equity

Noncontrolling interests
Total shareholders’ equity
Total liabilities and shareholders’ equity

See accompanying notes to consolidated financial statements.

93

At December 31,

2019

2018

$

$

$

5,683
2,373
19,617
17,516
5,113
50,302
17,314
12,044
20,860
79,749
33,121
4,459
4,600
222,449

10,492
13,601
6,879
2,991
12,133
1,830
1,596
—
3,781
53,303
18,926
64,699
7,294
4,459
7,436
2,162
158,279

4,059
2,522
17,631
16,450
4,581
45,243
15,732
11,349
—
78,678
36,524
3,884
5,046
196,456

8,925
11,365
6,147
2,939
10,711
1,937
—
720
1,265
44,009
—
71,444
7,677
3,884
8,119
2,780
137,913

—

—

45,972
(28,235)
45,108
1,019
63,864
306
64,170
222,449

$

45,440
(28,228)
40,911
102
58,225
318
58,543
196,456

$

$

$

$

 
Consolidated Statements of Cash Flows

In millions

Cash flows from operating activities:

Cash receipts from customers

Cash paid for inventory and prescriptions dispensed by retail network
pharmacies

Insurance benefits paid

Cash paid to other suppliers and employees

Interest and investment income received

Interest paid

Income taxes paid

Net cash provided by operating activities

Cash flows from investing activities:

Proceeds from sales and maturities of investments
Purchases of investments

Purchases of property and equipment

Proceeds from sale-leaseback transactions

Acquisitions (net of cash acquired)

Proceeds from sale of subsidiary and other assets

Other

Net cash used in investing activities

Cash flows from financing activities:

Net repayments of short-term debt

Proceeds from issuance of long-term debt

Repayments of long-term debt

Derivative settlements

Repurchase of common stock

Dividends paid

Proceeds from exercise of stock options

Payments for taxes related to net share settlement of equity awards

Other

Net cash provided by (used in) financing activities

Effect of exchange rate changes on cash, cash equivalents and restricted cash

Net increase (decrease) in cash, cash equivalents and restricted cash

Cash, cash equivalents and restricted cash at the beginning of the period

For the Years Ended December 31,

2019

2018

2017

$

248,393

$

186,519

$

176,594

(149,655)
(52,242)
(28,932)
955
(2,954)
(2,717)
12,848

(148,981)
(6,897)
(17,234)
644
(2,803)
(2,383)
8,865

(146,469)
(2,810)
(15,348)
21
(1,072)
(2,909)
8,007

7,049
(7,534)
(2,457)
5
(444)
—

42
(3,339)

(720)
3,736
(8,336)
(25)
—
(2,603)
210
(112)
—
(7,850)
—

1,659

4,295

817
(692)
(2,037)
—
(42,226)
832

21
(43,285)

(556)
44,343
(5,522)
446

—
(2,038)
242
(97)
1

36,819
(4)
2,395

1,900

61
(137)
(1,918)
265
(1,181)
—

33
(2,877)

(598)
—

—

—
(4,361)
(2,049)
329
(71)
(1)
(6,751)
1
(1,620)
3,520

1,900

Cash, cash equivalents and restricted cash at the end of the period

$

5,954

$

4,295

$

94

 
 
In millions

Reconciliation of net income (loss) to net cash provided by operating activities:

For the Years Ended December 31,

2019

2018

2017

Net income (loss)

$

6,631

$

(596) $

6,623

Adjustments required to reconcile net income (loss) to net cash provided by
operating activities:

Depreciation and amortization

Goodwill impairments

Loss on settlement of defined benefit pension plans

Stock-based compensation

Loss on sale of subsidiary

Loss on early extinguishment of debt

Deferred income taxes

Other noncash items

Change in operating assets and liabilities, net of effects from acquisitions:

Accounts receivable, net
Inventories

Other assets

Accounts payable and pharmacy claims and discounts payable

Health care costs payable and other insurance liabilities

Other liabilities

4,371

—

—

453

205

79
(654)
264

(2,158)
(1,075)
(614)
3,550

320

1,476

2,718

6,149

—

280

86

—

87

253

(1,139)
(1,153)
(3)
2,329
(311)
165

Net cash provided by operating activities

$

12,848

$

8,865

$

See accompanying notes to consolidated financial statements.

2,479

181

187

234

—

—
(1,334)
53

(941)
(514)
(338)
1,710

—
(333)
8,007

95

Consolidated Statements of Shareholders’ Equity

Attributable to CVS Health

Number of shares
outstanding

Common
Shares

Treasury
Shares (1)

Common 
Stock and
Capital
Surplus (2)

Treasury
Stock (1)

Retained
Earnings

Accumulated
Other 
Comprehensive
Income (Loss)

Total
CVS Health 
Shareholders’ 
Equity

Noncontrolling 
Interests 

Total 
Shareholders’
Equity

1,705

(644) $

31,635 $ (33,483) $ 38,983 $

(305) $

36,830 $

4 $

—

—

7

—

—

—

—

—

—

(54)

—

—

—

—

461

—

—

—

—

—

—

(4,313)

6,622

—

—

—

—

—

(2,049)

—

—

140

—

—

—

—

6,622

140

461

(4,313)

(2,049)

—

1,712

(698)

32,096

(37,796)

43,556

(165)

37,691

—

—

—

—

8

—

—

—

—

—

—

—

274

—

(1)

—

—

—

—

—

—

—

—

—

12,923

9,561

421

—

—

—

—

—

7

—

—

—

(6)

(594)

—

—

—

—

(2,045)

—

—

1,720

(425)

45,440

(28,228)

40,911

—

—

—

7

—

—

—

—

—

—

2

(2)

—

—

—

—

—

532

—

—

—

—

—

—

—

(7)

—

—

178

6,634

—

—

—

(2,615)

—

(7)

—

274

—

—

—

—

—

—

102

—

—

917

—

—

—

—

(13)

(594)

274

22,484

421

7

(2,045)

—

—

58,225

178

6,634

917

532

(7)

(2,615)

—

1

—

—

—

—

(1)

4

—

(2)

—

—

—

—

—

329

(13)

318

—

(3)

—

—

—

—

(9)

36,834

6,623

140

461

(4,313)

(2,049)

(1)

37,695

(13)

(596)

274

22,484

421

7

(2,045)

329

(13)

58,543

178

6,631

917

532

(7)

(2,615)

(9)

1,727

(425) $

45,972 $ (28,235) $ 45,108 $

1,019 $

63,864 $

306 $

64,170

In millions

Balance at December
31, 2016

Net income

Other comprehensive
income (Note 13)

Stock option activity,
stock awards and other

Purchase of treasury
shares, net of ESPP
issuances
Common stock dividends

Other decreases in
noncontrolling interests
Balance at December
31, 2017

Adoption of new 
accounting standards (3)
Net loss

Other comprehensive
income (Note 13)

Common shares issued to
acquire Aetna

Stock option activity,
stock awards and other

Purchase of treasury
shares, net of ESPP
issuances
Common stock dividends

Acquisition of
noncontrolling interests

Other decreases in
noncontrolling interests
Balance at December
31, 2018

Adoption of new
accounting standards
(Note 1)

Net income (loss)

Other comprehensive
income (Note 13)

Stock option activity,
stock awards and other

Purchase of treasury
shares, net of ESPP
issuances
Common stock dividends

Other decreases in
noncontrolling interests
Balance at December
31, 2019

_____________________________________________

(1)  Treasury shares include 1 million shares held in trust for each of the years ended December 31, 2019, 2018 and 2017. Treasury stock includes $29 million 
related to shares held in trust for each of the years ended December 31, 2019 and 2018 and $31 million related to shares held in trust for the year ended 
December 31, 2017. See Note 1 ‘‘Significant Accounting Policies’’ for additional information.

(2)  Common stock and capital surplus includes the par value of common stock of $17 million as of December 31, 2019, 2018 and 2017.
(3)  Reflects the adoption of Accounting Standards Update (“ASU”) 2014-09, Revenue from Contracts with Customers, which resulted in a reduction to retained 
earnings of $13 million and the adoption of ASU 2018-02, Income Statement - Reporting Comprehensive Income (Topic 220): Reclassification of Certain 
Tax Effects from Accumulated Other Comprehensive Income, which resulted in a reduction to accumulated other comprehensive income of $7 million and 
an increase to retained earnings of $7 million, each during the year ended December 31, 2018.

See accompanying notes to consolidated financial statements.

96

Notes to Consolidated Financial Statements

1. 

Significant Accounting Policies 

Description of Business  

CVS Health Corporation (“CVS Health”), together with its subsidiaries (collectively, “Company”), has approximately 9,900 
retail locations, approximately 1,100 walk-in medical clinics, a leading pharmacy benefits manager with approximately 105 
million plan members, a dedicated senior pharmacy care business serving more than one million patients per year and 
expanding specialty pharmacy services. CVS Health also serves an estimated 37 million people through traditional, voluntary 
and consumer-directed health insurance products and related services, including expanding Medicare Advantage offerings and a 
leading standalone Medicare Part D prescription drug plan (“PDP”). The Company believes its innovative health care model 
increases access to quality care, delivers better health outcomes and lowers overall health care costs.

On November 28, 2018 (the “Aetna Acquisition Date”), the Company acquired Aetna Inc. (“Aetna”). As a result of the 
acquisition of Aetna (the “Aetna Acquisition”), the Company added the Health Care Benefits segment. Certain aspects of 
Aetna’s operations, including products for which the Company no longer solicits or accepts new customers, such as large case 
pensions and long-term care insurance products, are included in the Company’s Corporate/Other segment. The consolidated 
financial statements reflect Aetna’s results subsequent to the Aetna Acquisition Date.

Effective for the first quarter of 2019, the Company realigned the composition of its segments to correspond with changes to its 
operating model and reflect how its Chief Operating Decision Maker (the “CODM”) reviews information and manages the 
business. As a result of this realignment, the Company’s SilverScript® PDP moved from the Pharmacy Services segment to the 
Health Care Benefits segment. In addition, the Company moved Aetna’s mail order and specialty pharmacy operations from the 
Health Care Benefits segment to the Pharmacy Services segment. Segment financial information has been retrospectively 
adjusted to reflect these changes. 

The Company has four reportable segments: Pharmacy Services, Retail/LTC, Health Care Benefits and Corporate/Other, which 
are described below. 

Pharmacy Services Segment
The Pharmacy Services segment provides a full range of pharmacy benefit management (“PBM”) solutions, including plan 
design offerings and administration, formulary management, retail pharmacy network management services, mail order 
pharmacy, specialty pharmacy and infusion services, clinical services, disease management services and medical spend 
management. The Pharmacy Services segment’s clients are primarily employers, insurance companies, unions, government 
employee groups, health plans, PDPs, Medicaid managed care plans, plans offered on public health insurance exchanges 
(“Public Exchanges”) and private health insurance exchanges, other sponsors of health benefit plans and individuals throughout 
the United States. The Pharmacy Services segment operates retail specialty pharmacy stores, specialty mail order pharmacies, 
mail order dispensing pharmacies, compounding pharmacies and branches for infusion and enteral nutrition services. 

Retail/LTC Segment
The Retail/LTC segment sells prescription drugs and a wide assortment of general merchandise, including over-the-counter 
drugs, beauty products, cosmetics and personal care products, provides health care services through its MinuteClinic® walk-in 
medical clinics and conducts long-term care pharmacy (“LTC”) operations, which distribute prescription drugs and provide 
related pharmacy consulting and other ancillary services to chronic care facilities and other care settings. As of December 31, 
2019, the Retail/LTC segment operated approximately 9,900 retail locations, approximately 1,100 MinuteClinic® locations as 
well as online retail pharmacy websites, LTC pharmacies and onsite pharmacies. 

Health Care Benefits Segment
The Health Care Benefits segment is one of the nation’s leading diversified health care benefits providers, serving an estimated 
37 million people as of December 31, 2019. The Health Care Benefits segment has the information and resources to help 
members, in consultation with their health care professionals, make more informed decisions about their health care. The Health 
Care Benefits segment offers a broad range of traditional, voluntary and consumer-directed health insurance products and 
related services, including medical, pharmacy, dental and behavioral health plans, medical management capabilities, Medicare 
Advantage and Medicare Supplement plans, PDPs, Medicaid health care management services, workers’ compensation 
administrative services and health information technology products and services. The Health Care Benefit segment’s customers 
include employer groups, individuals, college students, part-time and hourly workers, health plans, health care providers 
(“providers”), governmental units, government-sponsored plans, labor groups and expatriates. The Company refers to insurance 

97

products (where it assumes all or a majority of the risk for medical and dental care costs) as “Insured” and administrative 
services contract products (where the plan sponsor assumes all or a majority of the risk for medical and dental care costs) as 
“ASC.” For periods prior to November 28, 2018 (the Aetna Acquisition Date), the Health Care Benefits segment was comprised 
of the Company’s SilverScript PDP business. 

Corporate/Other Segment
The Company presents the remainder of its financial results in the Corporate/Other segment, which consists of:

•  Management and administrative expenses to support the overall operations of the Company, which include certain aspects 
of executive management and the corporate relations, legal, compliance, human resources, information technology and 
finance departments, expenses associated with the Company’s investments in its transformation and Enterprise 
modernization programs and acquisition-related transaction and integration costs; and

• 

Products for which the Company no longer solicits or accepts new customers such as its large case pensions and long-term 
care insurance products.

Basis of Presentation

The accompanying consolidated financial statements of CVS Health and its subsidiaries have been prepared in accordance with 
accounting principles generally accepted in the United States of America (“GAAP”). The consolidated financial statements 
include the accounts of the Company and its majority-owned subsidiaries and variable interest entities (“VIEs”) for which the 
Company is the primary beneficiary. All material intercompany balances and transactions have been eliminated.

Reclassifications

Certain prior year amounts have been reclassified to conform with the current year presentation.

Use of Estimates

The preparation of financial statements in conformity with GAAP requires management to make estimates and assumptions that 
affect the reported amounts in the consolidated financial statements and accompanying notes. Actual results could differ from 
those estimates. 

Cash and Cash Equivalents

Cash and cash equivalents consist of cash and temporary investments with maturities of three months or less when purchased. 
The Company invests in short-term money market funds, commercial paper and time deposits, as well as other debt securities 
that are classified as cash equivalents within the accompanying consolidated balance sheets, as these funds are highly liquid and 
readily convertible to known amounts of cash. 

Restricted Cash

Restricted cash included in other current assets on the consolidated balance sheets represents amounts held in escrow accounts 
in connection with certain recent acquisitions. Restricted cash included in other assets on the consolidated balance sheets 
represents amounts held in a trust in one of the Company’s captive insurance companies to satisfy collateral requirements 
associated with the assignment of certain insurance policies. All restricted cash is invested in time deposits, money market 
funds or commercial paper. 

The following is a reconciliation of cash and cash equivalents on the consolidated balance sheets to total cash, cash equivalents 
and restricted cash on the consolidated statements of cash flows as of December 31, 2019, 2018 and 2017:

In millions

Cash and cash equivalents

Restricted cash (included in other current assets)

Restricted cash (included in other assets)

2019

2018

2017

$

5,683

$

4,059

$

1,696

—

271

6

230

14

190

Total cash, cash equivalents and restricted cash at the end of the period in the
consolidated statements of cash flows

$

5,954

$

4,295

$

1,900

98

Investments

Debt Securities
Debt securities consist primarily of U.S. Treasury and agency securities, mortgage-backed securities, corporate and foreign 
bonds and other debt securities. Debt securities are classified as either current or long-term investments based on their 
contractual maturities unless the Company intends to sell an investment within the next twelve months, in which case it is 
classified as current on the consolidated balance sheets. Debt securities are classified as available for sale and are carried at fair 
value. See Note 4 ‘‘Fair Value’’ for additional information on how the Company estimates the fair value of these investments.

The cost for mortgage-backed and other asset-backed securities is adjusted for unamortized premiums and discounts, which are 
amortized using the interest method over the estimated remaining term of the securities, adjusted for anticipated prepayments. 

The Company regularly reviews its debt securities to determine whether a decline in fair value below the cost basis or carrying 
value is other-than-temporary. When a debt security is in an unrealized capital loss position, the Company monitors the duration 
and severity of the loss to determine if sufficient market recovery can occur within a reasonable period of time. If a decline in 
the fair value of a debt security is considered other-than-temporary, the cost basis or carrying value of the debt security is 
written down. The write-down is then bifurcated into its credit and non-credit related components. The amount of the credit-
related component is included in the Company’s net income (loss), and the amount of the non-credit related component is 
included in other comprehensive income (loss), unless the Company intends to sell the debt security or it is more likely than not 
that the Company will be required to sell the debt security prior to its anticipated recovery of the debt security’s amortized cost 
basis. Interest is not accrued on debt securities when management believes the collection of interest is unlikely. 

Equity Securities
Equity securities with readily available fair values are measured at fair value with changes in fair value recognized in net 
income (loss).

Mortgage Loans
Mortgage loan investments on the consolidated balance sheets are valued at the unpaid principal balance, net of impairment 
reserves. A mortgage loan may be impaired when it is a problem loan (i.e., more than 60 days delinquent, in bankruptcy or in 
process of foreclosure), a potential problem loan (i.e., high probability of default) or a restructured loan. For impaired loans, a 
specific impairment reserve is established for the difference between the recorded investment in the loan and the estimated fair 
value of the collateral. The Company applies its loan impairment policy individually to all loans in its portfolio.

The impairment evaluation described above also considers characteristics and risk factors attributable to the aggregate 
portfolio. An additional allowance for loan losses is established if it is probable that there will be a credit loss on a group of 
similar mortgage loans. The following characteristics and risk factors are considered when evaluating if a credit loss is probable 
on a group of similar mortgage loans: loan-to-value ratios, property type (e.g., office, retail, apartment, industrial), geographic 
location, vacancy rates and property condition. 

Full or partial impairments of loans are recorded at the time an event occurs affecting the legal status of the loan, typically at the 
time of foreclosure or upon a loan modification giving rise to forgiveness of debt. Interest income on a potential problem loan 
or restructured loan is accrued to the extent it is deemed to be collectible and the loan continues to perform under its original or 
restructured terms. Interest income on problem loans is recognized on a cash basis. Cash payments on loans in the process of 
foreclosure are treated as a return of principal. Mortgage loans with a maturity date or a committed prepayment date within 
twelve months are classified as current on the consolidated balance sheets.

Other Investments
Other investments consist primarily of the following:

• 

Private equity and hedge fund limited partnerships, which are accounted for using the equity method of accounting. Under 
this method, the carrying value of the investment is based on the value of the Company’s equity ownership of the 
underlying investment funds provided by the general partner or manager of the investments, the financial statements of 
which generally are audited. As a result of the timing of the receipt of the valuation information provided by the fund 
managers, these investments are generally reported on up to a three month lag. The Company reviews investments for 
impairment at least quarterly and monitors their performance throughout the year through discussions with the 
administrators, managers and/or general partners. If the Company becomes aware of an impairment of a limited 
partnership’s investments through its review or prior to receiving the limited partnership’s financial statements at the 

99

financial statement date, an impairment will be recognized by recording a reduction in the carrying value of the limited 
partnership with a corresponding charge to net investment income. 

• 

• 

Investment real estate, which is carried on the consolidated balance sheets at depreciated cost, including capital additions, 
net of write-downs for other-than-temporary declines in fair value. Depreciation is calculated using the straight-line method 
based on the estimated useful life of each asset. If any real estate investment is considered held-for-sale, it is carried at the 
lower of its carrying value or fair value less estimated selling costs. The Company generally estimates fair value using a 
discounted future cash flow analysis in conjunction with comparable sales information. At the time of the sale, the 
difference between the sales price and the carrying value is recorded as a realized capital gain or loss. 

Privately-placed equity securities, which are carried on the consolidated balance sheets at cost less impairments, plus or 
minus subsequent adjustments for observable price changes. Additionally, as a member of the Federal Home Loan Bank of 
Boston (“FHLBB”), a subsidiary of the Company is required to purchase and hold shares of the FHLBB. These shares are 
restricted and carried at cost. 

Net Investment Income
Net investment income on the Company’s investments is recorded when earned and is reflected in the Company’s net income 
(loss) (other than net investment income on assets supporting experience-rated products). Experience-rated products are 
products in the large case pensions business where the contract holder, not the Company, assumes investment and other risks, 
subject to, among other things, minimum guarantees provided by the Company. The effect of investment performance on 
experience-rated products is allocated to contract holders’ accounts daily, based on the underlying investment experience and, 
therefore, does not impact the Company’s net income (loss) (as long as the contract’s minimum guarantees are not triggered). 
Net investment income on assets supporting large case pensions’ experience-rated products is included in net investment 
income in the consolidated statements of operations and is credited to contract holders’ accounts through a charge to benefit 
costs.

Realized capital gains and losses on investments (other than realized capital gains and losses on investments supporting 
experience-rated products) are included as a component of net investment income in the consolidated statements of operations. 
Realized capital gains and losses are determined on a specific identification basis. Purchases and sales of debt and equity 
securities and alternative investments are reflected on the trade date. Purchases and sales of mortgage loans and investment real 
estate are reflected on the closing date.

Realized capital gains and losses on investments supporting large case pensions’ experience-rated products are not included in 
realized capital gains and losses in the consolidated statements of operations and instead are credited directly to contract 
holders’ accounts. The contract holders’ accounts are reflected in policyholders’ funds on the consolidated balance sheets.

Unrealized capital gains and losses on investments (other than unrealized capital gains and losses on investments supporting 
experience-rated products) are reflected in shareholders’ equity, net of tax, as a component of accumulated other comprehensive 
income. Unrealized capital gains and losses on investments supporting large case pensions’ experience-rated products are 
credited directly to contract holders’ accounts. The contract holders’ accounts are reflected in policyholders’ funds on the 
consolidated balance sheets.

Derivative Financial Instruments

The Company uses derivative financial instruments in order to manage interest rate and foreign exchange risk and credit 
exposure. The Company’s use of these derivatives is generally limited to hedging risk and has principally consisted of using 
interest rate swaps, treasury rate locks, forward contracts, futures contracts, warrants, put options and credit default swaps.

100

Accounts Receivable

Accounts receivable are stated net of allowances for doubtful accounts, customer credit allowances, contractual allowances and 
estimated terminations. Accounts receivable, net is composed of the following at December 31, 2019 and 2018:

In millions

Trade receivables

Vendor and manufacturer receivables

Premium receivables

Other receivables

   Total accounts receivable, net

2019

     2018

$

6,717

$

7,856

2,663

2,381

6,497

7,315

2,259

1,560

$

19,617

$

17,631

The activity in the allowance for doubtful accounts receivable for the years ended December 31, 2019, 2018 and 2017 is as 
follows:

In millions

Beginning balance

Additions charged to bad debt expense

Write-offs charged to allowance

Ending balance

Inventories 

2019

     2018

2017

$

$

287
111
(79)
319

$

$

162

$

162
(37)
287

$

158

139
(135)
162

Inventories are valued at the lower of cost or net realizable value using the weighted average cost method. Physical inventory 
counts are taken on a regular basis in each retail store and LTC pharmacy, and a continuous cycle count process is the primary 
procedure used to validate the inventory balances on hand in each distribution center and mail facility to ensure that the 
amounts reflected in the consolidated financial statements are properly stated. During the interim period between physical 
inventory counts, the Company accrues for anticipated physical inventory losses on a location-by-location basis based on 
historical results and current physical inventory trends. 

Reinsurance Recoverables 

The Company utilizes reinsurance agreements primarily to: (a) reduce required capital and (b) facilitate the acquisition or 
disposition of certain insurance contracts. Ceded reinsurance agreements permit the Company to recover a portion of its losses 
from reinsurers, although they do not discharge the Company’s primary liability as the direct insurer of the risks reinsured. 
Failure of reinsurers to indemnify the Company could result in losses; however, the Company does not expect charges for 
unrecoverable reinsurance to have a material effect on its consolidated operating results or financial condition. The Company 
evaluates the financial condition of its reinsurers and monitors concentrations of credit risk arising from similar geographic 
regions, activities or economic characteristics of its reinsurers. At December 31, 2019, the Company’s reinsurance recoverables 
consisted primarily of amounts due from third parties that are rated consistent with companies that are considered to have the 
ability to meet their obligations. Reinsurance recoverables are recorded as other current assets or other assets on the 
consolidated balance sheets.

Health Care Contract Acquisition Costs

Insurance products included in the Health Care Benefits segment are cancelable by either the customer or the member monthly 
upon written notice. Acquisition costs related to prepaid health care and health indemnity contracts are generally expensed as 
incurred. Acquisition costs for certain long-duration insurance contracts are deferred and are recorded as other current assets or 
other assets on the consolidated balance sheets and are amortized over the estimated life of the contracts. The amortization of 
deferred acquisition costs is recorded in operating expenses in the consolidated statements of operations. At December 31, 2019 
and 2018, the balance of deferred acquisition costs was $271 million and $22 million, respectively, comprised primarily of 
commissions paid on Medicare Supplement products within the Health Care Benefits segment. 

101

Property and Equipment

Property and equipment is reported at historical cost, net of accumulated depreciation. Property, equipment and improvements 
to leased premises are depreciated using the straight-line method over the estimated useful lives of the assets, or when 
applicable, the term of the lease, whichever is shorter. Estimated useful lives generally range from 1 to 40 years for buildings, 
building improvements and leasehold improvements and 3 to 10 years for fixtures, equipment and internally developed 
software. Repair and maintenance costs are charged directly to expense as incurred. Major renewals or replacements that 
substantially extend the useful life of an asset are capitalized and depreciated. Application development stage costs for 
significant internally developed software projects are capitalized and depreciated. 

Property and equipment consists of the following at December 31, 2019 and 2018: 

In millions

Land

Building and improvements

Fixtures and equipment

Leasehold improvements

Software

Total property and equipment

Accumulated depreciation and amortization

Property and equipment, net

2019

2018

$

1,981

$

4,068

13,807
5,611

3,467

1,872

3,785

13,028

5,384

2,800

28,934
(16,890)
12,044

$

26,869
(15,520)
11,349

$

Depreciation expense (which includes the amortization of property and equipment under finance or capital leases) totaled $1.9 
billion in the year ended December 31, 2019 and $1.7 billion in each of the years ended December 31, 2018 and 2017. See Note 
6 ‘‘Leases’’ for additional information about finance and capital leases. 

Right-of-Use Assets and Lease Liabilities

The Company determines if an arrangement contains a lease at the inception of a contract. Right-of-use assets represent the 
Company’s right to use an underlying asset for the lease term and lease liabilities represent the Company’s obligation to make 
lease payments arising from the lease. Right-of-use assets and lease liabilities are recognized at the commencement date of the 
lease, renewal date of the lease or significant remodeling of the lease space based on the present value of the remaining future 
minimum lease payments. As the interest rate implicit in the Company’s leases is not readily determinable, the Company 
utilizes its incremental borrowing rate, determined by class of underlying asset, to discount the lease payments. The operating 
lease right-of-use assets also include lease payments made before commencement and are reduced by lease incentives. 

The Company’s real estate leases typically contain options that permit renewals for additional periods of up to five years each. 
For real estate leases, the options to extend are not considered reasonably certain at lease commencement because the Company 
reevaluates each lease on a regular basis to consider the economic and strategic incentives of exercising the renewal options and 
regularly opens or closes stores to align with its operating strategy. Generally, the renewal option periods are not included 
within the lease term and the associated payments are not included in the measurement of the right-of-use asset and lease 
liability. Similarly, renewal options are not included in the lease term for non-real estate leases because they are not considered 
reasonably certain of being exercised at lease commencement. Leases with an initial term of 12 months or less are not recorded 
on the balance sheets, and lease expense is recognized on a straight-line basis over the term of the short-term lease.

For real estate leases, the Company accounts for lease components and nonlease components as a single lease component.  
Certain real estate leases require additional payments based on sales volume, as well as reimbursement for real estate taxes, 
common area maintenance and insurance, which are expensed as incurred as variable lease costs. Other real estate leases 
contain one fixed lease payment that includes real estate taxes, common area maintenance and insurance. These fixed payments 
are considered part of the lease payment and included in the right-of-use assets and lease liabilities.

See Note 6 ‘‘Leases’’ for additional information about right-of-use assets and lease liabilities. 

102

    
Goodwill 

The Company accounts for business combinations using the acquisition method of accounting, which requires the excess cost 
of an acquisition over the fair value of net assets acquired and identifiable intangible assets to be recorded as goodwill. 
Goodwill is not amortized, but is subject to impairment reviews annually, or more frequently if necessary, as further described 
below. See Note 5 ‘‘Goodwill and Other Intangibles’’ for additional information about goodwill. 

Intangible Assets

The Company’s identifiable intangible assets consist primarily of trademarks, trade names, customer contracts/relationships, 
covenants not to compete, technology, provider networks and value of business acquired (“VOBA”). These intangible assets 
arise primarily from the determination of their respective fair market values at the date of acquisition. Amounts assigned to 
identifiable intangible assets, and their related useful lives, are derived from established valuation techniques and management 
estimates.

The Company’s definite-lived intangible assets are amortized over their estimated useful lives based upon the pattern of future 
cash flows attributable to the asset. Other than VOBA, definite-lived intangible assets are amortized using the straight-line 
method. VOBA is amortized over the expected life of the acquired contracts in proportion to estimated premiums. Indefinite-
lived intangible assets are not amortized but are tested for impairment annually, or more frequently if necessary, as further 
described in “Long-Lived Asset Impairment” below.

See Note 5 ‘‘Goodwill and Other Intangibles’’ for additional information about intangible assets. 

Long-Lived Asset Impairment

The Company evaluates the recoverability of long-lived assets, excluding goodwill and indefinite-lived intangible assets, which 
are tested for impairment using separate tests described below, whenever events or changes in circumstances indicate that the 
carrying value of such asset may not be recoverable. The Company groups and evaluates these long-lived assets for impairment 
at the lowest level at which individual cash flows can be identified. If indicators of impairment are present, the Company first 
compares the carrying amount of the asset group to the estimated future cash flows associated with the asset group 
(undiscounted and without interest charges). If the estimated future cash flows used in this analysis are less than the carrying 
amount of the asset group, an impairment loss calculation is prepared. The impairment loss calculation compares the carrying 
amount of the asset group to the asset group’s estimated future cash flows (discounted and with interest charges). If required, an 
impairment loss is recorded for the portion of the asset group’s carrying value that exceeds the asset group’s estimated future 
cash flows (discounted and with interest charges). During the year ended December 31, 2019, the Company recorded store 
rationalization charges of $231 million, primarily related to operating lease right-of-use asset impairment charges. See Note 6 
‘‘Leases’’ for additional information about the right-of-use asset impairment charges. During the year ended December 31, 
2018, the Company recognized a $43 million long-lived asset impairment charge, primarily related to the impairment of 
property and equipment. There were no material impairment charges recognized on long-lived assets in the year ended 
December 31, 2017. 

When evaluating goodwill for potential impairment, the Company compares the fair value of its reporting units to their 
respective carrying amounts. The Company estimates the fair value of its reporting units using a combination of a discounted 
cash flow method and a market multiple method. If the carrying amount of a reporting unit exceeds its estimated fair value, an 
impairment loss is recognized in an amount equal to that excess. During the third quarter of 2019, the Company performed its 
required annual goodwill impairment tests and concluded there were no goodwill impairments as of the testing date. See Note 5 
‘‘Goodwill and Other Intangibles’’ for additional information about goodwill impairment charges recorded during the years 
ended December 31, 2018 and 2017. 

Indefinite-lived intangible assets are tested for impairment by comparing the estimated fair value of the asset to its carrying 
value. The Company estimates the fair value of its indefinite-lived trademarks using the relief from royalty method under the 
income approach. If the carrying value of the asset exceeds its estimated fair value, an impairment loss is recognized, and the 
asset is written down to its estimated fair value. There were no impairment losses recognized on indefinite-lived intangible 
assets in any of the years ended December 31, 2019, 2018 or 2017.

103

Separate Accounts

Separate Accounts assets and liabilities related to large case pensions products represent funds maintained to meet specific 
objectives of contract holders who bear the investment risk. These assets and liabilities are carried at fair value. Net investment 
income (including net realized capital gains and losses) accrue directly to such contract holders. The assets of each account are 
legally segregated and are not subject to claims arising from the Company’s other businesses. Deposits, withdrawals and net 
investment income (including net realized and net unrealized capital gains and losses) on Separate Accounts assets are not 
reflected in the consolidated statements of operations or cash flows. Management fees charged to contract holders are included 
in services revenue and recognized over the period earned.

Health Care Costs Payable

Health care costs payable consist principally of unpaid fee-for-service medical, dental and pharmacy claims, capitation costs, 
other amounts due to health care providers pursuant to risk-sharing arrangements related to the Health Care Benefits segment’s 
Insured Commercial, Medicare and Medicaid products and accruals for state assessments. Unpaid health care claims include an 
estimate of payments the Company will make for (i) services rendered to the Company’s Insured members but not yet reported 
to the Company and (ii) claims which have been reported to the Company but not yet paid, each as of the financial statement 
date (collectively, “IBNR”). Health care costs payable also include an estimate of the cost of services that will continue to be 
rendered after the financial statement date if the Company is obligated to pay for such services in accordance with contractual 
or regulatory requirements. Such estimates are developed using actuarial principles and assumptions which consider, among 
other things, historical and projected claim submission and processing patterns, assumed and historical medical cost trends, 
historical utilization of medical services, claim inventory levels, changes in Insured membership and product mix, seasonality 
and other relevant factors. The Company reflects changes in these estimates in benefit costs in the Company’s consolidated 
operating results in the period they are determined. Capitation costs represent contractual monthly fees paid to participating 
physicians and other medical providers for providing medical care, regardless of the volume of medical services provided to the 
Insured member. Amounts due under risk-sharing arrangements are based on the terms of the underlying contracts with the 
providers and consider claims experience under the contracts through the financial statement date.

The Company develops its estimate of IBNR using actuarial principles and assumptions that consider numerous factors. Of 
those factors, the Company considers the analysis of historical and projected claim payment patterns (including claims 
submission and processing patterns) and the assumed health care cost trend rate (the year-over-year change in per member per 
month health care costs) to be the most critical assumptions. In developing its IBNR estimate, the Company consistently applies 
these actuarial principles and assumptions each period, with consideration to the variability of related factors. There have been 
no significant changes to the methodologies or assumptions used to develop the Company’s estimate of IBNR in 2019.

The Company analyzes historical claim payment patterns by comparing claim incurred dates (i.e., the date services were 
provided) to claim payment dates to estimate “completion factors.” The Company uses completion factors predominantly to 
estimate the ultimate cost of claims incurred more than three months before the financial statement date. The Company 
estimates completion factors by aggregating claim data based on the month of service and month of claim payment and 
estimating the percentage of claims incurred for a given month that are complete by each month thereafter. For any given 
month, substantially all claims are paid within six months of the date of service, but it can take up to 48 months or longer after 
the date of service before all of the claims are completely resolved and paid. These historically-derived completion factors are 
then applied to claims paid through the financial statement date to estimate the ultimate claim cost for a given month’s incurred 
claim activity. The difference between the estimated ultimate claim cost and the claims paid through the financial statement date 
represents the Company’s estimate of claims remaining to be paid as of the financial statement date and is included in the 
Company’s health care costs payable. The completion factors the Company uses reflect judgments and possible adjustments 
based on data such as claim inventory levels, claim submission and processing patterns and, to a lesser extent, other factors 
such as changes in health care cost trend rates, changes in Insured membership and changes in product mix. If claims are 
submitted or processed on a faster (slower) pace than prior periods, the actual claims may be more (less) complete than 
originally estimated using the Company’s completion factors, which may result in reserves that are higher (lower) than the 
ultimate cost of claims.

Because claims incurred within three months before the financial statement date are less mature, the Company uses a 
combination of historically-derived completion factors and the assumed health care cost trend rate to estimate the ultimate cost 
of claims incurred for these months. The Company applies its actuarial judgment and places a greater emphasis on the assumed 
health care cost trend rate for the most recent claim incurred dates as these months may be influenced by seasonal patterns and 
changes in membership and product mix.

104

The Company’s health care cost trend rate is affected by changes in per member utilization of medical services as well as 
changes in the unit cost of such services. Many factors influence the health care cost trend rate, including the Company’s ability 
to manage benefit costs through product design, negotiation of favorable provider contracts and medical management programs, 
as well as the mix of the Company’s business. The health status of the Company’s Insured members, aging of the population 
and other demographic characteristics, advances in medical technology and other factors continue to contribute to rising per 
member utilization and unit costs. Changes in health care practices, inflation, new technologies, increases in the cost of 
prescription drugs (including specialty pharmacy drugs), direct-to-consumer marketing by pharmaceutical companies, clusters 
of high-cost cases, claim intensity, changes in the regulatory environment, health care provider or member fraud and numerous 
other factors also contribute to the cost of health care and the Company’s health care cost trend rate.

For each reporting period, the Company uses an extensive degree of judgment in the process of estimating its health care costs 
payable. As a result, considerable variability and uncertainty is inherent in such estimates, particularly with respect to claims 
with claim incurred dates of three months or less before the financial statement date; and the adequacy of such estimates is 
highly sensitive to changes in assumed completion factors and the assumed health care cost trend rates. For each reporting 
period the Company recognizes the actuarial best estimate of health care costs payable considering the potential volatility in 
assumed completion factors and health care cost trend rates, as well as other factors. The Company believes its estimate of 
health care costs payable is reasonable and adequate to cover its obligations at December 31, 2019; however, actual claim 
payments may differ from the Company’s estimates. A worsening (or improvement) of the Company’s health care cost trend 
rates or changes in completion factors from those that the Company assumed in estimating health care costs payable at 
December 31, 2019 would cause these estimates to change in the near term, and such a change could be material.

Each quarter, the Company re-examines previously established health care costs payable estimates based on actual claim 
payments for prior periods and other changes in facts and circumstances. Given the extensive degree of judgment in this 
estimate, it is possible that the Company’s estimates of health care costs payable could develop either favorably (that is, its 
actual benefit costs for the period were less than estimated) or unfavorably. The changes in the Company’s estimate of health 
care costs payable may relate to a prior quarter, prior year or earlier periods. For a roll forward of the Company’s health care 
costs payable, see Note 7 ‘‘Health Care Costs Payable.’’ The Company’s reserving practice is to consistently recognize the 
actuarial best estimate of its ultimate liability for health care costs payable.

Other Insurance Liabilities

Unpaid Claims
Unpaid claims consist primarily of reserves associated with certain short-duration group disability and term life insurance 
contracts, including an estimate for IBNR as of the financial statement date. Reserves associated with certain short-duration 
group disability and term life insurance contracts are based upon the Company’s estimate of the present value of future benefits, 
which is based on assumed investment yields and assumptions regarding mortality, morbidity and recoveries from the U.S. 
Social Security Administration. The Company develops its estimate of IBNR using actuarial principles and assumptions which 
consider, among other things, contractual requirements, claim incidence rates, claim recovery rates, seasonality and other 
relevant factors. The Company discounts certain claim liabilities related to group long-term disability and life insurance waiver 
of premium contracts. The discount rates generally reflect the Company’s expected investment returns for the investments 
supporting all incurral years of these liabilities. The discount rates for retrospectively-rated contracts are set at contractually 
specified levels. The Company’s estimates of unpaid claims are subject to change due to changes in the underlying experience 
of the insurance contracts, changes in investment yields or other factors, and these changes are recorded in current and future 
benefits in the consolidated statements of operations in the period they are determined. The Company estimates its reserve for 
claims IBNR for life products largely based on completion factors. The completion factors used are based on the Company’s 
historical experience and reflect judgments and possible adjustments based on data such as claim inventory levels, claim 
payment patterns, changes in business volume and other factors. If claims are submitted or processed on a faster (slower) pace 
than historical periods, the actual claims may be more (less) complete than originally estimated using completion factors, which 
may result in reserves that are higher (lower) than required to cover future life benefit payments. There have been no significant 
changes to the methodologies or assumptions used to develop the Company’s estimate of unpaid claims IBNR in 2019. As of 
December 31, 2019, unpaid claims balances of $704 million and $1.8 billion were recorded in other insurance liabilities and 
other long-term insurance liabilities, respectively. As of December 31, 2018, unpaid claims balances of $816 million and $1.9 
billion were recorded in other insurance liabilities and other long-term insurance liabilities, respectively.

Substantially all life and disability insurance liabilities have been fully ceded to unrelated third parties through indemnity 
reinsurance agreements; however, the Company remains directly obligated to the policyholders.

105

Future Policy Benefits
Future policy benefits consist primarily of reserves for limited payment pension and annuity contracts and long-term care 
insurance contracts. Reserves for limited payment pension and annuity contracts are computed using actuarial principles that 
consider, among other things, assumptions reflecting anticipated mortality, retirement, expense and interest rate experience. 
Such assumptions generally vary by plan, year of issue and policy duration. Assumed interest rates on such contracts ranged 
from 3.5% to 11.3% in the year ended December 31, 2019 and from the Aetna Acquisition Date through December 31, 2018. 
The Company periodically reviews mortality assumptions against both industry standards and its experience. Reserves for long-
duration long-term care contracts represent the Company’s estimate of the present value of future benefits to be paid to or on 
behalf of policyholders less the present value of future net premiums. The assumed interest rate on such contracts was 5.1% in 
the year ended December 31, 2019 and from the Aetna Acquisition Date through December 31, 2018. The Company’s estimate 
of the present value of future benefits under such contracts is based upon mortality, morbidity and interest rate assumptions. As 
of December 31, 2019, future policy benefits balances of $508 million and $5.6 billion were recorded in other insurance 
liabilities and other long-term insurance liabilities, respectively. As of December 31, 2018, future policy benefits balances of 
$536 million and $6.2 billion were recorded in other insurance liabilities and other long-term insurance liabilities, respectively. 

Premium Deficiency Reserves

The Company evaluates its insurance contracts to determine if it is probable that a loss will be incurred. A premium deficiency 
loss is recognized when it is probable that expected future claims, including maintenance costs (for example, direct costs such 
as claim processing costs), will exceed existing reserves plus anticipated future premiums and reinsurance recoveries. 
Anticipated investment income is considered in the calculation of premium deficiency losses for short-duration contracts. For 
purposes of determining premium deficiency losses, contracts are grouped consistent with the Company’s method of acquiring, 
servicing and measuring the profitability of such contracts. As of December 31, 2019 and 2018, the Company established a 
premium deficiency reserve of $4 million and $16 million, respectively, related to Medicaid products in the Health Care 
Benefits segment. 

Policyholders’ Funds

Policyholders’ funds consist primarily of reserves for pension and annuity investment contracts and customer funds associated 
with certain health contracts. Reserves for such contracts are equal to cumulative deposits less withdrawals and charges plus  
interest credited thereon, net of experience-rated adjustments. In 2019, interest rates for pension and annuity investment 
contracts ranged from 3.5% to 15.0%. From the Aetna Acquisition Date through December 31, 2018, interest rates for pension 
and annuity investment contracts ranged from 3.5% to 13.4%. Reserves for contracts subject to experience rating reflect the 
Company’s rights as well as the rights of policyholders and plan participants. The Company also holds funds for health savings 
accounts (“HSAs”) on behalf of members associated with high deductible health plans. These amounts are held to pay for 
qualified health care expenses incurred by these members. The HSA balances were approximately $2.2 billion and $2.1 billion 
at December 31, 2019 and 2018, respectively, and are reflected in other current assets with a corresponding liability in 
policyholders’ funds. 

Policyholders’ funds liabilities that are expected to be paid within twelve months from the balance sheet date are classified as 
current on the consolidated balance sheets. Policyholders’ funds liabilities that are expected to be paid greater than twelve 
months from the balance sheet date are included in other long-term liabilities on the consolidated balance sheets. 

Self-Insurance Liabilities

The Company is self-insured for certain losses related to general liability, workers’ compensation and auto liability. The 
Company obtains third party insurance coverage to limit exposure from these claims. The Company is also self-insured for 
certain losses related to health and medical liabilities. The Company’s self-insurance accruals, which include reported claims 
and claims incurred but not reported, are calculated using standard insurance industry actuarial assumptions and the Company’s 
historical claims experience. At December 31, 2019 and 2018, self-insurance liabilities totaled $856 million and $865 million, 
respectively, and were recorded as accrued expenses on the consolidated balance sheets.

Foreign Currency Translation and Transactions

For non-U.S. dollar functional currency locations, (i) assets and liabilities are translated at end-of-period exchange rates, (ii) 
revenues and expenses are translated at average exchange rates in effect during the period and (iii) equity is translated at 
historical exchange rates. The resulting cumulative translation adjustments are included as a component of accumulated other 
comprehensive income (loss).

106

For U.S. dollar functional currency locations, foreign currency assets and liabilities are remeasured into U.S. dollars at end-of-
period exchange rates, except for nonmonetary balance sheet accounts which are remeasured at historical exchange rates. 
Revenues and expenses are remeasured at average exchange rates in effect during each period, except for those expenses related 
to the nonmonetary balance sheet amounts which are remeasured at historical exchange rates. Gains or losses from foreign 
currency remeasurement are included in net income (loss).

On July 1, 2019, the Company sold its Brazilian subsidiary, Drogaria Onofre Ltda. (“Onofre”) for an immaterial amount. The 
Company recorded a loss on the divestiture, which included the elimination of the subsidiary’s $154 million cumulative 
translation adjustment from accumulated other comprehensive income. Gains and losses from foreign currency transactions and 
the effects of foreign currency remeasurements were not material in 2018 or 2017.

Revenue Recognition

Pharmacy Services Segment
The Pharmacy Services segment sells prescription drugs directly through its mail service dispensing pharmacies and indirectly 
through the Company’s retail pharmacy network. The Company’s pharmacy benefit arrangements are accounted for in a manner 
consistent with a master supply arrangement as there are no contractual minimum volumes and each prescription is considered 
a separate purchasing decision and distinct performance obligation transferred at a point in time. PBM services performed in 
connection with each prescription claim are considered part of a single performance obligation which culminates in the 
dispensing of prescription drugs.

The Company recognizes revenue using the gross method at the contract price negotiated with its clients when the Company 
has concluded it controls the prescription drug before it is transferred to the client plan members. The Company controls 
prescriptions dispensed indirectly through its retail pharmacy network because it has separate contractual arrangements with 
those pharmacies, has discretion in setting the price for the transaction and assumes primary responsibility for fulfilling the 
promise to provide prescription drugs to its client plan members while also performing the related PBM services.

Revenues include (i) the portion of the price the client pays directly to the Company, net of any discounts earned on brand name 
drugs or other discounts and refunds paid back to the client (see “Drug Discounts” and “Guarantees” below), (ii) the price paid 
to the Company by client plan members for mail order prescriptions and the price paid to retail network pharmacies by client 
plan members for retail prescriptions (“retail co-payments”), and (iii) claims based administrative fees for retail pharmacy 
network contracts. Sales taxes are not included in revenues. 

The Company recognizes revenue when control of the prescription drugs is transferred to customers, in an amount that reflects 
the consideration the Company expects to be entitled to receive in exchange for those prescription drugs. The Company has 
established the following revenue recognition policies for the Pharmacy Services segment:

•  Revenues generated from prescription drugs sold by mail service dispensing pharmacies are recognized when the 

prescription drug is delivered to the client plan member. At the time of delivery, the Company has performed substantially 
all of its performance obligations under its client contracts and does not experience a significant level of returns or 
reshipments.

•  Revenues generated from prescription drugs sold by third party pharmacies in the Company’s retail pharmacy network and 
associated administrative fees are recognized at the Company’s point-of-sale, which is when the claim is adjudicated by the 
Company’s online claims processing system and the Company has transferred control of the prescription drug and 
performed all of its performance obligations.

For contracts under which the Company acts as an agent or does not control the prescription drugs prior to transfer to the client 
plan member, revenue is recognized using the net method.

Drug Discounts
The Company records revenue net of manufacturers’ rebates earned by its clients based on their plan members’ utilization of 
brand-name formulary drugs. The Company estimates these rebates at period-end based on actual and estimated claims data and 
its estimates of the manufacturers’ rebates earned by its clients. The estimates are based on the best available data at period-end 
and recent history for the various factors that can affect the amount of rebates due to the client. The Company adjusts its rebates 
payable to clients to the actual amounts paid when these rebates are paid or as significant events occur. Any cumulative effect of 
these adjustments is recorded against revenues at the time it is identified. Adjustments generally result from contract changes 
with clients or manufacturers that have retroactive rebate adjustments, differences between the estimated and actual product 
mix subject to rebates, or whether the brand name drug was included in the applicable formulary. The effect of adjustments 

107

between estimated and actual manufacturers’ rebate amounts has not been material to the Company’s operating results or 
financial condition.

Guarantees
The Company also adjusts revenues for refunds owed to clients resulting from pricing guarantees and performance against 
defined service and performance metrics. The inputs to these estimates are not subject to a high degree of subjectivity or 
volatility. The effect of adjustments between estimated and actual pricing and performance refund amounts has not been 
material to the Company’s operating results or financial condition.

Retail/LTC Segment
Retail Pharmacy 
The Company’s retail drugstores recognize revenue at the time the customer takes possession of the merchandise. For pharmacy 
sales, each prescription claim is its own arrangement with the customer and is a performance obligation, separate and distinct 
from other prescription claims under other retail network arrangements. Revenues are adjusted for refunds owed to third party 
payers resulting from pricing guarantees and performance against defined value-based service and performance metrics. The 
inputs to these estimates are not subject to a high degree of subjectivity or volatility. The effect of adjustments between 
estimated and actual pricing and performance refund amounts has not been material to the Company’s operating results or 
financial condition.

Revenue from Company gift cards purchased by customers is deferred as a contract liability until goods or services are 
transferred. Any amounts not expected to be redeemed by customers (i.e., breakage) are recognized based on historical 
redemption patterns.

Customer returns are not material to the Company’s operating results or financial condition. Sales taxes are not included in 
revenues.

Loyalty and Other Programs
The Company’s customer loyalty program, ExtraCare®, consists of two components, ExtraSavingsTM and ExtraBucks® 
Rewards. ExtraSavings are coupons that are recorded as a reduction of revenue when redeemed as the Company concluded that 
they do not represent a promise to the customer to deliver additional goods or services at the time of issuance because they are 
not tied to a specific transaction or spending level. 

ExtraBucks Rewards are accumulated by customers based on their historical spending levels. Thus, the Company has 
determined that there is an additional performance obligation to those customers at the time of the initial transaction. The 
Company allocates the transaction price to the initial transaction and the ExtraBucks Rewards transaction based upon the 
relative standalone selling price, which considers historical redemption patterns for the rewards. Revenue allocated to 
ExtraBucks Rewards is recognized as those rewards are redeemed. At the end of each period, unredeemed ExtraBucks Rewards 
are reflected as a contract liability.

The Company also offers a subscription-based membership program, CarePass®, under which members are entitled to a suite of 
benefits delivered over the course of the subscription period, as well as a promotional reward that can be redeemed for future 
goods and services. Subscriptions are paid for on a monthly or annual basis at the time of or in advance of the Company 
delivering the goods and services. Revenue from these arrangements is recognized as the performance obligations are satisfied.

Long-term Care
Revenue is recognized when control of the promised goods or services is transferred to customers in an amount that reflects the 
consideration the Company expects to be entitled to receive in exchange for those goods or services. Each prescription claim 
represents a separate performance obligation of the Company, separate and distinct from other prescription claims under 
customer arrangements. A significant portion of Long-term Care revenue from sales of pharmaceutical and medical products is 
reimbursed by the federal Medicare Part D program and, to a lesser extent, state Medicaid programs. The Company monitors its 
revenues and receivables from these reimbursement sources, as well as long-term care facilities and other third party insurance 
payors, and reduces revenue at the revenue recognition date to properly account for the variable consideration due to anticipated 
differences between billed and reimbursed amounts. Accordingly, the total revenues and receivables reported in the Company’s 
consolidated financial statements are recorded at the amount expected to be ultimately received from these payors. 

Patient co-payments associated with Medicare Part D, certain state Medicaid programs, Medicare Part B and certain third party 
payors typically are not collected at the time products are delivered or services are rendered, but are billed to the individuals as 
part of normal billing procedures and subject to normal accounts receivable collections procedures.

108

Walk-In Medical Clinics
For services provided by the Company’s walk-in medical clinics, revenue recognition occurs for completed services provided to 
patients, with adjustments taken for third party payor contractual obligations and patient direct bill historical collection rates.

Health Care Benefits Segment
Health Care Benefits revenue is principally derived from insurance premiums and fees billed to customers. Revenue is 
recognized based on customer billings, which reflect contracted rates per employee and the number of covered employees 
recorded in the Company’s records at the time the billings are prepared. Billings are generally sent monthly for coverage during 
the following month. 

The Company’s billings may be subsequently adjusted to reflect enrollment changes due to member terminations or other 
factors. These adjustments are known as retroactivity adjustments. In each period, the Company estimates the amount of future 
retroactivity and adjusts the recorded revenue accordingly. As information regarding actual retroactivity amounts becomes 
known, the Company refines its estimates and records any required adjustments to revenues in the period in which they arise.

Premium Revenue
Premiums are recognized as revenue in the month in which the enrollee is entitled to receive health care services. Premiums are 
reported net of an allowance for estimated terminations and uncollectible amounts. Additionally, premium revenue subject to 
the Patient Protection and Affordable Care Act and the Health Care and Education Reconciliation Act of 2010’s (as amended, 
collectively, the “ACA’s”) minimum medical loss ratio (“MLR”) rebate requirements is recorded net of the estimated minimum 
MLR rebates for the current calendar year. Premiums related to unexpired contractual coverage periods (unearned premiums) 
are reported as other insurance liabilities on the consolidated balance sheets and recognized as revenue when earned.

Some of the Company’s contracts allow for premiums to be adjusted to reflect actual experience or the relative health status of 
Insured members. Such adjustments are reasonably estimable at the outset of the contract, and adjustments to those estimates 
are made based on actual experience of the customer emerging under the contract and the terms of the underlying contract.

Services Revenue
Services revenue relates to contracts that can include various combinations of services or series of services which generally are 
capable of being distinct and accounted for as separate performance obligations. The Health Care Benefits segment’s services 
revenue primarily consists of the following components:

•  ASC fees are received in exchange for performing certain claim processing and member services for ASC members. ASC 

fee revenue is recognized over the period the service is provided. Some of the Company’s administrative services contracts 
include guarantees with respect to certain functions, such as customer service response time, claim processing accuracy and 
claim processing turnaround time, as well as certain guarantees that a plan sponsor’s benefit claim experience will fall 
within a certain range. With any of these guarantees, the Company is financially at risk if the conditions of the 
arrangements are not met, although the maximum amount at risk typically is limited to a percentage of the fees otherwise 
payable to the Company by the customer involved. Each period the Company estimates its obligations under the terms of 
these guarantees and records its estimate as an offset to services revenues.

•  Workers’ compensation administrative services consist of fee-based managed care services. Workers’ compensation 

administrative services revenue is recognized once the service is provided.

Accounting for Medicare Part D 
Revenues include insurance premiums earned by the Company’s PDPs, which are determined based on the PDP’s annual bid 
and related contractual arrangements with the U.S. Centers for Medicare & Medicaid Services (“CMS”). The insurance 
premiums include a beneficiary premium, which is the responsibility of the PDP member, and can be subsidized by CMS in the 
case of low-income members, and a direct premium paid by CMS. Premiums collected in advance are initially recorded within 
other insurance liabilities and are then recognized ratably as revenue over the period in which members are entitled to receive 
benefits.

Revenues also include a risk-sharing feature of the Medicare Part D program design referred to as the risk corridor. The 
Company estimates variable consideration in the form of amounts payable to, or receivable from, CMS under the risk corridor, 
and adjusts revenue based on calculations of additional subsidies to be received from or owed to CMS at the end of the 
reporting year.

In addition to Medicare Part D premiums, the Company receives additional payments each month from CMS related to 
catastrophic reinsurance, low-income cost sharing subsidies and coverage gap benefits. If the subsidies received differ from the 

109

amounts earned from actual prescriptions transferred, the difference is recorded in either accounts receivable, net or accrued 
expenses.

Disaggregation of Revenue
The following table disaggregates the Company’s revenue by major source in each segment for the years ended December 31, 
2019 and 2018:

In millions
2019

Major goods/services lines:

Pharmacy

Front Store

Premiums

Net investment income

Other

Total

Pharmacy
Services

Retail/
LTC

Health Care
Benefits

Corporate/
Other

Intersegment
Eliminations

Consolidated
Totals

$ 140,896

$ 66,442

$

—

—

—

595

19,422

—

—

744

— $

—

63,031

599

5,974

— $

—

91

412

9

$ 141,491

$ 86,608

$

69,604

$

512

$

(41,439) $
—

—

—

—
(41,439) $

165,899

19,422

63,122

1,011

7,322

256,776

Pharmacy Services distribution channel:

Pharmacy network (1)
Mail choice (2)
Other

Total

2018

Major goods/services lines:

Pharmacy

Front Store

Premiums

Net investment income

Other

Total

$

88,755

52,141

595

$ 141,491

$ 134,216

$ 64,179

$

164

$

— $

—

—

—

520

19,055

—

—

755

—

8,180

58

560

—

4

602

—

$ 134,736

$ 83,989

$

8,962

$

606

$

(33,714) $
—

164,845

19,055

—

—

—
(33,714) $

8,184

660

1,835

194,579

Pharmacy Services distribution channel:

Pharmacy network (1) (3)
Mail choice (2) (3)
Other

Total

$

87,167

47,049

520

$ 134,736

_____________________________________________

(1)  Pharmacy Services pharmacy network is defined as claims filled at retail and specialty retail pharmacies, including the Company’s retail pharmacies and 

LTC pharmacies, but excluding Maintenance Choice® activity, which is included within the mail choice category. Maintenance choice permits eligible 
client plan members to fill their maintenance prescriptions through mail order delivery or at a CVS pharmacy retail store for the same price as mail order.

(2)  Pharmacy Services mail choice is defined as claims filled at a Pharmacy Services mail order facility, which includes specialty mail claims inclusive of 
Specialty Connect® claims picked up at a retail pharmacy, as well as prescriptions filled at the Company’s retail pharmacies under the Maintenance 
Choice program. 

(3)  Certain prior year amounts have been reclassified for consistency with the current period presentation. 

Contract Balances
Contract liabilities primarily represent the Company’s obligation to transfer additional goods or services to a customer for 
which the Company has received consideration, and include ExtraBucks Rewards and unredeemed Company gift cards. The 
consideration received remains a contract liability until goods or services have been provided to the customer. In addition, the 
Company recognizes breakage on Company gift cards based on historical redemption patterns.

110

    
    
    
The following table provides information about receivables and contract liabilities from contracts with customers as of 
December 31, 2019 and 2018:

In millions

Trade receivables (included in accounts receivable, net)

Contract liabilities (included in accrued expenses)

2019

     2018

$

6,717

$

6,497

73

67

During the year ended December 31, 2019, the contract liabilities balance includes increases related to customers’ earnings in 
ExtraBucks Rewards or issuances of Company gift cards and decreases for revenues recognized during the period as a result of 
the redemption of ExtraBucks Rewards or Company gift cards and breakage of Company gift cards. Below is a summary of 
such changes:

In millions

Balance at December 31, 2018

Adoption of ASU 2014-09

Rewards earnings and gift card issuances

Redemption and breakage

Balance at December 31, 2019

Cost of Products Sold

2019

     2018

$

$

67

—

365
(359)
73

$

$

53

17

332
(335)
67

The Company accounts for cost of products sold as follows:

Pharmacy Services Segment
Cost of products sold includes: (i) the cost of prescription drugs sold during the reporting period directly through the 
Company’s mail service dispensing pharmacies and indirectly through the Company’s retail pharmacy network, (ii) shipping 
and handling costs, and (iii) the operating costs of the Company’s mail service dispensing pharmacies and client service 
operations and related information technology support costs including depreciation and amortization. The cost of prescription 
drugs sold component of cost of products sold includes: (i) the cost of the prescription drugs purchased from manufacturers or 
distributors and shipped to members in clients’ benefit plans from the Company’s mail service dispensing pharmacies, net of 
any volume-related or other discounts (see “Vendor Allowances and Purchase Discounts” below) and (ii) the cost of 
prescription drugs sold (including retail co-payments) through the Company’s retail pharmacy network under contracts where 
the Company is the principal, net of any volume-related or other discounts. 

Retail/LTC Segment
Cost of products sold includes: the cost of merchandise sold during the reporting period, including prescription drug costs, and 
the related purchasing costs, warehousing and delivery costs (including depreciation and amortization) and actual and estimated 
inventory losses. 

Vendor Allowances and Purchase Discounts 

The Company accounts for vendor allowances and purchase discounts as follows: 

Pharmacy Services Segment
The Pharmacy Services segment receives purchase discounts on products purchased. Contractual arrangements with vendors, 
including manufacturers, wholesalers and retail pharmacies, normally provide for the Pharmacy Services segment to receive 
purchase discounts from established list prices in one, or a combination, of the following forms: (i) a direct discount at the time 
of purchase, (ii) a discount for the prompt payment of invoices or (iii) when products are purchased indirectly from a 
manufacturer (e.g., through a wholesaler or retail pharmacy), a discount (or rebate) paid subsequent to dispensing. These 
rebates are recognized when prescriptions are dispensed and are generally calculated and billed to manufacturers within 30 days 
of the end of each completed quarter. Historically, the effect of adjustments resulting from the reconciliation of rebates 
recognized to the amounts billed and collected has not been material to the Company’s operating results or financial condition. 
The Company accounts for the effect of any such differences as a change in accounting estimate in the period the reconciliation 
is completed. The Pharmacy Services segment also receives additional discounts under its wholesaler contracts if it exceeds 
contractually defined purchase volumes. In addition, the Pharmacy Services segment receives fees from pharmaceutical 

111

manufacturers for administrative services. Purchase discounts and administrative service fees are recorded as a reduction of cost 
of products sold. 

Retail/LTC Segment
Vendor allowances received by the Retail/LTC segment reduce the carrying cost of inventory and are recognized in cost of 
products sold when the related inventory is sold, unless they are specifically identified as a reimbursement of incremental costs 
for promotional programs and/or other services provided. Amounts that are directly linked to advertising commitments are 
recognized as a reduction of advertising expense (included in operating expenses) when the related advertising commitment is 
satisfied. Any such allowances received in excess of the actual cost incurred also reduce the carrying cost of inventory. The total 
value of any upfront payments received from vendors that are linked to purchase commitments is initially deferred. The 
deferred amounts are then amortized to reduce cost of products sold over the life of the contract based upon purchase volume. 
The total value of any upfront payments received from vendors that are not linked to purchase commitments is also initially 
deferred. The deferred amounts are then amortized to reduce cost of products sold on a straight-line basis over the life of the 
related contract. The total amortization of these upfront payments was not material to the Company’s consolidated financial 
statements in any of the periods presented. 

Health Care Reform

Health Insurer Fee
Since January 1, 2014, the ACA imposes an annual premium-based health insurer fee (“HIF”) for each calendar year payable in 
September which is not deductible for tax purposes. The Company is required to estimate a liability for the HIF at the 
beginning of the calendar year in which the fee is payable with a corresponding deferred asset that is amortized ratably to 
operating expenses over the calendar year. The Company records the liability for the HIF in accrued expenses and records the 
deferred asset in other current assets. There was no expense related to the HIF in 2019 and 2017, since the HIF was temporarily 
suspended for each of those periods. In 2018, operating expenses included $157 million related to the Company’s share of the 
HIF. The HIF applies for 2020, and in December 2019, the HIF was repealed for calendar years after 2020. 

Risk Adjustment 
The ACA established a permanent risk adjustment program to transfer funds from qualified individual and small group 
insurance plans with below average risk scores to plans with above average risk scores. Based on the risk of the Company’s 
qualified plan members relative to the average risk of members of other qualified plans in comparable markets, as defined by 
the ACA, the Company estimates its ultimate risk adjustment receivable (recorded in accounts receivable) or payable (recorded 
in accrued expenses) for the current calendar year and reflects the pro-rata year-to-date impact as an adjustment to premium 
revenue. 

Advertising Costs 

Advertising costs, which are reduced by the portion funded by vendors, are expensed when the related advertising takes place. 
Net advertising costs, which are included in operating expenses, were $396 million, $364 million and $230 million in 2019, 
2018 and 2017, respectively. 

Stock-Based Compensation

Stock-based compensation is measured at the grant date based on the fair value of the award and is recognized as an expense 
over the applicable requisite service period of the stock award (generally 3 to 5 years) using the straight-line method. 

Income Taxes

The Company accounts for income taxes under the asset and liability method, which requires the recognition of deferred tax 
assets and liabilities for the expected future tax consequences of events that have been included in the consolidated financial 
statements. Under this method, deferred tax assets and liabilities are determined on the basis of the differences between the 
consolidated financial statements and tax basis of assets and liabilities using enacted tax rates in effect for the year or years in 
which the differences are expected to reverse. The effect of a change in the tax rates on deferred tax assets and liabilities is 
recognized in income in the period that includes the enactment date of such change.

The Tax Cuts and Jobs Act (the “TCJA”) was enacted on December 22, 2017. Among numerous changes to existing tax laws, 
the TCJA permanently reduced the federal corporate income tax rate from 35% to 21% effective January 1, 2018. The effects of 
changes in tax rates on deferred tax balances are required to be taken into consideration in the period in which the changes are 

112

 
enacted, regardless of when they are effective. As a result of the reduction of the corporate income tax rate under the TCJA, the 
Company estimated the revaluation of its net deferred tax liabilities and recorded a provisional income tax benefit of 
approximately $1.5 billion for year ended December 31, 2017. In 2018, the Company completed its process of determining the 
TCJA’s final impact and recorded an additional income tax benefit of $100 million.

The Company recognizes deferred tax assets to the extent that it believes these assets are more likely than not to be realized. In 
making such a determination, the Company considers all available positive and negative evidence, including future reversals of 
existing taxable temporary differences, projected future taxable income, tax planning strategies, and the Company’s recent 
operating results. The Company establishes a valuation allowance when it does not consider it more likely than not that a 
deferred tax asset will be recovered. 

The Company records uncertain tax positions on the basis of a two-step process whereby (1) the Company determines whether 
it is more likely than not that the tax positions will be sustained on the basis of the technical merits of the position and (2) for 
those tax positions that meet the more-likely-than-not recognition threshold, the Company recognizes the largest amount of tax 
benefit that is more than 50% likely to be realized upon ultimate settlement with the related tax authority. 

Interest and/or penalties related to uncertain tax positions are recognized in the income tax provision. 

Measurement of Defined Benefit Pension and Other Postretirement Employee Benefit Plans

The Company sponsors defined benefit pension plans (“pension plans”) and other postretirement employee benefit plans 
(“OPEB plans”) for its employees and retirees. The Company recognizes the funded status of its pension and OPEB plans on 
the consolidated balance sheets based on the year-end measurements of plan assets and benefit obligations. When the fair value 
of plan assets are in excess of the plan benefit obligations, the amounts are reported in other current assets and other assets. 
When the fair value of plan benefit obligations are in excess of plan assets, the amounts are reported in accrued expenses and 
other long-term liabilities based on the amount by which the actuarial present value of benefits payable in the next twelve 
months included in the benefit obligation exceeds the fair value of plan assets. The net periodic benefit costs for the Company’s 
pension and OPEB plans do not contain a service cost component as these plans have been frozen for an extended period of 
time. Non-service cost components of pension and postretirement benefit cost are included in other expense (income) in the 
consolidated statements of operations.

Earnings (Loss) per Common Share

Earnings (loss) per share is computed using the two-class method. The Company calculates basic earnings (loss) per share 
based on the weighted average number of common shares outstanding for the period. See Note 14 ‘‘Earnings (Loss) Per Share’’ 
for additional information.

Shares Held in Trust

The Company maintains grantor trusts, which held approximately one million shares of its common stock at both December 31, 
2019 and 2018. These shares are designated for use under various employee compensation plans. Since the Company holds 
these shares, they are excluded from the computation of basic and diluted shares outstanding. 

Variable Interest Entities

The Company has investments in (i) a generic pharmaceutical sourcing entity, (ii) certain hedge fund and private equity 
investments and (iii) certain real estate partnerships that are considered VIE’s. The Company does not have a future obligation 
to fund losses or debts on behalf of these investments; however, it may voluntarily contribute funds. In evaluating whether the 
Company is the primary beneficiary of a VIE, the Company considers several factors, including whether the Company has (a) 
the power to direct the activities that most significantly impact the VIE’s economic performance and (b) the obligation to 
absorb losses and the right to receive benefits that could potentially be significant to the VIE. 

Variable Interest Entities - Primary Beneficiary
In 2014, the Company and Cardinal Health, Inc. (“Cardinal”) established Red Oak Sourcing, LLC (“Red Oak”), a generic 
pharmaceutical sourcing entity in which the Company and Cardinal each own 50%. The Red Oak arrangement has an initial 
term of 10 years. Under this arrangement, the Company and Cardinal contributed their sourcing and supply chain expertise to 
Red Oak and agreed to source and negotiate generic pharmaceutical supply contracts for both companies through Red Oak; 
however, Red Oak does not own or hold inventory on behalf of either company. No physical assets (e.g., property and 

113

equipment) were contributed to Red Oak by either company, and minimal funding was provided to capitalize Red Oak. The 
Company has determined that it is the primary beneficiary of this VIE because it has the ability to direct the activities of Red 
Oak. Consequently, the Company consolidates Red Oak in its consolidated financial statements within the Retail/LTC segment. 

Cardinal is required to pay the Company 39 quarterly payments beginning in October 2014. As milestones are met, the 
quarterly payments increase. The Company received from Cardinal $183 million during each of the years ended December 31, 
2019, 2018 and 2017. The payments reduce the Company’s carrying value of inventory and are recognized in cost of products 
sold when the related inventory is sold. Revenues associated with Red Oak expenses reimbursed by Cardinal for the years 
ended December 31, 2019, 2018 and 2017, and amounts due to or due from Cardinal at December 31, 2019 and 2018 were 
immaterial.

Variable Interest Entities - Other Variable Interest Holder
The Company has invested in certain VIEs for which it has determined that it is not the primary beneficiary, consisting of the 
following:

•  Hedge fund and private equity investments - The Company invests in hedge fund and private equity investments in order to 

generate investment returns for its investment portfolio supporting its insurance businesses.

•  Real estate partnerships - The Company invests in various real estate partnerships, including those that construct, own and 
manage low-income housing developments. For the low income housing development investments, substantially all of the 
projected benefits to the Company are from tax credits and other tax benefits. 

The Company is not the primary beneficiary of these VIEs because the nature of the Company’s involvement with the activities 
of these VIEs does not give the Company the power to direct the activities that most significantly impact their economic 
performance. The Company records the amount of its investment in these VIEs as long-term investments on the consolidated 
balance sheets and recognizes its share of each VIE’s income or losses in net income (loss). The Company’s maximum 
exposure to loss from these VIEs is limited to its investment balances as disclosed below and the risk of recapture of previously 
recognized tax credits related to the real estate partnerships, which the Company does not consider significant.

The total amount of other variable interest holder VIE assets included in long-term investments on the consolidated balance 
sheets at December 31, 2019 and 2018 was as follows:

In millions

Hedge fund investments

Private equity investments

Real estate partnerships

Total

Related Party Transactions

2019

2018

$

$

$

271

538

212

270

524

275

1,021

$

1,069

The Company has an equity method investment in SureScripts, LLC (“SureScripts”), which operates a clinical health 
information network. The Company utilizes this clinical health information network in providing services to its client plan 
members and retail customers. The Company expensed fees for the use of this network of $32 million, $45 million and $35 
million in the years ended December 31, 2019, 2018 and 2017, respectively. The Company’s investment in and equity in the 
earnings of SureScripts for all periods presented is immaterial.

The Company has an equity method investment in Heartland Healthcare Services (“Heartland”). Heartland operates several 
LTC pharmacies in four states. Heartland paid the Company $96 million, $135 million and $139 million for pharmaceutical 
inventory purchases during the years ended December 31, 2019, 2018 and 2017, respectively. Additionally, the Company 
performs certain collection functions for Heartland and then passes those customer cash collections back to Heartland. The 
Company’s investment in and equity in the earnings of Heartland for all periods presented is immaterial.

During the year ended December 31, 2019, the Company made a charitable contribution of $30 million to the CVS Health 
Foundation, a non-profit entity that focuses on health, education and community involvement programs. The charitable 
contribution will fund future charitable giving and was recorded as an operating expense in the consolidated statement of 
operations for the year ended December 31, 2019.

114

    
Discontinued Operations

In connection with certain business dispositions completed between 1995 and 1997, the Company retained guarantees on store 
lease obligations for a number of former subsidiaries, including Linens ‘n Things and Bob’s Stores, each of which subsequently 
filed for bankruptcy. The Company’s loss from discontinued operations primarily includes lease-related costs that the Company 
believes it will likely be required to satisfy pursuant to its Linens ‘n Things and Bob’s Stores lease guarantees. See “Lease 
Guarantees” in Note 16 ‘‘Commitments and Contingencies’’ for more information. 

Results from discontinued operations were immaterial for the years ended December 31, 2019 and 2018. Below is a summary 
of the results of discontinued operations for the year ended December 31, 2017: 

In millions

Loss from discontinued operations

Income tax benefit

Loss from discontinued operations, net of tax

New Accounting Pronouncements Recently Adopted 

2017

(13)
5
(8)

$

$

Leases
In February 2016, the Financial Accounting Standards Board (the “FASB”) issued ASU 2016-02, Leases (Topic 842). Under 
this accounting standard, lessees are required to recognize a right-of-use asset and a lease liability for virtually all of their leases 
(other than leases that meet the definition of a short-term lease). The liability is equal to the present value of lease payments. 
The asset is based on the liability, subject to certain adjustments, such as for initial direct costs. For income statement purposes, 
a dual model was retained, requiring leases to be classified as either operating or finance leases. Operating leases result in 
straight-line expense (similar to operating leases under the prior accounting standard), while finance leases result in a front-
loaded expense pattern (similar to capital leases under the prior accounting standard). Lessor accounting is similar to the prior 
model, but updated to align with certain changes to the lessee model (e.g., certain definitions, such as initial direct costs, have 
been updated) and the new revenue recognition standard that was adopted in 2018. 

The Company adopted this new accounting standard on January 1, 2019 on a modified retrospective basis and applied the new 
standard to all leases through a cumulative-effect adjustment to beginning retained earnings. As a result, comparative financial 
information has not been restated and continues to be reported under the accounting standards in effect for those periods. The 
Company elected the package of practical expedients permitted under the transition guidance within the new standard, which 
includes, among other things, the ability to carry forward the existing lease classification. On January 1, 2019, the Company 
recorded an after-tax transition adjustment to increase retained earnings by approximately $178 million ($241 million prior to 
tax effect). The new standard had a material impact on the Company’s consolidated balance sheet, but did not materially impact 
the Company’s consolidated operating results and had no impact on the Company’s cash flows. 

115

Impact of New Lease Standard on Balance Sheet Line Items
As a result of applying the new lease accounting standard using a modified retrospective method, the following adjustments 
were made to accounts on the consolidated balance sheet as of January 1, 2019:

In millions

Consolidated Balance Sheets:

Other current assets

Total current assets

Property and equipment, net

Operating lease right-of-use assets

Intangible assets, net

Other assets

Total assets

Accrued expenses

Current portion of operating lease liabilities

Current portion of long-term debt

Total current liabilities

Long-term operating lease liabilities

Long-term debt

Deferred income taxes

Other long-term liabilities

Total liabilities

Retained earnings

Total CVS Health shareholders’ equity

Total shareholders’ equity

Impact of Change in Accounting Policy

As Reported
December 31, 2018

Adjustments

As Adjusted
January 1, 2019

$

4,581

$

45,243

11,349

—

36,524

5,046

196,456

10,711

—

1,265

44,009

—

71,444

7,677

2,780

137,913

40,911

58,225

58,543

(48) $
(48)
11

20,987
(217)
(521)
20,212
(52)
1,803

2

1,753

18,832
(96)
63
(518)
20,034

178

178

178

4,533

45,195

11,360

20,987

36,307

4,525

216,668

10,659

1,803

1,267

45,762

18,832

71,348

7,740

2,262

157,947

41,089

58,403

58,721

Accounting for Interest Associated with the Purchase of Callable Debt Securities
In March 2017, the FASB issued ASU 2017-08, Accounting for Interest Associated with the Purchase of Callable Debt 
Securities (Topic 310). Under this standard, premiums on callable debt securities are amortized to the earliest call date rather 
than to the contractual maturity date. Callable debt securities held at a discount will continue to be amortized to the contractual 
maturity date. The Company adopted this new accounting standard on January 1, 2019 on a modified retrospective basis and 
recorded an immaterial cumulative effect adjustment from accumulated other comprehensive income to retained earnings on the 
consolidated balance sheet.

New Accounting Pronouncements Not Yet Adopted

Measurement of Credit Losses on Financial Instruments
In June 2016, the FASB issued ASU 2016-13, Financial Instruments - Credit Losses (Topic 326). This standard requires the use 
of a forward-looking expected credit loss impairment model for trade and other receivables, held-to-maturity debt securities, 
loans and other instruments. This standard also requires impairments and recoveries for available-for-sale debt securities to be 
recorded through an allowance account and revises certain disclosure requirements. The Company adopted this new accounting 
standard on January 1, 2020. The Company adopted the credit loss impairment model on a modified retrospective basis and 
recorded an immaterial cumulative effect adjustment to retained earnings as of the adoption date. The Company adopted the 
available-for-sale debt security impairment model on a prospective basis. The adoption of this standard did not have a material 
impact on the Company’s consolidated operating results, cash flows or financial condition.

Customer’s Accounting for Implementation Costs Incurred in a Cloud Computing Arrangement that is a Service Contract
In August 2018, the FASB issued ASU 2018-15, Intangibles - Goodwill and other - Internal-Use Software (Topic 350-40): 
Customer’s Accounting for Implementation Costs Incurred in a Cloud Computing Arrangement that is a Service Contract. This 
standard requires a customer in a cloud computing arrangement that is a service contract to follow the internal-use software 
guidance in Topic 350-40 to determine which implementation costs to capitalize as assets. The Company adopted this new 

116

accounting guidance on January 1, 2020 on a prospective basis. The implementation of this standard is not expected to have a 
material impact on the Company’s consolidated operating results, cash flows, financial condition or related disclosures.

Targeted Improvements to the Accounting for Long-Duration Insurance Contracts
In August 2018, the FASB issued ASU 2018-12, Targeted Improvements to the Accounting for Long-Duration Contracts (Topic 
944). This standard requires the Company to review cash flow assumptions for its long-duration insurance contracts at least 
annually and recognize the effect of changes in future cash flow assumptions in net income (loss). This standard also requires 
the Company to update discount rate assumptions quarterly and recognize the effect of changes in these assumptions in other 
comprehensive income. The rate used to discount the Company’s liability for future policy benefits will be based on an estimate 
of the yield for an upper-medium grade fixed-income instrument with a duration profile matching that of the Company’s 
liabilities. In addition, this standard changes the amortization method for deferred acquisition costs and requires additional 
disclosures regarding the long duration insurance contract liabilities in the Company’s interim and annual financial statements. 
The standard is effective for public companies for fiscal years, and interim periods within those fiscal years, beginning after 
December 15, 2021. The Company is currently evaluating the effect that implementation of this standard will have on the 
Company’s consolidated operating results, cash flows, financial condition and related disclosures.

Simplifying the Accounting for Income Taxes 
In December 2019, the FASB issued ASU 2019-12, Simplifying the Accounting for Income Taxes (Topic 740). This standard 
simplifies the accounting for income taxes by eliminating certain exceptions to the guidance in Accounting Standards 
Codification (“ASC”) 740 related to the approach for intraperiod tax allocation, the methodology for calculating income taxes 
in an interim period and the recognition of deferred tax liabilities for outside basis differences. The standard also simplifies 
aspects of the accounting for franchise taxes and enacted changes in tax laws or rates and clarifies the accounting for 
transactions that result in a step-up in the tax basis of goodwill. The standard is effective for public companies for fiscal years, 
and interim periods within those fiscal years, beginning after December 15, 2021. Early adoption is permitted. The Company is 
currently evaluating the effect that implementation of this standard will have on the Company’s consolidated operating results, 
cash flows, financial condition and related disclosures.

117

2. 

Acquisitions and Divestitures 

Acquisition of Aetna

On the Aetna Acquisition Date, the Company acquired 100% of the outstanding shares and voting interests of Aetna for a 
combination of cash and stock. Under the terms of the merger agreement, Aetna shareholders received $145.00 in cash and 
0.8378 CVS Health shares for each Aetna share. The transaction valued Aetna at approximately $212 per share or 
approximately $70 billion. Including the assumption of Aetna’s debt, the total value of the transaction was approximately $78 
billion. The Company financed the cash portion of the purchase price through a combination of cash on hand and by issuing 
approximately $45 billion of new debt, including senior notes and term loans. The Company acquired Aetna to help improve 
the consumer health care experience by combining Aetna’s health care benefits products and services with CVS Health’s 
approximately 9,900 retail locations, approximately 1,100 walk-in medical clinics and integrated pharmacy capabilities with the 
goal of becoming the new, trusted front door to health care.

The transaction has been accounted for using the acquisition method of accounting which requires, among other things, the 
assets acquired and liabilities assumed to be recognized at their fair values at the date of acquisition. The following table 
summarizes the fair values of the assets acquired and liabilities assumed at the date of acquisition:

In millions

Cash and cash equivalents

Accounts receivable

Other current assets

Investments (current and long-term)

Goodwill

Intangible assets

Other assets

Total assets acquired

Health care costs payable

Other current liabilities

Debt (current and long-term)

Deferred income taxes

Other long-term liabilities

Total liabilities assumed

Noncontrolling interests

Total consideration transferred

$

6,565

4,094

3,894

17,984

47,755

22,571

8,249
111,112

5,302

9,940

8,098

4,608

13,078

41,026

320

$

69,766

The Company’s assessment of the fair value of assets acquired and liabilities assumed was finalized during the fourth quarter of 
2019. Measurement period adjustments to assets acquired and liabilities assumed during the year ended December 31, 
2019 primarily were due to additional information received related to certain intangible asset valuations and contingencies and 
the related impact on the accounting for income taxes and goodwill. There were no material income statement measurement 
period adjustments recorded during the year ended December 31, 2019.

Consolidated Results of Operations
The Company’s consolidated operating results for the year ended December 31, 2018, included $5.6 billion of revenues and 
$146 million of income before income tax provision associated with the operating results of Aetna from the Aetna Acquisition 
Date to December 31, 2018. 

During the years ended December 31, 2018 and 2017, the Company incurred transaction costs of $147 million and $34 million, 
respectively, associated with the Aetna Acquisition that were recorded within operating expenses.

Unaudited Pro Forma Financial Information
The following unaudited pro forma information presents a summary of the Company’s combined operating results for the years 
ended December 31, 2018 and 2017 as if the Aetna acquisition and the related financing transactions had occurred on January 
1, 2017. The following pro forma financial information is not necessarily indicative of the Company’s operating results as they 

118

would have been had the acquisition been effected on the assumed date, nor is it necessarily an indication of trends in future 
results for a number of reasons, including differences between the assumptions used to prepare the pro forma financial 
information, basic shares outstanding and dilutive equivalents, cost savings from operating efficiencies, potential synergies, and 
the impact of incremental costs incurred in integrating the businesses.

In millions, except per share data

Total revenues

Income from continuing operations

Basic earnings per share from continuing operations attributable to CVS Health

Diluted earnings per share from continuing operations attributable to CVS Health

Year Ended December 31,

2018

243,232

1,152

0.89

0.88

$

$

$

2017

236,000

6,813

5.25

5.21

$

$

$

The pro forma results for the years ended December 31, 2018 and 2017 include adjustments related to the following purchase 
accounting and acquisition-related items:

•  Elimination of intercompany transactions between CVS Health and Aetna;
•  Elimination of estimated foregone interest income associated with (i) cash assumed to have been used to partially fund 
the Aetna Acquisition and (ii) adjusting the amortized cost of Aetna’s investment portfolio to fair value as of the 
completion of the Aetna Acquisition;

•  Elimination of historical intangible asset, deferred acquisition cost and capitalized software amortization expense and 

addition of amortization expense based on the values of identified intangible assets;

•  Additional interest expense from (i) the long-term debt issued to partially fund the Aetna Acquisition and (ii) the 

amortization of the fair value adjustment to assumed long-term debt.

•  Additional depreciation expense related to the adjustment of Aetna’s property and equipment to fair value;
•  Adjustments to align CVS Health’s and Aetna’s accounting policies;
•  Elimination of transaction related costs; and
•  Tax effects of the adjustments noted above.

Divestiture of Brazilian Subsidiary

On July 1, 2019, the Company sold its Brazilian subsidiary, Onofre, for an immaterial amount. Onofre operated 50 retail 
pharmacy stores, the results of which historically had been reported within the Retail/LTC segment. The Company recorded a 
pre-tax loss on the divestiture of $205 million in the year ended December 31, 2019, which primarily relates to the elimination 
of the cumulative translation adjustment from accumulated other comprehensive income and is reflected in operating expenses 
in the Company’s consolidated statements of operations within the Retail/LTC segment.

Divestiture of RxCrossroads Subsidiary

On January 2, 2018, the Company sold its RxCrossroads subsidiary, the results of which had historically been reported within 
the Retail/LTC segment, to McKesson Corporation for $725 million. The Company recorded a pre-tax loss on the divestiture of 
$86 million in the year ended December 31, 2018 and transaction costs associated with the sale of $9 million in the year ended 
December 31, 2017, each of which were reflected in operating expenses in the Company’s consolidated statements of 
operations within the Retail/LTC segment. 

3. 

Investments

Total investments at December 31, 2019 and 2018 were as follows:

2019

2018

In millions

Current

Long-term

Total

Current

Long-term

Total

Debt securities available for sale

Mortgage loans

Other investments

Total investments

$

$

2,251

$

14,671

$

16,922

$

2,359

$

12,896

$

15,255

122

—

1,091

1,552

1,213

1,552

145

18

1,216

1,620

1,361

1,638

2,373

$

17,314

$

19,687

$

2,522

$

15,732

$

18,254

119

 
 
At December 31, 2019 and 2018, the Company held investments of $537 million and $531 million, respectively, related to the 
2012 conversion of an existing group annuity contract from a participating to a non-participating contract. The conversion 
occurred prior to the Aetna Acquisition. These investments are included in the total investments of large case pensions 
supporting non-experience-rated products. Although these investments are not accounted for as Separate Accounts assets, they 
are legally segregated and are not subject to claims that arise out of the Company’s business and only support future policy 
benefits obligations under that group annuity contract. 

Debt Securities

Debt securities available for sale at December 31, 2019 and 2018 were as follows:

In millions
December 31, 2019

Debt securities:

Amortized
Cost

Gross
Unrealized
Gains

Gross
Unrealized
Losses

Fair
Value

U.S. government securities

$

1,791

$

62

$

States, municipalities and political subdivisions

U.S. corporate securities
Foreign securities

Residential mortgage-backed securities

Commercial mortgage-backed securities

Other asset-backed securities

Redeemable preferred securities

Total debt securities (1)

2,202

7,167
2,149

508

654

1,397

30

108

573
200

25

46

13

8

$

15,898

$

1,035

$

December 31, 2018

Debt securities:

U.S. government securities

$

1,662

$

States, municipalities and political subdivisions

U.S. corporate securities

Foreign securities

Residential mortgage-backed securities

Commercial mortgage-backed securities

Other asset-backed securities

Redeemable preferred securities

Total debt securities (1)
_____________________________________________

2,370

6,444

2,355

567

594

1,097

30
15,119

$

$

26

30

61

31

10

11

3

—
172

$

$

(1) $
(1)
(3)
(1)
—

—
(5)
—
(11) $

— $
(1)
(16)
(3)
—

—
(15)
(1)
(36) $

1,852

2,309

7,737
2,348

533

700

1,405

38

16,922

1,688

2,399

6,489

2,383

577

605

1,085

29
15,255

(1) 

Investment risks associated with the Company’s experience-rated products generally do not impact the Company’s consolidated operating results. At 
December 31, 2019, debt securities with a fair value of $965 million, gross unrealized capital gains of $83 million and no gross unrealized capital losses, 
and at December 31, 2018, debt securities with a fair value of $916 million, gross unrealized capital gains of $12 million and gross unrealized capital 
losses of $2 million were included in total debt securities, but support experience-rated products. Changes in net unrealized capital gains (losses) on these 
securities are not reflected in accumulated other comprehensive income.

120

 
 
 
   
 
 
 
   
The amortized cost and fair value of debt securities at December 31, 2019 are shown below by contractual maturity.  Actual 
maturities may differ from contractual maturities because securities may be restructured, called or prepaid, or the Company 
intends to sell a security prior to maturity.

In millions

Due to mature:

Less than one year

One year through five years

After five years through ten years

Greater than ten years

Residential mortgage-backed securities

Commercial mortgage-backed securities

Other asset-backed securities

Total

Amortized
Cost

Fair 
Value

$

1,028

$

5,507

3,081

3,723

508

654

1,397

$

15,898

$

1,034

5,702

3,296

4,252

533

700

1,405

16,922

Mortgage-Backed and Other Asset-Backed Securities
All of the Company’s residential mortgage-backed securities at December 31, 2019 were issued by the Government National 
Mortgage Association, the Federal National Mortgage Association or the Federal Home Loan Mortgage Corporation and carry 
agency guarantees and explicit or implicit guarantees by the U.S. Government. At December 31, 2019, the Company’s 
residential mortgage-backed securities had an average credit quality rating of AAA and a weighted average duration of 3.3 
years.

The Company’s commercial mortgage-backed securities have underlying loans that are dispersed throughout the United States. 
Significant market observable inputs used to value these securities include loss severity and probability of default. At 
December 31, 2019, these securities had an average credit quality rating of AAA and a weighted average duration of 6.1 years.

The Company’s other asset-backed securities have a variety of underlying collateral (e.g., automobile loans, credit card 
receivables, home equity loans and commercial loans). Significant market observable inputs used to value these securities 
include the unemployment rate, loss severity and probability of default. At December 31, 2019, these securities had an average 
credit quality rating of AA and a weighted average duration of 1.2 years.

121

 
Summarized below are the debt securities the Company held at December 31, 2019 and 2018 that were in an unrealized capital 
loss position, aggregated by the length of time the investments have been in that position:

Less than 12 months

Greater than 12 months

Total

Number
of
Securities

Fair
Value

Unrealized
Losses

Number
of
Securities

Fair
Value

Unrealized
Losses

Number
of
Securities

Fair
Value

Unrealized
Losses

In millions, except number of
securities
December 31, 2019

Debt securities:

U.S. government securities
States, municipalities and
political subdivisions
U.S. corporate securities

Foreign securities
Residential mortgage-
backed securities
Commercial mortgage-
backed securities
Other asset-backed
securities

Total debt securities

December 31, 2018

Debt securities:

U.S. government securities
States, municipalities and
political subdivisions
U.S. corporate securities

Foreign securities
Residential mortgage-
backed securities
Other asset-backed
securities
Redeemable preferred
securities

52

$ 168

$

66

181

39

30

16

138

522

115

305

75

16

49

254

$ 982

$

8

$

26

$

54

86

1,399

1,431

243

314

45

1

516

528

14

23

1

1

2

1

—

—

1

6

—

1

16

3

—

15

1

36

— $ — $

2

2

—

9

—

5

—

—

—

—

187

200

182

$ 187

$

— $ — $

—

—

—

—

—

—

—

—

—

—

—

—

— $ — $

—

—

1

—

—

—

4

5

—

—

—

—

—

—

—

—

52

$ 168

$

68

183

39

39

16

325

722

120

305

75

16

49

436

$ 1,169

$

8

$

26

$

54

86

1,399

1,431

243

314

45

1

516

528

14

23

2,279

$ 2,409

$

1

1

3

1

—

—

5

11

—

1

16

3

—

15

1

36

Total debt securities

2,279

$ 2,409

$

The Company reviewed the securities in the tables above and concluded that they are performing assets generating investment 
income to support the needs of the Company’s business. In performing this review, the Company considered factors such as the 
quality of the investment security based on research performed by the Company’s internal credit analysts and external rating 
agencies and the prospects of realizing the carrying value of the security based on the investment’s current prospects for 
recovery. As of December 31, 2019, the Company did not intend to sell these securities, and did not believe it was more likely 
than not that it would be required to sell these securities prior to the anticipated recovery of their amortized cost basis. Since 
Aetna’s investment portfolio was measured at fair value as of the Aetna Acquisition Date, each of the securities as of December 
31, 2018 were in an unrealized loss position for less than 12 months.

122

 
 
The maturity dates for debt securities in an unrealized capital loss position at December 31, 2019 were as follows:

In millions

Due to mature:

Supporting experience-
rated products

Supporting remaining
products

Total

Fair
Value

Unrealized
Losses

Fair
Value

Unrealized
Losses

Fair
Value

Unrealized
Losses

Less than one year

$

— $

— $

12

$

— $

12

$

One year through five years

After five years through ten years

Greater than ten years

Residential mortgage-backed
securities

Commercial mortgage-backed
securities

Other asset-backed securities

Total

$

3

9

11

—

—

10

33

Mortgage Loans

—

—

—

—

—

—

285

151

197

16

49

426

$

— $

1,136

$

1

2

3

—

—

5

11

288

160

208

16

49

436

$

1,169

$

The Company’s mortgage loans are collateralized by commercial real estate. During 2019 and subsequent to the Aetna 
Acquisition Date in 2018, the Company had the following activity in its mortgage loan portfolio:

In millions

New mortgage loans

Mortgage loans fully-repaid

Mortgage loans foreclosed

2019

2018

$

$

131

234

—

—

1

2

3

—

—

5

11

4

27

—

The Company assesses mortgage loans on a regular basis for credit impairments, and annually assigns a credit quality indicator 
to each loan. The Company’s credit quality indicator is internally developed and categorizes its portfolio on a scale from 1 to 
7. These indicators are based upon several factors, including current loan-to-value ratios, property condition, market trends, 
creditworthiness of the borrower and deal structure. 

•  Category 1 - Represents loans of superior quality.
•  Categories 2 to 4 - Represent loans where credit risk is minimal to acceptable; however, these loans may display some 

susceptibility to economic changes.

•  Categories 5 and 6 - Represent loans where credit risk is not substantial, but these loans warrant management’s close 

attention.

•  Category 7 - Represents loans where collections are potentially at risk; if necessary, an impairment is recorded.

Based upon the Company’s assessments at December 31, 2019 and 2018, the Company’s mortgage loans were given the 
following credit quality indicators:

In millions, except credit ratings indicator

1

2 to 4

5 and 6

7

Total

2019

2018

$

58

$

1,143

12

—

42

1,301

18

—

$

1,213

$

1,361

123

 
 
 
 
 
 
 
At December 31, 2019 scheduled mortgage loan principal repayments were as follows:

In millions

2020

2021

2022

2023

2024

Thereafter

Total

Net Investment Income

Sources of net investment income for the years ended December 31, 2019 and 2018 were as follows:

In millions
Debt securities
Mortgage loans
Other investments
Gross investment income
Investment expenses
Net investment income (excluding net realized capital gains or losses)
Net realized capital gains (1)
Net investment income (2)
_____________________________________________

$

122

235

200

81

193

382

$

1,213

2019

2018

$

$

589
71
194
854
(42)
812
199
1,011

$

$

61
6
593
660
(3)
657
3
660

(1)  Net realized capital gains are net of other-than-temporary impairment (“OTTI”) losses on debt securities recognized in the consolidated statements of 

operations of $24 million for the year ended December 31, 2019. There were no material OTTI losses on debt securities for the year ended December 31, 
2018. 

(2)  Net investment income includes $44 million and $4 million for 2019 and 2018, respectively, related to investments supporting experience-rated products. 

The Company’s net investment income was $21 million in 2017, relating to interest income on cash equivalents and debt 
securities. The Company did not have any material realized capital gains or losses during 2017. 

Capital gains and losses recognized during the year ended December 31, 2019 related to investments in equity securities held as 
of December 31, 2019 were not material.

Excluding amounts related to experience-rated products, proceeds from the sale of available for sale debt securities and the 
related gross realized capital gains and losses in the year ended December 31, 2019 and subsequent to the Aetna Acquisition 
Date in 2018 were as follows:

In millions

Proceeds from sales

Gross realized capital gains

Gross realized capital losses

4. 

Fair Value

2019

2018

$

4,773

$

389

146
(17)

2
(2)

The preparation of the Company’s consolidated financial statements in accordance with GAAP requires certain assets and 
liabilities to be reflected at their fair value and others to be reflected on another basis, such as an adjusted historical cost 
basis. In this note, the Company provides details on the fair value of financial assets and liabilities and how it determines those 
fair values. The Company presents this information for those financial instruments that are measured at fair value for which the 
change in fair value impacts net income (loss) attributable to CVS Health or other comprehensive income separately from other 
financial assets and liabilities.

124

Financial Instruments Measured at Fair Value on the Consolidated Balance Sheets

Certain of the Company’s financial instruments are measured at fair value on the consolidated balance sheets. The fair values of 
these instruments are based on valuations that include inputs that can be classified within one of three levels of a hierarchy 
established by GAAP.  The following are the levels of the hierarchy and a brief description of the type of valuation information 
(“valuation inputs”) that qualifies a financial asset or liability for each level:

•  Level 1 – Unadjusted quoted prices for identical assets or liabilities in active markets.

•  Level 2 – Valuation inputs other than Level 1 that are based on observable market data.  These include: quoted prices for 
similar assets in active markets, quoted prices for identical assets in inactive markets, valuation inputs that are observable 
that are not prices (such as interest rates and credit risks) and valuation inputs that are derived from or corroborated by 
observable markets.

•  Level 3 – Developed from unobservable data, reflecting the Company’s assumptions.

Financial assets and liabilities are classified based upon the lowest level of input that is significant to the valuation. When 
quoted prices in active markets for identical assets and liabilities are available, the Company uses these quoted market prices to 
determine the fair value of financial assets and liabilities and classifies these assets and liabilities in Level 1. In other cases 
where a quoted market price for identical assets and liabilities in an active market is either not available or not observable, the 
Company estimates fair value using valuation methodologies based on available and observable market information or by using 
a matrix pricing model. These financial assets and liabilities are classified in Level 2. If quoted market prices are not available, 
the Company determines fair value using broker quotes or an internal analysis of each investment’s financial performance and 
cash flow projections. Thus, financial assets and liabilities may be classified in Level 3 even though there may be some 
significant inputs that may be observable.

The following is a description of the valuation methodologies used for the Company’s financial assets and liabilities that are 
measured at fair value, including the general classification of such assets and liabilities pursuant to the valuation hierarchy.

Cash and Cash Equivalents – The carrying value of cash and cash equivalents approximates fair value as maturities 
are less than three months. When quoted prices are available in an active market, cash equivalents are classified in 
Level 1 of the fair value hierarchy. Fair values of cash equivalent instruments that do not trade on a regular basis in 
active markets are classified as Level 2.

Debt Securities – Where quoted prices are available in an active market, debt securities are classified in Level 1 of the 
fair value hierarchy. The Company’s Level 1 debt securities consist primarily of U.S. Treasury securities.

The fair values of the Company’s Level 2 debt securities are obtained using models, such as matrix pricing, which use 
quoted market prices of debt securities with similar characteristics or discounted cash flows to estimate fair value. The 
Company reviews these prices to ensure they are based on observable market inputs that include quoted prices for 
similar assets in active markets, quoted prices for identical assets in inactive markets and inputs that are observable 
that are not prices (such as interest rates and credit risks). The Company also reviews the methodologies and the 
assumptions used to calculate prices from these observable inputs. On a quarterly basis, the Company selects a sample 
of its Level 2 debt securities’ prices and compares them to prices provided by a secondary source. Variances over a 
specified threshold are identified and reviewed to confirm the price provided by the primary source represents an 
appropriate estimate of fair value. In addition, the Company’s internal investment team consistently compares the 
prices obtained for select Level 2 debt securities to the team’s own independent estimates of fair value for those 
securities. The Company obtained one price for each of its Level 2 debt securities and did not adjust any of those 
prices at December 31, 2019 or 2018. 

The Company also values certain debt securities using Level 3 inputs. For Level 3 debt securities, fair values are 
determined by outside brokers or, in the case of certain private placement securities, are priced internally. Outside 
brokers determine the value of these debt securities through a combination of their knowledge of the current pricing 
environment and market flows. The Company did not have any broker quoted debt securities at December 31, 2019. 
The total fair value of broker quoted debt securities at December 31, 2018 was $50 million. The Company obtained 
one non-binding broker quote for each of these Level 3 debt securities and did not adjust any of those quotes at 
December 31, 2018. Examples of these broker quoted Level 3 debt securities include certain U.S. and foreign 
corporate securities and certain of the Company’s commercial mortgage-backed securities as well as other asset-
backed securities. For some private placement securities, the Company’s internal staff determines the value of these 
debt securities by analyzing spreads of corporate and sector indices as well as interest spreads of comparable public 

125

bonds. Examples of these private placement Level 3 debt securities include certain U.S. and foreign securities and 
certain tax-exempt municipal securities.

Equity Securities – The Company currently has two classifications of equity securities: those that are publicly traded 
and those that are privately placed. Publicly-traded equity securities are classified in Level 1 because quoted prices are 
available for these securities in an active market. For privately placed equity securities, there is no active market; 
therefore, these securities are classified in Level 3 because the Company prices these securities through an internal 
analysis of each investment’s financial statements and cash flow projections. Significant unobservable inputs consist of 
earnings and revenue multiples, discount for lack of marketability and comparability adjustments. An increase or 
decrease in any of these unobservable inputs would result in a change in the fair value measurement, which may be 
significant. 

There were no financial liabilities measured at fair value on a recurring basis on the consolidated balance sheets at 
December 31, 2019 or 2018. Financial assets measured at fair value on a recurring basis on the consolidated balance sheets at 
December 31, 2019 and 2018 were as follows:

In millions
December 31, 2019

Cash and cash equivalents
Debt securities:

U.S. government securities

States, municipalities and political subdivisions

U.S. corporate securities

Foreign securities

Residential mortgage-backed securities

Commercial mortgage-backed securities

Other asset-backed securities

Redeemable preferred securities

Total debt securities

Equity securities

Total

December 31, 2018

Cash and cash equivalents

Debt securities:

U.S. government securities
States, municipalities and political subdivisions
U.S. corporate securities

Foreign securities

Residential mortgage-backed securities

Commercial mortgage-backed securities

Other asset-backed securities

Redeemable preferred securities

Total debt securities

Equity securities
Total

Level 1

Level 2

Level 3

Total

$

3,397

$

2,286

$

— $

5,683

1,785

—

—

—

—

—

—

—

1,785

34

67

2,309

7,700

2,348

533

700

1,405

26

15,088

—

$

5,216

$

17,374

$

—

—

37

—

—

—

—

12

49

39

88

1,852

2,309

7,737

2,348

533

700

1,405

38

16,922

73

$

22,678

$

2,619

$

1,440

$

— $

4,059

1,597
—
—

—

—

—

—

—

1,597

19
4,235

$

$

91
2,399
6,422

2,380

577

605

1,085

22

13,581

—
15,021

—
—
67

3

—

—

—

7

77

54
131

$

$

1,688
2,399
6,489

2,383

577

605

1,085

29

15,255

73
19,387

126

 
 
 
 
 
 
 
 
 
 
 
 
There were no transfers between Levels 1 and 2 during the years ended December 31, 2019 and 2018. The changes in the 
balances of Level 3 financial assets during 2019 were as follows:

In millions
Beginning balance
Net realized and unrealized capital gains (losses):

Included in earnings 
Included in other comprehensive income

Purchases
Sales
Settlements
 Transfers out of Level 3, net
Ending balance

Foreign
securities

U.S.
corporate
securities

Equity
securities

Redeemable
preferred
securities

Total

$

3

$

67

$

54

$

7

$

131

—
—
2
—
(1)
(4)
— $

(33)
18
3
(6)
(12)
—
37

$

13
—
13
(41)
—
—
39

$

—
5
—
—
—
—
12

$

The total gross transfers into (out of) Level 3 during the year ended December 31, 2019 were as follows:

In millions

Gross transfers into Level 3

Gross transfers out of Level 3

Net transfers out of Level 3

(20)
23
18
(47)
(13)
(4)
88

—
(4)
(4)

$

$

$

The increase in the balance of Level 3 financial assets during 2018 relates to investments acquired in the Aetna Acquisition, 
which occurred on November 28, 2018. There were no transfers into or out of Level 3 subsequent to the Aetna Acquisition Date 
in 2018.

Financial Instruments Not Measured at Fair Value on the Consolidated Balance Sheets

The carrying value and estimated fair value classified by level of fair value hierarchy for financial instruments carried on the 
consolidated balance sheets at adjusted cost or contract value at December 31, 2019 and 2018 were as follows:

In millions
December 31, 2019

Assets:

Mortgage loans
Equity securities (1)

Liabilities:

Investment contract liabilities:

With a fixed maturity

Without a fixed maturity

Long-term debt

Carrying
Value

 Estimated Fair Value

Level 1

Level 2

Level 3

Total

$

1,213

$

— $

— $

1,239

$

1,239

149

N/A

N/A

N/A

N/A

5

372

—

—

68,480

74,306

—

—

—

5

392

—

5

392

74,306

127

 
In millions
December 31, 2018

Assets:

Mortgage loans
Equity securities (1)

Liabilities:

Investment contract liabilities:

With a fixed maturity

Without a fixed maturity

Long-term debt

_____________________________________________

Carrying
Value

Level 1

 Estimated Fair Value
Level 3
Level 2

Total

$

1,361

$

— $

— $

1,366

$

1,366

140

N/A

N/A

N/A

N/A

5

382

—

—

72,709

71,252

—

—

—

5

357

—

5

357

71,252

(1) 

It was not practical to estimate the fair value of these cost-method investments as it represents shares of unlisted companies. See Note 1 ‘‘Significant 
Accounting Policies’’ for additional information regarding the valuation of cost method investments. 

Separate Accounts Measured at Fair Value on the Consolidated Balance Sheets

Separate Accounts assets relate to the Company’s large case pensions products which represent funds maintained to meet 
specific objectives of contract holders. Since contract holders bear the investment risk of these assets, a corresponding Separate 
Accounts liability has been established equal to the assets. These assets and liabilities are carried at fair value. Net investment 
income and capital gains and losses on Separate Accounts assets accrue directly to such contract holders. The assets of each 
account are legally segregated and are not subject to claims arising from the Company’s other businesses. Deposits, 
withdrawals, net investment income and realized and unrealized capital gains and losses on Separate Accounts assets are not 
reflected in the consolidated statements of operations, shareholders’ equity or cash flows.

Separate Accounts assets include debt and equity securities. The valuation methodologies used for these assets are similar to the 
methodologies described above in this Note 4 ‘‘Fair Value.’’ Separate Accounts assets also include investments in common/
collective trusts that are carried at fair value. Common/collective trusts invest in other investment funds otherwise known as the 
underlying funds. The Separate Accounts’ interests in the common/collective trust funds are based on the fair values of the 
investments of the underlying funds and therefore are classified in Level 2. The assets in the underlying funds primarily consist 
of equity securities. Investments in common/collective trust funds are valued at their respective net asset value (“NAV”) per 
share/unit on the valuation date.

Separate Accounts financial assets at December 31, 2019 and 2018 were as follows:

December 31, 2019

December 31, 2018

In millions

Level 1

Level 2

Level 3

Total

Level 1

Level 2

Level 3

Total

Cash and cash equivalents

$

2

$

143

$ — $

145

$

2

$

189

$ — $

191

Debt securities

Equity securities

Common/collective trusts

1,224

2,589

—

—

2

499

—

—

—

3,813

2

499

782

—

—

2,500

3

404

Total

$ 1,226

$ 3,233

$ — $ 4,459

$

784

$ 3,096

$

4

—

—

4

3,286

3

404

$ 3,884

During 2019 and 2018, there were no transfers of Separate Accounts financial assets between Levels 1 and 2. During 2019 and 
2018, the Company had an immaterial amount of gross transfers of Separate Accounts financial assets into or out of Level 3.

Offsetting Financial Assets and Liabilities
Certain financial assets and liabilities are offset in the Company’s consolidated balance sheets or are subject to master netting 
arrangements or similar agreements with the applicable counterparty. Financial liabilities subject to offsetting and enforceable 
master netting arrangements were $3 million as of December 31, 2019. Financial assets subject to offsetting and enforceable 
master netting arrangements were $13 million as of December 31, 2018. 

128

5. 

Goodwill and Other Intangibles

Goodwill

Below is a summary of the changes in the carrying amount of goodwill by segment for the years ended December 31, 2019 and 
2018:

In millions

Balance at December 31, 2017

Acquisitions

Foreign currency translation adjustments

Divestiture of RxCrossroads subsidiary

Impairments

Balance at December 31, 2018

Segment realignment

Purchase accounting adjustments

Other

Pharmacy
Services

Retail/
LTC

Health Care
Benefits

Total

$

21,819

$

16,632

$

— $

1,569

—

—

—

23,388

194

—
(1)
23,581

735
(14)
(398)
(6,149)
10,806

—

—

1
10,807

$

$

44,484

—

—

—

44,484
(194)
1,071

—
45,361

$

38,451

46,788
(14)
(398)
(6,149)
78,678

—

1,071

—
79,749

Balance at December 31, 2019

$

Cumulative goodwill impairments were $6.1 billion at both December 31, 2019 and 2018.

The changes in the carrying amount of goodwill during the years ended December 31, 2019 and 2018 reflect the following 
activity:

Segment Realignment
During 2019, the Company realigned the composition of its segments to correspond with changes to its operating model and 
reflect how the CODM reviews information and manages the business as discussed in Note 1 ‘‘Significant Accounting 
Policies.’’ As a result of this realignment, the Company reallocated the goodwill balance of the Pharmacy Services and Health 
Care Benefits segments based on a relative fair value approach. 

Aetna Acquisition
On November 28, 2018, the Company completed the Aetna Acquisition. The majority of the preliminary valuation of goodwill 
associated with the Aetna Acquisition was recorded in the Health Care Benefits segment. The Company also allocated a portion 
of such goodwill to the Retail/LTC and Pharmacy Services segments related to the fair value of identified synergies that are 
expected to directly benefit those segments. During 2019, the Company finalized its purchase accounting assessment and 
recorded the applicable measurement period adjustments, including an adjustment to the acquired goodwill. See Note 2 
‘‘Acquisitions and Divestitures’’ for further discussion regarding the Aetna Acquisition.

LTC
During 2018, the LTC reporting unit continued to experience industry-wide challenges that impacted management’s ability to 
grow the business at the rate that was originally estimated when the Company acquired Omnicare, Inc. (“Omnicare”) and when 
the 2017 annual goodwill impairment test was performed. Those challenges include lower client retention rates, lower 
occupancy rates in skilled nursing facilities, the deteriorating financial health of numerous skilled nursing facility customers 
which resulted in a number of customer bankruptcies in 2018, and continued facility reimbursement pressures. In June 2018, 
LTC management submitted its initial budget for 2019 and updated the 2018 annual forecast which showed a deterioration in 
the projected financial results for the remainder of 2018 and in 2019, which also caused management to update its long-term 
forecast beyond 2019. Based on these updated projections, management determined that there were indicators that the LTC 
reporting unit’s goodwill may be impaired and, accordingly, management performed an interim goodwill impairment test as of 
June 30, 2018. The results of that interim impairment test showed that the fair value of the LTC reporting unit was lower than 
the carrying value, resulting in a $3.9 billion pre-tax goodwill impairment charge in the second quarter of 2018. The fair value 
of the LTC reporting unit was determined using a combination of a discounted cash flow method and a market multiple method. 
In addition to the lower financial projections, changes in risk-free interest rates and lower market multiples of peer group 
companies contributed to the amount of the 2018 goodwill impairment charges. 

129

    
    
 
During the third quarter of 2018, the Company performed its required annual impairment tests of goodwill and concluded there 
was no impairment of goodwill or trade names. 

During the fourth quarter of 2018, the LTC reporting unit missed its forecast primarily due to operational issues and customer 
liquidity issues, including one significant customer bankruptcy. Additionally, LTC management submitted an updated final 
budget for 2019 which showed significant additional deterioration in the projected financial results for 2019 compared to the 
analyses performed in the second and third quarters of 2018 primarily due to continued industry and operational challenges, 
which also caused management to make further updates to its long-term forecast beyond 2019. The updated projections 
reflected continued industry wide challenges including lower occupancy rates in skilled nursing facilities, significant 
deterioration in the financial health of numerous skilled nursing facility customers and continued facility reimbursement 
pressures. Based on these updated projections, management determined that there were indicators that the LTC reporting unit’s 
goodwill may be further impaired and, accordingly, management performed an interim goodwill impairment test during the 
fourth quarter of 2018. The results of that interim impairment test showed that the fair value of the LTC reporting unit was 
lower than the carrying value, resulting in an additional $2.2 billion pre-tax goodwill impairment charge in the fourth quarter of 
2018. In addition to the lower financial projections, lower market multiples of peer group companies also contributed to the 
amount of the fourth quarter 2018 goodwill impairment charge. The fair value of the LTC reporting unit was determined using a 
methodology consistent with the methodology described above for the analyses performed during the second and third quarters 
of 2018.

During the third quarter of 2019, the Company performed its required annual impairment tests of goodwill. The results of these 
impairment tests indicated that there was no impairment of goodwill. As of December 31, 2019, the remaining goodwill balance 
in the LTC reporting unit was $431 million.

RxCrossroads 
During 2017, the Company began pursuing various strategic alternatives for its RxCrossroads reporting unit. In connection with 
this effort, the Company performed an interim goodwill impairment test in the second quarter of 2017. The results of that 
impairment test showed that the fair value of the RxCrossroads reporting unit was lower than the carrying value, resulting in a 
$135 million pre-tax goodwill impairment charge in the second quarter of 2017. 

The TCJA was enacted on December 22, 2017 and reduced the U.S. federal corporate income tax rate from 35% to 21% 
effective January 1, 2018 (see Note 10 ‘‘Income Taxes’’). As a result, the RxCrossroads deferred income tax liabilities were 
reduced by $47 million and an income tax benefit of $47 million was recorded in the 2017 statement of operations. The 
reduction in the deferred income tax liabilities increased the carrying value of the RxCrossroads reporting unit by $47 million 
which triggered an additional goodwill impairment charge in the RxCrossroads reporting unit of $46 million during the fourth 
quarter of 2017. 

On January 2, 2018, the Company sold its RxCrossroads subsidiary to McKesson Corporation for $725 million, at which time 
the remaining goodwill of this reporting unit was removed from the consolidated balance sheets. 

130

Intangible Assets

The following table is a summary of the Company’s intangible assets as of December 31, 2019 and 2018:

Gross
Carrying
Amount

Accumulated
Amortization

Net
Carrying
Amount

Weighted
Average
Life (years)

In millions, except weighted average life
2019

Trademarks (indefinite-lived)

Customer contracts/relationships and covenants not to compete

Technology

Provider networks

Value of Business Acquired

Other

Total

2018

$

10,498

$

25,447

1,060

4,200

590

364

$

42,159

$

Trademarks (indefinite-lived)
Customer contracts/relationships and covenants not to compete

$

$

10,498
26,213

Technology

Provider networks

Value of Business Acquired
Favorable leases and other (1)

Total

_____________________________________________

1,060

4,200

590

1,177

$

43,738

$

— $

(8,128)
(386)
(229)
(63)
(232)
(9,038) $

— $

(6,349)
(31)
(19)
(7)
(808)
(7,214) $

10,498

17,319

674

3,971

527

132

33,121

10,498
19,864

1,029

4,181

583

369

36,524

N/A

14.8

3.0

20.0

20.0

8.1

15.1

N/A
14.8

3.0

20.0

20.0

17.1

15.3

(1)  Upon adoption of ASU 2016-02, Leases, the Company’s favorable leases were reclassified from an intangible asset to a reduction of the right-of-use asset. 

Refer to Note 1 ‘‘Significant Accounting Policies’’ for additional information on the adoption of ASU 2016-02, Leases. 

Amortization expense for intangible assets totaled $2.4 billion, $1.0 billion and $817 million for the years ended December 31, 
2019, 2018 and 2017, respectively. The projected annual amortization expense for the Company’s intangible assets for the next 
five years is as follows:

In millions
2020
2021
2022
2023
2024

6. 

Leases

$

2,283
2,186
1,816
1,786
1,743

The Company adopted ASU 2016-02, Leases (Topic 842) (“ASC 842”) on January 1, 2019 on a modified retrospective basis. 
As a result, the Company’s lease disclosures as of and for the year ended December 31, 2019 are reported under ASC 842. 
Comparative financial information for prior periods has not been restated and continues to be reported under ASC 840, the lease 
accounting standard in effect for those periods. 

Disclosure Subsequent to the Adoption of the New Lease Accounting Standard (ASU 2016-02) 

The Company leases most of its retail stores and mail order facilities and certain distribution centers and corporate offices under 
operating or finance leases, typically with initial terms of 15 to 25 years. The Company also leases certain equipment and other 
assets under operating or finance leases, typically with initial terms of 3 to 10 years. 

In addition, the Company leases pharmacy space at the stores of another retail chain for which the noncancelable contractual 
term of the pharmacy lease arrangement exceeds the remaining estimated economic life of the buildings. For these pharmacy 

131

lease arrangements, the Company concluded that for accounting purposes the lease term was the remaining estimated economic 
life of the buildings. Consequently, most of these individual pharmacy leases are finance leases.

The following table is a summary of the components of net lease cost for the year ended December 31, 2019:

In millions

Operating lease cost

Finance lease cost:

Amortization of right-of-use assets

Interest on lease liabilities

Total finance lease costs

Short-term lease costs

Variable lease costs

Less: sublease income

Net lease cost

Supplemental cash flow information related to leases for the year ended December 31, 2019 is as follows:

In millions

Cash paid for amounts included in the measurement of lease liabilities:

Operating cash flows paid for operating leases

Operating cash flows paid for interest portion of finance leases

Financing cash flows paid for principal portion of finance leases

Right-of-use assets obtained in exchange for lease obligations:

Operating leases

Finance leases

2019

$

2,720

38

44

82

24

581

50

$

3,357

2019

$

2,701

44

26

1,824

283

132

Supplemental balance sheet information related to leases as of December 31, 2019 is as follows:

In millions, except remaining lease term and discount rate
Operating leases:

Operating lease right-of-use assets

Current portion of operating lease liabilities

Long-term operating lease liabilities

Total operating lease liabilities

Finance leases: (1)
Property and equipment, gross
Accumulated depreciation (2)
Property and equipment, net

Current portion of long-term debt

Long-term debt

Total finance lease liabilities

Weighted average remaining lease term (in years)

Operating leases

Finance leases

Weighted average discount rate

Operating leases

Finance leases
_____________________________________________

$

$

$

$

$

$

$

20,860

1,596

18,926

20,522

790
(38)
752

27

781

808

13.8

20.5

4.6%

6.7%

(1)  Finance lease right-of-use assets are included within property and equipment, net and the respective finance lease liabilities are included in current portion 

(2) 

of long-term debt and long-term debt on the consolidated balance sheets.
In accordance with ASC 842, upon adoption the net carrying value of the prior capital leases became the initial basis of the Company’s finance leases. As 
a result, upon adoption there was no accumulated amortization associated with such finance leases.

The following table summarizes the maturity of lease liabilities under finance and operating leases as of December 31, 2019:

In millions

2020

2021

2022

2023

2024

Thereafter

Total lease payments (2)
Less: imputed interest

Total lease liabilities

_____________________________________________

$

$

Finance
Leases

Operating
Leases (1)

Total

$

2,699

$

84

82

79

77

76

1,056

1,454
(646)
808

$

2,598

2,444

2,335

2,103

15,654

27,833
(7,311)
20,522

$

2,783

2,680

2,523

2,412

2,179

16,710

29,287
(7,957)
21,330

(1)  Future operating lease payments have not been reduced by minimum sublease rentals of $315 million due in the future under noncancelable subleases.
(2)  The Company leases pharmacy and clinic space from Target Corporation. Amounts related to such finance and operating leases are reflected above. 

Pharmacy lease amounts due in excess of the remaining estimated economic life of the buildings of approximately $2.2 billion are not reflected in this 
table since the estimated economic life of the buildings is shorter than the contractual term of the pharmacy lease arrangement.

133

Sale-Leaseback Transactions
The Company finances a portion of its store development program through sale-leaseback transactions. The properties are 
generally sold at net book value, which generally approximates fair value, and the resulting leases generally qualify and are 
accounted for as operating leases. The operating leases that resulted from these transactions are included in the tables above. 
The Company does not have any retained or contingent interests in the stores and does not provide any guarantees, other than a 
guarantee of lease payments, in connection with the sale-leaseback transactions. Proceeds from sale-leaseback transactions 
totaled $5 million in 2019.  

Store Rationalization Charges
During the first quarter of 2019, the Company performed a review of its retail stores and determined it would close 46 
underperforming retail pharmacy stores during the second quarter of 2019. As a result, management determined that there were 
indicators of impairment with respect to the impacted stores, including the associated operating lease right-of-use assets. 
Accordingly, an interim long-lived asset impairment test was performed. The results of the impairment test indicated that the 
fair value of each store asset group was lower than the carrying value. The fair value was determined using a discounted cash 
flow method based on estimated sublease income. In the three months ended March 31, 2019, the Company recorded a store 
rationalization charge of $135 million, primarily related to these operating lease right-of-use asset impairment charges, which 
was recorded within operating expenses in the Retail/LTC segment.

During the third quarter of 2019, in connection with its annual budgeting process, the Company performed an updated review 
of its retail stores and determined it would close an additional 22 underperforming retail pharmacy stores during the first quarter 
of 2020. As a result, management determined that there were indicators of impairment with respect to the impacted stores, 
including the associated operating lease right-of-use assets. Accordingly, an interim long-lived asset impairment test was 
performed. The results of the impairment test indicated that the fair value of each store asset group was lower than the carrying 
value. The fair value was determined using a discounted cash flow method based on estimated sublease income. In the three 
months ended September 30, 2019, the Company recorded a store rationalization charge of $96 million, primarily related to 
these operating lease right-of-use asset impairment charges, which was recorded within operating expenses in the Retail/LTC 
segment.

Comparative Disclosure Prior to the Adoption of the New Lease Accounting Standard (ASU 2016-02)

The following table is a summary of the Company’s net rental expense for operating leases for the years ended December 31, 
2018 and 2017:

In millions

Minimum rentals

Contingent rentals

Rental expense

Less: sublease income

Total rental expense, net

The amount of property and equipment under capital leases at December 31, 2018 was as follows:

In millions

Property and equipment under capital leases

Accumulated amortization of property and equipment under capital leases

Property and equipment under capital leases, net

2018

2017

$

2,528

$

2,455

28

2,556
(21)
2,535

$

29

2,484
(24)
2,460

2018

582
(163)
419

$

$

$

Sale-Leaseback Transactions
The Company finances a portion of its store development program through sale-leaseback transactions. The properties are 
generally sold at net book value, which generally approximates fair value, and the resulting leases generally qualify and are 
accounted for as operating leases. The Company does not have any retained or contingent interests in the stores and does not 
provide any guarantees, other than a guarantee of lease payments, in connection with the sale-leaseback transactions. There 
were no sale-leaseback transactions in 2018. Proceeds from sale-leaseback transactions totaled $265 million in 2017.

134

Store Rationalization Charges
Prior to the adoption of ASC 842, when the Company closed a facility, the present value of estimated unrecoverable costs, 
including the remaining lease obligation less estimated sublease income and the book value of abandoned property and 
equipment, were charged to expense. During the year ended December 31, 2018, the Company did not recognize any significant 
charges related to facility closing costs.

In December 2016, the Company announced an enterprise streamlining initiative designed to reduce costs and enhance 
operating efficiencies to allow the Company to be more competitive in the current health care environment. During the year 
ended December 31, 2017, in connection with that enterprise streamlining initiative, the Company closed 71 retail stores and 
recorded charges of $215 million within operating expenses in the Retail/LTC segment. The charges primarily consist of 
provisions for the present value of noncancelable lease obligations. The noncancelable lease obligations associated with stores 
closed during the year ended December 31, 2017 extend through the year 2039. 

The long-term portion of the lease obligations associated with all outstanding facility closings was $269 million as of 
December 31, 2018 and was recorded in other long-term liabilities on the consolidated balance sheets. Upon adoption of ASC 
842, the closed store lease obligation was reclassified from a liability to a reduction of the right-of-use asset. Refer to Note 1 
‘‘Significant Accounting Policies’’ for additional discussion regarding the adoption of ASC 842. 

7. 

Health Care Costs Payable

The following is information about incurred and cumulative paid health care claims development as of December 31, 2019, net 
of reinsurance, and the total IBNR liabilities plus expected development on reported claims included within the net incurred 
claims amounts. See Note 1 ‘‘Significant Accounting Policies’’ for information on how the Company estimates IBNR reserves 
and health care costs payable as well as changes to those methodologies, if any. The Company’s estimate of IBNR liabilities is 
primarily based on trend and completion factors. Claim frequency is not used in the calculation of the Company’s liability. In 
addition, it is impracticable to disclose claim frequency information for health care claims due to the Company’s inability to 
gather consistent claim frequency information across its multiple claims processing systems. Any claim frequency count 
disclosure would not be comparable across the Company’s different claim processing systems and would not be consistent from 
period to period based on the volume of claims processed through each system. As a result, health care claim count frequency is 
not included in the disclosures below.

The Company acquired Aetna on November 28, 2018. The information about incurred and cumulative paid health care claims 
development in the table below is presented on a retrospective basis, under which the Company included Aetna’s historical 
development of health care claims for all years presented in the table. The information about incurred and paid health care 
claims development for the year ended December 31, 2018 is presented as required unaudited supplemental information.

In millions

Date of Service

2018

2019

In millions

Date of Service

2018
2019

Incurred Health Care Claims,
Net of Reinsurance
For the Years Ended December 31,

2018

(Unaudited)

$

44,962

$

2019

Total $

44,621

51,426

96,047

Cumulative Paid Health Care Claims,
Net of Reinsurance
For the Years Ended December 31,

2018

(Unaudited)

$

39,440

$

2019

Total $

All outstanding liabilities for health care costs payable prior to 2018, net of reinsurance

Total outstanding liabilities for health care costs payable, net of reinsurance

$

135

44,373
44,987

89,360

56

6,743

At December 31, 2019, the Company’s liabilities for IBNR plus expected development on reported claims totaled 
approximately $5.0 billion. Substantially all of the Company’s liabilities for IBNR plus expected development on reported 
claims at December 31, 2019 related to the current calendar year.

The reconciliation of the December 31, 2019 health care net incurred and paid claims development tables to the health care 
costs payable liability on the consolidated balance sheet is as follows:

In millions
Short-duration health care costs payable, net of reinsurance
Reinsurance recoverables
Premium deficiency reserve
Insurance lines other than short duration

Total health care costs payable

December 31, 2019
6,743
$
5
4
127
6,879

$

Prior to the Aetna Acquisition on November 28, 2018, the Company’s health care costs payable balance was immaterial and 
related to unpaid pharmacy claims for its SilverScript PDP. Accordingly, the Company has not provided disclosures for health 
care costs payable for periods prior to 2018. The following table shows the components of the change in health care costs 
payable during 2019 and 2018:

In millions

Health care costs payable, beginning of the period

Less: Reinsurance recoverables

Health care costs payable, beginning of the period, net

Acquisitions, net
Reclassification from pharmacy claims and discounts payable (1)

Add: Components of incurred health care costs

  Current year

  Prior years

Total incurred health care costs (2)

Less: Claims paid

  Current year

  Prior years

Total claims paid

Add: Premium deficiency reserve

Health care costs payable, end of period, net

Add: Reinsurance recoverables

Health care costs payable, end of period
_____________________________________________

2019

2018

$

6,147

$

4

6,143

—

—

52,723
(524)
52,199

46,158

5,314

51,472

4

6,874

5

5

—

5

5,357

776

6,594
(42)
6,552

6,303

260

6,563

16

6,143

4

$

6,879

$

6,147

(1)  As of the Aetna Acquisition Date, the Company reclassified $776 million of the Pharmacy Services segment’s unpaid retail pharmacy claims to third 

parties from pharmacy claims and discounts payable to health care costs payable as the third party liability was incurred to support the Health Care 
Benefits segment’s insured members.

(2)  Total incurred health care costs for the year ended December 31, 2019 and 2018 in the table above exclude (i) $4 million and $16 million, respectively, 
related to a premium deficiency reserve related to the Company’s Medicaid products, (ii) $41 million and $4 million, respectively, of benefit costs 
recorded in the Health Care Benefits segment that are included in other insurance liabilities on the consolidated balance sheets and (iii) $285 million and 
$22 million, respectively, of benefit costs recorded in the Corporate/Other segment that are included in other insurance liabilities on the consolidated 
balance sheets.

The Company’s estimates of prior years’ health care costs payable decreased by $524 million in 2019 because claims were 
settled for amounts less than originally estimated (i.e., the amount of claims incurred was lower than originally estimated), 
primarily due to lower health care cost trends as well as the actual claim submission time being faster than originally assumed 
(i.e., the Company’s completion factors were higher than originally assumed) in estimating health care costs payable at the end 
of the prior year. This development does not directly correspond to an increase in the Company’s operating results as these 
reductions were offset by estimated current period health care costs when the Company established the estimate of the current 
year health care costs payable.

136

 
8. 

Borrowings and Credit Agreements

The following table is a summary of the Company’s borrowings as of December 31, 2019 and 2018:

In millions
Short-term debt

Commercial paper

Long-term debt

2.2% senior notes due March 2019
2.25% senior notes due August 2019
3.125% senior notes due March 2020
Floating rate notes due March 2020 (2.515% and 3.397% at December 31, 2019 and 2018)
2.8% senior notes due July 2020
3.35% senior notes due March 2021
Floating rate notes due March 2021 (2.605% and 3.487% at December 31, 2019 and 2018)
4.125% senior notes due May 2021
2.125% senior notes due June 2021
4.125% senior notes due June 2021
5.45% senior notes due June 2021
3-year tranche term loan due November 2021
3.5% senior notes due July 2022
2.75% senior notes due November 2022
2.75% senior notes due December 2022
4.75% senior notes due December 2022
3.7% senior notes due March 2023
2.8% senior notes due June 2023
4% senior notes due December 2023
2.625% senior notes due August 2024
3.375% senior notes due August 2024
3.5% senior notes due November 2024
5% senior notes due December 2024
4.1% senior notes due March 2025
3.875% senior notes due July 2025
2.875% senior notes due June 2026
3% senior notes due August 2026
6.25% senior notes due June 2027
4.3% senior notes due March 2028
3.25% senior notes due August 2029
4.875% senior notes due July 2035
6.625% senior notes due June 2036
6.75% senior notes due December 2037
4.78% senior notes due March 2038
6.125% senior notes due September 2039
5.75% senior notes due May 2041
4.5% senior notes due May 2042
4.125% senior notes due November 2042
5.3% senior notes due December 2043
4.75% senior notes due March 2044
5.125% senior notes due July 2045
3.875% senior notes due August 2047
5.05% senior notes due March 2048
Finance lease liabilities
Other

Total debt principal

Debt premiums
Debt discounts and deferred financing costs

Less:

Short-term debt (commercial paper)
Current portion of long-term debt

Long-term debt

2019

2018

$

— $

720

—
—
723
277
2,750
2,038
1,000
222
1,750
203
187
—
1,500
1,000
1,250
399
6,000
1,300
1,250
1,000
650
750
299
5,000
2,828
1,750
750
372
9,000
1,750
652
771
533
5,000
447
133
500
500
750
375
3,500
1,000
8,000
808
279
69,246
262
(1,028)
68,480

375
850
2,000
1,000
2,750
3,000
1,000
550
1,750
500
600
3,000
1,500
1,000
1,250
399
6,000
1,300
1,250
—
650
750
299
5,000
2,828
1,750
—
372
9,000
—
652
771
533
5,000
447
133
500
500
750
375
3,500
1,000
8,000
642
19
74,265
302
(1,138)
73,429

(720)
(1,265)
71,444

—
(3,781)
64,699

$

$

137

The following is a summary of the Company’s required repayments of debt principal due during each of the next five years and 
thereafter, as of December 31, 2019:

In millions

2020

2021

2022

2023

2024

Thereafter

Total

Finance lease liabilities (1)

Total debt principal

_____________________________________________

(1)  See Note 6 ‘‘Leases’’ for a summary of maturities of the Company’s finance lease liabilities.

Short-term Borrowings

$

3,754

5,404

4,153

8,554

2,704

43,869

68,438

808

$

69,246

Commercial Paper and Back-up Credit Facilities
The Company did not have any commercial paper outstanding as of December 31, 2019. The Company had $720 million of 
commercial paper outstanding at a weighted average interest rate of 2.8% as of December 31, 2018. In connection with its 
commercial paper program, the Company maintains a $1.0 billion 364-day unsecured back-up revolving credit facility, which 
expires on May 14, 2020, a $1.0 billion, five-year unsecured back-up revolving credit facility, which expires on May 18, 2022, 
a $2.0 billion, five-year unsecured back-up revolving credit facility, which expires on May 17, 2023 and a $2.0 billion, five-
year unsecured back-up revolving credit facility, which expires on May 16, 2024. The credit facilities allow for borrowings at 
various rates that are dependent, in part, on the Company’s public debt ratings and require the Company to pay a weighted 
average quarterly facility fee of approximately .03%, regardless of usage. As of December 31, 2019 and 2018, there were no 
borrowings outstanding under any of the Company’s back-up credit facilities.

Bridge Loan Facility
On December 3, 2017, in connection with the Aetna Acquisition, the Company entered into a $49.0 billion unsecured bridge 
loan facility commitment. The Company paid $221 million in fees upon entering into the agreement. The fees were capitalized 
in other current assets and were amortized as interest expense over the period the bridge loan facility commitment was 
outstanding. The bridge loan facility commitment was reduced to $44.0 billion on December 15, 2017 upon the Company 
entering into a $5.0 billion term loan agreement. The Company recorded $56 million of amortization of the bridge loan facility 
fees during the year ended December 31, 2017, which was recorded in interest expense in the consolidated statement of 
operations.

On March 9, 2018, the Company issued an aggregate of $40.0 billion principal amount of unsecured floating rate notes and 
unsecured fixed rate senior notes, collectively the “2018 Notes.” At that time, the bridge loan facility commitment was reduced 
to $4.0 billion, and the Company paid $8 million in fees to retain the bridge loan facility commitment through the Aetna 
Acquisition Date. Those fees were capitalized in other current assets and were amortized as interest expense over the period the 
bridge loan facility commitment was outstanding. The Company recorded $173 million of amortization of the bridge loan 
facility commitment fees during the year ended December 31, 2018, which was recorded in interest expense in the consolidated 
statement of operations. On October 26, 2018, the Company entered into a $4.0 billion unsecured 364-day bridge term loan 
agreement to formalize the bridge loan facility discussed above. On November 28, 2018, in connection with the Aetna 
Acquisition, the $4.0 billion unsecured 364-day bridge term loan agreement terminated.

Federal Home Loan Bank of Boston
Since the Aetna Acquisition Date, a subsidiary of the Company is a member of the FHLBB. As a member, the subsidiary has 
the ability to obtain cash advances, subject to certain minimum collateral requirements. The maximum borrowing capacity 
available from the FHLBB as of December 31, 2019 was approximately $850 million. At both December 31, 2019 and 2018, 
there were no outstanding advances from the FHLBB.

138

Long-term Borrowings

2019 Notes
On August 15, 2019, the Company issued $1.0 billion aggregate principal amount of 2.625% unsecured senior notes due August 
15, 2024, $750 million aggregate principal amount of 3% unsecured senior notes due August 15, 2026 and $1.75 billion 
aggregate principal amount of 3.25% unsecured senior notes due August 15, 2029 (collectively, the “2019 Notes”) for total 
proceeds of approximately $3.5 billion, net of discounts and underwriting fees. The net proceeds of the 2019 Notes were used 
to repay certain of the Company’s outstanding debt.

Beginning in July 2019, the Company entered into several interest rate swap and treasury lock transactions to manage interest 
rate risk. These agreements were designated as cash flow hedges and were used to hedge the exposure to variability in future 
cash flows resulting from changes in interest rates related to the anticipated issuance of the 2019 Notes. In connection with the 
issuance of the 2019 Notes, the Company terminated all outstanding cash flow hedges. The Company paid a net amount of $25 
million to the hedge counterparties upon termination, which was recorded as a loss, net of tax, of $18 million in accumulated 
other comprehensive income and will be reclassified as interest expense over the life of the 2019 Notes. See Note 13 ‘‘Other 
Comprehensive Income’’ for additional information. 

Early Extinguishment of Debt
In August 2019, the Company purchased $4.0 billion of its outstanding senior notes through cash tender offers. The senior notes 
purchased included the following: $1.3 billion of its 3.125% senior notes due 2020, $723 million of its floating rate notes due 
2020, $328 million of its 4.125% senior notes due 2021, $297 million of 4.125% senior notes due 2021 issued by Aetna, $413 
million of 5.45% senior notes due 2021 issued by Coventry Health Care, Inc., a wholly-owned subsidiary of Aetna, and $962 
million of its 3.35% senior notes due 2021. In connection with the purchase of such senior notes, the Company paid a premium 
of $76 million in excess of the aggregate principal amount of the senior notes that were purchased, incurred $8 million in fees 
and recognized a net gain of $5 million on the write-off of net unamortized deferred financing premiums, for a net loss on early 
extinguishment of debt of $79 million. 

2018 Notes
On March 9, 2018, the Company issued an aggregate of $40.0 billion in principal amount of the 2018 Notes for total proceeds 
of approximately $39.4 billion, net of discounts and underwriting fees. The net proceeds of the 2018 Notes were used to fund a 
portion of the Aetna Acquisition. The 2018 Notes consisted of the following at the time of issuance:

In millions

3.125% senior notes due March 2020

Floating rate notes due March 2020

3.35% senior notes due March 2021

Floating rate notes due March 2021

3.7% senior notes due March 2023

4.1% senior notes due March 2025
4.3% senior notes due March 2028

4.78% senior notes due March 2038

5.05% senior notes due March 2048

Total debt principal

$

2,000

1,000

3,000

1,000

6,000

5,000
9,000

5,000

8,000

$

40,000

From December 2017 through March 2018, the Company entered into several interest rate swap and treasury lock transactions 
to manage interest rate risk. These agreements were designated as cash flow hedges and were used to hedge the exposure to 
variability in future cash flows resulting from changes in interest rates related to the anticipated issuance of long-term debt to 
fund the Aetna Acquisition. 

In connection with the issuance of the 2018 Notes, the Company terminated all outstanding cash flow hedges. In connection 
with the hedge transactions, the Company received a net amount of $446 million from the hedge counterparties upon 
termination, which was recorded as a gain, net of tax, of $331 million in accumulated other comprehensive income and will be 
reclassified as a reduction of interest expense over the life of the 2018 Notes. See Note 13 ‘‘Other Comprehensive Income’’ for 
additional information. 

139

Term Loan Agreement
On December 15, 2017, in connection with the Aetna Acquisition, the Company entered into a $5.0 billion term loan 
agreement. The term loan agreement allowed for borrowings at various rates that were dependent, in part, on the Company’s 
debt ratings. In connection with the Aetna Acquisition, the Company borrowed $5.0 billion (a $3.0 billion three-year tranche 
and a $2.0 billion five-year tranche) under the term loan agreement in November 2018. The Company terminated the $2.0 
billion five-year tranche in December 2018 with the repayment of the borrowing. The Company made principal payments of 
$500 million in March 2019, $1.0 billion in May 2019 and $1.5 billion in July 2019 on the three-year tranche, and terminated 
the three-year tranche and the term loan agreement with the final repayment of the borrowing in July 2019, at which time the 
Company had repaid all term loans. 

Aetna Related Debt
Upon the closing of the Aetna Acquisition, the Company assumed long-term debt with a fair value of $8.1 billion, with stated 
interest rates ranging from 2.2% to 6.75%. The long-term debt assumed is included in the summary of the Company’s 
borrowings table above.

Debt Covenants

The Company’s back-up revolving credit facilities, unsecured senior notes and unsecured floating rate notes contain customary 
restrictive financial and operating covenants. These covenants do not include an acceleration of the Company’s debt maturities 
in the event of a downgrade in the Company’s credit ratings. The Company does not believe the restrictions contained in these 
covenants materially affect its financial or operating flexibility. As of December 31, 2019, the Company was in compliance 
with all of its debt covenants.

9. 

Pension Plans and Other Postretirement Benefits

Defined Contribution Plans

As of December 31, 2019, the Company sponsors several active 401(k) savings plans that cover all employees who meet plan 
eligibility requirements. The Company makes matching contributions consistent with the provisions of the respective plans. 

At the participant’s option, account balances, including the Company’s matching contribution, can be invested among various 
investment options under each plan. Two of the defined contribution plans offer the Company’s common stock fund as an 
investment option. The Company also maintains nonqualified, unfunded deferred compensation plans for certain key 
employees. The plans provide participants the opportunity to defer portions of their eligible compensation and for certain 
nonqualified plans, participants receive matching contributions equivalent to what they could have received under the CVS 
Health Future Fund 401(k) Plan or Aetna 401(k) Plan absent certain restrictions and limitations under the Internal Revenue 
Code. The Company’s contributions under the above defined contribution plans were $550 million, $334 million and $314 
million in 2019, 2018 and 2017, respectively. The Company’s contributions for the years ended December 31, 2019 and 2018 
include contributions to the Aetna Inc. 401(k) plan subsequent to the Aetna Acquisition Date. 

Defined Benefit Pension Plans

On November 28, 2018, the Company completed the Aetna Acquisition. Aetna sponsors a tax-qualified defined benefit pension 
plan that was frozen in 2010. Aetna also sponsors a nonqualified supplemental pension plan that was frozen in 2007. Aetna’s 
pension plan benefit obligations and the fair value of plan assets were remeasured as of the Aetna Acquisition Date.

Prior to the Aetna Acquisition, during the year ended December 31, 2017, the Company settled the pension obligations of its 
two existing tax-qualified defined benefit pension plans by irrevocably transferring pension liabilities to an insurance company 
through the purchase of group annuity contracts and through lump sum distributions. These purchases, funded with pension 
plan assets, resulted in pre-tax settlement losses of $187 million in the year ended December 31, 2017, related to the recognition 
of accumulated deferred actuarial losses. The settlement losses were recorded in other expense in the consolidated statement of 
operations. The Company also sponsors several other defined benefit pension plans that are unfunded nonqualified 
supplemental retirement plans. 

140

Pension Benefit Obligation and Plan Assets
The following tables outline the change in pension benefit obligation and plan assets over the specified periods:

In millions

Change in benefit obligation:

Benefit obligation, beginning of year

Acquired benefit obligations
Interest cost

Actuarial loss

Benefit payments

Benefit obligation, end of year

Change in plan assets:

Fair value of plan assets, beginning of year

Fair value of plan assets acquired

Actual return on plan assets

Employer contributions
Benefit payments

Fair value of plan assets, end of year

$

2019

2018

$

5,841
—
225

530
(357)
6,239

5,663

—

1,064

25
(357)
6,395

131
5,685
25

41
(41)
5,841

—

5,709
(17)
12
(41)
5,663

Funded status

$

156

$

(178)

The assets (liabilities) recognized on the consolidated balance sheets at December 31, 2019 and 2018 for the pension plans 
consisted of the following:

In millions

Non-current assets reflected in other assets

Current liabilities reflected in accrued expenses

Non-current liabilities reflected in other long-term liabilities

Net assets (liabilities)

2019

2018

$

$

494
(25)
(313)
156

$

$

147
(25)
(300)
(178)

Net Periodic Benefit Cost (Income)
The components of net periodic benefit cost (income) for the years ended December 31, 2019, 2018 and 2017 are shown below:

In millions

Components of net periodic benefit cost (income):

Interest cost

Expected return on plan assets

Amortization of net actuarial loss

Settlement losses

Net periodic benefit cost (income)

2019

2018

2017

$

$

$

225
(357)
1

—
(131) $

$

25
(33)
2

—
(6) $

20
(20)
21

187

208

141

Pension Plan Assumptions
The Company uses a series of actuarial assumptions to determine its benefit obligation and net periodic benefit cost (income), 
including discount rates and expected return on plan assets assumptions, as further detailed below. 

Discount Rates - The discount rate is determined using a yield curve as of the annual measurement date. The yield 
curve consists of a series of individual discount rates, with each discount rate corresponding to a single point in time, 
based on high-quality bonds. Projected benefit payments are discounted to the measurement date using the 
corresponding rate from the yield curve that is consistent with the maturity profile of the expected liability cash flows.

Expected Return on Plan Assets - The expected long-term rate of return on plan assets is determined by using the 
plan’s target allocation and return expectations based on many factors including forecasted long-term capital market 
real returns and the inflationary outlook on a plan by plan basis. See “Pension Plan Assets” below for additional details 
regarding the pension plan assets as of December 31, 2019 and 2018.

The Company determined its benefit obligation based on the following weighted average assumptions as of December 31, 2019 
and 2018:

Discount rate

2019

2018

3.2%

4.3%

The Company determined its net periodic benefit cost (income) based on the following weighted average assumptions for the 
years ended December 31, 2019, 2018 and 2017:

Discount rate

Expected long-term rate of return on plan assets

2019

2018

2017

4.0%
6.5%

4.0%

6.6%

4.0%

5.0%

Pension Plan Assets
As of December 31, 2017, the assets in the Company’s tax-qualified defined benefit pension plans had been fully liquidated to 
settle all plan obligations through the purchase of group annuity contracts and through lump sum distributions. Subsequent to 
the Aetna Acquisition Date, the Company’s pension plan assets primarily include debt and equity securities held in separate 
accounts, common/collective trusts and real estate investments. The valuation methodologies used to value these debt and 
equity securities and common/collective trusts are similar to the methodologies described in Note 4 “Fair Value.” Pension plan 
assets also include investments in other assets that are carried at fair value. The following is a description of the valuation 
methodologies used to value real estate investments and these additional investments, including the general classification 
pursuant to the fair value hierarchy.

Real Estate - Real estate investments are valued by independent third party appraisers. The appraisals comply with the 
Uniform Standards of Professional Appraisal Practice, which include, among other things, the income, cost, and sales 
comparison approaches to estimating property value. Therefore, these investments are classified in Level 3.

Private equity and hedge fund limited partnerships - Private equity and hedge fund limited partnerships are carried at 
fair value which is estimated using the NAV per unit as reported by the administrator of the underlying investment 
fund as a practical expedient to fair value. Therefore, these investments have been excluded from the fair value table 
below.

142

Pension plan assets with changes in fair value measured on a recurring basis at December 31, 2019 were as follows: 

In millions

Cash and cash equivalents

Debt securities:

    U.S. government securities

    States, municipalities and political subdivisions

    U.S. corporate securities

    Foreign securities

    Residential mortgage-backed securities

    Commercial mortgage-backed securities

    Other asset-backed securities

    Redeemable preferred securities

Total debt securities

Equity securities:

    U.S. domestic

    International

    Domestic real estate

Total equity securities

Other investments:

    Real estate
    Common/collective trusts (1)
    Derivatives

Total other investments
Total pension investments (2)
_____________________________________________

Level 1

Level 2

Level 3

Total

$

92

$

65

$

— $

157

592

—

—

—

—

—

—

—

592

931

481

25

1,437

—

—

—

—

31

157

1,849

178

385

89

150

5

2,844

1

—

—

1

—

288
(2)
286

$

2,121

$

3,196

$

—

—

1

—

—

—

—

—

1

—

—

—

—

353

—

—

353

354

623

157

1,850

178

385

89

150

5

3,437

932

481

25

1,438

353

288
(2)
639

$

5,671

(1)  The assets in the underlying funds of common/collective trusts consist of $137 million of equity securities and $151 million of debt securities. 
(2)  Excludes $540 million of private equity limited partnership investments and $184 million of hedge fund limited partnership investments as these amounts 

are measured at NAV per share or an equivalent and are not subject to leveling within the fair value hierarchy.

143

Pension plan assets with changes in fair value measured on a recurring basis at December 31, 2018 were as follows: 

In millions

Cash and cash equivalents

Debt securities:

    U.S. government securities

    States, municipalities and political subdivisions

    U.S. corporate securities

    Foreign securities

    Residential mortgage-backed securities

    Commercial mortgage-backed securities

    Other asset-backed securities

    Redeemable preferred securities

Total debt securities

Equity securities:

    U.S. domestic

    International

    Domestic real estate

Total equity securities

Other investments:

    Real estate
    Common/collective trusts (1)
    Derivatives

Total other investments
Total pension investments (2)
_____________________________________________

Level 1

Level 2

Level 3

Total

$

68

$

30

$

— $

98

511

—

—

—

—

—

—

—

511

744

356

30

1,130

—

—

—

—

38

147

1,671

177

339

70

162

6

2,610

—

—

—

—

—

253

2

255

$

1,709

$

2,895

$

—

—

5

—

—

—

—

—

5

—

—

—

—

425

—

—

425

430

549

147

1,676

177

339

70

162

6

3,126

744

356

30

1,130

425

253

2

680

$

5,034

(1)  The assets in the underlying funds of common/collective trusts consist of $109 million of equity securities and $144 million of debt securities. 
(2)  Excludes $465 million of private equity limited partnership investments and $164 million of hedge fund limited partnership investments as these amounts 

are measured at NAV per share or an equivalent and are not subject to leveling within the fair value hierarchy.

The changes in the balance of Level 3 pension plan assets during 2019 were as follows:

In millions

Beginning balance

Actual return on plan assets

Purchases, sales and settlements

Transfers into (out of) Level 3

Ending balance

2019

U.S. corporate
securities

Total

Real estate

425

$

5

$

5
(77)
—

—
(5)
1

353

$

1

$

$

$

430

5
(82)
1

354

The increase in the balance of Level 3 pension plan assets during 2018 relates to investments acquired in the Aetna Acquisition. 
There was an immaterial amount of transfers into or out of Level 3 from the Aetna Acquisition Date to December 31, 2018.

The Company’s pension plan invests in a diversified mix of assets intended to maximize long-term returns while recognizing 
the need for adequate liquidity to meet ongoing benefit and administrative obligations. The risk of unexpected investment and 
actuarial outcomes is regularly evaluated. This evaluation is performed through forecasting and assessing ranges of investment 
outcomes over short- and long-term horizons and by assessing the pension plan’s liability characteristics. Complementary 
investment styles and strategies are utilized by multiple investment management firms to further improve portfolio and 
operational risk characteristics. Public and private equity investments are used primarily to increase overall plan returns. Real 
estate investments are viewed favorably for their diversification benefits and above-average dividend generation. Fixed income 

144

investments provide diversification benefits and liability hedging attributes that are desirable, especially in falling interest rate 
environments.

At December 31, 2019, target investment allocations for the Company’s pension plan were: 33% in equity securities, 54% in 
debt securities, 6% in real estate, 4% in private equity limited partnerships and 3% in hedge funds. Actual asset allocations may 
differ from target allocations due to tactical decisions to overweight or underweight certain assets or as a result of normal 
fluctuations in asset values. Asset allocations are consistent with stated investment policies and, as a general rule, periodically 
rebalanced back to target asset allocations. Asset allocations and investment performance are formally reviewed periodically 
throughout the year by the pension plan’s Benefit Finance Committee. Forecasting of asset and liability growth is performed at 
least annually.

Cash Flows
The Company generally contributes to its tax-qualified pension plan based on minimum funding requirements determined under 
applicable federal laws and regulations. Employer contributions related to the nonqualified supplemental pension plans 
generally represent payments to retirees for current benefits. The Company contributed $25 million, $12 million and $46 
million to its pension plans during 2019, 2018 and 2017, respectively. No contributions are required for the tax-qualified 
pension plan in 2020. The Company expects to make an immaterial amount of contributions for all other pension plans in 2020. 
The Company estimates the following future benefit payments, which are calculated using the same actuarial assumptions used 
to measure the pension benefit obligation as of December 31, 2019: 

In millions

2020

2021

2022

2023

2024

2025-2029

$

373

415

379

384

380

1,851

Multiemployer Pension Plans
The Company also contributes to a number of multiemployer pension plans under the terms of collective-bargaining 
agreements that cover its union-represented employees. The risks of participating in these multiemployer plans are different 
from single-employer pension plans in the following respects: (i) assets contributed to the multiemployer plan by one employer 
may be used to provide benefits to employees of other participating employers, (ii) if a participating employer stops 
contributing to the plan, the unfunded obligations of the plan may be borne by the remaining participating employers, and (iii) 
if the Company chooses to stop participating in some of its multiemployer plans, the Company may be required to pay those 
plans an amount based on the underfunded status of the applicable plan, which is referred to as a withdrawal liability. 

None of the multiemployer pension plans in which the Company participates are individually significant to the Company. The 
Company’s contributions to multiemployer pension plans were $18 million, $18 million and $17 million in 2019, 2018 and 
2017, respectively. 

Other Postretirement Benefits

The Company provides postretirement health care and life insurance benefits to certain retirees who meet eligibility 
requirements. During 2018, the Company acquired additional OPEB plans in connection with the Aetna Acquisition. The 
Company’s funding policy is generally to pay covered expenses as they are incurred. For retiree medical plan accounting, the 
Company reviews external data and its own historical trends for health care costs to determine the health care cost trend rates. 
As of December 31, 2019 and 2018, the Company’s other postretirement benefits had an accumulated postretirement benefit 
obligation of $246 million and $228 million, respectively. Net periodic benefit costs related to these other postretirement 
benefits were $7 million, $2 million and $1 million in 2019, 2018 and 2017, respectively. 

145

The Company estimates the following future benefit payments, which are calculated using the same actuarial assumptions used 
to measure the accumulated other postretirement benefit obligation as of December 31, 2019: 

In millions

2020

2021

2022

2023

2024

2025-2029

$

15

15

15

15

15

72

Pursuant to various collective bargaining agreements, the Company also contributes to multiemployer health and welfare plans 
that cover certain union-represented employees. The plans provide postretirement health care and life insurance benefits to 
certain employees who meet eligibility requirements. The Company’s contributions to multiemployer health and welfare plans 
totaled $57 million, $58 million and $58 million in 2019, 2018 and 2017, respectively. 

10. 

Income Taxes

The income tax provision (benefit) for continuing operations consisted of the following for the years ended December 31, 2019, 
2018 and 2017:

In millions

Current:

Federal

State

Deferred:

Federal

State

Total

2019

     2018

     2017

$

2,450

$

1,480

$

2,594

565

3,015

(535)
(114)
(649)
2,366

$

499

1,979

22

1

23

$

2,002

$

464

3,058

(1,435)
14
(1,421)
1,637

The TCJA was enacted on December 22, 2017. Among numerous changes to existing tax laws, the TCJA permanently reduced 
the federal corporate income tax rate from 35% to 21% effective on January 1, 2018. The effects of changes in tax rates on 
deferred tax balances are required to be taken into consideration in the period in which the changes are enacted, regardless of 
when they are effective. As a result of the reduction of the corporate income tax rate under the TCJA, the Company estimated 
the revaluation of its net deferred tax liabilities and recorded a provisional income tax benefit of approximately $1.5 billion for 
year ended December 31, 2017. In 2018, the Company completed its process of determining the TCJA’s final impact and 
recorded an additional income tax benefit of $100 million.

The following table is a reconciliation of the statutory income tax rate to the Company’s effective income tax rate for 
continuing operations for the years ended December 31, 2019, 2018 and 2017:

Statutory income tax rate

State income taxes, net of federal tax benefit

Effect of the Tax Cuts and Jobs Act
Health insurer fee

Goodwill impairments

Sale of subsidiary

Other

Effective income tax rate

146

2019

     2018

     2017

21.0%

21.0%

35.0%

4.0

—
—

—

—

1.3

27.7
(7.1)
2.2

89.5

5.0

4.1

26.3%

142.4%

4.1
(18.3)
—

0.8

—
(1.8)
19.8%

The following table is a summary of the components of the Company’s deferred income tax assets and liabilities as of 
December 31, 2019 and 2018:

In millions

Deferred income tax assets:

Lease and rents

Inventory

Employee benefits

Bad debts and other allowances

Retirement benefits

Net operating loss and capital loss carryforwards

Deferred income

Insurance reserves

Investments

Other

Valuation allowance

Total deferred income tax assets

Deferred income tax liabilities:

Investments

Depreciation and amortization

Total deferred income tax liabilities

Net deferred income tax liabilities

2019

     2018

$

267

$

23

191

294

47

480

36

430

—

277

28

243

243

130

529

104

467

11

451
(374)
1,845

242
(520)
1,754

(289)
(8,850)
(9,139)
(7,294) $

—
(9,431)
(9,431)
(7,677)

$

As of December 31, 2019, the Company has net operating and capital loss carryovers of $480 million, which expire between 
2021 and 2038. The Company considers all available positive and negative evidence, including future reversals of existing 
taxable temporary differences, projected future taxable income, tax planning strategies and the Company’s recent operating 
results. The Company established a valuation allowance of $374 million because it does not consider it more likely than not that 
these deferred tax assets will be recovered.

A reconciliation of the beginning and ending amount of unrecognized tax benefits as of December 31, 2019, 2018 and 2017 is 
as follows:

In millions

Beginning balance

Additions based on tax positions related to the current year

Additions based on tax positions related to prior years

Reductions for tax positions of prior years

Expiration of statutes of limitation

Settlements

Ending balance

2019

     2018

     2017

$

661

$

344

$

4

115
(111)
(7)
(7)
655

$

1

324
(5)
(2)
(1)
661

$

$

307

62

32
(28)
(10)
(19)
344

The increase in the balance of unrecognized tax benefits in 2018 compared to 2017 was mainly due to the Aetna Acquisition.

The Company and most of its subsidiaries are subject to U.S. federal income tax as well as income tax of numerous state and 
local jurisdictions. The Company is a participant in the Compliance Assurance Process, which is a program made available by 
the U.S. Internal Revenue Service (“IRS”) to certain qualifying large taxpayers, under which participants work collaboratively 
with the IRS to identify and resolve potential tax issues through open, cooperative and transparent interaction prior to the 
annual filing of their federal income tax returns. The IRS has completed its examinations of the Company’s consolidated U.S. 
federal income tax returns through tax year 2013. The IRS has substantially completed its examinations of the Company’s 
consolidated U.S. federal income tax returns for tax years 2014 through 2018. The IRS is currently examining the Company’s 
2019 consolidated U.S. federal income tax return.

147

The Company and its subsidiaries are also currently under income tax examinations by a number of state and local tax 
authorities. As of December 31, 2019, no examination has resulted in any proposed adjustments that would result in a material 
change to the Company’s operating results, financial condition or liquidity.

Substantially all material state and local income tax matters have been concluded for fiscal years through 2014. Certain state 
exams are likely to be concluded and certain state statutes of limitations will lapse in 2020, but the change in the balance of the 
Company’s uncertain tax positions is projected to be immaterial. In addition, it is reasonably possible that the Company’s 
unrecognized tax benefits could change within the next twelve months due to the anticipated conclusion of various 
examinations with the IRS for various years. An estimate of the range of the possible change cannot be made at this time.

The Company records interest expense related to unrecognized tax benefits and penalties in the income tax provision. The 
Company accrued interest expense of approximately $49 million, $19 million and $11 million in 2019, 2018 and 2017, 
respectively. The Company had approximately $173 million and $80 million accrued for interest and penalties as of 
December 31, 2019 and 2018, respectively. 

As of December 31, 2019, the total amount of unrecognized tax benefits that, if recognized, would affect the Company’s 
effective income tax rate is approximately $532 million, after considering the federal benefit of state income taxes.

11. 

Stock Incentive Plans

The terms of the CVS Health 2017 Incentive Compensation Plan (“ICP”) provide for grants of annual incentive and long-term 
performance awards to executive officers and other officers and employees of the Company or any subsidiary of the Company, 
as well as equity compensation to outside directors of CVS Health. Payment of such annual incentive and long-term 
performance awards will be in cash, stock, other awards or other property, at the discretion of the Management Planning and 
Development Committee (the “MP&D Committee”) of CVS Health’s Board of Directors (the “Board”). The ICP allows for a 
maximum of 32 million shares of CVS Health common stock to be reserved and available for grants. Prior to the acquisition of 
Aetna in 2018, the ICP was the only compensation plan under which the Company granted stock options, restricted stock and 
other stock-based awards to its employees, with the exception of the Company’s Employee Stock Purchase Plan (“ESPP”). As 
of December 31, 2019, there were approximately 17 million shares of CVS Health common stock available for future grants 
under the ICP.

As of the Aetna Acquisition Date, approximately 22 million shares of Aetna common stock subject to awards outstanding under 
the Amended Aetna Inc. 2010 Stock Incentive Plan (“SIP”) were assumed by CVS Health. In addition, in accordance with the 
merger agreement, shares which were available for future issuance under the SIP were converted into approximately 32 million 
shares of CVS Health common stock reserved and available for issuance pursuant to future awards. As of December 31, 
2019, there were approximately 27 million shares of CVS Health common stock available for future grants under the SIP.

Stock-Based Compensation Expense

Stock-based compensation is measured at the grant date based on the fair value of the award and is recognized as expense over 
the requisite service period of the stock award (generally three to five years) using the straight-line method. The following table 
is a summary of stock-based compensation for the years ended December 31, 2019, 2018 and 2017:

In millions
Stock options and stock appreciation rights (“SARs”) (1) (2)
Restricted stock units and performance stock units (2)

Total stock-based compensation
_____________________________________________

2019

2018

2017

$

$

76

377

453

$

$

70

210

280

$

$

65

169

234

Includes the ESPP.

(1) 
(2)  Stock-based compensation for the year ended December 31, 2018 includes $14 million and $27 million associated with accelerated vesting of SARs and 

restricted stock replacement awards, respectively, issued to Aetna employees who were terminated subsequent to the Aetna Acquisition.

ESPP

The ESPP provides for the purchase of up to 30 million shares of CVS Health common stock. Under the ESPP, eligible 
employees may purchase common stock at the end of each six month offering period at a purchase price equal to 90% of the 
lower of the fair market value on the first day or the last day of the offering period. During 2019, approximately two million 

148

shares of common stock were purchased under the provisions of the ESPP at an average price of $53.29 per share. As of 
December 31, 2019, approximately seven million shares of common stock were available for issuance under the ESPP.

The fair value of stock-based compensation associated with the ESPP is estimated on the date of grant (the first day of the 
six month offering period) using the Black-Scholes option pricing model.

The following table is a summary of the assumptions used to value the ESPP awards for the years ended December 31, 2019, 
2018 and 2017:

Dividend yield (1)
Expected volatility (2)
Risk-free interest rate (3)
Expected life (in years) (4)
Weighted-average grant date fair value
_____________________________________________

2019

2018

2017

1.70%

27.96%

2.27%

0.5

1.45%

28.02%

1.87%

0.5

1.24%

22.70%

0.86%

0.5

$

10.51

$

12.26

$

13.01

(1)  The dividend yield is calculated based on semi-annual dividends paid and the fair market value of CVS Health stock at the grant date.
(2)  The expected volatility is estimated based on the historical volatility of CVS Health’s daily stock price over the previous six month period.
(3)  The risk-free interest rate is selected based on the Treasury constant maturity interest rate whose term is consistent with the expected term of ESPP 

purchases (i.e., six months).

(4)  The expected life is based on the semi-annual purchase period.

Restricted Stock Units and Performance Stock Units

The Company’s restricted stock units and performance stock units are considered nonvested share awards and require no 
payment from the employee. The fair value of the restricted stock units is based on the market price of CVS Health common 
stock on the grant date and is recognized on a straight-line basis over the vesting period. For each restricted stock unit granted, 
employees receive one share of common stock, net of taxes, at the end of the vesting period. 

The Company’s performance stock units contain performance vesting conditions in addition to a service vesting condition. 
Vesting of the Company’s performance stock units is dependent upon the degree to which the Company achieves its 
performance goals, which are generally set for a three-year performance period and are approved at the time of grant by the 
MP&D Committee. 

The fair value of performance stock units granted with service and performance vesting conditions is based on the market price 
of CVS Health common stock on the grant date and is recognized over the vesting period. Certain of the performance stock 
units also contain a market vesting condition based on the performance of CVS Health common stock relative to a comparator 
group. The fair value of these performance stock units is determined using a Monte Carlo simulation as of the grant date and is 
recognized over the vesting period. 

On November 28, 2018, the Company completed the Aetna Acquisition. All unvested Aetna performance stock unit and 
restricted stock unit awards as of the Aetna Acquisition Date were converted into replacement CVS Health restricted stock 
awards. 

As of December 31, 2019, there was $524 million of total unrecognized compensation cost related to the Company’s restricted 
stock units and performance stock units that are expected to vest. These costs are expected to be recognized over a weighted-
average period of 2.2 years. The total fair value of restricted stock units vested during 2019, 2018 and 2017 was $265 million, 
$262 million and $175 million, respectively.

149

The following table is a summary of the restricted stock unit and performance stock unit activity for the year ended 
December 31, 2019:

In thousands, except weighted average grant date fair value

Outstanding at beginning of year, nonvested

Granted

Vested

Forfeited

Outstanding at end of year, nonvested

Stock Options and SARs

Weighted Average
Grant Date
Fair Value

Units

11,005

$

7,644
$
(4,216) $
(1,308) $
$
13,125

76.18

54.34

62.59

58.73

61.57

All stock option grants are awarded at fair value on the date of grant. The fair value of stock options is estimated using the 
Black-Scholes option pricing model, and stock-based compensation is recognized on a straight-line basis over the requisite 
service period. Stock options granted generally become exercisable over a four-year period from the grant date. Stock options 
granted prior to 2019 generally expire seven years after the grant date. Stock options granted in 2019 expire ten years after the 
grant date.

On November 28, 2018, the Company completed the Aetna Acquisition. All unvested Aetna SARs outstanding as of the Aetna 
Acquisition Date were converted into replacement CVS Health SARs. The replacement SARs granted will be settled in CVS 
Health common stock, net of taxes, based on the appreciation of the stock price on the exercise date over the market price on 
the date of grant. The fair value of SARs is estimated using the Black-Scholes option pricing model, and stock-based 
compensation is recognized on a straight-line basis over the requisite service period. SARs generally become exercisable over a 
three-year period from the grant date. SARs generally expire ten years after the grant date.

The following table is a summary of stock option and SAR activity that occurred for the years ended December 31, 2019, 2018 
and 2017:

In millions

Cash received from stock options exercised (including ESPP)

$

Payments for taxes for net share settlement of equity awards

Intrinsic value of stock options and SARs exercised

Fair value of stock options and SARs vested

2019

2018

2017

210

112
30

467

$

242

$

97

79

324

329

71

176

341

The fair value of each stock option and SAR is estimated using the Black-Scholes option pricing model based on the following 
assumptions at the time of grant:

Dividend yield (1)
Expected volatility (2)
Risk-free interest rate (3)
Expected life (in years) (4)
Weighted-average grant date fair value
_____________________________________________

2019

2018

2017

3.68%

21.76%

0.56%

6.3

2.76%

21.27%

2.77%

4.8

2.56%

18.39%

1.77%

4.1

$

6.27

$

24.55

$

9.43

(1)  The dividend yield is based on annual dividends paid and the fair market value of CVS Health stock at the grant date.
(2)  The expected volatility is estimated based on the historical volatility of CVS Health’s daily stock price over a period equal to the expected life of each 

option or SAR grant after adjustments for infrequent events such as stock splits.

(3)  The risk-free interest rate is selected based on yields from U.S. Treasury zero-coupon issues with a remaining term equal to the expected term of the 

options or SARs being valued.

(4)  The expected life represents the number of years the options or SARs are expected to be outstanding from grant date based on historical option or SAR 

holder exercise experience.

The increase in the weighted-average grant date fair value in 2018 was due to the issuance of the replacement SARs in 
connection with the Aetna Acquisition. 

150

As of December 31, 2019, unrecognized compensation expense related to unvested stock options and SARs totaled $41 million, 
which the Company expects to be recognized over a weighted-average period of 2.1 years. After considering anticipated 
forfeitures, the Company expects approximately 10 million of the unvested stock options and SARs to vest over the requisite 
service period.

The following table is a summary of the Company’s stock option and SAR activity for the year ended December 31, 2019:

In thousands, except weighted average exercise price and remaining
contractual term

Shares

Weighted
Average
Exercise
 Price

Weighted
Average
Remaining
Contractual
Term

Aggregate
Intrinsic
Value

Outstanding at beginning of year

Granted

Exercised

Forfeited

Expired

Outstanding at end of year

Exercisable at end of year
Vested at end of year and expected to vest in the future

12. 

Shareholders’ Equity

Share Repurchases

22,909

$

6,538
$
(3,667) $
(769) $
(1,109) $
$
23,902

13,267
23,328

$
$

71.15

54.40

46.17

68.12

82.40

69.98  

77.48  
70.28  

$

4.76

2.73
4.67

274,987

109,765
265,128

The following share repurchase programs have been authorized by the Board:

In billions
Authorization Date

November 2, 2016 (“2016 Repurchase Program”)

December 15, 2014 (“2014 Repurchase Program”)

Authorized

Remaining as of
December 31, 2019

$

$

15.0

10.0

13.9

—

Each of the share Repurchase Programs was effective immediately. The 2014 Repurchase Program has been completed. The 
2016 Repurchase Program permits the Company to effect repurchases from time to time through a combination of open market 
repurchases, privately negotiated transactions, accelerated share repurchase (“ASR”) transactions, and/or other derivative 
transactions. The 2016 Repurchase Program can be modified or terminated by the Board at any time.

During the years ended December 31, 2019 and 2018, the Company did not repurchase any shares of common stock pursuant to 
the 2016 Repurchase Program. During the year ended December 31, 2017, the Company repurchased an aggregate of 55.4 
million shares of common stock for approximately $4.4 billion under the 2014 and 2016 Repurchase Programs, a significant 
portion of which were repurchased through two ASR transactions which are further described below. 

Pursuant to the authorization under the 2014 Repurchase Program, in August 2016, the Company entered into two fixed dollar 
ASRs with Barclays Bank PLC (“Barclays”) for a total of $3.6 billion. Upon payment of the $3.6 billion purchase price in 
January 2017, the Company received a number of shares of CVS Health common stock equal to 80% of the $3.6 billion 
notional amount of the ASRs or approximately 36.1 million shares, which were placed into treasury stock in January 2017. The 
ASRs were accounted for as an initial treasury stock transaction for $2.9 billion and a forward contract for $0.7 billion. In April 
2017, the Company received an additional 9.9 million shares of CVS Health common stock, representing the remaining 20% of 
the $3.6 billion notional amount of the ASRs, thereby concluding the ASRs. The additional 9.9 million shares of common stock 
delivered to the Company by Barclays were placed into treasury stock, and the forward contract was reclassified from capital 
surplus to treasury stock in April 2017.

Dividends

The quarterly cash dividend declared by the Board was $0.50 per share in 2019 and 2018. CVS Health has paid cash dividends 
every quarter since becoming a public company. Future dividend payments will depend on the Company’s earnings, capital 
requirements, financial condition and other factors considered relevant by the Board. 

151

Regulatory Requirements

On November 28, 2018, the Company completed the Aetna Acquisition. Aetna’s insurance business operations are conducted 
through subsidiaries that principally consist of HMOs and insurance companies. The Company’s HMO and insurance 
subsidiaries report their financial statements in accordance with accounting practices prescribed by state regulatory authorities 
which may differ from GAAP.

The combined statutory net income of the Company’s insurance and HMO subsidiaries for the year ended December 31, 2019 
was $2.8 billion and for the year ended December 31, 2018 (which includes Aetna and its subsidiaries from November 28, 2018 
to December 31, 2018) was not material. The estimated combined statutory capital and surplus at December 31, 2019 and 2018 
of the Company’s insurance and HMO subsidiaries was approximately $11.0 billion and $10.1 billion, respectively. The 
Company’s insurance and HMO subsidiaries paid $2.4 billion of gross dividends to the Company for the year ended 
December 31, 2019.

In addition to general state law restrictions on payments of dividends and other distributions to stockholders applicable to all 
corporations, HMOs and insurance companies are subject to further regulations that, among other things, may require those 
companies to maintain certain levels of equity and restrict the amount of dividends and other distributions that may be paid to 
their equity holders. In addition, in connection with the Aetna Acquisition, the Company made certain undertakings that require 
prior regulatory approval of dividends by certain of its HMOs and insurance companies. At December 31, 2019, these amounts 
were as follows:

In millions

Estimated minimum statutory surplus required by regulators

Investments on deposit with regulatory bodies

Estimated maximum dividend distributions permitted in 2020 without prior regulatory approval

$

5,841

672

366

Noncontrolling Interests

At December 31, 2019 and 2018, noncontrolling interests were $306 million and $318 million, respectively, primarily related to 
third party interests in the Company’s operating entities. The noncontrolling entities’ share is included in total shareholders’ 
equity on the consolidated balance sheets.

152

13.  Other Comprehensive Income

Shareholders’ equity included the following activity in accumulated other comprehensive income (loss) in 2019, 2018 and 
2017:

In millions
Net unrealized investment gains:

Beginning of year balance

Other comprehensive income before reclassifications ($927, $132 and $0 pretax)
Amounts reclassified from accumulated other comprehensive income ($(105), $1 and $0  
pretax) (1)

Other comprehensive income

End of year balance

Foreign currency translation adjustments:

Beginning of year balance

Other comprehensive income (loss) before reclassifications
Amounts reclassified from accumulated other comprehensive loss (2)

Other comprehensive income (loss)

End of year balance

Net cash flow hedges:

Beginning of year balance
Adoption of new accounting standard (3)

Other comprehensive income (loss) before reclassifications ($(25), $465 and $(18) 
pretax)
Amounts reclassified from accumulated other comprehensive income (loss) ($(20), $(19) 
and $2 pretax) (4)

Other comprehensive income (loss)

End of year balance

Pension and other postretirement benefits:

Beginning of year balance
Adoption of new accounting standard (3)

Other comprehensive income (loss) before reclassifications ($162, $(178) and $0 pretax)
Amounts reclassified from accumulated other comprehensive loss ($(12), $11 and $249 
pretax) (5)

Other comprehensive income (loss)

End of year balance

Total beginning of year accumulated other comprehensive income (loss)
Adoption of new accounting standard (3)
Total other comprehensive income

Total end of year accumulated other comprehensive income (loss)
_____________________________________________

At December 31,

2019

2018

2017

$

97

$

— $

763

(86)
677

774

(158)
8
154

162

4

312

—

(18)

(15)
(33)
279

(149)
—

120

(9)
111
(38)

102

—

917

97

—

97

97

(129)
(29)
—
(29)
(158)

(15)
(3)

344

(14)
330

312

(21)
(4)
(132)

8
(124)
(149)

(165)
(7)
274

$

1,019

$

102

$

—

—

—

—

—

(127)
(2)
—
(2)
(129)

(5)
—

(11)

1
(10)
(15)

(173)
—

—

152

152
(21)

(305)
—

140
(165)

(1)  Amounts reclassified from accumulated other comprehensive income for specifically identified debt securities are included in net investment income in 

the consolidated statements of operations. 

(2)  Amounts reclassified from accumulated other comprehensive loss represent the elimination of the cumulative translation adjustment associated with the 
sale of Onofre, which was sold on July 1, 2019. The loss on the divestiture of Onofre is reflected in operating expenses in the consolidated statements of 
operations.

(3)  Reflects the adoption of ASU 2018-02, Income Statement Reporting Comprehensive Income (Topic 220); Reclassification of Certain Tax Effects from 

Accumulated Other Comprehensive Income during the year ended December 31, 2018.

153

(4)  Amounts reclassified from accumulated other comprehensive income (loss) for specifically identified cash flow hedges are included within interest 

expense in the consolidated statements of operations. The Company expects to reclassify approximately $14 million, net of tax, in net gains associated 
with its cash flow hedges into net income within the next 12 months.

(5)  Amounts reclassified from accumulated other comprehensive loss for specifically identified pension and other postretirement benefits are included in 

other expense (income) in the consolidated statements of operations. 

14.  Earnings (Loss) Per Share

Earnings (loss) per share is computed using the two-class method. For periods in which the Company reports net income, 
diluted earnings per share is determined by using the weighted average number of common and dilutive common equivalent 
shares outstanding during the period, unless the effect is antidilutive. SARs and options to purchase 17 million shares of 
common stock were outstanding, but were excluded from the calculation of diluted earnings per share, for the year ended 
December 31, 2019 because the exercise prices of the SARs and options were greater than the average market price of the 
common shares and, therefore, the effect would be antidilutive. For the same reason, options to purchase 13 million and 10 
million shares of common stock were outstanding, but were excluded from the calculation of diluted earnings per share, for the 
years ended December 31, 2018 and 2017, respectively. In addition, due to the loss from continuing operations attributable to 
CVS Health in the year ended December 31, 2018, 3 million potentially dilutive common equivalent shares were excluded from 
the calculation of diluted earnings per share, as the impact of these shares was antidilutive for that period.

The following is a reconciliation of basic and diluted earnings (loss) per share from continuing operations for the years ended 
December 31, 2019, 2018 and 2017:

In millions, except per share amounts

Numerator for earnings (loss) per share calculation:

Income (loss) from continuing operations

Income allocated to participating securities

Net (income) loss attributable to noncontrolling interests

Income (loss) from continuing operations attributable to CVS Health

Denominator for earnings (loss) per share calculation:

Weighted average shares, basic

Effect of dilutive securities

Weighted average shares, diluted

Earnings (loss) per share from continuing operations:

Basic

Diluted

15.  Reinsurance

2019

2018

2017

$

6,631
(5)
3

6,629

$

(596) $
(3)
2
(597) $

1,301

4

1,305

1,044

—

1,044

6,631
(24)
(1)
6,606

1,020

4

1,024

5.10

5.08

$

$

(0.57) $
(0.57) $

6.48

6.45

$

$

$

$

The Company utilizes reinsurance agreements primarily to: (a) reduce required capital and (b) facilitate the acquisition or 
disposition of certain insurance contracts. Ceded reinsurance agreements permit the Company to recover a portion of its losses 
from reinsurers, although they do not discharge the Company’s primary liability as the direct insurer of the risks reinsured.

On November 30, 2018, the Company completed the sale of Aetna’s standalone Medicare Part D prescription drug plans to a 
subsidiary of WellCare Health Plans, Inc. (“WellCare”), effective December 31, 2018. In connection with that sale, subsidiaries 
of WellCare and Aetna entered into reinsurance agreements under which WellCare ceded to Aetna 100% of the insurance risk 
related to the divested standalone Medicare Part D prescription drug plans for the 2019 PDP plan year.

In January 2020, the Company entered into two four-year reinsurance agreements with an unrelated reinsurer that allow it to 
reduce required capital and provide collateralized excess of loss reinsurance coverage on a portion of the Health Care Benefits 
segment’s group Commercial Insured business.

154

 
Reinsurance recoverables (recorded as other current assets or other assets on the consolidated balance sheets) at December 31, 
2019 and 2018 were as follows:

In millions
Reinsurer

Hartford Life and Accident Insurance Company

Lincoln Life & Annuity Company of New York

WellCare Health Plans

VOYA Retirement Insurance and Annuity Company

All Other

Total

2019

2018

$ 3,085

$ 3,470

413

355

175

103

424

—

186

461

$ 4,131

$ 4,541

Prior to the Aetna Acquisition Date, the Company had no material assumed or ceded premiums or benefit costs. Accordingly, 
the Company has not provided disclosure of these amounts for periods prior to 2018. 

Direct, assumed and ceded premiums earned for the years ended December 31, 2019 and 2018 were as follows:

In millions
Direct
Assumed
Ceded

Net premiums

2019
$ 62,968
2,108
(1,954)
$ 63,122

2018
$ 8,365
38
(219)
$ 8,184

The impact of reinsurance on benefit costs for the years ended December 31, 2019 and 2018 were as follows:

In millions

Direct

Assumed

Ceded

Net benefit costs

2019

2018

$ 52,592

$ 6,773

1,562
(1,625)
$ 52,529

32
(211)
$ 6,594

There is not a material difference between premiums on a written basis versus an earned basis.

The Company also has various agreements with unrelated reinsurers that do not qualify for reinsurance accounting under 
GAAP, and consequently are accounted for using deposit accounting. The Company entered into these contracts to reduce the 
risk of catastrophic loss which in turn reduces the Company’s capital and surplus requirements. Total deposit assets and 
liabilities related to reinsurance agreements that do not qualify for reinsurance accounting under GAAP were not material as of 
December 31, 2019 or 2018.

16.  Commitments and Contingencies

Guarantees

The Company has the following significant guarantee arrangements at December 31, 2019:

•  ASC Claim Funding Accounts - The Company has arrangements with certain banks for the processing of claim payments 
for its ASC customers. The banks maintain accounts to fund claims of the Company’s ASC customers. The customer is 
responsible for funding the amount paid by the bank each day. In these arrangements, the Company guarantees that the 
banks will not sustain losses if the responsible ASC customer does not properly fund its account. The aggregate maximum 
exposure under these arrangements is generally limited to $250 million. The Company can limit its exposure to these 
guarantees by suspending the payment of claims for ASC customers that have not adequately funded the amount paid by 
the bank. 

• 

Separate Accounts Assets - Certain Separate Accounts assets associated with the large case pensions business in the 
Corporate/Other segment represent funds maintained as a contractual requirement to fund specific pension annuities that 
the Company has guaranteed. Minimum contractual obligations underlying the guaranteed benefits in these Separate 
155

Accounts were approximately $1.4 billion at both December 31, 2019 and 2018. See Note 1 ‘‘Significant Accounting 
Policies’’ for additional information on Separate Accounts. Contract holders assume all investment and mortality risk and 
are required to maintain Separate Accounts balances at or above a specified level. The level of required funds is a function 
of the risk underlying the Separate Account’s investment strategy. If contract holders do not maintain the required level of 
Separate Accounts assets to meet the annuity guarantees, the Company would establish an additional liability. Contract 
holders’ balances in the Separate Accounts at December 31, 2019 exceeded the value of the guaranteed benefit obligation. 
As a result, the Company was not required to maintain any additional liability for its related guarantees at December 31, 
2019. 

Lease Guarantees

Between 1995 and 1997, the Company sold or spun off a number of subsidiaries, including Bob’s Stores and Linens ‘n Things, 
each of which subsequently filed for bankruptcy, and Marshalls. In many cases, when a former subsidiary leased a store, the 
Company provided a guarantee of the former subsidiary’s lease obligations for the initial lease term and any extension thereof 
pursuant to a renewal option provided for in the lease prior to the time of the disposition. When the subsidiaries were disposed 
of and accounted for as discontinued operations, the Company’s guarantees remained in place, although each initial purchaser 
agreed to indemnify the Company for any lease obligations the Company was required to satisfy. If any of the purchasers or any 
of the former subsidiaries fail to make the required payments under a store lease, the Company could be required to satisfy 
those obligations. As of December 31, 2019, the Company guaranteed 79 such store leases (excluding the lease guarantees 
related to Linens ‘n Things, which have been recorded as a liability on the consolidated balance sheet), with the maximum 
remaining lease term extending through 2030.

Guaranty Fund Assessments, Market Stabilization and Other Non-Voluntary Risk Sharing Pools

Under guaranty fund laws existing in all states, insurers doing business in those states can be assessed (in most states up to 
prescribed limits) for certain obligations of insolvent insurance companies to policyholders and claimants. The life and health 
insurance guaranty associations in which the Company participates that operate under these laws respond to insolvencies of 
long-term care insurers as well as health insurers. The Company’s assessments generally are based on a formula relating to the 
Company’s health care premiums in the state compared to the premiums of other insurers. Certain states allow assessments to 
be recovered over time as offsets to premium taxes. Some states have similar laws relating to HMOs and/or other payors such 
as not-for-profit consumer-governed health plans established under the ACA.

In 2009, the Pennsylvania Insurance Commissioner placed long-term care insurer Penn Treaty Network America Insurance 
Company and one of its subsidiaries (collectively, “Penn Treaty”) in rehabilitation, an intermediate action before insolvency, 
and subsequently petitioned a state court to convert the rehabilitation into a liquidation. Penn Treaty was placed in liquidation in 
March 2017. The Company has recorded a liability for its estimated share of future assessments by applicable life and health 
guaranty associations. It is reasonably possible that in the future the Company may record a liability and expense relating to 
other insolvencies which could have a material adverse effect on the Company’s operating results, financial condition and cash 
flows. While historically the Company has ultimately recovered more than half of guaranty fund assessments through 
statutorily permitted premium tax offsets, significant increases in assessments could lead to legislative and/or regulatory actions 
that limit future offsets.

HMOs in certain states in which the Company does business are subject to assessments, including market stabilization and 
other risk-sharing pools, for which the Company is assessed charges based on incurred claims, demographic membership mix 
and other factors. The Company establishes liabilities for these assessments based on applicable laws and regulations. In certain 
states, the ultimate assessments the Company pays are dependent upon the Company’s experience relative to other entities 
subject to the assessment, and the ultimate liability is not known at the financial statement date. While the ultimate amount of 
the assessment is dependent upon the experience of all pool participants, the Company believes it has adequate reserves to 
cover such assessments.

The Company’s total guaranty fund assessments liability was $84 million and $90 million at December 31, 2019 and 2018, 
respectively, and was recorded in accrued expenses on the consolidated balance sheets.

Litigation and Regulatory Proceedings

The Company is a party to numerous legal proceedings, investigations, audits and claims arising, for the most part, in the 
ordinary course of its businesses, including the matters described below. The Company records accruals for outstanding legal 
matters when it believes it is probable that a loss will be incurred and the amount can be reasonably estimated. The Company 

156

evaluates, on a quarterly basis, developments in legal matters that could affect the amount of any accrual and developments that 
would make a loss contingency both probable and reasonably estimable. If a loss contingency is not both probable and 
reasonably estimable, the Company does not establish an accrued liability. None of the Company’s accruals for outstanding 
legal matters are material individually or in the aggregate to the Company’s financial condition.

Except as otherwise noted, the Company cannot predict with certainty the timing or outcome of the legal matters described 
below, and the Company is unable to reasonably estimate a possible loss or range of possible loss in excess of amounts already 
accrued for these matters. It is reasonably possible that the outcome of such legal matters could be material to the Company.

Usual and Customary Litigation

The Company is named as a defendant in a number of lawsuits that allege that the Company’s retail stores overcharged for 
prescription drugs by not providing the correct usual and customary charge.

Corcoran et al. v. CVS Health Corporation (U.S. District Court for the Northern District of California) and Podgorny et al. v. 
CVS Health Corporation (U.S. District Court for the Northern District of Illinois). These putative class actions were filed 
against the Company in July and September 2015. The cases were consolidated in the U.S. District Court for the Northern 
District of California. Plaintiffs seek damages and injunctive relief under the consumer protection statutes of certain states on 
behalf of a class of consumers who purchased certain prescription drugs. Several third-party payors filed similar putative class 
actions on behalf of payors captioned Sheet Metal Workers Local No. 20 Welfare and Benefit Fund v. CVS Health Corp. and 
Plumbers Welfare Fund, Local 130 v. CVS Health Corporation (both pending in the U.S. District Court for the District of 
Rhode Island) in February and August 2016. In all of these cases the plaintiffs allege the Company overcharged for certain 
prescription drugs by not submitting the price available to members of the CVS Health Savings Pass program as the pharmacy’s 
usual and customary price. In the Corcoran case, the U.S. District Court granted summary judgment to CVS on plaintiffs’ 
claims in their entirety and certified certain subclasses in September 2017. In June 2019, the U.S. Court of Appeals for the 
Ninth Circuit reversed the U.S. District Court’s grant of summary judgment and reversed the U.S. District Court’s narrowing of 
the requested class. The Corcoran case is proceeding to a trial on a six state class basis, and trial is scheduled to occur in 2020. 
The Sheet Metal Workers plaintiffs have amended their complaint to assert a claim under the federal Racketeer Influenced and 
Corrupt Organizations Act premised on an alleged conspiracy between the Company and other PBMs. The Company is 
defending itself against these claims.

State of California ex rel. Matthew Omlansky v. CVS Caremark Corporation (Superior Court of the State of California, County 
of Sacramento). In April 2016, the California Superior Court unsealed a first amended qui tam complaint filed in July 2013. The 
government has declined to intervene in this case. The relator alleges that the Company submitted false claims for payment to 
the California Medicaid program in connection with reimbursement for drugs available through the CVS Health Savings Pass 
program as well as certain other generic drugs. The case has been stayed pending the relator’s appeal of the judgment against 
him in a similar case against another retailer. The Company is defending itself against these claims.

State of Mississippi v. CVS Health Corporation, et al. (Circuit Court of DeSoto County, Mississippi, Third Judicial District). In 
July 2016, the Company was served with a complaint filed on behalf of the State of Mississippi. The complaint alleged that 
CVS retail pharmacies in Mississippi submitted false claims for reimbursement to the Mississippi Medicaid program by not 
submitting the price available to members of the CVS Health Savings Pass program as the pharmacy’s usual and customary 
price. In June 2019, the Company’s motion for judgment on the pleadings was granted in part and denied in part. Also in June 
2019, the State of Mississippi’s motion to dismiss the Company’s counterclaim for declaratory relief was granted. The 
Company is defending itself against these claims.

PBM Litigation and Investigations

The Company is named as a defendant in a number of lawsuits and is subject to a number of investigations concerning its PBM 
practices. 

Klein, et al. v. Prime Therapeutics, et al. (U.S. District Court for the District of Minnesota). This putative class action was filed 
against the Company and other PBMs in June 2017 on behalf of ERISA plan members who purchased and paid for EpiPen or 
EpiPen Jr. Plaintiffs allege that the PBMs are ERISA fiduciaries to plan members and have violated ERISA by allegedly 
causing higher inflated prices for EpiPens through the process of negotiating increased rebates from EpiPen manufacturer 
Mylan. This case has been consolidated with a similar matter and is now proceeding as In re EpiPen ERISA Litigation. The 
Company is defending itself against these claims.

157

County of Harris, Texas v. Eli Lilly and Company, et al. (U.S. District Court for the Southern District of Texas). This lawsuit 
was filed against Caremark, Aetna, the manufacturers of insulin and other PBMs in November 2019 by Harris County. Harris 
County alleges that it was overcharged for insulin as a result of a “price fixing conspiracy” between the manufacturers and 
PBMs to artificially increase the price of insulin and other diabetes medications. The complaint alleges that the manufacturers 
and PBMs engaged in an “Insulin Pricing Scheme” whereby the manufacturers artificially increased the reported prices of their 
insulin products while “secretly” paying rebates to the PBMs in exchange for preferred treatment on the PBMs’ drug 
formularies. The Company is defending itself against these claims.

In March 2017, Advanced Care Scripts, a subsidiary acquired in the Omnicare transaction that is now part of the Company’s 
PBM specialty operations, received a subpoena from the U.S. Department of Justice (the “DOJ”) requesting documents 
concerning its work with pharmaceutical manufacturers and charitable foundations that provide payment assistance to Medicare 
patients in connection with an investigation concerning potential violations of the federal Anti-Kickback Statute and/or federal 
False Claims Act. The Company has been cooperating with the government with respect to this subpoena and additional 
requests for information.

The Company has received subpoenas, CIDs and other requests for documents and information from, and is being investigated 
by, Attorneys General of several states regarding its PBM practices, including pricing and rebates. In addition, the Company has 
received inquiries from congressional committees regarding insulin pricing. The Company has been providing documents and 
information in response to these subpoenas, CIDs and requests for information.

Controlled Substances Litigation, Audits and Subpoenas

In December 2017, the U.S. Judicial Panel on Multidistrict Litigation consolidated numerous cases filed against various 
defendants by plaintiffs such as counties, cities, hospitals, Indian tribes and third-party payors, alleging claims generally 
concerning the impacts of widespread opioid abuse. The consolidated multidistrict litigation captioned In re National 
Prescription Opiate Litigation (MDL No. 2804) is pending in the U.S. District Court for the Northern District of Ohio. This 
multidistrict litigation presumptively includes hundreds of relevant federal court cases that name the Company as a defendant. 
A significant number of similar cases that name the Company as a defendant in some capacity are pending in state courts. In 
addition, the Company has been named as a defendant in similar cases brought by certain state Attorneys General. The 
Company is defending itself against all such claims. Additionally, the Company has received subpoenas, CIDs and/or other 
requests for information regarding opioids from state Attorneys General and insurance and other regulators of several states. 
The Company has been cooperating with the government with respect to these subpoenas, CIDs and other requests for 
information.

The Company routinely is audited by the U.S. Drug Enforcement Administration (the “DEA”). In some instances, the Company 
is in discussions with the DEA and U.S. Attorney’s Offices concerning allegations that the Company violated certain 
requirements of the federal Controlled Substances Act.

In September 2015, the DEA served the Company with an administrative subpoena. The subpoena seeks documents related to 
controlled substance policies, procedures and practices at eight Omnicare pharmacy locations from May 2012 to the present. In 
September 2017, the DEA expanded the investigation to include an additional Omnicare pharmacy location. The Company has 
been cooperating with the government and providing documents and witnesses in response to this subpoena.

In January 2020, the DOJ served the Company with a DEA administrative subpoena. The subpoena seeks documents relating to 
practices with respect to opioids and other controlled substances at CVS Pharmacy locations in connection with an investigation 
concerning potential violations of the federal Controlled Substances Act and the federal False Claims Act. The Company has 
been cooperating with the government with respect to this subpoena.

Prescription Processing Litigation and Investigations

U.S. ex rel. Bassan et al. v. Omnicare, Inc. and CVS Health Corp. and U.S. ex rel. Mohajer et al. v. Omnicare, Inc. and CVS Health 
Corp. (U.S. District Court for the Southern District of New York). In December 2019, the U.S. Attorney’s Office for the Southern 
District of New York (the “SDNY”) filed complaints-in-intervention in these two previously sealed qui tam cases. With respect 
to the Bassan complaint, all states except Washington, D.C. and Indiana have declined to intervene; Washington, D.C. has intervened, 
and Indiana has not filed a decision on intervention. The government’s investigation related to these complaints included the 
previously  disclosed  CID  that  the  Company  received  in  October  2015  from  the  SDNY  concerning  the  Company’s  Omnicare 
pharmacies’ cycle fill process for assisted living facilities. The complaints allege that for certain non-skilled nursing facilities, 

158

Omnicare improperly filled prescriptions beyond one year where a valid prescription did not exist and that these dispensing events 
violated the federal False Claims Act. The Company is defending itself against these claims.

In July 2017, the Company also received a subpoena from the California Department of Insurance requesting documents 
concerning the Company’s Omnicare pharmacies’ cycle fill process for assisted living facilities. The Company has been 
cooperating with the California Department of Insurance and providing documents and information in response to this 
subpoena.

In December 2016, the Company received a CID from the U.S. Attorney’s Office for the Northern District of New York 
requesting documents and information in connection with a federal False Claims Act investigation concerning whether the 
Company’s retail pharmacies improperly submitted certain insulin claims to Part D of the Medicare program rather than Part B 
of the Medicare program. The Company has been cooperating with the government and providing documents and information 
in response to this CID.

In May 2017, the Company received a CID from the SDNY requesting documents and information concerning possible false 
claims submitted to Medicare in connection with reimbursements for prescription drugs under the Medicare Part D program. 
The Company has been cooperating with the government and providing documents and information in response to this CID.

Provider Proceedings

The Company is named as a defendant in purported class actions and individual lawsuits arising out of its practices related to 
the payment of claims for services rendered to its members by health care providers with whom the Company has a contract 
and with whom the Company does not have a contract (“out-of-network providers”). Among other things, these lawsuits allege 
that the Company paid too little to its health plan members and/or providers for these services and/or otherwise allege that the 
Company failed to timely or appropriately pay or administer claims and benefits (including the Company’s post payment audit 
and collection practices and reductions in payments to providers due to sequestration). Other major health insurers are the 
subject of similar litigation or have settled similar litigation.

The Company also has received subpoenas and/or requests for documents and other information from, and been investigated by, 
state Attorneys General and other state and/or federal regulators, legislators and agencies relating to, and the Company is 
involved in other litigation regarding, its out-of-network benefit payment and administration practices. It is reasonably possible 
that others could initiate additional litigation or additional regulatory action against the Company with respect to its out-of-
network benefit payment and/or administration practices.

CMS Actions

CMS regularly audits the Company’s performance to determine its compliance with CMS’s regulations and its contracts with 
CMS and to assess the quality of services it provides to Medicare beneficiaries. CMS uses various payment mechanisms to 
allocate and adjust premium payments to the Company’s and other companies’ Medicare plans by considering the applicable 
health status of Medicare members as supported by information prepared, maintained and provided by health care providers. 
The Company collects claim and encounter data from providers and generally relies on providers to appropriately code their 
submissions to the Company and document their medical records, including the diagnosis data submitted to the Company with 
claims. CMS pays increased premiums to Medicare Advantage plans and Medicare PDP plans for members who have certain 
medical conditions identified with specific diagnosis codes. Federal regulators review and audit the providers’ medical records 
to determine whether those records support the related diagnosis codes that determine the members’ health status and the 
resulting risk-adjusted premium payments to the Company. In that regard, CMS has instituted risk adjustment data validation 
(“RADV”) audits of various Medicare Advantage plans, including certain of the Company’s plans, to validate coding practices 
and supporting medical record documentation maintained by health care providers and the resulting risk adjusted premium 
payments to the plans. CMS may require the Company to refund premium payments if the Company’s risk adjusted premiums 
are not properly supported by medical record data. The Office of the Inspector General of Health and Human Services (the 
“OIG”) also is auditing the Company’s risk adjustment-related data and that of other companies. The Company expects CMS 
and the OIG to continue these types of audits.

In 2012, CMS revised its audit methodology for RADV audits to determine refunds payable by Medicare Advantage plans for 
contract year 2011 and forward. Under the revised methodology, among other things, CMS will extrapolate the error rate 
identified in the audit sample of approximately 200 members to all risk adjusted premium payments made under the contract 
being audited. For contract years prior to 2011, CMS did not extrapolate sample error rates to the entire contract. As a result, the 
revised methodology may increase the Company’s exposure to premium refunds to CMS based on incomplete medical records 

159

maintained by providers. Since 2013, CMS has selected certain of the Company’s Medicare Advantage contracts for various 
contract years for RADV audit, and the number of RADV audits continues to increase. The Company is currently unable to 
predict which of its Medicare Advantage contracts will be selected for future audit, the amounts of any retroactive refunds of, or 
prospective adjustments to, Medicare Advantage premium payments made to the Company, the effect of any such refunds or 
adjustments on the actuarial soundness of the Company’s Medicare Advantage bids, or whether any RADV audit findings 
would require the Company to change its method of estimating future premium revenue in future bid submissions to CMS or 
compromise premium assumptions made in the Company’s bids for prior contract years, the current contract year or future 
contract years. Any premium or fee refunds or adjustments resulting from regulatory audits, whether as a result of RADV, 
Public Exchange related or other audits by CMS, the OIG, the U.S. Department of Health and Human Services or otherwise, 
including audits of the Company’s minimum MLR rebates, methodology and/or reports, could be material and could adversely 
affect the Company’s operating results, financial condition and/or cash flows.

Medicare CIDs

The Company has received CIDs from the Civil Division of the DOJ in connection with a current investigation of the 
Company’s patient chart review processes in connection with risk adjustment data submissions under Parts C and D of the 
Medicare program. The Company has been cooperating with the government and providing documents and information in 
response to these CIDs.

Stockholder Matters

The Company and/or its current and/or former directors and/or executive officers are named as defendants in a number of 
lawsuits and a request for access to information initiated by holders or putative holders of CVS Health common stock.

Between February and August 2019, six class action complaints were filed by putative plaintiffs against the Company and 
certain current and former officers and directors: Anarkat v. CVS Health Corp., et al. (U.S. District Court for the District of 
Rhode Island); Labourers’ Pension Fund of Central and Eastern Canada v. CVS Health Corp., et al. (New York Supreme 
Court); City of Warren Police and Fire Retirement Sys.v. CVS Health Corp., et. al. (Rhode Island Superior Court); Cambria Co. 
Employees Retirement Sys. v. CVS Health Corp., et al. (New York Supreme Court); Freundlich v. CVS Health Corp., et al. 
(Rhode Island Superior Court); and Waterford Twp. Police & Fire Retirement Sys. v. CVS Health Corp., et al. (U.S. District 
Court for the District of Rhode Island). The plaintiffs in these cases assert a variety of causes of action under federal securities 
laws that are premised on allegations that the defendants made certain omissions and misrepresentations relating to the 
performance of the Company’s LTC business unit, which allegedly injured investors who acquired CVS Health securities 
between February 9, 2016 and February 20, 2019. The Freundlich case also alleges that defendants misrepresented anticipated 
synergies of the Aetna Acquisition. Plaintiffs in the Freundlich and the City of Warren cases have filed a consolidated complaint 
that combines their allegations. The Company is defending itself against these claims.

In January 2020, a derivative complaint was filed against the Company’s directors and current and former executive officers in 
the U.S. District Court for the District of Rhode Island by a stockholder. Lovoi v. Aguirre, et al. makes allegations similar to 
those contained the six stockholder class action complaints described above, including that the Company made false or 
misleading statements about its LTC business unit’s financial health. The Lovoi complaint alleges claims for breach of fiduciary 
duty against the Company’s directors and certain of its current and former executive officers and for violation of the federal 
securities laws. The Lovoi complaint seeks damages, restitution and equitable relief on behalf of the Company. The Company’s 
directors and current and former executive officers are defending themselves against these claims.

In November 2019, the Company received a demand to inspect its books and records under Delaware General Corporation Law 
Section 220 from purported stockholder Judith B. Cohen. The demand seeks various documents related to the Company’s LTC 
operations, its financial condition and its goodwill impairment charges, as well as more general information regarding share 
repurchases, director nominations and charitable donations. The Company has objected to this request.

Other Legal and Regulatory Proceedings.

The Company is also a party to other legal proceedings and is subject to government investigations, inquiries and audits and has 
received and is cooperating with the government in response to CIDs, subpoenas or similar process from various governmental 
agencies requesting information, arising, for the most part, in the ordinary course of its businesses. These other legal 
proceedings and government actions include claims of or relating to bad faith, medical or professional malpractice, claims 
processing, dispensing of medications, non-compliance with state and federal regulatory regimes, marketing misconduct, failure 
to timely or appropriately pay or administer claims and benefits, provider network structure (including the use of performance-

160

based networks and termination of provider contracts), rescission of insurance coverage, improper disclosure or use of personal 
information, anticompetitive practices, general contractual matters, product liability, intellectual property litigation and 
employment litigation. Some of these other legal proceedings are or are purported to be class actions or derivative claims. The 
Company is defending itself against the claims brought in these matters.

Awards to the Company and others of certain government contracts, particularly Medicaid contracts and other contracts with 
government customers in the Company’s Health Care Benefits segment, frequently are subject to protests by unsuccessful 
bidders. These protests may result in awards to the Company being reversed, delayed or modified. The loss or delay in 
implementation of any government contract could adversely affect the Company’s operating results. The Company will 
continue to defend contract awards it receives.

There also continues to be a heightened level of review and/or audit by regulatory authorities and legislators of, and increased 
litigation regarding, the Company’s and the rest of the health care and related benefits industry’s business and reporting 
practices, including premium rate increases, utilization management, development and application of medical policies, 
complaint, grievance and appeal processing, information privacy, provider network structure (including provider network 
adequacy, the use of performance-based networks and termination of provider contracts), provider directory accuracy, 
calculation of minimum medical loss ratios and/or payment of related rebates, delegated arrangements, rescission of insurance 
coverage, limited benefit health products, student health products, pharmacy benefit management practices (including 
manufacturers’ rebates, pricing, the use of narrow networks and the placement of drugs in formulary tiers), sales practices, 
customer service practices, vendor oversight and claim payment practices (including payments to out-of-network providers).

As a leading national health care company, the Company regularly is the subject of government actions of the types described 
above. These government actions may prevent or delay the Company from implementing planned premium rate increases and 
may result, and have resulted, in restrictions on the Company’s businesses, changes to or clarifications of the Company’s 
business practices, retroactive adjustments to premiums, refunds or other payments to members, beneficiaries, states or the 
federal government, withholding of premium payments to the Company by government agencies, assessments of damages, civil 
or criminal fines or penalties, or other sanctions, including the possible suspension or loss of licensure and/or suspension or 
exclusion from participation in government programs.

The Company can give no assurance that its businesses, financial condition, operating results and/or cash flows will not be 
materially adversely affected, or that the Company will not be required to materially change its business practices, based on: 
(i) future enactment of new health care or other laws or regulations; (ii) the interpretation or application of existing laws or 
regulations as they may relate to one or more of the Company’s businesses, one or more of the industries in which the Company 
competes and/or the health care industry generally; (iii) pending or future federal or state government investigations of one or 
more of the Company’s businesses, one or more of the industries in which the Company competes and/or the health care 
industry generally; (iv) pending or future government audits, investigations or enforcement actions against the Company; 
(v) adverse developments in any pending qui tam lawsuit against the Company, whether sealed or unsealed, or in any future qui 
tam lawsuit that may be filed against the Company; or (vi) adverse developments in pending or future legal proceedings against 
the Company or affecting one or more of the industries in which the Company competes and/or the health care industry 
generally.

17. 

Segment Reporting

The Company has three operating segments, Pharmacy Services, Retail/LTC and Health Care Benefits, as well as a Corporate/
Other segment. The Company’s segments maintain separate financial information, and the CODM evaluates the segments’ 
operating results on a regular basis in deciding how to allocate resources among the segments and in assessing segment 
performance. The CODM evaluates the performance of the Company’s segments based on adjusted operating income. Effective 
for the first quarter of 2019, adjusted operating income is defined as operating income (GAAP measure) excluding the impact 
of amortization of intangible assets and other items, if any, that neither relate to the ordinary course of the Company’s business 
nor reflect the Company’s underlying business performance. Segment financial information has been retrospectively adjusted to 
conform with the current period presentation. See the reconciliation of consolidated operating income (GAAP measure) to 
adjusted operating income below for further context regarding the items excluded from operating income in determining 
adjusted operating income. The Company uses adjusted operating income as its principal measure of segment performance as it 
enhances the Company’s ability to compare past financial performance with current performance and analyze underlying 
business performance and trends. Non-GAAP financial measures the Company discloses, such as consolidated adjusted 
operating income, should not be considered a substitute for, or superior to, financial measures determined or calculated in 
accordance with GAAP.

161

Effective for the first quarter of 2019, the Company realigned the composition of its segments to correspond with changes to its 
operating model and reflect how its CODM reviews information and manages the business. See Note 1 ‘‘Significant 
Accounting Policies’’ for further discussion of this realignment. Segment financial information has been retrospectively 
adjusted to reflect these changes. 

In 2018 and 2017, approximately 9.8% and 12.3%, respectively, of the Company’s consolidated revenues were from Aetna, a 
Pharmacy Services segment client. On November 28, 2018, the Company completed the Aetna Acquisition. Subsequent to the 
Aetna Acquisition, transactions with Aetna continue to be reported within the Pharmacy Services segment, but are eliminated in 
the Company’s consolidated financial statements. 

In millions
2019:

Pharmacy 
Services (1)

Retail/
LTC

Health Care
Benefits

Corporate/
Other

Intersegment
Eliminations (2)

Consolidated
Totals

Revenues from customers

$

141,491

$

86,608

$

69,005

$

Net investment income

Total revenues

  Adjusted operating income (loss)

Depreciation and amortization

Additions to property and equipment

2018:

Revenues from customers

Net investment income

Total revenues

  Adjusted operating income (loss)

Depreciation and amortization

Additions to property and equipment

2017:

Revenues from customers

Net investment income

Total revenues

  Adjusted operating income (loss)

Depreciation and amortization

Additions to property and equipment

_____________________________________________

—

—

141,491

86,608

5,129

766

332

6,705

1,723

1,212

134,736

83,989

—

—

134,736

83,989

4,955

710

326

7,403

1,698

1,350

130,822

79,398

—

—

130,822

79,398

4,628

710

311

7,475

1,651

1,398

599

69,604

5,202

1,721

533

8,904

58

8,962

528

172

46

3,582

5

3,587

359

2

—

$

100

412

512
(1,000)
161

404

(41,439) $
—
(41,439)
(697)
—

—

4

602

606
(856)
138

401

—

16

16
(896)
116

340

(33,714)
—
(33,714)
(769)
—

—

(29,037)
—
(29,037)
(741)
—

—

255,765

1,011

256,776

15,339

4,371

2,481

193,919

660

194,579

11,261

2,718

2,123

184,765

21

184,786

10,825

2,479

2,049

(1)  Total revenues of the Pharmacy Services segment include approximately $11.5 billion, $11.4 billion and $10.8 billion of retail co-payments for 2019, 2018 

and 2017, respectively. See Note 1 ‘‘Significant Accounting Policies’’ for additional information about retail co-payments.

(2)  Intersegment eliminations relate to intersegment revenue generating activities that occur between the Pharmacy Services segment, the Retail/LTC segment 

and/or the Health Care Benefits segment.  

162

The following is a reconciliation of consolidated operating income to adjusted operating income for the years ended 
December 31, 2019, 2018 and 2017:

In millions

Operating income (GAAP measure)
Amortization of intangible assets (1)
Acquisition-related transaction and integration costs (2)
Store rationalization charges (3)
Loss on divestiture of subsidiary (4)
Goodwill impairments (5)
Impairment of long-lived assets (6)
Interest income on financing for the Aetna Acquisition (7)

Adjusted operating income
_____________________________________________

2019

2018

2017

$

11,987

$

4,021

$

9,538

2,436

480

231

205

—

—

—

$

15,339

$

1,006

492

—

86

6,149

43
(536)
11,261

817

65

215

9

181

—

—

$

10,825

(1)  The Company’s acquisition activities have resulted in the recognition of intangible assets as required under the acquisition method of accounting which 

consist primarily of trademarks, customer contracts/relationships, covenants not to compete, technology, provider networks and value of business acquired. 
Definite-lived intangible assets are amortized over their estimated useful lives and are tested for impairment when events indicate that the carrying value 
may not be recoverable. The amortization of intangible assets is reflected in the Company’s statements of operations in operating expenses within each 
segment. Although intangible assets contribute to the Company’s revenue generation, the amortization of intangible assets does not directly relate to the 
underwriting of the Company’s insurance products, the services performed for the Company’s customers or the sale of the Company’s products or services. 
Additionally, intangible asset amortization expense typically fluctuates based on the size and timing of the Company’s acquisition activity. Accordingly, the 
Company believes excluding the amortization of intangible assets enhances the Company’s and investors’ ability to compare the Company’s past financial 
performance with its current performance and to analyze underlying business performance and trends. Intangible asset amortization excluded from the 
related non-GAAP financial measure represents the entire amount recorded within the Company’s GAAP financial statements, and the revenue generated 
by the associated intangible assets has not been excluded from the related non-GAAP financial measure. Intangible asset amortization is excluded from the 
related non-GAAP financial measure because the amortization, unlike the related revenue, is not affected by operations of any particular period unless an 
intangible asset becomes impaired or the estimated useful life of an intangible asset is revised.  

(2)  In 2019, 2018 and 2017, acquisition-related transaction and integration costs relate to the Aetna Acquisition. In 2018 and 2017, acquisition-related 

transaction and integration costs also relate to the acquisition of Omnicare. The acquisition-related transaction and integration costs are reflected in the 
Company’s consolidated statements of operations in operating expenses within the Corporate/Other segment and the Retail/LTC segment.  

(3)  In 2019, the store rationalization charges relate to the planned closure of 46 underperforming retail pharmacy stores during the second quarter of 2019 and 
the planned closure of 22 underperforming retail pharmacy stores during the first quarter of 2020. In 2019, the store rationalization charges primarily relate 
to operating lease right-of-use asset impairment charges and are reflected in the Company’s consolidated statements of operations in operating expenses 
within the Retail/LTC segment. In 2017, the store rationalization charges related to the Company’s enterprise streamlining initiative and are reflected in the 
Company’s consolidated statements of operations in operating expenses within the Retail/LTC segment.   

(4)  In 2019, the loss on divestiture of subsidiary represents the pre-tax loss on the sale of Onofre, which occurred on July 1, 2019. The loss on divestiture 

primarily relates to the elimination of the cumulative translation adjustment from accumulated other comprehensive income. In 2018, the loss on divestiture 
of subsidiary represents the pre-tax loss on the sale of the Company’s RxCrossroads subsidiary for $725 million on January 2, 2018. In 2017, the loss on 
divestiture of subsidiary represents transaction costs associated with the sale of RxCrossroads. The losses on divestiture of subsidiary are reflected in the 
Company’s consolidated statements of operations in operating expenses within the Retail/LTC segment and Corporate/Other segment.  

(5)  In 2018, the goodwill impairments relate to the LTC reporting unit within the Retail/LTC segment. In 2017, the goodwill impairments relate to the 

RxCrossroads reporting unit within the Retail/LTC segment. 

(6)  In 2018, impairment of long-lived assets primarily relates to the impairment of property and equipment within the Retail/LTC segment and is reflected in 

operating expenses in the Company’s consolidated statements of operations. 

(7)  In 2018, the Company recorded interest income of $536 million on the proceeds of the $40 billion of unsecured senior notes it issued in March 2018 to 

partially fund the Aetna Acquisition. All amounts are for the periods prior to the close of the Aetna Acquisition, which occurred on November 28, 2018, and 
were recorded within the Corporate/Other segment.

163

Report of Independent Registered Public Accounting Firm

To the Shareholders and the Board of Directors of CVS Health Corporation

Opinion on Internal Control over Financial Reporting

We have audited CVS Health Corporation’s internal control over financial reporting as of December 31, 2019, based on criteria 
established in Internal Control-Integrated Framework issued by the Committee of Sponsoring Organizations of the Treadway 
Commission (2013 framework) (the COSO criteria). In our opinion, CVS Health Corporation (the Company) maintained, in all 
material respects, effective internal control over financial reporting as of December 31, 2019, based on the COSO criteria.

We also have audited, in accordance with the standards of the Public Company Accounting Oversight Board (United States) 
(PCAOB), the 2019 consolidated financial statements of the Company and our report dated February 18, 2020, expressed an 
unqualified opinion thereon.

Basis for Opinion

The Company’s management is responsible for maintaining effective internal control over financial reporting and for its 
assessment of the effectiveness of internal control over financial reporting included in the accompanying Management’s Report 
on Internal Control Over Financial Reporting. Our responsibility is to express an opinion on the Company’s internal control 
over financial reporting based on our audit. We are a public accounting firm registered with the PCAOB and are required to be 
independent with respect to the Company in accordance with the U.S. federal securities laws and the applicable rules and 
regulations of the Securities and Exchange Commission and the PCAOB.

We conducted our audit in accordance with the standards of the PCAOB. Those standards require that we plan and perform the 
audit to obtain reasonable assurance about whether effective internal control over financial reporting was maintained in all 
material respects. 

Our audit included obtaining an understanding of internal control over financial reporting, assessing the risk that a material 
weakness exists, testing and evaluating the design and operating effectiveness of internal control based on the assessed risk, and 
performing such other procedures as we considered necessary in the circumstances. We believe that our audit provides a 
reasonable basis for our opinion.

Definition and Limitations of Internal Control over Financial Reporting

A company’s internal control over financial reporting is a process designed to provide reasonable assurance regarding the 
reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally 
accepted accounting principles. A company’s internal control over financial reporting includes those policies and procedures 
that (1) pertain to the maintenance of records that, in reasonable detail, accurately and fairly reflect the transactions and 
dispositions of the assets of the company; (2) provide reasonable assurance that transactions are recorded as necessary to permit 
preparation of financial statements in accordance with generally accepted accounting principles, and that receipts and 
expenditures of the company are being made only in accordance with authorizations of management and directors of the 
company; and (3) provide reasonable assurance regarding prevention or timely detection of unauthorized acquisition, use, or 
disposition of the company’s assets that could have a material effect on the financial statements.

Because of its inherent limitations, internal control over financial reporting may not prevent or detect misstatements. Also, 
projections of any evaluation of effectiveness to future periods are subject to the risk that controls may become inadequate 
because of changes in conditions, or that the degree of compliance with the policies or procedures may deteriorate.

/s/ Ernst & Young LLP
Boston, Massachusetts
February 18, 2020 

164

 
 
 
 
 
 
 
 
 
 
 
 
Report of Independent Registered Public Accounting Firm 

To the Shareholders and the Board of Directors of CVS Health Corporation

Opinion on the Financial Statements

We have audited the accompanying consolidated balance sheets of CVS Health Corporation (the Company) as of December 31, 
2019 and 2018, the related consolidated statements of operations, comprehensive income (loss), shareholders’ equity and cash 
flows for each of the three years in the period ended December 31, 2019, and the related notes (collectively referred to as the 
“consolidated financial statements”). In our opinion, the consolidated financial statements present fairly, in all material respects, 
the financial position of the Company at December 31, 2019 and 2018, and the results of its operations and its cash flows for each 
of the three years in the period ended December 31, 2019, in conformity with U.S. generally accepted accounting principles. 

We  also  have  audited,  in  accordance  with  the  standards  of  the  Public  Company Accounting  Oversight  Board  (United  States) 
(PCAOB), the Company’s internal control over financial reporting as of December 31, 2019, based on criteria established in 
Internal Control-Integrated Framework issued by the Committee of Sponsoring Organizations of the Treadway Commission (2013 
framework) and our report dated February 18, 2020 expressed an unqualified opinion thereon.

Adoption of ASU 2016-02

As discussed in Note 1 to the consolidated financial statements, the Company changed its method of accounting for leases in 
2019 due to the adoption of ASU 2016-02, Leases.

Basis for Opinion

These financial statements are the responsibility of the Company’s management. Our responsibility is to express an opinion on 
the Company’s financial statements based on our audits. We are a public accounting firm registered with the PCAOB and are 
required to be independent with respect to the Company in accordance with the U.S. federal securities laws and the applicable 
rules and regulations of the Securities and Exchange Commission and the PCAOB.

We conducted our audits in accordance with the standards of the PCAOB. Those standards require that we plan and perform the 
audit to obtain reasonable assurance about whether the financial statements are free of material misstatement, whether due to 
error or fraud. Our audits included performing procedures to assess the risks of material misstatement of the financial 
statements, whether due to error or fraud, and performing procedures that respond to those risks. Such procedures included 
examining, on a test basis, evidence regarding the amounts and disclosures in the financial statements. Our audits also included 
evaluating the accounting principles used and significant estimates made by management, as well as evaluating the overall 
presentation of the financial statements. We believe that our audits provide a reasonable basis for our opinion.

Critical Audit Matters

The critical audit matters communicated below are matters arising from the current period audit of the financial statements that 
were communicated or required to be communicated to the audit committee and that: (1) relate to accounts or disclosures that are 
material  to  the  financial  statements  and  (2)  involved  our  especially  challenging,  subjective,  or  complex  judgments.  The 
communication of critical audit matters does not alter in any way our opinion on the consolidated financial statements, taken as a 
whole, and we are not, by communicating the critical audit matters below, providing separate opinions on the critical audit matters 
or on the accounts or disclosures to which they relate.

165

Impairment of goodwill

Description
of the Matter

At December 31, 2019, the Company’s goodwill allocated to the Long-term Care (“LTC”) and Commercial 
Business  reporting  units  was  $0.4  billion  and  $26.8  billion,  respectively. As  discussed  in  Note  1  to  the 
consolidated  financial  statements,  goodwill  is  not  amortized,  but rather  is  subject  to  an  annual  impairment 
review, or more frequent reviews, if events and circumstances indicate an impairment exists. 

How We
Addressed
the Matter in
Our Audit

Description 
of the Matter

Auditing management's annual goodwill impairment test related to the LTC and Commercial Business reporting 
units was complex and highly judgmental due to the significant estimation required to determine the fair value 
of the reporting units. In particular, the fair value estimate was sensitive to significant assumptions, such as 
changes in the discount rate, projected revenue and projected operating income that are forward-looking and 
affected by future economic and market conditions.  
We obtained an understanding, evaluated the design and tested the operating effectiveness of controls over the 
Company’s annual goodwill impairment review process, including controls over management’s review of the 
significant assumptions described above.

To  test  the  estimated  fair  value  of  the  LTC  and  Commercial  Business  reporting  units,  we  performed  audit 
procedures  that  included,  among  others,  assessing  methodologies  and  testing  the  significant  assumptions 
discussed above and the underlying data used by the Company in its analysis. We compared the significant 
assumptions to the reporting units’ historical results and third-party industry data. We performed sensitivity 
analyses of significant assumptions to evaluate the changes in the fair value of the reporting units that would 
result from changes in the key assumptions. We involved valuation specialists to assist in our assessment of the 
methodology and significant assumptions (such as discount rates), used by the Company. In addition, we tested 
management’s reconciliation of the fair value of all reporting units to the market capitalization of the Company. 

Valuation of health care costs payable

At  December  31,  2019,  the  incurred  but  not  reported  (“IBNR”)  liabilities  represented  $5.0  billion  of 
$6.9 billion of health care costs payable. As discussed in Note 1 to the financial statements, the Company’s 
liability for health care costs payable includes estimated payments for (1) services rendered to members but 
not yet reported and (2) claims that have been reported but not yet paid, each as of the financial statement date 
(collectively, “IBNR”). The estimated IBNR liability is developed utilizing actuarial principles and assumptions 
that include historical and projected claim submission and processing patterns, historical and assumed medical 
cost trends, historical utilization of medical services, claim inventory levels, changes in membership and product 
mix, seasonality and other relevant factors to record the actuarial best estimate of health care costs payable. 
There is significant uncertainty inherent in determining management’s actuarial best estimate of health care 
costs payable. In particular, the estimate is sensitive to the assumed completion factors and the assumed health 
care cost trend rates. 

Auditing management’s actuarial best estimate of IBNR reserves for health care costs payable for its products 
and services involved a high degree of subjectivity in evaluating management’s assumptions used in the valuation 
process.

How We 
Addressed 
the Matter in 
Our Audit

We obtained an understanding, evaluated the design and tested the operating effectiveness of controls over the 
process for estimating IBNR reserves. This included, among others, controls over the completeness and accuracy 
of data used in the actuarial projections, the transfer of data between underlying source systems, and the review 
and  approval  processes  that  management  has  in  place  for  the  actuarial  principles  and  assumptions  used  in 
estimating the health care costs payable.   

To test IBNR reserves, our audit procedures included, among others, testing the completeness and accuracy of 
the underlying claim and membership data used in the calculation of IBNR reserves. We involved actuarial 
specialists to assist with our audit procedures, which included, among others, evaluating the methodologies 
applied by the Company in determining the actuarially determined liability, evaluating management’s actuarial 
principles  and  assumptions  used  in  their  analysis  based  on  historical  claim  experience,  and  independently 
calculating a range of reserve estimates for comparison to management’s actuarial best estimate of the liability 
for health care costs payable. Additionally, we performed a review of the prior period liabilities for incurred 
but not paid claims to subsequent claims development. 

166

/s/ Ernst & Young LLP

We have served as the Company’s auditor since 2007.

Boston, Massachusetts
February 18, 2020

167

Quarterly Financial Information (Unaudited)

In millions, except per share amounts
2019:

Total revenues

Operating income

Income from continuing operations

Net income attributable to CVS Health

Per common share data:

Basic earnings per common share:

First
Quarter

Second
Quarter

Third
Quarter

Fourth
Quarter

Year

$ 61,646

$ 63,431

$ 64,810

$ 66,889

2,690

1,427

1,421

3,332

1,931

1,936

2,928

1,529

1,530

3,037

1,744

1,747

$ 256,776
11,987

6,631

6,634

Income from continuing operations attributable to CVS
Health

Income from discontinued operations attributable to CVS
Health

Net income attributable to CVS Health

Diluted earnings per common share:

Income from continuing operations attributable to CVS
Health

Income from discontinued operations attributable to CVS
Health

Net income attributable to CVS Health

Dividends per common share

$

$

$

$

$

$

$

1.09

$

1.49

$

1.17

$

1.34

$

5.10

— $

— $

— $

— $

1.09

$

1.49

$

1.17

$

1.34

$

—

5.10

1.09

$

1.49

$

1.17

$

1.33

$

5.08

— $

— $

— $

— $

1.09

0.50

$

$

1.49

0.50

$

$

1.17

0.50

$

$

1.33

0.50

$

$

—

5.08

2.00

168

In millions, except per share amounts
2018:

Total revenues

Operating income (loss)

Income (loss) from continuing operations

Net income (loss) attributable to CVS Health

Per common share data:

Basic earnings (loss) per common share:

First
Quarter

Second
Quarter

Third
Quarter

Fourth
Quarter

Year

$ 45,743

1,996

998

998

$ 46,922
(1,373)
(2,562)
(2,563)

$ 47,490

$ 54,424

$ 194,579

2,574

1,390

1,390

824
(422)
(419)

4,021
(596)
(594)

Income (loss) from continuing operations attributable to CVS
Health

Income (loss) from discontinued operations attributable to
CVS Health

Net income (loss) attributable to CVS Health

Diluted earnings (loss) per common share:

Income (loss) from continuing operations attributable to CVS
Health
Income (loss) from discontinued operations attributable to
CVS Health

Net income (loss) attributable to CVS Health

Dividends per common share

$

$

$

$

$

$

$

0.98

$

(2.52) $

1.36

$

(0.37) $

(0.57)

— $

0.98

$

— $
(2.52) $

— $

1.36

$

— $
(0.37) $

—
(0.57)

0.98

$

(2.52) $

1.36

$

(0.37) $

(0.57)

— $

0.98

0.50

$

$

— $
(2.52) $
$
0.50

— $

1.36

0.50

$

$

— $
(0.37) $
$
0.50

—
(0.57)
2.00

169

Item 9.  Changes in and Disagreements With Accountants on Accounting and Financial Disclosure.

None.

Item 9A.  Controls and Procedures.

Evaluation of disclosure controls and procedures

The Company’s Chief Executive Officer and Chief Financial Officer, after evaluating the effectiveness of the design and 
operation of the Company’s disclosure controls and procedures (as defined in Rules 13a-15 (f) and 15d-15(f) under the 
Securities Exchange Act of 1934) as of December 31, 2019, have concluded that as of such date the Company’s disclosure 
controls and procedures were adequate and effective at a reasonable assurance level and designed to ensure that material 
information relating to the Company and its consolidated subsidiaries would be made known to such officers on a timely basis.

Management’s report on internal control over financial reporting

Management is responsible for establishing and maintaining adequate internal control over financial reporting. The Company’s 
internal control over financial reporting includes those policies and procedures that (1) pertain to the maintenance of records 
that, in reasonable detail, accurately and fairly reflect the transactions and dispositions of the assets of the Company; (2) 
provide reasonable assurance that transactions are recorded as necessary to permit preparation of the Company’s consolidated 
financial statements in accordance with generally accepted accounting principles, and that receipts and expenditures of the 
Company are being made only in accordance with authorizations of management and directors of the Company; and (3) provide 
reasonable assurance regarding prevention or timely detection of unauthorized acquisition, use, or disposition of the Company’s 
assets that could have a material effect on the Company’s consolidated financial statements. In order to ensure the Company’s 
internal control over financial reporting is effective, management regularly assesses such control and did so most recently for its 
financial reporting as of December 31, 2019.

Management conducted an assessment of the effectiveness of the Company’s internal control over financial reporting based on 
the criteria established in Internal Control-Integrated Framework issued by the Committee of Sponsoring Organizations of the 
Treadway Commission (2013 Framework). This evaluation included review of the documentation, evaluation of the design 
effectiveness and testing of the operating effectiveness of controls. The Company’s system of internal control over financial 
reporting is enhanced by periodic reviews by the Company’s internal auditors, written policies and procedures and a written 
Code of Conduct adopted by CVS Health’s Board of Directors, applicable to all employees of the Company. In addition, the 
Company has an internal Disclosure Committee, comprised of management from each functional area within the Company, 
which performs a separate review of disclosure controls and procedures. There are inherent limitations in the effectiveness of 
any system of internal control over financial reporting.

Based on management’s assessment, management concluded that the Company’s internal control over financial reporting is 
effective and provides reasonable assurance that assets are safeguarded and that the financial records are reliable for preparing 
financial statements as of December 31, 2019.

Ernst & Young LLP, the Company’s independent registered public accounting firm, is appointed by CVS Health’s Board of 
Directors and ratified by CVS Health’s stockholders. They were engaged to render an opinion regarding the fair presentation of 
the Company’s consolidated financial statements as well as conducting an audit of internal control over financial reporting. 
Their reports included in Item 8 of this Form 10-K are based upon audits conducted in accordance with the standards of the 
Public Company Accounting Oversight Board (United States).

Changes in internal control over financial reporting

On November 28, 2018, the Company completed its acquisition of Aetna. During the fourth quarter ended December 31, 2019, 
the Company completed the process of integrating the internal control over financial reporting of Aetna with the rest of the 
Company. 

Other than the foregoing, there has been no change in the Company’s internal control over financial reporting identified in 
connection with the evaluation required by paragraph (d) of Rule 13a-15 or Rule 15d-15 that occurred during the fourth quarter 
ended December 31, 2019 that has materially affected, or is reasonably likely to materially affect, the Company’s internal 
control over financial reporting.

170

Item 9B.  Other Information.

No events have occurred during the fourth quarter ended December 31, 2019 that would require disclosure under this item.

Item 10.  Directors, Executive Officers and Corporate Governance.

PART III

Information concerning the Executive Officers of CVS Health Corporation is included in Part I of this 10-K pursuant to General 
Instruction G to Form 10-K. 

The sections of the Proxy Statement under the captions “Committees of the Board as of the Annual Meeting,” “Code of 
Conduct,” “Audit Committee Report,” and “Biographies of our Incumbent Board Nominees” are incorporated herein by 
reference. 

Item 11.  Executive Compensation.

The sections of the Proxy Statement under the captions “Non-Employee Director Compensation” and “Executive 
Compensation and Related Matters,” including “Letter from the Management Planning and Development Committee,” 
“Compensation Committee Report,” “Compensation Discussion and Analysis” and “Compensation of Named Executive 
Officers” are incorporated herein by reference.

Item 12.  Security Ownership of Certain Beneficial Owners and Management and Related Stockholder Matters.

The sections of the Proxy Statement under the captions “Share Ownership of Directors and Certain Executive Officers” and 
“Share Ownership of Principal Stockholders” are incorporated herein by reference. Those sections contain information 
concerning security ownership of certain beneficial owners and management and related stockholder matters.

The following table summarizes information about the registrants common stock that may be issued upon the exercise of 
options, warrants and rights under all of the Company’s equity compensation plans as of December 31, 2019:

Number of
securities to be
issued upon
exercise of
outstanding
options, warrants
and rights (1) (2)
(a)

Weighted
average exercise
price of
outstanding
options, warrants
and rights
(b)

Number of securities
remaining available for
future issuance under
equity compensation
plans (excluding
securities reflected in
first column) (1)
(c)

32,237

$

4,518
36,755

$

73.32  

43.46  
71.83  

17,152

26,849
44,001

Equity compensation plans approved by stockholders (3)
Equity compensation plans not approved by 
stockholders (4) (5)

Total

_____________________________________________

(1)  Shares in thousands.
(2)  Consists of: (i) 21,184 shares of common stock underlying outstanding options, (ii) 1,110 shares of common stock issuable upon the exercise of outstanding 
stock appreciation rights (“SARs”) and (iii) 14,461 shares of common stock issuable on the vesting of outstanding restricted stock units, deferred stock 
units and performance stock units, assuming target level performance in the case of performance stock units. The number of shares included with respect to 
outstanding SARs is the number of shares of CVS Health common stock that would have been issued had the SARs been exercised based on the closing 
price per share of CVS Health common stock on December 31, 2019, as reported on the NYSE, which was $74.29.  

(3)  Consists of the CVS Health 2017 Incentive Compensation Plan.
(4)  Consists of the Amended Aetna Inc. 2010 Stock Incentive Plan (the “Aetna Stock Plan”). 
(5)  Amount in column (c) consists of the maximum number of shares of CVS Health common stock available for future issuance under the Aetna Stock Plan as 

of December 31, 2019. 

The Aetna Stock Plan was last approved by Aetna’s shareholders at Aetna’s 2017 Annual Meeting on May 19, 2017. The 
Company elected to continue to grant awards under the Aetna Stock Plan to employees of Aetna and its subsidiaries following 
the completion of the Aetna Acquisition. The Aetna Stock Plan is designed to promote the Company’s interests and those of its 
stockholders and to further align the interests of stockholders and employees by tying awards to total return to stockholders, 
enabling plan participants to acquire additional equity interests in the Company and providing compensation opportunities 

171

dependent upon the Company’s performance. The Aetna Stock Plan has not been submitted to the Company’s stockholders and 
will expire on May 21, 2020. 

Under the Aetna Stock Plan, eligible participants can be granted stock options to purchase shares of CVS Health common stock, 
SARs, time-vesting and/or performance-vesting incentive stock or incentive units and other stock based awards. As of 
December 31, 2019, the maximum number of shares of CVS Health common stock that may be issued under the awards 
outstanding under the Aetna Stock Plan was 4.5 million shares, subject to adjustment for corporate transactions and 26.8 million 
shares remained available for future awards. If an award under the Aetna Stock Plan is paid solely in cash, no shares are 
deducted from the number of shares available for issuance under the Aetna Stock Plan.

Item 13.  Certain Relationships and Related Transactions, and Director Independence.

The sections of the Proxy Statement under the captions “Independence Determinations for Directors” and “Related Person 
Transaction Policy” are incorporated herein by reference.

Item 14.  Principal Accountant Fees and Services.

The section of the Proxy Statement under the caption “Item 2: Ratification of Appointment of Independent Registered Public 
Accounting Firm for 2020” is incorporated herein by reference.

172

Item 15.  Exhibits, Financial Statement Schedules.

The following documents are filed as part of this 10-K:

PART IV

1.  Financial Statements. See “Index to Consolidated Financial Statements” in Item 8 of this 10-K.

2.  Financial Statement Schedules. All financial statement schedules are omitted because they are not applicable, not 

required under the instructions, or the information is included in the consolidated financial statements or related notes.

3.  Exhibits. The exhibits listed in the “Index to Exhibits” in this Item 15 are filed or incorporated by reference as part of 
this 10-K. Exhibits marked with an asterisk (*) are management contracts or compensatory plans or arrangements. 
Exhibits other than those listed are omitted because they are not required to be listed or are not applicable. Pursuant to 
Item 601(b)(4)(iii) of Regulation S-K, the Registrant hereby agrees to furnish to the Securities and Exchange 
Commission a copy of any omitted instrument that is not required to be listed.

Exhibit
2
2.1

2.2

2.3

3
3.1

3.2

4
4.1

4.2

4.3

4.4

4.5

4.6

4.7

4.8

4.9

INDEX TO EXHIBITS

Description

Plan of acquisition, reorganization, arrangement, liquidation or succession

Agreement and Plan of Merger, dated as of May 20, 2015, among CVS Pharmacy, Inc., Tree Merger Sub, Inc. 
and Omnicare, Inc. (incorporated by reference to Exhibit 2.1 to the Registrant’s Current Report on Form 8-K 
filed May 21, 2015).

Master Transaction Agreement dated as of October 22, 2017, by and between Aetna Inc. and Hartford Life and 
Accident Insurance Company (incorporated by reference to Exhibit 2.3 to the Registrant’s Annual Report on 
Form 10-K for the fiscal year ended December 31, 2018).

Agreement and Plan of Merger, dated as of December 3, 2017, among CVS Health Corporation, Hudson 
Merger Sub Corp. and Aetna Inc. (incorporated by reference to Exhibit 2.1 to the Registrant’s Current Report 
on Form 8-K filed December 5, 2017).

Articles of Incorporation and Bylaws

Restated Certificate of Incorporation of the Registrant dated June 4, 2018 (incorporated by reference to 
Exhibit 3.1C of Registrant’s Current Report on Form 8-K filed June 5, 2018).

By-Laws of the Registrant, as amended and restated June 4, 2018 (incorporated by reference to Exhibit 3.2 to 
the Registrant’s Current Report on Form 8-K filed June 5, 2018).

Instruments defining the rights of security holders, including indentures

Specimen common stock certificate (incorporated by reference to Exhibit 4.1 to the Registration Statement of 
the Registrant ((then known as CVS Corporation) as successor to Melville Corporation) on Form 8-B filed 
November 4, 1996).

Senior Indenture dated August 15, 2006, between the Registrant and The Bank of New York Mellon Trust 
Company, N.A., as trustee (incorporated by reference to Exhibit 4.1 to the Registrant’s Current Report on Form 
8-K filed August 15, 2006).

Form of the Registrant’s 2020 Floating Rate Note (incorporated by reference to Exhibit 4.1 to the Registrant’s 
Current Report on Form 8-K filed March 12, 2018).

Form of the Registrant’s 2021 Floating Rate Note (incorporated by reference to Exhibit 4.2 to the Registrant’s 
Current Report on Form 8-K filed March 12, 2018).

Form of the Registrant’s 2020 Note (incorporated by reference to Exhibit 4.3 to the Registrant’s Current Report 
on Form 8-K filed March 12, 2018).

Form of the Registrant’s 2021 Note (incorporated by reference to Exhibit 4.4 to the Registrant’s Current Report 
on Form 8-K filed March 12, 2018).

Form of the Registrant’s 2023 Note (incorporated by reference to Exhibit 4.5 to the Registrant’s Current Report 
on Form 8-K filed March 12, 2018).

Form of the Registrant’s 2025 Note (incorporated by reference to Exhibit 4.6 to the Registrant’s Current Report 
on Form 8-K filed March 12, 2018).

Form of the Registrant’s 2028 Note (incorporated by reference to Exhibit 4.7 to the Registrant’s Current Report 
on Form 8-K filed March 12, 2018).

173

4.10

4.11

4.12

4.13

4.14

4.15

10
10.1

10.2

10.3

10.4

10.5

10.6

10.7

10.8

10.9*

10.10*

10.11*

10.12*

10.13*

10.14*

10.15*

10.16*

Form of the Registrant’s 2038 Note (incorporated by reference to Exhibit 4.8 to the Registrant’s Current Report 
on Form 8-K filed March 12, 2018).

Form of the Registrant’s 2048 Note (incorporated by reference to Exhibit 4.9 to the Registrant’s Current Report 
on Form 8-K filed March 12, 2018).

Form of the Registrant’s 2024 Note (incorporated by reference to Exhibit 4.1 to the Registrant’s Current Report 
on Form 8-K filed August 15, 2019).

Form of the Registrant’s 2026 Note (incorporated by reference to Exhibit 4.2 to the Registrant’s Current Report 
on Form 8-K filed August 15, 2019).

Form of the Registrant’s 2029 Note (incorporated by reference to Exhibit 4.3 to the Registrant’s Current Report 
on Form 8-K filed August 15, 2019).

Material terms of outstanding securities that are registered under Section 12 of the 1934 Act as required by Item 
202(a)-(d) and (f) of Regulation S-K.

Material Contracts

Five Year Credit Agreement, dated as of May 18, 2017, by and among the Registrant, the lenders party thereto 
and The Bank of New York Mellon, as Administrative Agent (incorporated by reference to Exhibit 10.2 to the 
Registrant’s Quarterly Report on Form 10-Q for the fiscal quarter ended June 30, 2017).

Amendment No. 1 to Five Year Credit Agreement dated as of December 15, 2017, to the Five Year Credit 
Agreement dated as of May 18, 2017, by and among the Registrant, the lenders party thereto and The Bank of 
New York Mellon, as Administrative Agent (incorporated by reference to Exhibit 10.3 to the Registrant’s 
Current Report on Form 8-K filed December 19, 2017).

Amendment No. 2 to Five Year Credit Agreement dated as of May 17, 2018, to the Five Year Credit Agreement 
dated as of May 18, 2017, by and among the Registrant, the lenders party thereto and The Bank of New York 
Mellon, as Administrative Agent (incorporated by reference to Exhibit 10.4 to the Registrant’s Quarterly Report 
on Form 10-Q for the fiscal quarter ended June 30, 2018).

Amendment No. 3, dated as of May 16, 2019, to the Five Year Credit Agreement dated as of May 18, 2017, by 
and among the Registrant, the lenders party thereto and The Bank of New York Mellon, as Administrative 
Agent (incorporated by reference to Exhibit 10.4 of the Registrant’s Quarterly Report on Form 10-Q for the 
fiscal quarter ended June 30, 2019).

Five Year Credit Agreement dated as of May 17, 2018, by and among the Registrant, the lenders party thereto 
and The Bank of New York Mellon, as Administrative Agent (incorporated by reference to Exhibit 10.2 to the 
Registrant’s Quarterly Report on Form 10-Q for the fiscal quarter ended June 30, 2018).

Amendment No. 1, dated as of May 16, 2019, to the Five Year Credit Agreement dated as of May 17, 2018, by 
and among the Registrant, the lenders party thereto and The Bank of New York Mellon, as Administrative 
Agent (incorporated by reference to Exhibit 10.3 of the Registrant’s Quarterly Report on Form 10-Q for the 
fiscal quarter ended June 30, 2019).

364-Day Credit Agreement dated as of May 16, 2019 by and among the Registrant, the lenders party thereto 
and Bank of America, N.A., as Administrative Agent (incorporated by reference to Exhibit 10.1 of the 
Registrant’s Quarterly Report on Form 10-Q for the fiscal quarter ended June 30, 2019).

Five Year Credit Agreement dated as of May 16, 2019 by and among the Registrant, the lenders party thereto 
and Bank of America, N.A., as Administrative Agent (incorporated by reference to Exhibit 10.2 of the 
Registrant’s Quarterly Report on Form 10-Q for the fiscal quarter ended June 30, 2019).

The Registrant’s Supplemental Retirement Plan I for Select Senior Management, as amended and restated as of 
December 31, 2008 (incorporated by reference to Exhibit 10.6 to the Registrant’s Quarterly Report on Form 10-
Q for the fiscal quarter ended June 30, 2009).

Form of Enterprise Non-Competition, Non-Disclosure and Developments Agreement between the Registrant 
and certain of the Registrant’s executive officers (incorporated by reference to Exhibit 10.25 of the Registrant’s 
Annual Report on Form 10-K for the fiscal year ended December 31, 2013).

The Registrant’s Deferred Stock Compensation Plan, as amended and restated.

The Registrant’s 2007 Employee Stock Purchase Plan, as amended (incorporated by reference to Exhibit 10.20 
to the Registrant’s Annual Report on Form 10-K for the fiscal year ended December 31, 2015).

Universal 409A Definition Document, as amended (incorporated by reference to Exhibit 10.28 to the 
Registrant’s Annual Report on Form 10-K for the fiscal year ended December 31, 2015).

The Registrant’s Deferred Compensation Plan, as amended and restated. 

The Registrant’s Partnership Equity Program, as amended (incorporated by reference to Exhibit 10.25 to the 
Registrant’s Annual Report on Form 10-K for the fiscal year ended December 31, 2016).

The Registrant’s Performance-Based Restricted Stock Unit Plan, as amended (incorporated by reference to 
Exhibit 10.27 to the Registrant’s Annual Report on Form 10-K for the fiscal year ended December 31, 2016).

174

10.17*

10.18*

10.19*

10.20*

10.21*

10.22*

10.23*

10.24*

10.25*

10.26*

10.27*

10.28*

10.29*

10.30*

10.31*

10.32*

10.33*

10.34*

10.35*

10.36*

10.37*

10.38*

The Registrant’s 2017 Incentive Compensation Plan (incorporated by reference to Exhibit A to the Registrant’s 
Definitive Proxy Statement on Form 14A filed March 31, 2017).

The Registrant’s Executive Incentive Plan, as amended (incorporated by reference to Exhibit 10.4 to the 
Registrant’s Quarterly Report on Form 10-Q for the fiscal quarter ended June 30, 2017).

The Registrant’s Long-Term Incentive Plan, as amended (incorporated by reference to Exhibit 10.5 to the 
Registrant’s Quarterly Report on Form 10-Q for the fiscal quarter ended June 30, 2017).

Form of Non-Qualified Stock Option Agreement between the Registrant and selected employees of the 
Registrant (incorporated by reference to Exhibit 10.29 to the Registrant’s Annual Report on Form 10-K for the 
fiscal year ended December 31, 2014).

Form of Restricted Stock Unit Agreement - Annual Grant - between the Registrant and selected employees of 
the Registrant (incorporated by reference to Exhibit 10.30 to the Registrant’s Annual Report on Form 10-K for 
the fiscal year ended December 31, 2014).

Form of Performance-Based Restricted Stock Unit Agreement between the Registrant and selected employees 
of the Registrant (incorporated by reference to Exhibit 10.31 to the Registrant’s Annual Report on Form 10-K 
for the fiscal year ended December 31, 2014).

Form of Partnership Equity Program Participant Purchased RSUs, Company Matching RSUs and Company 
Matching Options Agreement (Pre-Tax) (incorporated by reference to Exhibit 10.32 to the Registrant’s Annual 
Report on Form 10-K for the fiscal year ended December 31, 2014).

Form of Partnership Equity Program Participant Purchased RSUs, Company Matching RSUs and Company 
Matching Options Agreement (Post-Tax) (incorporated by reference to Exhibit 10.33 to the Registrant’s Annual 
Report on Form 10-K for the fiscal year ended December 31, 2014).

Form of Performance Stock Unit Agreement - Annual Grant between the Registrant and selected employees of 
the Registrant (incorporated by reference to Exhibit 10.1 to the Registrant’s Quarterly Report on Form 10-Q for 
the fiscal quarter ended March 31, 2018).

Form of Performance Stock Unit Agreement (LTIP) - Annual Grant between the Registrant and selected 
employees of the Registrant (incorporated by reference to Exhibit 10.2 to the Registrant’s Quarterly Report on 
Form 10-Q for the fiscal quarter ended March 31, 2018).

The Registrant’s Management Incentive Plan.

The Registrant’s Severance Plan for Non-Store Employees amended as of November 28, 2018 (incorporated by 
reference to Exhibit 10.37 to the Registrant’s Annual Report on Form 10-K for the fiscal year ended December 
31, 2018).

The Registrant’s Performance-Based Restricted Stock Unit Program, as amended (incorporated by reference to 
Exhibit 10.38 to the Registrant’s Annual Report on Form 10-K for the fiscal year ended December 31, 2018).

Form of Non-Qualified Stock Option Agreement between the Registrant and selected employees of the 
Registrant (incorporated by reference to Exhibit 10.39 to the Registrant’s Annual Report on Form 10-K for the 
fiscal year ended December 31, 2018).

Form of Restricted Stock Unit Agreement - Annual Grant - between the Registrant and selected employees of 
the Registrant (incorporated by reference to Exhibit 10.40 to the Registrant’s Annual Report on Form 10-K for 
the fiscal year ended December 31, 2018).

Form of Performance-Based Restricted Stock Unit Agreement between the Registrant and selected employees 
of the Registrant (incorporated by reference to Exhibit 10.41 to the Registrant’s Annual Report on Form 10-K 
for the fiscal year ended December 31, 2018).

Form of Partnership Equity Program Participant Purchased RSUs, Company Matching RSUs and Company 
Matching Options Agreement (Pre-Tax) (incorporated by reference to Exhibit 10.42 to the Registrant’s Annual 
Report on Form 10-K for the fiscal year ended December 31, 2018).

Form of Partnership Equity Program Participant Purchased RSUs, Company Matching RSUs and Company 
Matching Options Agreement (Post-Tax) (incorporated by reference to Exhibit 10.31 to the Registrant’s Annual 
Report on Form 10-K for the fiscal year ended December 31, 2013).
Form of Performance Stock Unit Agreement - Annual Grant between the Registrant and selected employees of 
the Registrant (incorporated by reference to Exhibit 10.5 of the Registrant’s Quarterly Report on Form 10-Q for 
the fiscal quarter ended June 30, 2019).

Amended Aetna Inc. 2010 Stock Incentive Plan, as amended May 19, 2017 (incorporated by reference to 
Exhibit 99.1 to the Registrant’s Registration Statement on Form S-8 filed November 30, 2018).

Form of Aetna Inc. 2010 Stock Incentive Plan - Market Stock Unit Terms of Award (incorporated by reference 
to Exhibit 10.45 to the Registrant’s Annual Report on Form 10-K for the fiscal year ended December 31, 2018).

Form of Aetna Inc. 2010 Stock Incentive Plan - Performance Stock Unit Terms of Award (2015) (incorporated 
by reference to Exhibit 10.46 to the Registrant’s Annual Report on Form 10-K for the fiscal year ended 
December 31, 2018).

175

10.39*

10.40*

10.41*

10.42*

10.43*

10.44*

10.45*

10.46*

10.47*

10.48*

10.49*

10.50*

10.51*

10.52*

10.53*

10.54*

10.55*

10.56*

10.57*

21
21.1

23
23.1

31
31.1

Form of Aetna Inc. 2010 Stock Incentive Plan - Executive Restricted Stock Unit Terms of Award (2015) 
(incorporated by reference to Exhibit 10.47 to the Registrant’s Annual Report on Form 10-K for the fiscal year 
ended December 31, 2018).

Form of Aetna Inc. 2010 Stock Incentive Plan - Stock Appreciation Right Terms of Award (2015) (incorporated 
by reference to Exhibit 10.48 to the Registrant’s Annual Report on Form 10-K for the fiscal year ended 
December 31, 2018).

Amended and Restated Employment Agreement between the Registrant and Larry Merlo (incorporated by 
reference to Exhibit 10.38 to the Registrant’s Annual Report on Form 10-K for the fiscal year ended 
December 31, 2008).

Amendment dated as of December 21, 2012 to the Amended and Restated Employment Agreement between the 
Registrant and Larry Merlo (incorporated by reference to Exhibit 10.31 to the Registrant’s Annual Report on 
Form 10-K for the fiscal year ended December 31, 2012).

Form of Non-Qualified Stock Option Agreement - Annual Grant between the Registrant and Larry Merlo 
(incorporated by reference to Exhibit 10.37 to the Registrant’s Annual Report on Form 10-K for the fiscal year 
ended December 31, 2016).

Form of Restricted Stock Unit Agreement - Annual Grant between the Registrant and Larry Merlo 
(incorporated by reference to Exhibit 10.38 to the Registrant’s Annual Report on Form 10-K for the fiscal year 
ended December 31, 2016).

Amendment dated January 22, 2015 to Nonqualified Stock Option Agreements between the Registrant and 
Larry Merlo (incorporated by reference to Exhibit 10.1 to the Registrant’s Current Report on Form 8-K filed 
January 23, 2015).

Form of Performance Stock Unit Agreement - Annual Grant between the Registrant and selected employees of 
the Registrant (incorporated by reference to Exhibit 10.5 to the Registrant’s Quarterly Report on Form 10-Q for 
the fiscal quarter ended June 30, 2019).
Change in Control Agreement effective as of July 19, 2010 between the Registrant and Eva Boratto 
(incorporated by reference to Exhibit 10.1 of the Registrant’s Quarterly Report on Form 10-Q for the fiscal 
quarter ended March 31, 2019).

Restrictive Covenant Agreement dated June 21, 2019 between the Registrant and Eva Boratto.

Change in Control Agreement dated December 22, 2008 between the Registrant and Jonathan Roberts 
(incorporated by reference to Exhibit 10.33 to the Registrant’s Annual Report on Form 10-K for the fiscal year 
ended December 31, 2012).

Amendment dated as of December 31, 2012 to the Change in Control Agreement dated December 22, 2008 
between the Registrant and Jonathan Roberts (incorporated by reference to Exhibit 10.34 to the Registrant’s 
Annual Report on Form 10-K for the fiscal year ended December 31, 2012).

Restricted Stock Unit Agreement - Annual Grant dated April 1, 2016 between the Registrant and Jonathan 
Roberts (incorporated by reference to Exhibit 10.44 to the Registrant’s Annual Report on Form 10-K for the 
fiscal year ended December 31, 2016).

Restrictive Covenant Agreement dated May 20, 2016 between the Registrant and Jonathan Roberts 
(incorporated by reference to Exhibit 10.45 to the Registrant’s Annual Report on Form 10-K for the fiscal year 
ended December 31, 2016).
Change in Control Agreement dated as of November 10, 2017 between the Registrant and Derica Rice 
(incorporated by reference to Exhibit 10.3 of the Registrant’s Quarterly Report on Form 10-Q for the fiscal 
quarter ended March 31, 2019).

Restrictive Covenant Agreement dated June 19, 2019 between the Registrant and Derica Rice. 

Change in Control Agreement dated October 1, 2012 between the Registrant and Thomas Moriarty 
(incorporated by reference to Exhibit 10.1 of the Registrant’s Quarterly Report on Form 10-Q for the fiscal 
quarter ended March 31, 2015).

Restrictive Covenant Agreement dated July 8, 2019 between the Registrant and Thomas Moriarty. 
Descriptions of certain arrangements not embodied in formal documents as described under the heading “Non-
Employee Director Compensation” are incorporated herein by reference to the Proxy Statement (when filed).

Subsidiaries of the registrant

Subsidiaries of CVS Health Corporation.

Consents of experts and counsel

Consent of Ernst & Young LLP.

Rule 13a-14(a)/15d-14(a) Certifications

Certification by the Chief Executive Officer.

176

31.2

32
32.1

32.2

101
101

104
104

Certification by the Chief Financial Officer.

Section 1350 Certifications

Certification by the Chief Executive Officer.

Certification by the Chief Financial Officer.

Interactive Data File

The following materials from the CVS Health Corporation Annual Report on Form 10-K for the fiscal year
ended December 31, 2019 formatted in Inline XBRL: (i) the Consolidated Statements of Operations, (ii) the
Consolidated Statements of Comprehensive Income (Loss), (iii) the Consolidated Balance Sheets, (iv) the
Consolidated Statements of Cash Flows, (v) the Consolidated Statements of Shareholders’ Equity and (vi) the
related Notes to Consolidated Financial Statements. The instance document does not appear in the Interactive
Data File because its XBRL tags are embedded within the Inline XBRL document.

Cover Page Interactive Data File - The cover page from the Company's Annual Report on Form 10-K for the
year ended December 31, 2019, formatted in Inline XBRL (included as Exhibit 101).

Item 16.  Form 10-K Summary.

None.

177

SIGNATURES
Pursuant to the requirements of Section 13 or 15(d) of the Securities Exchange Act of 1934, the registrant has duly caused this 
report to be signed on its behalf by the undersigned, thereunto duly authorized.

Date: February 18, 2020

CVS HEALTH CORPORATION
By:

/s/ EVA C. BORATTO
Eva C. Boratto
Executive Vice President and Chief Financial Officer

Pursuant to the requirements of the Securities Exchange Act of 1934, this report has been signed below by the following 
persons on behalf of the registrant and in the capacities and on the dates indicated.

Signature

Title(s)

/s/ FERNANDO AGUIRRE
Fernando Aguirre

/s/ RICHARD M. BRACKEN
Richard M. Bracken

/s/ C. DAVID BROWN II
C. David Brown II

/s/ EVA C. BORATTO
Eva C. Boratto

/s/ JAMES D. CLARK
James D. Clark

Director

Director

Director

Executive Vice President and Chief Financial
Officer (Principal Financial Officer)

Senior Vice President - Controller and Chief
Accounting Officer (Principal Accounting Officer)

/s/ ALECIA A. DECOUDREAUX
Alecia A. DeCoudreaux

/s/ NANCY-ANN M. DEPARLE
Nancy-Ann M. DeParle

Director

Director

Date

February 18, 2020

February 18, 2020

February 18, 2020

February 18, 2020

February 18, 2020

February 18, 2020

February 18, 2020

/s/ DAVID W. DORMAN
David W. Dorman

/s/ ROGER N. FARAH
Roger N. Farah

/s/ ANNE M. FINUCANE
Anne M. Finucane

/s/ EDWARD J. LUDWIG
Edward J. Ludwig

/s/ LARRY J. MERLO
Larry J. Merlo

/s/ JEAN-PIERRE MILLON
Jean-Pierre Millon

/s/ MARY L. SCHAPIRO
Mary L. Schapiro

/s/ RICHARD J. SWIFT
Richard J. Swift

/s/ WILLIAM C. WELDON
William C. Weldon

/s/ TONY L. WHITE
Tony L. White

Chair of the Board and Director

February 18, 2020

Director

Director

Director

President and Chief Executive Officer
(Principal Executive Officer) and Director

Director

Director

Director

Director

Director

February 18, 2020

February 18, 2020

February 18, 2020

February 18, 2020

February 18, 2020

February 18, 2020

February 18, 2020

February 18, 2020

February 18, 2020

    
    
Reconciliation  

Adjusted Earnings Per Share (Unaudited) 

CVS Health Corporation (“CVS Health”) uses non-GAAP financial measures to analyze underlying business performance 
and trends. CVS Health believes that providing these non-GAAP financial measures enhances CVS Health’s and investors’ 
ability to compare CVS Health’s past financial performance with its current performance. These non-GAAP financial 
measures are provided as supplemental information to the financial measures CVS Health discloses that are calculated and 
presented in accordance with GAAP. Non-GAAP financial measures should not be considered a substitute for, or superior to, 
financial measures determined or calculated in accordance with GAAP. CVS Health’s definitions of its non-GAAP financial 
measures may not be comparable to similarly titled measurements reported by other companies.  

CVS Health defines adjusted income from continuing operations attributable to CVS Health as income (loss) from continuing 
operations attributable to CVS Health (GAAP measure) excluding the impact of amortization of intangible assets and other 
items, if any, that neither relate to the ordinary course CVS Health’s business nor reflect CVS Health’s underlying business 
performance, such as acquisition-related transaction and integration costs, store rationalization charges, gains/losses on 
divestitures, losses on early extinguishment of debt, goodwill impairments, impairment of long-lived assets, losses on 
settlements of defined benefit pension plans, adjustments to legal reserves in connection with legal settlements, net interest 
expense on financings associated with proposed acquisitions (for periods prior to the acquisition), the corresponding tax 
benefit or expense related to the items excluded from adjusted income from continuing operations attributable to CVS Health, 
the corresponding impact to income allocable to participating securities, net of tax, related to the items excluded from income 
from continuing operations attributable to CVS Health in determining adjusted income from continuing operations 
attributable to CVS Health, and any other items specifically identified herein. GAAP diluted EPS from continuing operations 
and Adjusted EPS, respectively, are calculated by dividing income (loss) from continuing operations attributable to CVS 
Health and adjusted income from continuing operations attributable to CVS Health by CVS Health’s weighted average 
diluted shares outstanding.  

 
 
The following are reconciliations of income (loss) from continuing operations to adjusted income from continuing 
operations attributable to CVS Health and calculations of GAAP diluted EPS from continuing operations and        
Adjusted EPS:

In millions, except per share data
Income (loss) from continuing operations (GAAP measure)

Net loss (income) attributable to noncontrolling interests (GAAP measure)

Income allocable to participating securities (GAAP measure)

Income (loss) from continuing operations attributable to CVS Health (GAAP 
measure)

Non-GAAP adjustments:

Amortization of intangible assets  (1)
Acquisition-related transaction and integration costs (2)
Store rationalization charges (3)
Loss on divestiture of subsidiary  (4)
Loss on early extinguishment of debt  (5)
Goodwill impairments  (6)
Impairment of long-lived asset (7)
Losses on settlements of defined benefit pension plans  (8)
Adjustments to legal reserves in connection with legal settlements  (9)
Net interest expense on financing activities (10)
Income tax benefit (11)
Income allocable to participating securities, net of tax (12)

2019

Year Ended December 31, 
2017

2016

2018

2015

$          

6,631

$           

(596)

$          

6,631

$          

5,320

$          

5,230

3

(5)

2

(3)

(1)

(24)

(2)

(27)

(2)

(26)

6,629

(597)

6,606

5,291

5,202

2,436

480

231

205

79

—

—

—

—

—

(815)

(1)

1,006

492

—

86

—

6,149

43

—

—

894

(658)

(9)

817

65

215

9

—

181

—

187

—

56

(2,096)

2

795

291

34

—

643

—

—

—

(85)

—

(665)

(4)

611

220

—

—

—

—

—

—

90

52

(364)

(1)

Adjusted income from continuing operations attributable to CVS Health

$          

9,244

$          

7,406

$          

6,042

$          

6,300

$          

5,810

Weighted average diluted shares outstanding (GAAP) 
Adjusted weighted average diluted shares outstanding (non-GAAP) (13)

1,305

1,305

1,044

1,047

1,024

1,024

1,079

1,079

1,126

1,126

GAAP diluted earnings (loss) per share from continuing operations

$         

5.08

$        

(0.57)

$         

6.45

$         

4.91

$         

4.62

Adjusted EPS

$         

7.08

$         

7.08

$         

5.90

$         

5.84

$         

5.16

Footnotes: 

3) 

2) 

1)  CVS Health’s and its subsidiaries’ (collectively, the “Company’s”) acquisition activities have resulted in the recognition 
of intangible assets as required under the acquisition method of accounting which consist primarily of trademarks, 
customer contracts/relationships, covenants not to compete, technology, provider networks and value of business 
acquired. Definite-lived intangible assets are amortized over their estimated useful lives and are tested for impairment 
when events indicate that the carrying value may not be recoverable. The amortization of intangible assets is reflected in 
CVS Health’s statements of operations in operating expenses within each segment. Although intangible assets contribute 
to the Company’s revenue generation, the amortization of intangible assets does not directly relate to the underwriting of 
the Company’s insurance products, the services performed for the Company’s customers or the sale of the Company’s 
products or services. Additionally, intangible asset amortization expense typically fluctuates based on the size and timing 
of the Company’s acquisition activity. Accordingly, CVS Health believes excluding the amortization of intangible assets 
enhances CVS Health’s and investors’ ability to compare the Company’s past financial performance with its current 
performance and to analyze underlying business performance and trends. Intangible asset amortization excluded from the 
related non-GAAP financial measure represents the entire amount recorded within CVS Health’s GAAP financial 
statements, and the revenue generated by the associated intangible assets has not been excluded from the related non-
GAAP financial measure. Intangible asset amortization is excluded from the related non-GAAP financial measure 
because the amortization, unlike the related revenue, is not affected by operations of any particular period unless an 
intangible asset becomes impaired or the estimated useful life of an intangible asset is revised. 
In 2019, acquisition-related transaction and integration costs relate to the acquisition (the “Aetna Acquisition”) of Aetna 
Inc. (“Aetna”). In 2018 and 2017, acquisition-related transaction and integration costs relate to the Aetna Acquisition and 
the acquisition of Omnicare, Inc (“Omnicare”). In 2016 and 2015, acquisition-related integration costs relate to the 
acquisition of Omnicare and the pharmacies and clinics of Target. 
In 2019, the store rationalization charges relate to the planned closure of 22 underperforming retail pharmacy stores in 
the first quarter of 2020 and the planned closure of 46 underperforming retail pharmacy stores in the second quarter of 
2019. These store rationalization charges primarily relate to operating lease right-of-use asset impairment charges. In 
2017 and 2016, the store rationalization charges primarily represent charges for noncancelable lease obligations 
associated with stores closed in connection with the Company’s enterprise streamlining initiative. 
In 2019, the loss on divestiture of subsidiary represents the pre-tax loss on the sale of the Company’s Brazilian 
subsidiary, Drogaria Onofre Ltda. (“Onofre”), which occurred on July 1, 2019, and primarily relates to the elimination of 
the cumulative translation adjustment from accumulated other comprehensive income. In 2018, the loss on divestiture of 
subsidiary represents the pre-tax loss on the sale of the Company’s RxCrossroads subsidiary (“RxCrossroads”) for $725 
million on January 2, 2018. In 2017, the loss on divestiture of subsidiary represents transaction costs associated with the 
sale of RxCrossroads.  
In 2019, the loss on early extinguishment of debt related to the repayment of $4.0 billion of the Company’s outstanding 
senior notes in August 2019 pursuant to its tender offers for such senior notes. In 2016, the loss on early extinguishment 
of debt related to the repayment of $4.2 billion of the Company’s outstanding senior notes pursuant to its tender offer for 
such senior notes.  
In 2018, the goodwill impairments relate to the LTC reporting unit within the Retail/LTC segment. In 2017, the goodwill 
impairments relate to the RxCrossroads reporting unit within the Retail/LTC segment. 
In 2018, impairment of long-lived assets primarily relates to the impairment of property and equipment within the 
Retail/LTC segment.  
In 2017, the Company settled the pension obligations of its two tax-qualified pension plans by irrevocably transferring 
pension liabilities to an insurance company through the purchase of group annuity contracts and through lump sum 
distributions. These purchases, funded with the pension plan assets, resulted in pre-tax settlement losses related to the 
recognition of accumulated deferred actuarial losses.  
In 2016, adjustments to legal reserves represent legal charges of $3 million in the first quarter of 2016 in connection with 
a disputed 1999 legal settlement and an $88 million reversal of an accrual in connection with a legal settlement in the 
fourth quarter of 2016. In 2015, adjustments to legal reserves include a charge related to a legacy lawsuit challenging the 
1999 legal settlement by MedPartners, an acquired subsidiary, of various securities class actions and a related derivative 
claim.  

5) 

4) 

7) 

6) 

8) 

9) 

10)  In 2018, net interest expense on financing activities includes interest expense related to (i) bridge financing costs, (ii) 
interest expense on $40 billion of unsecured senior notes issued on March 9, 2018 (the “2018 Notes”) and (iii) interest 
expense on the Company’s $5 billion term loan facility relating to the Aetna Acquisition. The interest expense was 
reduced by related interest income earned on the proceeds of the 2018 Notes. All amounts are for the periods prior to the 
close of the Aetna Acquisition, which occurred on November 28, 2018. In 2017, net interest expense on financing 
activities includes bridge financing costs related to the Aetna Acquisition. In 2015, net interest expense on financing 
activities includes financing costs associated with the acquisitions of Omnicare and the pharmacies and clinics of Target. 

11)  Represents the corresponding tax benefit or expense related to the items excluded from adjusted income from continuing 

operations attributable to CVS Health and Adjusted EPS above. The nature of each non-GAAP adjustment is evaluated 
to determine whether a discrete adjustment should be made to the adjusted income tax provision. 

12)  Represents the corresponding impact to income allocable to participating securities, net of tax, related to the items above 
excluded from income (loss) from continuing operations attributable to CVS Health in determining adjusted income 
from continuing operations attributable to CVS Health and calculating Adjusted EPS above. 

13)  Adjusted EPS for the year ended December 31, 2018 is calculated utilizing adjusted weighted average diluted shares 
outstanding, which includes 3 million potential common equivalent shares, as the impact of these shares was dilutive. 
The potential common equivalent shares were excluded from the calculation of GAAP loss per share from continuing 
operations for the year ended December 31, 2018, as the shares would have had an anti-dilutive effect as a result of the 
GAAP net loss incurred. 

Officer, Director and Stockholder Information

Officers

Larry J. Merlo
President and Chief Executive Officer
Eva C. Boratto
Executive Vice President and  
Chief Financial Officer
Jonathan C. Roberts
Executive Vice President and  
Chief Operating Officer
Lisa G. Bisaccia
Executive Vice President and  
Chief Human Resources Officer
Troyen A. Brennan, M.D.
Executive Vice President and  
Chief Medical Officer
David A. Falkowski
Executive Vice President and  
Chief Compliance Officer
Joshua M. Flum
Executive Vice President –  
Enterprise Strategy and Digital

Richard M. Jelinek
Executive Vice President – Integration 
Alan M. Lotvin, M.D.
Executive Vice President and President –  
CVS Caremark
Karen S. Lynch
Executive Vice President and President – Aetna
Jonathan E. Mayhew
Executive Vice President – Transformation
Thomas M. Moriarty
Executive Vice President, Chief Policy and  
External Affairs Officer and General Counsel 
James D. Clark
Senior Vice President – Controller and  
Chief Accounting Officer
Carol A. DeNale
Senior Vice President and Treasurer

Valerie C. Haertel
Senior Vice President – Investor Relations 
John P. Kennedy
Senior Vice President and Chief Tax Officer
Colleen M. McIntosh
Senior Vice President, Corporate Secretary  
and Chief Governance Officer
Thomas S. Moffatt
Vice President, Assistant Secretary and Assistant 
General Counsel – Corporate Services

OFFICERS’ CERTIFICATIONS 
The Company has filed the required certifications under 
Section 302 of the Sarbanes-Oxley Act of 2002 regarding  
the quality of our public disclosures as Exhibits 31.1 and  
31.2 to our Annual Report on Form 10-K for the fiscal 
year ended December 31, 2019. After our 2019 annual 
meeting of stockholders, the Company filed with the New 
York Stock Exchange the CEO certification regarding its  
compliance with the NYSE corporate governance listing 
standards as required by NYSE Rule 303A.12(a).

Directors 

Fernando Aguirre (1) (5)
Former Chief Executive Officer and Chairman, 
Chiquita Brands International, Inc. 
Richard M. Bracken (2) (4) (6)
Former Chairman and Chief Executive Officer, 
HCA Holdings, Inc.
C. David Brown II (3) (5) (6)
Partner and Member of the Executive Committee,  
Nelson Mullins Riley & Scarborough LLP
Alecia A. DeCoudreaux (1) (4)
President Emerita, Mills College 
and Former Executive, Eli Lilly and Company
Nancy-Ann M. DeParle (4) (5) (6)
Managing Partner and Co-Founder, Consonance 
Capital Partners, LLC and Former Director of the 
White House Office of Health Reform

David W. Dorman (3) (5) (6)
Chair of the Board, CVS Health Corporation and 
Former Chairman and CEO, AT&T Corporation
Roger N. Farah (3) (4)
Chairman of the Board, Tiffany & Co. and  
Former Executive, Tory Burch and Ralph Lauren
Anne M. Finucane (2) (3)
Vice Chairman, Bank of America Corporation
Edward J. Ludwig (1) (2)
Former Chairman and Chief Executive Officer, 
Becton, Dickinson and Company
Larry J. Merlo (6)
President and Chief Executive Officer, 
CVS Health Corporation
Jean-Pierre Millon (1) (4)
Former President and Chief Executive Officer, 
PCS Health Systems, Inc.

Mary L. Schapiro (1) (2)
Vice Chair of Public Policy and Special Advisor  
to the Chairman, Bloomberg, L.P.
Richard J. Swift (1) (6)
Former Chairman, President and  
Chief Executive Officer, Foster Wheeler Ltd.
William C. Weldon (3) (5)
Former Chairman and Chief Executive Officer, 
Johnson & Johnson
Tony L. White (3) (4)
Former Chairman, President and 
Chief Executive Officer, Applied Biosystems, Inc. 

(1) Audit Committee

(2) Investment and Finance Committee

(3) Management Planning and Development Committee

(4) Medical Affairs Committee

(5) Nominating and Corporate Governance Committee

(6) Executive Committee

Stockholder Information 

Corporate Headquarters
CVS Health Corporation 
One CVS Drive, Woonsocket, RI 02895 
(401) 765-1500
Annual Stockholders’ Meeting*
May 14, 2020 
CVS Health Corporate Headquarters
Stock Market Listing
The New York Stock Exchange 
Symbol: CVS

*  As part of our precautions regarding the coronavirus 
or COVID-19, we are planning for the possibility that 
the Annual Meeting may be held solely by means of 
remote communication for the health and safety of 
our stockholders and employees. If we take this step, 
we will publicly announce the decision to do so in 
advance by press release, which will be posted on 
our website at www.cvshealth.com/newsroom/
press-releases, as soon as practicable before the 
Annual Meeting. In that event, the Annual Meeting 
would be conducted remotely via live audio webcast 
on the date listed above. Details on how stockholders 

designed and produced by see see eye

can participate in the Annual Meeting will be available 
at www.cvshealthannualmeeting.com, including if the 
Annual Meeting is held solely by means of remote 
communication, and including information on how 
stockholders entitled to vote at the Annual Meeting 
can vote their shares if they elect not to do so in 
advance of the Annual Meeting.

Annual Report on Form 10-K and  
Other Company Information

The Company’s Annual Report on Form 10-K  
will be sent without charge to any stockholder  
upon request by contacting:

CVS Health Corporation 
Investor Relations Office 
One CVS Drive, MC 1008 
Woonsocket, RI 02895 
(800) 201-0938

In addition, financial reports and recent filings  
with the Securities and Exchange Commission, 
including our Form 10-K, as well as other  
Company information, are available via the  
Internet at investors.cvshealth.com. 

Transfer Agent and Registrar
Questions regarding stock holdings, certificate 
replacement/transfer, dividends and address  
changes should be directed to:

EQ Shareowner Services 
P.O. Box 64874 
St. Paul, MN  55164-0874 
Toll-free: (877) CVS-PLAN (287-7526) 
International: +1 (651) 450-4064 
Email: stocktransfer@eq-us.com 
Website: www.shareowneronline.com
Direct Stock Purchase/Dividend  
Reinvestment Program
Shareowner Services Plus PlanSM provides a 
convenient and economical way for you to 
purchase your first shares or additional shares  
of CVS Health common stock. The program is 
sponsored and administered by EQ Shareowner 
Services. For more information, including an 
enrollment form, please contact EQ Shareowner 
Services at (877) 287-7526.

We are health
innovators

Our Purpose
Helping people 
 on their path   
to better health

Our Strategy
Creating unmatched 
 human connections   
to transform   
the health care   
experience

Our Values
Innovation 
Collaboration 
Caring 
Integrity 
Accountability

CVS Health, One CVS Drive, Woonsocket, RI 02895    |   401.765.1500   |   cvshealth.com

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