8-K

BRISTOL MYERS SQUIBB CO (BMY)

8-K 2020-08-06 For: 2020-08-06
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Added on April 02, 2026

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

_____________________________

FORM 8-K

_____________________________

CURRENT REPORT

Pursuant to Section 13 OR 15(d) of

The Securities Exchange Act of 1934

Date of Report (Date of earliest event reported): August 6, 2020

_____________________________

BRISTOL-MYERS SQUIBB COMPANY

(Exact name of registrant as specified in its charter)

_____________________________

Delaware 001-01136 22-0790350
(State or other jurisdiction of<br>incorporation or organization) (Commission File Number) (I.R.S Employer<br>Identification No.)

430 E. 29th Street, 14th Floor

New York, NY, 10016

(Address of principal executive offices) (zip code)

Registrant’s telephone number, including area code: (212) 546-4000

_____________________________

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General Instruction A.2. below):

☐ Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)

☐ Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)

☐ Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))

☐ Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

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

Title of each class Trading Symbol(s) Name of each exchange on which registered
Common Stock, $0.10 Par Value BMY New York Stock Exchange
1.000% Notes due 2025 BMY25 New York Stock Exchange
1.750% Notes due 2035 BMY35 New York Stock Exchange
Bristol-Myers Squibb Contingent Value Rights BMY RT New York Stock Exchange
Celgene Contingent Value Rights CELG RT New York Stock Exchange

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).

Emerging growth company ☐

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

Item 2.02 Results of Operations and Financial Condition.

On August 6, 2020, Bristol-Myers Squibb Company (the “Company”) issued a press release (the “Earnings Press Release”) announcing its financial results for the second quarter of 2020. A copy of the Earnings Press Release is furnished pursuant to this Item 2.02 as Exhibit 99.1 to this Current Report on Form 8-K and incorporated by reference herein in its entirety. Also furnished pursuant to this Item 2.02 as Exhibit 99.2 to this Current Report on Form 8-K and incorporated by reference herein in its entirety is certain supplemental information posted on the Company’s website at www.bms.com.

Item 9.01 Financial Statements and Exhibits.

(d) Exhibits

The following exhibits are furnished as part of this Current Report on Form 8-K:

Exhibit<br>No. Description
99.1 Press release of Bristol-Myers Squibb Company dated August 6, 2020.
99.2 Certain supplemental information posted on Bristol-Myers Squibb Company’s website at www.bms.com not included in the press release.
104 The cover page from this Current Report on Form 8-K formatted in Inline XBRL (included as Exhibit 101).

EXHIBIT INDEX

Exhibit<br>No. Description
99.1 Press release of Bristol-Myers Squibb Company dated August 6, 2020.
99.2 Certain supplemental information posted on Bristol-Myers Squibb Company’s website at www.bms.com not included in the press release.
104 The cover page from this Current Report on Form 8-K formatted in Inline XBRL (included as Exhibit 101).

SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, as amended, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

BRISTOL-MYERS SQUIBB COMPANY
Dated: August 6, 2020 By: /s/ Katherine R. Kelly
Name: Katherine R. Kelly
Title: Corporate Secretary

Document

Exhibit 99.1

bmslogo20201.jpg

Bristol Myers Squibb Reports Second Quarter 2020 Financial Results

•Reports Second Quarter Revenues of $10.1 Billion

•Posts GAAP Loss Per Share of $0.04 and Non-GAAP EPS of $1.63

•Advances Pipeline with Positive Topline Results for Zeposia in Ulcerative Colitis; Approvals for Opdivo plus Yervoy in Lung Cancer

•Updates 2020 GAAP EPS Guidance Range from $0.37-$0.57 to ($0.06)-$0.09 and Non-GAAP EPS Guidance Range from $6.00-$6.20 to $6.10-$6.25

(NEW YORK, August 6, 2020) – Bristol Myers Squibb (NYSE:BMY) today reports results for the second quarter of 2020, which reflect strong product sales, continued advancement of the pipeline and robust operating performance.

“Our second quarter results reflect the passion and focus of our employees, who continue to introduce new medicines, support patients with serious diseases and deliver strong results during the COVID-19 pandemic,” said Giovanni Caforio, M.D., chairman and chief executive officer, Bristol Myers Squibb. “Our teams drove strong commercial execution while continuing to progress our integration initiatives. With several new product launches and the achievement of multiple milestones from our late-stage pipeline, I am confident that we are building a leading biopharma with a renewed portfolio of transformational medicines. Our financial flexibility and continued opportunities to invest in innovation position us well to deliver for the long-term.”

amounts in millions, except per share amounts
2019 Change
Total Revenues $6,273 61 %
GAAP Diluted (Loss)/EPS 0.87 N/A
Non-GAAP Diluted EPS 1.18 38 %
Total Pro Forma Revenues* 10,160 0 %

All values are in US Dollars.

* The pro forma revenues assume the company’s acquisition of Celgene (Celgene Acquisition) and its divestiture of Otezla^®^ to Amgen Inc. (Otezla^®^ Divestiture) occurred on January 1, 2019 and exclude foreign currency hedge gains and losses. Management believes that measuring revenue rates on a comparable pro forma basis is an appropriate way for investors to best understand the underlying performance of the business. See “Worldwide Pro Forma Revenue” in Quarterly Package of Financial Information for this quarter, which is available on bms.com/investors/financial-reporting/quarterly-results, for information on the revenue of the company and Celgene on a stand-alone basis for the prior-year period. Otezla^®^ is a trademark of Amgen Inc.

SECOND QUARTER FINANCIAL RESULTS

All comparisons are made versus the same period in 2019 unless otherwise stated.

•Bristol Myers Squibb posted second quarter revenues of $10.1 billion, an increase of 61% on a reported basis, or 63% when adjusted for foreign exchange. The increase was driven primarily by the impact of the Celgene Acquisition, which was completed on November 20, 2019. Revenues remained consistent on a pro forma basis, as sales were estimated to be negatively impacted by approximately $600 million due mainly to COVID-19 related channel inventory work downs from the first quarter, as well as lower demand resulting from reduced new patient starts and fewer patient visits to physicians in the pandemic.

•U.S. revenues increased 77% to $6.5 billion in the quarter. International revenues increased 40% to $3.6 billion in the quarter. When adjusted for foreign exchange impact, international revenues increased 43%.

•Gross margin as a percentage of revenue increased from 68.6% to 73.4% in the quarter primarily due to product mix, partially offset by the unwinding of inventory purchase price accounting adjustments.

•Marketing, selling and administrative expenses increased 51% to $1.6 billion in the quarter primarily due to $600 million of costs associated with the broader portfolio resulting from the Celgene Acquisition.

•Research and development expenses increased 90% to $2.5 billion in the quarter primarily due to $1.1 billion of costs associated with the broader portfolio resulting from the Celgene Acquisition.

•Amortization of acquired intangible assets was $2.4 billion in the quarter primarily due to the Celgene Acquisition.

•Income taxes were $1.7 billion on pre-tax earnings of $1.6 billion in the quarter primarily due to tax charges resulting from an internal transfer of certain intangible assets and the Otezla^®^ Divestiture and purchase price adjustments. The effective tax rate was 19.0% in the same period a year ago.

•The company reported net loss attributable to Bristol Myers Squibb of $85 million, or $0.04 per share, in the second quarter, compared to net earnings of $1.4 billion, or $0.87 per share, for the same period a year ago. The results in the current quarter include costs and expenses resulting from purchase price accounting, contingent value rights fair value adjustments and other acquisition and integration expenses.

•The company reported non-GAAP net earnings attributable to Bristol Myers Squibb of $3.8 billion, or $1.63 per share, in the second quarter, compared to net earnings of $1.9 billion, or $1.18 per share, for the same period a year ago. A discussion of the non-GAAP financial measures is included under the “Use of Non-GAAP Financial Information” section.

•Cash, cash equivalents and marketable debt securities were $22.2 billion and debt was $46.7 billion, as of June 30, 2020.

SECOND QUARTER PRODUCT REVENUE HIGHLIGHTS

amounts in millions
Product % Change from Quarter Ended June 30, 2019 on Reported Basis % Change from Quarter Ended June 30, 2019 on Pro Forma Basis**
Revlimid N/A* 6%
Eliquis 6% 6%
Opdivo (9)% (9)%
Orencia (4)% (4)%
Pomalyst/Imnovid N/A* 21%
Sprycel (6)% (6)%
Yervoy 1% 1%
Abraxane N/A* (2)%
Empliciti 7% 7%
Reblozyl N/A* N/A
Inrebic N/A* N/A
Zeposia N/A* N/A

All values are in US Dollars.

* Products were acquired as part of the Celgene Acquisition.

** Pro forma product revenues assume the Celgene Acquisition and the Otezla^®^ Divestiture occurred on January 1, 2019 and exclude foreign currency hedge gains and losses. Management believes that measuring product revenue rates on a comparable pro forma basis is an appropriate way for investors to best understand the underlying performance of the business. See “Worldwide Pro Forma Revenues” in the Quarterly Package of Financial Information for this quarter, which is available on bms.com/investors/financial-reporting/quarterly-results, for information on the product revenue of the company and Celgene for the prior-year period.

FIRST HALF PRODUCT REVENUE HIGHLIGHTS

amounts in millions
Product % Change from Six Months Ended June 30, 2019 on Reported Basis % Change from Six Months Ended June 30, 2019 on Pro Forma Basis**
Revlimid N/A* 10%
Eliquis 21% 21%
Opdivo (6)% (6)%
Orencia 3% 3%
Pomalyst/Imnovid N/A* 25%
Sprycel 3% 3%
Yervoy 2% 2%
Abraxane N/A* 2%
Empliciti 11% 11%
Reblozyl N/A* N/A
Inrebic N/A* N/A
Zeposia N/A* N/A

All values are in US Dollars.

* Products were acquired as part of the Celgene Acquisition.

** Pro forma product revenues assume the Celgene Acquisition and the Otezla^®^ Divestiture occurred on January 1, 2019 and exclude foreign currency hedge gains and losses. Management believes that measuring product revenue rates on a comparable pro forma basis is an appropriate way for investors to best understand the underlying performance of the business. See “Worldwide Pro Forma Revenues” in the Quarterly Package of Financial Information for this quarter, which is available on bms.com/investors/financial-reporting/quarterly-results, for information on the product revenue of the company and Celgene for the prior-year period.

SECOND QUARTER PRODUCT AND PIPELINE UPDATE

Cardiovascular

Eliquis

Patent Update

•In August, the Bristol-Myers Squibb-Pfizer Alliance announced the U.S. District Court decision to uphold both the composition of matter patent (US 6,967,208) and formulation patent (US 9,326,945) covering Eliquis^®^ (apixaban). (link)

Oncology and Hematology

Opdivo

Regulatory

•In June, the company announced the U.S. Food and Drug Administration (U.S. FDA) approval of Opdivo (nivolumab) for the treatment of patients with unresectable advanced, recurrent or metastatic esophageal squamous cell carcinoma (ESCC) after prior fluoropyrimidine-and platinum-based chemotherapy. (link)

•In May, the company announced Opdivo plus Yervoy (ipilimumab) given with two cycles of platinum-doublet chemotherapy was approved by the U.S. FDA for the first-line treatment of adult patients with metastatic or recurrent non-small cell lung cancer (NSCLC) with no EGFR or ALK genomic tumor aberrations. This approval was based on the Phase 3 CheckMate -9LA study. (link)

•In May, the company announced the U.S. FDA approved Opdivo plus Yervoy for the first-line treatment of adult patients with metastatic NSCLC whose tumors express PD-LI>1% as determined by an FDA-approved test, with no EGFR or ALK genomic tumor aberrations. This approval was based on data from Part 1a of the Phase 3 Checkmate -227 study. (link)

Reblozyl

Regulatory

•In June, the company and Acceleron Pharma Inc. announced the European Commission (EC) approved Reblozyl (luspatercept) for the treatment of transfusion-dependent anemia in adult patients with myelodysplastic syndromes (MDS) or beta thalassemia. (link)

ide-cel

Regulatory

•In July, the company and bluebird bio, Inc. announced that the companies submitted the Biologics License Application (BLA) to the U.S. FDA for idecabtagene vicleucel (ide-cel; bb2121) for patients with heavily pre-treated relapsed and refractory multiple myeloma. This submission follows the company’s receipt of a Refusal to File letter from the U.S. FDA in May 2020 following the original BLA submission from March 2020. (link)

•In May, the company announced that the European Medicines Agency (EMA) validated its Marketing Authorization Application (MAA) for ide-cel; bb2121, the company’s investigational B-cell maturation antigen (BCMA)-directed chimeric antigen receptor (CAR) T cell immunotherapy co-developed with bluebird bio, Inc., for the treatment of adult patients with multiple myeloma who have received at least three prior therapies, including an immunomodulatory agent, a proteasome inhibitor and an anti-CD38 antibody. (link)

CC-486

Regulatory

•In May, the company announced that the EMA validated its MAA for CC-486 for the maintenance treatment of adult patients with acute myeloid leukemia (AML), who achieved complete remission (CR) or CR with incomplete blood count recovery (CRi), following induction therapy with or without consolidation treatment, and who are not candidates for, or who choose not to proceed to, hematopoietic stem cell transplantation. (link)

Pomalyst

Regulatory

•In May, the company announced that the U.S. FDA approved Pomalyst (pomalidomide) for patients with AIDS-related Kaposi sarcoma whose disease has become resistant to highly active antiretroviral therapy (HAART), or in patients with Kaposi sarcoma who are HIV-negative. (link)

Liso-cel

Regulatory

•In July, the company announced that the EMA validated the MAA for liso-cel (lisocabtagene maraleucel), a CD19-directed chimeric antigen receptor (CAR) T cell therapy for the treatment of adults with relapsed or refractory large B-cell lymphoma after at least two prior therapies. (link)

Medical Conferences

•In May, at the American Society of Clinical Oncology (ASCO) 2020 Virtual Scientific Program, the company announced important new data and analysis across its cancer portfolio (link), including:

◦First disclosure of data from the Phase 3 CheckMate -9LA trial evaluating Opdivo plus Yervoy given concomitantly with two cycles of chemotherapy, for the first-line treatment of metastatic NSCLC. (link)

◦Three-year follow-up results from the Phase 3 Checkmate -227 trial, demonstrating that Opdivo plus Yervoy provided sustained improvements in overall survival (OS) and additional efficacy measures as a first-line treatment for patients with metastatic NSCLC. (link)

◦First presentation of data from the Phase 2 KarMMA study with bluebird bio, Inc. evaluating the efficacy and safety of the companies’ investigational B-cell maturation antigen (BCMA)-directed chimeric antigen receptor (CAR) T cell immunotherapy, idecabtagene vicleucel (ide-cel; bb2121), in patients with relapsed and refractory multiple myeloma. (link)

•In June, at the 25^th^ European Hematology Association (EHA), the company announced important new data and analysis from 60 company-sponsored studies, highlighting the company’s approaches to treating blood cancers and other diseases. (link)

Immunology

Zeposia

Commercial

•In June, the company announced the commercial launch and availability of Zeposia (ozanimod), a new oral treatment for relapsing forms of multiple sclerosis, in the U.S. Zeposia was approved by the U.S. FDA on March 25, 2020. (link)

Regulatory

•In May, the company announced the EC approval Zeposia for the treatment of adult patients in the European Union with relapsing forms of multiple sclerosis. (link)

Clinical

•In June, the company announced results from True North, a pivotal Phase 3 trial evaluating oral Zeposia as an induction and maintenance therapy for adult patients with moderate to severe ulcerative colitis. True North met both primary endpoints of clinical remission in induction at Week 10 and in maintenance at Week 52. (link)

Orencia

Clinical

•In June, at the European E-Congress of Rheumatology (EULAR) 2020, the company announced results from the open-label switch period of Early AMPLE, a Phase IV exploratory biomarker study assessing the differences by which Orencia (abatacept) and adalimumab, interfere with disease progression in moderate-to-severe early rheumatoid arthritis (RA) patients who tested positive (seropositive) for certain autoantibodies. (link)

COVID-19 Pandemic Response

During the current world health crisis, the company continues to take all necessary actions to promote public health by carrying out its mission of providing life-saving medicines to the patients who depend on the company and supporting relief efforts across the globe. (link)

Financial Guidance

Bristol Myers Squibb is updating its 2020 GAAP EPS guidance range from $0.37 - $0.57 to ($0.06) - $0.09. In addition, the company is updating its 2020 non-GAAP EPS guidance range of $6.00 - $6.20 to $6.10 - $6.25. Adjusted 2020 GAAP and non-GAAP line items are:

GAAP non-GAAP
Revenue $40.5B - $42.0B $40.5B - $42.0B
Gross margin as a percentage of revenue Approximately 74% Approximately 80%
Marketing, selling, and administrative expense $6.5B - $6.7B $6.5B - $6.7B
Research and development expense $9.7B - $9.9B $9.2B - $9.4B
Other (income)/expense, net $0.9B - $1.1B ($0.1B) - $0.1B
Effective tax rate Approximately 100% 16-17%
Weighted average diluted shares Approximately 2.3 Billion Approximately 2.3 Billion
EPS guidance ($0.06) - $0.09 $6.10 - $6.25

The 2020 guidance assumes the peak impact of the current COVID-19 crisis on the business would occur in the second quarter of 2020, with a return to a more stable business environment in the third quarter and minimal impact from the fourth quarter of 2020 onwards. Additional key factors assumed in guidance now include:

•Mid-July foreign exchange and interest rates apply.

•Products that saw significant advanced buying at the end of the first quarter will see that inventory work-down during the rest of the year, mostly in the second quarter, which the company experienced, and to a lesser degree in the third and fourth quarters.

•A reduction in new-to-brand prescriptions, and on physician administered product demand during the second quarter, recovering during the third quarter and fully recovered in the fourth quarter.

•All clinical trial activities are planned to resume by the end of the year where local country restrictions have been lifted.

The financial guidance excludes the impact of any potential future strategic acquisitions and divestitures and any specified items that have not yet been identified and quantified. The 2020 non-GAAP EPS guidance further excludes other specified items as discussed under “Use of Non-GAAP Financial Information.” A reconciliation of non-GAAP financial measures to the most comparable GAAP measure and the reasons why management believes the use of these measures is important are provided in supplemental materials available on the company’s website. The financial guidance is subject to risks and uncertainties applicable to all forward-looking statements as described elsewhere in this press release.

Company and Conference Call Information

Bristol Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases. For more information about Bristol Myers Squibb, visit us at BMS.com or follow us on LinkedIn, Twitter, YouTube, Facebook, and Instagram.

There will be a conference call on August 6 at 8:30 a.m. ET during which company executives will review financial information and address inquiries from investors and analysts. Investors and the general public are invited to listen to a live webcast of the call at http://investor.bms.com or by dialing in the U.S. toll free 800-458-4121 or international 786-789-4772, confirmation code: 8970168, or using this link, which becomes active 15 minutes prior to the

scheduled start time and entering your information to be connected. Materials related to the call will be available at the same website prior to the conference call.

A replay of the call will be available beginning at 12:00 p.m. ET on August 6 through 12:00 p.m. ET on August 20, 2020. The replay will also be available through http://investor.bms.com or by dialing in the U.S. toll free 888-203-1112 or international 719-457-0820, confirmation code: 8970168.

Use of Non-GAAP Financial Information

This earnings release contains non-GAAP financial measures, including non-GAAP earnings and related EPS information that are adjusted to exclude certain costs, expenses, gains and losses and other specified items that are evaluated on an individual basis. Reconciliations of these non-GAAP financial measures to the most comparable GAAP measures are available on the company’s website at www.bms.com.

These non-GAAP items are adjusted 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 future operating results. Similar charges or gains were recognized in prior periods and will likely reoccur in future periods, including amortization of acquired intangible assets beginning in the fourth quarter of 2019, including product rights that generate a significant portion of our ongoing revenue, unwind of inventory fair value adjustments, acquisition and integration expenses, restructuring costs, accelerated depreciation and impairment of property, plant and equipment and intangible assets, R&D charges or other income resulting from upfront or contingent milestone payments in connection with the acquisition or licensing of third-party intellectual property rights, costs of acquiring a priority review voucher, divestiture gains or losses, stock compensation resulting from accelerated vesting of Celgene awards, certain retention-related employee compensation charges related to the Celgene Acquisition, pension, legal and other contractual settlement charges, interest expense on the notes issued in May 2019 incurred prior to the Celgene Acquisition and interest income earned on the net proceeds of those notes, equity investment and contingent value rights fair value adjustments 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 the overall tax expense, deductibility and jurisdictional tax rates. Certain other significant tax items are also excluded such as the impact resulting from internal transfer of intangible assets and the Otezla^®^ Divestiture. This earnings release also provides international revenues excluding the impact of foreign exchange.

Non-GAAP information is intended to portray the results of the company’s baseline performance, supplement or enhance management, analysts and investors overall understanding of the company’s underlying financial performance and facilitate comparisons among current, past and future periods. For example, non-GAAP earnings and EPS information are indications of the company’s baseline performance before items that are considered by us to not be reflective of the company’s ongoing results. In addition, this information is among the primary indicators that we use as a basis for evaluating performance, allocating resources, setting incentive compensation targets and planning and forecasting for future periods. This information is not intended to be

considered in isolation or as a substitute for net earnings or diluted EPS 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.

Amortization of acquired intangible assets were previously included in non-GAAP earnings and EPS information. These amounts have become significant to the financial results subsequent to the Celgene Acquisition and as a result, have been excluded in the non-GAAP results to better reflect our core operating performance. Comparable prior period non-GAAP results have not been revised to include this adjustment as the related amounts were insignificant ($24 million and $48 million for the three and six months ended June 30, 2019, respectively).

Website Information

We routinely post important information for investors on our website, 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, 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 are not incorporated by reference into, and are 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, statements relating to goals, plans and projections regarding the company’s financial position, results of operations, market position, product development and business strategy. These statements may be identified by the fact 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 expression in connection with any discussion of future operating or financial performance, although not all forward-looking statements contain such terms. One can also identify forward-looking statements by the fact that they do not relate strictly to historical or current facts. These statements are likely to relate to, among other things, the company’s ability to execute successfully its strategic plans, including its business development strategy generally and in relation to its ability to realize the projected benefits of the Celgene Acquisition, the full extent of the impact of the COVID-19 pandemic on the company’s operations and the development and commercialization of its products, the expiration of patents or data protection on certain products, including assumptions about the company’s ability to retain patent exclusivity of certain products and the impact, and the result of governmental investigations. No forward-looking statement can be guaranteed, including that the company’s future clinical studies will support the data described in this release, product candidates will receive necessary clinical and manufacturing regulatory approvals, pipeline products will prove to be commercially successful, clinical and manufacturing regulatory approvals

will be sought or obtained within currently expected timeframes or contractual milestones will be achieved.

Such forward-looking statements are based on historical performance and 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, risks relating to integrating the company’s and Celgene’s business and operations, including with respect to human capital management, portfolio rationalization, finance and accounting systems, sales operations and product distribution, pricing systems and methodologies, data security systems, compliance programs and internal controls processes, on the company’s ability to realize the anticipated benefits from the Celgene Acquisition; the impact of the company’s significant additional indebtedness that it incurred and its issuance of additional shares in connection with the Celgene Acquisition on its ability to operate the combined company; various risks related to public health outbreaks, epidemics and pandemics, including the impact of the COVID-19 pandemic on the company’s operations, the possibility of the COVID-19 pandemic delaying the timing of the FDA’s approval decisions and that the company cannot reasonably assess or predict at this time the full extent of the adverse effect that the COVID-19 pandemic will have on its business, financial condition, results of operations and cash flows; challenges inherent in new product development, including obtaining and maintaining regulatory approval; increasing pricing pressures from market access, pharmaceutical pricing controls and discounting and other restrictions in the United States, the European Union and other regions around the world (including changes in rules and practices of managed care organizations and institutional and governmental purchasers and the proposals contained in the “American Patient First Blueprint” and the executive orders issued by the U.S. federal government in July designed to regulate prices and payment for pharmaceutical products); the possibility of difficulties and delays in product introduction and commercialization; the company’s ability to obtain and protect market exclusivity rights and enforce patents and other intellectual property rights; the risk of certain novel approaches to disease treatment (such as CAR T therapy); industry competition from other manufacturers; the risk of an adverse patent litigation decision or settlement and exposure to other litigation and/or regulatory actions; the impact of any U.S. healthcare reform and legislation or regulatory action in the U.S. and markets outside the U.S. affecting pharmaceutical product pricing, reimbursement or access; changes in tax law and regulations; any decline in the company’s future royalty streams; 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 company’s ability to execute its financial, strategic and operational plans; the company’s ability to identify potential strategic acquisitions, licensing opportunities or other beneficial transactions; the company’s ability to attract and retain key personnel; the company’s ability to effectively manage acquisitions, divestitures, alliances and other portfolio actions and to successfully realize the expected benefits of such actions; the company’s dependency on several key products; potential difficulties, delays and disruptions in manufacturing, distribution or sale of products, including without limitation, interruptions caused by damage to the company’s and the company’s suppliers’ manufacturing sites; regulatory decisions impacting labeling, manufacturing processes and/or other matters; the impact on the company’s competitive position from counterfeit or unregistered versions of its products or stolen products; the adverse impact of cyber-attacks on the company’s information systems or products,

including unauthorized disclosure of trade secrets or other confidential data stored in the company’s information systems and networks; political and financial instability of international economies and sovereign risk; interest rate and currency exchange rate fluctuations, credit and foreign exchange risk management; and issuance of new or revised accounting standards. In addition, the 2020 financial guidance provided in this release relies on assumptions about the duration and severity of the COVID-19 pandemic, timing of the return to a more stable business environment, patient and physician behaviors, buying patterns and clinical trial activities (together, the “Recovery Process”), among other things. If the actual Recovery Process differs materially from our assumptions, the impact of COVID-19 on our business could be worse than expected and our results may be negatively impacted.

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, 2019, as updated by the company’s subsequent Quarterly Reports on Form 10-Q, Current Reports on Form 8-K and other filings with the Securities and Exchange Commission. 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

PRODUCT REVENUES

FOR THE THREE MONTHS ENDED JUNE 30, 2020 AND 2019

(Unaudited, dollars in millions)

Worldwide Revenues U.S. Revenues^(b)^
2020 2019 % Change 2020 2019 % Change
Prioritized Brands
Revlimid $ 2,884 $ N/A $ 2,048 $ N/A
Eliquis 2,163 2,042 6 % 1,363 1,269 7 %
Opdivo 1,653 1,823 (9) % 956 1,112 (14) %
Orencia 750 778 (4) % 554 566 (2) %
Pomalyst/Imnovid 745 N/A 522 N/A
Sprycel 511 544 (6) % 308 307
Yervoy 369 367 1 % 254 253
Abraxane 308 N/A 218 N/A
Empliciti 97 91 7 % 59 63 (6) %
Reblozyl 55 N/A 55 N/A
Inrebic 15 N/A 15 N/A
Zeposia 1 N/A 1 N/A
Established Brands
Baraclude 121 147 (18) % 3 7 (57) %
Vidaza 126 N/A N/A
Other Brands^(a)^ 331 481 (31) % 131 90 46 %
Total $ 10,129 $ 6,273 61 % $ 6,487 $ 3,667 77 %

(a) Includes Sustiva, Reyataz, Daklinza and all other BMS and Celgene products acquired as part of the Celgene acquisition that have lost exclusivity in major markets, over-the-counter brands and royalty revenue. Other Brands includes $83 million worldwide and $66 million U.S. revenues relating to Celgene products for the three months ended June 30, 2020.

(b) Includes Puerto Rico.

BRISTOL-MYERS SQUIBB COMPANY

PRODUCT REVENUES

FOR THE SIX MONTHS ENDED JUNE 30, 2020 AND 2019

(Unaudited, dollars in millions)

Worldwide Revenues U.S. Revenues^(b)^
2020 2019 % Change 2020 2019 % Change
Prioritized Brands
Revlimid $ 5,799 $ N/A $ 4,014 $ N/A
Eliquis 4,804 3,967 21 % 3,140 2,475 27 %
Opdivo 3,419 3,624 (6) % 1,964 2,236 (12) %
Orencia 1,464 1,418 3 % 1,054 1,015 4 %
Pomalyst/Imnovid 1,458 N/A 1,011 N/A
Sprycel 1,032 1,003 3 % 608 547 11 %
Yervoy 765 751 2 % 511 528 (3) %
Abraxane 608 N/A 423 N/A
Empliciti 194 174 11 % 118 121 (2) %
Reblozyl 63 N/A 63 N/A
Inrebic 27 N/A 27 N/A
Zeposia 1 N/A 1 N/A
Established Brands
Baraclude 243 288 (16) % 6 14 (57) %
Vidaza 284 N/A 2 N/A
Other Brands^(a)^ 749 968 (23) % 311 180 73 %
Total $ 20,910 $ 12,193 71 % $ 13,253 $ 7,116 86 %

(a) Includes Sustiva, Reyataz, Daklinza and all other BMS and Celgene products acquired as part of the Celgene acquisition that have lost exclusivity in major markets, over-the-counter brands and royalty revenue. Other Brands includes $205 million worldwide and $169 million U.S. revenues relating to Celgene products for the six months ended June 30, 2020.

(b) Includes Puerto Rico.

BRISTOL-MYERS SQUIBB COMPANY

CONSOLIDATED STATEMENTS OF EARNINGS

FOR THE THREE AND SIX MONTHS ENDED JUNE 30, 2020 AND 2019

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

Three Months Ended June 30, Six Months Ended June 30,
2020^(c)^ 2019 2020^(c)^ 2019
Net product sales $ 9,817 $ 6,031 $ 20,358 $ 11,744
Alliance and other revenues 312 242 552 449
Total Revenues 10,129 6,273 20,910 12,193
Cost of products sold^(a)^ 2,699 1,972 6,361 3,796
Marketing, selling and administrative 1,628 1,076 3,234 2,082
Research and development 2,522 1,325 4,894 2,673
Amortization of acquired intangible assets 2,389 24 4,671 48
Other (income)/expense, net (736) 100 427 (161)
Total Expenses 8,502 4,497 19,587 8,438
Earnings Before Income Taxes 1,627 1,776 1,323 3,755
Provision for Income Taxes 1,707 337 2,169 601
Net (Loss)/Earnings (80) 1,439 (846) 3,154
Noncontrolling Interest 5 7 14 12
Net (Loss)/Earnings Attributable to BMS $ (85) $ 1,432 $ (860) $ 3,142
Weighted-Average Common Shares Outstanding:
Basic 2,263 1,636 2,261 1,635
Diluted 2,263 1,637 2,261 1,637
(Loss)/Earnings per Common Share:
Basic $ (0.04) $ 0.88 $ (0.38) $ 1.92
Diluted (0.04) 0.87 (0.38) 1.92
Other (income)/expense, net
Interest expense^(b)^ $ 357 $ 123 $ 719 $ 168
Pension and postretirement (2) 26 (6) 70
Royalties and licensing income (311) (303) (721) (611)
Divestiture losses/(gains) 9 8 (7) 8
Acquisition expenses 303 468
Contingent consideration (165) 391
Investment income (25) (119) (86) (175)
Integration expenses 166 106 340 128
Provision for restructuring 115 10 275 22
Equity investment gains (818) (71) (479) (246)
Litigation and other settlements (1) 31 1
Transition and other service fees (50) (2) (111) (4)
Intangible asset impairment 21 15 21 15
Reversion excise tax 76
Other (32) 4 (16) (5)
Other (income)/expense, net $ (736) $ 100 $ 427 $ (161)

(a) Excludes amortization of acquired intangible assets.

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

(c) Includes Celgene results of operations for the entire period.

BRISTOL-MYERS SQUIBB COMPANY

SPECIFIED ITEMS

FOR THE THREE AND SIX MONTHS ENDED JUNE 30, 2020 AND 2019

(Unaudited, dollars in millions)

Three Months Ended June 30, Six Months Ended June 30,
2020^(b)^ 2019 2020^(b)^ 2019
Inventory purchase price accounting adjustments $ 714 $ $ 2,134 $
Employee compensation charges 1 3
Site exit and other costs 13 139 29 151
Cost of products sold 728 139 2,166 151
Employee compensation charges 12 27
Site exit and other costs (1) 5 1
Marketing, selling and administrative 11 32 1
License and asset acquisition charges 300 25 325 25
IPRD impairments 32
Inventory purchase price accounting adjustments 17
Employee compensation charges 15 33
Site exit and other costs 39 19 95 38
Research and development 354 44 470 95
Amortization of acquired intangible assets 2,389 4,671
Interest expense^(a)^ (41) 83 (82) 83
Pension and postretirement 44 93
Royalties and licensing income (18) (101)
Divestiture losses/(gains) 9 8 (7) 8
Acquisition expenses 303 468
Contingent consideration (165) 391
Investment income (54) (54)
Integration expenses 166 106 340 128
Provision for restructuring 115 10 275 22
Equity investment gains (818) (71) (479) (246)
Reversion excise tax 76
Other (income)/expense, net (752) 429 413 502
Increase to pretax income 2,730 612 7,752 749
Income taxes on items above (3) (105) (294) (148)
Income taxes attributed to Otezla^®^ divestiture 255 255
Income taxes attributed to internal transfer of intangible assets 853 853
Income taxes 1,105 (105) 814 (148)
Increase to net earnings $ 3,835 $ 507 $ 8,566 $ 601

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

(b) Includes Celgene results of operations for the entire period.

BRISTOL-MYERS SQUIBB COMPANY

RECONCILIATION OF CERTAIN GAAP LINE ITEMS TO CERTAIN NON-GAAP LINE ITEMS

FOR THE THREE AND SIX MONTHS ENDED JUNE 30, 2020 AND 2019

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

Three Months Ended June 30, 2020 Six Months Ended June 30, 2020
GAAP^(a)^ Specified Items^(a)(b)^ Non-GAAP^(a)^ GAAP Specified Items^(a)(b)^ Non-GAAP^(a)^
Gross Profit $ 7,430 $ 728 $ 8,158 $ 14,549 $ 2,166 $ 16,715
Marketing, selling and administrative 1,628 (11) 1,617 3,234 (32) 3,202
Research and development 2,522 (354) 2,168 4,894 (470) 4,424
Amortization of acquired intangible assets 2,389 (2,389) 4,671 (4,671)
Other (income)/expense, net (736) 752 16 427 (413) 14
Earnings Before Income Taxes 1,627 2,730 4,357 1,323 7,752 9,075
Provision for Income Taxes 1,707 (1,105) 602 2,169 (814) 1,355
Noncontrolling interest 5 5 14 14
Net (Loss)/Earnings Attributable to BMS used for Diluted EPS Calculation $ (85) $ 3,835 $ 3,750 $ (860) $ 8,566 $ 7,706
Weighted-Average Common Shares Outstanding - Diluted 2,263 2,297 2,297 2,261 2,298 2,298
Diluted (Loss)/Earnings Per Share $ (0.04) $ 1.67 $ 1.63 $ (0.38) $ 3.73 $ 3.35
Effective Tax Rate 104.9 % (91.1) % 13.8 % 163.9 % (149.0) % 14.9 %
Three Months Ended June 30, 2019 Six Months Ended June 30, 2019
GAAP Specified Items^(b)^ Non-GAAP GAAP Specified Items^(b)^ Non-GAAP
Gross Profit $ 4,301 $ 139 $ 4,440 $ 8,397 $ 151 $ 8,548
Marketing, selling and administrative 1,076 1,076 2,082 (1) 2,081
Research and development 1,325 (44) 1,281 2,673 (95) 2,578
Amortization of acquired intangible assets 24 24 48 48
Other (income)/expense, net 100 (429) (329) (161) (502) (663)
Earnings Before Income Taxes 1,776 612 2,388 3,755 749 4,504
Provision for Income Taxes 337 105 442 601 148 749
Noncontrolling interest 7 7 12 12
Net Earnings Attributable to BMS used for Diluted EPS Calculation $ 1,432 $ 507 $ 1,939 $ 3,142 $ 601 $ 3,743
Weighted-Average Common Shares Outstanding - Diluted 1,637 1,637 1,637 1,637 1,637 1,637
Diluted Earnings Per Share $ 0.87 $ 0.31 $ 1.18 $ 1.92 $ 0.37 $ 2.29
Effective Tax Rate 19.0 % (0.5) % 18.5 % 16.0 % 0.6 % 16.6 %

(a) Includes Celgene results of operations for the entire period.

(b) Refer to the Specified Items schedule for further details. Effective tax rate on the Specified Items represents the difference between the GAAP and Non-GAAP effective tax rate.

BRISTOL-MYERS SQUIBB COMPANY

NET DEBT CALCULATION

AS OF JUNE 30, 2020 AND DECEMBER 31, 2019

(Unaudited, dollars in millions)

June 30,<br>2020 December 31,<br>2019
Cash and cash equivalents $ 19,934 $ 12,346
Marketable debt securities - current 1,724 3,047
Marketable debt securities - non-current 523 767
Cash, cash equivalents and marketable debt securities 22,181 16,160
Short-term debt obligations (4,819) (3,346)
Long-term debt (41,853) (43,387)
Net debt position $ (24,491) $ (30,573)

Contact

Media: 609-252-3345, media@bms.com

Investor Relations: Tim Power, 609-252-7509, timothy.power@bms.com; Nina Goworek, 908-673-9711, nina.goworek@bms.com

20

Document

Exhibit 99.2

BRISTOL-MYERS SQUIBB COMPANY

QUARTERLY TREND ANALYSIS OF REVENUES

(Unaudited, dollars in millions)

Revenues 2019 2020 % Change FX Impact^(c)^
1st Qtr 2nd Qtr 6 Months 3rd Qtr 9 Months 4th Qtr^(a)^ Year^(a)^ 1st Qtr^(b)^ 2nd Qtr^(b)^ 6 Months^(b)^ 3rd Qtr 9 Months 4th Qtr Year Qtr vs. Qtr YTD vs. YTD Qtr vs. Qtr YTD vs. YTD
United States $ 3,449 $ 3,667 $ 7,116 $ 3,472 $ 10,588 $ 4,754 $ 15,342 $ 6,766 $ 6,487 $ 13,253 77% 86%
Europe 1,480 1,491 2,971 1,445 4,416 1,850 6,266 2,567 2,136 4,703 43% 58% (3)% (3)%
Rest of the World 874 988 1,862 976 2,838 1,175 4,013 1,335 1,334 2,669 35% 43% (4)% (4)%
Other 117 127 244 114 358 166 524 113 172 285 35% 17%
Total $ 5,920 $ 6,273 $ 12,193 $ 6,007 $ 18,200 $ 7,945 $ 26,145 $ 10,781 $ 10,129 $ 20,910 61% 71% (2)% (2)%
% of Revenues 2019 2020
1st Qtr 2nd Qtr 6 Months 3rd Qtr 9 Months 4th Qtr^(a)^ Year^(a)^ 1st Qtr^(b)^ 2nd Qtr^(b)^ 6 Months^(b)^ 3rd Qtr 9 Months 4th Qtr Year
United States 58.2 % 58.4 % 58.3 % 57.8 % 58.2 % 59.8 % 58.7 % 62.8 % 64.0 % 63.4 %
Europe 25.0 % 23.8 % 24.4 % 24.1 % 24.3 % 23.3 % 24.0 % 23.8 % 21.1 % 22.5 %
Rest of the World 14.8 % 15.8 % 15.3 % 16.2 % 15.6 % 14.8 % 15.3 % 12.4 % 13.2 % 12.8 %
Other 2.0 % 2.0 % 2.0 % 1.9 % 1.9 % 2.1 % 2.0 % 1.0 % 1.7 % 1.3 %
Total 100.0 % 100.0 % 100.0 % 100.0 % 100.0 % 100.0 % 100.0 % 100.0 % 100.0 % 100.0 %

(a) Includes Celgene product revenues from November 20, 2019 through December 31, 2019.

(b) Includes Celgene product revenues for the entire period.

(c) Foreign exchange impacts were derived by applying the prior period average currency rates to the current period sales.

BRISTOL-MYERS SQUIBB COMPANY

EARNINGS FROM OPERATIONS

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

2019 2020 % Change
1st Qtr 2nd Qtr 6 Months 3rd Qtr 9 Months 4th Qtr^(c)^ Year^(c)^ 1st Qtr^(d)^ 2nd Qtr^(d)^ 6 Months^(d)^ 3rd Qtr 9 Months 4th Qtr Year Qtr vs. Qtr YTD vs. YTD
Net product sales $ 5,713 $ 6,031 $ 11,744 $ 5,768 $ 17,512 $ 7,662 $ 25,174 $ 10,541 $ 9,817 $ 20,358 63% 73%
Alliance and other revenues 207 242 449 239 688 283 971 240 312 552 29% 23%
Total Revenues 5,920 6,273 12,193 6,007 18,200 7,945 26,145 10,781 10,129 20,910 61% 71%
Cost of products sold^(a)^ 1,824 1,972 3,796 1,790 5,586 2,492 8,078 3,662 2,699 6,361 37% 68%
Marketing, selling and administrative 1,006 1,076 2,082 1,055 3,137 1,734 4,871 1,606 1,628 3,234 51% 55%
Research and development 1,348 1,325 2,673 1,378 4,051 2,097 6,148 2,372 2,522 4,894 90% 83%
Amortization of acquired intangible assets 24 24 48 25 73 1,062 1,135 2,282 2,389 4,671 ** **
Other (income)/expense, net (261) 100 (161) 410 249 689 938 1,163 (736) 427 ** **
Total Expenses 3,941 4,497 8,438 4,658 13,096 8,074 21,170 11,085 8,502 19,587 89% **
Earnings/(Loss) Before Income Taxes 1,979 1,776 3,755 1,349 5,104 (129) 4,975 (304) 1,627 1,323 (8)% (65)%
Provision for Income Taxes 264 337 601 (17) 584 931 1,515 462 1,707 2,169 ** **
Net (Loss)/Earnings 1,715 1,439 3,154 1,366 4,520 (1,060) 3,460 (766) (80) (846) ** **
Noncontrolling Interest 5 7 12 13 25 (4) 21 9 5 14 (29)% 17%
Net (Loss)/Earnings Attributable to BMS $ 1,710 $ 1,432 $ 3,142 $ 1,353 $ 4,495 $ (1,056) $ 3,439 $ (775) $ (85) $ (860) ** **
Diluted (Loss)/Earnings per Common Share* $ 1.04 $ 0.87 $ 1.92 $ 0.83 $ 2.75 $ (0.55) $ 2.01 $ (0.34) $ (0.04) $ (0.38) ** **
Weighted-Average Common Shares Outstanding - Diluted 1,637 1,637 1,637 1,634 1,636 1,918 1,712 2,258 2,263 2,261
Dividends declared per common share $ 0.41 $ 0.41 $ 0.82 $ 0.41 $ 1.23 $ 0.45 $ 1.68 $ 0.45 $ 0.45 $ 0.90 10% 10%
2019 2020
% of Total Revenues 1st Qtr 2nd Qtr 6 Months 3rd Qtr 9 Months 4th Qtr^(c)^ Year^(c)^ 1st Qtr^(d)^ 2nd Qtr^(d)^ 6 Months^(d)^ 3rd Qtr 9 Months 4th Qtr Year
Gross Margin 69.2 % 68.6 % 68.9 % 70.2 % 69.3 % 68.6 % 69.1 % 66.0 % 73.4 % 69.6 %
Other Ratios
Effective tax rate 13.3 % 19.0 % 16.0 % (1.3) % 11.4 % (721.7) % 30.5 % (152.0) % 104.9 % 163.9 %
Other (income)/expense, net 2019 2020 % Change
1st Qtr 2nd Qtr 6 Months 3rd Qtr 9 Months 4th Qtr^(c)^ Year^(c)^ 1st Qtr^(d)^ 2nd Qtr^(d)^ 6 Months^(d)^ 3rd Qtr 9 Months 4th Qtr Year Qtr vs. Qtr YTD vs. YTD
Interest expense^(b)^ $ 45 $ 123 $ 168 $ 209 $ 377 $ 279 $ 656 $ 362 $ 357 $ 719 ** **
Pension and postretirement 44 26 70 1,537 1,607 (8) 1,599 (4) (2) (6) ** **
Royalties and licensing income (308) (303) (611) (356) (967) (393) (1,360) (410) (311) (721) 3% 18%
Divestiture losses/(gains) 8 8 (1,179) (1,171) 3 (1,168) (16) 9 (7) 13% **
Acquisition expenses 165 303 468 7 475 182 657 (100)% (100)%
Contingent consideration 523 523 556 (165) 391 N/A N/A
Investment income (56) (119) (175) (173) (348) (116) (464) (61) (25) (86) (79)% (51)%
Integration expenses 22 106 128 96 224 191 415 174 166 340 57% **
Provision for restructuring 12 10 22 10 32 269 301 160 115 275 ** **
Equity investment (gains)/losses (175) (71) (246) 261 15 (294) (279) 339 (818) (479) ** 95%
Litigation and other settlements 1 1 (1) 77 77 32 (1) 31 N/A **
Transition and other service fees (2) (2) (4) (7) (11) (26) (37) (61) (50) (111) ** **
Intangible asset impairment 15 15 15 15 21 21 40% 40%
Reversion excise tax 76 76 N/A N/A
Other (9) 4 (5) 6 1 2 3 16 (32) (16) ** **
Other (income)/expense, net $ (261) $ 100 $ (161) $ 410 $ 249 $ 689 $ 938 $ 1,163 $ (736) $ 427 ** **

* Quarterly amounts may not add to the year-to-date amounts, as each period is computed on a discrete basis.

** In excess of +/- 100%.

(a) Excludes amortization of acquired intangible assets.

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

(c) Includes Celgene results of operations from November 20, 2019 through December 31, 2019.

(d) Includes Celgene results of operations for the entire period.

BRISTOL-MYERS SQUIBB COMPANY

RECONCILIATION OF GAAP AND NON-GAAP GROWTH DOLLARS AND PERCENTAGES EXCLUDING FOREIGN EXCHANGE IMPACT

FOR THE PERIOD ENDED JUNE 30, 2020

(Unaudited, dollars in millions)

QUARTER-TO-DATE 2020^(b)^ 2019 Change % Change Favorable / (Unfavorable) FX Impact * 2020 Excluding FX Favorable / (Unfavorable) FX Impact %* % Change Excluding FX
Revenues $ 10,129 $ 6,273 61 % $ 10,214 (2) % 63 %
Gross profit 7,430 4,301 3,129 73 % N/A N/A N/A N/A
Gross profit excluding specified items^(a)^ 8,158 4,440 3,718 84 % N/A N/A N/A N/A
Gross profit excluding specified items as a % of revenues 80.5 % 70.8 %
Marketing, selling and administrative 1,628 1,076 552 51 % 17 1,645 2 % 53 %
Marketing, selling and administrative excluding specified items^(a)^ 1,617 1,076 541 50 % 17 1,634 2 % 52 %
Marketing, selling and administrative excluding specified items as a % of revenues 16.0 % 17.2 %
Research and development 2,522 1,325 1,197 90 % 6 2,528 1 % 91 %
Research and development excluding specified items^(a)^ 2,168 1,281 887 69 % 6 2,174 1 % 70 %
Research and development excluding specified items as a % of revenues 21.4 % 20.4 %
YEAR-TO-DATE 2020^(b)^ 2019 Change % Change Favorable / (Unfavorable) FX Impact * 2020 Excluding FX Favorable / (Unfavorable) FX Impact %* % Change Excluding FX
Revenues $ 20,910 $ 12,193 71 % $ 21,077 (2) % 73 %
Gross profit 14,549 8,397 6,152 73 % N/A N/A N/A N/A
Gross profit excluding specified items^(a)^ 16,715 8,548 8,167 96 % N/A N/A N/A N/A
Gross profit excluding specified items as a % of revenues 79.9 % 70.1 %
Marketing, selling and administrative 3,234 2,082 1,152 55 % 29 3,263 2 % 57 %
Marketing, selling and administrative excluding specified items^(a)^ 3,202 2,081 1,121 54 % 29 3,231 1 % 55 %
Marketing, selling and administrative excluding specified items as a % of revenues 15.3 % 17.1 %
Research and development 4,894 2,673 2,221 83 % 10 4,904 83 %
Research and development excluding specified items^(a)^ 4,424 2,578 1,846 72 % 10 4,434 72 %
Research and development excluding specified items as a % of revenues 21.2 % 21.1 %

All values are in US Dollars.

* Foreign exchange impacts were derived by applying the prior period average currency rates to the current period sales and expenses.

(a) Refer to the Specified Items schedule for further details.

(b) Includes Celgene results of operations for the entire period.

BRISTOL-MYERS SQUIBB COMPANY

WORLDWIDE REVENUES

QUARTERLY REVENUES TREND ANALYSIS

(Unaudited, dollars in millions)

2019 2020 $ Change % Change
1st Qtr 2nd Qtr 6 Months 3rd Qtr 9 Months 4th Qtr^(b)^ Year^(b)^ 1st Qtr^(c)^ 2nd Qtr^(c)^ 6 Months^(c)^ 3rd Qtr 9 Months 4th Qtr Year Qtr vs. Qtr YTD vs. YTD Qtr vs. Qtr YTD vs. YTD
Prioritized Brands
Revlimid $ $ $ $ $ $ 1,299 $ 1,299 $ 2,915 $ 2,884 $ 5,799 $ 2,884 $ 5,799 N/A N/A
Eliquis 1,925 2,042 3,967 1,928 5,895 2,034 7,929 2,641 2,163 4,804 121 837 6% 21%
Opdivo 1,801 1,823 3,624 1,817 5,441 1,763 7,204 1,766 1,653 3,419 (170) (205) (9)% (6)%
Orencia 640 778 1,418 767 2,185 792 2,977 714 750 1,464 (28) 46 (4)% 3%
Pomalyst/Imnovid 322 322 713 745 1,458 745 1,458 N/A N/A
Sprycel 459 544 1,003 558 1,561 549 2,110 521 511 1,032 (33) 29 (6)% 3%
Yervoy 384 367 751 353 1,104 385 1,489 396 369 765 2 14 1% 2%
Abraxane 166 166 300 308 608 308 608 N/A N/A
Empliciti 83 91 174 89 263 94 357 97 97 194 6 20 7% 11%
Reblozyl 8 55 63 55 63 N/A N/A
Inrebic 5 5 12 15 27 15 27 N/A N/A
Zeposia 1 1 1 1 N/A N/A
Established Brands
Baraclude 141 147 288 145 433 122 555 122 121 243 (26) (45) (18)% (16)%
Vidaza 58 58 158 126 284 126 284 N/A N/A
Other Brands^(a)^ 487 481 968 350 1,318 356 1,674 418 331 749 (150) (219) (31)% (23)%
Total $ 5,920 $ 6,273 $ 12,193 $ 6,007 $ 18,200 $ 7,945 $ 26,145 $ 10,781 $ 10,129 $ 20,910 $ 3,856 $ 8,717 61% 71%

(a) Includes Sustiva, Reyataz, Daklinza and all other BMS and Celgene products acquired as part of the Celgene acquisition that have lost exclusivity in major markets, over-the-counter (OTC) brands and royalty revenue. Other Brands includes $83 million and $205 million relating to Celgene products in the three and six months ended June 30, 2020, respectively.

(b) Includes Celgene product revenues from November 20, 2019 through December 31, 2019.

(c) Includes Celgene product revenues for the entire period.

BRISTOL-MYERS SQUIBB COMPANY

WORLDWIDE PRO FORMA REVENUES

QUARTERLY REVENUES TREND ANALYSIS

(Unaudited, dollars in millions)

2019 2020 $ Change % Change
1st Qtr 2nd Qtr 6 Months 3rd Qtr 9 Months 4th Qtr^(e)^ Year 1st Qtr 2nd Qtr 6 Months 3rd Qtr 9 Months 4th Qtr Year Qtr vs. Qtr YTD vs. YTD Qtr vs. Qtr YTD vs. YTD
Prioritized Brands
Revlimid^(a)^ $ 2,562 $ 2,718 $ 5,280 $ 2,758 $ 8,038 $ 2,785 $ 10,823 $ 2,915 $ 2,884 $ 5,799 $ 166 $ 519 6% 10%
Eliquis 1,925 2,042 3,967 1,928 5,895 2,034 7,929 2,641 2,163 4,804 121 837 6% 21%
Opdivo 1,801 1,823 3,624 1,817 5,441 1,763 7,204 1,766 1,653 3,419 (170) (205) (9)% (6)%
Orencia 640 778 1,418 767 2,185 792 2,977 714 750 1,464 (28) 46 (4)% 3%
Pomalyst/Imnovid^(a)^ 554 617 1,171 662 1,833 692 2,525 713 745 1,458 128 287 21% 25%
Sprycel 459 544 1,003 558 1,561 549 2,110 521 511 1,032 (33) 29 (6)% 3%
Yervoy 384 367 751 353 1,104 385 1,489 396 369 765 2 14 1% 2%
Abraxane^(a)^ 285 314 599 317 916 336 1,252 300 308 608 (6) 9 (2)% 2%
Empliciti 83 91 174 89 263 94 357 97 97 194 6 20 7% 11%
Reblozyl^(b)^ 8 55 63 55 63 N/A N/A
Inrebic^(b)^ 2 2 9 11 12 15 27 15 27 N/A N/A
Zeposia^(b)^ 1 1 1 1 N/A N/A
Established Brands
Baraclude 141 147 288 145 433 122 555 122 121 243 (26) (45) (18)% (16)%
Vidaza^(a)^ 148 162 310 146 456 149 605 158 126 284 (36) (26) (22)% (8)%
Other Brands^(c)^ 552 557 1,109 420 1,529 393 1,922 418 331 749 (226) (360) (41)% (32)%
Total^(d)^ $ 9,534 $ 10,160 $ 19,694 $ 9,962 $ 29,656 $ 10,103 $ 39,759 $ 10,781 $ 10,129 $ 20,910 $ (31) $ 1,216 6%

(a) Products were acquired as part of the Celgene acquisition. Reflects product revenues for the period prior to November 20, 2019, which was the date of the acquisition. All product revenues prior to November 20, 2019 have been recast to exclude foreign currency hedge gains and losses.

(b) Products were acquired as part of the Celgene acquisition. Reflects product revenues for the period prior to November 20, 2019, which was the date of the acquisition.

(c) Includes Sustiva, Reyataz, Daklinza and all other BMS and Celgene products acquired as part of the Celgene acquisition that have lost exclusivity in major markets, over-the-counter (OTC) brands and royalty revenue. Reflects Celgene product revenues for the period prior to November 20, 2019, which was the date of the acquisition, for such Celgene products.

(d) All historically reported Celgene revenues have been recast to exclude Otezla^®^ product revenues.

(e) Celgene product revenues for the period of October 1, 2019 through November 19, 2019 are included below:

Revlimid $ 1,486
Pomalyst/Imnovid 370
Abraxane 170
Inrebic 4
Vidaza 91
Other Brands 37
Total $ 2,158

BRISTOL-MYERS SQUIBB COMPANY

U.S. REVENUES

QUARTERLY REVENUES TREND ANALYSIS

(Unaudited, dollars in millions)

2019 2020 % Change
1st Qtr 2nd Qtr 6 Months 3rd Qtr 9 Months 4th Qtr^(c)^ Year^(c)^ 1st Qtr^(d)^ 2nd Qtr^(d)^ 6 Months^(d)^ 3rd Qtr 9 Months 4th Qtr Year Qtr vs. Qtr YTD vs. YTD
Prioritized Brands
Revlimid $ $ $ $ $ $ 899 $ 899 $ 1,966 $ 2,048 $ 4,014 N/A N/A
Eliquis 1,206 1,269 2,475 1,124 3,599 1,156 4,755 1,777 1,363 3,140 7% 27%
Opdivo 1,124 1,112 2,236 1,088 3,324 1,020 4,344 1,008 956 1,964 (14)% (12)%
Orencia 449 566 1,015 554 1,569 577 2,146 500 554 1,054 (2)% 4%
Pomalyst/Imnovid 226 226 489 522 1,011 N/A N/A
Sprycel 240 307 547 325 872 319 1,191 300 308 608 11%
Yervoy 275 253 528 222 750 254 1,004 257 254 511 (3)%
Abraxane 122 122 205 218 423 N/A N/A
Empliciti 58 63 121 62 183 63 246 59 59 118 (6)% (2)%
Reblozyl 8 55 63 N/A N/A
Inrebic 5 5 12 15 27 N/A N/A
Zeposia 1 1 N/A N/A
Established Brands
Baraclude 7 7 14 2 16 4 20 3 3 6 (57)% (57)%
Vidaza 1 1 2 2 N/A N/A
Other Brands^(a)^ 90 90 180 95 275 108 383 180 131 311 46% 73%
Total^(b)^ $ 3,449 $ 3,667 $ 7,116 $ 3,472 $ 10,588 $ 4,754 $ 15,342 $ 6,766 $ 6,487 $ 13,253 77% 86%

(a) Includes Sustiva, Reyataz, Daklinza and all other BMS and Celgene products acquired as part of the Celgene acquisition that have lost exclusivity in major markets, OTC brands and royalty revenue. Other Brands includes $66 million and $169 million relating to Celgene products in the three and six months ended June 30, 2020, respectively.

(b) Includes Puerto Rico.

(c) Includes Celgene product revenues from November 20, 2019 through December 31, 2019.

(d) Includes Celgene product revenues for the entire period.

BRISTOL-MYERS SQUIBB COMPANY

U.S. PRO FORMA REVENUES

QUARTERLY REVENUES TREND ANALYSIS

(Unaudited, dollars in millions)

2019 2020 % Change
1st Qtr 2nd Qtr 6 Months 3rd Qtr 9 Months 4th Qtr^(d)^ Year 1st Qtr 2nd Qtr 6 Months 3rd Qtr 9 Months 4th Qtr Year Qtr vs. Qtr YTD vs. YTD
Prioritized Brands
Revlimid^(a)^ $ 1,686 $ 1,810 $ 3,496 $ 1,902 $ 5,398 $ 1,914 $ 7,312 $ 1,966 $ 2,048 $ 4,014 13% 15%
Eliquis 1,206 1,269 2,475 1,124 3,599 1,156 4,755 1,777 1,363 3,140 7% 27%
Opdivo 1,124 1,112 2,236 1,088 3,324 1,020 4,344 1,008 956 1,964 (14)% (12)%
Orencia 449 566 1,015 554 1,569 577 2,146 500 554 1,054 (2)% 4%
Pomalyst/Imnovid^(a)^ 390 447 837 469 1,306 489 1,795 489 522 1,011 17% 21%
Sprycel 240 307 547 325 872 319 1,191 300 308 608 11%
Yervoy 275 253 528 222 750 254 1,004 257 254 511 (3)%
Abraxane^(a)^ 196 207 403 206 609 237 846 205 218 423 5% 5%
Empliciti 58 63 121 62 183 63 246 59 59 118 (6)% (2)%
Reblozyl^(a)^ 8 55 63 N/A N/A
Inrebic^(a)^ 2 2 9 11 12 15 27 N/A N/A
Zeposia^(a)^ 1 1 N/A N/A
Established Brands
Baraclude 7 7 14 2 16 4 20 3 3 6 (57)% (57)%
Vidaza^(a)^ 3 3 6 2 8 2 10 2 2 (100)% (67)%
Other Brands^(b)^ 135 145 280 147 427 136 563 180 131 311 (10)% 11%
Total^(c)^ $ 5,769 $ 6,189 $ 11,958 $ 6,105 $ 18,063 $ 6,180 $ 24,243 $ 6,766 $ 6,487 $ 13,253 5% 11%

(a) Products were acquired as part of the Celgene acquisition. Reflects product revenues for the period prior to November 20, 2019, which was the date of the acquisition.

(b) Includes Sustiva, Reyataz, Daklinza and all other BMS and Celgene products acquired as part of the Celgene acquisition that have lost exclusivity in major markets, OTC brands and royalty revenue. Reflects Celgene product revenues for the period prior to November 20, 2019, which was the date of the acquisition, for such Celgene products.

(c) Includes Puerto Rico. All historically reported Celgene revenues have been recast to exclude Otezla^®^ product revenues.

(d) Celgene product revenues for the period of October 1, 2019 through November 19, 2019 are included below:

Revlimid $ 1,015
Pomalyst/Imnovid 263
Abraxane 115
Inrebic 4
Vidaza 1
Other Brands 28
Total $ 1,426

BRISTOL-MYERS SQUIBB COMPANY

INTERNATIONAL REVENUES

QUARTERLY REVENUES TREND ANALYSIS

(Unaudited, dollars in millions)

2019 2020 % Change^(c)^
1st Qtr 2nd Qtr 6 Months 3rd Qtr 9 Months 4th Qtr^(b)^ Year^(b)^ 1st Qtr^(d)^ 2nd Qtr^(d)^ 6 Months^(d)^ 3rd Qtr 9 Months 4th Qtr Year Qtr vs. Qtr YTD vs. YTD
Prioritized Brands
Revlimid $ $ $ $ $ $ 400 $ 400 $ 949 $ 836 $ 1,785 N/A N/A
Eliquis 719 773 1,492 804 2,296 878 3,174 864 800 1,664 3% 12%
Opdivo 677 711 1,388 729 2,117 743 2,860 758 697 1,455 (2)% 5%
Orencia 191 212 403 213 616 215 831 214 196 410 (8)% 2%
Pomalyst/Imnovid 96 96 224 223 447 N/A N/A
Sprycel 219 237 456 233 689 230 919 221 203 424 (14)% (7)%
Yervoy 109 114 223 131 354 131 485 139 115 254 1% 14%
Abraxane 44 44 95 90 185 N/A N/A
Empliciti 25 28 53 27 80 31 111 38 38 76 36% 43%
Established Brands
Baraclude 134 140 274 143 417 118 535 119 118 237 (16)% (14)%
Vidaza 57 57 156 126 282 N/A N/A
Other Brands^(a)^ 397 391 788 255 1,043 248 1,291 238 200 438 (49)% (44)%
Total $ 2,471 $ 2,606 $ 5,077 $ 2,535 $ 7,612 $ 3,191 $ 10,803 $ 4,015 $ 3,642 $ 7,657 40% 51%

(a) Includes Sustiva, Reyataz, Daklinza and all other BMS and Celgene products acquired as part of the Celgene acquisition that have lost exclusivity in major markets, OTC brands and royalty revenue. Other Brands includes $17 million and $36 million relating to Celgene products in the three and six months ended June 30, 2020, respectively.

(b) Includes Celgene product revenues from November 20, 2019 through December 31, 2019.

(c) The foreign exchange impact on international revenues was unfavorable 3% for both the second quarter and year-to-date. The foreign exchange impact on Prioritized Brands is included below.

(d) Includes Celgene product revenues for the entire period.

Quarter-to-Date Year-to-Date
Revenue Change % Favorable/ (Unfavorable) FX Impact % Revenue Change % Excluding FX Revenue Change % Favorable/ (Unfavorable) FX Impact % Revenue Change % Excluding FX
Eliquis 3% (2)% 5% 12% (2)% 14%
Opdivo (2)% (5)% 3% 5% (5)% 10%
Orencia (8)% (3)% (5)% 2% (3)% 5%
Sprycel (14)% (3)% (11)% (7)% (3)% (4)%
Yervoy 1% (5)% 6% 14% (5)% 19%
Empliciti 36% 36% 43% (1)% 44%

BRISTOL-MYERS SQUIBB COMPANY

INTERNATIONAL PRO FORMA REVENUES

QUARTERLY REVENUES TREND ANALYSIS

(Unaudited, dollars in millions)

2019 2020 % Change
1st Qtr 2nd Qtr 6 Months 3rd Qtr 9 Months 4th Qtr^(d)^ Year 1st Qtr 2nd Qtr 6 Months 3rd Qtr 9 Months 4th Qtr Year Qtr vs. Qtr YTD vs. YTD
Prioritized Brands
Revlimid^(a)^ $ 876 $ 908 $ 1,784 $ 856 $ 2,640 $ 871 $ 3,511 $ 949 $ 836 $ 1,785 (8)%
Eliquis 719 773 1,492 804 2,296 878 3,174 864 800 1,664 3% 12%
Opdivo 677 711 1,388 729 2,117 743 2,860 758 697 1,455 (2)% 5%
Orencia 191 212 403 213 616 215 831 214 196 410 (8)% 2%
Pomalyst/Imnovid^(a)^ 164 170 334 193 527 203 730 224 223 447 31% 34%
Sprycel 219 237 456 233 689 230 919 221 203 424 (14)% (7)%
Yervoy 109 114 223 131 354 131 485 139 115 254 1% 14%
Abraxane^(a)^ 89 107 196 111 307 99 406 95 90 185 (16)% (6)%
Empliciti 25 28 53 27 80 31 111 38 38 76 36% 43%
Established Brands
Baraclude 134 140 274 143 417 118 535 119 118 237 (16)% (14)%
Vidaza^(a)^ 145 159 304 144 448 147 595 156 126 282 (21)% (7)%
Other Brands^(b)^ 417 412 829 273 1,102 257 1,359 238 200 438 (51)% (47)%
Total^(c)^ $ 3,765 $ 3,971 $ 7,736 $ 3,857 $ 11,593 $ 3,923 $ 15,516 $ 4,015 $ 3,642 $ 7,657 (8)% (1)%

(a) Products were acquired as part of the Celgene acquisition. Reflects product revenues for the period prior to November 20, 2019, which was the date of the acquisition. All product revenues prior to November 20, 2019 have been recast to exclude foreign currency hedge gains and losses.

(b) Includes Sustiva, Reyataz, Daklinza and all other BMS and Celgene products acquired as part of the Celgene acquisition that have lost exclusivity in major markets, OTC brands and royalty revenue. Reflects Celgene product revenues for the period prior to November 20, 2019, which was the date of the acquisition, for such Celgene products.

(c) All historically reported Celgene revenues have been recast to exclude Otezla^®^ product revenues.

(d) Celgene product revenues for the period of October 1, 2019 through November 19, 2019 are included below:

Revlimid $ 471
Pomalyst/Imnovid 107
Abraxane 55
Vidaza 90
Other Brands 9
Total $ 732

BRISTOL-MYERS SQUIBB COMPANY

SPECIFIED ITEMS

(Unaudited, dollars in millions)

2019 2020
1st Qtr 2nd Qtr 6 Months 3rd Qtr 9 Months 4th Qtr^(b)^ Year^(b)^ 1st Qtr^(c)^ 2nd Qtr^(c)^ 6 Months^(c)^ 3rd Qtr 9 Months 4th Qtr Year
Inventory purchase price accounting adjustments $ $ $ $ $ $ 660 $ 660 $ 1,420 $ 714 $ 2,134
Employee compensation charges 1 1 2 1 3
Site exit and other costs 12 139 151 22 173 24 197 16 13 29
Cost of products sold 12 139 151 22 173 685 858 1,438 728 2,166
Employee compensation charges 27 27 15 12 27
Site exit and other costs 1 1 1 8 9 6 (1) 5
Marketing, selling and administrative 1 1 1 35 36 21 11 32
License and asset acquisition charges 25 25 25 25 25 300 325
IPRD impairments 32 32 32 32
Inventory purchase price accounting adjustments 17 17
Employee compensation charges 33 33 18 15 33
Site exit and other costs 19 19 38 20 58 109 167 56 39 95
Research and development 51 44 95 20 115 142 257 116 354 470
Amortization of acquired intangible assets 1,062 1,062 2,282 2,389 4,671
Interest expense^(a)^ 83 83 166 249 73 322 (41) (41) (82)
Pension and postretirement 49 44 93 1,545 1,638 (3) 1,635
Royalties and licensing income (9) (9) (15) (24) (83) (18) (101)
Divestiture losses/(gains) 8 8 (1,179) (1,171) 3 (1,168) (16) 9 (7)
Acquisition expenses 165 303 468 7 475 182 657
Contingent consideration 523 523 556 (165) 391
Investment income (54) (54) (99) (153) (44) (197)
Integration expenses 22 106 128 96 224 191 415 174 166 340
Provision for restructuring 12 10 22 10 32 269 301 160 115 275
Equity investment (gains)/losses (175) (71) (246) 261 15 (294) (279) 339 (818) (479)
Litigation and other settlements 75 75
Reversion excise tax 76 76
Other 2 2
Other (income)/expense, net 73 429 502 798 1,300 962 2,262 1,165 (752) 413
Increase to pretax income 137 612 749 840 1,589 2,886 4,475 5,022 2,730 7,752
Income taxes on items above (43) (105) (148) (275) (423) (264) (687) (291) (3) (294)
Income taxes attributed to Otezla^®^ divestiture 808 808 255 255
Income taxes attributed to internal transfer of intangible assets 853 853
Income taxes (43) (105) (148) (275) (423) 544 121 (291) 1,105 814
Increase to net earnings $ 94 $ 507 $ 601 $ 565 $ 1,166 $ 3,430 $ 4,596 $ 4,731 $ 3,835 $ 8,566

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

(b) Includes Celgene results of operations from November 20, 2019 through December 31, 2019.

(c) Includes Celgene results of operations for the entire period.

BRISTOL-MYERS SQUIBB COMPANY

RECONCILIATION OF CERTAIN GAAP LINE ITEMS TO CERTAIN NON-GAAP LINE ITEMS

(Unaudited, dollars in millions)

2019 2020
1st Qtr 2nd Qtr 6 Months 3rd Qtr 9 Months 4th Qtr^(b)^ Year^(b)^ 1st Qtr^(c)^ 2nd Qtr^(c)^ 6 Months^(c)^ 3rd Qtr 9 Months 4th Qtr Year
Gross Profit $ 4,096 $ 4,301 $ 8,397 $ 4,217 $ 12,614 $ 5,453 $ 18,067 $ 7,119 $ 7,430 $ 14,549
Specified items^(a)^ 12 139 151 22 173 685 858 1,438 728 2,166
Gross profit excluding specified items 4,108 4,440 8,548 4,239 12,787 6,138 18,925 8,557 8,158 16,715
Marketing, selling and administrative 1,006 1,076 2,082 1,055 3,137 1,734 4,871 1,606 1,628 3,234
Specified items^(a)^ (1) (1) (1) (35) (36) (21) (11) (32)
Marketing, selling and administrative excluding specified items 1,005 1,076 2,081 1,055 3,136 1,699 4,835 1,585 1,617 3,202
Research and development 1,348 1,325 2,673 1,378 4,051 2,097 6,148 2,372 2,522 4,894
Specified items^(a)^ (51) (44) (95) (20) (115) (142) (257) (116) (354) (470)
Research and development excluding specified items 1,297 1,281 2,578 1,358 3,936 1,955 5,891 2,256 2,168 4,424
Amortization of acquired intangible assets 24 24 48 25 73 1,062 1,135 2,282 2,389 4,671
Specified items^(a)^ (1,062) (1,062) (2,282) (2,389) (4,671)
Amortization of acquired intangible assets excluding specified items 24 24 48 25 73 73
Other (income)/expense, net (261) 100 (161) 410 249 689 938 1,163 (736) 427
Specified items^(a)^ (73) (429) (502) (798) (1,300) (962) (2,262) (1,165) 752 (413)
Other expense/(income), net excluding specified items (334) (329) (663) (388) (1,051) (273) (1,324) (2) 16 14

(a) Refer to the Specified Items schedule for further details.

(b) Includes Celgene results of operations from November 20, 2019 through December 31, 2019.

(c) Includes Celgene results of operations for the entire period.

BRISTOL-MYERS SQUIBB COMPANY

RECONCILIATION OF GAAP TO NON-GAAP EPS

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

2019 2020
1st Qtr 2nd Qtr 6 Months 3rd Qtr 9 Months 4th Qtr^(b)^ Year^(b)^ 1st Qtr^(c)^ 2nd Qtr^(c)^ 6 Months^(c)^ 3rd Qtr 9 Months 4th Qtr Year
Earnings/(Loss) before income taxes $ 1,979 $ 1,776 $ 3,755 $ 1,349 $ 5,104 $ (129) $ 4,975 $ (304) $ 1,627 $ 1,323
Specified items^(a)^ 137 612 749 840 1,589 2,886 4,475 5,022 2,730 7,752
Earnings before income taxes excluding specified items 2,116 2,388 4,504 2,189 6,693 2,757 9,450 4,718 4,357 9,075
Provision for income taxes 264 337 601 (17) 584 931 1,515 462 1,707 2,169
Income taxes on specified items^(a)^ 43 105 148 275 423 264 687 291 3 294
Income taxes attributed to Otezla^®^ divestiture^(a)^ (808) (808) (255) (255)
Income taxes attributed to internal transfer of intangible assets^(a)^ (853) (853)
Provision for income taxes excluding tax on specified items and income taxes attributed to Otezla^®^ divestiture and internal transfer of intangible assets 307 442 749 258 1,007 387 1,394 753 602 1,355
Noncontrolling Interest 5 7 12 13 25 (4) 21 9 5 14
Specified items^(a)^
Noncontrolling Interest excluding specified items 5 7 12 13 25 (4) 21 9 5 14
Net (loss)/earnings attributable to BMS used for Diluted EPS Calculation - GAAP 1,710 1,432 3,142 1,353 4,495 (1,056) 3,439 (775) (85) (860)
Specified items^(a)^ 94 507 601 565 1,166 3,430 4,596 4,731 3,835 8,566
Net earnings attributable to BMS used for Diluted EPS Calculation excluding specified items - Non-GAAP 1,804 1,939 3,743 1,918 5,661 2,374 8,035 3,956 3,750 7,706
Weighted-average Common Shares Outstanding - Diluted-GAAP 1,637 1,637 1,637 1,634 1,636 1,918 1,712 2,258 2,263 2,261
Weighted-average Common Shares Outstanding - Diluted-Non-GAAP 1,637 1,637 1,637 1,634 1,636 1,941 1,712 2,298 2,297 2,298
Diluted (Loss)/Earnings Per Share - GAAP* $ 1.04 $ 0.87 $ 1.92 $ 0.83 $ 2.75 $ (0.55) $ 2.01 $ (0.34) $ (0.04) $ (0.38)
Diluted Earnings Per Share attributable to specified items^(a)^ 0.06 0.31 0.37 0.34 0.71 1.77 2.68 2.06 1.67 3.73
Diluted Earnings Per Share - Non-GAAP* $ 1.10 $ 1.18 $ 2.29 $ 1.17 $ 3.46 $ 1.22 $ 4.69 $ 1.72 $ 1.63 $ 3.35
Effective Tax Rate 13.3 % 19.0 % 16.0 % (1.3) % 11.4 % (721.7) % 30.5 % (152.0) % 104.9 % 163.9 %
Specified items^(a)^ 1.2 % (0.5) % 0.6 % 13.1 % 3.6 % 735.7 % (15.7) % 168.0 % (91.1) % (149.0) %
Effective Tax Rate excluding specified items 14.5 % 18.5 % 16.6 % 11.8 % 15.0 % 14.0 % 14.8 % 16.0 % 13.8 % 14.9 %

* Quarterly amounts may not add to the year-to-date amounts, as each period is computed on a discrete basis.

(a) Refer to the Specified Items schedule for further details. Effective tax rate on the Specified Items represents the difference between the GAAP and Non-GAAP effective tax rate.

(b) Includes Celgene results from operations from November 20, 2019 through December 31, 2019.

(c) Includes Celgene results of operations for the entire period.

BRISTOL-MYERS SQUIBB COMPANY

SELECTED BALANCE SHEET INFORMATION

(Unaudited, dollars in millions)

March 31,<br>2019 June 30,<br>2019 September 30,<br>2019 December 31,<br><br>2019^(a)^ March 31,<br>2020 June 30,<br>2020 September 30,<br>2020 December 31,<br>2020
Cash and cash equivalents $ 7,335 $ 28,404 $ 30,489 $ 12,346 $ 15,817 $ 19,934
Marketable debt securities - current 1,429 953 2,053 3,047 2,505 1,724
Marketable debt securities - non-current 1,233 994 925 767 651 523
Cash, cash equivalents and marketable debt securities 9,997 30,351 33,467 16,160 18,973 22,181
Short-term debt obligations (381) (545) (569) (3,346) (3,862) (4,819)
Long-term debt (5,635) (24,433) (24,390) (43,387) (42,844) (41,853)
Net (debt)/cash position $ 3,981 $ 5,373 $ 8,508 $ (30,573) $ (27,733) $ (24,491)

(a) Includes Celgene balances as of December 31, 2019.

BRISTOL-MYERS SQUIBB COMPANY

2020 FULL YEAR PROJECTED DILUTED EPS FROM OPERATIONS

EXCLUDING PROJECTED SPECIFIED ITEMS

Full Year 2020
Pre-tax Tax
Projected Diluted (Loss)/Earnings Attributable to Shareholders per Common Share - GAAP (0.06) to 0.09
Projected Specified Items:
Purchase price accounting adjustments^(a)^ 5.31 0.29 5.02
Acquisition, restructuring and integration expenses^(b)^ 0.61 0.13 0.48
Equity investment losses and contingent consideration (0.04) (0.06) 0.02
Research and development license and asset acquisition charges 0.15 0.15
Employee compensation charges^(c)^ 0.04 0.01 0.03
Divestiture gains and licensing income (0.03) (0.03)
Other 0.01 0.01
Income taxes attributed to Otezla^®^ divestiture and internal transfer of intangible assets (0.48) 0.48
Total 6.05 (0.11) 6.16
Projected Diluted Earnings Attributable to Shareholders per Common Share - Non-GAAP 6.10 to 6.25

All values are in US Dollars.

(a) Includes amortization of acquired intangible assets, unwind of inventory fair value adjustments and amortization of fair value adjustments of debt assumed from Celgene.

(b) Includes acquisition-related financing, transaction, restructuring and integration expenses recognized in Cost of products sold, Research and development and Other (income)/expense, net.

(c) Includes items recognized in Cost of products sold, Marketing, selling and administrative and Research and development.

The following table summarizes the company's 2020 financial guidance:
Line item GAAP Non-GAAP
Revenues $40.5 billion - $42.0 billion $40.5 billion - $42.0 billion
Gross margin as a percent of revenue Approximately 74% Approximately 80%
Marketing, selling and administrative expense $6.5 billion - $6.7 billion $6.5 billion - $6.7 billion
Research and development expense $9.7 billion - $9.9 billion $9.2 billion - $9.4 billion
Other (income)/expense, net $0.9 billion - $1.1 billion ($0.1 billion) - $0.1 billion
Effective tax rate Approximately 100% 16% - 17%
Weighted average diluted shares Approximately 2.3 billion Approximately 2.3 billion The GAAP financial results for the full year of 2020 will include specified items, including purchase price accounting adjustments, acquisition and integration expenses, charges associated with restructuring, downsizing and streamlining worldwide operations, research and development license and asset acquisition charges, divestiture gains or losses, stock compensation resulting from accelerated vesting of Celgene awards, certain retention-related employee compensation charges related to the Celgene transaction, equity investment and contingent value rights fair value adjustments and tax items resulting from internal transfer of intangible assets and the Otezla® divestiture, among other items. The financial guidance for 2020 excludes the impact of any potential future strategic acquisitions and divestitures and other specified items that have not yet been identified and quantified. For a fuller discussion of items that could impact full year GAAP results, as well as the use of non-GAAP financial information, see Bristol Myers Squibb Reports Second Quarter 2020 Financial Results on August 6, 2020, including “2020 Financial Guidance” and “Use of non-GAAP Financial Information” therein.
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