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Pfizer financials

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Pfizer financials
Our Values Table of Contents

Integrity 2 Letter to Shareholders

5 Creating the World’s Fastest-Growing

Innovation Pharmaceutical Company

8 Our Market-Leading Medicines

Respect for People 12 Our Global Presence

16 Our Commitment to R&D

Customer Focus 18 Review of Operations

27 Our Community Activities

Teamwork 28 Financial Review

37 Management’s Report

38 Audit Committee’s Report and

Leadership

Independent Auditors’ Report

39 Consolidated Statement of Income

Performance 40 Consolidated Balance Sheet

41 Consolidated Statement of Shareholders’ Equity

Community 42 Consolidated Statement of Cash Flows

43 Notes to Consolidated Financial Statements

61 Quarterly Consolidated Financial Data (Unaudited)

62 Financial Summary (1989 -1999)

63 Directors, Committees, and Officers

64 Corporate and Shareholder Information

65 Ensuring Access to Innovative Medicines

Financial Highlights

Year ended December 31

% Change

(millions, except per share data) 1999 1998 1997 99/98 98/97

Total revenues $16,204 $13,544 $11,055 20 23

Income from continuing operations before provision for

taxes on income and minority interests 4,448 2,594 2,867 71 (10)

Provision for taxes on income 1,244 642 775 94 (17)

Discontinued operations – net of tax (20) 1,401 131 – 972

Net income 3,179 3,351 2,213 (5) 51

Research and development expenses 2,776 2,279 1,805 22 26

Property, plant and equipment additions 1,561 1,198 878 30 36

Cash dividends paid 1,148 976 881 18 11

Diluted earnings per common share .82 .85 .57 (4) 50

Cash dividends paid per common share .30 2/3 .25 1/3 .22 2/3 21 12

Shareholders’ equity per common share 2.36 2.33 2.10 1 11

Weighted average shares – diluted 3,884 3,945 3,909 (2) 1

Number of common shares outstanding 3,847 3,883 3,883 (1) –

(thousands)

Number of shareholders 147 105 87 40 21

Number of employees 51 46 41 11 12

Percentages may reflect rounding adjustments.

All data throughout this report have been restated to reflect the 1999 three-for-one stock split in the form of a 200% stock dividend.





About Pfizer About the Cover

Pfizer Inc is a research-based global pharmaceutical company. We discover, In Santa Ana, California, Dale and Arlene Post enjoy an outing with

develop, manufacture, and market innovative medicines for humans and their family, including daughter Jody, grandchildren Spencer and Emily,

animals. In 1999, Pfizer celebrated its 150th anniversary. and best friend Keeler. Both Dale and Arlene suffer from atrial fibrilla-

tion, a common form of irregular heartbeat, and rely on Tikosyn to

treat it. Approved in 1999, Tikosyn is the latest addition to Pfizer’s

broad cardiovascular portfolio.

During the 1990s, 1999

Pfizer’s revenues $16.2 billion

grew by 284%.

Our growth has outpaced the

industry every year for the past

decade, and was more than double

the average in 1999.









1989

$4.2 billion

To Our Shareholders



F

or Pfizer and our shareholders,

1999 was an exceptional year,

capping a decade of extraordinary Pfizer’s exceptional performance

achievement. We ended the century has substantially benefited our shareholders.

on a high note — including our share of Our stock split four times in the 1990s:

the sales generated by our copromotion three times on a two-for-one basis —

activities, Pfizer became the world’s in 1991, 1995, and 1997 — and on a

number one pharmaceutical company in three-for-one basis in 1999. This achieve-

prescription sales. ment is unprecedented in Pfizer’s history

Over the last decade, our prescription and unequaled by any company in our

pharmaceutical revenue has quintupled, peer group.

our investment in R&D has sextupled, In January of 1999, we announced a

our reported net income has more than first-quarter dividend of 22 cents (7.33

quadrupled, and the price of our stock cents adjusted for the three-for-one stock

has increased more than ten times. The split), a 16% increase over 1998. This year,

growth of our pharmaceutical revenue we increased the first-quarter dividend to

exceeded that of the industry every year 9 cents, up 23% (adjusted for the three-

throughout the last decade, and in 1999, for-one stock split) over the same quarter

it more than doubled the industry rate. the year before.

In 1999, total revenues topped $16.2 Driven by the success of our innovative

billion, up 20% over 1998. Excluding the in-line and alliance products, Pfizer

impact of a charge taken in the third Pharmaceuticals Group’s revenues

quarter related to Trovan inventories, of increased 22% to $14.9 billion. In 1999,

certain significant prior-year charges, and Pfizer became the only company to have

of the 1998 divestiture of the Medical participated in all three of the industry’s

Technology Group, net income increased latest record-breaking launches. In 1997,

by 29% to almost $3.4 billion, and in concert with Warner-Lambert, the

diluted earnings per share increased by company that discovered Lipitor, we

30% to 87 cents. launched this innovative lipid-lowering

agent. In 1998, we introduced Pfizer’s

Viagra, the world’s leading treatment for

erectile dysfunction. In February 1999,









2

along with G.D. Searle & Co., the

pharmaceutical division of Monsanto

Company, we launched Celebrex, one of Despite challenging market conditions,

the world’s leading treatments for arthritis, our Animal Health Group’s sales increased

which was discovered by Searle. 2% to $1.3 billion. These results were

We set another record in 1999 when fueled by the increasing popularity of

Pfizer became the only company in our Rimadyl, a treatment for the relief of

industry to have seven medicines, including pain and inflammation associated with

those we copromote, each achieve annual osteoarthritis in dogs; and by the launch of

sales of $1 billion or more. The five medi- Revolution, Pfizer’s new,

cines discovered by Pfizer in this group — innovative antiparasitic We set another record in 1999

Norvasc, Zoloft, Zithromax, Viagra, and for dogs and cats —

when Pfizer became the only

Diflucan — grew at a combined annual hailed by many as the

rate of 18%. Norvasc, with yearly sales most successful launch company in our industry to have

exceeding $3 billion, maintained its in the history of the seven medicines — including those

position as the world’s number one anti- animal health industry.

hypertensive. Zoloft continued to be a Building on the we copromote — each achieve

leading antidepressant worldwide. strong base provided by annual sales of $1 billion or more.

Zithromax retained its rank as the most- our innovative pharma-

prescribed branded oral antibiotic in the ceuticals for humans and animals, Pfizer

United States. Viagra remained the world’s is forging ahead with an aggressive R&D Total Revenues (millions of dollars)



leading treatment for erectile dysfunction, program. In 1999, we invested almost

Total revenues have

and Diflucan held the lead as the world’s $2.8 billion in R&D, a 22% increase over increased at a

compound annual

largest-selling prescription antifungal. 1998. We currently have more than 200 growth rate of 19%

$16,204



Unfortunately, we also experienced a projects in discovery and development for over the past 5 years. $13,544



disappointment with Trovan. Although humans and animals, and this year, we $11,055

$9,864

this unique antibiotic has saved thousands expect to invest approximately $3.2 billion $8,684



of lives, rare cases of unanticipated severe in R&D.

liver injury associated with it resulted in To accommodate our extensive number

our relabeling Trovan in the United States of projects in discovery and development,

exclusively for use in serious infections and to provide the necessary support for 95 96 97 98 99

in institutional settings, and in its suspen- our in-line products, we have expanded

sion in Europe. our research centers in Groton, Connecticut;

In early October of 1999, the U.S. Sandwich, England; and Nagoya, Japan. R&D Expenses (millions of dollars)





Food and Drug Administration (FDA) We have also added to our field forces — Research and

approved Tikosyn, Pfizer’s new medicine which are the key link between our development expenses

have increased at a $2,776

for atrial fibrillation, and we anticipate research laboratories and the practicing compound annual

growth rate of 22%

launching it in the first quarter of this year. physician. Since 1994, we have doubled over the past 5 years.

$2,279



A few weeks later, we received an approv- the number of our sales representatives $1,805

$1,567

able letter from the FDA for Relpax, our in the United States, and in our industry’s $1,340



innovative remedy for migraines. In most prestigious survey, more than

December, Pfizer’s antidepressant Zoloft 10,000 doctors nationwide have recognized

became the first medicine approved by the the outstanding quality and training of

FDA for the treatment of posttraumatic our sales force by ranking it number one 95 96 97 98 99



stress disorder, and by midyear, we expect overall for five consecutive years.

to refile our application for Zeldox, our Pfizer is advancing in every area. Our

novel antipsychotic drug. fundamentals are strong. Our pipeline is

broad and deep, and our field forces are

second to none. Our company is increasingly



3

recognized as a world leader in the busi-

ness community. In 1999, Forbes selected

Pfizer “Company of the Year,” and Working

Mother ranked Pfizer one of the “100 Best

Companies for Working Mothers.” Just

last month, Fortune named Pfizer one of

the “100 Best Companies to Work For” Obviously, one of the most important

and number one in our industry, and events of 1999 was Pfizer’s proposal to

Business Week ranked Pfizer’s board as one acquire Warner-Lambert. As you know, a

of the 25 best in the world. few weeks ago, we announced that Pfizer

Pfizer takes an active role in corporate and Warner-Lambert, the two fastest-

governance, public policy debates, and growing major companies in our industry,

support of the community. In the current would join forces to create what I believe

discussions over Medicare, we have strongly will be the best pharmaceutical company

supported prescription drug coverage for in the world. The page following this

elderly Americans who do not have access letter explains in greater detail how this

to pharmaceuticals. The statement on acquisition will benefit both you and the

page 65 suggests the measures that we shareholders of Warner-Lambert.

believe would provide the necessary cover- As we look toward a bright future,

age and also enable our industry to carry I would like to say a word about succession

out the R&D that saves, protects, and planning, which I believe is one of a

enhances lives. Chairman’s most important duties. For

Commitment to the community at me, this has been made easier by the

every level is one of Pfizer’s eight core extraordinary quality of senior managers

values, and I believe that it grows natu- at Pfizer. On May 27, 1999, our board

rally out of our humanitarian mission. This elected Dr. Henry A. McKinnell president

commitment also plays an indispensable and chief operating officer of Pfizer Inc.

role in promoting our outstanding perfor- He has done a superb job of managing

mance. It helps us hire and retain the best our acquisition of Warner-Lambert and

people. It helps us motivate our employees. of planning the integration of our two

It enhances our company’s reputation and companies. Simultaneously, the board

improves our relations with the public, elected Dr. John Niblack vice chairman

as well as with doctors, patients, and of our company.

others in the medical community. This As Pfizer enters the twenty-first

commitment also produces the kind of century, we have never been stronger and

trust and goodwill that are invaluable in our prospects have never been brighter.

dealing with regulatory agencies and In 1999, we celebrated 150 years of

government officials. excellence and innovation — a proud

legacy that the outstanding people of

Pfizer are well prepared to take into the

next millennium.



William C. Steere, Jr.

Chairman of the Board and

Chief Executive Officer

February 14, 2000







4

Creating the World’s Fastest-Growing

Pharmaceutical Company



W

ith net income growth of 20% per The combined pharmaceutical product lines of

year anticipated for 2000 to 2002 as the two companies represent significant depth

a stand-alone company, Pfizer was and breadth, including seven billion-dollar prod-

in a strong position to continue our ucts. The new Pfizer will receive all revenues

successes of the 1990s. However, in late 1999, a from Lipitor, which is expected to achieve sales

unique opportunity arose that would allow us in 2000 in excess of $5 billion. The company

to achieve even faster earnings growth. Pfizer will also have a significant presence in consumer

made a bid in November 1999, subsequently health care, confectionery products, and animal

revised in February 2000, to merge with medicines. The combined R&D operations will

Warner-Lambert, the only major pharmaceutical have a worldwide scientific staff of more than

company growing faster than we were. 12,000 and $4.7 billion in anticipated annual

Under terms of the agreement, Pfizer expenditures in 2000, the largest investment

will exchange 2.75 shares of Pfizer voting in the industry. We expect the combined

common stock for each outstanding share of company will have anticipated annual cost

Warner-Lambert voting stock. Approved by savings and efficiencies of $1.6 billion by 2002

the boards of both companies, the merger ($200 million of these savings are expected to

agreement is conditional upon the use of be achieved in 2000, $1 billion in 2001, and

pooling-of-interests $1.6 billion in 2002). Diluted earnings per

Pfizer and Warner-Lambert accounting, qualifying as a share of the combined company over that

represent a new competitive tax-free reorganization, the period are expected to accelerate from 20% for

approval of shareholders of Pfizer alone to 25% for Pfizer combined with

standard for our industry.

both companies, and the Warner-Lambert. These earnings projections

usual regulatory approvals. It is expected to include the $1.6 billion of cost savings phased

close in mid-2000. in over this time period, but do not include

The new company will retain the name sales opportunities achievable by bringing

Pfizer Inc. Up to eight independent directors together the two organizations, anticipated

from Warner-Lambert’s board of directors will restructuring charges and transaction fees of

be invited to join Pfizer’s board. Mr. Steere will $1.7 billion to $2.2 billion, and the termination

be chairman and chief executive officer, and fee paid by Warner-Lambert to American

Dr. McKinnell will be president and chief Home Products Corporation.

operating officer. Three members of the The new Pfizer will have the industry’s

Warner-Lambert management team will join broadest range of products that treat diseases

Pfizer’s Corporate Management Committee. associated with cardiovascular risks, a signifi-

Corporate headquarters will remain in New cantly expanded program in treating central

York. The worldwide and U.S. pharmaceutical nervous system disorders, a vastly expanded

division headquarters will also be in New York. portfolio of products for infectious diseases,

The Warner-Lambert Consumer Health Care and important medicines in women’s health.

Division, along with the other consumer The Pfizer and Warner-Lambert organiza-

businesses and selected additional functions, tions will work together in a spirit of collabora-

will be located at Warner-Lambert’s offices in tion and mutual respect to capitalize on the

Morris Plains, New Jersey. extraordinary opportunity now before us. The

The new Pfizer will have annual revenues combined talents of Pfizer and Warner-Lambert

in 2000 of approximately $31 billion, including people will make us not just bigger, but better.

$24 billion in prescription pharmaceutical sales. 5

By 2025, the number

in the

will double to

6

Athletes race toward the finish notion of an “Olympics for older

line in the 200-meter dash at people” would have been

the Pfizer-sponsored Senior unthinkable. Today, thanks in

Games. Held in Orlando, Florida, part to pharmaceutical

the 1999 event brought companies like Pfizer, millions





of peopletogether 12,000 men and

women ranging in age from

50 to 99. Not so long ago, the

of people realize that growing

old doesn’t have to mean

slowing down.









world age 65 and over

800 million.

7

G

ood health is the key to a good For example, several of the medicines

life. To do the things you love to we offer treat risk factors for heart disease,

do. To be productive at work. To one of the world’s leading killers. Backed

see your children have children. by award-winning patient and physician

Pfizer is committed to the pursuit of education programs, these drugs are helping

medicines that help ensure good health, millions of people “get to goal” — be it

and our products treat some of the world’s lower blood pressure (Norvasc), lower

most widespread diseases and conditions. cholesterol (Lipitor), or controlled blood









Pfizer medicines keep millio sugar levels (Glucotrol XL). Both Norvasc

and Lipitor had 1999 revenues in

excess of $3 billion,





ranking

them among the

world’s most successful

medicines of any kind.

Zoloft is a leading treatment

for depression, which is estimated to affect

more than 10% of the world’s population

— about 600 million people. In 1999,

Zoloft was approved for posttraumatic

stress disorder (PTSD), a debilitating





What could be better than winning the World

Series? For New York Yankee second baseman

Chuck Knoblauch, it was having the chance

to share that victory with his father, Ray, a

victim of Alzheimer’s disease. “In the 1998

season, my dad came out to the stadium and

took great joy in watching me play,”

Knoblauch says. “I’m not sure he would have

been able to do that if he wasn’t taking

Aricept. That’s why I’m happy to be working

with Pfizer and Eisai on an awareness

campaign stressing the need for early

diagnosis and treatment.” Discovered

and developed by Eisai Co., Ltd.,

and copromoted by Pfizer,

Aricept is the world’s leading

Alzheimer’s medicine.









8

condition triggered by exposure to an

extreme traumatic event. Approximately

half of all people will experience, witness, or

learn about such an event during their

lifetime; 10% to 20% of these people will Seven of the medicines we offer generated

develop PTSD.

1999 revenues of over $1 billion. No other



ons healthy pharmaceutical company has such a powerful

product portfolio.





throughout their lives.

Arthritis is another common condition

Global statistics are difficult to come by, but the high prevalence in

that Pfizer is helping to combat. In 1999,

the United States of many diseases — and the fact that so many

G.D. Searle & Co. and Pfizer introduced who suffer from them remain undiagnosed and untreated —

Celebrex, which delivers relief from underscores the importance of the work we are doing:

arthritis pain, inflammation, and stiffness. • One in four has high blood pressure.

Powered by an excellent efficacy and side- • One in three has high cholesterol.

effect profile, Celebrex set a new record as • One in sixteen has diabetes.

• One in six will suffer from depression.

the most successful U.S. product launch

• One in six has arthritis.

in industry history. • One in ten over age 65 has Alzheimer’s disease.

Building on our years of expertise in • Four in ten have allergies.

livestock products, Pfizer has also • Half of all men 40 to 70 years old will experience

established leadership in the fast-growing erectile dysfunction.

category of medicines for pets. The bond

between people and their pets is extremely

powerful. A Gallup poll of dog owners, Carole Gatti has owned and

for example, showed that 92% consider operated Florida’s Winstar

their pet to be a member of the family. Farm since 1988. She

relies on Pfizer’s animal

Pfizer’s newest companion animal medicine

health products to

is Revolution (marketed as Stronghold in care for the horses

Europe), the first and only product that she boards, as well

protects dogs and cats from both internal as for her own pets,

and external parasites, including heart- including dachshunds

worms and fleas, with just a single monthly Odie and Samantha.

topically applied dose. This unique medi-

cine has enjoyed one of the most successful

launches in animal health industry history.









9

By 2003,rising

global pharmaceutical

than it is today.



10

demand will create a

market one third larger

The subways of Tokyo are the overall Japanese market for

bursting with energy, even as 70 straight months. In fact,

Japan wrestles with caring for Pfizer now ranks as the number

what is the world’s most rapidly one non-Japanese-owned

aging population. Pfizer began pharmaceutical company.

doing business in Japan more The 1999 introduction of Viagra

than 40 years ago, and today it and the Alzheimer’s medicine

ranks as our second-largest Aricept, coupled with our plans

market, accounting for over to launch several new medi-

$1.2 billion in annual revenues. cines over the next few years,

In December, Pfizer Japan should ensure continued

achieved its “Super 70” goal — strong growth for Pfizer in this

growing revenues faster than important market.



11

T

he desire to live a healthy, produc-

tive life knows no borders. Pfizer

was one of the first in the industry

to recognize the tremendous

potential for success outside our home

country, and we now do business in more The following year, Aricept was intro-

than 150 countries. duced in Europe, where a similar strategy

While each market is unique, we yielded equally strong results. In 1999,

have been working to share best practices Aricept was launched in Japan, and Pfizer

on a global basis. In 1997, for example, and Eisai teams there met with their

we launched the Alzheimer’s medicine counterparts from France and the United

Aricept in the United States, along with States to learn from their success. The end

our copromotion partner Eisai. Aricept result is that well over a million people

quickly became the country’s most widely around the world have now been helped

prescribed Alzheimer’s treatment, as we by this powerful medicine.

worked to educate patients, physicians, and In 1998, Pfizer launched Viagra in the

advocacy groups about this effective treat- United States, triggering what can only be

ment for a terrible disease. described as a global phenomenon. For all









Pfizer brings good health

to every corn In 1999, Pfizer celebrated its 150th anniver-

sary as an American company and marked a

number of international milestones as well.

Forty-five years in France, Sweden, the

Philippines, and the Netherlands. Forty years

in Finland, Norway, and Portugal. Thirty-five

years in Korea, Singapore, and Malaysia. Ten

years in China — where DanLong Feng, who

works closely with the media and govern-

ment, was Pfizer’s first employee. Today, a

decade later, she is excited about the role

Pfizer is playing in bringing better health

care to her country. “More than 1.2 billion

people live here,” she says. “And they are

just as interested in living healthy lives as

people in every other part of the world.”









12

While “direct-to-consumer” advertising for

prescription pharmaceuticals is increasingly

common in the United States, it is still a new

concept in many other parts of the world.

Pfizer has pioneered the use of such ads to

raise awareness about erectile dysfunction, a

the attention, however, Viagra and erectile condition that affects an estimated 100 million

men and their partners worldwide. By show-

dysfunction (ED) are still frequently

casing the many faces of ED, Pfizer has taken

misunderstood. Pfizer has been educating this condition out of the shadows and given

men, doctors, and insurers that ED is a men the knowledge — and the courage —

common and treatable condition and one they need to seek treatment.

that can often be traced to even more serious

medical problems, such as high blood

pressure, high cholesterol, and diabetes.

This strategy, conceived and executed

globally, enabled Viagra to top the billion

dollar sales mark in 1999, its first full Italy

year on the market. More importantly, it

has helped more than six million men

and their partners in the United States

recapture an important part of their lives.









Brazil









rner of the world.

We are a truly global company,

doing business in more than

150 countries. In 1999, our

revenues exceeded $100 million

in 12 different countries outside

the United States.





United States









13

The sequencing

will increase the number

The odds against bringing an drug discovery and is still there machine that analyzes cells at

innovative new medicine to today. By forging alliances with a rate of 10,000 per second and

market are daunting. New tech- leading biotech companies and sorts out only those that react to

nologies are improving the investing in new facilities of our a specific compound.This allows

likelihood of success, however, own, we are redefining the R&D us to identify promising new drug

and that is good news for process. At our Discovery Tech- targets roughly eight times faster

pharmaceutical companies and nology Center in Cambridge, than conventional methods.

patients alike. Pfizer has long Massachusetts, scientist Mark

14 been on the cutting edge of Roth uses a state-of-the-art

of the human genome

of drug targets

from 500 to 10,000.

15

Our pipeline is full of exciting candidates,

including several medicines in late-stage

development with peak annual sales

potential of more than $1 billion.





Pfizer is leading the

T

remendous strides have been





way to a h

made against dozens of diseases

during the past several decades,

but much work remains to be

done. While we celebrate victories over

twentieth-century scourges like smallpox and we have assembled the strongest, most

and polio, we also watch with concern consistently productive global research and

the growing global ranks of those con- development operation in the industry to

fronting other dreaded illnesses, such do it. In the next few years alone, we expect

as diabetes and cancer. to launch as many as six new medicines

Pfizer is committed to discovering the to treat diseases and conditions affecting

wonder drugs of the twenty-first century, hundreds of millions of people.

At our research campus in

Groton, Connecticut, senior

scientist Barbara Foster is

part of a growing team of

Pfizer researchers working

to discover new cancer med-

icines. Pfizer has several

promising candidates in its

pipeline to prevent and treat

this disease. “Because we all

know colleagues and friends

whose cancer did not

respond to current therapies,

we take the challenge of

finding effective new drugs

very seriously,” Foster says.

“Every day we come to

work wanting to win. Our

scientists take great pride in

doing their best, and in

doing so, we inspire each

other to meet the challenge

before us.”









16

We have new chemical entities in early

development to treat these conditions:

Relpax, for example, our new medicine

to treat migraine headaches, is currently Alzheimer’s Disease Head Trauma

Anxiety Infection

under regulatory review. Relpax has Arthritis Ischemic Reperfusion Injury

demonstrated powerful pain relief in Asthma Lipid Modulation

Benign Prostatic Hyperplasia Migraine

comparative trials against the current market Bone Restoration Nicotine Addiction

leader. Because of this, we believe Relpax Cancer Obesity

will be welcome news to the world’s 240 Chronic Obstructive Pulmonary Disease Osteoporosis

Depression Pain

million migraine sufferers — 85% of Dermal Scarring Sleep Disorders

whom are not treated with a prescription Diabetes Stroke

Erectile Dysfunction Transplant Rejection

medicine, despite the incapacitating nature Frailty Wound Healing

of these headaches.









a healthier tomorrow.

We are equally optimistic about the for many of our currently marketed

prospects for a new “inhaled insulin” tech- medicines. Zithromax, for example, has

nology to treat diabetes that we are devel- been a very successful antibiotic for many

oping in collaboration with Aventis Pharma years. Today, Pfizer scientists are also

and Inhale Therapeutic Systems, Inc. The studying whether Zithromax might be

global incidence of diabetes is growing effective in preventing cardiac events in

rapidly, yet most people with the disease post-heart-attack patients.

are either undiagnosed or not adequately Looking farther into the future, Pfizer

controlling their blood sugar levels. This has more drug candidates in early develop-

new patient-friendly treatment option ment than ever before. They cover a broad

provides the means by which patients may range of therapeutic areas, including cancer,

better manage their diabetes and improve post-menopausal disorders, frailty, and brain

control of this debilitating disease. injury caused by stroke or trauma.

Inhaled insulin minimizes the need for Pfizer also leads the world in R&D

painful and inconvenient insulin injections dedicated to animal health. Our pipeline

and thus removes the psychological barrier of product candidates, which has tripled

to adequate administration of insulin. in number in the last three years, exploits

Clinical trials have shown inhaled novel gene therapies and vaccine technolo-

insulin to be effective in and of itself as gies and benefits from synergies with our

well as in conjunction with oral medicines. human health research. Between now and

Phase III studies are now under way at 120 2005, we estimate that our animal health

sites worldwide, and Pfizer and Aventis division will expand rapidly.

Pharma are constructing a state-of-the-art

insulin plant in Frankfurt, Germany.

To further drive near-term growth, we

are exploring new uses and formulations









17

Review of the proposed merger with Warner-Lambert,

we expect further profit margin expansion, 16%







Operations revenue growth, and 20% earnings per share

growth in 2000.

Pfizer set records in each of the past three

years with the most successful product launches in

pharmaceutical history — Lipitor, Viagra, and

Celebrex. These three young blockbusters joined







P

fizer completed its rise to the top of the seven strong growth products — Norvasc, Zoloft,

worldwide pharmaceutical rankings in Zithromax, Diflucan, Zyrtec, Aricept, and

1999. Culminating a decade of extraordi- Glucotrol XL — to produce total company

nary growth, the company’s sales of revenue growth of 20% to $16.2 billion in 1999.

prescription drugs, including our share of the Each of these 10 products is number one or

sales of copromoted products, were the highest number two in its field, with U.S. patent protection

in the industry. until at least 2004.

Pfizer’s performance is characterized not Our pipeline of new products shows great

only by size, but also by superior growth. In 1999, promise. One new product, Tikosyn, was approved

Pfizer had 20% revenue growth, the highest by the FDA, and another, Relpax, received an

among the world’s top 10 pharmaceutical approvable letter. We intend to refile Zeldox by

companies. Our pharmaceutical revenue growth midyear, and filings of four other candidates are

exceeded that of the industry every year this expected by 2002. These seven late-stage prod-

decade, and in 1999 was more than two times ucts include four with peak annual sales potential

the industry rate. of a billion dollars or more — Relpax, Zeldox,

Our profit margins expanded in 1999, as valdecoxib, and inhaled insulin — and two others —

we leveraged substantial recent investments in Vfend and darifenacin — with sales potential

sales, marketing, and R&D. For Pfizer, excluding approaching this level. In addition, we anticipate

20 filings for supplemental indications or presenta-

tions of marketed products during this period. In

Worldwide Revenues of Therapeutic Lines and Major Products total, our pipeline of human medicines has more

% Change than 90 programs in development to treat diseases

(millions of dollars) 1999 1998 1997 99/98 98/97

such as osteoporosis, frailty, cancer, head trauma,

stroke, diabetes, asthma, and erectile dysfunction.

Worldwide Pharmaceuticals $14,859 $ 12,230 $ 9,726 + 22 + 26

Cardiovascular Diseases 4,635 4,186 3,806 + 11 + 10 Cardiovascular Diseases

Norvasc 3,030 2,575 2,217 + 18 + 16

Cardura 794 688 626 + 15 + 10

Although substantial progress has been made

Procardia XL 521 714 822 - 27 - 13 in recent decades, cardiovascular diseases (CVD)

Infectious Diseases 3,145 2,822 2,475 + 11 + 14 remain the leading cause of death in the developed

Zithromax 1,333 1,041 821 + 28 + 27 world. Of the 2.3 million American deaths

Diflucan 1,002 916 881 + 9 + 4 every year, more than 41% are primarily attribut-

Unasyn 349 327 346 + 7 - 5

Sulperazon 158 133 139 + 19 - 4

able to CVD, and more than 60% have CVD as

Central Nervous System Disorders 2,156 1,924 1,553 + 12 + 24 a contributing cause.

Zoloft 2,034 1,836 1,507 + 11 + 22 Mortality rates from coronary heart disease

Diabetes 297 273 234 + 9 + 17 and stroke have been cut in half in the past

Glucotrol XL 262 226 175 + 16 + 29 20 years, in part due to improved treatment of

Viagra 1,033 788 – + 31 –

Allergy 557 422 273 + 32 + 55

hypertension. However, improvements have

Zyrtec/Reactine 552 416 265 + 33 + 57 stopped in recent years, and many of the 50 million

Arthritis/Inflammation 222 234 271 - 5 - 14 Americans afflicted by hypertension go undiag-

Feldene 179 201 236 - 11 - 15 nosed or inadequately treated. The NHANES III

Alliance Revenue 2,071 867 316 + 139 + 175 survey, for example, concluded that fewer than

Consumer Health Care 561 526 584 + 7 - 10

70% of hypertensive patients were aware of their

Percentages may reflect rounding adjustments. condition, fewer than 55% were receiving

Certain prior year data have been reclassified to conform to the current year presentation. treatment, and fewer than 30% had their blood

pressure under control.





18

Pfizer markets Norvasc, the world’s largest-

selling medicine for hypertension and angina.

Sales of Norvasc increased 18% to over $3.0 billion

in 1999. Since its introduction in 1990, Norvasc

has had more than 12 billion patient days of

therapy worldwide. Its success has been driven by

its outstanding efficacy, once-daily dosing, consis-

tent 24-hour control of hypertension and angina,

and excellent safety and tolerability. It is the

only drug in its class that can be safely used by

congestive heart failure patients.

The results of more than 190 clinical trials

support Norvasc’s profile. For example, in the

PREVENT clinical

trial, a three-year

study involving 825

patients with coro-

“It’s made

nary artery disease,

patients receiving a real difference Jessica Vance is a busy woman. She is a self-

employed event planner who enjoys painting,

hiking, dancing, and spending time with her

Norvasc experi-

enced significantly

fewer cardiovascular

in my life.” four grandchildren. Like millions of others, however, Jessica has high

blood pressure. Diagnosed in 1992, she tried several different antihyper-

tensives, but none worked for her until she began taking Norvasc in 1998.

procedures or events, such as angioplasties, bypass

“It’s made a real difference in my life,” Jessica says. “I can concentrate on

surgeries, and hospitalizations for severe angina or

building my business and doing the things I love without having to worry

heart failure, compared to those receiving placebo.

about my health all the time.”

Pfizer is currently undertaking a two-year,

3,000-patient study, CAMELOT, comparing

Norvasc with the ACE inhibitor enalapril in the Sales of Procardia XL for hypertension and

reduction of cardiovascular events and the angina declined 27% to $521 million, due in part

progression of atherosclerosis in patients with to doctors’ increasing emphasis on Norvasc.

coronary artery disease. Norvasc is also being Sales of Cardura, an alpha blocker offering

studied in the largest trial ever undertaken in clinicians and patients a unique, cost-effective

hypertension, the five-year, 43,000-patient option for treating hypertension and benign

ALLHAT trial begun in 1994 under the auspices prostatic hyperplasia (BPH), increased 15% to

of the National Heart, Lung, and Blood Institute. $794 million in 1999. Studies have found that

The five-year, 18,000-patient ASCOT clinical more than 40% of men diagnosed with BPH also

trial will test whether Norvasc and other newer have hypertension. Cardura can be used to treat

antihypertensive therapies can show reduced rates patients with BPH who also have hyperlipidemia,

of heart attacks compared with older therapies. insulin resistance, and diabetes. Cardura patients

ASCOT will also examine whether combination of in the PREDICT trial, a one-year, 1,089-patient

the lipid-lowering agent Lipitor with Norvasc study, experienced significantly better relief of

reduces the rates of heart attacks. BPH symptoms than patients on finasteride. An

extended-release formulation, Cardura XL, which

has been launched in some European countries,

may reduce the need for dose titration.

Blood cholesterol levels are an important and

underappreciated risk factor for heart disease.

Studies have shown that a 1% decrease in

cholesterol levels leads to a 2% decrease in the

risk of heart disease.









19

Lipitor is the most-prescribed cholesterol-

lowering product in the United States, receiving

more than 43% of weekly new prescriptions for all

cholesterol-lowering agents. Worldwide sales of

Lipitor, discovered and developed by the Parke-

Davis Division of Warner-Lambert and copromoted

by Pfizer, totaled $3.7 billion in 1999.

In clinical studies, Lipitor, as an adjunct to

diet, has demonstrated the ability to significantly The American Stroke Association estimates

reduce cholesterol levels. In fact, 72% of Lipitor that 600,000 Americans suffer a stroke every

patients studied reached their National Cholesterol year, more than one quarter of whom die.

Education Program goal for LDL cholesterol on Neutrophil inhibitory factor (NIF), a biological

the 10 mg starting dose. discovered by Corvas that is produced by the

In the AVERT trial, Lipitor demonstrated a canine hookworm, may be useful in preventing

36% reduction in the combined incidence of brain damage that occurs in stroke. Pfizer is

cardiovascular events, such as death, nonfatal conducting Phase II clinical trials of this com-

heart attack, bypass surgery, revascularization, pound and, pending their success, may accelerate

and worsening angina, compared with patients this product’s development.

receiving angioplasty followed by usual care.

Pfizer and Warner-Lambert are continuing Diabetes

a broad clinical program for Lipitor. The TNT People with diabetes are two to four times more

(Treating to New Targets) trial is a five-year likely than non-diabetics to have heart disease

study enrolling 8,600 patients at 250 sites to or suffer a stroke. Worldwide, the incidence of

determine whether there are further benefits diabetes is estimated to grow from 175 million

to using higher doses of Lipitor to bring LDL today to 240 million people in the next decade.

cholesterol below current guidelines. Glucotrol XL, Pfizer’s oral treatment for

Pfizer and Warner-Lambert have also begun Type 2 diabetes, stimulates the pancreas to release

development programs for a single product that insulin, with convenient once-daily dosing, no

combines the active ingredients of Lipitor and weight gain, and no adverse effects on blood

Norvasc. In the United States, 27 million patients lipids. Sales in 1999 rose 16% to $262 million.

suffer from both high blood pressure and high We are developing an inhalable form of

cholesterol. With only about 15% of these insulin in collaboration with Aventis Pharma and

patients being treated for both conditions, a vast Inhale Therapeutic Systems. Our clinical data in

number of patients may benefit from a single Type 1 diabetics show this patient-friendly

combination therapy. insulin delivery system to be as effective as subcu-

Pfizer will add to its cardiovascular product taneous injections of short-acting insulin. In Type

line with the first-quarter 2000 launch of 2 diabetes, we are demonstrating that inhaled

Tikosyn. This product is indicated for conversion insulin can be used as monotherapy or as an

to, and maintenance of, normal sinus rhythm in adjunct to oral hypoglycemic agents. The prod-

highly symptomatic patients with atrial fibrilla- uct, expected to be the first of its kind to reach

tion (AF)/atrial flutter of greater than one week the market, is in Phase III clinical trials, with a

duration. Pfizer has developed a comprehensive regulatory filing expected in 2001.

program to educate institutions and health care Pfizer is also pursuing an innovative approach

professionals on the required in-hospital initiation to treatment of Type 2 diabetes with the develop-

of the drug and use of its unique dosing algorithm. ment of CP-368,296. This compound inhibits the

Patients with AF suffer from rapid and irregular enzyme responsible for the release of glucose into

heartbeats in the upper chambers of the heart. the blood from stored glycogen in the liver.

Many experience debilitating chest pain, short- Clinical trials indicate that CP-368,296 causes a

ness of breath, fatigue, and anxiety. highly significant dose-dependent decrease in fast-

ing morning glucose levels after two weeks of

administration without the accompanying risk

of hypoglycemia.









20

Infectious Diseases

Pfizer’s Zithromax is the most-prescribed brand-

name oral antibiotic in the United States. Diflucan, the world’s best-selling prescrip-

Worldwide sales grew 28% to $1.3 billion in tion antifungal product, achieved 9% growth in

1999, driven by the product’s broad efficacy, sales to over $1.0 billion in 1999. This robust

compliance advantages, favorable side-effect profile, growth after 12 years on the market reflects the

and a good-tasting liquid formulation for children. unique properties of Diflucan and the growing

Zithromax treats most respiratory infections in medical need that it continues to fulfill. It treats

adults and children with once-daily dosing for

just three to five days. It is also used for skin As a working mother at Pfizer, Nancy Knowles

infections in adults, middle ear infections and understands the challenge of balancing the

strep pharyngitis in children, and a broad range demands of career and family — especially when

of other illnesses. one of her children is sick. Seen here at the

The 3,500-patient WIZARD study is testing “Pfizer Kids” child care center in New York City

whether 600 mg of Zithromax taken once weekly with Carly and Sean, Nancy says, “Sean’s ear

reduces cardiac events in post-heart-attack infection was really slowing him down. Zithromax

patients with atherosclerosis who are positive for has him laughing again.” Zithromax’s efficacy

previous Chlamydia presence. Chlamydia has been and convenient once-a-day-for-five-days dosing

observed in arterial plaques, where it may con- has helped it become the most-prescribed

tribute to plaque instability, rupture, and heart branded oral antibiotic in the

attack. Zithromax’s unique long tissue half-life

and high antichlamydial potency make it the

United States. Family-friendly

measures like our child “Zithromax

ideal agent for this condition. A new indication

for treatment of Mycobacterium avium complex and

a three-day dosing regimen for the U.S. market

care center contributed to

Pfizer being named one of

the “100 Best Companies

has Sean laughing

are also in advanced development.

again.”

to Work For” by Fortune magazine and one of the

“100 Best Companies for Working Mothers” by

Working Mother magazine.









21

Central Nervous System Disorders

While diseases of the central nervous system can

be difficult to recognize, they have devastating

effects on people’s lives. About 18 million people

systemic fungal infections, often present in in the United States suffer from depression at any

critically ill AIDS, cancer, transplant, and other given time, and up to 25% of women and up to

immunocompromised patients. Such infections 12% of men in the United States will experience

are difficult to diagnose and, if not treated early, a major depression during their lives. Pfizer’s

can result in high mortality. Diflucan is also Zoloft treats depression and panic disorder as well

effective as an oral treatment for vaginal candidi- as obsessive-compulsive disorder in adults and

asis and other non-life-threatening infections. children with strong efficacy and a favorable

Pfizer is completing clinical testing of Vfend safety and tolerability profile. The results of

(voriconazole), a powerful antifungal that it outcomes research studies have demonstrated that

expects to file with regulatory authorities during Zoloft patients have lower discontinuation rates

2000. The compound is targeted to treat a broad and better treatment compliance in comparison to

range of patients for invasive infections, includ- some other antidepressants.

ing aspergillosis and candidiasis. In 1999, Zoloft became the second Pfizer-

Sales of Trovan were $86 million in 1999. developed product to achieve $2 billion in annual

In June 1999, based on reports of rare liver side sales. An oral liquid dosage form, which provides

effects, European medical authorities suspended more convenient dosing in children and patients

the European Union licenses of Trovan for 12 who have difficulty swallowing pills, and an indi-

months. In the rest of the world, including the cation for posttraumatic stress disorder (PTSD)

United States, the use of Trovan is limited to were approved by the FDA in December 1999.

serious infections in institutionalized patients. Approximately 8% of the population will suffer

from PTSD at some point in their lifetimes.

Pfizer is also testing Zoloft for social phobia and

pediatric depression.

“It was a long,



“Today I’m better, hard road,” says

Lyn Whitten,

Approximately 10% of people over 65 suffer

from Alzheimer’s disease, including 4 million

Americans. Aricept has been taken by more

a lot better.” reflecting upon

the past few years of her life. “But today

I’m better, a lot better.” Lyn is one of more

than a million patients with mild-to-moderate

Alzheimer’s disease to enhance or maintain cogni-

tion. Discovered and developed by Eisai Co.,

than a million uninsured patients who have

Ltd., and copromoted by Pfizer,

received the most advanced Pfizer

the product preserves levels of

medicines at no charge through our

a neurotransmitter in the

Sharing the Care program. Following

brain. Total worldwide sales

the loss of a good job in California’s

grew 49% to $551 million

aerospace industry and the

in 1999. Together with

death of her mother, Lyn found

our partner Eisai, we

herself battling severe depres-

recently concluded

sion and anxiety, struggling to

make ends meet, and wonder-

ing where to turn for help. She

has been taking the antide-

pressant Zoloft for about a

year, and is gradually

getting her life back on

track. “I owe thanks to

the many people who

have helped me

along the way,” she

says. “I feel truly

blessed.”









22

two landmark one-year studies that demonstrate

Aricept’s benefit in maintaining patient function

and delaying institutionalization. It is also the

subject of a three-year, 720-patient study

designed to investigate whether Aricept can delay each year in the United States. Pfizer’s Phase II

the onset of Alzheimer’s disease in patients with compound CP-101,606 shows promise as a

mild cognitive impairment. treatment for brain trauma. If pivotal trials are

Clinical development of Zeldox, for the successful, this candidate has the potential for

manifestation of psychosis, advanced in 1999. accelerated development.

One psychotic disorder, schizophrenia, affects

approximately 1% of the world’s population. It is Metabolic Disorders

characterized by symptoms such as hallucinations, The National Institutes of Health estimate that

delusions, social withdrawal, and cognitive 10 million Americans suffer from osteoporosis,

impairment. Zeldox is effective in treating a a disease characterized by deterioration of bone

broad spectrum of symptoms, both in the short mass. The Pfizer-developed compound lasofoxifene

and long term, causing little or no weight gain has shown promise in prevention and treatment

and having a favorable effect on blood lipids. It of osteoporosis, lowering of harmful blood lipids,

has a unique intramuscular form for initiation of and prevention of breast cancer. In Phase II clinical

therapy for control of acute exacerbations. trials, 0.25 mg of lasofoxifene increased bone

Following consultation with the FDA, after mineral density in the lumbar spine more than

the agency issued a non-approvable letter for 60 mg of raloxifene after six months. Lasofoxifene

Zeldox, we undertook a unique clinical trial to also lowered LDL cholesterol by 25%.

characterize the modest electrocardiogram (ECG) Loss of bone and muscle mass throughout life

changes that were seen with the drug. Data from can lead to frailty and greatly reduced quality of

this trial and the clinical development program life in the elderly. CP-424,391, a Phase II Pfizer

support the absence of a significant risk associated compound, has demonstrated good efficacy, safety,

with the ECG changes seen with Zeldox. We and tolerability in increasing levels of the growth

anticipate refiling our new drug application for hormone that preserves bone and muscle mass.

Zeldox by midyear.

Migraine is one of the most common Arthritis

medical problems, experienced by 18% of women About one person in six suffers from arthritis.

and 6% of men. In spite of the incapacitating Rheumatoid arthritis (RA) affects about 1% of

nature of migraines — symptoms of which the population and results when the immune sys-

include severe headache pain, nausea, and sensitivity tem attacks a person’s own joints. Osteoarthritis

to light or sound — the vast majority of sufferers (OA) results from wear and tear on the joints.

have never been diagnosed or treated with pre- Celebrex, a new pharmaceutical copromoted

scription medicines. by Pfizer and the G.D. Searle division of

In October 1999, Pfizer received an approvable Monsanto Company, which discovered the drug,

letter from the FDA for Relpax, our new treatment relieves the pain, inflammation, and stiffness of

for migraine. Clinical data show that within an OA and RA. In clinical trials, Celebrex was shown

hour of taking an oral dose of Relpax, up to 40% to be as effective as the maximum recommended

of patients with moderate or severe migraine dose of the prescription-strength nonsteroidal

experience significant or complete headache relief, anti-inflammatory drug (NSAID) naproxen in

and up to 70% of patients experience relief treating arthritis pain and inflammation. Celebrex

within two hours. The Relpax clinical program works by inhibiting the enzyme cyclo-oxygenase-2

consisted of seven controlled clinical trials, three of (COX-2), which plays a role in arthritis pain and

which compared Relpax to the current leading inflammation, without inhibiting cyclo-oxygenase-1

prescription treatment for migraine. (COX-1), which helps maintain the stomach lining.

Brain trauma from motor vehicle accidents, NSAIDs in general inhibit both COX enzymes, so

sports injuries, and other causes results in about they treat arthritis pain and inflammation, but

300,000 hospitalizations and 50,000 deaths may damage the stomach lining, potentially leading

to ulcers in some patients.









23

“I just love seeing Ed

be himself again.” In New York’s Central Park, Ed and Shaila Small

enjoy an afternoon of ice skating. The Smalls have

always been extremely active people, but Ed’s

arthritic knee was beginning to slow him down.

He began taking Celebrex in February 1999 and

has been feeling better ever since. “I am the

director of a track and field center during the

week and keep busy during my days off, too,” Ed

says. “If my knee is holding me back, I can’t live

my life.” Shaila noticed the difference Celebrex

made right away. “I could see how hard it was for

him to deal with the pain,” she says. “I just love

seeing Ed be himself again.”





Cancer

Cancer is the second leading cause of death in

the United States, with 1.2 million new cases

and 600,000 deaths every year.

In December 1999, the FDA approved

Celebrex as the first COX-2 specific inhibitor

approved for treatment of familial adenomatous

polyposis (FAP), a rare and devastating genetic

disease characterized by the development of

hundreds to thousands of polyps in the colon and

rectum. Left untreated, virtually all patients with

FAP develop colorectal cancer by age 40 to 50.

Celebrex is being tested for several other cancers.



Erectile Dysfunction

The 1998 launch of Viagra for erectile dysfunction

(ED) was one of the most talked-about medical

advances of our time. The product made further

progress in 1999, with a worldwide rollout and

sales topping $1 billion. Since launch, physicians

have written more than 17 million prescriptions

for Viagra for more than 6 million patients in the

United States alone. More than 150 million

tablets have been dispensed worldwide.

Viagra allows many men with ED to achieve

With sales of $1.5 billion in 1999, Celebrex erections in response to sexual stimulation. It

was the most successful drug launch in pharma- improves erections in up to 82% of men who take

ceutical industry history. In its first year, more it, is effective in a broad range of patients, and

than 19 million prescriptions were written for offers the convenience of a pill. At the 1999 annual

Celebrex worldwide. meeting of the American Urological Association,

Pfizer and G.D. Searle & Co. are actively Pfizer reported that 93% of 401 patients who

engaged in a program to broaden the clinical pro- participated in a Viagra study remained satisfied

file of Celebrex, including potential new uses for with the drug after two years.

treatment of pain and several types of cancer.

In addition, Pfizer and Searle are testing the

second-generation compound valdecoxib for

treatment of RA, OA, and pain.



24

The division is also working today to plan

Allergy for future switches of prescription-only medicines

Pfizer’s antihistamine Zyrtec, marketed as Reactine to over-the-counter (OTC) brands. With experience

in Canada, provides strong, rapid, and long-lasting gained by the successful OTC switch of Reactine

relief for seasonal and perennial allergies and hives in Canada and Diflucan One in the United

with once-daily dosing. Sales in the United States Kingdom, Pfizer is well positioned to expand its

and Canada grew 33% to $552 million in 1999. OTC portfolio in coming years.

In two clinical studies conducted in an artificially

controlled pollen environment, Zyrtec began Animal Health

working in about one hour, compared to about Pfizer’s Animal Health Group (AHG) is a

three hours for Claritin. In a survey of 623 allergy global supplier of animal medicines unmatched

sufferers, 93% wanted fast relief most. Zyrtec is in product-line or geographic breadth. AHG

the only prescription antihistamine approved for revenues grew 2% to $1.3 billion in 1999.

children as young as two years old. Zyrtec syrup The $1.3 billion worldwide pet antiparasitic

is the most-prescribed antihistamine syrup in the market consists of medicines for external parasites

United States. A formulation with a decongestant such as fleas and ticks, treatments for gastroin-

is in advanced development. testinal worms, and heartworm preventatives.

Revolution, marketed as Stronghold in Europe, is

Urology the first product to treat all three problems, and

More than 50 million people in the United States, its U.S. launch was one of the most successful in

Europe, and Japan suffer from overactive bladder, a the history of animal health. This once-a-month,

condition characterized by increased frequency and simple-to-administer topical liquid protects

urgency of bladder activity and incontinent events.

Pfizer expects its compound darifenacin to provide

a therapeutic profile superior to the therapies What moves at 180 miles-per-hour and gets the red out

currently available. Darifenacin progressed into even faster? It’s the new Visine-sponsored race car, which

Phrase III testing during 1999. is tearing up tracks across America in 2000 as part of the





“Visine helps me stay

NASCAR Busch

Consumer Health Care Grand National

Pfizer’s Consumer Health Care Group (CHC)

markets a broad range of self-medication products.

CHC sales, which are reflected in pharmaceutical focused on the

sales, increased 7% in 1999 to $561 million.

Six of CHC’s nine major brands — including

BenGay for the pain of minor arthritis and muscle

checkered flag.”

Series. A second car,

sponsored by Viagra,

is racing on NASCAR’s Winston Cup circuit. NASCAR auto

aches, and Visine eye care products, which

provide fast relief for redness, dryness, and now racing is the fastest-growing spectator sport in the world.

allergies — are number one in their category. One fan of Visine is driver Matt Kenseth, who especially

Other CHC brands include Cortizone anti-itch likes the brand’s newest formulation, Visine Tears. “My eyes

products, Desitin diaper rash products, Unisom can get pretty dry, especially when we race in places like

sleep aids, RID head lice treatments, Barbasol Arizona and California,” he says. “Visine

shaving cream, and Plax pre-brushing dental rinse. helps me stay focused on the checkered flag.”









25

provides relief from acute



“Ezra and Ivan are

Lisa Neuman owns two dogs and cares for

dozens more every day as a veterinarian at and chronic pain associated

the Miracle with osteoarthritis. A new



more than just my dogs. Mile Animal

Clinic in Ft.

chewable form provides the

pet owner with greater con-

venience of administration.



They’re my friends.”

Myers,

Florida. “I know how important it is to Other important Pfizer

keep pets healthy,” she says. “Ezra and companion animal products

Ivan are more than just my dogs. They’re my friends.” Dr. Neuman include Vanguard vaccines

protects them from harmful parasites — inside and out — with for canine enteric disease,

Revolution, a new Pfizer medicine developed specifically for dogs Leukocell vaccines for feline

and cats. “As a veterinarian, it’s great to be able to prescribe a single leukemia, Clavamox anti-

product that does so many things so effectively. It’s great as a pet infectives, and Anipryl for

owner, too. One spot of Revolution a month on the back of their Cushing’s disease and

necks, and these guys are good to go.” Cognitive Dysfunction

Syndrome in dogs.

against internal and external parasites, including AHG produces leading antiparasitics, vaccines,

heartworm, fleas, and ear mites in both dogs and and anti-infectives for cattle, swine, and poultry.

cats; American dog ticks and sarcoptic mange in Dectomax, AHG’s largest-selling product, pro-

dogs; and hookworm and roundworm in cats. tects cattle, swine, and sheep from both internal

There are nearly 53 million dogs and nearly 60 and external parasites, providing the broadest

million cats in the United States alone. More than spectrum of control available. It can be adminis-

half of all dogs and three-quarters of all cats are tered either by injection or topically. RespiSure/

not adequately protected against these parasites. Stellamune vaccines help prevent a type of

Since its introduction in 1997, nearly 5 mil- pneumonia and the related problems of slow

lion arthritic dogs worldwide have been treated weight gain, decreased feed efficiency, and lack

with Rimadyl. About 15% of all dogs suffer of uniformity in size in swine.

from osteoarthritis, a condition characterized by

worsening pain, stiffness, and lameness. Rimadyl

26

A Helping Hand



I

n country after country, through the

donations of our medicines and the

volunteer efforts of our employees, Pfizer

is bringing improved health — and

renewed hope — to those in need.

In the United States, Pfizer’s largest

philanthropic program is Sharing the

Care, through which uninsured patients

receive our innovative medicines at

no charge.

“I speak on behalf of all governors

when I say we are proud of Sharing the

Care and its commitment to helping

more than a million of the nation’s medically



“My own son is blind,

Phat Tran, left,

underserved lead healthier, more productive lives,” and Chieck

said Thomas Carper, governor Kieta work at

of Delaware and 1999 chairman

of the National Governors’

Association, which is partnering

so I understand Pfizer’s plant in Brooklyn, New York, where our

trachoma-fighting antibiotic Zithromax is manu-





how precious sight is.”

factured for ship-

with Pfizer on the program. ment around the

Access to medicines is no less of an issue world. Tran is a

outside the United States, a fact tragically native of Vietnam, Kieta of Mali—two of the five devel-

illustrated by trachoma, a disease that has already the wake of natural oping nations that Pfizer is working with to eliminate

claimed the sight of 6 million people — mostly disasters in Turkey, this blinding disease. “You can tell when people have

women and children — and threatens a staggering Taiwan, Venezuela, trachoma,” says Kieta, who recently returned to Mali

540 million more. and the United States.for a visit. “Their eyes are open, but they cannot see.

In 1998, Pfizer joined with the Edna Aiding refugees in There’s great satisfaction in knowing you are making

McConnell Clark Foundation to found the war-torn Kosovo and a medicine that will help people in your homeland.”

International Trachoma Initiative. One of the Indonesia. Bringing Tran agrees. “My own son is blind, so I understand how

cornerstones of the program is Pfizer’s donation smiles to the faces ofprecious sight is,” he says. “I’m very proud to be a

of the antibiotic Zithromax to five developing sick children around part of a company that is helping to fight blindness

countries where the disease is endemic. We have the world. Visiting around the world.”

already provided more than a million doses of this classrooms to inspire

powerful medicine, which has proven to be the the scientists of tomorrow.

most effective way to combat trachoma. As one Pfizer employee said after a day of

“The donation of Zithromax will help us to volunteering with his family at a children’s

reduce significantly the number of new trachoma hospital in Atlanta, Georgia: “My eight-year-old

cases in Morocco and save the sight of many son was impressed that Pfizer does more than

of our citizens,” said Dr. Abdelwahed El Fassi, just make medicines for sick people; we also

Morocco’s Minister of Public Health. help people by being there when needed. I

In addition to large-scale programs, Pfizer think that sums up who we are better than just

employees continue to find hundreds of ways to about anything.”

make the world a better place. Providing relief in 27

Financial Review





Proposed Merger with Warner-Lambert Company inventories. Our 1998 operating results reflect:

• the sale of our Medical Technology Group (MTG)

On February 7, 2000, we announced an agreement to merge

• the recording of certain significant charges associated

with Warner-Lambert Company (Warner-Lambert). Under

with adjustments to asset values, the exiting of certain

terms of the merger agreement, which has been approved by

product lines, plant rationalizations, severance payments,

the Board of Directors of both Pfizer and Warner-Lambert,

co-promotion payments to Searle, a contribution to The

we will exchange 2.75 shares of Pfizer voting common stock

Pfizer Foundation and other miscellaneous charges

for each outstanding share of Warner-Lambert voting common

stock in a tax-free transaction valued at $98.31 per Warner- Analysis of the Consolidated Statement of Income

Lambert share, or an equity value of $90 billion based on the

closing price of our stock on February 4, 2000 of $35.75 per % Change

share. Customary and usual provisions will be made for (millions of dollars) 1999 1998 1997 99/98 98/97

outstanding options and warrants. Net sales $14,133 $12,677 $10,739 11 18

The combined company, which will be called Pfizer Inc, Alliance revenue 2,071 867 316 139 175

is expected to have (excluding any impact of anticipated

Total revenues 16,204 13,544 11,055 20 23

restructuring charges and transaction fees of $1.7 billion to Cost of sales 2,528 2,094 1,776 21 18

$2.2 billion): Selling, informational and

• compounded annual revenue growth of 13% and earnings administrative expenses 6,351 5,568 4,401 14 27

growth of 25% through 2002 % of total revenues 39.2% 41.1% 39.8%

• $4.7 billion in annual research and development expenses R&D expenses 2,776 2,279 1,805 22 26

in 2000 % of total revenues 17.1% 16.8% 16.3%

• anticipated annual cost savings and efficiencies of Other deductions — net 101 1,009 206 (90) 391

$1.6 billion by 2002 ($200 million of these savings are Income from continuing

expected to be achieved in 2000, $1 billion in 2001 and operations before taxes $ 4,448 $ 2,594 $ 2,867 71 (10)

$1.6 billion in 2002) % of total revenues 27.5% 19.2% 25.9%

• diluted earnings per share of $.98 on a pro forma basis in Taxes on income $ 1,244 $ 642 $ 775 94 (17)

Effective tax rate 28.0% 24.8% 27.0%

2000, $1.27 for 2001 and $1.56 for 2002 (these numbers

Income from continuing

include the $1.6 billion of cost savings phased in over this operations $ 3,199 $ 1,950 $ 2,082 64 (6)

time period, but do not include any increased sales from % of total revenues 19.7% 14.4% 18.8%

collaborative activities and the $1.8 billion termination Discontinued

fee paid by Warner-Lambert to American Home operations — net of tax (20) 1,401 131 — 972

Products Corporation) Net income $ 3,179 $ 3,351 $ 2,213 (5) 51

This transaction is subject to customary conditions, % of total revenues 19.6% 24.7% 20.0%

including the use of pooling-of-interests accounting, qualifying

Percentages may reflect rounding adjustments.

as a tax-free reorganization, shareholder approval at both

companies and usual regulatory approvals. The transaction is Total Revenues

expected to close in mid-2000.

The following financial review reflects the results of Total revenues increased 20% or $2,660 million in 1999 and

operations and financial condition of Pfizer and does not consider 23% or $2,489 million in 1998. Revenue increases in both

the impact of the proposed merger with Warner-Lambert. years were primarily due to sales volume growth of our in-line

products and revenue generated from product alliances

Overview of Consolidated Operating Results (alliance revenue).

Revenue growth in 1999 was not significantly impacted

In 1999, total revenues grew 20% to $16,204 million, reflecting

by foreign exchange. Total revenues grew by 26% in 1998

the strong worldwide demand for our in-line products, as well

excluding the impact of foreign exchange.

as our alliance products. Our operating results in 1999 were

impacted by the recording of a charge to write off certain Trovan









28

Pfizer Inc and Subsidiary Companies







introduction of Viagra accounts for 12 percentage points of the

Elements of Total Revenue Growth 1998 U.S. growth. Pharmaceutical revenue growth in 1999 was

not significantly impacted by foreign exchange. In 1998,

Volume has been the major pharmaceutical revenue grew 29% excluding the impact of

24.8%

contributor to total revenue foreign exchange. The currency impact on the 1998 revenue

growth in each of the last growth reflects the strengthening of the dollar relative to the

three years. 19.6%

Japanese yen, as well as several European and other Asian

14.0% currencies.

In 1999, we had seven products, including alliance

products, with sales to third parties in excess of $1 billion each.

Volume The five Pfizer-discovered products in this group — Norvasc,

Price 1.2% 1.6% Zoloft, Zithromax, Viagra and Diflucan — grew at a combined

0.5%

Currency annual rate of 18% in 1999 and are patent-protected well into

(0.5)% this decade, or beyond.

(3.5)% (3.5)%

Net Sales — Major Pharmaceutical Products

99 98 97

% Increase

(millions of dollars) 1999 1998 1997 99/98 98/97

Percentage Change in Total Revenues

Cardiovascular Diseases: $4,635 $4,186 $3,806 11 10

Norvasc 3,030 2,575 2,217 18 16

Analysis of % Change

Total % Cardura 794 688 626 15 10

Change Volume Price Currency

Infectious Diseases: 3,145 2,822 2,475 11 14

Pharmaceutical

Zithromax 1,333 1,041 821 28 27

1999 vs. 1998 21.5 21.1 0.5 (0.1)

Diflucan 1,002 916 881 9 4

1998 vs. 1997 25.8 28.1 1.0 (3.3)

Animal Health Central Nervous System

1999 vs. 1998 2.4 4.9 1.2 (3.7) Disorders: 2,156 1,924 1,553 12 24

1998 vs. 1997 (1.1) 0.6 2.4 (4.1) Zoloft 2,034 1,836 1,507 11 22

Total

Viagra 1,033 788 — 31 —

1999 vs. 1998 19.6 19.6 0.5 (0.5)

1998 vs. 1997 22.5 24.8 1.2 (3.5) Allergy: 557 422 273 32 55

Zyrtec/Reactine 552 416 265 33 57

Certain prior year data have been reclassified to conform to the current year

presentation.

Total Revenues by Business Segment

(% of total revenue) Pharmaceutical Animal Health In June 1999, the European Union’s Committee for

8% 10% 12% Proprietary Medicinal Products suspended the European Union

(EU) licenses of the oral and intravenous formulations of our

antibiotic Trovan for 12 months. In the rest of the world,

including the U.S., the use of Trovan is limited to serious

infections in institutionalized patients. As a result of these

92% 88%

limitations, Trovan net sales declined to $86 million in 1999

90%

1999 1998 1997 from $160 million in 1998. See “Cost of sales” for a discussion

(millions of dollars)

of a charge recorded in 1999 to write off certain Trovan

inventories.

% Change % Change % Change

99/98 98/97 97/96

Alliance revenue was $2,071 million in 1999, reflecting

$14,859 22 $12,230 26 $ 9,726 13 revenue associated with the co-promotion of Lipitor, Aricept

1,345 2 1,314 (1) 1,329 9

and our new alliance product, Celebrex.

Total $16,204 20 $13,544 23 $11,055 12 In February 1999, we launched Celebrex with G.D. Searle

& Co. (Searle), the pharmaceutical division of Monsanto

Company, which discovered and developed the drug. Celebrex

Pharmaceutical revenues increased 22% to $14,859 million in is used for the relief of symptoms of adult rheumatoid arthritis

1999 and 26% to $12,230 million in 1998. In the U.S. market, and osteoarthritis. During 1999, Celebrex achieved total global

revenue growth was 21% in 1999 and 38% in 1998, while sales of approximately $1.5 billion.

international growth was 22% in 1999 and 10% in 1998. The









29

Pfizer Inc and Subsidiary Companies







Together with our alliance partner, the Parke-Davis Net sales decreased 1% in 1998 due to a weak livestock

Division of Warner-Lambert, the company that discovered and market in the U.S. and poor Asian economies.

developed Lipitor, we co-promote this product in most major

world markets. During 1999, Lipitor achieved third-party sales Total Revenues by Country

of approximately $3.7 billion.

(% of total revenue) United States Japan All Other Countries

These alliances allow us to co-promote or license these 8% 7% 9%

products for sale in certain countries. Under the co-promotion 31% 32% 36%

agreements, these products are marketed and promoted with

our alliance partners. We provide cash, staff and other resources

to sell, market, promote and further develop these products.

Revenue from co-promotion agreements is reported in the

61% 61% 55%

Statement of Income as Alliance revenue. 1999 1998 1997

Certain alliance agreements include additional provisions (millions of dollars)

that enable our product alliance partners the right to negotiate % Change % Change % Change

to co-promote certain specified Pfizer-discovered products. 99/98 98/97 97/96

$ 9,896 21 $ 8,205 35 $ 6,089 17

Rebates under Medicaid and related state programs 1,249 32 943 (1) 949 3

reduced revenues by $146 million in 1999, $150 million in 5,059 15 4,396 9 4,017 7

1998 and $99 million in 1997. The 1998 increase in rebates

Total $16,204 20 $13,544 23 $11,055 12

reflects growth of in-line products and the introduction in

1998 of two products — Trovan and Viagra. We also provided

to the federal government legislatively mandated discounts of Revenues were in excess of $100 million in each of 12

$95 million in 1999, $105 million in 1998 and $88 million countries outside the U.S. in 1999. The U.S. was the only

in 1997. Performance-based contracts also provide rebates to country to contribute more than 10% to total revenues.

several customers as a result of the increasing influence of

managed care groups on the pricing of our products. Percentage Change in Geographic Total Revenues

by Business Segment

In the fourth quarter of 1999, we sold the Bain de Soleil

sun care product line for $26 million in cash to Schering- % Change in Total Revenues

Plough HealthCare Products, Inc. Proceeds from the sale U.S. International

approximated the total of the carrying value of net assets 99/98 98/97 99/98 98/97

associated with this product line and selling costs. The sale of

Pharmaceutical 21 38 22 10

Bain de Soleil will not have a material impact on our future

Animal Health 14 3 (7) (4)

results of operations. Total 21 35 18 8

Animal Health net sales increased 2% to $1,345 million

in 1999 and decreased 1% to $1,314 million in 1998. Excluding Product Developments

the impact of foreign exchange, net sales increased 6% in 1999 We continue to invest in R&D to provide future sources

and 3% in 1998. The increase in net sales in 1999 was due to: of revenue through the development of new products, as well

• the performance of the companion animal business as through additional uses for existing in-line and alliance

partially offset by products. Certain significant regulatory actions by, and filings

• the continuing weakness in the livestock market in the pending with, the U.S. Food and Drug Administration (FDA)

U.S. and Europe follow:

• the decision of the European Commission to ban certain

antibiotic feed additives, including Stafac (virginiamycin) U.S. FDA Approvals

in the EU after June 30, 1999

Product Indication Date Approved

We do not expect the ban on sales of virginiamycin to have Zoloft Posttraumatic stress disorder (PTSD) December 1999

a material effect on our future results of operations. Zoloft Oral liquid dosage form December 1999

Sales of companion animal products increased by 30% in Celebrex Familial adenomatous polyposis December 1999

1999 primarily due to the launch of Revolution and the growth (a rare and devastating hereditary

of Rimadyl. Revolution was approved in the U.S. in July 1999 disease that, left untreated, almost

always leads to colorectal cancer)

as the first and only topically applied medication for dogs and

Tikosyn Atrial fibrillation October 1999

cats that is effective against heartworm, fleas and many other

parasites. Rimadyl is a treatment for the relief of pain and

inflammation associated with osteoarthritis in dogs.









30

Pfizer Inc and Subsidiary Companies







Zoloft is the first and only medicine to receive FDA Ongoing or planned clinical trials for new product

approval for the treatment of PTSD. development programs include:

We have developed a comprehensive program to educate

Product Indication

institutions and health care professionals on the required in-

hospital initiation and dosing regimen for Tikosyn. We expect lasofoxifene Prevention and treatment of osteoporosis

Prevention of breast cancer

to launch Tikosyn in the U.S. in the first quarter of 2000, and Reduction of risk of coronary heart disease

it will be available to those prescribers and hospitals that have

Vfend (voriconazole) Serious systemic fungal infections

participated in this educational program.

darifenacin Overactive bladder

Pending U.S. New Drug Applications

inhaled insulin Diabetes

Product Indication Date Filed valdecoxib (under Osteoarthritis

co-development Rheumatoid arthritis

Relpax Migraine headaches October 1998

with Searle) Pain

Zeldox Psychotic disorders — December 1997

intramuscular dosage form

Zeldox Psychotic disorders — March 1997 Additional product development programs are in various

oral dosage form stages of discovery.

In 1998, we entered into worldwide agreements with

In October 1999, we received an approvable letter from the Aventis Pharma to manufacture insulin and co-develop and

FDA for Relpax for the treatment of migraines. Regulatory co-promote inhaled insulin. Under the agreements, Aventis

review is continuing in Europe. Pharma and Pfizer will contribute expertise in the development

We received a non-approvable letter from the FDA and production of insulin products, as well as selling and

for Zeldox in 1998. Analysis and interpretation of the results marketing resources. We bring to the alliance our development

of a recently completed study on the effects of Zeldox will be of inhaled insulin from our collaboration with Inhale

included in an amended New Drug Application, which Therapeutic Systems, Inc. Together with Aventis Pharma we

we expect to file by midyear 2000. are building a new insulin manufacturing plant in Frankfurt,

Ongoing or planned clinical trials for additional uses and Germany, to support the product currently in development.

dosage forms for our currently marketed products include: We have decided not to pursue further development of

ezlopitant for the treatment of chemotherapy-induced nausea

Product Indication

and vomiting in cancer patients, as well as Alond for the

Norvasc Pediatric hypertension treatment of diabetic neuropathy.

Zithromax Decrease cardiovascular risk in patients with

atherosclerosis (a process in which fatty substances are Costs and Expenses

deposited within blood vessels) caused by certain

infections In 1999, we substantially completed the actions under the

Treatment of mycobacterium avium complex restructuring plans announced in 1998.

Accelerated dosing regimen (three-day treatment)

In 1998, we recorded charges for the restructuring in

Viagra Female sexual arousal disorder addition to charges for certain asset impairments. These pre-tax

Zoloft Pediatric depression charges were recorded in the 1998 Statement of Income as

Social phobia follows:

Zyrtec Decongestant formulation

Pediatric (millions of dollars) Total COS* SI&A* R&D OD*

Lipitor Broad cardiovascular-care clinical program Restructuring charges $177 $68 $17 $1 $ 91

Aricept Oral liquid dosage form Asset impairments 213 18 — — 195

Celebrex Sporadic adenomatous polyposis * COS — Cost of sales; SI&A — Selling, informational and administrative expenses; OD —

Pain Other deductions — net.





Together with Warner-Lambert, we are jointly exploring

potential Lipitor line extensions and product combinations and

other areas of mutual interest. This includes a program to

develop a combination product that contains the cholesterol-

lowering and antihypertensive medications in Lipitor and

Norvasc — two of the world’s most widely prescribed medicines.









31

Pfizer Inc and Subsidiary Companies







The components of the 1998 restructuring charges follow: SI&A increased 14% in 1999 and 27% in 1998. These

increases reflect support for previously introduced products and

Utilization

new products. Such support included substantial global

(millions of dollars) Charges in 1998 1998 1999 Beyond investments, begun in 1998, in our pharmaceutical sales force,

Property, plant including the creation of a new U.S. primary-care sales force

and equipment $ 49 $ 49 $— $— and a new U.S. specialty sales force dedicated to rheumatology.

Write-down of intangibles 44 44 — — In addition, personnel increases in other specialty sales forces

Employee termination costs 40 12 28 — in the U.S. and the expansion of international sales forces

Other 44 11 17 16

contributed to the increase in SI&A. Our past investments in

Total $177 $116 $45 $16 SI&A are enabling us to maximize the financial return realized

from our products.

As a result of the restructuring, our workforce was reduced

by approximately 500 manufacturing, sales and corporate R&D increased 22% in 1999 and 26% in 1998. These

personnel. In 1998, restructuring charges of $90 million are expenditures were necessary to support the advancement of

reflected in the pharmaceutical segment and $87 million are in potential drug candidates in all stages of development

the animal health segment. (from initial discovery through final regulatory approval). In

In 1998, we recorded an impairment charge of 2000, we expect total R&D spending to be about $3.2 billion.

$110 million in the pharmaceutical segment to adjust See “Proposed Merger with Warner-Lambert Company” for the

intangible asset values, primarily goodwill and trademarks, expected R&D spending in 2000 of a combined Pfizer/Warner-

related to consumer health care product lines. These charges Lambert entity.

resulted from significant changes in the marketplace and a Other deductions —net decreased 90% in 1999 due to

revision of our strategies. the absence of certain significant charges recorded in 1998 of

As noted in our discussion of revenues, our animal health $883 million.

antibiotic feed additive Stafac was banned throughout the EU, Other deductions — net increased substantially in 1998

resulting in 1998 asset impairment charges of $103 million primarily due to:

($85 million to adjust intangible asset values, primarily • asset impairments — $195 million

goodwill and trademarks, and $18 million to adjust the • restructuring charges — $91 million

carrying value of machinery and equipment in the • co-promotion payments to Searle for rights to

pharmaceutical segment). Celebrex — $240 million

In 1999, revenues declined approximately $41 million • a contribution to The Pfizer Foundation —

as a result of exiting certain product lines. In 1999, as a result $300 million

of the restructuring activities and the asset impairments, • legal settlements involving the brand-name prescription

we realized cost savings of approximately $39 million and a drug antitrust litigation — $57 million

reduction in amortization and depreciation expense of partially offset by

approximately $12 million. • an increase in interest income on the investment of cash

Cost of sales increased 21% in 1999 and 18% in 1998. generated from operations and the divestiture of MTG

Based on our evaluation of the actions noted in our discussion • foreign exchange effects

of revenues, we determined that it was unlikely that certain Our overall effective tax rate was 28.1% in 1999 and

Trovan inventories of finished goods, bulk, work-in-process 35.4% in 1998. This decrease was due mainly to the 1998 gain

and raw materials will be used. Accordingly, in the third on the disposal of MTG being recognized in jurisdictions with

quarter of 1999, we recorded a charge of $310 million in Cost of higher tax rates.

sales to write off Trovan inventories in excess of the amount The effective tax rate for continuing operations was 28.0%

required to support expected sales. Also included in Cost of sales in 1999 and 24.8% in 1998. Significant charges in both 1999

for 1999 is a benefit of $6.6 million related to the change in and 1998 were recorded in jurisdictions with higher tax rates.

accounting for the cost of inventories from the “Last-in, first- However, the level of these charges was greater in 1998 than in

out” method to the “First-in, first-out” method. Excluding the 1999. Excluding these charges in 1999 and 1998, the effective

Trovan inventory charge and the benefit related to the tax rate was 28.4% in 1999 and 28.0% in 1998. This increase

accounting change for inventories in 1999 and the asset in 1999 was primarily due to the mix of income by country.

impairments and restructuring charges in 1998, cost of sales We have received and are protesting assessments from the

increased 11%, comparable to the increase in 1999 net sales. Belgian tax authorities. For additional details, see note 9,

Excluding the 1998 asset impairments and restructuring “Taxes on Income,” beginning on page 49.

charges, cost of sales increased 13% in 1998 as compared to an

increase in net sales of 18%.









32

Pfizer Inc and Subsidiary Companies







Discontinued Operations Financial Condition, Liquidity and

In 1999, we agreed to pay a fine of $20 million to settle Capital Resources

antitrust charges involving our former Food Science Group. Our net financial asset position as of December 31 was as

This charge is reflected in Discontinued operations — net of tax. follows:

For additional details, see note 18, “Litigation,” beginning on

page 54. (millions of dollars) 1999 1998 1997

During 1998, we exited the medical devices business with Financial assets* $6,436 $5,835 $3,034

the sale of our remaining MTG businesses: Short- and long-term debt 5,526 3,256 2,976

• Howmedica to Stryker Corporation in December for Net financial assets $ 910 $2,579 $ 58

$1.65 billion in cash

* Consists of cash and cash equivalents, short-term loans and investments, and long-

• Schneider to Boston Scientific Corporation in September term loans and investments.

for $2.1 billion in cash

• American Medical Systems to E.M. Warburg, Pincus & Selected Measures of Liquidity and

Co., LLC, in September for $130 million in cash Capital Resources

• Valleylab to U.S. Surgical Corporation in January for

$425 million in cash 1999 1998 1997

The net proceeds from these divestitures were used for Cash and cash equivalents and

general corporate purposes, including the repayment of short-term loans and

commercial paper borrowings. Net income of these businesses investments (millions of dollars)* $4,715 $4,079 $1,704

Working capital (millions of dollars) 2,006 2,739 2,448

up to the date of their divestiture and divestiture gains are

Current ratio 1.22:1 1.38:1 1.49:1

included in Discontinued operations — net of tax.

Shareholders’ equity per

common share** $ 2.36 $ 2.33 $ 2.10

Net Income

* Cash is managed jurisdictionally and is not always available to be used in every

Net income for 1999 decreased 5% from 1998. Diluted location throughout the world. When necessary, we utilize short-term borrowings for

earnings per share were $.82 and decreased by 4% from 1998. various corporate purposes.

Excluding the impact of the 1999 Trovan inventory charge and ** Represents shareholders’ equity divided by the actual number of common shares

outstanding (which excludes treasury shares and those held by the employee benefit

certain significant charges and discontinued operations in 1998, trusts).

net income increased by 29% in 1999 over 1998. On that same

basis, diluted earnings per share were $.87 in 1999 and The decrease in working capital from 1998 to 1999 was

increased by 30% over 1998. The 1998 pre-tax significant primarily due to the following:

charges related to: • Decrease in Inventories — due to the writeoff of Trovan

• asset impairments — $213 million inventory

• restructuring charges — $177 million • Increase in Short-term borrowings — primarily to fund

• co-promotion payments to Searle — $240 million common stock purchases of $2.5 billion

• contribution to The Pfizer Foundation — $300 million offset by

• other, which is primarily related to legal settlements — • Net increase in Cash and cash equivalents and Short-term

$126 million investments — mainly from profits earned overseas

• Increase in Accounts receivable — resulting from growth in

sales volume and higher alliance revenue receivables due to

sales growth of alliance products and the launch of

Celebrex in February 1999

• Decrease in Income taxes payable









33

Pfizer Inc and Subsidiary Companies







The increase in working capital from 1997 to 1998 was divestitures, partially offset by tax benefits associated with

primarily due to the following: charges for asset impairment, restructuring, co-promotion

• Increase in Cash and cash equivalents and Short-term payments to Searle and the contribution to The Pfizer

investments — due to the receipt of cash from the MTG Foundation

divestiture • higher compensation related accruals

• Increase in Accounts receivable — due to the alliance revenue reduced by

receivables and growth in sales volume • higher receivable and inventory levels related to new

• Increase in Inventories — due to higher pharmaceutical products

inventory levels as a result of new products

offset by Net cash used in investing activities in 1999 changed

• Decrease in Net assets of discontinued operations — due to the primarily due to:

sale of the MTG businesses • the absence of proceeds from the sale of MTG which

• Increase in Short-term borrowings — due to an increase in occurred in 1998

funding for common stock purchases at a higher average • increased purchases of property, plant and equipment

price net of repayments made with cash received from the in 1999

MTG divestiture

• Increase in Dividends payable — related to the first-quarter Net cash used in investing activities decreased in 1998

1999 dividend declared in December 1998 primarily due to:

• Increase in Income taxes payable — primarily due to changes • proceeds from the sale of the MTG businesses, some of

in operations and the divestiture of the MTG businesses which accounts for our increase in short-term investments

• Increase in Other current liabilities — primarily due to reduced by

accrued charges associated with the divestiture of the • increased long-term investments

MTG businesses and our plan to exit certain product lines • increased purchases of property, plant and equipment



The decline in the current ratio from 1998 to 1999 was Net cash used in financing activities decreased in 1999

primarily due to higher short-term borrowings due to an primarily due to:

increase in funding for common stock purchases. The increase • increased short-term borrowings for common stock

in shareholders’ equity per common share in 1998 was purchases

primarily due to growth in net income. reduced by

• higher dividend payments to our shareholders

Summary of Cash Flows

Net cash used in financing activities increased in 1998

(millions of dollars) 1999 1998 1997 primarily due to:

Cash provided by/(used in): • the increase in common stock purchases at a

Operating activities $ 3,076 $ 3,282 $ 1,580 higher average price

Investing activities (2,768) (335) (963) • higher dividend payments to our shareholders

Financing activities (1,127) (2,277) (981) reduced by

Discontinued operations (20) 4 118 • more cash received from employee stock option exercises

Effect of exchange-rate changes on

cash and cash equivalents 26 1 (27)

Under the current share-purchase program begun in

Net (decrease)/increase in cash September 1998, we are authorized to purchase up to

and cash equivalents $ (813) $ 675 $ (273)

$5 billion of our common stock. In 1999, we purchased

approximately 65.6 million shares of our common stock in

Net cash provided by operating activities decreased in the open market for approximately $2.5 billion. Since the

1999 primarily due to: beginning of this program, we have purchased 80.4 million

• higher receivable levels related to increased sales and shares of our common stock for approximately $3 billion. In

alliance revenue September 1998, we completed a program under which we

• higher taxes paid purchased 79.2 million shares of our common stock at a total

reduced by cost of $2 billion. Purchased shares are available for general

• higher income from continuing operations corporate purposes.

Net cash provided by operating activities increased in We have available lines of credit and revolving-credit

1998 primarily due to: agreements with a select group of banks and other financial

• higher taxes payable associated with sales growth of intermediaries. Major unused lines of credit totaled

existing and new products as well as the MTG approximately $1.5 billion at December 31, 1999.









34

Pfizer Inc and Subsidiary Companies







Our short-term debt has been rated P1 by Moody’s geographic location. PIBE continues to have S&P’s highest

Investors Services (Moody’s) and A-1+ by Standard and Poor’s short-term rating of A-1+.

(S&P). Also, our long-term debt has been rated Aaa by The net income of PIBE is affected by changes in market

Moody’s and AAA by S&P for the past 14 years. Moody’s and interest rates because of repricing and maturity mismatches

S&P are the major corporate debt-rating organizations and between its interest-sensitive assets and liabilities. PIBE is

these are their highest ratings. currently asset sensitive (more assets than liabilities repricing

in a given period) and, therefore, we expect that in an

Cash Dividends Paid Per Common Share environment of increasing interest rates, net income would

increase. PIBE’s asset and liability management reflects its

(dollars)

liquidity, interest-rate outlook and general market conditions.

The 1999 cash dividends paid

represented the 32nd consecutive $.30 2/3 For additional details regarding our banking operation, see

year of dividend increases. note 3, “Financial Subsidiaries,” beginning on page 44.

$.25 1/3

$.22 2/3 Forward-Looking Information and

$.20 Factors That May Affect Future Results

$.17 1/3

The Securities and Exchange Commission encourages

companies to disclose forward-looking information so that

investors can better understand a company’s future prospects

and make informed investment decisions. This annual

report and other written and oral statements that we make

from time to time contain such forward-looking statements

95 96 97 98 99

that set out anticipated results based on management’s

plans and assumptions. We have tried, wherever possible, to

identify such statements by using words such as “anticipate,”

Dividends on Common Stock “estimate,” “expects,” “projects,” “intends,” “plans,” “believes”

and words and terms of similar substance in connection with

Our dividend payout ratio, which represents cash dividends any discussion of future operating or financial performance.

paid per common share divided by diluted earnings per We cannot guarantee that any forward-looking statement

common share, was approximately 37% in 1999, 30% in 1998 will be realized, although we believe we have been prudent in

and 40% in 1997. In 1999, excluding the effect on net income of our plans and assumptions. Achievement of future results is

the Trovan inventory charge, the dividend payout ratio was subject to risks, uncertainties and inaccurate assumptions.

approximately 35%. In 1998, excluding the effects on net Should known or unknown risks or uncertainties materialize, or

income of discontinued operations and charges for asset should underlying assumptions prove inaccurate, actual results

impairment, restructuring, co-promotion payments to Searle and could vary materially from those anticipated, estimated or

the contribution to The Pfizer Foundation, the dividend payout projected. Investors should bear this in mind as they consider

ratio was 38%. In December 1999, the Board of Directors forward-looking statements.

declared a first-quarter 2000 dividend of $.09. The first-quarter We undertake no obligation to publicly update forward-

2000 cash dividend will mark the 33rd consecutive year of looking statements, whether as a result of new information,

quarterly dividend increases. future events or otherwise.

Banking Operation Certain risks, uncertainties and assumptions are discussed

here and under the heading entitled “Cautionary Factors That

Our international banking operation, Pfizer International May Affect Future Results” in Item 1 of our annual report on

Bank Europe (PIBE), operates under a full banking license Form 10-K for the year ended December 31, 1999, which will

from the Central Bank of Ireland. The results of its operations be filed at the end of March 2000.

are included in Other deductions — net. Prior to the filing of Form 10-K, you should refer to the

PIBE extends credit to financially strong borrowers, discussion under the same heading in our quarterly report on

largely through U.S. dollar loans made primarily for short and Form 10-Q for the quarter ended October 3, 1999, and to the

medium terms, with floating interest rates. Generally, loans extent incorporated by reference therein, in our Form 10-K

are made on an unsecured basis. When deemed appropriate, filing for 1998. This discussion of potential risks and

guarantees and certain covenants may be obtained as a uncertainties is by no means complete but is designed to

condition to the extension of credit. highlight important factors that may impact our outlook.

To reduce credit risk, PIBE has established credit approval

guidelines, borrowing limits and monitoring procedures. Competition and the Health Care Environment

Credit risk is further reduced through an active policy of In the U.S., many pharmaceutical products are subject to

diversification with respect to borrower, industry and increasing pricing pressures, which could be significantly

impacted by the current national debate over Medicare reform.





35

Pfizer Inc and Subsidiary Companies







If the Medicare program provided outpatient pharmaceutical • foreign receivables, payables, debt and loans — changes in

coverage for its beneficiaries, the federal government, through its exchange rates

enormous purchasing power under the program, could demand In our sensitivity analysis, we assumed that the change

discounts from pharmaceutical companies that may implicitly in one currency’s rate relative to the U.S. dollar would not have

create price controls on prescription drugs. On the other hand, an effect on other currencies’ rates relative to the U.S. dollar.

a Medicare drug reimbursement provision may increase the All other factors were held constant.

volume of pharmaceutical drug purchases, offsetting at least in If there were an adverse change in foreign exchange rates

part these potential price discounts. In addition, managed care of 10%, the expected effect on net income related to

organizations, institutions and other government agencies our financial instruments would be immaterial. For additional

continue to seek price discounts. Government efforts to reduce details, see note 4-D, “Derivative Financial Instruments —

Medicare and Medicaid expenses are expected to increase the use Accounting Policies,” on page 46.

of managed care organizations. This may result in managed care

influencing prescription decisions for a larger segment of the Interest Rate Risk

population. International operations are also subject to price and Our U.S. dollar interest-bearing investments, loans and

market regulations. As a result, it is expected that pressures on borrowings are subject to interest rate risk. We invest and

pricing and operating results will continue. borrow primarily on a short-term or variable-rate basis. We are

also subject to interest rate risk on Japanese yen and on euro

Financial Risk Management short-term borrowings. Under certain market conditions,

The overall objective of our financial risk management interest rate swap contracts are used to adjust interest-sensitive

program is to seek a reduction in the potential negative assets and liabilities.

earnings effects from changes in foreign exchange and interest Our financial instrument holdings at year-end were

rates arising in our business activities. We manage these analyzed to determine their sensitivity to interest rate changes.

financial exposures through operational means and by using The fair values of these instruments were determined by net

various financial instruments. These practices may change as present values.

economic conditions change. In our sensitivity analysis, we used the same change in

interest rate for all maturities. All other factors were held

Foreign Exchange Risk constant. If interest rates increased by 10%, the expected effect

A significant portion of our revenues and earnings are exposed on net income related to our financial instruments would be

to changes in foreign exchange rates. Where practical, we seek immaterial.

to relate expected local currency revenues with local currency

costs and local currency assets with local currency liabilities. International Markets

Generally, we do not use financial instruments for trading Thirty-nine percent of our 1999 revenues arise from

activities. international operations and we expect revenue and net income

Foreign exchange risk is also managed through the use of growth in 2000 to be impacted by changes in foreign

foreign currency forward-exchange contracts. These contracts exchange rates.

are used to offset the potential earnings effects from short-term Revenues from Asia comprised approximately 11% of total

foreign currency assets and liabilities that arise during revenues in 1999, including 8% from Japan.

operations. For additional details on foreign exchange

exposures, see note 4-D, “Derivative Financial Instruments — European Currency

Instruments Outstanding,” on page 47. A new European currency (euro) was introduced in January

In addition, foreign currency put options are purchased to 1999 to replace the separate currencies of 11 individual

reduce a portion of the potential negative effects on earnings countries. The major changes during its first year of existence

related to certain of our significant anticipated intercompany have occurred in the banking and financial sectors. The impact

inventory purchases for up to one year. These purchased options at the commercial and retail level has been limited but is

hedge Japanese yen versus the U.S. dollar. expected to increase during the next two years through

Also, under certain market conditions, we protect December 31, 2001, when the separate currencies will cease to

against possible declines in the reported net assets of our exist. We are modifying systems and commercial arrangements

subsidiaries in Japan and in countries that are a member of the to deal with the new currency, including the availability of

European Monetary Union. We do this through currency swaps dual currency processes to permit transactions to be

and borrowing in Japanese yen and borrowing in euros. denominated in the separate currencies, as well as the euro. The

Our financial instrument holdings at year-end were cost of this effort is not expected to have a material effect on

analyzed to determine their sensitivity to foreign exchange rate our businesses or results of operations. We continue to evaluate

changes. The fair values of these instruments were determined the economic and operational impact of the euro, including its

as follows: impact on competition, pricing and foreign currency exchange

• forward-exchange contracts and currency swaps — net risks. There is no guarantee, however, that all problems have

present values been foreseen and corrected, or that no material disruption will

• purchased foreign currency options — foreign exchange occur in our businesses.

option pricing model



36

Pfizer Inc and Subsidiary Companies







Tax Legislation Litigation, Tax and Environmental Matters

Pursuant to the Small Jobs Protection Act of 1996 (the Act), Claims have been brought against us and our subsidiaries for

Section 936 of the Internal Revenue Code (the U.S. possessions various legal and tax matters. In addition, our operations are

corporation income tax credit) was repealed for tax years subject to international, federal, state and local environmental

beginning after December 31, 1995. The Act allows us to laws and regulations. It is possible that our cash flows and

continue using the credit against the tax arising from results of operations could be affected by the one-time impact

manufacturing income earned in a U.S. possession for an of the resolution of these contingencies. We believe that

additional 10-year period. The amount of manufacturing the ultimate disposition of these matters to the extent not

income eligible for the credit during this additional period is previously provided for will not have a material impact on our

subject to a cap based on income earned prior to 1996 in the financial condition, results of operations or cash flows, except

U.S. possession. This 10-year extension period does not apply where specifically commented on in note 18, “Litigation,”

to investment income earned in a U.S. possession, the credit on beginning on page 54 and note 9, “Taxes on Income,”

which expired as of July 1, 1996. The Act does not affect the beginning on page 49.

amendments made to Section 936 by the 1993 Omnibus

Budget Reconciliation Act, which provided for a five-year

phase-down of the U.S. possession tax credit from 100% to

40%. In addition, the Act permitted the extension of the R&D

tax credit through June 30, 1998. In 1998, this credit was

again extended to June 30, 1999, and in 1999, it was further

extended to June 30, 2004.

Recently Issued Accounting Standards Management’s Report

In June 1999, the Financial Accounting Standards Board We prepared and are responsible for the financial statements

issued Statement of Financial Accounting Standards (SFAS) that appear on pages 39 to 61. These financial statements are

No. 137, Accounting for Derivative Instruments and Hedging in conformity with generally accepted accounting principles

Activities — Deferral of the Effective Date of FASB Statement and, therefore, include amounts based on informed judgments

No. 133. This pronouncement requires us to adopt SFAS and estimates. We also accept responsibility for the preparation

No. 133, Accounting for Derivative Instruments and Hedging of other financial information that is included in this

Activities, on January 1, 2001. SFAS No. 133 requires a document.

company to recognize all derivative instruments as assets or We have designed a system of internal control to:

liabilities in its balance sheet and measure them at fair value. • safeguard the Company’s assets,

We do not expect the adoption of SFAS No. 133 to have a • ensure that transactions are properly authorized, and

material impact on our financial position, results of operations • provide reasonable assurance, at reasonable cost, of the

or cash flows. integrity, objectivity and reliability of the financial

information.

Year 2000 An effective internal control system has inherent

We have not experienced any operational problems as a result limitations no matter how well designed and, therefore, can

of Year 2000 issues, and Year 2000 had no material effect on provide only reasonable assurance with respect to financial

our revenues. Although the transition from 1999 to 2000 did statement preparation. The system is built on a business ethics

not adversely impact our company, there can be no assurances policy that requires all employees to maintain the highest

that we will not experience any negative effects or disruptions ethical standards in conducting Company affairs. Our system

in our businesses in the future as a result of Year 2000 issues. of internal control includes:

The total cost of our Year 2000 Program was • careful selection, training and development of financial

$130 million, of which we incurred $94 million in 1999, managers,

$31 million in 1998 and $5 million in 1997. These costs were • an organizational structure that segregates responsibilities,

expensed as incurred, except for capitalizable hardware of • a communications program which ensures that the

approximately $8 million in 1999, $4 million in 1998 and Company’s policies and procedures are well understood

$1 million in 1997 and were funded through operating cash throughout the organization, and

flows. Such costs did not include normal system upgrades and • an extensive program of internal audits, with prompt

replacements. Immaterial costs may be incurred in 2000 to follow-up, including reviews of separate operations and

address remaining non-critical Year 2000 issues. functions around the world.









37

Pfizer Inc and Subsidiary Companies







Our independent certified public accountants, management present, to discuss the results of their

KPMG LLP, have audited the annual financial statements in examinations, the evaluations of the Company’s internal

accordance with generally accepted auditing standards. The controls, and the overall quality of the Company’s financial

independent auditors’ report expresses an informed judgment reporting. In reliance on the reviews and discussions referred

as to the fair presentation of the Company’s reported operating to above, the Committee recommended to the Board of

results, financial position and cash flows. Their judgment is Directors, and the Board has approved, that the audited

based on the results of auditing procedures performed and financial statements be included in the Company’s Annual

such other tests that they deemed necessary, including their Report on Form 10-K for the year ended December 31, 1999,

consideration of our internal control structure. for filing with the Securities and Exchange Commission. The

We consider and take appropriate action on recom- Committee and the Board also have recommended, subject to

mendations made by KPMG LLP and our internal auditors. shareholder approval, the selection of the Company’s

We believe that our system of internal control is effective independent auditors.

and adequate to accomplish the objectives discussed above.

G. B. Harvey, Chair, Audit Committee

W. C. Steere, Jr., Principal Executive Officer February 14, 2000



D. L. Shedlarz, Principal Financial Officer



L. V. Cangialosi, Principal Accounting Officer

February 14, 2000

Independent Auditors’ Report







To the Shareholders and Board of Directors of Pfizer Inc:

Audit Committee’s Report

The Audit Committee reviews the Company’s financial We have audited the accompanying consolidated balance sheets

reporting process on behalf of the Board of Directors. of Pfizer Inc and subsidiary companies as of December 31,

Management has the primary responsibility for the financial 1999, 1998 and 1997 and the related consolidated statements

statements and the reporting process, including the system of income, shareholders’ equity and cash flows for each of the

of internal controls. In this context, the Committee has met years then ended. These consolidated financial statements are

and held discussions with management and the independent the responsibility of the Company’s management. Our

auditors. Management represented to the Committee that the responsibility is to express an opinion on these consolidated

Company’s consolidated financial statements were prepared in financial statements based on our audits.

accordance with generally accepted accounting principles, and We conducted our audits in accordance with generally

the Committee has reviewed and discussed the consolidated accepted auditing standards. Those standards require that we

financial statements with management and the independent plan and perform the audit to obtain reasonable assurance

auditors. The Committee discussed with the independent about whether the consolidated financial statements are

auditors matters required to be discussed by Statement free of material misstatement. An audit includes examining,

of Auditing Standards No. 61 (Communication With Audit on a test basis, evidence supporting the amounts and

Committees). In addition, the Committee has discussed with disclosures in the consolidated financial statements. An

the independent auditors, the auditors’ independence from the audit also includes assessing the accounting principles

Company and its management, including the matters in the used and significant estimates made by management, as

written disclosures required by the Independence Standards well as evaluating the overall consolidated financial

Board Standard No. 1 (Independence Discussions with Audit statement presentation. We believe that our audits provide

Committees). The Committee discussed with the Company’s a reasonable basis for our opinion.

internal and independent auditors the overall scope and plans In our opinion, the consolidated financial statements

for their respective audits. The Committee meets with the referred to above present fairly, in all material respects, the

internal and independent auditors, with and without financial position of Pfizer Inc and subsidiary companies at

December 31, 1999, 1998 and 1997, and the results of their

operations and their cash flows for each of the years then ended,

in conformity with generally accepted accounting principles.







New York, NY

February 14, 2000









38

Pfizer Inc and Subsidiary Companies









Consolidated Statement of Income

Year ended December 31



(millions, except per share data) 1999 1998 1997

Net sales $14,133 $12,677 $10,739

Alliance revenue 2,071 867 316

Total revenues 16,204 13,544 11,055

Costs and expenses:

Cost of sales 2,528 2,094 1,776

Selling, informational and administrative expenses 6,351 5,568 4,401

Research and development expenses 2,776 2,279 1,805

Other deductions Ñ net 101 1,009 206

Income from continuing operations before provision

for taxes on income and minority interests 4,448 2,594 2,867

Provision for taxes on income 1,244 642 775

Minority interests 5 2 10

Income from continuing operations 3,199 1,950 2,082

Discontinued operations Ñ net of tax (20) 1,401 131

Net income $ 3,179 $ 3,351 $ 2,213





Earnings per common share Ñ basic

Income from continuing operations $ .85 $ .51 $ .55

Discontinued operations Ñ net of tax (.01) .37 .04

Net income $ .84 $ .88 $ .59





Earnings per common share Ñ diluted

Income from continuing operations $ .82 $ .49 $ .53

Discontinued operations Ñ net of tax Ñ .36 .04

Net income $ .82 $ .85 $ .57





Weighted average shares Ñ basic 3,775 3,789 3,771

Weighted average shares Ñ diluted 3,884 3,945 3,909

See Notes to Consolidated Financial Statements which are an integral part of these statements.









39

Pfizer Inc and Subsidiary Companies









Consolidated Balance Sheet

December 31



(millions, except per share data) 1999 1998 1997

Assets

Current Assets

Cash and cash equivalents $ 739 $ 1,552 $ 877

Short-term investments 3,703 2,377 712

Accounts receivable, less allowance for doubtful accounts:

1999 Ñ $68; 1998 Ñ $67; 1997 Ñ $35 3,864 2,914 2,220

Short-term loans 273 150 115

Inventories

Finished goods 650 697 442

Work in process 711 890 808

Raw materials and supplies 293 241 211

Total inventories 1,654 1,828 1,461

Prepaid expenses and taxes 958 1,110 637

Net assets of discontinued operations Ñ Ñ 1,420

Total current assets 11,191 9,931 7,442

Long-term loans and investments 1,721 1,756 1,330

Property, plant and equipment, less accumulated depreciation 5,343 4,415 3,793

Goodwill, less accumulated amortization:

1999 Ñ $129; 1998 Ñ $109; 1997 Ñ $90 763 813 989

Other assets, deferred taxes and deferred charges 1,556 1,387 1,437

Total assets $20,574 $18,302 $14,991

Liabilities and ShareholdersÕ Equity

Current Liabilities

Short-term borrowings, including current portion of long-term debt $ 5,001 $ 2,729 $ 2,251

Accounts payable 951 971 660

Dividends payable 349 285 Ñ

Income taxes payable 869 1,162 729

Accrued compensation and related items 669 614 456

Other current liabilities 1,346 1,431 898

Total current liabilities 9,185 7,192 4,994

Long-term debt 525 527 725

Postretirement benefit obligation other than pension plans 346 359 394

Deferred taxes on income 301 197 127

Other noncurrent liabilities 1,330 1,217 818

Total liabilities 11,687 9,492 7,058

ShareholdersÕ Equity

Preferred stock, without par value; 12 shares authorized, none issued Ñ Ñ Ñ

Common stock, $.05 par value; 9,000 shares authorized;

issued: 1999 Ñ 4,260; 1998 Ñ 4,222; 1997 Ñ 4,165 213 210 207

Additional paid-in capital 5,416 5,506 3,101

Retained earnings 13,396 11,439 9,349

Accumulated other comprehensive expense (399) (234) (85)

Employee benefit trusts (2,888) (4,200) (2,646)

Treasury stock, at cost:

1999 Ñ 413; 1998 Ñ 339; 1997Ñ 283 (6,851) (3,911) (1,993)

Total shareholdersÕ equity 8,887 8,810 7,933

Total liabilities and shareholdersÕ equity $20,574 $18,302 $14,991

See Notes to Consolidated Financial Statements which are an integral part of these statements.









40

Pfizer Inc and Subsidiary Companies









Consolidated Statement of ShareholdersÕ Equity

Accum.

Employee

Additional Other Com-

Common Stock Benefit Trusts Treasury Stock

Paid-In Retained prehensive

(millions) Shares Par Value Capital Shares Fair Value Shares Cost Earnings Inc./(Exp.) Total

Balance January 1, 1997 1,378 $ 69 $1,693 (36) $(1,488) (87) $(1,482) $ 8,017 $ 145 $6,954

Restatement for the 1999 stock split 2,756 138 (138) (72) Ñ (175) Ñ Ñ Ñ Ñ

Balance January 1, 1997, as restated 4,134 207 1,555 (108) (1,488) (262) (1,482) 8,017 145 6,954

Comprehensive income:

Net income 2,213 2,213

Other comprehensive expense Ñ

net of tax:

Currency translation adjustment (253) (253)

Net unrealized gain on available-

for-sale securities 20 20

Minimum pension liability 3 3

Total other comprehensive expense (230) (230)

Total comprehensive income 1,983

Cash dividends declared (881) (881)

Stock option transactions 29 Ñ 343 13 68 411

Purchases of common stock (34) (586) (586)

Employee benefit trusts

transactions Ñ net 1,177 1 (1,158) Ñ 7 26

Other 2 Ñ 26 26

Balance December 31, 1997 4,165 207 3,101 (107) (2,646) (283) (1,993) 9,349 (85) 7,933

Comprehensive income:

Net income 3,351 3,351

Other comprehensive expense Ñ

net of tax:

Currency translation adjustment (74) (74)

Net unrealized loss on available-

for-sale securities (2) (2)

Minimum pension liability (73) (73)

Total other comprehensive expense (149) (149)

Total comprehensive income 3,202

Cash dividends declared (1,261) (1,261)

Stock option transactions 55 3 745 Ñ (18) 730

Purchases of common stock (58) (1,912) (1,912)

Employee benefit trusts

transactions Ñ net 1,633 5 (1,554) 2 12 91

Other 2 Ñ 27 27

Balance December 31, 1998 4,222 210 5,506 (102) (4,200) (339) (3,911) 11,439 (234) 8,810

Comprehensive income:

Net income 3,179 3,179

Other comprehensive expense Ñ

net of tax:

Currency translation adjustment (222) (222)

Net unrealized gain on available-

for-sale securities 81 81

Minimum pension liability (24) (24)

Total other comprehensive expense (165) (165)

Total comprehensive income 3,014

Cash dividends declared (1,222) (1,222)

Stock option transactions 35 3 526 Ñ (16) 513

Purchases of common stock (66) (2,500) (2,500)

Employee benefit trusts

transactions Ñ net (735) 13 1,312 (8) (424) 153

Other 3 Ñ 119 119

Balance December 31, 1999 4,260 $213 $5,416 (89) $(2,888) (413) $ (6,851) $13,396 $(399) $8,887

See Notes to Consolidated Financial Statements which are an integral part of these statements.









41

Pf i z e r I n c a n d S u b s i d i a r y C o m p a n i e s









Consolidated Statement of Cash Flows

Year ended December 31



(millions of dollars) 1999 1998 1997

Operating Activities

Income from continuing operations $ 3,199 $ 1,950 $2,082

Adjustments to reconcile income from continuing operations

to net cash provided by operating activities:

Depreciation and amortization 542 489 428

Trovan inventory write-off 310 Ñ Ñ

Asset impairments and restructuring charges Ñ 323 Ñ

Deferred taxes and other 286 22 83

Changes in assets and liabilities, net of effect of businesses divested:

Accounts receivable (978) (765) (477)

Inventories (240) (439) (350)

Prepaid and other assets 68 (350) (128)

Accounts payable and accrued liabilities 61 628 (63)

Income taxes payable (179) 951 (54)

Other deferred items 7 473 59

Net cash provided by operating activities 3,076 3,282 1,580

Investing Activities

Purchases of property, plant and equipment (1,561) (1,198) (878)

Proceeds from disposals of property, plant and equipment 71 79 47

Purchases net of maturities of short-term investments (8,633) (5,845) (221)

Proceeds from redemptions of short-term investments 7,309 4,209 28

Proceeds from sales of businesses Ñ net 26 3,059 21

Purchases of long-term investments (322) (752) (74)

Other investing activities 342 113 114

Net cash used in investing activities (2,768) (335) (963)

Financing Activities

Repayments of long-term debt (4) (202) (269)

Increase in short-term debt Ñ net 2,083 402 325

Proceeds from stock issuances 62 Ñ Ñ

Purchases of common stock (2,500) (1,912) (586)

Cash dividends paid (1,148) (976) (881)

Stock option transactions and other 380 411 430

Net cash used in financing activities (1,127) (2,277) (981)

Net cash (used in)/provided by discontinued operations (20) 4 118

Effect of exchange-rate changes on cash and cash equivalents 26 1 (27)

Net (decrease)/increase in cash and cash equivalents (813) 675 (273)

Cash and cash equivalents at beginning of year 1,552 877 1,150

Cash and cash equivalents at end of year $ 739 $ 1,552 $ 877

Supplemental Cash Flow Information

Cash paid during the period for:

Income taxes $ 1,293 $ 1,073 $ 809

Interest 238 155 149

See Notes to Consolidated Financial Statements which are an integral part of these statements.









42

Pfizer Inc and Subsidiary Companies









Notes to Consolidated Financial Statements





1 Significant Accounting Policies D — Long-Lived Assets

Long-lived assets include:

A — Consolidation and Basis of Presentation • property, plant and equipment — These assets are recorded

The consolidated financial statements include the parent at original cost and increased by the cost of any significant

company and all significant subsidiaries, including those improvements after purchase. We depreciate the cost

operating outside the U.S. Balance sheet amounts for the evenly over the assets’ estimated useful lives. For tax

international operations are as of November 30 of each year and purposes, accelerated depreciation methods are used as

income statement amounts are for the full-year periods ending allowed by tax laws.

on the same date. Substantially all unremitted earnings of • goodwill — Goodwill represents the difference between the

international subsidiaries are free of legal and contractual purchase price of acquired businesses and the fair value of

restrictions. All significant transactions among our businesses their net assets when accounted for by the purchase

have been eliminated. We made certain reclassifications to the method. We amortize goodwill evenly over periods not

1998 and 1997 financial statements to conform to the 1999 exceeding 40 years. The average amortization period is

presentation. 37 years.

In preparing the financial statements, we must use some • other intangible assets — Other intangible assets are

estimates and assumptions that may affect reported amounts included in Other assets, deferred taxes and deferred charges.

and disclosures. Estimates are used when accounting for We amortize these assets evenly over their estimated

depreciation, amortization, employee benefits and asset useful lives.

valuation allowances. We are also subject to risks and

uncertainties that may cause actual results to differ from We review long-lived assets to assess recoverability from

estimated results, such as changes in the health care future operations using undiscounted cash flows. When

environment, competition, foreign exchange and legislation. necessary, we record charges for impairments of long-lived

“Forward-Looking Information and Factors That May Affect assets for the amount by which the present value of future cash

Future Results,” beginning on page 35, discusses these and flows exceeds the carrying value of these assets.

other uncertainties.

E — Foreign Currency Translation

B — Cash Equivalents For most international operations, local currencies are

Cash equivalents include items almost as liquid as cash, such as considered their functional currencies. We translate assets and

certificates of deposit and time deposits with maturity periods liabilities to their U.S. dollar equivalents at rates in effect at

of three months or less when purchased. If items meeting this the balance sheet date and record translation adjustments in

definition are part of a larger investment pool, we classify them Shareholders’ Equity. We translate Statement of Income accounts

as Short-term investments. at average rates for the period. Transaction adjustments are

C — Inventories recorded in Other deductions —net.

We value inventories at cost or fair value, if lower. Cost is For operations in highly inflationary economies, we

determined as follows: translate the balance sheet items as follows:

• finished goods and work-in-process at average actual cost • monetary items (that is, assets and liabilities that will

• raw materials and supplies at average or latest actual cost be settled for cash) at rates in effect at the balance sheet

date, with translation adjustments recorded in Other

In 1999, we changed the method of determining the cost deductions —net

of all of our remaining inventories previously on the “Last-in, • non-monetary items at historical rates (that is, those

first-out” (LIFO) method to the “First-in, first-out” (FIFO) rates in effect when the items were first recorded)

method. Those inventories consisted of U.S. sourced

pharmaceuticals and part of the animal health inventories. We

believe that the change in accounting for inventories from

LIFO to FIFO is preferable because inventory costs are stable

and substantially unaffected by inflation. The change in the

method of inventory costing resulted in a pre-tax benefit of

$6.6 million included in Cost of sales for 1999.







43

Pfizer Inc and Subsidiary Companies







F — Product Alliances In 1997, we sold Strato/Infusaid to Horizon Medical

We have agreements to promote pharmaceutical Products and Arrow International for $21 million in cash.

products developed by other companies. Alliance revenue

represents revenue recorded under these co-promotion The contractual net assets identified as part of the

agreements and is derived from the sale of products. The disposition of Valleylab, Schneider, AMS and Howmedica are

revenue is earned when our co-promotion partners ship the recorded as Net assets of discontinued operations at December 31,

related goods and the sale is consummated with a third party. 1997. The net cash flows of our discontinued operations are

Such revenue is based in most cases upon a percentage of our reported as Net cash (used in)/provided by discontinued operations.

co-promotion partners’ net sales. Selling, informational and Net assets of discontinued operations consisted of the

administrative expenses in most cases includes other expenses for following:

selling and marketing these products.

We have license agreements in certain foreign countries (millions of dollars) 1997

for these products. When products are sold under license Net current assets $ 397

agreements, we record Net sales instead of Alliance revenue and Property, plant and equipment — net 383

record related costs and expenses in the appropriate caption in Other net noncurrent assets

and liabilities 640

the Statement of Income.

Net assets of discontinued operations $1,420

G — Stock-Based Compensation

In accordance with Statement of Financial Accounting

Standards No. 123, Accounting for Stock-Based Compensation, we Discontinued operations —net of tax were as follows:

elected to account for our stock-based compensation under (millions of dollars) 1999 1998 1997

Accounting Principles Board Opinion No. 25, Accounting for

Net sales $ — $1,160 $1,449

Stock Issued to Employees.

The exercise price of stock options granted equals the Pre-tax income/(loss) $(20) $ 92 $ 232

market price on the date of grant. In general, there is no Provision for taxes on income — 57 93

recorded expense related to stock options. Income/(loss) from operations of

discontinued businesses — net of tax (20) 35 139

H — Advertising Expense

We record advertising expense as follows: Pre-tax gain/(loss) on disposal of

discontinued businesses — 2,504 (11)

• production costs as incurred

Provision/(benefit) for taxes on

• costs of radio time, television time and space in

gain/(loss) — 1,138 (3)

publications are deferred until the advertising first occurs

Gain/(loss) on disposal of discontinued

businesses — net of tax — 1,366 (8)

Advertising expense totaled $1,310 million in 1999,

$1,139 million in 1998, and $898 million in 1997. Discontinued operations — net of tax $(20) $1,401 $ 131



2 Discontinued Operations 3 Financial Subsidiaries

In 1999, we agreed to pay a fine of $20 million to settle Our financial subsidiaries include Pfizer International Bank

antitrust charges involving our former Food Science Group, Europe (PIBE) and a small captive insurance company. PIBE

divested in 1996. For additional details, see note 18, periodically adjusts its loan portfolio to meet its business

“Litigation.” needs. Information about these subsidiaries follows:

In 1998, we completed the sale of the Medical Technology

Group (MTG) segment. Accordingly, the consolidated financial Condensed Balance Sheet

statements and related notes reflect the results of operations (millions of dollars) 1999 1998 1997

and net assets of the MTG businesses — Valleylab, Schneider,

Cash and interest-bearing deposits $114 $103 $115

American Medical Systems (AMS), Howmedica and

Loans — net 380 433 408

Strato/Infusaid — as discontinued operations. We completed the Other assets 13 15 8

sales of:

Total assets $507 $551 $531

• Howmedica to Stryker Corporation in December for

$1.65 billion in cash Certificates of deposit and

• Schneider to Boston Scientific Corporation in September other liabilities $ 24 $ 97 $ 73

for $2.1 billion in cash Shareholders’ equity 483 454 458

• AMS to E.M. Warburg, Pincus & Co., LLC in September Total liabilities and

for $130 million in cash shareholders’ equity $507 $551 $531

• Valleylab to U.S. Surgical Corporation in January for

$425 million in cash









44

Pfizer Inc and Subsidiary Companies







Condensed Statement of Income The contractual maturities of the held-to-maturity and

available-for-sale debt securities as of December 31, 1999, were

(millions of dollars) 1999 1998 1997

as follows:

Interest income $27 $30 $29

Interest expense (2) (2) (2) Years

Other income — net 8 1 13 Over 1 Over 5

(millions of dollars) Within 1 to 5 to 10 Over 10 Total

Net income $33 $29 $40

Held-to-maturity

debt securities:

4 Financial Instruments Corporate debt $3,590 $ 34 $ — $— $3,624

Most of our financial instruments are recorded in the Certificates of deposit 443 2 — — 445

Other — 2 8 9 19

Balance Sheet. Several “derivative” financial instruments

Available-for-sale

are “off-balance-sheet” items. debt securities:

A — Investments in Debt and Equity Securities Certificates of deposit — 370 75 — 445

Information about our investments follows: Corporate debt — 91 150 — 241

Total debt securities $4,033 $499 $233 $9 $4,774

(millions of dollars) 1999 1998 1997 Available-for-sale

Trading securities $ 113 $ 99 $ — equity securities 290

Trading securities 113

Amortized cost and fair value of

held-to-maturity debt securities:* Total investments $5,177

Corporate debt 3,624 2,306 626

Certificates of deposit 445 670 655 B — Short-Term Borrowings

Municipals — — 56 The weighted average effective interest rate on short-term

Other 19 21 104 borrowings outstanding at December 31 was 4.3% in 1999,

Total held-to-maturity debt securities 4,088 2,997 1,441 3.7% in 1998 and 2.9% in 1997. We had approximately

Cost and fair value of available-for-sale

$1.5 billion available to borrow under lines of credit at

debt securities* 686 686 686 December 31, 1999.

Cost of available-for-sale equity C — Long-Term Debt

securities 60 54 81

Gross unrealized gains 230 106 106 (millions of dollars) 1999 1998 1997

Gross unrealized losses — (8) (4) Floating-rate unsecured notes $491 $491 $686

Fair value of available-for-sale equity Other borrowings and mortgages 34 36 39

securities 290 152 183 Total long-term debt $525 $527 $725

Total investments $5,177 $3,934 $2,310 Current portion not included above $ 2 $ 4 $ 4

* Gross unrealized gains and losses are not significant.

The floating-rate unsecured notes mature on various dates

These investments are in the following captions in the from 2001 to 2005 and bear interest at a defined variable rate

Balance Sheet: based on the commercial paper borrowing rate. The weighted

(millions of dollars) 1999 1998 1997

average interest rate was 6.1% at December 31, 1999. These

notes minimize credit risk on certain available-for-sale debt

Cash and cash equivalents $ 443 $ 660 $ 636

securities that may be used to satisfy the notes at maturity. In

Short-term investments 3,703 2,377 712

September 1998, we repaid $195 million of the outstanding

Long-term loans and investments 1,031 897 962

floating-rate unsecured notes prior to their scheduled maturity

Total investments $5,177 $3,934 $2,310 by using the proceeds from the issuance of short-term

commercial paper.

Long-term debt outstanding at December 31, 1999,

matures as follows:

After

(millions of dollars) 2001 2002 2003 2004 2004

Maturities $131 $161 $— $— $233









45

Pfizer Inc and Subsidiary Companies







D — Derivative Financial Instruments Other deductions —net includes:

Purpose • changes in the fair value of foreign exchange contracts

“Forward-exchange contracts,” “currency swaps” and and changes in foreign currency assets and liabilities

“purchased currency options” are used to reduce exposure to • payments under swap contracts to offset, primarily,

foreign exchange risks. Also, “interest rate swap” contracts are interest expense or, to a lesser extent, net foreign

used to adjust interest rate exposures. exchange losses

• amortization of discounts or premiums on currencies

Accounting Policies sold under forward-exchange contracts

We consider derivative financial instruments to be “hedges”

(that is, an offset of foreign exchange and interest rate risks) Our criteria to qualify for hedge accounting are:

when certain criteria are met. Under hedge accounting Foreign currency instruments must:

for a purchased currency option, its impact on earnings is • relate to a foreign currency asset, liability or an

deferred until the recognition of the underlying hedged item anticipated transaction that is probable and whose

(inventory) in earnings. We recognize the earnings impact characteristics and terms have been identified

of the other instruments during the terms of the contracts, • involve the same currency as the hedged item

along with the earnings impact of the items they offset. • reduce the risk of foreign currency exchange

Purchased currency options are recorded at cost and movements on our operations

amortized evenly to operations through the expected inventory

delivery date. Gains at the transaction date are included in the Interest rate instruments must:

cost of the related inventory purchased. • relate to an asset or a liability

As interest rates change, we accrue the difference • change the character of the interest rate by converting

between the debt interest rates recognized in the Statement a variable rate to a fixed rate or vice versa

of Income and the amounts payable to or receivable from

counterparties under interest rate swap contracts. Likewise, The following table summarizes the exposures hedged

amounts arising from currency swap contracts are accrued as or offset by the various instruments we use:

exchange rates change.

Maximum Maturity in Years

The financial statements include the following items

related to derivative and other financial instruments serving as Instrument Exposure 1999 1998 1997

hedges or offsets: Forward-exchange Foreign currency

Prepaid expenses and taxes includes: contracts assets and liabilities .5 .5 .5

• purchased currency options Currency swaps Net investments 4 5 —

Loans .3 1 2

Other current liabilities includes: Purchased Inventory purchases

• fair value of forward-exchange contracts currency options and sales .9 1 1

• net amounts payable related to interest rate swap

Interest rate swaps Debt interest 4 5 1

contracts



Other noncurrent liabilities includes:

• net amounts payable related to currency

swap contracts



Accumulated other comprehensive expense includes changes in

the:

• foreign exchange translation of currency swaps and

foreign debt

• fair value of forward-exchange contracts for net

investment hedges









46

Pfizer Inc and Subsidiary Companies







Instruments Outstanding The Japanese yen for U.S. dollar currency swaps require

The notional amounts of derivative financial instruments, that we make interim payments of a fixed rate of 1.1% on the

except for currency swaps, do not represent actual amounts Japanese yen payable and have interim receipts of a variable

exchanged by the parties, but instead represent the amount rate based on a commercial paper rate on the U.S. dollar

of the item on which the contracts are based. receivable. These currency swaps replaced $625 million

The notional amounts of our foreign currency and interest of Japanese yen debt, which previously served as a hedge

rate contracts follow: of our net investments in Japan, as well as related interest

rate swaps.

(millions of dollars) 1999 1998 1997

The Japanese yen and Swiss franc interest rate swaps

Foreign currency contracts: effectively fixed the interest rate on floating rate debt as

Commitments to sell foreign follows:

currencies, primarily in exchange • the Japanese yen debt at 1.4% in 1999, 1998 and 1997

for U.S. dollars:

• the Swiss franc debt at 2.1% in 1997

Euro* $1,050 $ — $ —

U.K. pounds 781 482 548

Japanese yen 412 298 224 The floating interest rates were based on “LIBOR” rates

Irish punt* 91 61 107 related to the contract currencies. In connection with the sale

Australian dollars 76 98 59 of the Schneider Swiss subsidiary in 1998, we terminated the

German marks* 39 50 158 Swiss franc interest rate swap contracts and ceased borrowing

Netherlands guilders* — 316 4 Swiss francs.

French francs* — 216 134

Other currencies 192 201 240 E — Fair Value

Commitments to purchase foreign The following methods and assumptions were used to estimate

currencies, primarily in exchange the fair value of derivative and other financial instruments at

for U.S. dollars: the balance sheet date:

Euro* 339 — — • short-term financial instruments (cash equivalents,

U.K. pounds 101 53 60 accounts receivable and payable, forward-exchange

Irish punt* 50 532 92 contracts, short-term investments and borrowings) —

German marks* 47 67 73

cost approximates fair value because of the short maturity

Netherlands guilders* — 156 4

Swiss francs — 8 187

period

Other currencies 196 144 136 • loans —cost approximates fair value because of the short

interest reset period

Total forward-exchange contracts $3,374 $2,682 $2,026

• long-term investments, long-term debt, forward-exchange

Currency swaps: contracts and purchased currency options—fair value is

Japanese yen $ 829 $ 754 $ — based on market or dealer quotes

U.K. pounds 40 40 40

• interest rate and currency swap agreements—fair value is

Total currency swaps $ 869 $ 794 $ 40 based on estimated cost to terminate the agreements

Purchased currency options, (taking into account broker quotes, current interest

primarily for U.S. dollars: rates and the counterparties’ creditworthiness)

Japanese yen $ 393 $ 364 $ 198

German marks — — 130 The differences between fair and carrying values of our

French francs — — 46

derivative and other financial instruments were not material at

Belgian francs — — 29

December 31, 1999, 1998 and 1997, except for a difference of

Other currencies 30 25 61

$230 million at December 31, 1999 for available-for-sale

Total purchased currency options $ 423 $ 389 $ 464 equity securities.

Interest rate swap contracts:

F — Credit Risk

Japanese yen $ 353 $ 321 $ 814

Swiss francs — — 405

We periodically review the creditworthiness of counterparties

to foreign exchange and interest rate agreements and do not

Total interest rate swaps $ 353 $ 321 $1,219

expect to incur a loss from failure of any counterparties

*On January 1, 1999, members of the European Monetary Union were permitted to use to perform under the agreements. In general, there is no

the new currency, the euro, or their old currency.

requirement for collateral from customers. There are

no significant concentrations of credit risk related to our

financial instruments. No individual counterparty credit

exposure exceeded 10% of our consolidated Shareholders’ Equity

at December 31, 1999.









47

Pfizer Inc and Subsidiary Companies







5 Comprehensive Income 7 Property, Plant and Equipment

Changes in accumulated other comprehensive income/ The major categories of property, plant and equipment follow:

(expense) follow:

Useful

Net Accumulated Lives

Unrealized Other Com- (millions of dollars) (years) 1999 1998 1997

Currency Gain/(Loss) on Minimum prehensive Land — $ 174 $ 151 $ 126

Translation Available-For- Pension Income/

Buildings 331⁄3 2,008 1,669 1,534

(millions of dollars) Adjustment Sale Securities Liability (Expense)*

Machinery and

Balance equipment 8–20 3,040 2,685 2,459

January 1, Furniture, fixtures

1997 $ 174 $ 40 $ (69) $ 145 and other 3–121⁄ 2 1,618 1,383 1,232

Period change (253) 20 3 (230) Construction in

Balance progress — 1,197 956 516

December 31, 8,037 6,844 5,867

1997 (79) 60 (66) (85) Less: accumulated

Period change (74) (2) (73) (149) depreciation 2,694 2,429 2,074

Balance Total property, plant

December 31, and equipment $5,343 $4,415 $3,793

1998 (153) 58 (139) (234)

Period change (222) 81 (24) (165)

8 Other Deductions — Net

Balance

December 31, The components of other deductions —net follow:

1999 $(375) $139 $(163) $(399)

(millions of dollars) 1999 1998 1997

* Income tax benefit for other comprehensive expense was $76 million in 1997,

$116 million in 1998 and $33 million in 1999. Interest income $(301) $ (185) $(156)

Interest expense 236 143 149

6 Inventories Interest expense capitalized (13) (7) (2)

Net interest income (78) (49) (9)

In June 1999, the European Union’s Committee for Proprietary

Co-promotion payments to Searle — 240 —

Medicinal Products suspended the European Union licenses of

Contribution to The

the oral and intravenous formulations of Trovan for 12 months. Pfizer Foundation — 300 —

Based on our evaluation of these events and related matters, we Legal settlements involving the

determined that it was unlikely that certain Trovan inventories brand-name prescription drug

of finished goods, bulk, work-in-process, and raw materials will antitrust litigation 2 57 —

be used. Accordingly, in the third quarter of 1999, we recorded Amortization of goodwill and other

a charge of $310 million ($205 million after-tax, or $.05 after- intangibles 43 45 48

tax per diluted share) in Cost of sales to write off Trovan Net exchange (gains)/losses (20) (16) 26

Other, net 154 432 141

inventories in excess of the amount required to support

expected sales. Other deductions — net $ 101 $1,009 $ 206





In 1999, we substantially completed the actions under the

restructuring plans announced in 1998.

In 1998, we recorded charges for the restructuring in

addition to charges for certain asset impairments. The

components of these pre-tax charges follow:



(millions of dollars) Total COS* SI&A* R&D OD*



Restructuring charges $177 $68 $17 $1 $ 91

Asset impairments 213 18 — — 195

* COS —Cost of sales; SI&A —Selling, informational and administrative expenses; OD —

Other deductions-net.









48

Pfizer Inc and Subsidiary Companies







The components of the 1998 restructuring charges follow: In 1998, our animal health antibiotic feed additive, Stafac,

was banned, effective in mid-1999, throughout the European

Utilization

Union, resulting in asset impairment charges of $103 million

(millions of dollars) Charges in 1998 1998 1999 Beyond ($85 million was to adjust intangible asset values, primarily

Property, plant goodwill and trademarks, and $18 million was to adjust the

and equipment $ 49 $ 49 $— $— carrying value of machinery and equipment in the

Write-down of intangibles 44 44 — — pharmaceutical segment).

Employee termination costs 40 12 28 —

Other 44 11 17 16 9 Taxes on Income

Total $177 $116 $45 $16 Income from continuing operations before taxes consisted of

the following:

These charges resulted from a review of our global

operations to increase efficiencies and return on assets, thereby (millions of dollars) 1999 1998 1997

resulting in plant and product line rationalizations. In addition United States $2,557 $1,184 $1,215

to the disposition of our MTG businesses, we exited certain International 1,891 1,410 1,652

product lines including certain lines associated with our animal Total income from continuing

health business and certain of our fermentation operations. operations before taxes $4,448 $2,594 $2,867

We wrote off assets related to the product lines we exited,

including inventory, intangible assets—primarily goodwill—as The provision for taxes on income from continuing

well as certain buildings, machinery and equipment which we operations consisted of the following:

do not plan to use or sell.

As a result of the restructuring, our work force was (millions of dollars) 1999 1998 1997

reduced by approximately 500 manufacturing, sales and United States:

corporate personnel. Employee termination costs represent Taxes currently payable:

payments for severance, outplacement counseling fees, medical Federal $ 621 $ 344 $344

and other benefits and a $5 million noncash charge for the State and local 38 24 9

acceleration of nonvested employee stock options. Deferred income taxes (72) (162) (23)

Other restructuring charges consist of charges for Total U.S. tax provision 587 206 330

inventory for product lines we have exited—$12 million, International:

contract termination payments—$9 million, facility closure Taxes currently payable 606 550 462

costs—$7 million and environmental remediation costs Deferred income taxes 51 (114) (17)

associated with the disposal of certain facilities—$16 million. Total international tax provision 657 436 445

In 1998, we recorded an impairment charge of

Total provision for taxes on income $1,244 $ 642 $775

$110 million in the pharmaceutical segment to adjust

intangible asset values, primarily goodwill and trademarks,

related to consumer health care product lines. These charges Amounts are reflected in the preceding tables based on the

resulted from significant changes in the marketplace and a location of the taxing authorities. As of December 31, 1999, we

revision of our strategies, including: have not made a U.S. tax provision of approximately

• the decision to redeploy resources from personal care and $1.9 billion for approximately $8.2 billion of unremitted

minor brands to over-the-counter switches of prescription earnings of our international subsidiaries. These earnings are

products expected, for the most part, to be reinvested overseas.

• the withdrawal of one of our major over-the-counter We operate a manufacturing subsidiary in Puerto Rico

products in Italy that benefits from a Puerto Rican incentive grant in effect

• an acquired product line which experienced declines through the end of 2002. Under this grant, we are partially

in market share exempt from income, property and municipal taxes. For further

information on U.S. taxation of Puerto Rican operations, see

“Tax Legislation” on page 37.









49

Pfizer Inc and Subsidiary Companies







Reconciliation of the U.S. statutory income tax rate to our A valuation allowance is recorded because some items

effective tax rate for continuing operations follows: recorded as foreign deferred tax assets may not be deductible

or creditable. The “foreign tax credit carryforwards” were

(percentages) 1999 1998 1997 generated from dividends paid or deemed to be paid by

U.S. statutory income tax rate 35.0 35.0 35.0 subsidiaries to the parent company between 1997 and 1999. We

Effect of partially tax-exempt can carry these credits forward for five years from the year of

operations in Puerto Rico (1.5) (2.2) (1.8) actual payment and apply them to certain U.S. tax liabilities.

Effect of international operations (4.8) (5.5) (5.0)

The Internal Revenue Service (IRS) has completed and

All other — net (0.7) (2.5) (1.2)

closed its audits of our tax returns through 1992. The IRS

Effective tax rate for continuing completed its audits in January 2000 of our tax returns for

operations 28.0 24.8 27.0 1993 through 1995. We are awaiting the agent’s final report for

those years. We do not expect any material adjustments to be

Deferred taxes arise because of different treatment between proposed.

financial statement accounting and tax accounting, known as In November 1994, Belgian tax authorities notified Pfizer

“temporary differences.” We record the tax effect of these Research and Development Company N.V./S.A. (PRDCO),

temporary differences as “deferred tax assets” (generally items an indirect, wholly owned subsidiary of our company, of a

that can be used as a tax deduction or credit in future periods) proposed adjustment to the taxable income of PRDCO for

and “deferred tax liabilities” (generally items that we received fiscal year 1992. The proposed adjustment arises from an

a tax deduction for, but have not yet been recorded in the assertion by the Belgian tax authorities of jurisdiction with

Statement of Income). respect to income resulting primarily from certain transfers

The tax effects of the major items recorded as deferred tax of property by our non-Belgian subsidiaries to the Irish branch

assets and liabilities are: of PRDCO. In January 1995, PRDCO received an assessment

from the tax authorities for additional taxes and interest of

1999 1998 1997

Deferred Tax Deferred Tax Deferred Tax

approximately $432 million and $97 million, respectively,

relating to these matters. In January 1996, PRDCO received

(millions of dollars) Assets Liabs. Assets Liabs. Assets Liabs.

an assessment from the tax authorities, for fiscal year 1993, for

Prepaid/deferred items $ 361 $ 197 $ 411 $ 169 $ 252 $189 additional taxes and interest of approximately $86 million and

Inventories 471 109 322 72 218 60 $18 million, respectively. The additional assessment arises from

Property, plant and

the same assertion by the Belgian tax authorities of jurisdiction

equipment 22 514 39 433 30 350

Employee benefits 544 131 391 97 297 113

with respect to all income of the Irish branch of PRDCO.

Restructurings and Based upon the relevant facts regarding the Irish branch of

special charge* 244 — 301 — 133 — PRDCO and the provisions of the Belgian tax laws and the

Foreign tax credit written opinions of outside counsel, we believe that the

carryforwards 181 — 117 — 159 — assessments are without merit.

Other carryforwards 165 — 97 — 135 — We believe that our accrued tax liabilities are adequate for

Unremitted earnings — 335 — 335 — — all years.

All other 121 170 169 73 119 76

Subtotal 2,109 1,456 1,847 1,179 1,343 788 10 Benefit Plans

Valuation allowance (27) — (30) — (27) —

Our pension plans cover most employees worldwide. Our

Total deferred taxes $2,082 $1,456 $1,817 $1,179 $1,316 $788 postretirement plans provide medical and life insurance

Net deferred tax asset $ 626 $ 638 $ 528 benefits to retirees and their eligible dependents.

* Includes tax effect of the 1991 charge for potential future Shiley C/C heart valve

Information regarding our pension and postretirement

fracture claims. benefit obligation follows:



These amounts, netted by taxing location, are in the Pension Postretirement

following captions in the Balance Sheet: (percentages) 1999 1998 1997 1999 1998 1997



(millions of dollars) 1999 1998 1997 Weighted-average

assumptions:

Prepaid expenses and taxes $ 744 $ 809 $ 425 Discount rate:

Other assets, deferred taxes and U.S. plans 7.5 6.8 7.0 7.5 6.8 7.0

deferred charges 183 26 230 International plans 5.1 5.3 5.9

Deferred taxes on income (301) (197) (127) Rate of compensation

Net deferred tax asset $ 626 $ 638 $ 528 increase:

U.S. plans 4.5 4.5 4.5

International plans 3.7 3.4 3.9









50

Pfizer Inc and Subsidiary Companies







The following tables present reconciliations of the benefit The components in the balance sheet consist of:

obligation of the plans; the plan assets of the pension plans and

Pension Postretirement

the funded status of the plans:

(millions of dollars) 1999 1998 1997 1999 1998 1997

Pension Postretirement

Prepaid benefit cost $ 537 $ 504 $ 499 $ — $ — $ —

(millions of dollars) 1999 1998 1997 1999 1998 1997 Accrued benefit

Change in benefit liability (655) (562) (362) (346) (359) (394)

obligation Intangible asset 79 71 53 — — —

Benefit obligation at Accumulated other

beginning of year $3,177 $2,674 $2,130 $ 286 $ 287 $ 285 comprehensive

Service cost 169 151 105 7 10 7 income 317 249 143 — — —

Interest cost 192 181 145 18 20 19 Net amount

Employee recognized $ 278 $ 262 $ 333 $(346) $(359) $(394)

contributions 9 6 6

Plan amendments 13 15 274 2 — —

Information related primarily to International plans:

Plan net (gains)/losses 87 354 240 (30) (3) (7)

Foreign exchange Pension

impact 28 36 (103)

Acquisitions — — 3 — — — (millions of dollars) 1999 1998 1997

Divestitures (42) (26) — — — — Pension plans with an accumulated benefit

Curtailments — (26) (1) — (10) — obligation in excess of plan assets:

Settlements (1) (10) (1) — — — Fair value of plan assets $400 $323 $294

Benefits paid (221) (178) (124) (20) (18) (17) Accumulated benefit obligation 752 693 553

Benefit obligation at Pension plans with a benefit obligation in

end of year $3,411 $3,177 $2,674 $ 263 $ 286 $ 287 excess of plan assets:

Fair value of plan assets $496 $435 $422

Change in Benefit obligation 949 901 774

plan assets

Fair value of plan

assets at beginning

At December 31, 1999, the major U.S. pension plan held

of year $3,194 $2,793 $2,410 approximately 6.8 million shares of our common stock with a

Actual return on plan fair value of approximately $220 million. The Plan received

assets 464 530 491 approximately $2 million in dividends on these shares in 1999.

Company The assumptions used and the annual cost related to these

contributions 76 63 50 plans follow:

Employee

contributions 9 6 6 Pension Postretirement

Foreign exchange

(percentages) 1999 1998 1997 1999 1998 1997

impact 26 3 (57)

Acquisitions — — 1 Weighted average

Divestitures (34) (23) — assumptions:

Settlements (1) (13) (1) Expected return on

Benefits paid (206) (165) (107) plan assets:

U.S. plans 10.0 10.0 10.0

Fair value of plan

International plans 7.3 8.1 7.5

assets at end of year $3,528 $3,194 $2,793

(millions of dollars)

Funded status:

Plan assets in excess Service cost $169 $ 151 $ 105 $ 7 $ 10 $ 7

of/(less than) Interest cost 192 181 145 18 20 19

benefit Expected return on

obligation $ 117 $ 17 $ 119 $(263) $(286) $(287) plan assets (275) (249) (208)

Unrecognized: Amortization of:

Net transition asset (4) (4) (10) — — — Prior service costs/

Net (gains)/ (gains) 19 24 34 (18) (24) (24)

losses (75) 1 (86) (56) (26) (24) Net transition asset (5) (6) (5) — — —

Prior service Net losses/(gains) 12 10 2 — (1) (1)

costs/(gains) 240 248 310 (27) (47) (83) Curtailments and

settlements— net* — 28 — — (22) —

Net amount

recognized $ 278 $ 262 $ 333 $(346) $(359) $(394) Net periodic benefit

cost/(gain) $112 $ 139 $ 73 $ 7 $(17) $ 1

* Includes approximately $12 million of special termination pension benefits for certain

MTG employees in 1998.







51

Pfizer Inc and Subsidiary Companies







An average increase of 6.9% in the cost of health care 13 Preferred Stock Purchase Rights

benefits was assumed for 2000 and is projected to decrease over

Preferred Stock Purchase Rights have a scheduled term

the next five years to 5.2% and to then remain at that level.

through October 2007, although the term may be extended or

A 1% change in the medical trend rate assumed for

the Rights may be redeemed prior to expiration. One right was

postretirement benefits would have the following effects

issued for each share of common stock issued by our company.

at December 31, 1999:

These rights are not exercisable unless certain change-in-

(millions of dollars) 1% Increase 1% Decrease control events transpire, such as a person acquiring or

Total of service and interest

obtaining the right to acquire beneficial ownership of 15% or

cost components $ 1 $ (1) more of our outstanding common stock or an announcement of

Postretirement benefit obligation 13 (12) a tender offer for at least 30% of our stock. The rights are

evidenced by corresponding common stock certificates and

We have savings and investment plans for most employees automatically trade with the common stock unless an event

in the U.S., Puerto Rico, the U.K. and Ireland. Employees may transpires that makes them exercisable. If the rights become

contribute a portion of their salaries to the plans and we match exercisable, separate certificates evidencing the rights will be

a portion of the employee contributions. Our contributions distributed and each right will entitle the holder to purchase a

were $50 million in 1999, $48 million in 1998 and $43 million new series of preferred stock at a defined price from our

in 1997. company. The preferred stock, in addition to preferred

dividend and liquidation rights, will entitle the holder to vote

11 Lease Commitments with the company’s common stock.

The rights are redeemable by us at a fixed price until

We lease properties for use in our operations. In addition to

10 days, or longer as determined by the Board, after

rent, the leases require us to pay directly for taxes, insurance,

certain defined events, or at any time prior to the expiration of

maintenance and other operating expenses, or to pay higher

the rights.

rent when operating expenses increase. Rental expense, net

We have reserved 3.0 million preferred shares to be issued

of sublease income, was $158 million in 1999, $131 million in

pursuant to these rights. No such shares have yet been issued.

1998 and $127 million in 1997. This table shows future

At the present time, the rights have no dilutive effect on the

minimum rental commitments under noncancellable leases

earnings per common share calculation.

at December 31, 1999:



After

14 Employee Benefit Trusts

(millions of dollars) 2000 2001 2002 2003 2004 2004 In 1993, we sold 120 million shares of treasury stock to the

Lease commitments $54 $45 $40 $29 $27 $286 Pfizer Inc. Grantor Trust in exchange for a $600 million note.

The Trust was established primarily to fund our employee

12 Common Stock benefit plans. In February 1999, the Trust transferred 10

million shares to us to satisfy the balance due on its note and

We effected a three-for-one stock split of our common stock in contributed its remaining 90 million shares to the newly

the form of a 200% stock dividend in 1999 and a two-for-one established Pfizer Inc. Employee Benefit Trust (EBT). The

split of our common stock in the form of a 100% stock Grantor Trust was then dissolved and the shares of the EBT

dividend in 1997. All share and per share information in this will now be used to fund employee benefit plans. The Balance

report reflects both splits. Per share data may reflect rounding Sheet reflects the fair value of the shares owned by the EBT as a

adjustments as a result of the three-for-one split. reduction of Shareholders’ Equity.

Under the current share-purchase program begun in

September 1998, we are authorized to purchase up to $5 billion

of our common stock. In 1999, we purchased approximately

65.6 million shares of our common stock in the open market at

an average price of $38 per share. Since the beginning of this

program, we have purchased 80.4 million shares of our

common stock for approximately $3 billion. In September

1998, we completed a program under which we purchased

79.2 million shares of our common stock at a total cost of

$2 billion. In 1998, we purchased approximately 57.8 million

shares of our common stock at an average price of $33 per share

under these share-purchase programs. Of the 57.8 million

shares repurchased in 1998, 14.8 million shares were

repurchased under the share-purchase program which started in

September 1998, for a total cost of $525 million.







52

Pfizer Inc and Subsidiary Companies







15 Earnings Per Share The following table summarizes information concerning

options outstanding under the Plan at December 31, 1999:

The weighted average common shares used in the

computations of basic earnings per common share and earnings (thousands

per common share assuming dilution were as follows: of shares) Options Outstanding Options Exercisable

Weighted

(millions, except per share data) 1999 1998 1997 Average Weighted Weighted

Number Remaining Average Number Average

Earnings:

Range of Outstanding Contractual Exercise Exercisable Exercise

Income from continuing operations $3,199 $1,950 $2,082 Exercise Prices at 12/31/99 Term (years) Price at 12/31/99 Price

Discontinued operations— net of tax (20) 1,401 131

$ 0 – $10 85,308 4.0 $ 6.40 84,401 $ 6.38

Net income $3,179 $3,351 $2,213 10 – 15 36,677 6.6 12.42 34,439 12.42

Basic: 15 – 20 35,486 7.7 18.34 21,145 18.35

Weighted average number of 20 – 40 48,730 8.7 35.18 14,114 35.18

common shares outstanding 3,775 3,789 3,771 over 40 66,904 9.2 42.07 — —

Earnings per common share

Income from continuing operations $ .85 $ .51 $ .55 The following table summarizes the activity for the Plan:

Discontinued operations— net of tax (.01) .37 .04

Under Option

Net income $ .84 $ .88 $ .59

Shares Weighted

Diluted: Available for Average Exercise

Weighted average number of (thousands of shares) Grant Shares Price Per Share

common shares outstanding 3,775 3,789 3,771 Balance January 1, 1997 105,042 259,284 $ 7.21

Common share equivalents— Granted (42,612) 42,612 18.35

stock options and stock issuable Exercised — (46,983) 5.38

under employee compensation plans 109 156 138 Cancelled 1,959 (2,016) 12.89

Weighted average number of Balance December 31, 1997 64,389 252,897 9.39

common shares and common Granted (52,860) 52,860 35.21

share equivalents 3,884 3,945 3,909 Exercised — (54,888) 7.04

Earnings per common share Cancelled 1,212 (1,257) 19.91

Income from continuing operations $ .82 $ .49 $ .53 Balance December 31, 1998 12,741 249,612 15.32

Discontinued operations— net of tax — .36 .04 Authorized 165,000 — —

Net income $ .82 $ .85 $ .57 Granted (67,963) 67,963 42.07

Exercised — (41,524) 9.57

Cancelled 2,928 (2,946) 35.41

Options to purchase 115 million shares were outstanding

during 1999 but were not included in the computation of Balance December 31, 1999 112,706 273,105 22.63

diluted earnings per share because the options’ exercise prices Options granted in 1999 include options for 450 shares granted to every eligible

were greater than the average market price of the common employee worldwide in celebration of our 150th Anniversary.



shares. The tax benefits related to certain stock option transactions were $228 million in 1999,

$274 million in 1998 and $88 million in 1997.

16 Stock Option and Performance Awards

The weighted-average fair value per stock option granted

We may grant stock options to any employee, including was $13.57 for 1999 options, $11.31 for 1998 options and $5.59

officers, under our Stock and Incentive Plan. Options are for the 1997 options. We estimated the fair values using the

exercisable after five years or less, subject to continuous Black-Scholes option pricing model, modified for dividends

employment and certain other conditions and expire 10 years and using the following assumptions:

after the grant date. Once exercisable, the employee can

purchase shares of our common stock at the market price on 1999 1998 1997

the date we granted the option. Expected dividend yield 1.02% 1.02% 1.76%

The Plan also allows for stock appreciation rights, Risk-free interest rate 5.26% 5.23% 6.23%

stock awards and performance awards. In 1999, shareholders Expected stock price volatility 25.98% 26.29% 25.56%

approved amendments to increase the shares available in Expected term until exercise (years) 5.75 5.75 5.50

the Plan and to extend its term through 2008.









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Pfizer Inc and Subsidiary Companies







The following table summarizes results as if we had 18 Litigation

recorded compensation expense for the 1999, 1998 and 1997

The Company is involved in a number of claims and

option grants:

litigations, including product liability claims and litigations

(millions of dollars, except per share data) 1999 1998 1997 considered normal in the nature of its businesses. These include

Net income:

suits involving various pharmaceutical and hospital products

As reported $3,179 $3,351 $2,213 that allege either reaction to or injury from use of the product.

Pro forma 2,750 3,149 2,087 In addition, from time to time the Company is involved in, or

Basic earnings per share: is the subject of, various governmental or agency inquiries or

As reported $ .84 $ .88 $ .59 investigations relating to its businesses.

Pro forma .73 .83 .55 In 1999, the Company pleaded guilty to one count of price

Diluted earnings per share: fixing of sodium erythorbate from July 1992 until December

As reported $ .82 $ .85 $ .57

1994, and one count of market allocation of maltol from

Pro forma .71 .80 .53

December 1989 until December 1995, and paid a total fine of

$20 million. The activities at issue involved the Company’s

The Performance-Contingent Share Award Program former Food Science Group, a division that manufactured food

was established effective in 1993 to provide executives and additives and that the Company divested in 1996. The

other key employees the right to earn common stock awards. Department of Justice has stated that no further antitrust

We determine the award payouts after the performance period charges will be brought against the Company relating to the

ends, based on specific performance criteria. Under the former Food Science Group, that no antitrust charges will be

Program, up to 120 million shares may be awarded. We brought against any current director, officer or employee of the

awarded approximately 2,276,000 shares in 1999, Company for conduct related to the products of the former

approximately 1,959,000 shares in 1998 and approximately Food Science Group, and that none of the Company’s current

1,347,000 shares in 1997. At December 31, 1999, program directors, officers or employees was aware of any aspect of the

participants had the right to earn up to 12.3 million additional activity that gave rise to the violations. Five purported class

shares. Compensation expense related to the Program was action suits involving these products have been filed against

$64 million in 1999, $202 million in 1998 and $74 million the Company; two in California State Court, and three in New

in 1997. York Federal Court. The Company does not believe that this

We entered into two forward-purchase contracts in 1998 plea and settlement, or civil litigation involving these

and on maturity they were extended. These contracts offset the products, will have a material effect on its business or results of

potential impact on net income of our liability under the operations.

Program. At settlement date we will, at the option of the On June 9, 1997, the Company received notice of the

counterparty to the contract, either receive our own stock or filing of an Abbreviated New Drug Application (ANDA) by

settle the contracts for cash. Other contract terms are as Mylan Pharmaceuticals for a sustained-release nifedipine

follows: product asserted to be bioequivalent to Procardia XL. Mylan’s

Maximum Maturity notice asserted that the proposed formulation does not infringe

in Years relevant licensed Alza and Bayer patents and thus that approval

Number of Shares (thousands) Per Share 1999 1998 of their ANDA should be granted before patent expiration. On

3,000 $33.73 — .9 July 18, 1997, the Company, together with Bayer AG and Bayer

3,017 33.75 .9 — Corporation, filed a patent-infringement suit against Mylan

Pharmaceuticals Inc. and Mylan Laboratories Inc. in the United

The financial statements include the following items States District Court for the Western District of Pennsylvania

related to these contracts: with respect to Mylan’s ANDA. Suit was filed under Bayer

Prepaid expenses and taxes includes: AG’s U.S. Patent No. 5,264,446, licensed to the Company,

• fair value of these contracts relating to nifedipine of a specified particle size range. Mylan

Other deductions—net includes: has filed its answer denying infringement and a scheduling

• changes in the fair value of these contracts order has been entered. On December 17, 1999, Mylan received

final approval from the FDA for its 30 mg. extended-release

17 Insurance nifedipine tablet. On March 16, 1999, the United States

We maintain insurance coverage adequate for our needs. Under District Court granted Mylan’s motion to file an amended

our insurance contracts, we usually accept self-insured answer and antitrust counterclaims. All discovery on the

retentions appropriate for our specific business risks. antitrust counterclaims is stayed pending resolution of the

patent misuse claims. On March 29, 1999, Mylan filed a

motion for summary judgment based on an adverse decision

against Bayer in Bayer’s litigation against Elan Pharmaceutical

Research Corp. which involved the same nifedipine particle size







54

Pfizer Inc and Subsidiary Companies







patent. Discovery has been essentially completed and the complete discovery of parties and fact witnesses and February

parties dispositive motions were filed by an extended deadline 29, 2000, to complete discovery of expert witnesses. On

of July 19, 1999, including Pfizer and Bayer’s summary December 20, 1999, the court extended the date to complete

judgment motion seeking to dismiss Mylan’s patent misuse fact discovery to January 28, 2000, and that of expert discovery

defenses and counterclaims. On December 13, 1999, Mylan to March 15, 2000. A status conference with the court is

filed its opposition to plaintiffs’ motion for summary judgment scheduled for March 17, 2000.

dismissing Mylan’s patent misuse defense and counterclaim, On April 2, 1998, the Company received notice from Lek

and Bayer and the Company filed their opposition to Mylan’s U.S.A. Inc. of its filing of an ANDA for a 60 mg. formulation

motion for summary judgment of non-infringement. The of nifedipine alleged to be bioequivalent to Procardia XL. On

parties reply memoranda in support of their motions were filed May 14, 1998, Bayer and Pfizer commenced suit against Lek for

on December 28, 1999. infringement of Bayer’s U.S. Patent No. 5,264,446, as well as

On or about February 23, 1998, Bayer AG received notice for infringement of a second Bayer patent, No. 4,412,986

that Biovail Laboratories Incorporated had filed an ANDA for a relating to combinations of nifedipine with certain polymeric

sustained-release nifedipine product asserted to be materials. On September 14, 1998, Lek was served with the

bioequivalent to one dosage strength (60 mg.) of Procardia XL. summons and complaint. Plaintiffs amended the complaint on

The notice was subsequently received by the Company as well. November 10, 1998, limiting the action to infringement of

The notice asserts that the Biovail product does not infringe U.S. Patent 4,412,986. On January 19, 1999, Lek filed a motion

Bayer’s U.S. Patent No. 5,264,446. On March 26, 1998, the to dismiss the complaint alleging infringement of U.S. Patent

Company received notice of the filing of an ANDA by Biovail 4,412,986. Pfizer responded to this motion and oral argument

Laboratories of a 30 mg. dosage formulation of nifedipine has been held in abeyance pending a settlement conference. In

alleged to be bioequivalent to Procardia XL. On April 2, 1998, September 1999, a settlement agreement was entered into

Bayer and Pfizer filed a patent-infringement action against among the parties staying this litigation until the expiration of

Biovail, relating to their 60 mg. nifedipine product, in the U.S. Patent No. 4,412,986 on November 2, 2000.

United States District Court for the District of Puerto Rico. On February 10, 1999, the Company received a notice from

On May 6, 1998, Bayer and Pfizer filed a second patent Lek U.S.A. of its filing of an ANDA for a 90 mg. formulation

infringement action in Puerto Rico against Biovail under the of nifedipine alleged to be bioequivalent to Procardia XL. On

same patent with respect to Biovail’s 30 mg. nifedipine March 25, 1999, Bayer and Pfizer commenced suit against Lek

product. These actions have been consolidated for discovery and for infringement of the same two Bayer patents originally

trial. On April 24, 1998, Biovail Laboratories Inc. brought suit asserted against Lek’s 60 mg. formulation. This case was also

in the United States District Court for the Western District of the subject of a settlement conference. In September, 1999, a

Pennsylvania against the Company and Bayer seeking a settlement agreement was entered into among the parties

declaratory judgment of invalidity of and/or non-infringement staying this litigation until the expiration of U.S. patent No.

of the 5,264,446 nifedipine patent as well as a finding of 4,412,986 on November 2, 2000.

violation of the antitrust laws. Biovail has also moved to On November 9, 1998, Pfizer received an ANDA notice

transfer the patent infringement actions from Puerto Rico to letter from Martec Pharmaceutical, Inc. for generic versions (30

the Western District of Pennsylvania. Pfizer has opposed this mg., 60 mg., 90 mg.) of Procardia XL. On or about December

motion to transfer and on June 19, 1998, moved to dismiss 18, 1998, Pfizer received a new ANDA certification letter

Biovail’s declaratory judgment action and antitrust action in stating that the ANDA had actually been filed in the name of

the Western District of Pennsylvania, or in the alternative, to Martec Scientific, Inc. On December 23, 1998, Pfizer brought

stay the action pending the outcome of the infringement an action against Martec Pharmaceutical, Inc. and Martec

actions in Puerto Rico. On January 4, 1999, the District Court Scientific, Inc. in the Western District of Missouri for

in Pennsylvania granted Pfizer’s motion for a stay of the infringement of Bayer’s patent relating to nifedipine of a

antitrust action pending the outcome of the infringement specific particle size. On January 26, 1999, a second complaint

actions in Puerto Rico. On January 29, 1999, the District was filed against Martec Scientific in the Western District of

Court in Puerto Rico denied Biovail’s motion to transfer the Missouri based on Martec’s new ANDA certification letter.

patent infringement actions from Puerto Rico to the Western Martec filed its response to this complaint on February 26,

District of Pennsylvania. On April 12, 1999, Biovail filed a 1999. A hearing to determine claim scope is scheduled for

motion for summary judgment also based in part on the June 1, 2000.

summary judgment motion granted to Elan in the Bayer v. Pfizer filed suit on July 8, 1997, against the FDA in the

Elan litigation in the Northern District of Georgia. Pfizer and United States District Court for the District of Columbia,

Bayer’s response was filed on April 26, 1999. On September 20, seeking a declaratory judgment and injunctive relief enjoining

1999, the United States District Court in Puerto Rico denied the FDA from processing Mylan’s ANDA or any other ANDA

Biovail’s motion for summary judgment without prejudice to submission referencing Procardia XL that uses a different

their refiling after completion of discovery in the Procardia XL extended-release mechanism. Pfizer’s suit alleges that extended-

patent-infringement litigation. The court set an expedited release mechanisms that are not identical to the osmotic pump

discovery schedule with a deadline of December 30, 1999, to mechanism of Procardia XL constitute different dosage forms





55

Pfizer Inc and Subsidiary Companies







requiring the filing and approval of suitability petitions under On May 19, 1999, Abbott Laboratories filed an action

the Food Drug and Cosmetics Act before the FDA can accept against the Company in the United States District Court of the

an ANDA for filing. Mylan intervened in Pfizer’s suit. On Northern District of Illinois alleging that the Company’s use,

March 31, 1998, the U.S. District Judge granted the sale or manufacture of trovafloxacin infringes Abbott’s United

government’s motion for summary judgment against the States Patent No. 4,616,019 claiming naphthyriding antibiotics

Company. On July 16, 1999, the D.C. Court of Appeals and seeking a permanent injunction and damages. An answer

dismissed the appeal on the ground that since the FDA had not denying these allegations was filed on June 9, 1999. Discovery

approved any ANDA referencing Procardia XL that uses a is in progress.

different extended-release mechanism than the osmotic pump On December 17, 1999, the Company received notice of

mechanism of Procardia XL, it was premature to maintain this the filing of an ANDA by Zenith Goldline Pharmaceuticals

action, stating that Pfizer has the right to bring such an action for 50 mg. and 100 mg. tablets of sertraline hydrochloride

if, and when, the FDA approves such an ANDA. Subsequent to alleged to be bioequivalent to Zoloft. Zenith has certified to

FDA’s final approval of Mylan’s ANDA, on December 18, 1999 the FDA that it will not engage in the manufacture, use or sale

Pfizer filed suit against FDA in the United States District of sertraline hydrochloride until the expiration of Pfizer’s U.S.

Court for the District of Delaware. The suit alleges that FDA Patent 4,536,518, which covers sertraline per se and expires

unlawfully approved Mylan’s 30 mg. extended release product December 30, 2005. Zenith has also alleged in its certification

because FDA had not granted an ANDA suitability petition to the FDA that the manufacture, use and sale of Zenith’s

reflecting a difference in dosage form from Procardia XL. product will not infringe Pfizer’s U.S. Patent 4,962,128, which

On March 31, 1999, the Company received notice from covers methods of treating an anxiety-related disorder or

TorPharm of its filing, through its U.S. agent Apotex Corp., of Pfizer’s U.S. Patent 5,248,699, which covers a crystalline

an ANDA for 1 mg., 2 mg., 4 mg. and 8 mg. tablets alleged to polymorph of sertraline hydrochloride. These patents expire in

be bioequivalent to Cardura (doxazosin mesylate). The notice November 2009 and August 2012, respectively. On January 28,

letter alleges that Pfizer’s patent on doxazosin is invalid in view 2000, the Company filed a patent infringement action against

of certain prior art references. Following a review of these Zenith Goldline and its parent Ivax Corporation in the United

allegations, suit was filed in the United States District Court States District Court for the District of New Jersey for

for the Northern District of Illinois against TorPharm and infringement of the ’128 and ’699 patents.

Apotex Corp. on May 14, 1999. The defendants requested a 90- On February 1, 2000, the Company received notice of the

day period in which to file their answer. The request was filing of an ANDA by Novopharm Limited for 50 mg, 100 mg,

granted and TorPharm/Apotex’s answer was filed by August 150 mg and 200 mg tablets of fluconazole alleged to be

19, 1999. Discovery is in progress. On June 2, 1999, FDA was bioequivalent to DIFLUCAN. Novopharm has certified to the

notified that given the patent litigation and pursuant to FDA its position that the Company’s U.S. Patent 4,404,216,

provisions of the Federal Food Drug and Cosmetic Act, the which covers fluconazole, is invalid. This patent expires in

FDA may not approve the TorPharm application for thirty January 2004. The Company is evaluating Novopharm’s notice.

months from filing or resolution of the litigation. In pre-existing litigation between Pioneer Hi-Bred

On May 5, 1999, the Company filed an action against Sibia International, Inc. and DeKalb Genetics Corporation in the

Neurosciences, Inc. in the United States District Court for the United States District Court for the Southern District of Iowa,

District of Delaware seeking a declaratory judgment that two the court granted on October 8, 1999 Pioneer’s motion to add

Sibia patents claiming reporter gene drug screening assays are additional parties, including Pfizer Inc. and Monsanto Co. (the

invalid, not infringed by the Company, and unenforceable due present owner of DeKalb Genetics Corporation), as codefendant

to Sibia’s misuse of its patent rights in seeking certain license parties. The amended complaint, which claims violations of the

terms. On May 27, 1999, Sibia Neurosciences, Inc. filed an federal Lanham Act and Iowa state law stemming from the

answer to the Company’s declaratory judgment action in which codefendants’ alleged use of Pioneer’s corn seed germplasm in

Sibia denies that a prior case or controversy existed, but admits the development of competitive corn seed products, was served

that a case or controversy does now exist regarding at least one on the Company on October 19. The Company filed its answer

patent in suit, denies the invalidity, unenforceability and non- on December 15, 1999.

infringement of the patents in suit, and asserts various On September 22, 1999, the jury in a trademark-

jurisdictional and equitable defenses, affirmative defenses, and infringement litigation brought against the Company by

lack of standing by the Company to assert patent misuse. Sibia Trovan Ltd. and Electronic Identification Devices, Ltd. relating

Neurosciences also filed a counterclaim alleging willful to use of the TROVAN mark for trovafloxacin issued a verdict

infringement by the Company of one of the patents in suit. A in favor of the plaintiffs with respect to liability, holding that

reply to that counterclaim denying Sibia’s allegation has been the Company had infringed Trovan Ltd.’s mark and had acted

filed. The parties submitted a joint status report to the court in bad faith. Following a further damage trial, on October 12,

on December 14, 1999, in which the parties agreed to complete 1999, the jury awarded Trovan Ltd. a total of $143 million in

fact discovery by August 21, 2000, and commence trial on

January 8, 2001.









56

Pfizer Inc and Subsidiary Companies







damages, comprised of $5 million actual damages, $3 million responsible party or participant with respect to several waste

as a reasonable royalty and $135 million in punitive damages. site matters in foreign jurisdictions. Such claims have been

The court held a hearing on December 27, 1999, on whether to made by the filing of a complaint, the issuance of an

award the plaintiffs profits based on the Company’s sales of administrative directive or order, or the issuance of a notice or

Trovan and, if so, the amount of same. The Company’s motion demand letter. These claims are in various stages of

for mistrial remains outstanding. administrative or judicial proceedings. They include demands

As previously disclosed, a number of lawsuits and claims for recovery of past governmental costs and for future

have been brought against the Company and Shiley investigative or remedial actions. In many cases, the dollar

Incorporated, a wholly owned subsidiary, alleging either amount of the claim is not specified. In most cases, claims have

personal injury from fracture of 60° or 70° Shiley Convexo been asserted against a number of other entities for the same

Concave (“C/C”) heart valves, or anxiety that properly recovery or other relief as was asserted against the Company.

functioning implanted valves might fracture in the future, or The Company is currently participating in remedial action at a

personal injury from a prophylactic replacement of a number of sites under federal, state, local and foreign laws.

functioning valve. To the extent possible with the limited amount of

In an attempt to resolve all claims alleging anxiety that information available at this time, the Company has evaluated

properly functioning valves might fracture in the future, the its responsibility for costs and related liability with respect to

Company entered into a settlement agreement in January 1992 the above sites and is of the opinion that the Company’s liability

in Bowling v. Shiley, et al., a case brought in the United States with respect to these sites should not have a material adverse

District Court for the Southern District of Ohio, that effect on the financial position or the results of operations of the

established a worldwide settlement class of people with C/C Company. In arriving at this conclusion, the Company has

heart valves and their spouses, except those who elected to considered, among other things, the payments that have been

exclude themselves. The settlement provided for a Consultation made with respect to the sites in the past; the factors, such as

Fund of $90 million, which was fixed by the number of claims volume and relative toxicity, ordinarily applied to allocate

filed, from which valve recipients received payments that are defense and remedial costs at such sites; the probable costs to be

intended to cover their cost of consultation with cardiologists paid by the other potentially responsible parties; total projected

or other health care providers with respect to their valves. The remedial costs for a site, if known; existing technology; and the

settlement agreement established a second fund of at least $75 currently enacted laws and regulations. The Company

million to support C/C valve-related research, including the anticipates that a portion of these costs and related liability will

development of techniques to identify valve recipients who may be covered by available insurance.

have significant risk of fracture, and to cover the unreimbursed Through the early 1970s, Pfizer Inc. (Minerals Division)

medical expenses that valve recipients may incur for certain and Quigley Company, Inc. (“Quigley”), a wholly owned

procedures related to the valves. The Company’s obligation as subsidiary, sold a minimal amount of one construction product

to coverage of these unreimbursed medical expenses is not and several refractory products containing some asbestos. These

subject to any dollar limitation. Following a hearing on the sales were discontinued thereafter. Although these sales

fairness of the settlement, it was approved by the court on represented a minor market share, the Company has been

August 19, 1992, and all appeals have been exhausted. named as one of a number of defendants in numerous lawsuits.

Generally, the plaintiffs in all of the pending heart valve These actions, and actions related to the Company’s sale of talc

litigations seek money damages. Based on the experience of the products in the past, claim personal injury resulting from

Company in defending these claims to date, including exposure to asbestos-containing products, and nearly all seek

insurance proceeds and reserves, the Company is of the opinion general and punitive damages. In these actions, the Company

that these actions should not have a material adverse effect on or Quigley is typically one of a number of defendants, and both

the financial position or the results of operations of the are members of the Center for Claims Resolution (the “CCR”),

Company. Litigation involving insurance coverage for the a joint defense organization of sixteen defendants that is

Company’s heart valve liabilities has been resolved. defending these claims. The Company and Quigley are

The Company’s operations are subject to federal, state, responsible for varying percentages of defense and liability

local and foreign environmental laws and regulations. Under payments for all members of the CCR. A number of cases

the Comprehensive Environmental Response Compensation and alleging property damage from asbestos-containing products

Liability Act of 1980, as amended (“CERCLA” or “Superfund”), installed in buildings have also been brought against the

the Company has been designated as a potentially responsible Company, but most have been resolved.

party by the United States Environmental Protection Agency As of January 29, 2000, there were 57,328 personal injury

with respect to certain waste sites with which the Company claims pending against Quigley and 26,890 such claims

may have had direct or indirect involvement. Similar against the Company (excluding those that are inactive or have

designations have been made by some state environmental been settled in principle), and 68 talc cases against the

agencies under applicable state Superfund laws. Such Company.

designations are made regardless of the extent of the Company’s The Company believes that its costs incurred in defending

involvement. There are also claims that the Company may be a and ultimately disposing of the asbestos personal injury claims,





57

Pfizer Inc and Subsidiary Companies







as well as the property damage and talc claims, will be largely The Federal Trade Commission opened an investigation

covered by insurance policies issued by several primary focusing on the pricing practices at issue in the above

insurance carriers and a number of excess carriers that have pharmacy antitrust litigation. In July 1996, the Commission

agreed to provide coverage, subject to deductibles, exclusions, issued a subpoena for documents to the Company, among

retentions and policy limits. Litigation against excess insurance others, to which the Company responded. A second subpoena

carriers seeking damages and/or declaratory relief to secure was issued to the Company for documents in May 1997 and the

their coverage obligations has now been largely resolved, Company again responded. We are not aware of any further

although claims against several of such insureds do remain activity.

pending. Based on the Company’s experience in defending the FDA administrative proceedings relating to Plax are

claims to date and the amount of insurance coverage available, pending, principally an industry-wide call for data on all anti-

the Company is of the opinion that the actions should not plaque products by the FDA. The call-for-data notice specified

ultimately have a material adverse effect on the financial that products that have been marketed for a material time and

position or the results of operations of the Company. to a material extent may remain on the market pending FDA

In 1993, the Company was named, together with review of the data, provided the manufacturer has a good faith

numerous other manufacturers of brand-name prescription belief that the product is generally recognized as safe and

drugs and certain companies that distribute brand-name effective and is not misbranded. The Company believes that

prescription drugs, in suits in federal and state courts brought Plax satisfied these requirements and prepared a response to the

by various groups of retail pharmacy companies, alleging that FDA’s request, which was filed on June 17, 1991. This filing, as

the manufacturers violated the Sherman Act by agreeing not to well as the filings of other manufacturers, is still under review

give retailers certain discounts and that the failure to give such and is currently being considered by an FDA Advisory

discounts violated the Robinson Patman Act. A class action Committee. The Committee has issued a draft report

was brought on the Sherman Act claim, as well as additional recommending that plaque removal claims should not be

actions by approximately 3,500 individual retail pharmacies permitted in the absence of data establishing efficacy against

and a group of chain and supermarket pharmacies (the gingivitis. The process of incorporating the Advisory

“individual actions”) on both the Sherman Act and Robinson Committee recommendations into a final monograph is

Patman Act claims. A retailer class was certified in 1994 (the expected to take several years. If the draft recommendation is

“Federal Class Action”). In 1996, fifteen manufacturer ultimately accepted in the final monograph, although it would

defendants, including the Company, settled the Federal Class have a negative impact on sales of Plax, it will not have a

Action. The Company’s share was $31.25 million, payable in material adverse effect on the sales, financial position or

four annual installments without interest. Trial began in operations of the Company.

September 1998 for the class case against the non-settlers, and On January 15, 1997, an action was filed in Circuit Court,

the District Court also permitted the opt-out plaintiffs to add Chambers County, Alabama, purportedly on behalf of a class of

the wholesalers as named defendants in their cases. The District consumers, variously defined by the laws or types of laws

Court dismissed the case at the close of the plaintiffs’ evidence. governing their rights and encompassing residents of up to 47

The plaintiffs appealed and, on July 13, 1999, the Court of states. The complaint alleges that the Company’s claims for

Appeals upheld most of the dismissal but remanded on one Plax were untrue, entitling them to a refund of their purchase

issue, while expressing doubts that the plaintiffs could prove price for purchases since 1988. A hearing on Plaintiffs’ motion

any damages. to certify the class was held on June 2, 1998. We are awaiting

Retail pharmacy cases also have been filed in state courts the Court’s decision. The Company believes the complaint is

in five states, and consumer class actions were filed in state without merit.

courts in fourteen states and the District of Columbia alleging Since December 1998, four actions have been filed, in state

injury to consumers from the failure to give discounts to retail courts in Houston, San Francisco, Chicago and New Orleans,

pharmacy companies. purportedly on behalf of statewide (California) or nationwide

In addition to its settlement of the retailer Federal Class (Houston, Chicago and New Orleans) classes of consumers who

Action (see above), the Company has also settled several major allege that the Company’s and other manufacturers’ advertising

opt-out retail cases, and along with other manufacturers: (1) has and promotional claims for Rid and other pediculicides were

entered into an agreement to settle all outstanding consumer untrue, entitling them to refunds, other damages and/or

class actions (except Alabama, California and North Dakota), injunctive relief. The Houston case has been voluntarily

which settlement is going through the approval process in the dismissed and proceedings in the San Francisco, Chicago and

various courts in which the actions are pending; and (2) has New Orleans cases are still in early stages of the proceedings.

entered into an agreement to settle the California consumer The Company believes the complaints are without merit.

case, which has been approved by the Court there. In December, 1999 and January, 2000, two suits were filed

The Company believes that these brand-name prescription in California state courts against the Company and other

drug antitrust cases, which generally seek damages and certain manufacturers of zinc oxide-containing powders. The first suit

injunctive relief, are without merit. was filed by the Center for Environmental Health and the

second was filed by an individual plaintiff on behalf of a





58

Pfizer Inc and Subsidiary Companies







purported class of purchasers of baby powder products. The of a purported class of people whose dogs had suffered injury or

suits generally allege that the label of Desitin powder violates death after ingesting Rimadyl, an antiarthritic medication for

California’s “Proposition 65” by failing to warn of the presence older dogs. The suit, which was filed in state court in South

of lead, which is alleged to be a carcinogen. In January, 2000, Carolina, is in the early pretrial stages. The Company believes

the Company received a notice from a California environmental it is without merit.

group alleging that the labeling of Desitin ointment and During 1998, the Company completed the sale of all of the

powder violates Proposition 65 by failing to warn of the businesses and companies that were part of the Medical

presence of cadmium, which is alleged to be a carcinogen. Technology Group. As part of the sale provisions, the Company

Several other manufacturers of zinc oxide-containing topical has retained responsibility for certain items, including matters

baby products have received similar notices. The Company related to the sale of MTG products sold by the Company

believes that the labeling for Desitin complies with applicable before the sale of the MTG businesses. A number of cases have

legal requirements. been brought against Howmedica Inc. (some of which also

In April 1996, the Company received a Warning Letter name the Company) alleging that P.C.A. one-piece acetabular

from the FDA relating to the timeliness and completeness of hip prostheses sold from 1983 through 1990 were defectively

required post-marketing reports for pharmaceutical products. designed and manufactured and pose undisclosed risks to

The letter did not raise any safety issue about Pfizer drugs. The implantees. These cases have now been resolved. Between 1994

Company has been implementing remedial actions designed to and 1996, seven class actions alleging various injuries arising

remedy the issues raised in the letter. During 1997, the from implantable penile prostheses manufactured by American

Company met with the FDA to apprise them of the scope and Medical Systems were filed and ultimately dismissed or

status of these activities. A review of the Company’s new discontinued. Thereafter, between late 1996 and early 1998,

procedures was undertaken by FDA in 1999. The Company and approximately 700 former members of one or more of the

Agency met to review the findings of this review and agreed purported classes, represented by some of the same lawyers who

that commitments and remedial measures undertaken by the filed the class actions, filed individual suits in Circuit Court in

Company related to the Warning Letter have been Minneapolis alleging damages from their use of implantable

accomplished. The Company agreed to keep the Agency penile prostheses. Most of these claims, along with a number of

informed of its activities as it continues to modify its processes filed and unfiled claims from other jurisdictions, have now

and procedures. been resolved. The Company believes that most if not all of

During May and June, 1999, the FDA and the European these cases are without merit.

Union’s Committee for Proprietary Medicinal Products (CPMP) In June 1993, the Ministry of Justice of the State of Sao

reconsidered the approvals to market Trovan, a broad-spectrum Paulo, Brazil, commenced a civil public action against the

antibiotic, following post-market reports of severe adverse liver Company’s Brazilian subsidiary, Laboratorios Pfizer Ltda.

reactions to the drug. On June 9, the Company announced (“Pfizer Brazil”) asserting that during a period in 1991 Pfizer

that, regarding the marketing of Trovan in the United States, it Brazil withheld sale of the pharmaceutical product Diabinese

had agreed to restrict the indications, limit product in violation of antitrust and consumer protection laws. The

distribution, make certain other labeling changes and to action sought the award of moral, economic and personal

communicate revised warnings to health care professionals in damages to individuals and the payment to a public reserve

the United States. On July 1, Pfizer received the opinion of the fund. In February 1996, the trial court issued a decision

CPMP recommending a one-year suspension of the licenses to holding Pfizer Brazil liable. The trial court’s opinion also

market Trovan in the European Union. The CPMP opinion has established the amount of moral damages for individuals who

been finalized in a Final Decision by the European might make claims later in the proceeding and set out a

Commission. Since June, 1999, three suits and several claims formula for calculating the payment into the public reserve

have been received by the Company alleging liver injuries due fund which could have resulted in a sum of approximately $88

to the ingestion of Trovan. The majority of these claims have million. Pfizer Brazil appealed this decision. In September

been resolved without litigation. In June and July, 1999, two of 1999, the appeals court issued a ruling upholding the trial

the lawsuits were filed in the Circuit Court, Hampton County, court’s decision as to liability. However, the appeals court

South Carolina on behalf of a purported class of all persons who decision overturned the trial court’s decision concerning

received Trovan, seeking compensatory and punitive damages damages, ruling that criteria to apply in the calculation of

and injunctive relief. One of the suits, seeking injunctive relief, damages, both as to individuals and as to payment of any

has been dismissed. No substantitive proceedings have yet amounts to the reserve fund, should be established only in a

occurred in the other suit and the Company believes that it is later stage of the proceeding. The Company believes that this

not properly maintainable as a class action, and will defend action should not have a material adverse effect on the financial

against it accordingly. position or the results of operations of the Company.

In October 1999 the Company was sued in an action

seeking unspecified damages, costs and attorney’s fees on behalf









59

Pfizer Inc and Subsidiary Companies







19 Segment Information and Geographic Data Each separately managed segment offers different products

requiring different marketing and distribution strategies.

We operate in the following two business segments:

We sell our products primarily to customers in the

• pharmaceutical — including treatments for heart diseases,

wholesale sector. In 1999, sales to our two largest wholesalers

infectious diseases, central nervous system disorders,

accounted for 14% and 12% of total revenues. These sales were

diabetes, arthritis, erectile dysfunction and allergies, as

concentrated in the pharmaceutical segment.

well as self-medications

Revenues were in excess of $100 million in each of

• animal health — products for food animals and companion

12 countries outside the U.S. in 1999. The U.S. was the only

animals, including antibiotics, vaccines and other

country to contribute more than 10% to total revenues. The

veterinary items

following tables present segment and geographic information:



Segment Information

Animal Corporate/

(millions of dollars) Pharmaceutical Health Other Consolidated



Total revenues 1999 $14,859 $1,345 $ — $16,204

1998 12,230 1,314 — 13,544

1997 9,726 1,329 — 11,055

Segment profit 1999 4,898(1) 67 (517)(2) 4,448(3)

1998 3,574 (77) (903)(2) 2,594(3)

1997 3,129 112 (374)(2) 2,867(3)

Identifiable assets(4) 1999 9,723 2,144 8,707 20,574

1998 7,987 2,109 8,206 18,302

1997 6,464 2,197 6,330(5) 14,991

Property, plant and equipment additions(4) 1999 1,387 90 84 1,561

1998 991 97 110 1,198

1997 687 69 122 878

Depreciation and amortization(4) 1999 438 74 30 542

1998 386 82 21 489

1997 337 75 16 428





Geographic Data

All

United Other

(millions of dollars) States(6) Japan Countries Consolidated



Total revenues 1999 $9,896 $1,249 $5,059 $16,204

1998 8,205 943 4,396 13,544

1997 6,089 949 4,017 11,055

Long-lived assets 1999 3,430 487 2,750 6,667

1998 2,905 369 2,499 5,773

1997 2,910 283 2,155 5,348

(1)

Includes $310 million charge to write off Trovan inventories.

(2)

Includes interest income/(expense) and corporate expenses. Corporate also includes other income/(expense) of the financial subsidiaries (see note 3,“Financial Subsidiaries”) and

certain performance-based compensation expenses not allocated to the operating segments.

(3)

Consolidated total equals income from continuing operations before provision for taxes on income and minority interests.

(4)

Certain production facilities are shared by various segments. Property, plant and equipment, as well as capital additions and depreciation, are allocated based on physical

production. Corporate assets are primarily cash, short-term investments and long-term loans and investments.

(5)

Includes net assets of discontinued operations.

(6)

Includes operations in Puerto Rico.



20 Subsequent Event Lambert share, or an equity value of $90 billion based on the

closing price of our stock on February 4, 2000 of $35.75 per

On February 7, 2000, we announced an agreement to merge

share. Customary and usual provisions will be made for

with Warner-Lambert Company (Warner-Lambert). Under

outstanding options and warrants.

terms of the merger agreement, which has been approved by

This transaction is subject to customary conditions,

the Board of Directors of both Pfizer and Warner-Lambert, we

including the use of pooling-of-interests accounting, qualifying

will exchange 2.75 shares of Pfizer voting common stock for

as a tax-free reorganization, shareholder approval at both

each outstanding share of Warner-Lambert voting common

companies and usual regulatory approvals. The transaction is

stock in a tax-free transaction valued at $98.31 per Warner-

expected to close in mid-2000.



60

Pfizer Inc and Subsidiary

Companies







Quarterly Consolidated Financial Data (Unaudited)

Quarter

(millions of dollars, except per share data) First Second Third Fourth

1999

Net sales $3,524 $3,298 $3,423 $3,887

Alliance revenue 403 481 569 619

Total revenues 3,927 3,779 3,992 4,506

Costs and expenses 2,778 2,751 3,025 3,202

Income from continuing operations before provision

for taxes on income and minority interests 1,149 1,028 967 1,304

Provision for taxes on income 333 298 265 348

Minority interests 1 1 1 2

Income from continuing operations 815 729 701 954

Discontinued operations Ñ net of tax Ñ (20) Ñ Ñ

Net income $ 815 $ 709 $ 701 $ 954

Earnings per common share Ñ basic

Income from continuing operations $ .22 $ .19 $ .19 $ .25

Discontinued operations Ñ net of tax Ñ (.01) Ñ Ñ

Net income $ .22 $ .18 $ .19 $ .25

Earnings per common share Ñ diluted

Income from continuing operations $ .21 $ .18 $ .18 $ .25

Discontinued operations Ñ net of tax Ñ Ñ Ñ Ñ

Net income $ .21 $ .18 $ .18 $ .25

Cash dividends paid per common share $ .07 1Ú3 $ .07 1Ú3 $ .08 $ .08

Stock prices

High $ 48 11Ú64 $ 50 3Ú64 $ 40 11Ú16 $ 42 1Ú4

Low $ 36 33Ú64 $ 31 35Ú64 $ 32 $ 32 3Ú16





1998

Net sales $ 2,886 $ 3,114 $ 3,110 $ 3,567

Alliance revenue 150 198 220 299

Total revenues 3,036 3,312 3,330 3,866

Costs and expenses 2,294 2,468 2,628 3,560

Income from continuing operations before provision

for taxes on income and minority interests 742 844 702 306

Provision for taxes on income 206 249 186 1

Minority interests 1 1 1 (1)

Income from continuing operations 535 594 515 306

Discontinued operations Ñ net of tax 157 34 882 328

Net income $ 692 $ 628 $ 1,397 $ 634

Earnings per common share Ñ basic

Income from continuing operations $ .14 $ .16 $ .13 $ .08

Discontinued operations Ñ net of tax .04 .01 .24 .08

Net income $ .18 $ .17 $ .37 $ .16

Earnings per common share Ñ diluted

Income from continuing operations $ .14 $ .15 $ .13 $ .07

Discontinued operations Ñ net of tax .04 Ñ .23 .09

Net income $ .18 $ .15 $ .36 $ .16

Cash dividends paid per common share $ .06 1Ú3 $ .06 1Ú3 $ .06 1Ú3 $ .06 1Ú3

Stock prices

High $ 32 1Ú2 $ 40 37Ú64 $ 40 13Ú64 $ 42 63Ú64

Low $ 23 11Ú16 $ 32 1Ú8 $ 30 43Ú64 $ 28 43Ú64

All data reflects the 1999 three-for-one stock split.

As of January 31, 2000, there were 149,747 record holders of our common stock (symbol PFE).





61

Pfizer Inc and Subsidiary Companies









Financial Summary

Year Ended December 31

(millions, except per share data) 1999 1998 1997 1996 1995 1994 1993 1992 1991 1990 1989

Net sales $14,133 12,677 10,739 9,864 8,684 6,825 6,080 5,816 5,352 4,757 4,220

Alliance revenue 2,071 867 316 Ñ Ñ Ñ Ñ Ñ Ñ Ñ Ñ

Total revenues 16,204 13,544 11,055 9,864 8,684 6,825 6,080 5,816 5,352 4,757 4,220

Research and development 2,776 2,279 1,805 1,567 1,340 1,036 880 776 654 545 449

Other costs and expenses 8,980 8,671 6,383 5,769 5,327 4,212 3,822 3,829 3,675 3,288 3,045

Divestitures, restructuring and unusual items Ñ net(1) Ñ Ñ Ñ Ñ Ñ Ñ 741 (141) 300 Ñ Ñ

Income from continuing operations

before taxes and minority interests $ 4,448 2,594 2,867 2,528 2,017 1,577 637 1,352 723 924 726

Provision for taxes on income $ 1,244 642 775 758 609 445 106 368 141 235 171

Income from continuing operations before

cumulative effect of accounting changes $ 3,199 1,950 2,082 1,764 1,401 1,127 529 981 579 684 551

Discontinued operations Ñ net of tax (20) 1,401 131 165 172 171 129 113 143 117 130

Cumulative effect of accounting changes Ñ Ñ Ñ Ñ Ñ Ñ Ñ (283)(2) Ñ Ñ Ñ

Net income $ 3,179 3,351 2,213 1,929 1,573 1,298 658 811 722 801 681

Effective tax rate Ñ continuing operations 28.0% 24.8% 27.0% 30.0% 30.2% 28.2% 16.6% 27.2% 19.5% 25.4% 23.6%

Depreciation $ 473 420 363 309 277 236 206 209 183 167 160

Property, plant and equipment additions 1,561 1,198 878 690 635 620 575 592 505 466 388

Cash dividends paid 1,148 976 881 771 659 594 536 487 437 397 364

As of December 31

Working capital(3) $ 2,006 2,739 2,448 1,914 1,787 1,582 1,875 2,749 1,978 1,920 2,026

Property, plant and equipment Ñ net 5,343 4,415 3,793 3,456 3,113 2,747 2,320 1,994 2,061 1,808 1,565

Total assets(3) 20,574 18,302 14,991 14,251 12,339 10,797 8,986 9,346 9,387 8,782 8,099

Long-term debt 525 527 725 681 828 604 571 571 393 189 181

Long-term capital(4) 9,738 9,551 8,819 7,907 6,518 5,150 4,643 5,453 5,725 5,643 5,034

ShareholdersÕ equity 8,887 8,810 7,933 6,954 5,506 4,324 3,866 4,719 5,026 5,092 4,536

Per common share data:

Basic:

Income from continuing operations

before effect of accounting changes $ .85 .51 .55 .47 .38 .31 .14 .25 .15 .17 .14

Discontinued operations Ñ net of tax (.01) .37 .04 .05 .05 .04 .03 (.04)(2) .03 .03 .03

Net income $ .84 .88 .59 .52 .43 .35 .17 .21 .18 .20 .17

Diluted:

Income from continuing operations

before effect of accounting changes $ .82 .49 .53 .46 .37 .30 .14 .24 .14 .17 .14

Discontinued operations Ñ net of tax Ñ .36 .04 .04 .05 .05 .03 (.04)(2) .04 .03 .03

Net income $ .82 .85 .57 .50 .42 .35 .17 .20 .18 .20 .17

Market value per share (December 31) $ 32.44 41.67 24.85 13.83 10.50 6.44 5.75 6.04 7.00 3.37 2.90

Return on shareholdersÕ equity 35.9% 40.0% 29.7% 31.0% 32.0% 31.7% 15.3% 16.6% 14.3% 16.6% 15.4%

Cash dividends paid per share $ .302Ú3 .251Ú3 .222Ú3 .20 .171Ú3 .152Ú3 .14 .121Ú3 .11 .10 .091Ú3

ShareholdersÕ equity per share $ 2.36 2.33 2.10 1.85 1.48 1.18 1.04 1.21 1.27 1.29 1.14

Current ratio 1.22:1 1.38:1 1.49:1 1.36:1 1.37:1 1.35:1 1.60:1 1.92:1 1.62:1 1.67:1 1.75:1

Weighted average shares used to calculate:

Basic earnings per share amounts 3,775 3,789 3,771 3,743 3,687 3,670 3,785 3,948 3,963 3,966 3,972

Diluted earnings per share amounts 3,884 3,945 3,909 3,864 3,777 3,729 3,845 4,038 4,072 4,046 4,073

Employees of continuing operations (thousands) 51 46 41 39 37 34 33 33 35 33 33

Total revenues per employee (thousands) $ 318 292 269 256 238 202 184 177 154 145 129

All financial information reflects the divestitures of our MTG and food science businesses as discontinued operations.

We have restated all common share and per share data for the 1999, 1997, 1995 and 1991 stock splits.

(1)

Divestitures, restructuring and unusual items Ñ net includes the following:

1993 Ñ Pre-tax charges of approximately $745 million and $56 million to cover worldwide restructuring programs, as well as unusual items and a gain of

approximately $60 million realized on the sale of our remaining interest in Minerals Technologies Inc.

1992Ñ Pre-tax gain of $259 million on the sale of a business, offset by pre-tax charges of $175 million for restructuring, consolidating and streamlining.

In addition, it includes pre-tax curtailment gains of $57 million associated with postretirement benefits other than pensions of divested operations.

1991Ñ A pre-tax charge of $300 million for potential future Shiley C/C heart valve fracture claims.

(2)

Accounting changes adopted January 1, 1992: SFAS No. 106 Ñ charge of $313 million or $.08 per share; SFAS No. 109 Ñ credit of $30 million or $.01 per share.

Per share amounts of accounting changes are included in per share amounts presented for discontinued operations.

(3)

Includes net assets of discontinued operations of our MTG businesses through 1997.

(4)

Defined as long-term debt, deferred taxes on income, minority interests and shareholdersÕ equity.







62

Directors, Committees, and Officers

Pfizer’s Board of Directors is frequently recognized as one of the best in the

United States. In 1999, for example, the Pfizer Board was named one of “Five

Champion Boards” by Corporate Board Member magazine. In 2000, Business

Week magazine named the Pfizer Board to its “Top 25 Best Boards” list.







Board of Directors William C. Steere, Jr. (1) Loretta V. Cangialosi

Chairman and Chief Executive Officer – Vice President and Controller

Michael S. Brown, M.D. (4)

Pfizer Inc Gary N. Jortner

Distinguished Chair – Biomedical Sciences;

Regental Professor – University of Texas Jean-Paul Vallès, Ph.D. (2) Vice President; Senior Vice President,

Southwestern Medical Center Chairman and Chief Executive Officer – Product Development –

Minerals Technologies Inc. Pfizer Pharmaceuticals Group

M. Anthony Burns (1, 3)

Chairman and Chief Executive Officer – J. Patrick Kelly

Ryder System, Inc. Vice President; Senior Vice President,

Elected Corporate Officers Worldwide Marketing –

W. Don Cornwell (2)

Pfizer Pharmaceuticals Group

Chairman and Chief Executive Officer – William C. Steere, Jr.**

Granite Broadcasting Corporation Chairman of the Board and Chief Alan G. Levin

Executive Officer Vice President and Treasurer

George B. Harvey (2)

Former Chairman, President, and Chief Henry A. McKinnell, Ph.D.** Craig Saxton, M.D.

Executive Officer – Pitney Bowes Inc. President and Chief Operating Officer; Vice President; Executive Vice President –

President – Central Research

Constance J. Horner (1, 4)

Guest Scholar – The Brookings Pfizer Pharmaceuticals Group Mohand Sidi Said

Institution; Former Assistant to the John F. Niblack, Ph.D.** Vice President; Senior Vice President –

President of the United States Vice Chairman Pfizer Pharmaceuticals Group and Area

President, Asia/Africa/Middle East

Stanley O. Ikenberry, Ph.D. (1, 4) C. L. Clemente**

President – Executive Vice President – Corporate Frederick W. Telling, Ph.D.

American Council on Education Affairs; Secretary and Corporate Counsel Vice President – Corporate Strategic

Planning and Policy

Harry P. Kamen (4) Karen L. Katen**

Former Chairman, President, and Chief Senior Vice President; Executive Vice

Executive Officer – Metropolitan Life President – Pfizer Pharmaceuticals (1) Executive Committee*

Insurance Company Group and President – (2) Audit Committee

Thomas G. Labrecque (3) U.S. Pharmaceuticals

(3) Executive Compensation Committee

Former Chairman – Paul S. Miller** (4) Corporate Governance Committee

The Chase Manhattan Corporation Executive Vice President;

Henry A. McKinnell, Ph.D. General Counsel All directors are alternate members of the

*

President and Chief Operating Officer – George M. Milne, Jr., Ph.D.** Executive Committee

Pfizer Inc; President, Pfizer Senior Vice President; President – ** Member, Corporate Management

Pharmaceuticals Group Central Research Committee



Dana G. Mead, Ph.D. (3) William J. Robison**

Chairman – Tenneco Automotive Inc. Executive Vice President –

and Pactiv Corporation Employee Resources

John F. Niblack, Ph.D. David L. Shedlarz**

Vice Chairman – Pfizer Inc Executive Vice President –

Franklin D. Raines (2) Chief Financial Officer

Chairman and Chief Executive Officer – Brian W. Barrett

Fannie Mae Vice President; President –

Ruth J. Simmons, Ph.D. (2) Animal Health Group

President – Smith College M. Kenneth Bowler, Ph.D.

Vice President –

Federal Government Relations 63

Corporate and Shareholder Information

Stock Listings Annual Meeting of Shareholders Help Lines

Our Common Stock is listed on the New Our Annual Meeting will be held on Consumers or health care professionals

York Stock Exchange. It is also listed on the Thursday, April 27, 2000, at 10:00 a.m., who have questions about any of our

London, Paris, Brussels, and Swiss stock in The Empire State Ballroom, The medicines should call: (800) 438 1985.

exchanges. Our Common Stock is also Grand Hyatt, 42nd Street at Lexington People interested in receiving literature

traded on various United States regional Avenue, New York City. Detailed infor- about us should call: (800) PFE 4717.

stock exchanges. mation about the meeting is contained

in our Notice of Annual Meeting and The Legend of Pfizer

Shareholder Services and Programs joint proxy statement/prospectus. The Legend of Pfizer, part of a series of

All inquiries concerning shareholder corporate profiles by Jeffrey L. Rodengen,

accounts and stock transfer matters, Political Action Committee chronicles Pfizer’s evolution from a small

including direct deposit of dividends and You can receive a copy of the report of fine-chemicals company founded in 1849

the elimination of duplicate mailings of campaign contributions made by the

Annual Reports, should be directed to Company’s Political Action Committee

our Transfer Agent and Registrar: in 1999 by contacting the office of the

First Chicago Trust Company, Secretary, Pfizer Inc.

a division of EquiServe

P.O. Box 2500 1999 Environmental, Health and

Jersey City, NJ 07303-2500 Safety Report

Telephone: (800) PFE 9393 Pfizer takes great pride in its environ-

Internet: www.fctc.com mental, health and safety performance.

A new report has been published detailing

Direct Purchase Program the Company’s efforts to protect the

You may purchase your first shares of environment and provide a safe and

Pfizer directly through our Shareholder healthy workplace for employees. You

Investment Program. Other features of can receive a copy of the report by

the Program include dividend reinvest- calling (800) PFE 4717.

ment, weekly purchases of stock, and to its current position as a world

automatic monthly investments by elec- leader in pharmaceuticals. This 160-page

tronic bank debit. Contact First Chicago book includes a foreword by Pfizer

at the address given on this page for a Chairman William C. Steere, Jr., and is

Shareholder Investment Program illustrated with black-and-white and

prospectus and enrollment form. color photography. You may purchase a

copy at discount from the publisher,

Form 10-K Write Stuff Syndicate, Inc., by calling

Upon written request, we will provide (800) 900 2665, or ordering online at

without charge to each shareholder a copy www.writestuffbooks.com. Mention

of our Annual Report on Securities and Pfizer’s Annual Report to receive 15%

Exchange Commission Form 10-K for off the $39.95 cover price.

the fiscal year ended December 31, 1999.

Requests should be directed to:

Secretary

All trademarks in this publication are or have

Pfizer Inc been used by Pfizer Inc, with the exception of the

235 East 42nd Street following: Aricept is a trademark of Eisai Co., Ltd.;

New York, NY 10017-5755 Celebrex is a trademark of G.D. Searle & Co.,

a division of Monsanto Company; Lipitor is a

The report will also be available on trademark of Warner-Lambert Company.

the Securities and Exchange

Commission’s EDGAR database at Design: Conceptual Annual Reports/Hoi L. Chu, NYC.

Photography: principal, Neil Selkirk; additional,

www.sec.gov/edgarhp.htm. William Vázquez; Bruce Johnson; Stone – Chad

Ehlers; PF Sports Images.



10 %

TOTAL RECOVERED FIBER







64

Ensuring Access to Innovative Medicines

“Lifesaving drugs are an indispensable part yield new drugs to treat virtually every Canadian government’s top priority.

of modern medicine,” President Clinton disease. Heavy-handed government Frustrated with an overburdened public

said in his most recent State of the Union interference would stifle the discovery of health system, which now has surgery

address. And he’s absolutely right. those new medicines by diminishing the waiting lists stretching for months,

That’s the main reason why Americans resources available for research. many Canadians travel to the United

are spending more on pharmaceuticals. And significant resources are required. States to seek private care. While

It has little to do with higher prices for On average, it takes $500 million to bring American health care delivery is not

medicines. Pfizer’s price increases have one new drug to market. Last year alone, perfect, it is still the envy of the world.

been less than the overall rate of inflation Pfizer invested about $2.8 billion to Nonetheless, we must continue to

since 1994, accounting for discounts to discover new medicines. In the absence improve access. It must be adjusted to

federal buyers and Medicaid. What is of rigorous reinvestment, new drugs will meet the needs of those seniors who are

driving pharmaceutical spending growth be delayed or simply go undiscovered. without prescription drug coverage, but

in the United States is a significant In Canada, the government-controlled the issue is not one fundamentally of

increase in the utilization of medicines. health care system has depressed R&D prices. For its part, Pfizer has announced

Medicines such as Lipitor, Zoloft, and and resulted in significant delays in the that there will be no price increases for

Celebrex mark significant improvements approvals of innovative medicines from three of its pharmaceuticals sold in the

over previous therapies, and more and the United States. When governments set U.S. market in 2000 and only a modest

more Americans are relying on these and the price of pharmaceuticals, bureaucrats 3.1% increase for our other medicines.

dozens of other breakthrough pharmaceu- often use the

ticals to live longer and healthier lives. approval and reim- What is driving pharmaceutical

The question before the nation now bursement process

is how best to provide access to these as a cost-savings spending growth in the United

medicines for the seniors who need them.

In developing such a policy, it’s important

device by keeping

new products off

States is a significant increase in

to keep in mind that two thirds of seniors the markets. For the utilization of medicines.

already have prescription drug coverage. instance, six medi-

There’s no need to revamp a system cines recently introduced in the United Our best estimate is that these price

that’s already working for most of its States, five of which have no therapeutic changes, combined with the impact of

participants. But there is need to fine-tune alternative, are not available in Canada. discounts to federal buyers and the

it so the remaining senior population — On average, Canadians wait a full year Medicaid program, will result in an

about 13 million people — can also have longer than Americans before new effective average price increase of 2.5%,

access to all FDA-approved medicines. pharmaceuticals are approved and reim- which is equal to the December 1999

Pfizer supports a variety of approaches, bursed by the government, if they are Blue Chip Consensus forecast of the

including: approved at all. By delaying and denying change in the Consumer Price Index for

• Expanded Insurance Alternatives — access to innovative medicines, the the year 2000.

These could be developed by private Canadian health care system has narrowed We are on the threshold of a phar-

insurers with subsidies given to low- the range of medicines available to patients. maceutical revolution in the treatment of

income elderly. Yet, despite stringent government disease. By pursuing — in a spirit of

• Tax Code Changes — Credits or control, Canadians still pay about the compromise and pragmatism — proposals

deductions could subsidize the cost of same percentage of their income as that expand access while preserving

prescription drug insurance. Americans to purchase pharmaceuticals. incentives for research, the United States

• State-based Solutions — Federal While it’s true many things cost less in can provide prescription drug coverage

grants to the 50 states could provide Canada — such as fast food, a quality for seniors who need it and maintain our

funds to create drug-access programs university education, and some pharma- status as the world’s leader in pharma-

for low-income residents. ceuticals — it’s also true that Canadians ceutical innovation.

Whatever approach is adopted, it’s earn considerably less than Americans. These issues will have tremendous

essential that it preserve the research Nor have price controls improved impact on the owners of Pfizer, not only

pharmaceutical industry’s capacity to overall medical services in Canada. In a as shareholders but also as patients and

discover new medicines. Not only has recent survey, most Canadians polled taxpayers. If you’d like to learn more and

the industry significantly extended and said their nation’s health care system was find out how you can become involved,

enhanced human life, it’s now poised to “in crisis.” In another survey, 93% said fill out and return either or both of the

enter a golden age of discovery that will that improving health care should be the attached response cards.





65


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