PFIZER INC
For the period ended Sep 28, 2025. Filed Nov 4, 2025.
View on SEC.govAbout this filing
A company's report for each of its first three quarters. The financial statements are not audited. It shows how the business has moved since the last annual report, and what management says changed.
Sep 28, 2025 · Filed Nov 4, 2025
Extracted filing text, with the paragraph anchors used by the comparison.
See the whole filing, with its images and exhibitsContents
Total Revenues––Selected Product Discussion
Biopharma
| (MILLIONS) · Revenue · % Change | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Product · Period · GlobalRevenues · Region · Sept. 28, 2025 · Sept. 29, 2024 · Total · Oper. · Operational Results Commentary | ||||||||||||
| Eliquis | QTD | $2,015Up 22%(operationally) | U.S. | $1,292 | $1,002 | 29 | QTD growth primarily driven by higher demand globally and favorable net price in the U.S. as a result of the expected favorable year-over-year impact of the elimination of the coverage gap as part of the IRA Medicare Part D Redesign, partially offset by generic entry and price erosion in certain international markets.YTD growth driven by higher demand globally, partially offset by lower net price in the U.S., including the impact of higher chargebacks, generic entry and price erosion in certain international markets. | |||||
| Int’l. | 723 | 616 | 17 | 11 | ||||||||
| Worldwide | $2,015 | $1,617 | 25 | 22 | ||||||||
| YTD | $5,941Up 7%(operationally) | U.S. | $3,913 | $3,677 | 6 | |||||||
| Int’l. | 2,028 | 1,857 | 9 | 8 | ||||||||
| Worldwide | $5,941 | $5,534 | 7 | 7 | ||||||||
| (MILLIONS) · Revenue · % Change | |||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Product · Period · GlobalRevenues · Region · Sept. 28, 2025 · Sept. 29, 2024 · Total · Oper. · Operational Results Commentary | |||||||||||||||
| Prevnar family | QTD | $1,742Down 4%(operationally) | U.S. | $1,155 | $1,308 | (12) | QTD decline primarily driven by timing of pediatric CDC shipments in the U.S., coupled with lower demand, partially offset by higher market share and timing of shipments in the pediatric indication in certain international markets, continued uptake of the adult indication in the U.S. as a result of strong demand following the CDC’s recommendation for ages 50-64 and strong uptake of the adult indication in certain international markets.YTD decline primarily driven by worldwide lower pediatric indication sales mostly due to timing of CDC shipments in the U.S., as well as timing of shipments and competitive pressure in certain international markets, partially offset by strong uptake of the adult indication in the U.S. as a result of strong demand following the CDC’s recommendation for ages 50-64, coupled with strong uptake of the adult indication in certain international developed markets as well as new launches of the pediatric indication in certain emerging markets. | ||||||||
| Int’l. | 587 | 495 | 18 | 17 | |||||||||||
| Worldwide | $1,742 | $1,803 | (3) | (4) | |||||||||||
| YTD | $4,786Down 1%(operationally) | U.S. | $3,185 | $3,289 | (3) | ||||||||||
| Int’l. | 1,601 | 1,564 | 2 | 3 | |||||||||||
| Worldwide | $4,786 | $4,853 | (1) | (1) | |||||||||||
| Vyndaqel family | QTD | $1,591Up 7%(operationally) | U.S. | $948 | $960 | (1) | Growth primarily driven by strong demand with continuing uptake in patient diagnosis primarily in the U.S. and certain international developed markets, as well as improved patient affordability in the U.S., partially offset by lower net price in the U.S. mostly due to the impact of higher manufacturer discounts resulting from the IRA Medicare Part D Redesign as well as new payer contracts. | ||||||||
| Int’l. | 643 | 486 | 32 | 25 | |||||||||||
| Worldwide | $1,591 | $1,447 | 10 | 7 | |||||||||||
| YTD | $4,692Up 19%(operationally) | U.S. | $2,924 | $2,572 | 14 | ||||||||||
| Int’l. | 1,767 | 1,334 | 32 | 31 | |||||||||||
| Worldwide | $4,692 | $3,907 | 20 | 19 | |||||||||||
| Ibrance | QTD | $1,057Down 5%(operationally) | U.S. | $670 | $717 | (7) | Declines primarily driven by lower net price in the U.S. largely due to the impact of higher manufacturer discounts resulting from the IRA Medicare Part D Redesign, as well as generic entry in certain international markets, partially offset by a favorable one-time adjustment of rebate accruals related to prior periods internationally recorded in the third quarter of the current year as well as improved patient affordability in the U.S. | ||||||||
| Int’l. | 387 | 371 | 4 | (1) | |||||||||||
| Worldwide | $1,057 | $1,087 | (3) | (5) | |||||||||||
| YTD | $3,083Down 6%(operationally) | U.S. | $2,024 | $2,136 | (5) | ||||||||||
| Int’l. | 1,058 | 1,135 | (7) | (8) | |||||||||||
| Worldwide | $3,083 | $3,272 | (6) | (6) | |||||||||||
| Paxlovid | QTD | $1,225Down 55%(operationally) | U.S. | $1,122 | $2,313 | (52) | QTD and YTD declines primarily driven by:• lower COVID-19 infections across U.S. and international markets and lower international government purchases; and• the non-recurrence of a $442 million favorable U.S. government stockpile purchase in the third quarter of 2024,partially offset by:• favorable adjustments of rebate accruals related to prior periods, as well as higher net price in the U.S. following transition from the U.S. government agreement.YTD decline also driven by the non-recurrence of a $771 million favorable final adjustment recorded in the first quarter of 2024 to the estimated non-cash revenue reversal of $3.5 billion recorded in the fourth quarter of 2023. | ||||||||
| Int’l. | 104 | 389 | (73) | (73) | |||||||||||
| Worldwide | $1,225 | $2,703 | (55) | (55) | |||||||||||
| YTD | $2,144Down 57%(operationally) | U.S. | $1,796 | $4,181 | (57) | ||||||||||
| Int’l. | 347 | 807 | (57) | (56) | |||||||||||
| Worldwide | $2,144 | $4,989 | (57) | (57) | |||||||||||
| Comirnaty | QTD | $1,151Down 20%(operationally) | U.S. | $870 | $1,164 | (25) | QTD decline mainly due to a narrower recommendation for vaccination in the U.S., as well as delayed approval of the new variant vaccine, partially offset by a lower returns provision and higher market share in the U.S., as well as higher contractual deliveries in certain international marketsYTD growth primarily driven by higher contractual deliveries in certain international markets and favorable returns reserve reversal and higher market share in the U.S., partially offset by delayed approval of the new variant vaccine as well as a narrower recommendation for vaccination in the U.S. | ||||||||
| Int’l. | 282 | 258 | 9 | 5 | |||||||||||
| Worldwide | $1,151 | $1,422 | (19) | (20) | |||||||||||
| YTD | $2,097Up 6% (operationally) | U.S. | $1,275 | $1,339 | (5) | ||||||||||
| Int’l. | 821 | 631 | 30 | 30 | |||||||||||
| Worldwide | $2,097 | $1,970 | 6 | 6 | |||||||||||
| Xtandi | QTD | $578Up 3%(operationally) | U.S. | $578 | $561 | 3 | Growth mainly driven by strong demand, in part due to improved patient affordability in the U.S., partially offset by unfavorable buying patterns and lower net price partly due to the impact of higher manufacturer discounts resulting from the IRA Medicare Part D Redesign. | ||||||||
| Int’l. | — | — | — | — | |||||||||||
| Worldwide | $578 | $561 | 3 | 3 | |||||||||||
| YTD | $1,602Up 9%(operationally) | U.S. | $1,602 | $1,474 | 9 | ||||||||||
| Int’l. | — | — | — | — | |||||||||||
| Worldwide | $1,602 | $1,474 | 9 | 9 | |||||||||||
| Padcev | QTD | $464Up 13%(operationally) | U.S. | $449 | $407 | 10 | QTD and YTD growth primarily driven by increased market share in first line locally advanced or metastatic urothelial cancer (la/mUC).YTD growth also driven by a one-time favorable impact associated with transition to a wholesaler distribution model in the U.S. | ||||||||
| Int’l. | 16 | 2 | * | * | |||||||||||
| Worldwide | $464 | $409 | 13 | 13 | |||||||||||
| YTD | $1,432Up 25%(operationally) | U.S. | $1,402 | $1,128 | 24 | ||||||||||
| Int’l. | 30 | 16 | 88 | 89 | |||||||||||
| Worldwide | $1,432 | $1,144 | 25 | 25 | |||||||||||
| (MILLIONS) · Revenue · % Change | ||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Product · Period · GlobalRevenues · Region · Sept. 28, 2025 · Sept. 29, 2024 · Total · Oper. · Operational Results Commentary | ||||||||||||||
| Nurtec ODT/Vydura | QTD | $412Up 22%(operationally) | U.S. | $383 | $314 | 22 | Growth primarily driven by strong demand in the U.S. and recent launches in certain international markets, partially offset by lower net price in the U.S. mainly due to unfavorable changes in channel mix. | |||||||
| Int’l. | 29 | 23 | 26 | 22 | ||||||||||
| Worldwide | $412 | $337 | 22 | 22 | ||||||||||
| YTD | $1,019Up 17%(operationally) | U.S. | $945 | $820 | 15 | |||||||||
| Int’l. | 74 | 50 | 49 | 48 | ||||||||||
| Worldwide | $1,019 | $870 | 17 | 17 | ||||||||||
| Xeljanz | QTD | $313Down 4%(operationally) | U.S. | $205 | $203 | 1 | Declines primarily driven by lower demand and price erosion across international developed markets, lower net price in the U.S. due to unfavorable changes in channel mix as well as the impact of higher manufacturer discounts resulting from the IRA Medicare Part D Redesign, partially offset by higher volumes in the U.S. | |||||||
| Int’l. | 108 | 118 | (9) | (13) | ||||||||||
| Worldwide | $313 | $321 | (3) | (4) | ||||||||||
| YTD | $763Down 7%(operationally) | U.S. | $431 | $459 | (6) | |||||||||
| Int’l. | 331 | 360 | (8) | (8) | ||||||||||
| Worldwide | $763 | $818 | (7) | (7) | ||||||||||
| Lorbrena | QTD | $268Up 28%(operationally) | U.S. | $103 | $82 | 25 | Growth primarily driven by increased patient share in the first-line ALK+ metastatic NSCLC treatment setting in the U.S., China and certain other international markets, partially offset by lower net price in the U.S. mainly due to the impact of higher manufacturer discounts resulting from the IRA Medicare Part D Redesign. | |||||||
| Int’l. | 165 | 124 | 34 | 30 | ||||||||||
| Worldwide | $268 | $206 | 30 | 28 | ||||||||||
| YTD | $741Up 38%(operationally) | U.S. | $294 | $211 | 39 | |||||||||
| Int’l. | 447 | 327 | 37 | 37 | ||||||||||
| Worldwide | $741 | $538 | 38 | 38 | ||||||||||
| Adcetris | QTD | $215Down 20%(operationally) | U.S. | $210 | $260 | (19) | QTD and YTD declines primarily driven by lower volume due to competitive pressures in the U.S. as a result of changes of guidelines in 2024. The YTD decline was partially offset by a one-time favorable impact associated with transition to a wholesaler distribution model in the U.S. | |||||||
| Int’l. | 5 | 8 | (37) | (37) | ||||||||||
| Worldwide | $215 | $268 | (20) | (20) | ||||||||||
| YTD | $687Down 14%(operationally) | U.S. | $671 | $784 | (14) | |||||||||
| Int’l. | 16 | 20 | (21) | (18) | ||||||||||
| Worldwide | $687 | $804 | (15) | (14) | ||||||||||
| Abrysvo | QTD | $279Down 22%(operationally) | U.S. | $210 | $318 | (34) | QTD decline primarily driven by lower vaccination rates for the older adult indication in the U.S. following an updated ACIP recommendation, partially offset by launch uptake for both the maternal and adult indications in certain international markets.YTD performance primarily driven by lower vaccination rates for the older adult indication following an updated ACIP recommendation in the U.S., offset by increased market share in the adult indication, higher demand in the maternal indication —both in the U.S.— and launch uptake for both adult and maternal indications in certain international markets. | |||||||
| Int’l. | 68 | 38 | 81 | 75 | ||||||||||
| Worldwide | $279 | $356 | (22) | (22) | ||||||||||
| YTD | $553Flat(operationally) | U.S. | $374 | $490 | (24) | |||||||||
| Int’l. | 178 | 66 | * | * | ||||||||||
| Worldwide | $553 | $557 | (1) | — | ||||||||||
Pfizer CentreOne
| (MILLIONS) · Revenue · % Change | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Operating Segment · Period · GlobalRevenues · Region · Sept. 28, 2025 · Sept. 29, 2024 · Total · Oper. · Operational Results Commentary | |||||||||
| PC1 | QTD | $344Up 18%(operationally) | U.S. | $92 | $76 | 21 | Growth driven by higher manufacturing of third-party products under manufacturing and supply agreements, higher manufacturing-related services and higher active pharmaceutical ingredient sales. | ||
| Int’l. | 253 | 210 | 21 | 17 | |||||
| Worldwide | $344 | $285 | 21 | 18 | |||||
| YTD | $929Up 13%(operationally) | U.S. | $245 | $195 | 25 | ||||
| Int’l. | 684 | 625 | 9 | 9 | |||||
| Worldwide | $929 | $820 | 13 | 13 | |||||
See the Item 1. Business—Patents and Other Intellectual Property Rights section of our 2024 Form 10-K for information regarding the expiration of various patent rights, Note 12 for a discussion of recent developments concerning patent and product litigation relating to certain of the products discussed above and Note 13C for additional information regarding the primary indications or class of the selected products discussed above.
Costs and Expenses
| Three Months Ended · Nine Months Ended | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| (MILLIONS) · September 28,2025 · September 29,2024 · % Change · September 28,2025 · September 29,2024 · % Change | |||||||||
| Cost of sales | $4,172 | $5,263 | (21) | $10,795 | $11,942 | (10) | |||
| Percentage of Total revenues | 25.0% | 29.7% | 24.0% | 26.0% | |||||
| Selling, informational and administrative expenses | 3,186 | 3,244 | (2) | 9,632 | 10,456 | (8) | |||
| Research and development expenses | 2,546 | 2,598 | (2) | 7,231 | 7,787 | (7) | |||
| Acquired in-process research and development expenses | 1,390 | 13 | * | 1,401 | 20 | * | |||
| Amortization of intangible assets | 1,223 | 1,312 | (7) | 3,644 | 3,927 | (7) | |||
| Restructuring charges and certain acquisition-related costs | 286 | 313 | (9) | 945 | 1,669 | (43) | |||
| Other (income)/deductions—net | 517 | 243 | * | 2,210 | 2,030 | 9 | |||
Third Quarter of 2025 vs. Third Quarter of 2024 and First Nine Months of 2025 vs. First Nine Months of 2024
Cost of Sales
Cost of sales decreased $1.1 billion in the third quarter of 2025, primarily due to:
a favorable change in sales mix of $760 million, driven by lower sales of Comirnaty and Paxlovid, including the non-recurrence of a charge recorded in the third quarter of 2024 that was included in the 50% gross profit split with BioNTech and applicable royalty expenses;
a favorable revision of our estimate of accrued royalties; and
a decrease of $230 million due to lower amortization from the step-up of acquired inventory,
partially offset by:
a $260 million unfavorable impact of foreign exchange.
The decrease in Cost of sales as a percentage of revenues in the third quarter of 2025 was primarily due to the factors mentioned above.
Cost of sales decreased $1.1 billion in the first nine months of 2025, primarily due to:
a decrease of $540 million due to lower amortization from the step-up of acquired inventory;
the non-recurrence of charges in the first nine months of 2024 that were included in the 50% gross profit split with BioNTech and applicable royalty expenses; and
net favorable revisions to our estimate of accrued royalties.
The decrease in Cost of sales as a percentage of revenues in the first nine months of 2025 was primarily due to all the factors discussed above, partially offset by the non-recurrence of the Paxlovid favorable final adjustment of $771 million recorded in the first quarter of 2024 to the estimated non-cash Paxlovid revenue reversal recorded in the fourth quarter of 2023 and unfavorable sales mix.
Certain of our vaccines, including Comirnaty, are subject to seasonality of demand, with a greater portion of revenues and related cost of sales anticipated in the fall and winter seasons.
See also the Overview of Our Performance, Operating Environment, Strategy and Outlook—The Global Economic Environment––COVID-19 section for information about our COVID-19 products.
Selling, Informational and Administrative Expenses
Selling, informational and administrative expenses decreased $59 million in the third quarter and $824 million in the first nine months of 2025, primarily reflecting focused investments and ongoing productivity improvements as part of our cost realignment program that drove:
a decrease of $260 million in the third quarter and $720 million in the first nine months in marketing and promotional spend on various products; and
lower spending of $85 million in the third quarter and $370 million in the first nine months in corporate enabling functions,
partially offset by:
increases of $260 million in the third quarter and $235 million in the first nine months due to a favorable adjustment of U.S. healthcare reform fees recorded in the third quarter of 2024 primarily related to Paxlovid and Comirnaty.
Research and Development Expenses
Research and development expenses decreased $52 million in the third quarter and $556 million in the first nine months of 2025 primarily driven by a net decrease in spending of $90 million in the third quarter and $590 million in the first nine months due to pipeline focus and optimization including the expansion of our digital capabilities, as well as lower compensation-related expenses.
Acquired In-Process Research and Development Expenses
Acquired in-process research and development expenses increased $1.4 billion in the third quarter and in the first nine months of 2025 primarily driven by a $1.35 billion charge related to an in-licensing agreement with 3SBio.
Restructuring Charges and Other Costs Associated with Acquisitions and Cost-Reduction/Productivity Initiatives
Realigning Our Cost Base Program––This program is expected to deliver total net cost savings of approximately $5.7 billion through 2027. The total net cost savings are composed of: (i) net cost savings of $4.5 billion expected to be achieved by the end of 2025, most of which was achieved by year-end 2024, and (ii) our additional anticipated net cost savings of $1.2 billion, primarily in SI&A, expected to be achieved by the end of 2027. In addition, we expect cost savings of approximately $500 million from the expansion of this program in the first quarter of 2025 related to our R&D re-organization to be fully realized by the end of 2026, with the savings expected to be reinvested in R&D programs by the end of 2026.
Manufacturing Optimization Program––The first phase of this multi phased program is on track to deliver approximately $1.5 billion in net cost savings by the end of 2027, contributing savings in the third quarter of 2025.
Certain qualifying costs for these programs in all periods since inception were recorded and reflected as Certain Significant Items and excluded from our non-GAAP measure of Adjusted Income. See the Non-GAAP Financial Measure: Adjusted Income section within MD&A.
For a description of our programs, as well as the anticipated and actual costs, see Note 3. The program savings discussed above may be rounded and represent approximations. In addition to these programs, we continuously monitor our operations for cost reduction and/or productivity opportunities, especially in light of patent-based and regulatory exclusivity expiries as well as the expiration of collaborative arrangements for various products. Long-term improvement in gross margin will remain a key focus for the Company over the next few years.
Seagen acquisition––In connection with our acquisition of Seagen, we are focusing our efforts on achieving an appropriate cost structure for the combined company. We expect to generate approximately $1 billion of annual cost synergies, to be achieved by the end of 2026. The one-time costs to generate these synergies are expected to be approximately $1.7 billion, incurred primarily from 2023 through 2025.
Other (Income)/Deductions—Net
The unfavorable period-over-period change of $275 million in the third quarter of 2025 was primarily driven by (i) an intangible asset impairment charge in the third quarter of 2025, (ii) lower net gains on equity securities, (iii) the non-recurrence of equity method income in the third quarter of 2024 from our previous investment in Haleon and (iv) higher charges for certain legal matters, partially offset by (v) a non-recurrence of a charge in the third quarter of 2024 related to the expected sale of one of our facilities resulting from the discontinuation of our DMD program and (vi) lower net interest expense.
The unfavorable period-over-period change of $180 million for the first nine months of 2025 was primarily driven by (i) higher charges for certain legal matters, (ii) higher intangible asset impairments, (iii) net losses on equity securities in 2025 versus net gains on equity securities in 2024, (iv) the non-recurrence of a realized gain on the partial sale of our previous investment in Haleon recorded in the first quarter of 2024 and (v) the non-recurrence of equity method income from our previous investment in Haleon, partially offset by (vi) lower net interest expense and (vii) a non-recurrence of a charge in the third quarter of 2024 related to the expected sale of one of our facilities resulting from the discontinuation of our DMD program. See Note 4.
The text of this filing, as the company filed it with the SEC, without its images or exhibits. This is not investment advice.