Bristol Myers Squibb · Earnings release · 8-K Exhibit 99

EX-99.12a2025q3ex991.htmPRESS RELEASE OF BRISTOL-MYERS SQUIBB COMPANY DATED OCTOBER 30, 2025 Document

Bristol Myers Squibb Reports Third Quarter Financial Results for 2025

Performance Marked by Continued Growth Portfolio Momentum, Pipeline Advancements and Strategic Business Development

•Third quarter revenues increased 3% (+2% Ex-FX) to $12.2 billion

◦Growth Portfolio revenues increased 18% (+17% Ex-FX) to $6.9 billion

•GAAP EPS was $1.08 and non-GAAP EPS was $1.63; Both figures include net impact of $(0.20) due to the Acquired IPRD charges and licensing income

•T1Raising 2025 revenue guidance to a range of ~$47.5 billion to $48.0 billion; Updating non-GAAP EPS range to $6.40 to $6.60, inclusive of an $(0.80) per share net impact from Acquired IPRD charges and licensing income

(PRINCETON, N.J., October 30, 2025) – Bristol Myers Squibb (NYSE: BMY) today reports results for the third quarter of 2025.

“We delivered strong results this quarter as a result of continued execution across the business and ongoing Growth Portfolio momentum,” said Christopher Boerner, Ph.D., board chair and chief executive officer, Bristol Myers Squibb. “We're focused on building for the future by accelerating innovation, advancing our pipeline, staying agile and delivering more transformational medicines to more patients."

Third Quarter Results

$ in millions, except per share amounts

Change

Change Excl. FX**

Total Revenues

3

%

2

%

Earnings/(Loss) Per Share - GAAP*

%

N/A

Earnings/(Loss) Per Share - Non-GAAP*

(9)

%

N/A

Acquired IPRD Charges and Licensing Income Net Impact on Earnings/(Loss) Per Share

N/A

N/A

*GAAP and Non-GAAP earnings/(loss) per share include the net impact of Acquired IPRD charges and licensing income.

**See "Use of Non-GAAP Financial Information".

1

THIRD QUARTER RESULTS

All comparisons are made versus the same period in 2024 unless otherwise stated.

•Growth Portfolio revenues of $6.9 billion increased 18%, or 17% Ex-FX. Revenue growth was primarily driven by our immuno-oncology (IO) portfolio, Reblozyl, Camzyos and Breyanzi.

•T2Legacy Portfolio revenues of $5.4 billion decreased 12%, or 13% Ex-FX. Demand increased for Eliquis, which was more than offset by expected continued generic impact across the remainder of the Legacy Portfolio.

•Total revenues of $12.2 billion increased 3%, or 2% Ex-FX.

◦U.S. revenues of $8.3 billion increased 1%.

◦International revenues of $3.9 billion increased 6%, or 3% Ex-FX.

THIRD QUARTER PRODUCT REVENUE HIGHLIGHTS(d)

($ amounts in millions)

% Change from Quarter Ended September 30, 2024

% Change from Quarter Ended September 30, 2024 Ex-FX**

U.S.

Int'l

WW(c)

U.S.

Int'l

WW(c)

Int'l

WW(c)

Growth Portfolio

Opdivo

$

$

$

6

%

8

%

7

%

6

%

6

%

Opdivo Qvantig

7

N/A

N/A

N/A

N/A

N/A

Orencia

2

%

6

%

3

%

3

%

2

%

Yervoy

%

%

%

%

%

Reblozyl

%

%

%

%

%

Opdualag

%

%

%

%

%

Breyanzi

%

%

%

%

%

Camzyos

%

%

%

%

%

Zeposia

8

%

%

9

%

6

%

7

%

Abecma

%

%

9

%

%

6

%

Sotyktu

—

%

%

%

%

%

Krazati

5

%

%

%

%

%

Cobenfy

—

N/A

N/A

N/A

N/A

N/A

Other Growth Products(a)

8

%

%

%

%

%

Total Growth Portfolio

%

%

%

%

%

Legacy Portfolio

Eliquis

%

%

%

%

%

Revlimid

%

%

%

%

%

Pomalyst/Imnovid

%

%

%

%

%

Sprycel

%

%

%

%

%

Abraxane

%

%

%

%

%

Other Legacy Products(b)

%

%

%

%

%

Total Legacy Portfolio

%

%

%

%

%

Total Revenues

$

$

$

1

%

6

%

3

%

3

%

2

%

** See "Use of Non-GAAP Financial Information".

(a) Includes Augtyro, Onureg, Inrebic, Nulojix, Empliciti and royalty revenues.

(b) Includes other mature brands.

(c) Worldwide (WW) includes U.S. and International (Int'l).

(d) For the above table and all subsequent tables, certain totals may not sum due to rounding. Percentages have been calculated using unrounded amounts.

2

THIRD QUARTER COST & EXPENSES

All comparisons are made versus the same period in 2024 unless otherwise stated.

The table below presents selected line-item information.

($ amounts in millions)

GAAP

Specified Items**

Non-GAAP

GAAP

Specified Items**

Non-GAAP

Cost of products sold

$

$

$

$

Gross margin(a)

%

%

%

%

Selling, general and administrative

(1)

(7)

Research and development

Acquired IPRD

—

—

Amortization of acquired intangible assets

—

—

Other (income)/expense, net

Effective tax rate

%

%

%

%

%

%

**See "Use of Non-GAAP Financial Information" and refer to the Specified Items schedule below for further detail.

(a) Represents revenue minus cost of products sold divided by revenue.

•Gross margin on a GAAP and non-GAAP basis was 71.9% and 72.9% in 2025, and 75.1% and 76.0% in 2024, respectively, reflecting the change in product mix.

•Selling, general and administrative expenses of $1.8 billion decreased 10% on a GAAP and non-GAAP basis, primarily driven by our ongoing strategic productivity initiative.

•Research and development expenses of $2.5 billion increased 6% on a GAAP basis, primarily due to an IPRD impairment charge. Non-GAAP research and development expenses of $2.4 billion increased 3%, primarily due to the impact of recent acquisitions, partially offset by our ongoing strategic productivity initiative.

•T3Acquired IPRD charges of $633 million increased from $262 million on a GAAP and non-GAAP basis, primarily driven by the Philochem licensing arrangement and achievement of a milestone under the SystImmune collaboration. Licensing income increased from $25 million to $107 million on a GAAP and non-GAAP basis, primarily reflecting the execution of an out-licensing arrangement in 2025.

•Amortization of acquired intangible assets of $831 million decreased 65% on a GAAP basis, primarily due to lower amortization expense related to Revlimid.

•Effective tax rate increased from 27.5% to 29.5% on a GAAP basis, and from 18.5% to 22.3% on a non-GAAP basis. The increase in the non-GAAP effective tax rate was driven by jurisdictional earnings mix.

•Net income attributable to Bristol Myers Squibb of $2.2 billion, or $1.08 per share, increased from $1.2 billion, or $0.60 per share, on a GAAP basis. On a non-GAAP basis, net income attributable to Bristol Myers Squibb of $3.3 billion, or $1.63 per share, decreased from

3

$3.7 billion, or $1.80 per share. GAAP and non-GAAP EPS include the impacts of Acquired IPRD charges and licensing income.

PRODUCT AND PIPELINE UPDATES

Entries organized by date and inclusive of third quarter and recent updates.

Asset(s)

Date Announced

Milestone

Sotyktu® (deucravacitinib)

52-week data from the pivotal Phase 3 POETYK PsA-1 trial demonstrated that Sotyktu improved and maintained meaningful clinical responses, inhibition of radiographic progression and patient-reported outcomes in adults with active psoriatic arthritis.

In addition, data from an integrated analysis of the Phase 2 PAISLEY-SLE and PAISLEY long-term extension studies supported the safety and efficacy with up to four years of Sotyktu treatment for moderate-to-severe systemic lupus erythematosus (SLE).

Announced positive, updated data and early results from the Phase 1 Breakfree-1 study evaluating BMS-986353, an investigational, autologous CD19-targeted NEX-T CAR T cell therapy, across the systemic sclerosis, SLE and idiopathic inflammatory myopathies cohorts. The preliminary Phase 1 safety and efficacy results are consistent with the potential for immune reset, showing robust CAR T cell expansion, complete B cell depletion and re-emergence of a naive B cell phenotype across all three cohorts.

izalontamab brengitecan

(iza-bren)

First disclosure of safety and efficacy data presented with SystImmune from the global Phase I US-Lung-101 study of iza-bren, a potentially first-in-class EGFR x HER3 bispecific antibody-drug conjugate, demonstrated promising antitumor activity in heavily pre-treated patients across multiple tumor types, as well as a manageable safety profile.

October 1

The U.S. Food and Drug Administration (FDA) granted Fast Track Designation to BMS-986446, a potential best-in-class, anti-microtubule binding region-tau antibody currently in Phase 2 development for the treatment of early Alzheimer’s disease.

Sotyktu

Announced an expansion of the company's direct-to-patient offerings, providing eligible U.S. patients with steeply discounted prices for Sotyktu via the new BMS Patient Connect platform, beginning January 2026.

iberdomide

The Phase 3 EXCALIBER-RRMM study evaluating iberdomide, an investigational cereblon E3 ligase modulator (CELMoD™), combined with standard therapies (daratumumab + dexamethasone) in patients with relapsed or refractory multiple myeloma demonstrated a statistically significant improvement in minimal residual disease (MRD) negativity rates, compared with the control arm, in a planned interim analysis of the MRD endpoint.

4

September 8

First disclosure of data presented with BioNTech SE from the global randomized Phase 2 trial (NCT06449209) evaluating pumitamig, an investigational bispecific antibody targeting PD-L1 x VEGF-A, plus chemotherapy in patients with extensive-stage small cell lung cancer demonstrated encouraging anti-tumor responses with a positive trend in the secondary endpoint of progression free survival.

Additionally, this week pivotal studies for pumitamig and chemotherapy combinations are now initiating in first-line (1L) microsatellite stable colorectal cancer and 1L gastric cancer.

Camzyos® (mavacamten)

Results from the global, retrospective COLLIGO-HCM study showed that Camzyos was associated with reductions in left ventricular outflow tract obstruction and improvements in symptom burden in a racially diverse population of patients with symptomatic obstructive hypertrophic cardiomyopathy treated in an international, real-world setting.

iza-bren

The FDA granted Breakthrough Therapy Designation to iza-bren for the treatment of locally advanced or metastatic non-small cell lung cancer with epidermal growth factor (EGFR) exon 19 deletions or exon 21 L858R substitution mutations whose disease has progressed on or after treatment with an EGFR tyrosine kinase inhibitor and platinum-based chemotherapy.

Breyanzi® (lisocabtagene maraleucel)

August 4

The FDA accepted the supplemental biologics license application for Breyanzi as a potential treatment for adult patients with relapsed or refractory marginal zone lymphoma who have received at least two prior lines of systemic therapy. The FDA granted the application Priority Review and assigned a Prescription Drug User Fee Act goal date of December 5, 2025.

Business Development

In October 2025, the company announced a definitive agreement to acquire Orbital Therapeutics. The acquisition includes OTX-201, Orbital’s lead RNA immunotherapy preclinical candidate currently in IND-enabling studies. This investigational, next-generation CAR T-cell therapy is designed to reprogram cells in vivo and has the potential to offer a best-in-class profile for treating autoimmune diseases, aligned with Bristol Myers Squibb’s overall immune reset strategy. This in vivo approach, in which the patient’s own body serves as the manufacturer of CAR T-cells, has the potential to offer a reduced treatment burden, added convenience and improved accessibility compared to ex vivo CAR T-cell therapies. Bristol Myers Squibb will also gain access to Orbital’s differentiated RNA technology platform that integrates advanced RNA engineering and delivery methods, offering the potential to expand therapeutic applications and address additional diseases. The transaction is subject to the satisfaction of customary closing conditions.

5

Financial Guidance

Bristol Myers Squibb is increasing its full-year 2025 non-GAAP revenue guidance from a range of approximately $46.5 billion to $47.5 billion, to a range of approximately $47.5 billion to $48.0 billion. This update primarily reflects the continued strong performance of our Growth Portfolio.

Full-year other income and expense in 2025 is now expected to be approximately $500 million of income due to higher-than-anticipated royalties and licensing income, as well as favorable interest income.

Non-GAAP EPS is now expected to be in the range of $6.40 - $6.60, inclusive of an $(0.80) per share net impact related to Acquired IPRD charges and licensing income.

July

(Prior)

October

(Updated)

G1Total Revenues

(Reported & Ex-FX)

G2Gross Margin %

No change

G3Operating Expenses1

No change

G4Other income/(expense)

G5Effective tax rate

No change

G6Diluted EPS

Acquired IPRD Charges and Licensing Income Included in Diluted EPS

1 Operating Expenses = SG&A and R&D.

2 See "Use of Non-GAAP Financial Information."

3 July was calculated using foreign exchange rates as of July 25, 2025, and October was calculated using foreign

The 2025 financial guidance excludes the impact of any potential future strategic acquisitions, including Orbital Therapeutics, which is expected to close in the fourth quarter of 2025, divestitures, specified items that have not yet been identified and quantified, and the impact of future Acquired IPRD charges and licensing income. To the extent we have quantified the impact of significant R&D charges or other income resulting from upfront or contingent milestone payments in connection with asset acquisitions or licensing of third-party intellectual property rights, we may update this information from time to time on our website, www.bms.com, in the "Investors" section. Non-GAAP guidance assumes exchange rates as of the date noted. The financial guidance is subject to risks and uncertainties applicable to all forward-looking statements as described elsewhere in this press release.

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A reconciliation of forward-looking non-GAAP measures, including non-GAAP EPS, to the most directly comparable GAAP measures is not provided because comparable GAAP measures for such measures are not reasonably accessible or reliable due to the inherent difficulty in forecasting and quantifying measures that would be necessary for such reconciliation. Namely, we are not, without unreasonable effort, able to reliably predict the impact of accelerated depreciation and impairment charges, legal and other settlements, gains and losses from equity investments and other adjustments. In addition, the company believes such a reconciliation would imply a degree of precision and certainty that could be confusing to investors. These items are uncertain, depend on various factors and may have a material impact on our future GAAP results. See "Cautionary Statement Regarding Forward-Looking Statements" and "Use of Non-GAAP Financial Information."

Conference Call Information

Bristol Myers Squibb will host a conference call today, Thursday, October 30, 2025, at 8:00 a.m. ET, during which company executives will review financial results with the investment community.

Investors and the general public are invited to listen to a live webcast of the call at http://investor.bms.com. Materials related to the call will be available at http://investor.bms.com prior to the start of the conference call.

A replay of the webcast will be available at http://investor.bms.com approximately three hours after the conference call concludes.

About Bristol Myers Squibb: Transforming Patients' Lives Through Science

At Bristol Myers Squibb, our mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases. We are pursuing bold science to define what's possible for the future of medicine and the patients we serve. For more information, visit us at BMS.com and follow us on LinkedIn, X, YouTube, Facebook and Instagram.

###

corporatefinancial-news

For more information, contact:

Media Relations: media@bms.com

Investor Relations: investor.relations@bms.com

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Use of Non-GAAP Financial Information

In discussing financial results and guidance, the company refers to financial measures that are not in accordance with U.S. Generally Accepted Accounting Principles (GAAP). The non-GAAP financial measures are provided as supplemental information to the financial measures presented in this press release that are calculated and presented in accordance with GAAP and are presented because management has evaluated the company’s financial results both including and excluding the adjusted items or the effects of foreign currency translation, as applicable, and believes that the non-GAAP financial measures presented portray the results of the company's baseline performance, supplement or enhance management's, analysts' and investors' overall understanding of the company’s underlying financial performance and trends and facilitate comparisons among current, past and future periods.

In addition, non-GAAP gross margin, which is gross profit excluding certain specified items, as a percentage of revenues, non-GAAP operating margin, which is gross profit less selling, general and administrative expenses and research and development expenses excluding certain specified items as a percentage of revenues, non-GAAP operating expenses, which is selling, general and administrative and research and development expenses excluding certain specified items, non-GAAP selling, general and administrative expenses, which is selling, general and administrative expenses excluding certain specified items, and non-GAAP research and development expenses, which is research and development expenses excluding certain specified items, are relevant and useful for investors because they allow investors to view performance in a manner similar to the method used by our management and make it easier for investors, analysts and peers to compare our operating performance to other companies in our industry and to compare our year-over-year results.

This earnings release and the accompanying tables also provide certain revenues and expenses, as well as non-GAAP measures, excluding the impact of foreign exchange ("Ex-Fx"). We calculate foreign exchange impacts by converting our current-period local currency financial results using the prior period average currency rates and comparing these adjusted amounts to our current-period results. Ex-Fx financial measures are not accounted for according to GAAP because they remove the effects of currency movements from GAAP results.

Non-GAAP financial measures, such as non-GAAP earnings and related EPS information, are adjusted to exclude certain costs, expenses, gains and losses and other specified items that are evaluated on an individual basis after considering their quantitative and qualitative aspects and typically have one or more of the following characteristics, such as being highly variable, difficult to project, unusual in nature, significant to the results of a particular period or not indicative of past or future operating results. These items are excluded from non-GAAP earnings and related EPS information because the company believes they neither relate to the ordinary course of the company’s business nor reflect the company’s underlying business performance.

Similar charges or gains were recognized in prior periods and will likely reoccur in future periods, including amortization of acquired intangible assets, including product rights that generate a significant portion of our ongoing revenue and will recur until the intangible assets are fully amortized, unwinding of inventory purchase price adjustments, acquisition and integration expenses, restructuring costs, accelerated depreciation and impairment of property, plant and equipment and intangible assets, divestiture gains or losses, stock compensation resulting from acquisition-related equity awards, pension, legal and other contractual settlement charges, equity investment and contingent value rights fair value adjustments (including fair value adjustments attributed to limited partnership and other investments), and amortization of fair value adjustments of debt acquired from Celgene in our 2019 exchange offer, among other items. Deferred and current income taxes attributed to these items are also adjusted for considering their individual impact to

8

the overall tax expense, deductibility and jurisdictional tax rates, as well as certain other significant tax items.

Because the non-GAAP financial measures are not calculated in accordance with GAAP, they should not be considered superior to and are not intended to be considered in isolation or as a substitute for the related financial measures presented in the press release that are prepared in accordance with GAAP and may not be the same as or comparable to similarly titled measures presented by other companies due to possible differences in method and in the items being adjusted. We encourage investors to review our financial statements and publicly-filed reports in their entirety and not to rely on any single financial measure.

Reconciliations of the non-GAAP financial measures to the most comparable GAAP measures are provided in the accompanying financial tables and will also be available on the company’s website at www.bms.com. Within the accompanying financial tables presented, certain columns and rows may not add due to the use of rounded numbers. Percentages and EPS amounts presented are calculated from the underlying amounts.

A reconciliation of forward-looking non-GAAP measures, including non-GAAP EPS, to the most directly comparable GAAP measures is not provided because comparable GAAP measures for such measures are not reasonably accessible or reliable due to the inherent difficulty in forecasting and quantifying measures that would be necessary for such reconciliation. Namely, we are not, without unreasonable effort, able to reliably predict the impact of accelerated depreciation and impairment charges, legal and other settlements, gains and losses from equity investments and other adjustments. In addition, the company believes such a reconciliation would imply a degree of precision and certainty that could be confusing to investors. These items are uncertain, depend on various factors and may have a material impact on our future GAAP results.

Website Information

We routinely post important information for investors on our website, www.bms.com, in the “Investors” section. We may use this website as a means of disclosing material, non-public information and for complying with our disclosure obligations under Regulation FD. Accordingly, investors should monitor the Investors section of our website, in addition to following our press releases, Securities and Exchange Commission (SEC) filings, public conference calls, presentations and webcasts. We may also use social media channels to communicate with our investors and the public about our company, our products and other matters, and those communications could be deemed to be material information. The information contained on, or that may be accessed through, our website or social media channels is not incorporated by reference into, and is not a part of, this document.

Cautionary Statement Regarding Forward-Looking Statements

This earnings release and the related attachments (as well as the oral statements made with respect to information contained in this release and the attachments) contain certain “forward-looking” statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, regarding, among other things, the company’s 2025 financial guidance, its business development and capital allocation strategy, anticipated developments in the company’s pipeline, expectations with respect to the company’s future market position and the projected benefits of the company’s alliances and other business development activities. These statements may be identified by the fact that they use words such as “should,” “could,” “expect,” “anticipate,” “estimate,” “target,” “may,” “project,” “guidance,” “intend,” “plan,” “believe,” “will” and other words and terms of similar meaning and

9

expression in connection with any discussion of future operating or financial performance, although not all forward-looking statements contain such terms. All statements that are not statements of historical facts are, or may be deemed to be, forward-looking statements. No forward-looking statement can be guaranteed, and there is no assurance that the company will achieve its financial guidance and long-term targets, that the company’s future clinical studies will support the data described in this release, that the company’s product candidates will receive necessary clinical and manufacturing regulatory approvals, that the company’s pipeline products will prove to be commercially successful, that clinical and manufacturing regulatory approvals will be sought or obtained within currently expected timeframes, or that contractual milestones will be achieved.

Forward-looking statements are based on current expectations and projections about the company’s future financial results, goals, plans and objectives and involve inherent risks, assumptions and uncertainties, including internal or external factors that could delay, divert or change any of them in the next several years, that are difficult to predict, may be beyond the company’s control and could cause the company’s future financial results, goals, plans and objectives to differ materially from those expressed in, or implied by, the statements. Such risks, uncertainties and other matters include, but are not limited to: increasing pricing pressures from market access, pharmaceutical pricing controls and discounting, including the potential for international reference pricing and most-favored nation drug pricing for our products; market actions taken by private and government payers to manage drug utilization and contain costs; government actions relating to the imposition of new tariffs, trade restrictions and export regulations; the company’s ability to retain patent and market exclusivity for certain products; regulatory changes that result in lower prices, lower reimbursement rates and smaller populations for whom payers will reimburse; changes under the 340B Drug Pricing Program; the company’s ability to obtain and maintain regulatory approval for its product candidates; the possibility of difficulties and delays in product introduction and commercialization; increasing industry competition; potential difficulties, delays and disruptions in manufacturing, distribution or sale of products; the company’s ability to identify potential strategic acquisitions, licensing opportunities or other beneficial transactions; failure to complete, or delays in completing, collaborations, acquisitions, divestitures, alliances and other portfolio actions and the failure to achieve anticipated benefits from such transactions and actions; exposure to litigation and/or regulatory actions or investigations; the impact of any healthcare reform and legislation or regulatory action in the United States and international markets; increasing market penetration of lower-priced generic products; the failure of the company’s suppliers, vendors, outsourcing partners, alliance partners and other third parties to meet their contractual, regulatory and other obligations; the impact of counterfeit or unregistered versions of the company’s products and from stolen products; product label changes or other measures that could result in declining sales; safety or efficacy concerns regarding the company’s products or any product in the same class as the company’s products; the risk of cyber-attacks and unauthorized disclosure of trade secrets or other confidential data; the company’s ability to execute its financial, strategic and operational plans; the company’s ability to attract and retain key personnel; the impact of the company’s significant indebtedness; political and financial instability of international economies and sovereign risk; interest rate and currency exchange rate fluctuations, credit and foreign exchange risk management; risks relating to the use of social media platforms; issuance of new or revised accounting standards; and risks relating to public health outbreaks, epidemics and pandemics.

Forward-looking statements in this earnings release should be evaluated together with the many risks and uncertainties that affect the company’s business and market, particularly those identified in the cautionary statement and risk factors discussion in the company’s Annual Report on Form 10-K for the year ended December 31, 2024, as updated by the company’s subsequent Quarterly Reports on Form 10-Q, Current Reports on Form 8-K and other filings with the SEC. The forward-looking statements included in this document are made only as of the date of this document and

except as otherwise required by applicable law, the company undertakes no obligation to publicly update or revise any forward-looking statement, whether as a result of new information, future events, changed circumstances or otherwise.

BRISTOL-MYERS SQUIBB COMPANY

CONSOLIDATED STATEMENTS OF EARNINGS

(Unaudited, dollars and shares in millions except per share data)

Three Months Ended September 30,

Nine Months Ended September 30,

Net product sales

$

$

$

$

Alliance and other revenues

Total Revenues

Cost of products sold(a)

Selling, general and administrative

Research and development

Acquired IPRD

Amortization of acquired intangible assets

Other (income)/expense, net

Total Expenses

Earnings/(Loss) Before Income Taxes

Income tax provision

Net Earnings/(Loss)

Noncontrolling Interest

(6)

4

3

Net Earnings/(Loss) Attributable to BMS

$

$

$

$

Weighted-Average Common Shares Outstanding:

Basic

Diluted

Earnings/(Loss) per Common Share:

Basic

$

$

$

$

Diluted

Other (income)/expense, net

Interest expense(b)

$

$

$

$

Royalty income - divestitures

Royalty and licensing income

Provision for restructuring

Investment income

Integration expenses

Litigation and other settlements

—

Acquisition expense

—

—

5

Intangible asset impairments

—

—

Equity investment (gains)/losses

Contingent consideration

—

—

—

Other

Other (income)/expense, net

$

$

$

$

(a) Excludes amortization of acquired intangible assets.

(b) Includes amortization of purchase price adjustments to Celgene debt.

BRISTOL-MYERS SQUIBB COMPANY

PRODUCT REVENUES

(Unaudited, dollars in millions)

GAAP

Excl. F/X**

U.S.

Int'l(c)

WW(d)

U.S.

Int'l(c)

WW(d)

U.S.

Int'l(c)

WW(d)

U.S.

Int'l(c)

WW(d)

Growth Portfolio

Opdivo

$

$

$

$

$

$

6

%

8

%

7

%

6

%

6

%

6

%

Opdivo Qvantig

7

—

—

—

N/A

N/A

N/A

N/A

N/A

N/A

Orencia

2

%

6

%

3

%

2

%

3

%

2

%

Yervoy

%

%

%

%

%

%

Reblozyl

%

%

%

%

%

%

Opdualag

%

%

%

%

%

%

Breyanzi

%

%

%

%

%

%

Camzyos

%

%

%

%

%

%

Zeposia

8

%

%

9

%

8

%

6

%

7

%

Abecma

%

%

9

%

%

%

6

%

Sotyktu

—

%

%

%

—

%

%

%

Krazati

5

2

%

%

%

%

%

%

Cobenfy

—

—

—

—

N/A

N/A

N/A

N/A

N/A

N/A

Other Growth Products(a)

8

%

%

%

8

%

%

%

Total Growth Portfolio

%

%

%

%

%

%

Legacy Portfolio

Eliquis

%

%

%

%

%

%

Revlimid

%

%

%

%

%

%

Pomalyst/Imnovid

%

%

%

%

%

%

Sprycel

%

%

%

%

%

%

Abraxane

%

%

%

%

%

%

Other Legacy Products(b)

%

%

%

%

%

%

Total Legacy Portfolio

%

%

%

%

%

%

Total Revenues

$

$

$

$

$

$

1

%

6

%

3

%

1

%

3

%

2

%

** See "Use of Non-GAAP Financial Information".

(a) Includes Augtyro, Onureg, Inrebic, Nulojix, Empliciti and royalty revenues.

(b) Includes other mature brands.

(c) Includes Puerto Rico.

(d) Worldwide (WW) includes U.S. and International (Int'l).

BRISTOL-MYERS SQUIBB COMPANY

PRODUCT REVENUES

(Unaudited, dollars in millions)

GAAP

Excl. F/X**

U.S.

Int'l(c)

WW(d)

U.S.

Int'l(c)

WW(d)

U.S.

Int'l(c)

WW(d)

U.S.

Int'l(c)

WW(d)

Growth Portfolio

Opdivo

$

$

$

$

$

$

9

%

6

%

8

%

9

%

7

%

8

%

Opdivo Qvantig

8

—

—

—

N/A

N/A

N/A

N/A

N/A

N/A

Orencia

(2)

%

7

%

1

%

(2)

%

7

%

—

%

Yervoy

%

%

%

%

%

%

Reblozyl

%

%

%

%

%

%

Opdualag

%

%

%

%

%

%

Breyanzi

%

%

%

%

%

%

Camzyos

%

%

%

%

Zeposia

(3)

%

%

2

%

(3)

%

%

2

%

Abecma

%

%

8

%

%

%

7

%

Sotyktu

—

%

%

%

—

%

%

%

Krazati

5

%

%

%

%

%

%

Cobenfy

—

—

—

—

N/A

N/A

N/A

N/A

N/A

N/A

Other Growth Products(a)

%

%

%

%

%

%

Total Growth Portfolio

%

%

%

%

%

%

Legacy Portfolio

Eliquis

7

%

%

8

%

7

%

9

%

8

%

Revlimid

%

%

%

%

%

%

Pomalyst/Imnovid

%

%

%

%

%

%

Sprycel

%

%

%

%

%

%

Abraxane

%

%

%

%

%

%

Other Legacy Products(b)

(7)

%

%

%

(7)

%

%

%

Total Legacy Portfolio

%

%

%

%

%

%

Total Revenues

$

$

$

$

$

$

(3)

%

5

%

(1)

%

(3)

%

4

%

(1)

%

** See "Use of Non-GAAP Financial Information".

(a) Includes Augtyro, Onureg, Inrebic, Nulojix, Empliciti and royalty revenues.

(b) Includes other mature brands.

(c) Includes Puerto Rico.

(d) Worldwide (WW) includes U.S. and International (Int'l).

BRISTOL-MYERS SQUIBB COMPANY

INTERNATIONAL REVENUES(a)

FOREIGN EXCHANGE IMPACT (%)

(Unaudited)

Revenue Change %

F/X % Favorable/ (Unfavorable) **

Revenue Change % Ex- F/X **

Revenue Change %

F/X % Favorable/ (Unfavorable) **

Revenue Change % Ex- F/X **

Growth Portfolio

Opdivo

8%

3%

6%

6%

(1)%

7%

Opdivo Qvantig

N/A

N/A

N/A

N/A

N/A

N/A

Orencia

6%

2%

3%

7%

—%

7%

Yervoy

4%

—%

Reblozyl

4%

2%

Opdualag

7%

4%

Breyanzi

8%

Camzyos

9%

NM

Zeposia

6%

6%

3%

Abecma

9%

4%

Sotyktu

4%

2%

Krazati

3%

Cobenfy

N/A

N/A

N/A

N/A

N/A

N/A

Other Growth Products(b)

1%

—%

Total Growth Portfolio

3%

—%

Legacy Portfolio

Eliquis

6%

3%

9%

Revlimid

—%

(1)%

Pomalyst/Imnovid

1%

—%

Sprycel

1%

(1)%

Abraxane

(1)%

(2)%

Other Legacy Products(c)

1%

—%

Total Legacy Portfolio

3%

1%

Total Revenues

6%

3%

3%

5%

1%

4%

NM Not meaningful

** See "Use of Non-GAAP Financial Information".

(a) Includes Puerto Rico.

(b) Includes Augtyro, Onureg, Inrebic, Nulojix, Empliciti and royalty revenues.

(c) Includes other mature brands.

BRISTOL-MYERS SQUIBB COMPANY

WORLDWIDE REVENUES(a)

FOREIGN EXCHANGE IMPACT (%)

(Unaudited)

Revenue Change %

F/X % Favorable/ (Unfavorable) **

Revenue Change % Ex- F/X **

Revenue Change %

F/X % Favorable/ (Unfavorable) **

Revenue Change % Ex- F/X **

Growth Portfolio

Opdivo

7%

1%

6%

8%

—%

8%

Opdivo Qvantig

N/A

N/A

N/A

N/A

N/A

N/A

Orencia

3%

1%

2%

1%

—%

—%

Yervoy

1%

—%

Reblozyl

1%

—%

Opdualag

1%

—%

Breyanzi

2%

2%

Camzyos

1%

1%

Zeposia

9%

2%

7%

2%

1%

2%

Abecma

9%

4%

6%

8%

2%

7%

Sotyktu