bmy-20230202
0000014272false00000142722023-02-022023-02-020000014272bmy:CommonStock0.10ParValueMember2023-02-022023-02-020000014272bmy:A1.000Notesdue2025Member2023-02-022023-02-020000014272bmy:A1.750Notesdue2035Member2023-02-022023-02-020000014272bmy:CelgeneContingentValueRightsMember2023-02-022023-02-02

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): February 2, 2023

_____________________________
BRISTOL-MYERS SQUIBB COMPANY
(Exact name of registrant as specified in its charter)
_____________________________
Delaware001-0113622-0790350
(State or other jurisdiction of
incorporation or organization)
(Commission File Number)(I.R.S Employer
Identification No.)
430 E. 29th Street, 14th Floor
New York, New York, 10016
(Address of principal executive offices) (zip code)

Registrant’s telephone number, including area code: (212546-4200
_____________________________

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 classTrading Symbol(s)Name of each exchange on which registered
Common Stock, $0.10 Par ValueBMYNew York Stock Exchange
1.000% Notes due 2025BMY25New York Stock Exchange
1.750% Notes due 2035BMY35New York Stock Exchange
Celgene Contingent Value RightsCELG RTNew 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 February 2, 2023, Bristol-Myers Squibb Company (the “Company”) issued a press release (the “Earnings Press Release”) announcing its financial results for the fourth quarter of 2022 and full year of 2022. 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 (the “Supplemental Information”) posted on the Company’s website at www.bms.com.

Item 7.01 Regulation FD Disclosure.

On February 2, 2023, the Company posted on its website at www.bms.com a presentation (the “Bristol Myers Presentation”) on certain financial and operating initiatives available for viewing during the Company’s conference call and webcast announcing its financial results for the fourth quarter of 2022 and full year of 2022 at 9:00 a.m. Eastern time on February 2, 2023. A copy of the Bristol Myers Presentation is furnished pursuant to this Item 7.01 as Exhibit 99.3 to this Current Report on Form 8-K and incorporated by reference herein in its entirety. The Earnings Press Release and the Bristol Myers Presentation includes references to non-GAAP financial information. Reconciliations between the non-GAAP financial measures and the comparable GAAP financial measures are available in the Supplemental Information, which is included as Exhibit 99.2 hereto, and the reasons for the presentation of such non-GAAP financial measures are available in the Earnings Press Release, which is included as Exhibit 99.1 hereto. The Bristol Myers Presentation should be read in conjunction with the Supplemental Information and the Earnings Press Release. The Company reserves the right to discontinue availability of the Bristol Myers Presentation from its website at any time.

Pursuant to General Instruction B.2. to Form 8-K, the information set forth in this Item 7.01 of this Current Report on Form 8-K, including Exhibits 99.1, 99.2 and 99.3, shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities thereof, nor shall it be incorporated by reference into future filings by the Company under the Exchange Act or under the Securities Act of 1933, as amended, except to the extent specifically provided in any such filing. Additionally, the submission of the information set forth in this Item 7.01 is not deemed an admission as to the materiality of any information in this Current Report on Form 8-K that is required to be disclosed solely by Regulation FD.

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
No.
Description
99.1
Press release of Bristol-Myers Squibb Company dated February 2, 2023.
99.2Certain supplemental information posted on Bristol-Myers Squibb Company’s website at www.bms.com not included in the press release.
99.3
Presentation Materials of Bristol-Myers Squibb Company dated February 2, 2023.
104The cover page from this Current Report on Form 8-K formatted in Inline XBRL (included as Exhibit 101).
EXHIBIT INDEX
Exhibit
No.
Description
99.1
99.2
99.3
104The 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: February 2, 2023
By: /s/ Kimberly M. Jablonski
Name: Kimberly M. Jablonski
Title:Corporate Secretary


Exhibit 99.1
bmslogo2021.jpg

Bristol Myers Squibb Reports Fourth Quarter and Full-Year Financial Results for 2022
Reports Fourth Quarter Revenues of $11.4 Billion; Full-Year Revenues of $46.2 Billion
Fourth Quarter Revenues from In-Line Products and New Product Portfolio were $9.0 Billion, an Increase of 7%, or 12% When Adjusted for Foreign Exchange
Full-Year Revenues from In-Line Products and New Product Portfolio were $35.4 Billion, an Increase of 9%, or 13% When Adjusted for Foreign Exchange
Posts Fourth Quarter GAAP EPS of $0.95 and Non-GAAP EPS of $1.82; Includes Net Impact of ($0.01) Per Share for GAAP and Non-GAAP EPS Due to Acquired IPRD Charges and Licensing Income
Reports Full-Year GAAP EPS of $2.95 and Non-GAAP EPS of $7.70; Includes Net Impact of ($0.24) Per Share for GAAP and Non-GAAP EPS Due to Acquired IPRD Charges and Licensing Income
Provides GAAP and Non-GAAP Financial Guidance for 2023 Reflecting Continued Revenue and Earnings Growth

(NEW YORK, February 2, 2023) – Bristol Myers Squibb (NYSE:BMY) today reports results for the fourth quarter and full year of 2022, which reflect robust growth of the in-line and new product portfolios, driven by strong commercial execution and continued progress of the company's pipeline.

“2022 was a successful year for our company, one of significant clinical and regulatory achievements that broadened our product portfolio and advanced our pipeline,” said Giovanni Caforio, M.D., board chair and chief executive officer, Bristol Myers Squibb. “We are especially proud to have launched three first-in-class medicines that address serious unmet medical needs for patients. Our financial strength, talented workforce and proven ability to execute will enable us to continue to progress our pipeline and invest in future sources of innovation. With a younger and more diversified portfolio, promising mid-to-late stage registrational assets and a deep early-stage pipeline, I am confident that the company is well positioned for multiple waves of innovation that will support long-term growth.”

1



Fourth Quarter
$ amounts in millions, except per share amounts20222021ChangeChange
Excl. F/X**
Total Revenues$11,406 $11,985 (5)%(1)%
Earnings Per Share - GAAP*0.95 1.07 (11)%N/A
Earnings Per Share - Non-GAAP*1.82 1.84 (1)%N/A
* GAAP and non-GAAP earnings per share include the net impact of Acquired IPRD charges and licensing income of ($0.01) per share in the fourth quarter of 2022 and 2021.
** See "Use of Non-GAAP Financial Information."

Full Year
$ amounts in millions, except per share amounts20222021ChangeChange
Excl. F/X**
Total Revenues$46,159 $46,385 — %
Earnings Per Share - GAAP*2.95 3.12 (5)%N/A
Earnings Per Share - Non-GAAP*7.70 7.16 %N/A
* GAAP and non-GAAP earnings per share include the net impact of Acquired IPRD charges and licensing income of ($0.24) per share in 2022 compared to ($0.40) per share in 2021.
** See "Use of Non-GAAP Financial Information."


FOURTH QUARTER FINANCIAL RESULTS

All comparisons are made versus the same period in 2021 unless otherwise stated.

Bristol Myers Squibb posted revenues of $11.4 billion, a decrease of 5%, driven by recent LOE products (primarily Revlimid) and foreign exchange impacts, partially offset by in-line products (primarily Opdivo) and our new product portfolio (primarily Opdualag and Abecma). When adjusted for foreign exchange, revenues decreased 1%. Our in-line products and new product portfolio increased 7% to $9.0 billion, or 12% when adjusted for foreign exchange.
U.S. revenues increased 5% to $7.9 billion. International revenues decreased 22% to $3.5 billion. When adjusted for foreign exchange, international revenues decreased 13%, primarily due to lower demand for Revlimid as a result of generic erosion, partially offset by in-line products (primarily Opdivo) and our new product portfolio.
Gross margin decreased from 80.3% to 77.3% and decreased from 80.3% to 77.9% on a non-GAAP basis primarily due to product mix and higher manufacturing costs.
2



On a GAAP and non-GAAP basis, marketing, selling and administrative expenses decreased 4% to $2.3 billion primarily due to foreign exchange.
On a GAAP and non-GAAP basis, research and development expenses remained constant at $2.5 billion.
Acquired IPRD expenses decreased from $89 million in 2021 to $52 million in 2022.
Amortization of acquired intangible assets decreased 3% to $2.3 billion, due to expiration of Abraxane market exclusivity.
Income tax benefit was $166 million despite pre-tax earnings of $1.9 billion primarily due to the release of income tax reserves. On a non-GAAP basis, the effective tax rate decreased from 15.1% to 10.9% primarily due to the release of income tax reserves, partially offset by jurisdictional earnings mix.
The company reported net earnings attributable to Bristol Myers Squibb of $2.0 billion, or $0.95 per share, compared to $2.4 billion, or $1.07 per share. In addition to the items discussed above, the net earnings include the impact of fair value adjustments on equity investments in both periods.
The company reported non-GAAP net earnings attributable to Bristol Myers Squibb of $3.9 billion, or $1.82 per share, compared to non-GAAP net earnings of $4.1 billion, or $1.84 per share.
In addition to the items discussed above, the earnings per share results in 2022 include the impact of lower weighted-average common shares outstanding.


3



FOURTH QUARTER PRODUCT REVENUE HIGHLIGHTS
$ amounts in millions
Quarter Ended
December 31, 2022
Quarter Ended
December 31, 2021
% Change from Quarter Ended December 31, 2021% Change from Quarter Ended December 31, 2021 (Excl. F/X Impact)**
In-Line Products
Eliquis$2,688$2,6711%6%
Opdivo$2,216$1,98811%16%
Pomalyst/Imnovid$877$8543%6%
Orencia$913$8646%9%
Sprycel$578$5554%8%
Yervoy$568$5454%9%
Empliciti$71$81(12)%(7)%
Mature and Other Products*$411$441(7)%(2)%
Total In-Line Products Revenue$8,322$7,9994%9%
New Product Portfolio
Reblozyl$199$15132%34%
Abecma$125$6981%87%
Opdualag$104N/AN/A
Zeposia$79$4865%69%
Breyanzi$55$4038%48%
Onureg$37$2548%52%
Inrebic$23$2015%15%
Camzyos$16N/AN/A
Sotyktu$7N/AN/A
Total New Product Portfolio Revenue$645$35383%87%
Total In-Line Products and New Product Portfolio Revenue$8,967$8,3527%12%
Recent LOE Products
Revlimid$2,260$3,328(32)%(31)%
Abraxane$179$305(41)%(39)%
Total Recent LOE Products Revenue$2,439$3,633(33)%(32)%
Total Revenue$11,406$11,985(5)%(1)%
*    Includes over-the-counter (OTC) products, royalty revenue and other mature products.
** See "Use of Non-GAAP Financial Information."

FOURTH QUARTER REVENUE HIGHLIGHTS

In-Line Products
Revenues for in-line products were $8.3 billion compared to $8.0 billion, representing an increase of 4%, or 9% when adjusted for foreign exchange. In-line products revenue was largely driven by:
Eliquis revenues grew 1%, or 6% when adjusted for foreign exchange. U.S. revenues were $1.7 billion compared to $1.5 billion, representing an increase of 15% driven primarily by demand growth and favorable gross to net adjustments. International revenues were $970
4



million compared to $1.2 billion, representing a decrease of 17% driven by foreign exchange impacts and lower average net selling prices. When adjusted for foreign exchange impacts, Eliquis' international revenues declined 6%.
Opdivo revenues increased 11%, or 16% when adjusted for foreign exchange. U.S. revenues were $1.3 billion compared to $1.1 billion, representing an increase of 13% driven by higher demand for our newer metastatic and adjuvant indications, partially offset by declining second-line eligibility across tumors and increased competition. International revenues were $951 million compared to $868 million, representing an increase of 10% driven by higher demand as a result of launches for additional indications and core indications and timing of shipments, partially offset by foreign exchange impacts. When adjusted for foreign exchange impacts, Opdivo's international revenues increased 20%.

New Product Portfolio
New product portfolio revenues grew to $645 million compared to $353 million, representing growth of 83% driven by the launch of Opdualag and higher demand for Abecma and Reblozyl. Excluding foreign exchange, new product portfolio revenues grew 87%.

Recent LOE Products
Revlimid revenues declined by 32% primarily due to lower demand as a result of generic erosion.

5



FOURTH QUARTER PRODUCT AND PIPELINE UPDATE

Hematology
CategoryAssetMilestone
RegulatoryReblozyl®* (luspatercept)
The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has recommended approval of Reblozyl as a treatment for adult patients with anemia associated with non transfusion-dependent beta thalassemia. Reblozyl is being developed and commercialized through a global collaboration with Merck following Merck’s acquisition of Acceleron Pharma, Inc. in November 2021.
Breyanzi® (lisocabtagene maraleucel)
Japan’s Ministry of Health, Labour and Welfare approved Breyanzi for use in the second-line treatment of patients with relapsed or refractory large B-cell lymphoma regardless of whether autologous hematopoietic stem-cell transplantation is intended. The approval is based on the results of clinical trials in patients with relapsed or refractory aggressive B-cell non-Hodgkin lymphoma after first-line therapy, including global Phase III clinical trials (JCAR017-BCM-003) in patients intended for autologous hematopoietic stem-cell transplantation, Phase II clinical trials (017006) in the United States in patients not intended for autologous hematopoietic stem-cell transplantation, and cohort 2 of Phase II clinical trials (JCAR017-BCM-001) in Europe and Japan.
Clinical & Research
Breyanzi*
Positive topline results from the Phase 2 portion of the TRANSCEND CLL 004, a Phase 1/2, open-label, single-arm, multicenter study evaluating Breyanzi in adults with relapsed or refractory chronic lymphocytic leukemia or small lymphocytic lymphoma, showed that the study met the primary endpoint of complete response rate compared to historical control. No new safety signals were reported for Breyanzi in this study.
Reblozyl
Phase 3 COMMANDS trial met its primary endpoint, demonstrating a highly statistically significant and clinically meaningful improvement in red blood cell transfusion independence with concurrent hemoglobin increase in the first-line treatment of adults with very low-, low-, or intermediate-risk myelodysplastic syndromes who require red blood cell transfusions. No new safety signals were reported.
PipelineMultiple Myeloma Portfolio
In December, the company presented new data from across its multiple myeloma portfolio at the 64th American Society of Hematology Annual Meeting and Exposition, including:
Abecma(R) (idecabtagene vicleucel)
Two first disclosures of Phase 2 KarMMa-2 trial evaluating Abecma, demonstrating durable responses and predictable safety in patients with multiple myeloma after early relapse from or suboptimal response to stem cell transplant.
alnuctamab
First multicenter results from the Phase 1 study of bispecific TCE alnuctamab, administered subcutaneously every four weeks after six months, showed a reduction in inflammatory toxicity relative to intravenous administration, while maintaining anti-tumor activity with deep responses.
6



GPRC5D CAR T (BMS-986393/CC-95266)
First disclosure of Phase 1 study for GPRC5D CAR T (BMS-986393/CC-95266) demonstrating deep and durable responses with a manageable safety profile across all dose levels, including patients previously treated with a B-cell maturation antigen-directed CAR T cell therapy.
mezigdomide
First results from the dose expansion cohort of the Phase 1/2 study evaluating the novel oral CELMoD agent, mezigdomide with dexamethasone (DEX), showing durable efficacy and a manageable safety profile in patients who were highly refractory to multiple prior therapies.
iberdomide
New results from a cohort with patients previously exposed to a BCMA-targeted therapy of iberdomide Phase 1/2 study, evaluating the novel oral CELMoD agent with DEX, demonstrating clinically meaningful efficacy and safety regardless of type of prior anti-BCMA treatment.

Immunology
CategoryAssetMilestone
Regulatory
SotyktuTM* (deucrava-citinib)
The CHMP of the EMA has recommended the approval of Sotyktu for the treatment of adults with moderate-to-severe plaque psoriasis. The CHMP recommendation will now be reviewed by the European Commission, which has the authority to approve medicines for the European Union.
Clinical & Research
Zeposia® (ozanimod)
New retrospective analyses from the ongoing Phase 3 DAYBREAK open-label extension (OLE) study of Zeposia in relapsing multiple sclerosis showed that more than 92% of participants who received Zeposia mounted a serological response following COVID-19 vaccination. Interim analyses of the ongoing Phase 3 DAYBREAK OLE study showed that 68% of participants were relapse-free at up to 74 months of treatment. Post hoc analyses of the Phase 3 SUNBEAM, RADIANCE and DAYBREAK OLE studies demonstrated that a greater proportion of patients treated with Zeposia versus interferon beta-1a had a lower annualized rate of brain volume loss.
*Announced in January 2023.
7



FULL YEAR FINANCIAL RESULTS
All comparisons are made versus the same period in 2021 unless otherwise stated.
Bristol Myers Squibb posted revenues of $46.2 billion, consistent with the prior year, driven by in-line products (primarily Eliquis and Opdivo) and our new product portfolio (primarily Opdualag, Abecma and Reblozyl), offset by recent LOE products (primarily Revlimid) and foreign exchange. When adjusted for foreign exchange, revenues increased 3%. Our in-line products and new product portfolio increased 9% to $35.4 billion, or 13% when adjusted for foreign exchange.
U.S. revenues increased 9% to $31.8 billion. International revenues decreased 17% to $14.3 billion. When adjusted for foreign exchange, international revenues decreased 8%, primarily due to lower demand for Revlimid as a result of generic erosion, partially offset by in-line products (primarily Opdivo) and our new product portfolio.
Gross margin decreased from 78.6% to 78.0% and decreased from 79.9% to 78.8% on a non-GAAP basis primarily due to product mix, higher manufacturing costs, partially offset by foreign exchange.
On a GAAP basis, marketing, selling and administrative expenses increased 2% to $7.8 billion. On a non-GAAP basis, marketing, selling and administrative expenses increased 1% to $7.7 billion.
On a GAAP basis, research and development expenses decreased 7% to $9.5 billion primarily due to an IPRD impairment charge in 2021. On a non-GAAP basis, research and development expenses decreased 2% to $9.2 billion.
Acquired IPRD expenses decreased from $1.2 billion to $815 million. Acquired IPRD in 2022 was primarily related to a buyout of a future royalty obligation related to mavacamten and upfront and milestone charges relating to Dragonfly licensing arrangement. Acquired IPRD in 2021 was primarily related to a collaboration agreement with Eisai and Agenus licensing transaction.
Amortization of acquired intangible assets decreased 4% to $9.6 billion, due to a change in the expected expiration of the market exclusivity period for Pomalyst to the first quarter of 2026 and the expiration of Abraxane market exclusivity.
The GAAP effective tax rate increased from 13.4% to 17.7% primarily due to an income tax benefit of $1.0 billion in 2021 related to internal transfers of certain intangible assets, partially offset by the release of income tax reserves and jurisdictional earnings mix. The
8



non-GAAP effective tax rate decreased from 16.0% to 15.3% for the full year primarily due to the release of income tax reserves, partially offset by jurisdictional earnings mix.
The company reported net earnings attributable to Bristol Myers Squibb of $6.3 billion, or $2.95 per share, compared to $7.0 billion, or $3.12 per share. In addition to the items discussed above, the net earnings include the impact of fair value adjustments on equity investments in both periods and contingent value rights in 2021.
The company reported non-GAAP net earnings attributable to Bristol Myers Squibb of $16.5 billion, or $7.70 per share, compared to non-GAAP net earnings of $16.1 billion, or $7.16 per share. In addition to the items discussed above, the earnings per share results in 2022 include the impact of lower weighted-average common shares outstanding.

Beginning with the first quarter of 2022, 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 are no longer excluded from non-GAAP results. These R&D charges that were previously specified are now presented in a new financial statement line item labeled Acquired IPRD. GAAP and non-GAAP earnings per share include the net impact of Acquired IPRD charges and licensing income of ($0.01) per share in the fourth quarter for both periods. GAAP and non-GAAP earnings per share include the net impact of Acquired IPRD charges and licensing income of ($0.24) per share in full-year 2022 and ($0.40) per share in full-year 2021. For purposes of comparability, the non-GAAP financial results for the fourth quarter of 2021 have been updated to reflect this change. A discussion of the non-GAAP financial measures is included under the “Use of Non-GAAP Financial Information” section.

9



FULL YEAR PRODUCT REVENUE HIGHLIGHTS
$ amounts in millions
Full Year Ended
December 31, 2022
Full Year Ended December 31, 2021
% Change from Full Year Ended December 31, 2021 % Change from Full Year Ended December 31, 2021 (Excl. F/X Impact)***
In-Line Products
Eliquis$11,789$10,76210%14%
Opdivo$8,249$7,52310%14%
Pomalyst/Imnovid$3,497$3,3325%8%
Orencia$3,464$3,3065%8%
Sprycel$2,165$2,1172%6%
Yervoy$2,131$2,0265%10%
Empliciti$296$334(11)%(7)%
Mature and Other Products*$1,749$1,900(8)%(5)%
Total In-Line Products Revenues$33,340$31,3007%11%
New Product Portfolio
Reblozyl$717$55130%32%
Abecma$388$164****
Opdualag$252N/AN/A
Zeposia$250$13487%93%
Breyanzi$182$87****
Onureg$124$7370%74%
Inrebic$85$7415%16%
Camzyos$24N/AN/A
Sotyktu$8N/AN/A
Total New Product Portfolio Revenues$2,030$1,08387%92%
Total In-Line Products and New Product Portfolio Revenues$35,370$32,3839%13%
Recent LOE Products
Revlimid$9,978$12,821(22)%(21)%
Abraxane$811$1,181(31)%(30)%
Total Recent LOE Products Revenues$10,789$14,002(23)%(22)%
Total Revenue$46,159$46,3853%
*    Includes OTC products, royalty revenue and other mature products.
**    In excess of +100%.
*** See "Use of Non-GAAP Financial Information."

FULL YEAR REVENUE HIGHLIGHTS

In-Line Products
Revenues for in-line products were $33.3 billion compared to $31.3 billion, representing an increase of 7% or 11% when adjusted for foreign exchange. In-line products revenue was largely driven by:
Eliquis revenues grew 10%, or 14% when adjusted for foreign exchange. U.S. revenues were $7.8 billion compared to $6.5 billion, representing an increase of 21% driven primarily by
10



favorable gross to net adjustments and demand growth. International revenues were $4.0 billion compared to $4.3 billion, representing a decrease of 7% driven primarily by foreign exchange impacts and lower average net selling prices. When adjusted for foreign exchange impacts, Eliquis' international revenues increased 4%.
Opdivo revenues increased 10%, or 14% when adjusted for foreign exchange. U.S. revenues were $4.8 billion compared to $4.2 billion, representing an increase of 15% driven by higher demand for our newer metastatic and adjuvant indications, partially offset by declining second-line eligibility across tumors and increased competition. International revenues were $3.4 billion compared to $3.3 billion, representing an increase of 3% driven by higher demand as a result of launches for additional indications and core indications, partially offset by foreign exchange impacts. When adjusted for foreign exchange impacts, Opdivo's international revenues increased 14%.

New Product Portfolio
New product portfolio revenues grew to $2.0 billion compared to $1.1 billion, representing growth of 87% driven by the launch of Opdualag and higher demand for Abecma and Reblozyl. Excluding foreign exchange, new product portfolio revenues grew 92%.

Recent LOE Products
Revlimid revenues declined by 22% primarily due to lower demand as a result of generic erosion.

Environmental, Social & Governance (ESG)

As a leading biopharma company, we understand our responsibility extends well beyond the discovery, development, and delivery of innovative medicines. Our evolving Environmental, Social, and Governance (ESG) strategy builds on a legacy of comprehensive and global sustainability efforts. To learn more about our priorities and goals, please visit our latest ESG report.
11



Financial Guidance
Bristol Myers Squibb provides its 2023 GAAP EPS guidance range of $4.03 - $4.33 and its non-GAAP EPS guidance range of $7.95 - $8.25. Key 2023 GAAP and non-GAAP line-item guidance assumptions are:
Total revenues are expected to increase by approximately 2% at reported rates and approximately 2% excluding foreign exchange.
Revenues from Revlimid are expected to be approximately $6.5 billion.
Gross margin is expected to be approximately 77% for GAAP and for non-GAAP.
Operating expenses1 are expected to decrease by mid-single digits for GAAP and decrease by low single digits for non-GAAP.
An effective tax rate of approximately 22% for GAAP and approximately 17% for non-GAAP.
1 Consists of MS&A and R&D, excluding Acquired IPRD and Amortization of acquired intangible assets.

The 2023 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 and impact of future Acquired IPRD charges. To the extent in the future we quantify 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. GAAP and non-GAAP guidance assume current exchange rates. The 2023 non-GAAP EPS guidance is further explained under “Use of Non-GAAP Financial Information.” The financial guidance is subject to risks and uncertainties applicable to all forward-looking statements as described elsewhere in this press release.
12




Conference Call Information
Bristol Myers Squibb will host a conference call today at 9:00 a.m. ET during which company executives will review financial results 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.

Investors and the public can also access the live conference call by dialing in the U.S. toll free 888-300-3045 or international +1 646-568-1027, conference code: 3734085. 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 on http://investor.bms.com approximately three hours after the conference call concludes. A replay of the conference call will be available beginning at 11:30 a.m. ET on February 2 through 11:30 a.m. ET on February 16, 2023, by dialing in the U.S. toll free 800-770-2030 or international +1 647-362-9199, conference code: 3734085.

About Bristol Myers Squibb
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.

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, 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 marketing, selling and administrative expense and research and development expense excluding certain specified items as a percentage of revenues, non-GAAP operating expenses, which is marketing, selling and administrative and research and development expenses
13



excluding certain specified items, non-GAAP marketing, selling and administrative expenses, which is marketing, selling and administrative expense 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, unwind 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 equity method 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 the overall tax expense, deductibility and jurisdictional tax rates.

Beginning with the first quarter of 2022, 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 are no longer excluded from our non-GAAP financial measures. We made these changes to our presentation of non-GAAP financial measures following comments from and discussions with the U.S. Securities and Exchange Commission. For purposes of comparability, the non-GAAP financial measures for the prior periods have been updated to reflect this change.

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
14



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 attached financial tables presented, certain columns and rows may not add due to the use of rounded numbers. Percentages and earnings per share amounts presented are calculated from the underlying amounts.

Also note that a reconciliation of forward-looking non-GAAP gross margin, non-GAAP operating expenses and non-GAAP tax rate 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 able to reliably predict the impact of the unwind of inventory purchase price adjustments, accelerated depreciation and impairment of property, plant and equipment and intangible assets, and stock compensation resulting from acquisition-related equity awards, or currency exchange rates beyond the next twelve months. In addition, the company believes such a reconciliation would imply a degree of precision and certainty that could be confusing to investors. The variability of the specified items may have a significant and unpredictable impact on our future GAAP results.

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, the Company’s 2023 financial guidance, plans and strategy, including its business development and capital allocation strategy, anticipated developments in the company’s pipeline and expectations with respect to the company’s future market position. 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. 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
15



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; market actions taken by private and government payers to manage drug utilization and contain costs; the company’s ability to retain patent exclusivity of 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 company’s ability to obtain and protect market exclusivity rights and enforce patents and other intellectual property rights; 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; the risk of an adverse patent litigation decision or settlement and exposure to other 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 reduce the product's market acceptance for the company's products and 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 on the company’s information systems or products 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 dependency on several key products; any decline in the company’s future royalty streams; 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 including as a result of the Russian Federation-Ukraine conflict; interest rate and currency exchange rate fluctuations, credit and foreign exchange risk management; risks relating to the use of social media platforms; the impact of our exclusive forum provision in our by-laws for certain lawsuits on our stockholders’ ability to obtain a judicial forum that it finds favorable for such lawsuits; issuance of new or revised accounting standards; and risks relating to public health outbreaks, epidemics and pandemics, including the impact of the COVID-19 pandemic on the company’s operations.

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
16



in the cautionary statement and risk factors discussion in the company’s Annual Report on Form 10-K for the year ended December 31, 2021, 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.



17



BRISTOL-MYERS SQUIBB COMPANY
PRODUCT REVENUES
FOR THE THREE MONTHS ENDED DECEMBER 31, 2022 AND 2021
(Unaudited, dollars in millions)
Worldwide Revenues
U.S. Revenues(c)
20222021% Change20222021% Change
In-Line Products
Eliquis$2,688 $2,671 %$1,718 $1,496 15 %
Opdivo2,216 1,988 11 %1,265 1,120 13 %
Pomalyst/Imnovid877 854 %625 584 %
Orencia913 864 %710 637 11 %
Sprycel578 555 %418 351 19 %
Yervoy568 545 %345 330 %
Empliciti71 81 (12)%44 50 (12)%
Mature and other products(a)
411 441 (7)%141 146 (3)%
Total In-Line Products8,322 7,999 %5,266 4,714 12 %
New Product Portfolio
Reblozyl199 151 32 %157 130 21 %
Abecma125 69 81 %94 67 40 %
Opdualag104 — N/A104 — N/A
Zeposia79 48 65 %58 34 71 %
Breyanzi55 40 38 %42 38 11 %
Onureg37 25 48 %27 22 23 %
Inrebic23 20 15 %17 17 — 
Camzyos16 — N/A16 — N/A
Sotyktu— N/A— N/A
Total New Product Portfolio645 353 83 %522 308 69 %
Total In-Line and New Product Portfolio8,967 8,352 %5,788 5,022 15 %
Recent LOE Products(b)
Revlimid2,260 3,328 (32)%2,021 2,270 (11)%
Abraxane179 305 (41)%116 228 (49)%
Total Recent LOE Products2,439 3,633 (33)%2,137 2,498 (14)%
Total Revenues$11,406 $11,985 (5)%$7,925 $7,520 %
(a)    Includes over-the-counter (OTC) products, royalty revenue and mature products.
(b)    Recent LOE Products include products with significant expected decline in revenue from a prior reporting period as a result of a loss of exclusivity.
(c)    Includes Puerto Rico.
18



BRISTOL-MYERS SQUIBB COMPANY
PRODUCT REVENUES
FOR THE TWELVE MONTHS ENDED DECEMBER 31, 2022 AND 2021
(Unaudited, dollars in millions)
Worldwide Revenues
U.S. Revenues(c)
20222021% Change20222021% Change
In-Line Products
Eliquis$11,789 $10,762 10 %$7,786 $6,456 21 %
Opdivo8,249 7,523 10 %4,812 4,202 15 %
Pomalyst/Imnovid3,497 3,332 %2,438 2,249 %
Orencia3,464 3,306 %2,638 2,410 %
Sprycel2,165 2,117 %1,497 1,297 15 %
Yervoy2,131 2,026 %1,304 1,265 %
Empliciti296 334 (11)%185 200 (8)%
Mature and other products(a)
1,749 1,900 (8)%565 580 (3)%
Total In-Line Products33,340 31,300 %21,225 18,659 14 %
New Product Portfolio
Reblozyl717 551 30 %591 485 22 %
Abecma388 164 **297 158 88 %
Opdualag252 — N/A252 — N/A
Zeposia250 134 87 %177 99 79 %
Breyanzi182 87 **151 84 80 %
Onureg124 73 70 %95 69 38 %
Inrebic85 74 15 %69 67 %
Camzyos24 — N/A24 — N/A
Sotyktu— N/A— N/A
Total New Product Portfolio2,030 1,083 87 %1,664 962 73 %
Total In-Line and New Product Portfolio35,370 32,383 %22,889 19,621 17 %
Recent LOE Products(b)
Revlimid9,978 12,821 (22)%8,359 8,695 (4)%
Abraxane811 1,181 (31)%580 898 (35)%
Total Recent LOE Products10,789 14,002 (23)%8,939 9,593 (7)%
Total Revenues$46,159 $46,385 — $31,828 $29,214 %
**    In excess of +/- 100%
(a)    Includes OTC products, royalty revenue and mature products.
(b)    Recent LOE Products includes products with significant expected decline in revenue from a prior reporting period as a result of a loss of exclusivity.
(c)    Includes Puerto Rico.

19



BRISTOL-MYERS SQUIBB COMPANY
CONSOLIDATED STATEMENTS OF EARNINGS
FOR THE THREE AND TWELVE MONTHS ENDED DECEMBER 31, 2022 AND 2021
(Unaudited, dollars and shares in millions except per share data)
 
 Three Months Ended December 31,Twelve Months Ended December 31,
 2022
2021
2022
2021
Net product sales$11,065 $11,609 $44,671 $45,055 
Alliance and other revenues341 376 1,488 1,330 
Total Revenues11,406 11,985 46,159 46,385 
Cost of products sold(a)
2,593 2,356 10,137 9,940 
Marketing, selling and administrative2,266 2,354 7,814 7,690 
Research and development(b)
2,510 2,518 9,509 10,195 
Acquired IPRD(b)
52 89 815 1,159 
Amortization of acquired intangible assets2,343 2,417 9,595 10,023 
Other (income)/expense, net(217)393 576 (720)
Total Expenses9,547 10,127 38,446 38,287 
Earnings Before Income Taxes1,859 1,858 7,713 8,098 
(Benefit)/Provision for Income Taxes(166)(514)1,368 1,084 
Net Earnings2,025 2,372 6,345 7,014 
Noncontrolling Interest— 18 20 
Net Earnings Attributable to BMS $2,022 $2,372 $6,327 $6,994 
Weighted-Average Common Shares Outstanding:
Basic2,108 2,202 2,130 2,221 
Diluted2,124 2,219 2,146 2,245 
Earnings per Common Share:
Basic$0.96 $1.08 $2.97 $3.15 
Diluted0.95 1.07 2.95 3.12 
Other (income)/expense, net
Interest expense(c)
$294 $323 $1,232 $1,334 
Royalties and licensing income(316)(317)(1,283)(1,067)
Royalty income - divestitures(235)(219)(832)(666)
Equity investment (income)/losses(165)469 801 (745)
Integration expenses97 130 440 564 
Loss on debt redemption— — 266 281 
Divestiture gains— — (211)(9)
Litigation and other settlements146 33 178 82 
Investment income(82)(6)(171)(39)
Provision for restructuring15 19 75 169 
Contingent consideration(10)(32)(9)(542)
Other39 (7)90 (82)
Other (income)/expense, net$(217)$393 $576 $(720)
(a)    Excludes amortization of acquired intangible assets.
(b)    Research and development charges resulting from upfront or contingent milestone payments in connection with asset acquisitions or licensing of third-party intellectual property rights have been reclassified to the Acquired IPRD line item beginning with the first quarter of 2022. Prior period results have been revised for comparability.
(c)    Includes amortization of purchase price adjustments to Celgene debt.
20



BRISTOL-MYERS SQUIBB COMPANY
SPECIFIED ITEMS
FOR THE THREE AND TWELVE MONTHS ENDED DECEMBER 31, 2022 AND 2021
(Unaudited, dollars in millions)
 
 Three Months Ended December 31,Twelve Months Ended December 31,
 2022
2021(a)
2022
2021(a)
Inventory purchase price accounting adjustments$53 $— $293 $264 
Intangible asset impairment— — — 315 
Site exit and other costs20 — 63 24 
Cost of products sold73 — 356 603 
Employee compensation charges— — 73 
Site exit and other costs— 
Marketing, selling and administrative— 79 
IPRD impairments— — 98 840 
Inventory purchase price accounting adjustments— — 130 
Employee compensation charges— — 80 
Site exit and other costs— — — 
Research and development— — 308 843 
Amortization of acquired intangible assets2,343 2,417 9,595 10,023 
Interest expense(b)
(17)(29)(83)(120)
Equity investment losses/(income)(163)469 799 (758)
Integration expenses97 130 440 564 
Loss on debt redemption— — 266 281 
Divestiture gains— — (211)(9)
Litigation and other settlements144 — 140 — 
Provision for restructuring15 19 75 169 
Contingent consideration— (32)— (542)
Other— 71 — 
Other (income)/expense, net77 557 1,497 (415)
Increase to pretax income2,493 2,976 11,835 11,057 
Income taxes on items above(345)(261)(1,332)(993)
Income tax reserve release attributed to Mead Johnson (225)— (225)— 
Income taxes attributed to internal transfers of intangible assets(72)(983)(72)(983)
Income taxes(642)(1,244)(1,629)(1,976)
Increase to net earnings$1,851 $1,732 $10,206 $9,081 
(a)    Revised to exclude significant R&D charges or other income resulting from upfront and contingent milestone payments in connection with asset acquisitions or licensing of third-party intellectual property rights (including related income tax impacts).
(b)    Includes amortization of purchase price adjustments to Celgene debt.

21



BRISTOL-MYERS SQUIBB COMPANY
RECONCILIATION OF CERTAIN GAAP LINE ITEMS TO CERTAIN NON-GAAP LINE ITEMS
FOR THE THREE AND TWELVE MONTHS ENDED DECEMBER 31, 2022 AND 2021
(Unaudited, dollars and shares in millions except per share data)

Three Months Ended December 31, 2022Twelve Months Ended December 31, 2022
GAAP
Specified Items(a)
Non-GAAPGAAP
Specified Items(a)
Non-GAAP
Gross Profit$8,813 $73 $8,886 $36,022 $356 $36,378 
Marketing, selling and administrative2,266 — 2,266 7,814 (79)7,735 
Research and development2,510 — 2,510 9,509 (308)9,201 
Amortization of acquired intangible assets2,343 (2,343)— 9,595 (9,595)— 
Other (income)/expense, net(217)(77)(294)576 (1,497)(921)
Earnings Before Income Taxes1,859 2,493 4,352 7,713 11,835 19,548 
(Benefit)/Provision for Income Taxes(166)642 476 1,368 1,629 2,997 
Net Earnings Attributable to BMS used for Diluted EPS Calculation$2,022 $1,851 $3,873 $6,327 $10,206 $16,533 
Weighted-Average Common Shares Outstanding - Diluted2,124 2,124 2,124 2,146 2,146 2,146 
Diluted Earnings Per Share$0.95 $0.87 $1.82 $2.95 $4.75 $7.70 
Effective Tax Rate(8.9)%19.8 %10.9 %17.7 %(2.4)%15.3 %
Three Months Ended December 31, 2021Twelve Months Ended December 31, 2021
GAAP
Specified Items(a)
Non-GAAPGAAP
Specified Items(a)
Non-GAAP
Gross Profit$9,629 $— $9,629 $36,445 $603 $37,048 
Marketing, selling and administrative2,354 (2)2,352 7,690 (3)7,687 
Research and development2,518 — 2,518 10,195 (843)9,352 
Amortization of acquired intangible assets2,417 (2,417)— 10,023 (10,023)— 
Other (income)/expense, net393 (557)(164)(720)415 (305)
Earnings Before Income Taxes1,858 2,976 4,834 8,098 11,057 19,155 
(Benefit)/Provision for Income Taxes(514)1,244 730 1,084 1,976 3,060 
Net Earnings Attributable to BMS used for Diluted EPS Calculation$2,372 $1,732 $4,104 $6,994 $9,081 $16,075 
Weighted-Average Common Shares Outstanding - Diluted2,219 2,219 2,219 2,245 2,245 2,245 
Diluted Earnings Per Share$1.07 $0.77 $1.84 $3.12 $4.04 $7.16 
Effective Tax Rate(27.7)%42.8 %15.1 %13.4 %2.6 %16.0 %
(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.

22



BRISTOL-MYERS SQUIBB COMPANY
NET DEBT CALCULATION
AS OF DECEMBER 31, 2022 AND DECEMBER 31, 2021
(Unaudited, dollars in millions)
 
December 31, 2022December 31, 2021
Cash and cash equivalents$9,123 $13,979 
Marketable debt securities 130 2,987 
Cash, cash equivalents and marketable debt securities9,253 16,966 
Short-term debt obligations(4,264)(4,948)
Long-term debt(35,056)(39,605)
Net debt position$(30,067)$(27,587)
23





Media: [email protected]
Investor Relations: [email protected]

24

Exhibit 99.2
BRISTOL-MYERS SQUIBB COMPANY
QUARTERLY TREND ANALYSIS OF REVENUES
(Unaudited, dollars in millions)
Revenues
2021
2022
% Change
FX Impact(b)
 1st Qtr2nd Qtr6 Months3rd Qtr9 Months4th QtrYear1st Qtr2nd Qtr6 Months3rd Qtr9 Months4th QtrYearQtr vs. QtrYTD vs. YTDQtr vs. QtrYTD vs. YTD
United States$7,010 $7,388 $14,398 $7,296 $21,694 $7,520 $29,214 $7,694 $8,268 $15,962 $7,941 $23,903 $7,925 $31,828 5 %9 %  
International3,899 4,124 8,023 4,052 12,075 4,244 16,319 3,727 3,427 7,154 3,062 10,216 3,281 13,497 (22)%(17)%(9)%(9)%
Other(a)
164 191 355 276 631 221 852 227 192 419 215 634 200 834 (10)%(2)%  
Total$11,073 $11,703 $22,776 $11,624 $34,400 $11,985 $46,385 $11,648 $11,887 $23,535 $11,218 $34,753 $11,406 $46,159 (5)% (4)%(3)%
% of Revenues
2021
2022
 1st Qtr2nd Qtr6 Months3rd Qtr9 Months4th QtrYear1st Qtr2nd Qtr6 Months3rd Qtr9 Months4th QtrYear
United States63.3 %63.1 %63.2 %62.8 %63.1 %62.7 %63.0 %66.1 %69.6 %67.8 %70.8 %68.8 %69.5 %69.0 %
International35.3 %35.3 %35.2 %34.9 %35.1 %35.4 %35.1 %32.0 %28.8 %30.4 %27.3 %29.4 %28.8 %29.2 %
Other(a)
1.4 %1.6 %1.6 %2.3 %1.8 %1.9 %1.9 %1.9 %1.6 %1.8 %1.9 %1.8 %1.7 %1.8 %
Total100 %100 %100 %100 %100 %100 %100 %100 %100 %100 %100 %100 %100 %100 %
(a)    Other revenues include royalties and alliance-related revenues for products not sold by our regional commercial organizations.
(b)    Foreign exchange impacts were derived 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.

1


BRISTOL-MYERS SQUIBB COMPANY
EARNINGS FROM OPERATIONS
(Unaudited, dollars and shares in millions except per share data)
 
2021
2022
% Change
 1st Qtr2nd Qtr6 Months3rd Qtr9 Months4th QtrYear1st Qtr2nd Qtr6 Months3rd Qtr9 Months4th QtrYearQtr vs. QtrYTD vs. YTD
Net product sales$10,798 $11,405 $22,203 $11,243 $33,446 $11,609 $45,055 $11,308 $11,485 $22,793 $10,813 $33,606 $11,065 $44,671 (5)%(1)%
Alliance and other revenues275 298 573 381 954 376 1,330 340 402 742 405 1,147 341 1,488 (9)%12 %
Total Revenues11,073 11,703 22,776 11,624 34,400 11,985 46,385 11,648 11,887 23,535 11,218 34,753 11,406 46,159 (5)% 
Cost of products sold(a)
2,841 2,452 5,293 2,291 7,584 2,356 9,940 2,471 2,720 5,191 2,353 7,544 2,593 10,137 10 %2 %
Marketing, selling and administrative1,666 1,882 3,548 1,788 5,336 2,354 7,690 1,831 1,787 3,618 1,930 5,548 2,266 7,814 (4)%2 %
Research and development(b)
2,219 2,478 4,697 2,980 7,677 2,518 10,195 2,260 2,321 4,581 2,418 6,999 2,510 9,509  (7)%
Acquired IPRD(b)
793 799 271 1,070 89 1,159 333 400 733 30 763 52 815 (42)%(30)%
Amortization of acquired intangible assets2,513 2,547 5,060 2,546 7,606 2,417 10,023 2,417 2,417 4,834 2,418 7,252 2,343 9,595 (3)%(4)%
Other (income)/expense, net(702)(2)(704)(409)(1,113)393 (720)649 284 933 (140)793 (217)576 ****
Total Expenses8,543 10,150 18,693 9,467 28,160 10,127 38,287 9,961 9,929 19,890 9,009 28,899 9,547 38,446 (6)% 
Earnings before income taxes2,530 1,553 4,083 2,157 6,240 1,858 8,098 1,687 1,958 3,645 2,209 5,854 1,859 7,713  (5)%
Provision/(benefit) for income taxes501 492 993 605 1,598 (514)1,084 404 529 933 601 1,534 (166)1,368 (68)%26 %
Net Earnings2,029 1,061 3,090 1,552 4,642 2,372 7,014 1,283 1,429 2,712 1,608 4,320 2,025 6,345 (15)%(10)%
Noncontrolling interest14 20  20 13 15 3 18 N/A(10)%
Net Earnings Attributable to BMS$2,021 $1,055 $3,076 $1,546 $4,622 $2,372 $6,994 $1,278 $1,421 $2,699 $1,606 $4,305 $2,022 $6,327 (15)%(10)%
Diluted earnings per common share*$0.89 $0.47 $1.36 $0.69 $2.05 $1.07 $3.12 $0.59 $0.66 $1.25 $0.75 $2.00 $0.95 $2.95 (11)%(5)%
Weighted-average common shares outstanding - diluted2,265 2,252 2,258 2,243 2,253 2,219 2,245 2,164 2,149 2,157 2,148 2,154 2,124 2,146 
Dividends declared per common share$0.49 $0.49 $0.98 $0.49 $1.47 $0.54 $2.01 $0.54 $0.54 $1.08 $0.54 $1.62 $0.57 $2.19 6 %9 %
2021
2022
% of Total Revenues1st Qtr2nd Qtr6 Months3rd Qtr9 Months4th QtrYear1st Qtr2nd Qtr6 Months3rd Qtr9 Months4th QtrYear
Gross margin74.3 %79.0 %76.8 %80.3 %78.0 %80.3 %78.6 %78.8 %77.1 %77.9 %79.0 %78.3 %77.3 %78.0 %
Other Ratios
Effective tax rate19.8 %31.7 %24.3 %28.0 %25.6 %(27.7)%13.4 %23.9 %27.0 %25.6 %27.2 %26.2 %(8.9)%17.7 %
Other (income)/expense, net
2021
2022
% Change
1st Qtr2nd Qtr6 Months3rd Qtr9 Months4th QtrYear1st Qtr2nd Qtr6 Months3rd Qtr9 Months4th QtrYearQtr vs. QtrYTD vs. YTD
Interest expense(c)
$353 $330 $683 $328 $1,011 $323 $1,334 $326 $313 $639 $299 $938 $294 $1,232 (9)% (8)%
Royalties and licensing income (232)(253)(485)(265)(750)(317)(1,067)(306)(287)(593)(374)(967)(316)(1,283) 20 %
Royalty income - divestiture(135)(152)(287)(160)(447)(219)(666)(171)(221)(392)(205)(597)(235)(832)7 %25 %
Equity investment losses/(income)(601)(148)(749)(465)(1,214)469 (745)644 308 952 14 966 (165)801 ** **
Integration expenses141 152 293 141 434 130 564 105 124 229 114 343 97 440 (25)% (22)%
Loss/(gain) on debt redemption281 — 281 — 281  281 275 (9)266 — 266  266 N/A (5)%
Divestiture (gains)/losses— (11)(11)(9) (9)(211)— (211)— (211) (211)N/A **
Investment income(9)(12)(21)(12)(33)(6)(39)(10)(27)(37)(52)(89)(82)(171)****
Litigation and other settlements(8)44 36 13 49 33 82 (37)25 (12)44 32 146 178 ** **
Provision for restructuring45 78 123 27 150 19 169 23 20 43 17 60 15 75 (21)%(56)%
Contingent consideration(510)— (510)— (510)(32)(542)— — (10)(9)(69)% (98)%
Other(27)(30)(57)(18)(75)(7)(82)10 38 48 51 39 90 ** **
Other (income)/expense, net$(702)$(2)$(704)$(409)$(1,113)$393 $(720)$649 $284 $933 $(140)$793 $(217)$576 ** **
*    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)    Research and development charges resulting from upfront or contingent milestone payments in connection with asset acquisitions or licensing of third-party intellectual property rights have been reclassified to the Acquired IPRD line item beginning with the first quarter of 2022. Prior period results have been revised for comparability.
(c)    Includes amortization of purchase price adjustments to Celgene debt.


2


BRISTOL-MYERS SQUIBB COMPANY
RECONCILIATION OF GAAP AND NON-GAAP GROWTH DOLLARS AND PERCENTAGES EXCLUDING FOREIGN EXCHANGE IMPACT
FOR THE PERIOD ENDED DECEMBER 31, 2022
(Unaudited, dollars in millions)
QUARTER-TO-DATE
2022
2021
$ Change% ChangeFavorable/(Unfavorable) FX Impact $*2022 Excluding FXFavorable/(Unfavorable) FX Impact %*% Change Excluding FX
Revenues$11,406 $11,985 $(579)(5)%$(410)$11,816 (4)%(1)%
Gross profit8,813 9,629 (816)(8)%N/AN/AN/AN/A
Gross profit excluding specified items(a)
8,886 9,629 (743)(8)%N/AN/AN/AN/A
Gross profit excluding specified items as a % of revenues77.9 %80.3 %
Marketing, selling and administrative2,266 2,354 (88)(4)%70 2,336 %(1)%
Marketing, selling and administrative excluding specified items(a)
2,266 2,352 (86)(4)%70 2,336 %(1)%
Marketing, selling and administrative excluding specified items as a % of revenues19.9 %19.6 %
Research and development2,510 2,518 (8)— 28 2,538 %%
Research and development excluding specified items(a)
2,510 2,518 (8)— 28 2,538 %%
Research and development excluding specified items as a % of revenues22.0 %21.0 %
YEAR-TO-DATE
2022
2021
$ Change% ChangeFavorable/(Unfavorable) FX Impact $*2022 Excluding FXFavorable/(Unfavorable) FX Impact %*% Change Excluding FX
Revenues$46,159 $46,385 $(226)— $(1,464)$47,623 (3)%%
Gross profit36,022 36,445 (423)(1)%N/A N/A N/AN/A
Gross profit excluding specified items(a)
36,378 37,048 (670)(2)%N/A N/A N/AN/A
Gross profit excluding specified items as a % of revenues78.8 %79.9 %
Marketing, selling and administrative7,814 7,690 124 %207 8,021 %%
Marketing, selling and administrative excluding specified items(a)
7,735 7,687 48 %207 7,942 %%
Marketing, selling and administrative excluding specified items as a % of revenues16.8 %16.6 %
Research and development9,509 10,195 (686)(7)%102 9,611 %(6)%
Research and development excluding specified items(a)
9,201 9,352 (151)(2)%102 9,303 %(1)%
Research and development excluding specified items as a % of revenues19.9 %20.2 %
*    Foreign exchange impacts were derived 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.
(a)    Refer to the Specified Items schedule for further details.


3


BRISTOL-MYERS SQUIBB COMPANY
WORLDWIDE REVENUES
QUARTERLY REVENUES TREND ANALYSIS
(Unaudited, dollars in millions)
 
2021
2022
$ Change% Change
 1st Qtr2nd Qtr6 Months3rd Qtr9 Months4th QtrYear1st Qtr2nd Qtr6 Months3rd Qtr9 Months4th QtrYearQtr vs. QtrYTD vs. YTDQtr vs. QtrYTD vs. YTD
In-Line Products
Eliquis$2,886 $2,792 $5,678 $2,413 $8,091 $2,671 $10,762 $3,211 $3,235 $6,446 $2,655 $9,101 $2,688 $11,789 $17  $1,027 1 %10 %
Opdivo1,720 1,910 3,630 1,905 5,535 1,988 7,523 1,923 2,063 3,986 2,047 6,033 2,216 8,249 228 726 11 %10 %
Pomalyst/Imnovid773 854 1,627 851 2,478 854 3,332 826 908 1,734 886 2,620 877 3,497 23 165 3 %5 %
Orencia758 814 1,572 870 2,442 864 3,306 792 876 1,668 883 2,551 913 3,464 49 158 6 %5 %
Sprycel470 541 1,011 551 1,562 555 2,117 483 544 1,027 560 1,587 578 2,165 23 48 4 %2 %
Yervoy456 510 966 515 1,481 545 2,026 515 525 1,040 523 1,563 568 2,131 23 105 4 %5 %
Empliciti85 86 171 82 253 81 334 75 77 152 73 225 71 296 (10)(38)(12)%(11)%
Mature and other products(a)
506 473 979 480 1,459 441 1,900 462 435 897 441 1,338 411 1,749 (30)(151)(7)%(8)%
Total In-Line Products7,654 7,980 15,634 7,667 23,301 7,999 31,300 8,287 8,663 16,950 8,068 25,018 $8,322 33,340 323 2,040 4 %7 %
New Product Portfolio
Reblozyl112 128 240 160 400 151 551 156 172 328 190 518 199 717 48 166 32 %30 %
Abecma— 24 24 71 95 69 164 67 89 156 107 263 125 388 56 224 81 %**
Opdualag— —  —  —  —   58 64 84 148 104 252 104 252 N/AN/A
Zeposia18 28 46 40 86 48 134 36 66 102 69 171 79 250 31 116 65 %87 %
Breyanzi— 17 17 30 47 40 87 44 39 83 44 127 55 182 15 95 38 %**
Onureg15 12 27 21 48 25 73 23 32 55 32 87 37 124 12 51 48 %70 %
Inrebic16 16 32 22 54 20 74 18 23 41 21 62 23 85 3 11 15 %15 %
Camzyos— —  —  —  —   — 16 24 16 24 N/AN/A
Sotyktu— —  —  —  —   — — — 7 8 7 8 N/AN/A
Total New Product Portfolio161 225 386 344 730 353 1,083 350 482 832 553 1,385 645 2,030 292 947 83 %87 %
Total In-Line Products and New Product Portfolio7,815 8,205 16,020 8,011 24,031 8,352 32,383 8,637 9,145 17,782 8,621 26,403 8,967 35,370 615 2,987 7 %9 %
Recent LOE Products(b)
Revlimid2,944 3,202 6,146 3,347 9,493 3,328 12,821 2,797 2,501 5,298 2,420 7,718 2,260 9,978 (1,068)(2,843)(32)%(22)%
Abraxane314 296 610 266 876 305 1,181 214 241 455 177 632 179 811 (126)(370)(41)%(31)%
Total Recent LOE Products3,258 3,498 6,756 3,613 10,369 3,633 14,002 3,011 2,742 5,753 2,597 8,350 2,439 10,789 (1,194)(3,213)(33)%(23)%
Total$11,073 $11,703 $22,776 $11,624 $34,400 $11,985 $46,385 $11,648 $11,887 $23,535 $11,218 $34,753 $11,406 $46,159 $(579)$(226)(5)% 
**    In excess of +/- 100%.
(a)    Includes OTC products, royalty revenue and other mature products.
(b)    Recent LOE products include products with significant expected decline in revenue from a prior reporting period as a result of a loss of exclusivity.
4


BRISTOL-MYERS SQUIBB COMPANY
WORLDWIDE REVENUES
FOREIGN EXCHANGE IMPACT (%)
(Unaudited)
Three Months Ended December 31, 2022Twelve Months Ended December 31, 2022
Revenue Change %Favorable/ (Unfavorable) FX Impact % *Revenue Change % Excluding FXRevenue Change %Favorable/ (Unfavorable) FX Impact % *Revenue Change % Excluding FX
In-Line Products
Eliquis1%(5)%6%10%(4)%14%
Opdivo11%(5)%16%10%(4)%14%
Pomalyst/Imnovid3%(3)%6%5%(3)%8%
Orencia6%(3)%9%5%(3)%8%
Sprycel4%(4)%8%2%(4)%6%
Yervoy4%(5)%9%5%(5)%10%
Empliciti(12)%(5)%(7)%(11)%(4)%(7)%
Mature and other products(a)
(7)%(5)%(2)%(8)%(3)%(5)%
Total In-Line Products4%(5)%9%7%(4)%11%
New Product Portfolio
Reblozyl32%(2)%34%30%(2)%32%
Abecma81%(6)%87%******
OpdualagN/AN/AN/AN/AN/AN/A
Zeposia65%(4)%69%87%(6)%93%
Breyanzi38%(10)%48%******
Onureg48%(4)%52%70%(4)%74%
Inrebic15%15%15%(1)%16%
CamzyosN/AN/AN/AN/AN/AN/A
SotyktuN/AN/AN/AN/AN/AN/A
Total New Product Portfolio83%(4)%87%87%(5)%92%
Total In-Line Products and New Product Portfolio7%(5)%12%9%(4)%13%
Recent LOE Products(b)
Revlimid(32)%(1)%(31)%(22)%(1)%(21)%
Abraxane(41)%(2)%(39)%(31)%(1)%(30)%
Total Recent LOE Products(33)%(1)%(32)%(23)%(1)%(22)%
Total (5)%(4)%(1)%(3)%3%
*    Foreign exchange impacts were derived 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.
**    In excess of +/- 100%.
(a)    Includes over-the-counter (OTC) products, royalty revenue and other mature products.
(b)    Recent LOE products include products with significant expected decline in revenue from a prior reporting period as a result of a loss of exclusivity.
5


BRISTOL-MYERS SQUIBB COMPANY
U.S. REVENUES
QUARTERLY REVENUES TREND ANALYSIS
(Unaudited, dollars in millions)
 
2021
2022
% Change
 1st Qtr2nd Qtr6 Months3rd Qtr9 Months4th QtrYear1st Qtr2nd Qtr6 Months3rd Qtr9 Months4th QtrYearQtr vs. QtrYTD vs. YTD
In-Line Products
Eliquis$1,923 $1,722 $3,645 $1,315 $4,960 $1,496 $6,456 $2,147 $2,192 $4,339 $1,729 $6,068 $1,718 $7,786 15 %21 %
Opdivo944 1,076 2,020 1,062 3,082 1,120 4,202 1,099 1,205 2,304 1,243 3,547 1,265 4,812 13 %15 %
Pomalyst/Imnovid512 567 1,079 586 1,665 584 2,249 557 616 1,173 640 1,813 625 2,438 7 %8 %
Orencia536 593 1,129 644 1,773 637 2,410 592 654 1,246 682 1,928 710 2,638 11 %9 %
Sprycel275 325 600 346 946 351 1,297 305 372 677 402 1,079 418 1,497 19 %15 %
Yervoy294 328 622 313 935 330 1,265 311 326 637 322 959 345 1,304 5 %3 %
Empliciti51 51 102 48 150 50 200 47 47 94 47 141 44 185 (12)%(8)%
Mature and other products(a)
152 130 282 152 434 146 580 133 147 280 144 424 141 565 (3)%(3)%
Total In-Line Products4,687 4,792 9,479 4,466 13,945 4,714 18,659 5,191 5,559 10,750 5,209 15,959 5,266 21,225 12 %14 %
New Product Portfolio
Reblozyl98 110 208 147 355 130 485 134 144 278 156 434 157 591 21 %22 %
Abecma— 24 24 67 91 67 158 56 72 128 75 203 94 297 40 %88 %
Opdualag — — — —   58 64 84 148 104 252 N/AN/A
Zeposia13 20 33 32 65 34 99 21 48 69 50 119 58 177 71 %79 %
Breyanzi— 17 17 29 46 38 84 41 33 74 35 109 42 151 11 %80 %
Onureg14 12 26 21 47 22 69 19 25 44 24 68 27 95 23 %38 %
Inrebic15 15 30 20 50 17 67 15 20 35 17 52 17 69  3 %
Camzyos — — — —   — 16 24 N/AN/A
Sotyktu— — — — —   — — — 7 8 N/AN/A
Total New Product Portfolio140 198 338 316 654 308 962 292 403 695 447 1,142 522 1,664 69 %73 %
Total In-Line Products and New Product Portfolio4,827 4,990 9,817 4,782 14,599 5,022 19,621 5,483 5,962 11,445 5,656 17,101 5,788 22,889 15 %17 %
Recent LOE Products(b)
Revlimid1,958 2,164 4,122 2,303 6,425 2,270 8,695 2,038 2,130 4,168 2,170 6,338 2,021 8,359 (11)%(4)%
Abraxane225 234 459 211 670 228 898 173 176 349 115 464 116 580 (49)%(35)%
Total Recent LOE Products2,183 2,398 4,581 2,514 7,095 2,498 9,593 2,211 2,306 4,517 2,285 6,802 2,137 8,939 (14)%(7)%
Total(c)
$7,010 $7,388 $14,398 $7,296 $21,694 $7,520 $29,214 $7,694 $8,268 $15,962 $7,941 $23,903 $7,925 $31,828 5 %9 %
**    In excess of +/- 100%.
(a)    Includes OTC products, royalty revenue and other mature products.
(b)    Recent LOE Products include products with significant expected decline in revenue from a prior reporting period as a result of a loss of exclusivity.
(c)    Includes Puerto Rico.
6


BRISTOL-MYERS SQUIBB COMPANY
INTERNATIONAL REVENUES
QUARTERLY REVENUES TREND ANALYSIS
(Unaudited, dollars in millions)
2021
2022
% Change
1st Qtr2nd Qtr6 Months3rd Qtr9 Months4th QtrYear1st Qtr2nd Qtr6 Months3rd Qtr9 Months4th QtrYearQtr vs. QtrYTD vs. YTD
In-Line Products
Eliquis$963 $1,070 $2,033 $1,098 $3,131 $1,175 $4,306 $1,064 $1,043 $2,107 $926 $3,033 $970 $4,003 (17)%(7)%
Opdivo776 834 1,610 843 2,453 868 3,321 824 858 1,682 804 2,486 951 3,437 10 %3 %
Pomalyst/Imnovid261 287 548 265 813 270 1,083 269 292 561 246 807 252 1,059 (7)%(2)%
Orencia222 221 443 226 669 227 896 200 222 422 201 623 203 826 (11)%(8)%
Sprycel195 216 411 205 616 204 820 178 172 350 158 508 160 668 (22)%(19)%
Yervoy162 182 344 202 546 215 761 204 199 403 201 604 223 827 4 %9 %
Empliciti34 35 69 34 103 31 134 28 30 58 26 84 27 111 (13)%(17)%
Mature and other products(a)
354 343 697 328 1,025 295 1,320 329 288 617 297 914 270 1,184 (8)%(10)%
Total In-Line Products2,967 3,188 6,155 3,201 9,356 3,285 12,641 3,096 3,104 6,200 2,859 9,059 $3,056 $12,115 (7)%(4)%
New Product Portfolio
Reblozyl14 18 32 13 45 21 66 22 28 50 34 84 42 126 100 %91 %
Abecma— — — 2 6 11 17 28 32 60 31 91 ****
Zeposia13 21 14 35 15 18 33 19 52 21 73 50 %**
Breyanzi— — — 2 3 18 13 31 ****
Onureg— — 3 4 11 19 10 29 ****
Inrebic3 7 10 6 16 100 %**
Total New Product Portfolio21 27 48 28 76 45 121 58 79 137 106 243 123 366 ****
Total In-Line Products and New Product Portfolio2,988 3,215 6,203 3,229 9,432 3,330 12,762 3,154 3,183 6,337 2,965 9,302 3,179 12,481 (5)%(2)%
Recent LOE Products(b)
Revlimid986 1,038 2,024 1,044 3,068 1,058 4,126 759 371 1,130 250 1,380 239 1,619 (77)%(61)%
Abraxane89 62 151 55 206 77 283 41 65 106 62 168 63 231 (18)%(18)%
Total Recent LOE Products1,075 1,100 2,175 1,099 3,274 1,135 4,409 800 436 1,236 312 1,548 302 1,850 (73)%(58)%
Total$4,063 $4,315 $8,378 $4,328 $12,706 $4,465 $17,171 $3,954 $3,619 $7,573 $3,277 $10,850 $3,481 $14,331 (22)%(17)%
**    In excess of +/- 100%.
(a)    Includes OTC products, royalty revenue and other mature products.
(b)    Recent LOE products include products with significant expected decline in revenue from a prior reporting period as a result of a loss of market exclusivity.

7


BRISTOL-MYERS SQUIBB COMPANY
INTERNATIONAL REVENUES
FOREIGN EXCHANGE IMPACT (%)
(Unaudited)

Three Months Ended December 31, 2022Twelve Months Ended December 31, 2022
Revenue Change %Favorable/ (Unfavorable) FX Impact % *Revenue Change % Excluding FXRevenue Change %Favorable/ (Unfavorable) FX Impact % *Revenue Change % Excluding FX
In-Line Products
Eliquis(17)%(11)%(6)%(7)%(11)%4%
Opdivo10%(10)%20%3%(11)%14%
Pomalyst/Imnovid(7)%(11)%4%(2)%(10)%8%
Orencia(11)%(13)%2%(8)%(11)%3%
Sprycel(22)%(12)%(10)%(19)%(11)%(8)%
Yervoy4%(13)%17%9%(12)%21%
Empliciti(13)%(13)%(17)%(12)%(5)%
Mature and other products(a)
(8)%(8)%(10)%(5)%(5)%
Total In-Line Products(7)%(11)%4%(4)%(10)%6%
New Product Portfolio
Reblozyl100%(14)%**91%(18)%**
Abecma************
Zeposia50%(14)%64%******
Breyanzi************
Onureg************
Inrebic100%100%******
Total New Product Portfolio************
Total In-Line Products and New Product Portfolio(5)%(12)%7%(2)%(10)%8%
Recent LOE Products(b)
Revlimid(77)%(2)%(75)%(61)%(4)%(57)%
Abraxane(18)%(8)%(10)%(18)%(5)%(13)%
Total Recent LOE Products(73)%(3)%(70)%(58)%(3)%(55)%
Total (22)%(9)%(13)%(17)%(9)%(8)%
*    Foreign exchange impacts were derived 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.
**    In excess of +/- 100%.
(a)    Includes over-the-counter (OTC) products, royalty revenue and other mature products.
(b)    Recent LOE products include products with significant expected decline in revenue from a prior reporting period as a result of a loss of exclusivity.

8


BRISTOL-MYERS SQUIBB COMPANY
SPECIFIED ITEMS
(Unaudited, dollars in millions)
 
2021(a)
2022
1st Qtr2nd Qtr6 Months3rd Qtr9 Months4th QtrYear1st Qtr2nd Qtr6 Months3rd Qtr9 Months4th QtrYear
Inventory purchase price accounting adjustments$79 $88 $167 $97 $264 $ $264 $52 $102 $154 $86 $240 $53 $293 
Intangible asset impairment315 — 315 — 315  315 — — — — —   
Site exit and other costs23 24 — 24  24 — 43 43 — 43 20 63 
Cost of products sold417 89 506 97 603  603 52 145 197 86 283 73 356 
Employee compensation charges— —  1 — — — 73 73  73 
Site exit and other costs(1)— (1)— 2 2 —  6 
Marketing, selling and administrative(1)— 2 3 73 79  79 
IPRD impairments— 230 230 610 840  840 40 — 40 58 98  98 
Inventory purchase price accounting adjustments— — —  1 87 21 108 22 130  130 
Employee compensation charges— —  1 — — — 80 80  80 
Site exit and other costs— — —  1 — — — — —   
Research and development230 231 612 843  843 127 21 148 160 308  308 
Amortization of acquired intangible assets2,513 2,547 5,060 2,546 7,606 2,417 10,023 2,417 2,417 4,834 2,418 7,252 2,343 9,595 
Interest expense(b)
(34)(28)(62)(29)(91)(29)(120)(27)(21)(48)(18)(66)(17)(83)
Equity investment (income)/losses(608)(154)(762)(465)(1,227)469 (758)643 307 950 12 962 (163)799 
Integration expenses141 152 293 141 434 130 564 105 124 229 114 343 97 440 
Loss/(gain) on debt redemption281 — 281 — 281  281 275 (9)266 — 266  266 
Divestiture (gains)/losses— (11)(11)(9) (9)(211)— (211)— (211) (211)
Litigation and other settlements— — — — —   (40)— (40)36 (4)144 140 
Provision for restructuring45 78 123 27 150 19 169 23 20 43 17 60 15 75 
Contingent consideration(510)— (510)— (510)(32)(542)— — — — —   
Other— — — — —   — 42 42 28 70 1 71 
Other (income)/expense, net(685)37 (648)(324)(972)557 (415)768 463 1,231 189 1,420 77 1,497 
Increase to pretax income2,245 2,904 5,149 2,932 8,081 2,976 11,057 3,366 3,050 6,416 2,926 9,342 2,493 11,835 
Income taxes on items above(303)(292)(595)(137)(732)(261)(993)(398)(321)(719)(268)(987)(345)(1,332)
Income tax reserve release attributed to Mead Johnson— — — — —   — — — — — (225)(225)
Income taxes attributed to internal transfers of certain assets— — — — — (983)(983)— — — — — (72)(72)
Income taxes(303)(292)(595)(137)(732)(1,244)(1,976)(398)(321)(719)(268)(987)(642)(1,629)
Increase to net earnings$1,942 $2,612 $4,554 $2,795 $7,349 $1,732 $9,081 $2,968 $2,729 $5,697 $2,658 $8,355 $1,851 $10,206 
(a)    Revised to exclude significant R&D charges or other income resulting from up-front and contingent milestone payments in connection with asset acquisitions or licensing of third-party intellectual property rights (including related income tax impacts).
(b)    Includes amortization of purchase price adjustments to Celgene debt.

9


BRISTOL-MYERS SQUIBB COMPANY
RECONCILIATION OF CERTAIN GAAP LINE ITEMS TO CERTAIN NON-GAAP LINE ITEMS
(Unaudited, dollars in millions)
 
2021
2022
 1st Qtr2nd Qtr6 Months3rd Qtr9 Months4th QtrYear1st Qtr2nd Qtr6 Months3rd Qtr9 Months4th QtrYear
Gross Profit$8,232 $9,251 $17,483 $9,333 $26,816 $9,629 $36,445 $9,177 $9,167 $18,344 $8,865 $27,209 $8,813 $36,022 
Specified items(a)
417 89 506 97 603  603 52 145 197 86 283 73 356 
Gross profit excluding specified items8,649 9,340 17,989 9,430 27,419 9,629 37,048 9,229 9,312 18,541 8,951 27,492 8,886 36,378 
Marketing, selling and administrative1,666 1,882 3,548 1,788 5,336 2,354 7,690 1,831 1,787 3,618 1,930 5,548 2,266 7,814 
Specified items(a)
(1)— (1)(1)(2)(3)(2)(4)(6)(73)(79) (79)
Marketing, selling and administrative excluding specified items1,667 1,881 3,548 1,787 5,335 2,352 7,687 1,829 1,783 3,612 1,857 5,469 2,266 7,735 
Research and development2,219 2,478 4,697 2,980 7,677 2,518 10,195 2,260 2,321 4,581 2,418 6,999 2,510 9,509 
Specified items(a)
(1)(230)(231)(612)(843) (843)(127)(21)(148)(160)(308) (308)
Research and development excluding specified items2,218 2,248 4,466 2,368 6,834 2,518 9,352 2,133 2,300 4,433 2,258 6,691 2,510 9,201 
Amortization of acquired intangible assets2,513 2,547 5,060 2,546 7,606 2,417 10,023 2,417 2,417 4,834 2,418 7,252 2,343 9,595 
Specified items(a)
(2,513)(2,547)(5,060)(2,546)(7,606)(2,417)(10,023)(2,417)(2,417)(4,834)(2,418)(7,252)(2,343)(9,595)
Amortization of acquired intangible assets excluding specified items— — — — —   — — — — —   
Other (income)/expense, net(702)(2)(704)(409)(1,113)393 (720)649 284 933 (140)793 (217)576 
Specified items(a)
685 (37)648 324 972 (557)415 (768)(463)(1,231)(189)(1,420)(77)(1,497)
Other (income)/expense, net excluding specified items(17)(39)(56)(85)(141)(164)(305)(119)(179)(298)(329)(627)(294)(921)
(a)    Refer to the Specified Items schedule for further details. For a description of Non-GAAP financial information, see Bristol Myers Squibb "Use of non-GAAP Financial Information" herein.

10


BRISTOL-MYERS SQUIBB COMPANY
RECONCILIATION OF GAAP TO NON-GAAP EPS
(Unaudited, dollars and shares in millions except per share data)
 
2021
2022
 1st Qtr2nd Qtr6 Months3rd Qtr9 Months4th QtrYear1st Qtr2nd Qtr6 Months3rd Qtr9 Months4th QtrYear
Earnings before income taxes$2,530 $1,553 $4,083 $2,157 $6,240 $1,858 $8,098 $1,687 $1,958 $3,645 $2,209 $5,854 $1,859 $7,713 
Specified items(a)
2,245 2,904 5,149 2,932 8,081 2,976 11,057 3,366 3,050 6,416 2,926 9,342 2,493 11,835 
Earnings before income taxes excluding specified items4,775 4,457 9,232 5,089 14,321 4,834 19,155 5,053 5,008 10,061 5,135 15,196 4,352 19,548 
Provision/(benefit) for income taxes501 492 993 605 1,598 (514)1,084 404 529 933 601 1,534 (166)1,368 
Income taxes on specified items(a)
303 292 595 137 732 261 993 398 321 719 268 987 345 1,332 
Income tax reserve release attributed to Mead Johnson(a)
— — — — —   — — — — — 225 225 
Income taxes attributed to internal transfer of certain assets(a)
— — — — — 983 983 — — — — — 72 72 
Provision for income taxes excluding tax on specified items, income tax reserve release attributed to Mead Johnson and income taxes attributed to internal transfer of certain assets804 784 1,588 742 2,330 730 3,060 802 850 1,652 869 2,521 476 2,997 
Net earnings attributable to BMS used for diluted EPS calculation - GAAP2,021 1,055 3,076 1,546 4,622 2,372 6,994 1,278 1,421 2,699 1,606 4,305 2,022 6,327 
Specified items(a)
1,942 2,612 4,554 2,795 7,349 1,732 9,081 2,968 2,729 5,697 2,658 8,355 1,851 10,206 
Net earnings attributable to BMS used for diluted EPS calculation excluding specified items - non-GAAP3,963 3,667 7,630 4,341 11,971 4,104 16,075 4,246 4,150 8,396 4,264 12,660 3,873 16,533 
Weighted-average common shares outstanding - diluted-GAAP2,265 2,252 2,258 2,243 2,253 2,219 2,245 2,164 2,149 2,157 2,148 2,154 2,124 2,146 
Weighted-average common shares outstanding - diluted-non-GAAP2,265 2,252 2,258 2,243 2,253 2,219 2,245 2,164 2,149 2,157 2,148 2,154 2,124 2,146 
Diluted earnings per share - GAAP*$0.89 $0.47 $1.36 $0.69 $2.05 $1.07 $3.12 $0.59 $0.66 $1.25 $0.75 $2.00 $0.95 $2.95 
Diluted earnings per share attributable to specified items(a)
0.85 1.16 2.02 1.24 3.26 0.77 4.04 1.37 1.27 2.64 1.24 3.88 0.87 4.75 
Diluted earnings per share - non-GAAP*$1.74 $1.63 $3.38 $1.93 $5.31 $1.84 $7.16 $1.96 $1.93 $3.89 $1.99 $5.88 $1.82 $7.70 
Effective tax rate19.8 %31.7 %24.3 %28.0 %25.6 %(27.7)%13.4 %23.9 %27.0 %25.6 %27.2 %26.2 %(8.9)%17.7 %
Specified items(a)
(3.0)%(14.1)%(7.1)%(13.4)%(9.3)%42.8 %2.6 %(8.0)%(10.0)%(9.2)%(10.3)%(9.6)%19.8 %(2.4)%
Effective tax rate excluding specified items16.8 %17.6 %17.2 %14.6 %16.3 %15.1 %16.0 %15.9 %17.0 %16.4 %16.9 %16.6 %10.9 %15.3 %
*    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. For a description of Non-GAAP financial information, see Bristol Myers Squibb "Use of non-GAAP Financial Information" herein.



11


BRISTOL-MYERS SQUIBB COMPANY
SELECTED BALANCE SHEET INFORMATION
(Unaudited, dollars in millions)
March 31,
2021
June 30,
2021
September 30,
2021
December 31, 2021March 31,
2022
June 30,
2022
September 30,
2022
December 31, 2022
Cash and cash equivalents$10,982 $11,024 $13,540 $13,979 $12,369 $10,750 $7,734 $9,123 
Marketable debt securities - current1,948 1,946 2,123 2,987 2,599 2,478 1,293 130 
Marketable debt securities - non-current288 143 46 — — — — — 
Cash, Cash Equivalents and Marketable Debt Securities13,218 13,113 15,709 16,966 14,968 13,228 9,027  9,253 
Short-term debt obligations(1,777)(2,655)(5,065)(4,948)(7,522)(4,953)(2,132)(4,264)
Long-term debt(44,505)(42,503)(39,677)(39,605)(37,450)(37,107)(36,966)(35,056)
Net Debt Position$(33,064)$(32,045)$(29,033)$(27,587)$(30,004)$(28,832)$(30,071) $(30,067)




12


BRISTOL-MYERS SQUIBB COMPANY
2023 FULL YEAR PROJECTED DILUTED EPS FROM OPERATIONS
EXCLUDING PROJECTED SPECIFIED ITEMS
Full Year 2023
Pre-taxTaxAfter-tax
Projected Diluted Earnings Attributable to Shareholders per Common Share - GAAP$4.03 to $4.33
Projected Specified Items:
Purchase price accounting adjustments(a)
4.26 0.44 3.82 
Acquisition, restructuring and integration expenses(b)
0.13 0.03 0.10 
Total4.39 0.47 3.92 
Projected Diluted Earnings Attributable to Shareholders per Common Share - Non-GAAP$7.95 to $8.25
(a)    Includes amortization of acquired intangible assets, unwind of inventory purchase price adjustments and amortization of fair value adjustments of debt assumed from Celgene.
(b)    Includes acquisition-related restructuring and integration expenses recognized primarily in Other (income)/expense, net.

The following table summarizes the company's 2023 financial guidance:
Line itemGAAPNon-GAAP
Total reported revenues~ 2% increase~ 2% increase
Total revenues Ex-FX(c)
~ 2% increase~ 2% increase
Revlimid~ $6.5 billion~ $6.5 billion
Gross margin~ 77%~ 77%
Operating expenses(d)
Mid single-digit declineLow single-digit decline
Effective tax rate~ 22%~ 17%
(c)    Ex-FX excludes the impact of foreign exchange calculated by converting our current-period local currency financial results using the prior period average currency rates and comparing these adjusted amounts to our prior-period results.
(d)    Operating expenses consist of Marketing, selling and administrative expenses and Research and development expenses, excluding Acquired IPRD expenses.
The GAAP financial results for the full year of 2023 will include specified items, including purchase price accounting adjustments, acquisition and integration expenses, charges associated with restructuring, downsizing and streamlining worldwide operations, impairment of intangible assets, loss on debt redemption, divestiture gains or losses and equity investment (including fair value adjustments attributed to limited partnership equity method investments) and Turning Point related charges, among other items. The 2023 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. 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 Fourth Quarter and Full Year Financial Results for 2022 on February 2, 2023, including “2023 Financial Guidance” and “Use of non-GAAP Financial Information” therein.
13


BRISTOL-MYERS SQUIBB COMPANY
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 supplementary information to the earnings 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, 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 marketing, selling and administrative expense and research and development expense excluding certain specified items as a percentage of revenues, non-GAAP operating expenses, which is marketing, selling and administrative and research and development expenses excluding certain specified items, non-GAAP marketing, selling and administrative expenses, which is marketing, selling and administrative expense 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 supplementary information to the earnings release also provides 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, unwind 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 equity method investments) and amortization of fair value adjustments of debt acquired from Celgene in our 2019 exchange offer, among other items. Certain other significant tax items are also excluded such as the impact resulting from the release of income tax reserves related to the Mead Johnson split-off transaction, internal transfers of certain assets to streamline our legal entity structure subsequent to the Celgene acquisition. 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.

Beginning with the first quarter of 2022, 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 are no longer excluded from our non-GAAP financial measures. We made these changes to our presentation of non-GAAP financial measures following comments from and discussions with the U.S. Securities and Exchange Commission. For purposes of comparability, the non-GAAP financial measures for the prior periods have been updated to reflect this change.

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 earnings per share amounts presented are calculated from the underlying amounts.

Also note that a reconciliation of forward-looking non-GAAP gross margin, non-GAAP operating expenses and non-GAAP tax rate 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 able to reliably predict the impact of the unwind of inventory purchase price adjustments, accelerated depreciation and impairment of property, plant and equipment and intangible assets, and stock
14


compensation resulting from acquisition-related equity awards, or currency exchange rates beyond the next twelve months. In addition, the company believes such a reconciliation would imply a degree of precision and certainty that could be confusing to investors. The variability of the specified items may have a significant and unpredictable impact on our future GAAP results.
15
Q4 2022 Results February 2, 2023


 
Q4 2022 Results Not for Product Promotional Use Forward Looking Statements and Non-GAAP Financial Information 2 This presentation contains statements about Bristol-Myers Squibb Company’s (the “Company”) future financial results, plans, business development strategy, anticipated clinical trials, results and regulatory approvals that constitute forward-looking statements for purposes of the safe harbor provisions under the Private Securities Litigation Reform Act of 1995. All statements that are not statements of historical facts are, or may be deemed to be, forward-looking statements. Actual results may differ materially from those expressed in, or implied by, these statements as a result of various factors, including, but not limited to, (i) new laws and regulations, (ii) our ability to obtain, protect and maintain market exclusivity rights and enforce patents and other intellectual property rights, (iii) our ability to achieve expected clinical, regulatory and contractual milestones on expected timelines or at all, (iv) difficulties or delays in the development and commercialization of new products, (v) difficulties or delays in our clinical trials and the manufacturing, distribution and sale of our products, (vi) adverse outcomes in legal or regulatory proceedings, (vii) risks relating to acquisitions, divestitures, alliances, joint ventures and other portfolio actions and (viii) political and financial instability, including changes in general economic conditions. These and other important factors are discussed in the Company’s most recent annual report on Form 10-K and reports on Forms 10-Q and 8-K. These documents are available on the U.S. Securities and Exchange Commission’s website, on the Company’s website or from Bristol-Myers Squibb Investor Relations. No forward-looking statements can be guaranteed. In addition, any forward-looking statements and clinical data included herein are presented only as of the date hereof. Except as otherwise required by applicable law, the Company undertakes no obligation to publicly update any of the provided information, whether as a result of new information, future events, changed circumstances or otherwise. This presentation includes certain non-generally accepted accounting principles (“GAAP”) financial measures that we use to describe the Company’s performance. The non-GAAP financial measures are provided as supplemental information 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. This presentation also provides certain revenues and expenses 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. The non-GAAP information presented herein provides investors with additional useful information but should not be considered in isolation or as substitutes for the related GAAP measures. Moreover, other companies may define non-GAAP measures differently, which limits the usefulness of these measures for comparisons with such other companies. We encourage investors to review our financial statements and publicly filed reports in their entirety and not to rely on any single financial measure. An explanation of these non-GAAP financial measures and a reconciliation to the most directly comparable financial measure are available on our website at www.bms.com/investors. Also note that a reconciliation of forward-looking non-GAAP operating margin is not provided because a comparable GAAP measure is 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 the unwind of inventory purchase price adjustments, accelerated depreciation and impairment of property, plant and equipment and intangible assets, and stock compensation resulting from acquisition-related equity awards, or currency exchange rates. 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.


 
Giovanni Caforio, MD Chairman of the Board and Chief Executive Officer 3


 
Q4 2022 Results Not for Product Promotional Use Q4 & Full Year 2022 Performance 4 Strong Commercial Execution Global Net Sales 3 first-in-class medicines launched in 2022 Q4:~$11.4B (5%) YoY; (1%) Ex-FX* Earnings Per Share (EPS) Q4: GAAP $0.95, (11%) YoY Non-GAAP* $1.82, (1%) YoY Strong Financial Execution In-Line Brands & New Product Portfolio: FY: GAAP $2.95, (5%) YoY; Non-GAAP* $7.70, +8% YoY +9% YoY; +13% Ex-FX*FY:~$35.4B 1Sales growth on reported & ex-FX basis 2023 Guidance Total Sales Non-GAAP EPS* Reflects continued top & bottom-line growth ~2% YoY Growth1 $7.95 - $8.25 $4.03 - $4.33 FY:~$46.2B in-line YoY; +3% Ex-FX* +7% YoY; +12% Ex-FX*Q4:~$9.0B *See “Forward-Looking Statements and Non-GAAP Financial Information” GAAP EPS*


 
Q4 2022 Results Not for Product Promotional Use Key Milestones in 2022 Opdivo (+/- Yervoy) U.S./EU expected approvals:  1L ESCC (CM-648)  Neo-adj lung EFS (CM-816) (U.S.)  Adj. RCC (CM-914) Opdualag  1L melanoma U.S. approval  1L melanoma EU approval  Initiation 2L+ CRC Ph3 bempeg  1L melanoma  1L renal  1L bladder  Neo-adj. cis-ineligible MIBC Breyanzi  2L LBCL U.S. approval  3L+ LBCL EU approval Abecma  2L+ MM Ph2 (KarMMa-2)  3L-5L MM Ph3 (KarMMa-3) iberdomide  Initiation 2L+ MM Ph3 (EXCALIBER) Delivered on Our Commitments 5 Milestones represent data readouts unless otherwise specified To be expanded to include regulatory milestones pending future registrational successes Reblozyl  1L MDS Ph3 (COMMANDS) mezigdomide  4L+ MM Ph1/2  Initiation triplet 2L+ MM Ph3 Sotyktu  PsO U.S. approval  SLE Ph2 cendakimab  AD Ph21 Camzyos  oHCM U.S. approval  oHCM Ph3 (VALOR)  Initiation nHCM Ph3 (ODYSSEY- HCM) milvexian  SSP Ph2 1Met primary endpoint; no plan to move to registrational trials


 
Not for Product Promotional UseQ4 2022 Results • Camzyos nHCM • Sotyktu SLE • Opdualag 1L NSCLC  Breyanzi 3L+ CLL1 • Breyanzi 3L+ iNHL • Reblozyl MF Planned Next 1-2 Years • Sotyktu PsA • Zeposia CD Milestones Already Delivered that De-Risk 2025–2030 and Beyond  Zeposia MS  Reblozyl 2L TD MDS  Breyanzi 3L+ LBCL  Abecma 5L+  Zeposia UC  Camzyos oHCM  Sotyktu PsO  Opdualag 1L Mel FDC  Breyanzi 2L LBCL  Abecma 3-5L1  Reblozyl 1L MDS1  Onureg AML maint. New Product Portfolio Significantly De-Risked with Important Catalysts Ahead 6 Camzyos Reblozyl Breyanzi Zeposia Sotyktu Other** 2025 $10B - $13B Risk-Adjusted Sales $25B+ Non-Risk Adjusted* 2030 $4B+ $4B+ $4B+ $4B+ $3B+ $3B+ $1B+ Key Milestones Beyond • Opdualag Adj. Mel • Opdualag 2L+ MSS CRC *Non-risk adjusted revenue potential, subject to positive registrational trials and health authority approval **Other includes: Abecma, Onureg, Inrebic, and Opdualag Financial projections may contain non promoted sales, BMS promotes only according to label 1Data in-house, subject to regulatory approval


 
Q4 2022 Results Not for Product Promotional Use 2023 Key Milestones Opdivo (+/- Yervoy) Early Stage:  Neo-adjuvant NSCLC Ph3 (CM-816) approval in EU Metastatic  1L mCRPC Ph3 (CM-7DX) Opdualag  1L NSCLC Ph2 repotrectinib  ROS1+ NSCLC (TRIDENT-1) U.S. filing Abecma  3-5L MM Ph3 (KarMMa-3) filing  Initiation NDMM Ph3 (KarMMa-9) Breyanzi  2L TE LBCL EU approval  3L+ CLL Ph1/2 (TRANSCEND-CLL)  3L+ FL Ph2 (TRANSCEND- FL) Near-term Catalysts Across Diversified Portfolio 7Milestones represent data read-outs unless otherwise specified To be expanded to include regulatory milestones pending future registrational successes iberdomide  Initiation of pivotal post-transplant maintenance H2H vs Revlimid Reblozyl  1L MDS (COMMANDS) U.S. filing Sotyktu  Mod-to-severe PsO EU approval1  CD Ph2 (IM011-023)  UC Ph2 (IM011-127) LPA1 Antagonist  Initiation IPF Ph3  PPF Ph2 (IM027- 040) Camzyos  oHCM EU approval milvexian  Initiation Ph3 program2,3 2024/2025 Key Milestones Opdivo (+/- Yervoy) Metastatic:  1L HCC Ph3 (CM-9DW)  1L+ MSI High CRC Ph3 (CM-8HW) Early Stage:  Peri-adj NSCLC Ph3 (CM-77T)  Peri-adj MIBC Ph3 (CM-078)  Adj HCC Ph3 (CM-9DX)  Stage III Unresectable NSCLC Ph3 (CM-73L)  Adj NSCLC Ph3 (ANVIL, co-op group) Opdualag  1L HCC Ph2  2L HCC Ph2  2L+ MSS mCRC Ph3 alnuctamab BCMA TCE  Initiation MM Ph3 Reblozyl  1L MF Ph3 (INDEPENDENCE) cendakimab  EoE Ph3 Sotyktu  PsA Ph3 Zeposia  CD maintenance Ph3 (YELLOWSTONE) 1Positive CHMP opinion received in Jan. ’23 2SSP, ACS, AF trials conducted by Janssen 3SSP Phase 3 trial initiated in Jan. ’23


 
Q4 2022 Results Not for Product Promotional Use MYOK, TPTX 15+ Delivered Significant Financial & Portfolio Milestones Through Strong Execution 8 Sales growth High single-digit Non-GAAP EPS growth2 Mid-20s Cost synergies $3B+ $40B+ Significant Operating Cash Flow3 3 First-in-Class Assets Approved in 2022 BD execution Added new indications across portfolio 9New products delivered ~3 Year Financial Achievements1 ~3 Year Portfolio Achievements4 Strengthens Foundation for Portfolio Renewal & Long-Term Growth 3Operating cashflow generated from 2020 to 2022 4Portfolio Achievements from 2H’19 – 2022 1Financial Achievements from 2020-2022; Sales and Non-GAAP EPS based on non-compounded growth 2Non-GAAP EPS calculation excludes Acquired IPR&D impact from the MYOK acquisition in 2020; including this impact, the non-GAAP EPS growth rate would be in excess of 500%


 
Q4 2022 Results Not for Product Promotional Use Multiple Paths for Long-Term Growth 9 On track to deliver • Low-to-mid single digit revenue CAGR* • $8B - 10B growth from in-line brands (primarily I-O & Eliquis) • $10B - 13B from New Product Portfolio • 40%+ operating margin** 2025 Revenues LOE Brands 2030 Revenues Additional growth from New Product Portfolio Next Wave of innovation: 6 registrational stage assets Optionality from early- stage pipeline & BD 2025-2030 2020-2025 *At constant exchange rates on a risk-adjusted basis; **See "Forward-Looking Statements and Non-GAAP Financial Information“ and “Bristol Myers Squibb Company Reconciliation of Certain GAAP Line Items to Certain Non-GAAP Line Items” Financial projections may contain non promoted sales, BMS promotes only according to label Continued growth reflected in 2023 guidance


 
David Elkins Executive Vice President and Chief Financial Officer 10


 
Not for Product Promotional UseQ4 2022 Results Strong Total Company Performance 11 Total Company Sales ~$46.2B in-line YoY, +3% ex-FX $B FY 22 Net Sales* YoY % Ex-FX % Total Company $46.2 - +3% In-Line Products $33.3 +7% +11% New Product Portfolio $2.0 +87% +92% In-Line Products & New Product Portfolio $35.4 +9% +13% Recent LOEs1 $10.8 (23%) (22%) 1Recent LOE Brands = Revlimid & Abraxane $32.4 $35.4 $14.0 $10.8 2021 2022 Recent LOEs In-Line & New Products *Amounts may not add due to rounding


 
Not for Product Promotional UseQ4 2022 Results $151 $199 $69 $125 $104 $48 $79 $40 $55 $25 $37 $20 $23 $353 $645 Q4 2021 Q4 2022 $M Reblozyl Abecma Opdualag Zeposia Breyanzi Onureg Inrebic Camzyos Sotyktu $16 New Product Portfolio Sales Performance 12 Sales nearly doubled vs PY $551 $717 $164 $388 $252 $134 $250 $87 $182 $73 $124 $74 $85 $1,083 $2,030 FY 2021 FY 2022 $M Reblozyl Abecma Opdualag Zeposia Breyanzi Onureg Inrebic Camzyos Sotyktu $24 $8 $7


 
Not for Product Promotional UseQ4 2022 Results Q4 & Full Year 2022 Solid Tumor product summary 13 Opdivo • U.S. growth driven by demand in 1L lung, 1L renal, 1L gastric, adj. esophageal, adj. bladder cancer & neoadjuvant lung • Ex-U.S. growth from 1L lung, upper GI cancers & timing of shipments vs PY • Continued growth expected from current & expanded indications Opdualag • 3rd approved I-O agent; potential to be a new SOC in 1L melanoma • U.S. growth driven by strong demand; share in the high teens YoY Ex-FX YoY Ex-FX $2,216 +11% +16% $8,249 +10% +14% $568 +4% +9% $2,131 +5% +10% $179 (41%) (39%) $811 (31%) (30%) $104 --- --- $252 --- --- Q4 2022 FY 2022 Global Net Sales ($M)


 
Q4 2022 Results Not for Product Promotional Use Q4 & Full Year 2022 Cardiovascular product summary 14 • U.S. robust demand & gross-to-net adjustments offset by timing of wholesaler buying patterns in Q4’22 vs PY • Ex-U.S. continues to be #1 OAC in key international markets; impacted by some generic entry (UK/NL & Canada) & pricing measures ````` YoY Ex-FX YoY Ex-FX $2,688 +1% +6% $11,789 +10% +14% • Significant increase in REMS certified HCPs, total treated patients & commercial dispensed patients • EU approval in oHCM expected mid-year • VALOR: U.S. PDUFA date June 16, 2023 As of Sept 30, 20221 As of Dec 31, 20221 REMS Certified physicians >2000 >2600 Patients in Hub >1100 >1800 Patients on commercial drug >350 >900 First-in-class myosin inhibitorBest-in-class & leading OAC within category Q4 2022 FY 2022 Global Net Sales ($M) ````` YoY Ex-FX YoY Ex-FX $16 -- -- $24 -- -- Q4 2022 FY 2022 1Source: BMS Internal Analysis


 
Q4 2022 Results Not for Product Promotional Use Q4 & Full Year 2022 Hematology product summary 15 Revlimid – Impact from Gx entry; FY 2023 revenue projection ~$6.5B Pomalyst – Increased demand as patients move into earlier lines, extending treatment duration % YoY Ex-FX YoY Ex-FX $2,260 (32%) (31%) $9,978 (22%) (21%) $877 +3% +6% $3,497 +5% +8% $578 +4% +8% $2,165 +2% +6% $71 (12%) (7%) $296 (11%) (7%) Q4 2022 FY 2022 YoY Ex-FX YoY Ex-FX $199 +32% +34% $717 +30% +32% $125 +81% +87% $388 ** ** $55 +38% +48% $182 ** ** $37 +48% +52% $124 +70% +74% $23 +15% +15% $85 +15% +16% Q4 2022 FY 2022 **In excess of 100% Reblozyl • Robust U.S. demand with progress in increasing treatment duration & patient adherence • Continued expansion in international markets based on reimbursement timing Abecma & Breyanzi – Strong demand supported by increased manufacturing capacity Global Net Sales ($M)


 
Q4 2022 Results Not for Product Promotional Use Q4 & Full Year 2022 Immunology product summary 16 Zeposia • Strong demand growth including expansion into UC • Continuing to improve formulary access; achieved 0 or 1 step edit across several plans • Very encouraging HCP feedback & strong early adoption • Focused on driving demand to enable broader access in 2024 • Positive CHMP Opinion in mod-to-severe PsO in Jan. ’23 First-in-class selective allosteric TYK2 inhibitor % YoY % Ex-FX % YoY % Ex-FX % $913 +6% +9% $3,464 +5% +8% $79 +65% +69% $250 +87% +93% As of Dec 31, 20221 Volume >2000 TRx Equivalent Market Share2 ~25-30% Source of Business • Systemic-naïve (~1/3) • Otezla-experienced (~1/3) • Biologic-experienced (~1/3) Q4 2022 FY 2022 Global Net Sales ($M) 2Market share of written oral prescriptions in NBRx sourced from BrandImpact ````` YoY Ex-FX YoY Ex-FX $7 -- -- $8 -- -- Q4 2022 FY 2022 1Source: BMS Internal Analysis


 
Q4 2022 Results Not for Product Promotional Use US GAAP Non-GAAP $ in billions, except EPS Q4 2022 FY 2022 Q4 2022 FY 2022 Total Revenues, net 11.4 46.2 11.4 46.2 Gross Margin % 77.3% 78% 77.9% 78.8% Operating Expenses1 4.8 17.3 4.8 16.9 Acquired IPR&D 0.1 0.8 0.1 0.8 Amortization of Acquired Intangibles 2.3 9.6 - - Effective Tax Rate (8.9%) 17.7% 10.9% 15.3% Diluted EPS 0.95 2.95 1.82 7.70 Diluted Shares Outstanding (# in millions) 2,124 2,146 2,124 2,146 Q4 & Full Year 2022 Financial Performance 17 US P Non- P* Diluted EPS Impact from Acquired IPR&D2 (0.01) (0.24) (0.01) (0.24) 1 Operating Expenses = MS&A and R&D 2Comprises the net impact from Acquired IPRD & Licensing income *See “Forward-Looking Statements and Non-GAAP Financial Information”


 
Q4 2022 Results Not for Product Promotional Use Balanced Approach to Capital Allocation 18 *Cash includes cash, cash equivalents and marketable debt securities **Subject to Board approval $B Q4 2022 Total Cash* ~$9.3B Total Debt ~$39.3B • Prioritize opportunities to further diversify portfolio & strengthen long-term outlook • Debt reduction: ~$5B debt paid in 2022 • Maintain strong investment-grade credit rating Business Development Balance Sheet Strength Returning Cash to Shareholders • Continued annual dividend growth** ‒ 14th consecutive dividend increase • Opportunistic share repurchase ‒ ~$7.2B remaining authorizationStrong operating cash flow generation $4.1 $3.8 $2.3 $3.7 $3.3 Cash flow from Operations $B Q4 2021 Q1 2022 Q2 2022 Q3 2022 Q4 2022


 
Q4 2022 Results Not for Product Promotional Use Total Net Sales Reported Rates ~2% increase ~2% increase Total Net Sales Ex-FX ~2% increase ~2% increase Revlimid ~$6.5 billion ~$6.5 billion Gross Margin % ~77% ~77% Operating Expenses1 Mid-single digit decline Low-single digit decline Tax Rate ~22% ~17% Diluted EPS $4.03 - $4.33 $7.95 - $8.25 2023 Guidance 19 US GAAP* Non-GAAP* 1Operating Expenses = MS&A and R&D, excluding Acquired IPR&D and Amortization of acquired intangibles *See “Forward-Looking Statements and Non-GAAP Financial Information”


 
20 Giovanni Caforio, MD Chairman of the Board, Chief Executive Officer Chris Boerner, PhD Executive VP, Chief Commercialization Officer David Elkins Executive VP, Chief Financial Officer Samit Hirawat, MD Executive VP, Chief Medical Officer, Global Drug Development


 
Q4 2022 Results Not for Product Promotional Use Year-Ended December 31 2020 2021 2022 Total Revenues $42,518 $46,385 $46,159 Gross Profit $30,745 $36,445 $36,022 Specified items (a) $3,300 $603 $356 Gross Profit excluding specified items $34,045 $37,048 $36,378 Marketing, Selling and Administrative $7,661 $7,690 $7,814 Specified items (a) ($279) ($3) ($79) Marketing, Selling and Administrative excluding specified items $7,382 $7,687 $7,735 Research and Development $10,048 $10,195 $9,509 Specified items (a) ($903) ($843) ($308) Research and Development excluding specified items $9,145 $9,352 $9,201 Operating margin 31% 40% 41% Specified items (a) 10% 3% 1% Operating margin excluding specified items (b) 41% 43% 42% Bristol Myers Squibb Company Reconciliation of Certain GAAP Line Items to Certain Non-GAAP Line Items 21 (a): An explanation of these non-GAAP financial measures and a reconciliation to the most directly comparable GAAP financial measure are available on our website at bms.com/investors. (b): Operating margin on Specified Items represents the difference between the GAAP and Non-GAAP operating margin (Unaudited, dollars in millions)