Cover Page
Cover Page - shares | 3 Months Ended | |
Mar. 31, 2020 | Apr. 30, 2020 | |
Entity Information [Line Items] | ||
Document Type | 10-Q | |
Document Quarterly Report | true | |
Document Period End Date | Mar. 31, 2020 | |
Document Transition Report | false | |
Entity File Number | 1-6571 | |
Entity Registrant Name | Merck & Co., Inc. | |
Entity Incorporation, State or Country Code | NJ | |
Entity Tax Identification Number | 22-1918501 | |
Entity Address, Address Line One | 2000 Galloping Hill Road | |
Entity Address, City or Town | Kenilworth | |
Entity Address, State or Province | NJ | |
Entity Address, Postal Zip Code | 07033 | |
City Area Code | (908) | |
Local Phone Number | 740-4000 | |
Entity Current Reporting Status | Yes | |
Entity Interactive Data Current | Yes | |
Entity Filer Category | Large Accelerated Filer | |
Entity Small Business | false | |
Entity Emerging Growth Company | false | |
Entity Shell Company | false | |
Entity Common Stock, Shares Outstanding | 2,524,101,191 | |
Amendment Flag | false | |
Document Fiscal Year Focus | 2020 | |
Document Fiscal Period Focus | Q1 | |
Entity Central Index Key | 0000310158 | |
Current Fiscal Year End Date | --12-31 | |
Common Stock | ||
Entity Information [Line Items] | ||
Title of 12(b) Security | Common Stock ($0.50 par value) | |
Trading Symbol | MRK | |
Security Exchange Name | NYSE | |
1.125% Notes due 2021 | ||
Entity Information [Line Items] | ||
Title of 12(b) Security | 1.125% Notes due 2021 | |
Trading Symbol | MRK/21 | |
Security Exchange Name | NYSE | |
0.500% Notes due 2024 | ||
Entity Information [Line Items] | ||
Title of 12(b) Security | 0.500% Notes due 2024 | |
Trading Symbol | MRK 24 | |
Security Exchange Name | NYSE | |
1.875% Notes due 2026 | ||
Entity Information [Line Items] | ||
Title of 12(b) Security | 1.875% Notes due 2026 | |
Trading Symbol | MRK/26 | |
Security Exchange Name | NYSE | |
2.500% Notes due 2034 | ||
Entity Information [Line Items] | ||
Title of 12(b) Security | 2.500% Notes due 2034 | |
Trading Symbol | MRK/34 | |
Security Exchange Name | NYSE | |
1.375% Notes due 2036 | ||
Entity Information [Line Items] | ||
Title of 12(b) Security | 1.375% Notes due 2036 | |
Trading Symbol | MRK 36A | |
Security Exchange Name | NYSE |
CONDENSED CONSOLIDATED STATEMEN
CONDENSED CONSOLIDATED STATEMENT OF INCOME - USD ($) $ in Millions | 3 Months Ended | |
Mar. 31, 2020 | Mar. 31, 2019 | |
Income Statement [Abstract] | ||
Sales | $ 12,057 | $ 10,816 |
Costs, Expenses and Other | ||
Cost of sales | 3,312 | 3,052 |
Selling, general and administrative | 2,555 | 2,425 |
Research and development | 2,209 | 1,931 |
Restructuring costs | 72 | 153 |
Other (income) expense, net | 71 | 188 |
Total Costs, Expenses and Other | 8,219 | 7,749 |
Income Before Taxes | 3,838 | 3,067 |
Taxes on Income | 619 | 205 |
Net Income | 3,219 | 2,862 |
Less: Net Loss Attributable to Noncontrolling Interests | 0 | (53) |
Net Income Attributable to Merck & Co., Inc. | $ 3,219 | $ 2,915 |
Basic Earnings per Common Share Attributable to Merck & Co., Inc. Common Shareholders (in dollars per share) | $ 1.27 | $ 1.13 |
Earnings per Common Share Assuming Dilution Attributable to Merck & Co., Inc. Common Shareholders (in dollars per share) | $ 1.26 | $ 1.12 |
CONDENSED CONSOLIDATED STATEM_2
CONDENSED CONSOLIDATED STATEMENT OF COMPREHENSIVE INCOME - USD ($) $ in Millions | 3 Months Ended | |
Mar. 31, 2020 | Mar. 31, 2019 | |
Statement of Comprehensive Income [Abstract] | ||
Net Income Attributable to Merck & Co., Inc. | $ 3,219 | $ 2,915 |
Other Comprehensive (Loss) Income Net of Taxes: | ||
Net unrealized gain (loss) on derivatives, net of reclassifications | 104 | (48) |
Net unrealized (loss) gain on investments, net of reclassifications | (18) | 82 |
Benefit plan net gain and prior service credit, net of amortization | 60 | 15 |
Cumulative translation adjustment | (344) | 150 |
Other comprehensive income (loss), net of taxes | (198) | 199 |
Comprehensive Income Attributable to Merck & Co., Inc. | $ 3,021 | $ 3,114 |
CONDENSED CONSOLIDATED BALANCE
CONDENSED CONSOLIDATED BALANCE SHEET - USD ($) $ in Millions | Mar. 31, 2020 | Dec. 31, 2019 |
Current Assets | ||
Cash and cash equivalents | $ 7,425 | $ 9,676 |
Short-term investments | 7 | 774 |
Accounts receivable (net of allowance for doubtful accounts of $89 in 2020 and $86 in 2019) | 8,182 | 6,778 |
Inventories (excludes inventories of $1,630 in 2020 and $1,480 in 2019 classified in Other assets - see Note 6) | 5,846 | 5,978 |
Other current assets | 4,714 | 4,277 |
Total current assets | 26,174 | 27,483 |
Investments | 555 | 1,469 |
Property, Plant and Equipment, at cost, net of accumulated depreciation of $17,706 in 2020 and $17,686 in 2019 | 15,269 | 15,053 |
Goodwill | 19,767 | 19,425 |
Other Intangibles, Net | 16,096 | 14,196 |
Other Assets | 7,052 | 6,771 |
Total Assets | 84,913 | 84,397 |
Current Liabilities | ||
Loans payable and current portion of long-term debt | 6,361 | 3,610 |
Trade accounts payable | 3,572 | 3,738 |
Accrued and other current liabilities | 10,932 | 12,549 |
Income taxes payable | 1,033 | 736 |
Dividends payable | 1,585 | 1,587 |
Total current liabilities | 23,483 | 22,220 |
Long-Term Debt | 21,637 | 22,736 |
Deferred Income Taxes | 1,943 | 1,470 |
Other Noncurrent Liabilities | 11,550 | 11,970 |
Merck & Co., Inc. Stockholders’ Equity | ||
Common stock, $0.50 par value Authorized - 6,500,000,000 shares Issued - 3,577,103,522 shares in 2020 and 2019 | 1,788 | 1,788 |
Other paid-in capital | 39,697 | 39,660 |
Retained earnings | 48,272 | 46,602 |
Accumulated other comprehensive loss | (6,391) | (6,193) |
Stockholders' equity before deduction for treasury stock | 83,366 | 81,857 |
Less treasury stock, at cost: 1,053,090,194 shares in 2020 and 1,038,087,496 shares in 2019 | 57,161 | 55,950 |
Total Merck & Co., Inc. stockholders’ equity | 26,205 | 25,907 |
Noncontrolling Interests | 95 | 94 |
Total equity | 26,300 | 26,001 |
Liabilities and Equity | $ 84,913 | $ 84,397 |
CONDENSED CONSOLIDATED BALANC_2
CONDENSED CONSOLIDATED BALANCE SHEET (Parenthetical) - USD ($) $ in Millions | Mar. 31, 2020 | Dec. 31, 2019 |
Statement of Financial Position [Abstract] | ||
Allowance for doubtful accounts | $ 89 | $ 86 |
Inventories classified in Other assets | 1,630 | 1,480 |
Accumulated depreciation | $ 17,706 | $ 17,686 |
Common stock, par value (in dollars per share) | $ 0.50 | $ 0.50 |
Common stock, shares authorized (shares) | 6,500,000,000 | 6,500,000,000 |
Common stock, shares issued (in shares) | 3,577,103,522 | 3,577,103,522 |
Treasury stock, shares (shares) | 1,053,090,194 | 1,038,087,496 |
CONDENSED CONSOLIDATED STATEM_3
CONDENSED CONSOLIDATED STATEMENT OF CASH FLOWS - USD ($) $ in Millions | 3 Months Ended | |
Mar. 31, 2020 | Mar. 31, 2019 | |
Cash Flows from Operating Activities | ||
Net income | $ 3,219 | $ 2,862 |
Adjustments to reconcile net income to net cash provided by operating activities: | ||
Depreciation and amortization | 821 | 898 |
Intangible asset impairment charges | 0 | 104 |
Deferred income taxes | 82 | 194 |
Share-based compensation | 108 | 93 |
Other | 143 | 120 |
Net changes in assets and liabilities | (3,666) | (2,935) |
Net Cash Provided by Operating Activities | 707 | 1,336 |
Cash Flows from Investing Activities | ||
Capital expenditures | (986) | (595) |
Purchases of securities and other investments | (49) | (974) |
Proceeds from sales of securities and other investments | 1,816 | 1,899 |
Acquisition of ArQule, Inc., net of cash acquired | (2,545) | 0 |
Other | 136 | 38 |
Net Cash (Used in) Provided by Investing Activities | (1,628) | 368 |
Cash Flows from Financing Activities | ||
Net change in short-term borrowings | 3,583 | (4,135) |
Payments on debt | (1,951) | 0 |
Proceeds from issuance of debt | 0 | 4,958 |
Purchases of treasury stock | (1,281) | (1,090) |
Dividends paid to stockholders | (1,551) | (1,428) |
Proceeds from exercise of stock options | 26 | 173 |
Other | (316) | (92) |
Net Cash Used in Financing Activities | (1,490) | (1,614) |
Effect of Exchange Rate Changes on Cash, Cash Equivalents and Restricted Cash | (63) | 20 |
Net (Decrease) Increase in Cash, Cash Equivalents and Restricted Cash | (2,474) | 110 |
Cash, Cash Equivalents and Restricted Cash at Beginning of Year (includes restricted cash of $258 million at January 1, 2020 included in Other Assets) | 9,934 | 7,967 |
Cash, Cash Equivalents and Restricted Cash at End of Period (includes restricted cash of $35 million at March 31, 2020 included in Other Assets) | $ 7,460 | $ 8,077 |
CONDENSED CONSOLIDATED STATEM_4
CONDENSED CONSOLIDATED STATEMENT OF CASH FLOWS (Parenthetical) - USD ($) $ in Millions | Mar. 31, 2020 | Dec. 31, 2019 |
Statement of Cash Flows [Abstract] | ||
Restricted cash | $ 35 | $ 258 |
Basis of Presentation
Basis of Presentation | 3 Months Ended |
Mar. 31, 2020 | |
Organization, Consolidation and Presentation of Financial Statements [Abstract] | |
Basis of Presentation | Basis of Presentation The accompanying unaudited condensed consolidated financial statements of Merck & Co., Inc. (Merck or the Company) have been prepared pursuant to the rules and regulations for reporting on Form 10-Q. Accordingly, certain information and disclosures required by accounting principles generally accepted in the United States (GAAP) for complete consolidated financial statements are not included herein. These interim statements should be read in conjunction with the audited financial statements and notes thereto included in Merck’s Form 10-K filed on February 26, 2020. The results of operations of any interim period are not necessarily indicative of the results of operations for the full year. In the Company’s opinion, all adjustments necessary for a fair statement of these interim statements have been included and are of a normal and recurring nature. Planned Spin-Off of Women’s Health, Legacy Brands and Biosimilars into New Company In February 2020, Merck announced its intention to spin-off products from its women’s health, trusted legacy brands and biosimilars businesses into a new, independent, publicly traded company named Organon & Co. (Organon) through a distribution of Organon’s publicly traded stock to Company shareholders. The distribution is expected to qualify as tax-free to the Company and its shareholders for U.S. federal income tax purposes. The legacy brands included in the transaction consist of dermatology, non-opioid pain, respiratory, and select cardiovascular products including Zetia (ezetimibe) and Vytorin (ezetimibe and simvastatin), as well as the rest of Merck’s diversified brands franchise. Merck’s existing research pipeline programs will continue to be owned and developed within Merck as planned. Organon will have development capabilities initially focused on late-stage development and life-cycle management and is expected over time to develop research capabilities in selected therapeutic areas. The spin-off is expected to be completed in the first half of 2021, subject to market and certain other conditions. Subsequent to the spin-off, the historical results of the women’s health, legacy brands and biosimilars businesses will be reflected as discontinued operations in the Company’s consolidated financial statements. Recently Adopted Accounting Standards In June 2016, the FASB issued new guidance on the accounting for credit losses on financial instruments. The new guidance introduces an expected loss model for estimating credit losses, replacing the incurred loss model. The new guidance also changes the impairment model for available-for-sale debt securities, requiring the use of an allowance to record estimated credit losses (and subsequent recoveries). The Company adopted the new guidance effective January 1, 2020. There was no impact to the Company’s consolidated financial statements upon adoption. In November 2018, the FASB issued new guidance for collaborative arrangements intended to reduce diversity in practice by clarifying whether certain transactions between collaborative arrangement participants should be accounted for under revenue recognition guidance (ASC 606). The Company adopted the new guidance effective January 1, 2020, which resulted in minor changes to the presentation of information related to the Company’s collaborative arrangements. Recently Issued Accounting Standards Not Yet Adopted In December 2019, the FASB issued amended guidance on the accounting and reporting of income taxes. The guidance is intended to simplify the accounting for income taxes by removing exceptions related to certain intraperiod tax allocations and deferred tax liabilities; clarifying guidance primarily related to evaluating the step-up tax basis for goodwill in a business combination; and reflecting enacted changes in tax laws or rates in the annual effective tax rate. The amended guidance is effective for interim and annual periods in 2021. Early adoption is permitted. The amendments in the new guidance are to be applied on a retrospective basis, on a modified retrospective basis through a cumulative-effect adjustment to retained earnings or prospectively, depending on the amendment. The Company is currently evaluating the impact of adoption on its consolidated financial statements. In January 2020, the FASB issued new guidance intended to clarify certain interactions between accounting standards related to equity securities, equity method investments and certain derivatives. The guidance addresses accounting for the transition into and out of the equity method of accounting and measuring certain purchased options and forward contracts to acquire investments. The new guidance is effective for interim and annual periods in 2021 and is to be applied prospectively. Early adoption is permitted. The Company is currently evaluating the impact of adoption on its consolidated financial statements. In March 2020, the FASB issued optional guidance to ease the potential burden in accounting for (or recognizing the effects of) reference rate reform on financial reporting. The guidance provides optional expedients and exceptions for applying GAAP to contracts, hedging relationships, and other transactions affected by reference rate reform. The optional guidance is effective upon issuance and can be applied on a prospective basis at any time between January 1, 2020 through December 31, 2022. The Company is currently evaluating the impact of adoption on its consolidated financial statements. |
Acquisitions, Research Collabor
Acquisitions, Research Collaborations and License Agreements | 3 Months Ended |
Mar. 31, 2020 | |
Business Combinations [Abstract] | |
Acquisitions, Divestitures, Research Collaborations and License Agreements | Acquisitions, Research Collaborations and License Agreements The Company continues to pursue acquisitions and the establishment of external alliances such as research collaborations and licensing agreements to complement its internal research capabilities. These arrangements often include upfront payments, as well as expense reimbursements or payments to the third party, and milestone, royalty or profit share arrangements, contingent upon the occurrence of certain future events linked to the success of the asset in development. The Company also reviews its marketed products and pipeline to examine candidates which may provide more value through out-licensing and, as part of its portfolio assessment process, may also divest certain assets. Pro forma financial information for acquired businesses is not presented if the historical financial results of the acquired entity are not significant when compared with the Company’s financial results. In January 2020, Merck acquired ArQule, Inc. (ArQule), a publicly traded biopharmaceutical company focused on kinase inhibitor discovery and development for the treatment of patients with cancer and other diseases. Total consideration paid of $2.7 billion included $138 million of share-based compensation payments to settle equity awards attributable to precombination service and cash paid for transaction costs on behalf of ArQule. The Company incurred $95 million of transaction costs directly related to the acquisition of ArQule, consisting almost entirely of share-based compensation payments to settle non-vested equity awards attributable to postcombination service. These costs were included in Selling, general and administrative expenses in the first quarter of 2020. ArQule’s lead investigational candidate, MK-1026 (formerly ARQ 531), is a novel, oral Bruton’s tyrosine kinase (BTK) inhibitor currently being evaluated for the treatment of B-cell malignancies. The estimated fair value of assets acquired and liabilities assumed from ArQule is as follows: ($ in millions) January 16, 2020 Cash and cash equivalents $ 145 IPR&D MK-1026 (formerly ARQ 531) (1) 2,280 IPR&D MK-7075 (formerly ARQ 092) (1) 170 Licensing arrangement for ARQ 087 80 Deferred income tax liabilities (434 ) Other assets and liabilities, net 35 Total identifiable net assets 2,276 Goodwill (2) 414 Consideration transferred $ 2,690 (1) The fair values of the identifiable intangible assets related to in-process research and development (IPR&D) were determined using an income approach. The future net cash flows were discounted to present value utilizing a discount rate of 12.5% . Actual cash flows are likely to be different than those assumed. (2) The goodwill was allocated to the Pharmaceutical segment and is not deductible for tax purposes. |
Collaborative Arrangements
Collaborative Arrangements | 3 Months Ended |
Mar. 31, 2020 | |
Collaborative Arrangements [Abstract] | |
Collaborative Arrangements | Collaborative Arrangements Merck has entered into collaborative arrangements that provide the Company with varying rights to develop, produce and market products together with its collaborative partners. Both parties in these arrangements are active participants and exposed to significant risks and rewards dependent on the commercial success of the activities of the collaboration. Merck’s more significant collaborative arrangements are discussed below. AstraZeneca In July 2017, Merck and AstraZeneca PLC (AstraZeneca) entered into a global strategic oncology collaboration to co-develop and co-commercialize AstraZeneca’s Lynparza (olaparib) for multiple cancer types. Lynparza is an oral poly (ADP-ribose) polymerase (PARP) inhibitor currently approved for certain types of advanced ovarian, breast and pancreatic cancers. The companies are jointly developing and commercializing Lynparza, both as monotherapy and in combination trials with other potential medicines. Independently, Merck and AstraZeneca will develop and commercialize Lynparza in combinations with their respective PD-1 and PD-L1 medicines, Keytruda (pembrolizumab) and Imfinzi. The companies will also jointly develop and commercialize AstraZeneca’s Koselugo (selumetinib), an oral, selective inhibitor of MEK, part of the mitogen-activated protein kinase (MAPK) pathway, currently being developed for multiple indications. In April 2020, Koselugo was approved for the treatment of pediatric patients two years of age and older with neurofibromatosis type 1 who have symptomatic, inoperable plexiform neurofibromas. Under the terms of the agreement, AstraZeneca and Merck will share the development and commercialization costs for Lynparza and Koselugo monotherapy and non-PD-L1/PD-1 combination therapy opportunities. Profits from Lynparza and Koselugo product sales generated through monotherapies or combination therapies are shared equally. Merck will fund all development and commercialization costs of Keytruda in combination with Lynparza or Koselugo. AstraZeneca will fund all development and commercialization costs of Imfinzi in combination with Lynparza or Koselugo. AstraZeneca is the principal on Lynparza sales transactions. Merck records its share of Lynparza and Koselugo product sales, net of cost of sales and commercialization costs, as alliance revenue and its share of development costs associated with the collaboration as part of Research and development expenses. Reimbursements received from AstraZeneca for research and development expenses are recognized as reductions to Research and development costs. As part of the agreement, Merck made an upfront payment to AstraZeneca of $1.6 billion in 2017 and made payments of $750 million over a multi-year period for certain license options. In addition, the agreement provides for additional contingent payments from Merck to AstraZeneca related to the successful achievement of sales-based and regulatory milestones. Prior to 2020, Merck accrued sales-based milestone payments aggregating $1.0 billion related to Lynparza, of which $200 million and $250 million was paid to AstraZeneca in 2019 and 2018, respectively, and $250 million was paid in the first quarter of 2020. Potential future sales-based milestone payments of $3.1 billion have not yet been accrued as they are not deemed by the Company to be probable at this time. In 2019 and 2018, Lynparza received regulatory approvals triggering capitalized milestone payments of $60 million and $140 million , respectively, in the aggregate from Merck to AstraZeneca. Potential future regulatory milestone payments of $1.7 billion remain under the agreement. The intangible asset balance related to Lynparza (which includes capitalized sales-based and regulatory milestone payments) was $928 million at March 31, 2020 and is included in Other Intangibles, Net on the Consolidated Balance Sheet. The amount is being amortized over its estimated useful life through 2028 as supported by projected future cash flows, subject to impairment testing. Summarized financial information related to this collaboration is as follows: Three Months Ended ($ in millions) 2020 2019 Alliance revenue $ 145 $ 79 Cost of sales (1) 28 19 Selling, general and administrative 33 27 Research and development 36 45 ($ in millions) March 31, 2020 December 31, 2019 Receivables from AstraZeneca included in Other current assets $ 142 $ 128 Payables to AstraZeneca included in Accrued and other current liabilities (2) 326 577 (1) Represents amortization of capitalized milestone payments. (2) Includes accrued milestone payments. Eisai In March 2018, Merck and Eisai Co., Ltd. (Eisai) announced a strategic collaboration for the worldwide co-development and co-commercialization of Lenvima (lenvatinib), an orally available tyrosine kinase inhibitor discovered by Eisai. Lenvima is currently approved for the treatment of certain types of thyroid cancer, hepatocellular carcinoma, in combination with everolimus for certain patients with renal cell carcinoma, and in combination with Keytruda for the treatment of certain patients with endometrial carcinoma. Under the agreement, Merck and Eisai will develop and commercialize Lenvima jointly, both as monotherapy and in combination with Keytruda . Eisai records Lenvima product sales globally (Eisai is the principal on Lenvima sales transactions), and Merck and Eisai share profits equally. Merck records its share of Lenvima product sales, net of cost of sales and commercialization costs, as alliance revenue. Expenses incurred during co-development, including for studies evaluating Lenvima as monotherapy, are shared equally by the two companies and reflected in Research and development expenses. Under the agreement, Merck made an upfront payment to Eisai of $750 million and agreed to make payments of up to $650 million for certain option rights through 2021 (of which $325 million was paid in March 2019, $200 million was paid in March 2020 and $125 million is expected to be paid in March 2021). In addition, the agreement provides for additional contingent payments from Merck to Eisai related to the successful achievement of sales-based and regulatory milestones. Prior to 2020, Merck accrued sales-based milestone payments aggregating $950 million related to Lenvima. Of these amounts, $50 million was paid to Eisai in 2019 and an additional $300 million was paid in the first quarter of 2020. Potential future sales-based milestone payments of $3.0 billion have not yet been accrued as they are not deemed by the Company to be probable at this time. In 2018, Lenvima received regulatory approvals triggering capitalized milestone payments of $250 million in the aggregate from Merck to Eisai. Potential future regulatory milestone payments of $135 million remain under the agreement. The intangible asset balance related to Lenvima (which includes capitalized sales-based and regulatory milestone payments) was $921 million at March 31, 2020 and is included in Other Intangibles, Net on the Consolidated Balance Sheet. The amount is being amortized over its estimated useful life through 2026 as supported by projected future cash flows, subject to impairment testing. Summarized financial information related to this collaboration is as follows: Three Months Ended ($ in millions) 2020 2019 Alliance revenue $ 128 $ 74 Cost of sales (1) 35 51 Selling, general and administrative 11 19 Research and development 64 47 ($ in millions) March 31, 2020 December 31, 2019 Receivables from Eisai included in Other current assets $ 140 $ 150 Payables to Eisai included in Accrued and other current liabilities (2) 425 700 Payables to Eisai included in Other Noncurrent Liabilities (3) 300 525 (1) Represents amortization of capitalized milestone payments. (2) Includes accrued milestone and future option payments. (3) Includes accrued milestone payments. Bayer AG In 2014, the Company entered into a worldwide clinical development collaboration with Bayer AG (Bayer) to market and develop soluble guanylate cyclase (sGC) modulators including Bayer’s Adempas (riociguat), which is approved to treat pulmonary arterial hypertension and chronic thromboembolic pulmonary hypertension. The two companies have implemented a joint development and commercialization strategy. The collaboration also includes clinical development of Bayer’s vericiguat, which is in development for the potential treatment of worsening heart failure. Under the agreement, Bayer leads commercialization of Adempas in the Americas, while Merck leads commercialization in the rest of the world. For vericiguat, if approved, Bayer will lead commercialization in the rest of world and Merck will lead in the Americas. Both companies share in development costs and profits on sales and have the right to co-promote in territories where they are not the lead. Merck records sales of Adempas in its marketing territories, as well as alliance revenue, which is Merck’s share of profits from the sale of Adempas in Bayer’s marketing territories. In addition, the agreement provides for additional contingent payments from Merck to Bayer related to the successful achievement of sales-based milestones. Prior to 2020, Merck accrued $725 million of sales-based milestone payments for this collaboration, of which $350 million was paid to Bayer in 2018. There is an additional $400 million potential future sales-based milestone payment that has not yet been accrued as it is not deemed by the Company to be probable at this time. The intangible asset balance related to this collaboration (which includes the acquired intangible asset balance, as well as capitalized sales-based milestone payments) was $844 million at March 31, 2020 and is included in Other Intangibles, Net on the Consolidated Balance Sheet. The amount is being amortized over its estimated useful life through 2027 as supported by projected future cash flows, subject to impairment testing. Summarized financial information related to this collaboration is as follows: Three Months Ended ($ in millions) 2020 2019 Net sales of Adempas recorded by Merck $ 56 $ 48 Alliance revenue 53 42 Total sales 109 90 Cost of sales (1) 28 29 Selling, general and administrative 15 8 Research and development 25 30 ($ in millions) March 31, 2020 December 31, 2019 Receivables from Bayer included in Other current assets $ 50 $ 49 Payables to Bayer included in Other Noncurrent Liabilities (2) 375 375 (1) Includes amortization of intangible assets. (2) Represents accrued milestone payment. |
Restructuring
Restructuring | 3 Months Ended |
Mar. 31, 2020 | |
Restructuring and Related Activities [Abstract] | |
Restructuring | Restructuring In early 2019, Merck approved a new global restructuring program (Restructuring Program) as part of a worldwide initiative focused on further optimizing the Company’s manufacturing and supply network, as well as reducing its global real estate footprint. This program is a continuation of the Company’s plant rationalization, builds on prior restructuring programs and does not include any actions associated with the planned spin-off of Organon. As the Company continues to evaluate its global footprint and overall operating model, it subsequently identified additional actions under the Restructuring Program, and could identify further actions over time. The actions currently contemplated under the Restructuring Program are expected to be substantially completed by the end of 2023, with the cumulative pretax costs to be incurred by the Company to implement the program estimated to be approximately $2.5 billion . The Company estimates that approximately 60% of the cumulative pretax costs will result in cash outlays, primarily related to employee separation expense and facility shut-down costs. Approximately 40% of the cumulative pretax costs will be non-cash, relating primarily to the accelerated depreciation of facilities to be closed or divested. The Company expects to record charges of approximately $800 million in 2020 related to the Restructuring Program. Actions under previous global restructuring programs have been substantially completed. The Company recorded total pretax costs of $168 million and $187 million in the first quarter of 2020 and 2019 , respectively, related to restructuring program activities. Since inception of the Restructuring Program through March 31, 2020 , Merck has recorded total pretax accumulated costs of approximately $1.1 billion . For segment reporting, restructuring charges are unallocated expenses. The following tables summarize the charges related to restructuring program activities by type of cost: Three Months Ended March 31, 2020 ($ in millions) Separation Costs Accelerated Depreciation Other Total Cost of sales $ — $ 25 $ 43 $ 68 Selling, general and administrative — 11 — 11 Research and development — 17 — 17 Restructuring costs 47 — 25 72 $ 47 $ 53 $ 68 $ 168 Three Months Ended March 31, 2019 ($ in millions) Separation Costs Accelerated Depreciation Other Total Cost of sales $ — $ 34 $ — $ 34 Restructuring costs 128 — 25 153 $ 128 $ 34 $ 25 $ 187 Separation costs are associated with actual headcount reductions, as well as those headcount reductions which were probable and could be reasonably estimated. Accelerated depreciation costs primarily relate to manufacturing, research and administrative facilities and equipment to be sold or closed as part of the programs. Accelerated depreciation costs represent the difference between the depreciation expense to be recognized over the revised useful life of the asset, based upon the anticipated date the site will be closed or divested or the equipment disposed of, and depreciation expense as determined utilizing the useful life prior to the restructuring actions. All the sites have and will continue to operate up through the respective closure dates and, since future undiscounted cash flows are sufficient to recover the respective book values, Merck is recording accelerated depreciation over the revised useful life of the site assets. Anticipated site closure dates, particularly related to manufacturing locations, have been and may continue to be adjusted to reflect changes resulting from regulatory or other factors. Other activity in 2020 and 2019 includes asset abandonment, facility shut-down and other related costs, as well as pretax gains and losses resulting from the sales of facilities and related assets. Additionally, other activity includes certain employee-related costs associated with pension and other postretirement benefit plans (see Note 10) and share-based compensation. The following table summarizes the charges and spending relating to restructuring program activities for the three months ended March 31, 2020 : ($ in millions) Separation Costs Accelerated Depreciation Other Total Restructuring reserves January 1, 2020 $ 690 $ — $ 69 $ 759 Expense 47 53 68 168 (Payments) receipts, net (168 ) — (122 ) (290 ) Non-cash activity — (53 ) 42 (11 ) Restructuring reserves March 31, 2020 (1) $ 569 $ — $ 57 $ 626 (1) |
Financial Instruments
Financial Instruments | 3 Months Ended |
Mar. 31, 2020 | |
Derivative Instruments and Hedging Activities Disclosure [Abstract] | |
Financial Instruments | Financial Instruments Derivative Instruments and Hedging Activities The Company manages the impact of foreign exchange rate movements and interest rate movements on its earnings, cash flows and fair values of assets and liabilities through operational means and through the use of various financial instruments, including derivative instruments. A significant portion of the Company’s revenues and earnings in foreign affiliates is exposed to changes in foreign exchange rates. The objectives and accounting related to the Company’s foreign currency risk management program, as well as its interest rate risk management activities are discussed below. Foreign Currency Risk Management The Company has established revenue hedging, balance sheet risk management and net investment hedging programs to protect against volatility of future foreign currency cash flows and changes in fair value caused by changes in foreign exchange rates. The objective of the revenue hedging program is to reduce the variability caused by changes in foreign exchange rates that would affect the U.S. dollar value of future cash flows derived from foreign currency denominated sales, primarily the euro, Japanese yen and Chinese renminbi. To achieve this objective, the Company will hedge a portion of its forecasted foreign currency denominated third-party and intercompany distributor entity sales (forecasted sales) that are expected to occur over its planning cycle, typically no more than two years into the future. The Company will layer in hedges over time, increasing the portion of forecasted sales hedged as it gets closer to the expected date of the forecasted sales. The portion of forecasted sales hedged is based on assessments of cost-benefit profiles that consider natural offsetting exposures, revenue and exchange rate volatilities and correlations, and the cost of hedging instruments. The Company manages its anticipated transaction exposure principally with purchased local currency put options, forward contracts and purchased collar options. The fair values of these derivative contracts are recorded as either assets (gain positions) or liabilities (loss positions) in the Condensed Consolidated Balance Sheet. Changes in the fair value of derivative contracts are recorded each period in either current earnings or Other comprehensive income ( OCI ), depending on whether the derivative is designated as part of a hedge transaction and, if so, the type of hedge transaction. For derivatives that are designated as cash flow hedges, the unrealized gains or losses on these contracts are recorded in Accumulated other comprehensive income ( AOCI ) and reclassified into Sales when the hedged anticipated revenue is recognized. For those derivatives which are not designated as cash flow hedges, but serve as economic hedges of forecasted sales, unrealized gains or losses are recorded in Sales each period. The cash flows from both designated and non-designated contracts are reported as operating activities in the Condensed Consolidated Statement of Cash Flows. The Company does not enter into derivatives for trading or speculative purposes. The Company manages operating activities and net asset positions at each local subsidiary in order to mitigate the effects of exchange on monetary assets and liabilities. The Company also uses a balance sheet risk management program to mitigate the exposure of net monetary assets that are denominated in a currency other than a subsidiary’s functional currency from the effects of volatility in foreign exchange. In these instances, Merck principally utilizes forward exchange contracts to offset the effects of exchange on exposures denominated in developed country currencies, primarily the euro and Japanese yen. For exposures in developing country currencies, the Company will enter into forward contracts to partially offset the effects of exchange on exposures when it is deemed economical to do so based on a cost-benefit analysis that considers the magnitude of the exposure, the volatility of the exchange rate and the cost of the hedging instrument. The cash flows from these contracts are reported as operating activities in the Condensed Consolidated Statement of Cash Flows. Monetary assets and liabilities denominated in a currency other than the functional currency of a given subsidiary are remeasured at spot rates in effect on the balance sheet date with the effects of changes in spot rates reported in Other (income) expense, net . The forward contracts are not designated as hedges and are marked to market through Other (income) expense, net . Accordingly, fair value changes in the forward contracts help mitigate the changes in the value of the remeasured assets and liabilities attributable to changes in foreign currency exchange rates, except to the extent of the spot-forward differences. These differences are not significant due to the short-term nature of the contracts, which typically have average maturities at inception of less than one year . The Company also uses forward exchange contracts to hedge a portion of its net investment in foreign operations against movements in exchange rates. The forward contracts are designated as hedges of the net investment in a foreign operation. The unrealized gains or losses on these contracts are recorded in foreign currency translation adjustment within OCI and remain in AOCI until either the sale or complete or substantially complete liquidation of the subsidiary. The Company excludes certain portions of the change in fair value of its derivative instruments from the assessment of hedge effectiveness (excluded component). Changes in fair value of the excluded components are recognized in OCI . The Company recognizes in earnings the initial value of the excluded component on a straight-line basis over the life of the derivative instrument, rather than using the mark-to-market approach. The cash flows from these contracts are reported as investing activities in the Condensed Consolidated Statement of Cash Flows. Foreign exchange risk is also managed through the use of foreign currency debt. The Company’s senior unsecured euro-denominated notes have been designated as, and are effective as, economic hedges of the net investment in a foreign operation. Accordingly, foreign currency transaction gains or losses due to spot rate fluctuations on the euro-denominated debt instruments are included in foreign currency translation adjustment within OCI . The effects of the Company’s net investment hedges on OCI and the Consolidated Statement of Income are shown below: Amount of Pretax (Gain) Loss Recognized in Other Comprehensive Income (1) Amount of Pretax (Gain) Loss Recognized in Other (income) expense, net for Amounts Excluded from Effectiveness Testing Three Months Ended March 31, Three Months Ended March 31, ($ in millions) 2020 2019 2020 2019 Net Investment Hedging Relationships Foreign exchange contracts $ (3 ) $ (11 ) $ (8 ) $ (8 ) Euro-denominated notes (51 ) (30 ) — — (1) No amounts were reclassified from AOCI into income related to the sale of a subsidiary. Interest Rate Risk Management The Company may use interest rate swap contracts on certain investing and borrowing transactions to manage its net exposure to interest rate changes and to reduce its overall cost of borrowing. The Company does not use leveraged swaps and, in general, does not leverage any of its investment activities that would put principal capital at risk. In February 2020, five interest rate swaps with notional amounts of $250 million each matured. These swaps effectively converted the Company’s $1.25 billion , 1.85% fixed-rate notes due 2020 to variable rate debt. At March 31, 2020 , the Company was a party to 14 pay-floating, receive-fixed interest rate swap contracts designated as fair value hedges of fixed-rate notes in which the notional amounts match the amount of the hedged fixed-rate notes as detailed in the table below. March 31, 2020 ($ in millions) Par Value of Debt Number of Interest Rate Swaps Held Total Swap Notional Amount 3.875% notes due 2021 $ 1,150 5 $ 1,150 2.40% notes due 2022 1,000 4 1,000 2.35% notes due 2022 1,250 5 1,250 The interest rate swap contracts are designated hedges of the fair value changes in the notes attributable to changes in the benchmark London Interbank Offered Rate (LIBOR) swap rate. The fair value changes in the notes attributable to changes in the LIBOR swap rate are recorded in interest expense along with the offsetting fair value changes in the swap contracts. The cash flows from these contracts are reported as operating activities in the Condensed Consolidated Statement of Cash Flows. The table below presents the location of amounts recorded on the Consolidated Balance Sheet related to cumulative basis adjustments for fair value hedges: Carrying Amount of Hedged Liabilities Cumulative Amount of Fair Value Hedging Adjustment Increase (Decrease) Included in the Carrying Amount ($ in millions) March 31, 2020 December 31, 2019 March 31, 2020 December 31, 2019 Balance Sheet Line Item in which Hedged Item is Included Loans payable and current portion of long-term debt $ 1,160 $ 1,249 $ 11 $ (1 ) Long-Term Debt 2,315 3,409 69 14 Presented in the table below is the fair value of derivatives on a gross basis segregated between those derivatives that are designated as hedging instruments and those that are not designated as hedging instruments: March 31, 2020 December 31, 2019 Fair Value of Derivative U.S. Dollar Notional Fair Value of Derivative U.S. Dollar Notional ($ in millions) Balance Sheet Caption Asset Liability Asset Liability Derivatives Designated as Hedging Instruments Interest rate swap contracts Other current assets $ 11 $ — $ 1,150 $ — $ — $ — Interest rate swap contracts Other Assets 70 — 2,250 15 — 3,400 Interest rate swap contracts Accrued and other current liabilities — — — — 1 1,250 Foreign exchange contracts Other current assets 194 — 6,546 152 — 6,117 Foreign exchange contracts Other Assets 88 — 2,064 55 — 2,160 Foreign exchange contracts Accrued and other current liabilities — 7 734 — 22 1,748 Foreign exchange contracts Other Noncurrent Liabilities — 1 5 — 1 53 $ 363 $ 8 $ 12,749 $ 222 $ 24 $ 14,728 Derivatives Not Designated as Hedging Instruments Foreign exchange contracts Other current assets $ 347 $ — $ 10,039 $ 66 $ — $ 7,245 Foreign exchange contracts Accrued and other current liabilities — 85 4,665 — 73 8,693 $ 347 $ 85 $ 14,704 $ 66 $ 73 $ 15,938 $ 710 $ 93 $ 27,453 $ 288 $ 97 $ 30,666 As noted above, the Company records its derivatives on a gross basis in the Condensed Consolidated Balance Sheet. The Company has master netting agreements with several of its financial institution counterparties (see Concentrations of Credit Risk below). The following table provides information on the Company’s derivative positions subject to these master netting arrangements as if they were presented on a net basis, allowing for the right of offset by counterparty and cash collateral exchanged per the master agreements and related credit support annexes: March 31, 2020 December 31, 2019 ($ in millions) Asset Liability Asset Liability Gross amounts recognized in the condensed consolidated balance sheet $ 710 $ 93 $ 288 $ 97 Gross amounts subject to offset in master netting arrangements not offset in the condensed consolidated balance sheet (89 ) (89 ) (84 ) (84 ) Cash collateral received (216 ) — (34 ) — Net amounts $ 405 $ 4 $ 170 $ 13 The table below provides information regarding the location and amount of pretax (gains) losses of derivatives designated in fair value or cash flow hedging relationships: Sales Other (income) expense, net (1) Other comprehensive income (loss) Three Months Ended March 31, Three Months Ended March 31, Three Months Ended March 31, ($ in millions) 2020 2019 2020 2019 2020 2019 Financial Statement Line Items in which Effects of Fair Value or Cash Flow Hedges are Recorded $ 12,057 $ 10,816 $ 71 $ 188 $ (198 ) $ 199 (Gain) loss on fair value hedging relationships Interest rate swap contracts Hedged items — — 67 33 — — Derivatives designated as hedging instruments — — (67 ) (23 ) — — Impact of cash flow hedging relationships Foreign exchange contracts Amount of gain (loss) recognized in OCI on derivatives — — — — 178 (13 ) Increase (decrease) in Sales as a result of AOCI reclassifications 46 44 — — (46 ) (44 ) Interest rate contracts Amount of gain recognized in Other (income) expense, net on derivatives — — (1 ) (1 ) — — Amount of loss recognized in OCI on derivatives — — — — (1 ) (4 ) (1) Interest expense is a component of Other (income) expense, net. The table below provides information regarding the income statement effects of derivatives not designated as hedging instruments: Amount of Derivative Pretax (Gain) Loss Recognized in Income Three Months Ended March 31, ($ in millions) Income Statement Caption 2020 2019 Derivatives Not Designated as Hedging Instruments Foreign exchange contracts (1) Other (income) expense, net $ (180 ) $ 118 Foreign exchange contracts (2) Sales (7 ) 10 (1) These derivative contracts mitigate changes in the value of remeasured foreign currency denominated monetary assets and liabilities attributable to changes in foreign currency exchange rates. (2) These derivative contracts serve as economic hedges of forecasted transactions. At March 31, 2020 , the Company estimates $136 million of pretax net unrealized gains on derivatives maturing within the next 12 months that hedge foreign currency denominated sales over that same period will be reclassified from AOCI to Sales . The amount ultimately reclassified to Sales may differ as foreign exchange rates change. Realized gains and losses are ultimately determined by actual exchange rates at maturity. Investments in Debt and Equity Securities Information on investments in debt and equity securities is as follows: March 31, 2020 December 31, 2019 Amortized Cost Gross Unrealized Fair Value Amortized Cost Gross Unrealized Fair Value ($ in millions) Gains Losses Gains Losses U.S. government and agency securities $ 62 $ — $ — $ 62 $ 266 $ 3 $ — $ 269 Foreign government bonds 2 — — 2 — — — — Commercial paper — — — — 668 — — 668 Corporate notes and bonds — — — — 608 13 — 621 Asset-backed securities — — — — 226 1 — 227 Total debt securities $ 64 $ — $ — $ 64 $ 1,768 $ 17 $ — $ 1,785 Publicly traded equity securities (1) 779 838 Total debt and publicly traded equity securities $ 843 $ 2,623 (1) Unrealized net losses recognized in Other (income) expense, net on equity securities still held at March 31, 2020 were $4 million in the first quarter of 2020 . Unrealized net gains recognized in Other (income) expense, net on equity securities still held at March 31, 2019 were $114 million in the first quarter of 2019 . At March 31, 2020 and March 31, 2019 , the Company also had $450 million and $542 million , respectively, of equity investments without readily determinable fair values included in Other Assets . During the first three months of 2019 , the Company recognized unrealized losses of $9 million in Other (income) expense, net related to certain of these investments held at March 31, 2019 based on unfavorable observable price changes. Cumulative unrealized gains and cumulative unrealized losses based on observable prices changes for investments in equity investments without readily determinable fair values still held at March 31, 2020 were $109 million and $21 million , respectively. Fair Value Measurements Fair value is defined as the exchange price that would be received for an asset or paid to transfer a liability (an exit price) in the principal or most advantageous market for the asset or liability in an orderly transaction between market participants on the measurement date. The Company uses a fair value hierarchy which maximizes the use of observable inputs and minimizes the use of unobservable inputs when measuring fair value. There are three levels of inputs used to measure fair value with Level 1 having the highest priority and Level 3 having the lowest: Level 1 - Quoted prices (unadjusted) in active markets for identical assets or liabilities, Level 2 - Observable inputs other than Level 1 prices, such as quoted prices for similar assets or liabilities, or other inputs that are observable or can be corroborated by observable market data for substantially the full term of the assets or liabilities, Level 3 - Unobservable inputs that are supported by little or no market activity. Level 3 assets or liabilities are those whose values are determined using pricing models, discounted cash flow methodologies, or similar techniques with significant unobservable inputs, as well as assets or liabilities for which the determination of fair value requires significant judgment or estimation. If the inputs used to measure the financial assets and liabilities fall within more than one level described above, the categorization is based on the lowest level input that is significant to the fair value measurement of the instrument. Financial Assets and Liabilities Measured at Fair Value on a Recurring Basis Financial assets and liabilities measured at fair value on a recurring basis are summarized below: Fair Value Measurements Using Fair Value Measurements Using Level 1 Level 2 Level 3 Total Level 1 Level 2 Level 3 Total ($ in millions) March 31, 2020 December 31, 2019 Assets Investments Foreign government bonds $ — $ 2 $ — $ 2 $ — $ — $ — $ — Commercial paper — — — — — 668 — 668 Corporate notes and bonds — — — — — 621 — 621 Asset-backed securities (1) — — — — — 227 — 227 U.S. government and agency securities — — — — — 209 — 209 Publicly traded equity securities 560 — — 560 518 — — 518 560 2 — 562 518 1,725 — 2,243 Other assets (2) U.S. government and agency securities 62 — — 62 60 — — 60 Publicly traded equity securities 219 — — 219 320 — — 320 281 — — 281 380 — — 380 Derivative assets (3) Forward exchange contracts — 455 — 455 — 169 — 169 Purchased currency options — 174 — 174 — 104 — 104 Interest rate swaps — 81 — 81 — 15 — 15 — 710 — 710 — 288 — 288 Total assets $ 841 $ 712 $ — $ 1,553 $ 898 $ 2,013 $ — $ 2,911 Liabilities Other liabilities Contingent consideration $ — $ — $ 694 $ 694 $ — $ — $ 767 $ 767 Derivative liabilities (3) Forward exchange contracts — 90 — 90 — 95 — 95 Written currency options — 3 — 3 — 1 — 1 Interest rate swaps — — — — — 1 — 1 — 93 — 93 — 97 — 97 Total liabilities $ — $ 93 $ 694 $ 787 $ — $ 97 $ 767 $ 864 (1) Primarily all of the asset-backed securities were highly-rated (Standard & Poor’s rating of AAA and Moody’s Investors Service rating of Aaa), secured primarily by auto loan, credit card and student loan receivables, with weighted-average lives of primarily 5 years or less. (2) Investments included in other assets are restricted as to use, including for the payment of benefits under employee benefit plans. (3) The fair value determination of derivatives includes the impact of the credit risk of counterparties to the derivatives and the Company’s own credit risk, the effects of which were not significant. As of March 31, 2020 and December 31, 2019 , Cash and cash equivalents included $6.8 billion and $8.9 billion of cash equivalents, respectively (which would be considered Level 2 in the fair value hierarchy). Contingent Consideration Summarized information about the changes in liabilities for contingent consideration associated with business acquisitions is as follows: Three Months Ended March 31, ($ in millions) 2020 2019 Fair value January 1 $ 767 $ 788 Changes in estimated fair value (1) 33 (36 ) Payments (106 ) (85 ) Fair value March 31 (2)(3) $ 694 $ 667 (1) Recorded in Cost of sales, Research and development expenses, and Other (income) expense, net . Includes cumulative translation adjustments. (2) Balance at March 31, 2020 includes $119 million recorded as a current liability for amounts expected to be paid within the next 12 months. (3) At March 31, 2020 and December 31, 2019 , $520 million and $625 million , respectively, of the liabilities relate to the termination of the Sanofi-Pasteur MSD joint venture in 2016. As part of the termination, Merck recorded a liability for contingent future royalty payments of 11.5% on net sales of all Merck products that were previously sold by the joint venture through December 31, 2024. The fair value of this liability is determined utilizing the estimated amount and timing of projected cash flows using a risk-adjusted discount rate of 8% to present value the cash flows. The increase in the estimated fair value of liabilities for contingent consideration in the first quarter of 2020 primarily relates to MK-7264 (gefapixant), a program obtained in connection with the acquisition of Afferent Pharmaceuticals, following the conclusion of Phase 3 studies evaluating gefapixant for the treatment of chronic cough. The decline in the estimated fair value of liabilities for contingent consideration in the first quarter of 2019 primarily relates to a decision not to pursue an acute cough indication for gefapixant. The payments of contingent consideration in both periods relate to liabilities recorded in connection with the termination of the Sanofi-Pasteur MSD joint venture in 2016. Other Fair Value Measurements Some of the Company’s financial instruments, such as cash and cash equivalents, receivables and payables, are reflected in the balance sheet at carrying value, which approximates fair value due to their short-term nature. The estimated fair value of loans payable and long-term debt (including current portion) at March 31, 2020 , was $30.6 billion compared with a carrying value of $28.0 billion and at December 31, 2019 , was $28.8 billion compared with a carrying value of $26.3 billion . Fair value was estimated using recent observable market prices and would be considered Level 2 in the fair value hierarchy. Concentrations of Credit Risk On an ongoing basis, the Company monitors concentrations of credit risk associated with corporate and government issuers of securities and financial institutions with which it conducts business. Credit exposure limits are established to limit a concentration with any single issuer or institution. Cash and investments are placed in instruments that meet high credit quality standards as specified in the Company’s investment policy guidelines. The majority of the Company’s accounts receivable arise from product sales in the United States, Europe and China and are primarily due from drug wholesalers and retailers, hospitals, government agencies, managed health care providers and pharmacy benefit managers. The Company monitors the financial performance and creditworthiness of its customers so that it can properly assess and respond to changes in their credit profile. The Company also continues to monitor global economic conditions, including the volatility associated with international sovereign economies, and associated impacts on the financial markets and its business. The Company has accounts receivable factoring agreements with financial institutions in certain countries to sell accounts receivable. The Company factored $1.9 billion and $2.7 billion of accounts receivable in the first quarter of 2020 and the fourth quarter of 2019 , respectively, under these factoring arrangements, which reduced outstanding accounts receivable. The cash received from the financial institutions is reported within operating activities in the Consolidated Statement of Cash Flows. In certain of these factoring arrangements, for ease of administration, the Company will collect customer payments related to the factored receivables, which it then remits to the financial institutions. The net cash flows relating to these collections are reported as financing activities in the Consolidated Statement of Cash Flows. The cost of factoring such accounts receivable was de minimis . Derivative financial instruments are executed under International Swaps and Derivatives Association master agreements. The master agreements with several of the Company’s financial institution counterparties also include credit support annexes. These annexes contain provisions that require collateral to be exchanged depending on the value of the derivative assets and liabilities, the Company’s credit rating, and the credit rating of the counterparty. Cash collateral received by the Company from various counterparties was $216 million and $34 million at March 31, 2020 and December 31, 2019 , respectively. The obligation to return such collateral is recorded in Accrued and other current liabilities . No cash collateral was advanced by the Company to counterparties as of March 31, 2020 or December 31, 2019 . |
Inventories
Inventories | 3 Months Ended |
Mar. 31, 2020 | |
Inventory Disclosure [Abstract] | |
Inventories | Inventories Inventories consisted of: ($ in millions) March 31, 2020 December 31, 2019 Finished goods $ 1,753 $ 1,772 Raw materials and work in process 5,629 5,650 Supplies 232 207 Total (approximates current cost) 7,614 7,629 Decrease to LIFO cost (138 ) (171 ) $ 7,476 $ 7,458 Recognized as: Inventories $ 5,846 $ 5,978 Other assets 1,630 1,480 Amounts recognized as Other Assets are comprised almost entirely of raw materials and work in process inventories. At March 31, 2020 and December 31, 2019 , these amounts included $1.4 billion and $1.3 billion , respectively, of inventories not expected to be sold within one year. In addition, these amounts included $258 million and $168 million at March 31, 2020 and December 31, 2019 , respectively, of inventories produced in preparation for product launches. |
Contingencies
Contingencies | 3 Months Ended |
Mar. 31, 2020 | |
Commitments and Contingencies Disclosure [Abstract] | |
Contingencies | Contingencies The Company is involved in various claims and legal proceedings of a nature considered normal to its business, including product liability, intellectual property, and commercial litigation, as well as certain additional matters including governmental and environmental matters. In the opinion of the Company, it is unlikely that the resolution of these matters will be material to the Company’s financial condition, results of operations or cash flows. Given the nature of the litigation discussed below and the complexities involved in these matters, the Company is unable to reasonably estimate a possible loss or range of possible loss for such matters until the Company knows, among other factors, (i) what claims, if any, will survive dispositive motion practice, (ii) the extent of the claims, including the size of any potential class, particularly when damages are not specified or are indeterminate, (iii) how the discovery process will affect the litigation, (iv) the settlement posture of the other parties to the litigation and (v) any other factors that may have a material effect on the litigation. The Company records accruals for contingencies when it is probable that a liability has been incurred and the amount can be reasonably estimated. These accruals are adjusted periodically as assessments change or additional information becomes available. For product liability claims, a portion of the overall accrual is actuarially determined and considers such factors as past experience, number of claims reported and estimates of claims incurred but not yet reported. Individually significant contingent losses are accrued when probable and reasonably estimable. Legal defense costs expected to be incurred in connection with a loss contingency are accrued when probable and reasonably estimable. The Company’s decision to obtain insurance coverage is dependent on market conditions, including cost and availability, existing at the time such decisions are made. The Company has evaluated its risks and has determined that the cost of obtaining product liability insurance outweighs the likely benefits of the coverage that is available and, as such, has no insurance for most product liabilities. Product Liability Litigation Fosamax As previously disclosed, Merck is a defendant in product liability lawsuits in the United States involving Fosamax ( Fosamax Litigation). As of March 31, 2020 , approximately 3,590 cases are pending against Merck in either federal or state court. Plaintiffs in the vast majority of these cases generally allege that they sustained femur fractures and/or other bone injuries (Femur Fractures) in association with the use of Fosamax . All federal cases involving allegations of Femur Fractures have been or will be transferred to a multidistrict litigation in the District of New Jersey (Femur Fracture MDL). In the only bellwether case tried to date in the Femur Fracture MDL, Glynn v. Merck , the jury returned a verdict in Merck’s favor. In addition, in June 2013, the Femur Fracture MDL court granted Merck’s motion for judgment as a matter of law in the Glynn case and held that the plaintiff’s failure to warn claim was preempted by federal law. In August 2013, the Femur Fracture MDL court entered an order requiring plaintiffs in the Femur Fracture MDL to show cause why those cases asserting claims for a femur fracture injury that took place prior to September 14, 2010, should not be dismissed based on the court’s preemption decision in the Glynn case. Pursuant to the show cause order, in March 2014, the Femur Fracture MDL court dismissed with prejudice approximately 650 cases on preemption grounds. Plaintiffs in approximately 515 of those cases appealed that decision to the U.S. Court of Appeals for the Third Circuit (Third Circuit). In March 2017, the Third Circuit issued a decision reversing the Femur Fracture MDL court’s preemption ruling and remanding the appealed cases back to the Femur Fracture MDL court. In May 2019, the U.S. Supreme Court decided that the Third Circuit had incorrectly concluded that the issue of preemption should be resolved by a jury, and accordingly vacated the judgment of the Third Circuit and remanded the proceedings back to the Third Circuit to address the issue in a manner consistent with the Supreme Court’s opinion. In November 2019, the Third Circuit remanded the cases back to the District Court in order to allow that court to determine in the first instance whether the plaintiffs’ state law claims are preempted by federal law under the standards described by the Supreme Court in its opinion. Merck filed its initial brief on February 21, 2020, as required by the District Court. Accordingly, as of March 31, 2020 , approximately 970 cases were actively pending in the Femur Fracture MDL. As of March 31, 2020 , approximately 2,345 cases alleging Femur Fractures have been filed in New Jersey state court and are pending before Judge James Hyland in Middlesex County. The parties selected an initial group of cases to be reviewed through fact discovery, and Merck has continued to select additional cases to be reviewed. As of March 31, 2020 , approximately 275 cases alleging Femur Fractures have been filed and are pending in California state court. All of the Femur Fracture cases filed in California state court have been coordinated before a single judge in Orange County, California. Additionally, there are four Femur Fracture cases pending in other state courts. Discovery is presently stayed in the Femur Fracture MDL and in the state court in California. Merck intends to defend against these lawsuits. Januvia/Janumet As previously disclosed, Merck is a defendant in product liability lawsuits in the United States involving Januvia and/or Janumet . As of March 31, 2020 , Merck is aware of approximately 1,410 product users alleging that Januvia and/or Janumet caused the development of pancreatic cancer and other injuries. Most claims have been filed in multidistrict litigation before the U.S. District Court for the Southern District of California (MDL). Outside of the MDL, the majority of claims have been filed in coordinated proceedings before the Superior Court of California, County of Los Angeles (California State Court). In November 2015, the MDL and California State Court–in separate opinions–granted summary judgment to defendants on grounds of federal preemption. Plaintiffs appealed in both forums. In November 2017, the U.S. Court of Appeals for the Ninth Circuit vacated the judgment and remanded for further discovery. In November 2018, the California state appellate court reversed and remanded on similar grounds. In March 2019, the parties in the MDL and the California coordinated proceeding agreed to coordinate and adopt a schedule for completing discovery on general causation and preemption issues and for renewing summary judgment and Daubert motions. Under the stipulated case management schedule, the hearings for Daubert and summary judgment motions are expected to take place in the second half of 2020. As of March 31, 2020 , six product users have claims pending against Merck in state courts other than California, including Illinois. In June 2017, the Illinois trial court denied Merck’s motion for summary judgment based on federal preemption. Merck appealed, and the Illinois appellate court affirmed in December 2018. Merck filed a petition for leave to appeal to the Illinois Supreme Court in February 2019. In April 2019, the Illinois Supreme Court stayed consideration of the pending petition to appeal until the U.S. Supreme Court issued its opinion in Merck Sharp & Dohme Corp. v. Albrecht (relating to the Fosamax matter discussed above). Merck filed the opinion in Albrecht with the Illinois Supreme Court in June 2019. The petition for leave to appeal was decided in September 2019, in which the Illinois Supreme Court directed the intermediate appellate court to reconsider its earlier ruling. The Illinois Appellate Court issued a favorable decision concluding, consistent with Albrecht , that preemption presents a legal question to be resolved by the court. In addition to the claims noted above, the Company has agreed to toll the statute of limitations for approximately 50 additional claims. The Company intends to continue defending against these lawsuits. Vioxx As previously disclosed, Merck is a defendant in a lawsuit brought by the Attorney General of Utah alleging that Merck misrepresented the safety of Vioxx . The lawsuit is pending in Utah state court. Utah seeks damages and penalties under the Utah False Claims Act. A bench trial in this matter has been rescheduled for April 6, 2021. Governmental Proceedings As previously disclosed, in April 2019, Merck received a set of investigative interrogatories from the California Attorney General’s Office pursuant to its investigation of conduct and agreements that allegedly affected or delayed competition to Lantus in the insulin market. The interrogatories seek information concerning Merck’s development of an insulin glargine product, and its subsequent termination, as well as Merck’s patent litigation against Sanofi S.A. concerning Lantus and the resolution of that litigation. In February 2020, Merck received a subpoena for documents. Merck is cooperating with the California Attorney General’s investigation. As previously disclosed, the Company’s subsidiaries in China have received and may continue to receive inquiries regarding their operations from various Chinese governmental agencies. Some of these inquiries may be related to matters involving other multinational pharmaceutical companies, as well as Chinese entities doing business with such companies. The Company’s policy is to cooperate with these authorities and to provide responses as appropriate. As previously disclosed, from time to time, the Company receives inquiries and is the subject of preliminary investigation activities from competition and other governmental authorities in markets outside the United States. These authorities may include regulators, administrative authorities, and law enforcement and other similar officials, and these preliminary investigation activities may include site visits, formal or informal requests or demands for documents or materials, inquiries or interviews and similar matters. Certain of these preliminary inquiries or activities may lead to the commencement of formal proceedings. Should those proceedings be determined adversely to the Company, monetary fines and/or remedial undertakings may be required. Commercial and Other Litigation Zetia Antitrust Litigation As previously disclosed, Merck, MSD, Schering Corporation and MSP Singapore Company LLC (collectively, the Merck Defendants) are defendants in putative class action and opt-out lawsuits filed in 2018 on behalf of direct and indirect purchasers of Zetia alleging violations of federal and state antitrust laws, as well as other state statutory and common law causes of action. The cases have been consolidated for pretrial purposes in a federal multidistrict litigation before Judge Rebecca Beach Smith in the Eastern District of Virginia. In December 2018, the court denied the Merck Defendants’ motions to dismiss or stay the direct purchaser putative class actions pending bilateral arbitration. In August 2019, the district court adopted in full the report and recommendation of the magistrate judge with respect to the Merck Defendants’ motions to dismiss on non-arbitration issues, thereby granting in part and denying in part Merck Defendants’ motions to dismiss. In addition, in June 2019, the representatives of the putative direct purchaser class filed an amended complaint, and in August 2019, retailer opt-out plaintiffs filed an amended complaint. The Merck Defendants moved to dismiss the new allegations in both complaints. In October 2019, the magistrate judge issued a report and recommendation recommending that the district judge grant the motions in their entirety. In December 2019, the district court adopted this report and recommendation in part. The district court granted the Merck Defendants’ motion to dismiss to the extent the motion sought dismissal of claims for overcharges paid by entities that purchased generic ezetimibe from Par Pharmaceutical, Inc. (Par Pharmaceutical) and dismissed any claims for such overcharges. Trial in this matter has been rescheduled to begin on February 23, 2021. Bravecto Litigation In January 2020, the Company was served with a complaint in the United States District Court for the District of New Jersey, seeking to certify a nationwide class action of purchasers or users of Bravecto (fluralaner) products in the United States or its territories between May 1, 2014 and December 27, 2019. The complaint contends Bravecto causes neurological events and alleges violations of the New Jersey Consumer Fraud Act, Breach of Warranty, Product Liability, and related theories. A similar case was filed in Quebec, Canada in May 2019. Patent Litigation From time to time, generic manufacturers of pharmaceutical products file abbreviated New Drug Applications (NDAs) with the U.S. Food and Drug Administration (FDA) seeking to market generic forms of the Company’s products prior to the expiration of relevant patents owned by the Company. To protect its patent rights, the Company may file patent infringement lawsuits against such generic companies. Similar lawsuits defending the Company’s patent rights may exist in other countries. The Company intends to vigorously defend its patents, which it believes are valid, against infringement by companies attempting to market products prior to the expiration of such patents. As with any litigation, there can be no assurance of the outcomes, which, if adverse, could result in significantly shortened periods of exclusivity for these products and, with respect to products acquired through acquisitions, potentially significant intangible asset impairment charges. Bridion — Between January and March 2020, the Company received multiple Paragraph IV Certification Letters under the Hatch-Waxman Act notifying the Company that generic drug companies have filed applications to the FDA seeking pre-patent expiry approval to sell generic versions of Bridion (sugammadex) Injection. In March and April 2020, the Company filed patent infringement lawsuits in the U.S. District Courts for the District of New Jersey and the Northern District of West Virginia against those generic companies. These lawsuits, which assert one or more patents covering sugammadex and methods of using sugammadex, automatically stay FDA approval of the generic applications until June 2023 or until adverse court decisions, if any, whichever may occur earlier. No schedule for the cases has been set by the courts. Januvia, Janumet, Janumet XR — In February 2019, Par Pharmaceutical filed suit against the Company in the U.S. District Court for the District of New Jersey, seeking a declaratory judgment of invalidity of a patent owned by the Company covering certain salt and polymorphic forms of sitagliptin that expires in 2026. In response, the Company filed a patent infringement lawsuit in the U.S. District Court for the District of Delaware against Par Pharmaceutical and additional companies that also indicated an intent to market generic versions of Januvia , Janumet , and Janumet XR following expiration of key patent protection in 2022, but prior to the expiration of the later-granted patent owned by the Company covering certain salt and polymorphic forms of sitagliptin that expires in 2026, and a later granted patent owned by the Company covering the Janumet formulation which expires in 2028. Par Pharmaceutical dismissed its case in the U.S. District Court for the District of New Jersey against the Company and will litigate the action in the U.S. District Court for the District of Delaware. The Company filed a patent infringement lawsuit against Mylan Pharmaceuticals Inc. and Mylan Inc. (Mylan) in the Northern District of West Virginia. The Judicial Panel of Multidistrict Litigation entered an order transferring the Company’s lawsuit against Mylan to the U.S. District Court for the District of Delaware for coordinated and consolidated pretrial proceedings with the other cases pending in that district. In February 2020, the Company amended its complaint against one defendant, Teva Pharmaceuticals USA, Inc., to add patent infringement claims related to a patent that expires in 2025 and covers certain processes for manufacturing sitagliptin. The U.S. District Court for the District of Delaware has scheduled the lawsuits for a single 3-day trial on invalidity issues in October 2021. The Court will schedule separate 1-day trials on infringement issues if necessary. In the Company’s case against Mylan, the U.S. District Court for the Northern District of West Virginia has conditionally scheduled a three-day trial in December 2021 on all issues. The Company has settled with three generic companies such that these generic companies can bring their products to the market in November 2026 or earlier under certain circumstances. In October 2019, Mylan filed a petition for Inter Partes Review (IPR) at the United States Patent and Trademark Office (USPTO) seeking invalidity of the 2026 patent. The Company filed a Patent Owner Preliminary Response in the IPR proceeding in February 2020. The Company expects the USPTO to determine whether it will institute the IPR proceeding in May 2020. In Germany, a generic company has sought the revocation of the Supplementary Protection Certificate (SPC) for Janumet . If the generic company is successful, Janumet could lose market exclusivity in Germany as early as July 2022. It is possible that challenges to the Janumet SPC could occur in other European countries. Other Litigation There are various other pending legal proceedings involving the Company, principally product liability and intellectual property lawsuits. While it is not feasible to predict the outcome of such proceedings, in the opinion of the Company, either the likelihood of loss is remote or any reasonably possible loss associated with the resolution of such proceedings is not expected to be material to the Company’s financial condition, results of operations or cash flows either individually or in the aggregate. Legal Defense Reserves Legal defense costs expected to be incurred in connection with a loss contingency are accrued when probable and reasonably estimable. Some of the significant factors considered in the review of these legal defense reserves are as follows: the actual costs incurred by the Company; the development of the Company’s legal defense strategy and structure in light of the scope of its litigation; the number of cases being brought against the Company; the costs and outcomes of completed trials and the most current information regarding anticipated timing, progression, and related costs of pre-trial activities and trials in the associated litigation. The amount of legal defense reserves as of March 31, 2020 and December 31, 2019 of approximately $255 million and $240 million , respectively, represents the Company’s best estimate of the minimum amount of defense costs to be incurred in connection with its outstanding litigation; however, events such as additional trials and other events that could arise in the course of its litigation could affect the ultimate amount of legal defense costs to be incurred by the Company. The Company will continue to monitor its legal defense costs and review the adequacy of the associated reserves and may determine to increase the reserves at any time in the future if, based upon the factors set forth, it believes it would be appropriate to do so. |
Equity
Equity | 3 Months Ended |
Mar. 31, 2020 | |
Equity [Abstract] | |
Equity | Equity Three Months Ended March 31, Common Stock Other Paid-In Capital Retained Earnings Accumulated Other Comprehensive Loss Treasury Stock Non- controlling Interests Total ($ and shares in millions except per share amounts) Shares Par Value Shares Cost Balance at January 1, 2019 3,577 $ 1,788 $ 38,808 $ 42,579 $ (5,545 ) 985 $ (50,929 ) $ 181 $ 26,882 Net income attributable to Merck & Co., Inc. — — — 2,915 — — — — 2,915 Other comprehensive income, net of taxes — — — — 199 — — — 199 Cash dividends declared on common stock ($0.55 per share) — — — (1,429 ) — — — — (1,429 ) Treasury stock shares purchased — — — — — 14 (1,090 ) — (1,090 ) Share-based compensation plans and other — — (40 ) — — (5 ) 283 — 243 Net loss attributable to noncontrolling interests — — — — — — — (53 ) (53 ) Other changes in noncontrolling ownership interests — — — — — — — 3 3 Balance at March 31, 2019 3,577 $ 1,788 $ 38,768 $ 44,065 $ (5,346 ) 994 $ (51,736 ) $ 131 $ 27,670 Balance at January 1, 2020 3,577 $ 1,788 $ 39,660 $ 46,602 $ (6,193 ) 1,038 $ (55,950 ) $ 94 $ 26,001 Net income attributable to Merck & Co., Inc. — — — 3,219 — — — — 3,219 Other comprehensive loss, net of taxes — — — — (198 ) — — — (198 ) Cash dividends declared on common stock ($0.61 per share) — — — (1,549 ) — — — — (1,549 ) Treasury stock shares purchased — — — — — 16 (1,281 ) — (1,281 ) Share-based compensation plans and other — — 37 — — (1 ) 70 — 107 Other changes in noncontrolling ownership interests — — — — — — — 1 1 Balance at March 31, 2020 3,577 $ 1,788 $ 39,697 $ 48,272 $ (6,391 ) 1,053 $ (57,161 ) $ 95 $ 26,300 |
Share-Based Compensation Plans
Share-Based Compensation Plans | 3 Months Ended |
Mar. 31, 2020 | |
Share-based Payment Arrangement [Abstract] | |
Share-Based Compensation Plans | Share-Based Compensation Plans The Company has share-based compensation plans under which the Company grants restricted stock units (RSUs) and performance share units (PSUs) to certain management level employees. In addition, employees and non-employee directors may be granted options to purchase shares of Company common stock at the fair market value at the time of grant. The following table provides the amounts of share-based compensation cost recorded in the Condensed Consolidated Statement of Income: Three Months Ended ($ in millions) 2020 2019 Pretax share-based compensation expense $ 108 $ 93 Income tax benefit (15 ) (14 ) Total share-based compensation expense, net of taxes $ 93 $ 79 During the first three months of 2020 , the Company granted 58 thousand RSUs with a weighted-average grant date fair value of $85.66 per RSU and during the first three months of 2019 granted 70 thousand RSUs with a weighted-average grant date fair value of $77.39 per RSU. During the first three months of 2020 , the Company granted 770 thousand PSUs with a weighted-average grant date fair value of $75.65 per PSU and during the first three months of 2019 granted 609 thousand PSUs with a weighted-average grant date fair value of $90.50 per PSU. The Company did not grant any stock options during the first three months of 2020 or 2019. At March 31, 2020 , there was $1.1 billion of total pretax unrecognized compensation expense related to nonvested stock options, RSU and PSU awards which will be recognized over a weighted-average period of 2.4 years . The Company typically communicates the value of annual share-based compensation awards to employees during the first quarter, but the related share amounts are not established and communicated until early May. Therefore, while the number of RSU, PSU and stock option grants disclosed above do not reflect any amounts relating to the annual grants, share-based compensation costs for the first quarter of 2020 and 2019 and unrecognized compensation expense at March 31, 2020 reflect an impact relating to the awards communicated to employees. For segment reporting, share-based compensation costs are unallocated expenses. |
Pension and Other Postretiremen
Pension and Other Postretirement Benefit Plans | 3 Months Ended |
Mar. 31, 2020 | |
Retirement Benefits [Abstract] | |
Pension and Other Postretirement Benefit Plans | Pension and Other Postretirement Benefit Plans The Company has defined benefit pension plans covering eligible employees in the United States and in certain of its international subsidiaries. The net periodic benefit cost of such plans consisted of the following components: Three Months Ended 2020 2019 ($ in millions) U.S. International U.S. International Service cost $ 86 $ 74 $ 71 $ 60 Interest cost 109 34 114 45 Expected return on plan assets (194 ) (103 ) (206 ) (108 ) Amortization of unrecognized prior service credit (12 ) (3 ) (12 ) (3 ) Net loss amortization 75 31 35 16 Termination benefits 3 1 2 — Curtailments 2 (1 ) — — $ 69 $ 33 $ 4 $ 10 The Company provides medical benefits, principally to its eligible U.S. retirees and similar benefits to their dependents, through its other postretirement benefit plans. The net credit of such plans consisted of the following components: Three Months Ended ($ in millions) 2020 2019 Service cost $ 13 $ 12 Interest cost 14 17 Expected return on plan assets (19 ) (18 ) Amortization of unrecognized prior service credit (22 ) (21 ) $ (14 ) $ (10 ) In connection with restructuring actions (see Note 4), termination charges were recorded on pension plans related to expanded eligibility for certain employees exiting Merck. Also, in connection with these restructuring actions, curtailments were recorded on pension plans as reflected in the tables above. The components of net periodic benefit cost (credit) other than the service cost component are included in Other (income) expense, net (see Note 11), with the exception of certain amounts for termination benefits and curtailments, which are recorded in Restructuring costs if the event giving rise to the termination benefits or curtailment is related to restructuring actions as noted above. |
Other (Income) Expense, Net
Other (Income) Expense, Net | 3 Months Ended |
Mar. 31, 2020 | |
Other Income and Expenses [Abstract] | |
Other (Income) Expense, Net | Other (Income) Expense, Net Other (income) expense, net, consisted of: Three Months Ended ($ in millions) 2020 2019 Interest income $ (25 ) $ (89 ) Interest expense 212 209 Exchange losses 54 101 (Income) loss from investments in equity securities, net (1) (52 ) 25 Net periodic defined benefit plan (credit) cost other than service cost (90 ) (141 ) Other, net (28 ) 83 $ 71 $ 188 (1) Includes net realized and unrealized gains and losses from investments in equity securities either owned directly or through ownership interests in investment funds. The higher exchange losses in the first quarter of 2019 reflect losses on forward exchange contracts related to the acquisition of Antelliq Corporation. Other, net (as reflected in the table above) in the first quarter of 2019 includes $84 million of goodwill impairment charges related to certain businesses in the Healthcare Services segment. Interest paid for the three months ended March 31, 2020 and 2019 was $250 million and $195 million , respectively. |
Taxes on Income
Taxes on Income | 3 Months Ended |
Mar. 31, 2020 | |
Income Tax Disclosure [Abstract] | |
Taxes on Income | Taxes on Income The effective income tax rates of 16.1% and 6.7% for the first quarter of 2020 and 2019 , respectively, reflect the impacts of acquisition and divestiture-related costs and restructuring costs, partially offset by the beneficial impact of foreign earnings. In addition, the effective income tax rate for the first quarter of 2019 reflects the favorable impact of a $360 million net tax benefit related to the settlement of certain federal income tax matters. In the first quarter of 2019, the Internal Revenue Service (IRS) concluded its examinations of Merck’s 2012-2014 U.S. federal income tax returns. As a result, the Company was required to make a payment of $107 million . The Company’s reserves for unrecognized tax benefits for the years under examination exceeded the adjustments relating to this examination period and therefore the Company recorded a $360 million net tax benefit in the first quarter of 2019. This net benefit reflects reductions in reserves for unrecognized tax benefits for tax positions relating to the years that were under examination, partially offset by additional reserves for tax positions not previously reserved for. |
Earnings Per Share
Earnings Per Share | 3 Months Ended |
Mar. 31, 2020 | |
Earnings Per Share [Abstract] | |
Earnings Per Share | Earnings Per Share The calculations of earnings per share are as follows: Three Months Ended ($ and shares in millions except per share amounts) 2020 2019 Net income attributable to Merck & Co., Inc. $ 3,219 $ 2,915 Average common shares outstanding 2,533 2,585 Common shares issuable (1) 14 18 Average common shares outstanding assuming dilution 2,547 2,603 Basic earnings per common share attributable to Merck & Co., Inc. common shareholders $ 1.27 $ 1.13 Earnings per common share assuming dilution attributable to Merck & Co., Inc. common shareholders $ 1.26 $ 1.12 (1) Issuable primarily under share-based compensation plans. For both the first quarter of 2020 and 2019 , 2 million |
Other Comprehensive Income (Los
Other Comprehensive Income (Loss) | 3 Months Ended |
Mar. 31, 2020 | |
Equity [Abstract] | |
Other Comprehensive Income (Loss) | Other Comprehensive Income (Loss) Changes in AOCI by component are as follows: Three Months Ended March 31, ($ in millions) Derivatives Investments Employee Benefit Plans Cumulative Translation Adjustment Accumulated Other Comprehensive Income (Loss) Balance January 1, 2019, net of taxes $ 166 $ (78 ) $ (3,556 ) $ (2,077 ) $ (5,545 ) Other comprehensive income (loss) before reclassification adjustments, pretax (13 ) 76 (1 ) 156 218 Tax 3 — 6 (6 ) 3 Other comprehensive income (loss) before reclassification adjustments, net of taxes (10 ) 76 5 150 221 Reclassification adjustments, pretax (48 ) (1) 6 (2) 14 (3) — (28 ) Tax 10 — (4 ) — 6 Reclassification adjustments, net of taxes (38 ) 6 10 — (22 ) Other comprehensive income (loss), net of taxes (48 ) 82 15 150 199 Balance March 31, 2019, net of taxes $ 118 $ 4 $ (3,541 ) $ (1,927 ) $ (5,346 ) Balance January 1, 2020, net of taxes $ 31 $ 18 $ (4,261 ) $ (1,981 ) $ (6,193 ) Other comprehensive income (loss) before reclassification adjustments, pretax 178 3 — (333 ) (152 ) Tax (37 ) — 5 (11 ) (43 ) Other comprehensive income (loss) before reclassification adjustments, net of taxes 141 3 5 (344 ) (195 ) Reclassification adjustments, pretax (47 ) (1) (21 ) (2) 69 (3) — 1 Tax 10 — (14 ) — (4 ) Reclassification adjustments, net of taxes (37 ) (21 ) 55 — (3 ) Other comprehensive income (loss), net of taxes 104 (18 ) 60 (344 ) (198 ) Balance March 31, 2020, net of taxes $ 135 $ — $ (4,201 ) $ (2,325 ) $ (6,391 ) (1) Relates to foreign currency cash flow hedges that were reclassified from AOCI to Sales . (2) Represents net realized (gains) losses on the sales of available-for-sale debt securities that were reclassified from AOCI to Other (income) expense, net . (3) Includes net amortization of prior service cost and actuarial gains and losses included in net periodic benefit cost (see Note 10). |
Segment Reporting
Segment Reporting | 3 Months Ended |
Mar. 31, 2020 | |
Segment Reporting [Abstract] | |
Segment Reporting | Segment Reporting The Company’s operations are principally managed on a products basis and include three operating segments, which are the Pharmaceutical, Animal Health and Healthcare Services segments. The Pharmaceutical and Animal Health segments are the only reportable segments. The Pharmaceutical segment includes human health pharmaceutical and vaccine products. Human health pharmaceutical products consist of therapeutic and preventive agents, generally sold by prescription, for the treatment of human disorders. The Company sells these human health pharmaceutical products primarily to drug wholesalers and retailers, hospitals, government agencies and managed health care providers such as health maintenance organizations, pharmacy benefit managers and other institutions. Human health vaccine products consist of preventive pediatric, adolescent and adult vaccines, primarily administered at physician offices. The Company sells these human health vaccines primarily to physicians, wholesalers, physician distributors and government entities. A large component of pediatric and adolescent vaccine sales are made to the U.S. Centers for Disease Control and Prevention Vaccines for Children program, which is funded by the U.S. government. Additionally, the Company sells vaccines to the Federal government for placement into vaccine stockpiles. The Animal Health segment discovers, develops, manufactures and markets a wide range of veterinary pharmaceutical and vaccine products, as well as health management solutions and services, for the prevention, treatment and control of disease in all major livestock and companion animal species. The Company also offers an extensive suite of digitally connected identification, traceability and monitoring products. The Company sells its products to veterinarians, distributors and animal producers. The Healthcare Services segment provided services and solutions that focus on engagement, health analytics and clinical services to improve the value of care delivered to patients. The Company has been in the process of divesting the businesses in the Healthcare Services segment. The remaining businesses were divested during the first quarter of 2020. Sales of the Company’s products were as follows: Three Months Ended March 31, 2020 2019 ($ in millions) U.S. Int’l Total U.S. Int’l Total Pharmaceutical: Oncology Keytruda $ 1,906 $ 1,378 $ 3,284 $ 1,284 $ 985 $ 2,269 Alliance revenue - Lynparza (1) 85 60 145 50 29 79 Alliance revenue - Lenvima (1) 90 38 128 50 24 74 Emend 5 38 43 63 53 117 Vaccines Gardasil/Gardasil 9 461 636 1,097 362 476 838 ProQuad/M-M-R II /Varivax 333 102 435 343 153 496 Pneumovax 23 182 75 256 125 59 185 RotaTeq 140 82 222 154 57 211 Vaqta 30 30 60 29 18 47 Hospital Acute Care Bridion 143 157 299 119 136 255 Noxafil 8 87 94 91 99 190 Invanz 6 59 64 14 58 72 Prevymis 26 33 60 18 14 32 Cancidas 3 52 55 1 60 61 Primaxin — 51 51 — 59 59 Cubicin 15 31 46 42 46 88 Zerbaxa 20 16 37 12 14 26 Immunology Simponi — 215 215 — 208 208 Remicade — 88 88 — 123 123 Neuroscience Belsomra 27 53 79 24 44 67 Virology Isentress/Isentress HD 75 170 245 108 147 255 Zepatier 18 37 55 33 81 114 Cardiovascular Zetia (2 ) 147 145 — 140 140 Vytorin 3 50 53 3 94 97 Atozet — 122 122 — 94 94 Adempas — 56 56 — 48 48 Alliance revenue - Adempas (2) 49 5 53 40 2 42 Diabetes Januvia 355 419 774 384 440 824 Janumet 113 390 503 167 364 530 Women’s Health Implanon/Nexplanon 149 45 195 149 50 199 NuvaRing 26 37 63 185 34 219 Diversified Brands Singulair 5 151 155 5 186 191 Cozaar/Hyzaar 7 95 102 4 99 103 Nasonex 6 65 71 (1 ) 97 96 Arcoxia — 70 70 — 75 75 Follistim AQ 21 21 41 29 28 57 Other pharmaceutical (3) 409 780 1,194 328 754 1,082 Total Pharmaceutical segment sales 4,714 5,941 10,655 4,215 5,448 9,663 Animal Health: Livestock 162 577 739 117 494 611 Companion Animals 222 253 475 177 237 414 Total Animal Health segment sales 384 830 1,214 294 731 1,025 Other segment sales (4) 23 — 23 39 — 39 Total segment sales 5,121 6,771 11,892 4,548 6,179 10,727 Other (5) 16 149 165 7 82 89 $ 5,137 $ 6,920 $ 12,057 $ 4,555 $ 6,261 $ 10,816 U.S. plus international may not equal total due to rounding. (1) Alliance revenue represents Merck’s share of profits, which are product sales net of cost of sales and commercialization costs (see Note 3). (2) Alliance revenue represents Merck’s share of profits from sales in Bayer’s marketing territories, which are product sales net of cost of sales and commercialization costs (see Note 3). (3) Other pharmaceutical primarily reflects sales of other human health pharmaceutical products, including products within the franchises not listed separately. (4) Represents sales for the Healthcare Services segment. All the businesses in the Healthcare Services segment were divested as of March 31, 2020. (5) Other is primarily comprised of miscellaneous corporate revenues, including revenue hedging activities, as well as third-party manufacturing sales. Other in the first quarter of 2020 and 2019 also includes approximately $75 million and $15 million , respectively, related to the sale of the marketing rights for certain products. Product sales are recorded net of the provision for discounts, including chargebacks, which are customer discounts that occur when a contracted customer purchases through an intermediary wholesale purchaser, and rebates that are owed based upon definitive contractual agreements or legal requirements with private sector and public sector (Medicaid and Medicare Part D) benefit providers, after the final dispensing of the product by a pharmacy to a benefit plan participant. These discounts, in the aggregate, reduced U.S. sales by $3.2 billion and $2.6 billion for the three months ended March 31, 2020 and 2019 , respectively. Consolidated sales by geographic area where derived are as follows: Three Months Ended ($ in millions) 2020 2019 United States $ 5,137 $ 4,555 Europe, Middle East and Africa 3,534 3,103 China 864 746 Japan 811 799 Asia Pacific (other than China and Japan) 728 745 Latin America 556 561 Other 427 307 $ 12,057 $ 10,816 A reconciliation of segment profits to Income before taxes is as follows: Three Months Ended ($ in millions) 2020 2019 Segment profits: Pharmaceutical segment $ 7,477 $ 6,574 Animal Health segment 478 415 Other segment 1 2 Total segment profits 7,956 6,991 Other profits 139 30 Unallocated: Interest income 25 89 Interest expense (212 ) (209 ) Depreciation and amortization (381 ) (359 ) Research and development (2,097 ) (1,843 ) Amortization of purchase accounting adjustments (295 ) (397 ) Restructuring costs (72 ) (153 ) Other unallocated, net (1,225 ) (1,082 ) $ 3,838 $ 3,067 Pharmaceutical segment profits are comprised of segment sales less standard costs, as well as selling, general and administrative expenses directly incurred by the segment. Animal Health segment profits are comprised of segment sales, less all cost of sales, as well as selling, general and administrative expenses and research and development costs directly incurred by the segment. For internal management reporting presented to the chief operating decision maker, Merck does not allocate the remaining cost of sales not included in segment profits as described above, research and development expenses incurred in Merck Research Laboratories, the Company’s research and development division that focuses on human health-related activities, or general and administrative expenses, nor the cost of financing these activities. Separate divisions maintain responsibility for monitoring and managing these costs, including depreciation related to fixed assets utilized by these divisions and, therefore, they are not included in segment profits. In addition, costs related to restructuring activities, as well as the amortization of purchase accounting adjustments are not allocated to segments. Other profits are primarily comprised of miscellaneous corporate profits, as well as operating profits related to third-party manufacturing sales. Other unallocated, net, includes expenses from corporate and manufacturing cost centers, goodwill and other intangible asset impairment charges, gains or losses on sales of businesses, expense or income related to changes in the estimated fair value measurement of liabilities for contingent consideration, and other miscellaneous income or expense items. |
Basis of Presentation (Policies
Basis of Presentation (Policies) | 3 Months Ended |
Mar. 31, 2020 | |
Organization, Consolidation and Presentation of Financial Statements [Abstract] | |
Basis of Presentation | Basis of Presentation The accompanying unaudited condensed consolidated financial statements of Merck & Co., Inc. (Merck or the Company) have been prepared pursuant to the rules and regulations for reporting on Form 10-Q. Accordingly, certain information and disclosures required by accounting principles generally accepted in the United States (GAAP) for complete consolidated financial statements are not included herein. These interim statements should be read in conjunction with the audited financial statements and notes thereto included in Merck’s Form 10-K filed on February 26, 2020. The results of operations of any interim period are not necessarily indicative of the results of operations for the full year. In the Company’s opinion, all adjustments necessary for a fair statement of these interim statements have been included and are of a normal and recurring nature. |
Recently Adopted and Issued Accounting Standards | Recently Adopted Accounting Standards In June 2016, the FASB issued new guidance on the accounting for credit losses on financial instruments. The new guidance introduces an expected loss model for estimating credit losses, replacing the incurred loss model. The new guidance also changes the impairment model for available-for-sale debt securities, requiring the use of an allowance to record estimated credit losses (and subsequent recoveries). The Company adopted the new guidance effective January 1, 2020. There was no impact to the Company’s consolidated financial statements upon adoption. In November 2018, the FASB issued new guidance for collaborative arrangements intended to reduce diversity in practice by clarifying whether certain transactions between collaborative arrangement participants should be accounted for under revenue recognition guidance (ASC 606). The Company adopted the new guidance effective January 1, 2020, which resulted in minor changes to the presentation of information related to the Company’s collaborative arrangements. Recently Issued Accounting Standards Not Yet Adopted In December 2019, the FASB issued amended guidance on the accounting and reporting of income taxes. The guidance is intended to simplify the accounting for income taxes by removing exceptions related to certain intraperiod tax allocations and deferred tax liabilities; clarifying guidance primarily related to evaluating the step-up tax basis for goodwill in a business combination; and reflecting enacted changes in tax laws or rates in the annual effective tax rate. The amended guidance is effective for interim and annual periods in 2021. Early adoption is permitted. The amendments in the new guidance are to be applied on a retrospective basis, on a modified retrospective basis through a cumulative-effect adjustment to retained earnings or prospectively, depending on the amendment. The Company is currently evaluating the impact of adoption on its consolidated financial statements. In January 2020, the FASB issued new guidance intended to clarify certain interactions between accounting standards related to equity securities, equity method investments and certain derivatives. The guidance addresses accounting for the transition into and out of the equity method of accounting and measuring certain purchased options and forward contracts to acquire investments. The new guidance is effective for interim and annual periods in 2021 and is to be applied prospectively. Early adoption is permitted. The Company is currently evaluating the impact of adoption on its consolidated financial statements. In March 2020, the FASB issued optional guidance to ease the potential burden in accounting for (or recognizing the effects of) reference rate reform on financial reporting. The guidance provides optional expedients and exceptions for applying GAAP to contracts, hedging relationships, and other transactions affected by reference rate reform. The optional guidance is effective upon issuance and can be applied on a prospective basis at any time between January 1, 2020 through December 31, 2022. The Company is currently evaluating the impact of adoption on its consolidated financial statements. |
Contingencies Commitments and C
Contingencies Commitments and Contingencies (Policies) | 3 Months Ended |
Mar. 31, 2020 | |
Commitments and Contingencies Disclosure [Abstract] | |
Legal Costs, Policy | Legal defense costs expected to be incurred in connection with a loss contingency are accrued when probable and reasonably estimable. |
Acquisitions, Research Collab_2
Acquisitions, Research Collaborations and License Agreements (Tables) | 3 Months Ended |
Mar. 31, 2020 | |
Business Combinations [Abstract] | |
Fair Value of Assets Acquired and Liabilities Assumed | The estimated fair value of assets acquired and liabilities assumed from ArQule is as follows: ($ in millions) January 16, 2020 Cash and cash equivalents $ 145 IPR&D MK-1026 (formerly ARQ 531) (1) 2,280 IPR&D MK-7075 (formerly ARQ 092) (1) 170 Licensing arrangement for ARQ 087 80 Deferred income tax liabilities (434 ) Other assets and liabilities, net 35 Total identifiable net assets 2,276 Goodwill (2) 414 Consideration transferred $ 2,690 (1) The fair values of the identifiable intangible assets related to in-process research and development (IPR&D) were determined using an income approach. The future net cash flows were discounted to present value utilizing a discount rate of 12.5% . Actual cash flows are likely to be different than those assumed. (2) The goodwill was allocated to the Pharmaceutical segment and is not deductible for tax purposes. |
Collaborative Arrangements (Tab
Collaborative Arrangements (Tables) | 3 Months Ended |
Mar. 31, 2020 | |
Collaborative Arrangements [Abstract] | |
Collaboration Arrangements | Summarized financial information related to this collaboration is as follows: Three Months Ended ($ in millions) 2020 2019 Alliance revenue $ 145 $ 79 Cost of sales (1) 28 19 Selling, general and administrative 33 27 Research and development 36 45 ($ in millions) March 31, 2020 December 31, 2019 Receivables from AstraZeneca included in Other current assets $ 142 $ 128 Payables to AstraZeneca included in Accrued and other current liabilities (2) 326 577 (1) Represents amortization of capitalized milestone payments. (2) Includes accrued milestone payments. Summarized financial information related to this collaboration is as follows: Three Months Ended ($ in millions) 2020 2019 Alliance revenue $ 128 $ 74 Cost of sales (1) 35 51 Selling, general and administrative 11 19 Research and development 64 47 ($ in millions) March 31, 2020 December 31, 2019 Receivables from Eisai included in Other current assets $ 140 $ 150 Payables to Eisai included in Accrued and other current liabilities (2) 425 700 Payables to Eisai included in Other Noncurrent Liabilities (3) 300 525 (1) Represents amortization of capitalized milestone payments. (2) Includes accrued milestone and future option payments. (3) Includes accrued milestone payments. Summarized financial information related to this collaboration is as follows: Three Months Ended ($ in millions) 2020 2019 Net sales of Adempas recorded by Merck $ 56 $ 48 Alliance revenue 53 42 Total sales 109 90 Cost of sales (1) 28 29 Selling, general and administrative 15 8 Research and development 25 30 ($ in millions) March 31, 2020 December 31, 2019 Receivables from Bayer included in Other current assets $ 50 $ 49 Payables to Bayer included in Other Noncurrent Liabilities (2) 375 375 (1) Includes amortization of intangible assets. (2) Represents accrued milestone payment. |
Restructuring (Tables)
Restructuring (Tables) | 3 Months Ended |
Mar. 31, 2020 | |
Restructuring and Related Activities [Abstract] | |
Charges Related to Restructuring Program Activities by Type of Cost | The following tables summarize the charges related to restructuring program activities by type of cost: Three Months Ended March 31, 2020 ($ in millions) Separation Costs Accelerated Depreciation Other Total Cost of sales $ — $ 25 $ 43 $ 68 Selling, general and administrative — 11 — 11 Research and development — 17 — 17 Restructuring costs 47 — 25 72 $ 47 $ 53 $ 68 $ 168 Three Months Ended March 31, 2019 ($ in millions) Separation Costs Accelerated Depreciation Other Total Cost of sales $ — $ 34 $ — $ 34 Restructuring costs 128 — 25 153 $ 128 $ 34 $ 25 $ 187 |
Charges and Spending Relating to Restructuring Activities by Program | The following table summarizes the charges and spending relating to restructuring program activities for the three months ended March 31, 2020 : ($ in millions) Separation Costs Accelerated Depreciation Other Total Restructuring reserves January 1, 2020 $ 690 $ — $ 69 $ 759 Expense 47 53 68 168 (Payments) receipts, net (168 ) — (122 ) (290 ) Non-cash activity — (53 ) 42 (11 ) Restructuring reserves March 31, 2020 (1) $ 569 $ — $ 57 $ 626 (1) |
Financial Instruments (Tables)
Financial Instruments (Tables) | 3 Months Ended |
Mar. 31, 2020 | |
Derivative Instruments and Hedging Activities Disclosure [Abstract] | |
Effect of Net Investment Hedges on OCI and the Consolidated Statement of Income | The effects of the Company’s net investment hedges on OCI and the Consolidated Statement of Income are shown below: Amount of Pretax (Gain) Loss Recognized in Other Comprehensive Income (1) Amount of Pretax (Gain) Loss Recognized in Other (income) expense, net for Amounts Excluded from Effectiveness Testing Three Months Ended March 31, Three Months Ended March 31, ($ in millions) 2020 2019 2020 2019 Net Investment Hedging Relationships Foreign exchange contracts $ (3 ) $ (11 ) $ (8 ) $ (8 ) Euro-denominated notes (51 ) (30 ) — — (1) No amounts were reclassified from AOCI into income related to the sale of a subsidiary. |
Summary of Interest Rate Swaps Held | At March 31, 2020 , the Company was a party to 14 pay-floating, receive-fixed interest rate swap contracts designated as fair value hedges of fixed-rate notes in which the notional amounts match the amount of the hedged fixed-rate notes as detailed in the table below. March 31, 2020 ($ in millions) Par Value of Debt Number of Interest Rate Swaps Held Total Swap Notional Amount 3.875% notes due 2021 $ 1,150 5 $ 1,150 2.40% notes due 2022 1,000 4 1,000 2.35% notes due 2022 1,250 5 1,250 |
Amounts Recorded on Balance Sheet Related to Fair Value Hedges | The table below presents the location of amounts recorded on the Consolidated Balance Sheet related to cumulative basis adjustments for fair value hedges: Carrying Amount of Hedged Liabilities Cumulative Amount of Fair Value Hedging Adjustment Increase (Decrease) Included in the Carrying Amount ($ in millions) March 31, 2020 December 31, 2019 March 31, 2020 December 31, 2019 Balance Sheet Line Item in which Hedged Item is Included Loans payable and current portion of long-term debt $ 1,160 $ 1,249 $ 11 $ (1 ) Long-Term Debt 2,315 3,409 69 14 |
Fair Value of Derivatives on a Gross Basis Segregated between those Derivatives that are Designated as Hedging Instruments and those that are Not Designated as Hedging Instruments | Presented in the table below is the fair value of derivatives on a gross basis segregated between those derivatives that are designated as hedging instruments and those that are not designated as hedging instruments: March 31, 2020 December 31, 2019 Fair Value of Derivative U.S. Dollar Notional Fair Value of Derivative U.S. Dollar Notional ($ in millions) Balance Sheet Caption Asset Liability Asset Liability Derivatives Designated as Hedging Instruments Interest rate swap contracts Other current assets $ 11 $ — $ 1,150 $ — $ — $ — Interest rate swap contracts Other Assets 70 — 2,250 15 — 3,400 Interest rate swap contracts Accrued and other current liabilities — — — — 1 1,250 Foreign exchange contracts Other current assets 194 — 6,546 152 — 6,117 Foreign exchange contracts Other Assets 88 — 2,064 55 — 2,160 Foreign exchange contracts Accrued and other current liabilities — 7 734 — 22 1,748 Foreign exchange contracts Other Noncurrent Liabilities — 1 5 — 1 53 $ 363 $ 8 $ 12,749 $ 222 $ 24 $ 14,728 Derivatives Not Designated as Hedging Instruments Foreign exchange contracts Other current assets $ 347 $ — $ 10,039 $ 66 $ — $ 7,245 Foreign exchange contracts Accrued and other current liabilities — 85 4,665 — 73 8,693 $ 347 $ 85 $ 14,704 $ 66 $ 73 $ 15,938 $ 710 $ 93 $ 27,453 $ 288 $ 97 $ 30,666 |
Information on Derivative Positions Subject to Master Netting Arrangements as if they were Presented on a Net Basis | The following table provides information on the Company’s derivative positions subject to these master netting arrangements as if they were presented on a net basis, allowing for the right of offset by counterparty and cash collateral exchanged per the master agreements and related credit support annexes: March 31, 2020 December 31, 2019 ($ in millions) Asset Liability Asset Liability Gross amounts recognized in the condensed consolidated balance sheet $ 710 $ 93 $ 288 $ 97 Gross amounts subject to offset in master netting arrangements not offset in the condensed consolidated balance sheet (89 ) (89 ) (84 ) (84 ) Cash collateral received (216 ) — (34 ) — Net amounts $ 405 $ 4 $ 170 $ 13 |
Location and Amount of Pretax (Gains) Losses of Derivatives | The table below provides information regarding the location and amount of pretax (gains) losses of derivatives designated in fair value or cash flow hedging relationships: Sales Other (income) expense, net (1) Other comprehensive income (loss) Three Months Ended March 31, Three Months Ended March 31, Three Months Ended March 31, ($ in millions) 2020 2019 2020 2019 2020 2019 Financial Statement Line Items in which Effects of Fair Value or Cash Flow Hedges are Recorded $ 12,057 $ 10,816 $ 71 $ 188 $ (198 ) $ 199 (Gain) loss on fair value hedging relationships Interest rate swap contracts Hedged items — — 67 33 — — Derivatives designated as hedging instruments — — (67 ) (23 ) — — Impact of cash flow hedging relationships Foreign exchange contracts Amount of gain (loss) recognized in OCI on derivatives — — — — 178 (13 ) Increase (decrease) in Sales as a result of AOCI reclassifications 46 44 — — (46 ) (44 ) Interest rate contracts Amount of gain recognized in Other (income) expense, net on derivatives — — (1 ) (1 ) — — Amount of loss recognized in OCI on derivatives — — — — (1 ) (4 ) (1) Interest expense is a component of Other (income) expense, net. |
Income Statement Effects of Derivatives Not Designated as Hedging Instruments | The table below provides information regarding the income statement effects of derivatives not designated as hedging instruments: Amount of Derivative Pretax (Gain) Loss Recognized in Income Three Months Ended March 31, ($ in millions) Income Statement Caption 2020 2019 Derivatives Not Designated as Hedging Instruments Foreign exchange contracts (1) Other (income) expense, net $ (180 ) $ 118 Foreign exchange contracts (2) Sales (7 ) 10 (1) These derivative contracts mitigate changes in the value of remeasured foreign currency denominated monetary assets and liabilities attributable to changes in foreign currency exchange rates. (2) These derivative contracts serve as economic hedges of forecasted transactions. |
Information on Investments in Debt and Equity Securities | Information on investments in debt and equity securities is as follows: March 31, 2020 December 31, 2019 Amortized Cost Gross Unrealized Fair Value Amortized Cost Gross Unrealized Fair Value ($ in millions) Gains Losses Gains Losses U.S. government and agency securities $ 62 $ — $ — $ 62 $ 266 $ 3 $ — $ 269 Foreign government bonds 2 — — 2 — — — — Commercial paper — — — — 668 — — 668 Corporate notes and bonds — — — — 608 13 — 621 Asset-backed securities — — — — 226 1 — 227 Total debt securities $ 64 $ — $ — $ 64 $ 1,768 $ 17 $ — $ 1,785 Publicly traded equity securities (1) 779 838 Total debt and publicly traded equity securities $ 843 $ 2,623 (1) Unrealized net losses recognized in Other (income) expense, net on equity securities still held at March 31, 2020 were $4 million in the first quarter of 2020 . Unrealized net gains recognized in Other (income) expense, net on equity securities still held at March 31, 2019 were $114 million in the first quarter of 2019 . |
Financial Assets and Liabilities Measured at Fair Value on a Recurring Basis | Financial assets and liabilities measured at fair value on a recurring basis are summarized below: Fair Value Measurements Using Fair Value Measurements Using Level 1 Level 2 Level 3 Total Level 1 Level 2 Level 3 Total ($ in millions) March 31, 2020 December 31, 2019 Assets Investments Foreign government bonds $ — $ 2 $ — $ 2 $ — $ — $ — $ — Commercial paper — — — — — 668 — 668 Corporate notes and bonds — — — — — 621 — 621 Asset-backed securities (1) — — — — — 227 — 227 U.S. government and agency securities — — — — — 209 — 209 Publicly traded equity securities 560 — — 560 518 — — 518 560 2 — 562 518 1,725 — 2,243 Other assets (2) U.S. government and agency securities 62 — — 62 60 — — 60 Publicly traded equity securities 219 — — 219 320 — — 320 281 — — 281 380 — — 380 Derivative assets (3) Forward exchange contracts — 455 — 455 — 169 — 169 Purchased currency options — 174 — 174 — 104 — 104 Interest rate swaps — 81 — 81 — 15 — 15 — 710 — 710 — 288 — 288 Total assets $ 841 $ 712 $ — $ 1,553 $ 898 $ 2,013 $ — $ 2,911 Liabilities Other liabilities Contingent consideration $ — $ — $ 694 $ 694 $ — $ — $ 767 $ 767 Derivative liabilities (3) Forward exchange contracts — 90 — 90 — 95 — 95 Written currency options — 3 — 3 — 1 — 1 Interest rate swaps — — — — — 1 — 1 — 93 — 93 — 97 — 97 Total liabilities $ — $ 93 $ 694 $ 787 $ — $ 97 $ 767 $ 864 (1) Primarily all of the asset-backed securities were highly-rated (Standard & Poor’s rating of AAA and Moody’s Investors Service rating of Aaa), secured primarily by auto loan, credit card and student loan receivables, with weighted-average lives of primarily 5 years or less. (2) Investments included in other assets are restricted as to use, including for the payment of benefits under employee benefit plans. (3) The fair value determination of derivatives includes the impact of the credit risk of counterparties to the derivatives and the Company’s own credit risk, the effects of which were not significant. |
Information About the Changes in Liabilities for Contingent Consideration | Summarized information about the changes in liabilities for contingent consideration associated with business acquisitions is as follows: Three Months Ended March 31, ($ in millions) 2020 2019 Fair value January 1 $ 767 $ 788 Changes in estimated fair value (1) 33 (36 ) Payments (106 ) (85 ) Fair value March 31 (2)(3) $ 694 $ 667 (1) Recorded in Cost of sales, Research and development expenses, and Other (income) expense, net . Includes cumulative translation adjustments. (2) Balance at March 31, 2020 includes $119 million recorded as a current liability for amounts expected to be paid within the next 12 months. (3) At March 31, 2020 and December 31, 2019 , $520 million and $625 million , respectively, of the liabilities relate to the termination of the Sanofi-Pasteur MSD joint venture in 2016. As part of the termination, Merck recorded a liability for contingent future royalty payments of 11.5% on net sales of all Merck products that were previously sold by the joint venture through December 31, 2024. The fair value of this liability is determined utilizing the estimated amount and timing of projected cash flows using a risk-adjusted discount rate of 8% to present value the cash flows. |
Inventories (Tables)
Inventories (Tables) | 3 Months Ended |
Mar. 31, 2020 | |
Inventory Disclosure [Abstract] | |
Schedule of Inventories | Inventories consisted of: ($ in millions) March 31, 2020 December 31, 2019 Finished goods $ 1,753 $ 1,772 Raw materials and work in process 5,629 5,650 Supplies 232 207 Total (approximates current cost) 7,614 7,629 Decrease to LIFO cost (138 ) (171 ) $ 7,476 $ 7,458 Recognized as: Inventories $ 5,846 $ 5,978 Other assets 1,630 1,480 |
Equity (Tables)
Equity (Tables) | 3 Months Ended |
Mar. 31, 2020 | |
Equity [Abstract] | |
Equity | Three Months Ended March 31, Common Stock Other Paid-In Capital Retained Earnings Accumulated Other Comprehensive Loss Treasury Stock Non- controlling Interests Total ($ and shares in millions except per share amounts) Shares Par Value Shares Cost Balance at January 1, 2019 3,577 $ 1,788 $ 38,808 $ 42,579 $ (5,545 ) 985 $ (50,929 ) $ 181 $ 26,882 Net income attributable to Merck & Co., Inc. — — — 2,915 — — — — 2,915 Other comprehensive income, net of taxes — — — — 199 — — — 199 Cash dividends declared on common stock ($0.55 per share) — — — (1,429 ) — — — — (1,429 ) Treasury stock shares purchased — — — — — 14 (1,090 ) — (1,090 ) Share-based compensation plans and other — — (40 ) — — (5 ) 283 — 243 Net loss attributable to noncontrolling interests — — — — — — — (53 ) (53 ) Other changes in noncontrolling ownership interests — — — — — — — 3 3 Balance at March 31, 2019 3,577 $ 1,788 $ 38,768 $ 44,065 $ (5,346 ) 994 $ (51,736 ) $ 131 $ 27,670 Balance at January 1, 2020 3,577 $ 1,788 $ 39,660 $ 46,602 $ (6,193 ) 1,038 $ (55,950 ) $ 94 $ 26,001 Net income attributable to Merck & Co., Inc. — — — 3,219 — — — — 3,219 Other comprehensive loss, net of taxes — — — — (198 ) — — — (198 ) Cash dividends declared on common stock ($0.61 per share) — — — (1,549 ) — — — — (1,549 ) Treasury stock shares purchased — — — — — 16 (1,281 ) — (1,281 ) Share-based compensation plans and other — — 37 — — (1 ) 70 — 107 Other changes in noncontrolling ownership interests — — — — — — — 1 1 Balance at March 31, 2020 3,577 $ 1,788 $ 39,697 $ 48,272 $ (6,391 ) 1,053 $ (57,161 ) $ 95 $ 26,300 |
Share-Based Compensation Plans
Share-Based Compensation Plans (Tables) | 3 Months Ended |
Mar. 31, 2020 | |
Share-based Payment Arrangement [Abstract] | |
Amounts of Share-Based Compensation Cost Recorded in Consolidated Statement of Income | The following table provides the amounts of share-based compensation cost recorded in the Condensed Consolidated Statement of Income: Three Months Ended ($ in millions) 2020 2019 Pretax share-based compensation expense $ 108 $ 93 Income tax benefit (15 ) (14 ) Total share-based compensation expense, net of taxes $ 93 $ 79 |
Assumptions Used to Determine Weighted-Average Fair Value of Options Granted | The Company did not grant any stock options during the first three months of 2020 or 2019. At March 31, 2020 , there was $1.1 billion of total pretax unrecognized compensation expense related to nonvested stock options, RSU and PSU awards which will be recognized over a weighted-average period of 2.4 years . The Company typically communicates the value of annual share-based compensation awards to employees during the first quarter, but the related share amounts are not established and communicated until early May. Therefore, while the number of RSU, PSU and stock option grants disclosed above do not reflect any amounts relating to the annual grants, share-based compensation costs for the first quarter of 2020 and 2019 and unrecognized compensation expense at March 31, 2020 reflect an impact relating to the awards communicated to employees. For segment reporting, share-based compensation costs are unallocated expenses. |
Pension and Other Postretirem_2
Pension and Other Postretirement Benefit Plans (Tables) | 3 Months Ended |
Mar. 31, 2020 | |
Pension Plans | |
Defined Benefit Plan Disclosure [Line Items] | |
Components of net cost of defined benefit plans | The Company has defined benefit pension plans covering eligible employees in the United States and in certain of its international subsidiaries. The net periodic benefit cost of such plans consisted of the following components: Three Months Ended 2020 2019 ($ in millions) U.S. International U.S. International Service cost $ 86 $ 74 $ 71 $ 60 Interest cost 109 34 114 45 Expected return on plan assets (194 ) (103 ) (206 ) (108 ) Amortization of unrecognized prior service credit (12 ) (3 ) (12 ) (3 ) Net loss amortization 75 31 35 16 Termination benefits 3 1 2 — Curtailments 2 (1 ) — — $ 69 $ 33 $ 4 $ 10 |
Other Postretirement Benefit Plans | |
Defined Benefit Plan Disclosure [Line Items] | |
Components of net cost of defined benefit plans | The Company provides medical benefits, principally to its eligible U.S. retirees and similar benefits to their dependents, through its other postretirement benefit plans. The net credit of such plans consisted of the following components: Three Months Ended ($ in millions) 2020 2019 Service cost $ 13 $ 12 Interest cost 14 17 Expected return on plan assets (19 ) (18 ) Amortization of unrecognized prior service credit (22 ) (21 ) $ (14 ) $ (10 ) |
Other (Income) Expense, Net (Ta
Other (Income) Expense, Net (Tables) | 3 Months Ended |
Mar. 31, 2020 | |
Other Income and Expenses [Abstract] | |
Other (Income) Expense, Net | Other (income) expense, net, consisted of: Three Months Ended ($ in millions) 2020 2019 Interest income $ (25 ) $ (89 ) Interest expense 212 209 Exchange losses 54 101 (Income) loss from investments in equity securities, net (1) (52 ) 25 Net periodic defined benefit plan (credit) cost other than service cost (90 ) (141 ) Other, net (28 ) 83 $ 71 $ 188 (1) Includes net realized and unrealized gains and losses from investments in equity securities either owned directly or through ownership interests in investment funds. |
Earnings Per Share (Tables)
Earnings Per Share (Tables) | 3 Months Ended |
Mar. 31, 2020 | |
Earnings Per Share [Abstract] | |
Calculations of Earnings Per Share | The calculations of earnings per share are as follows: Three Months Ended ($ and shares in millions except per share amounts) 2020 2019 Net income attributable to Merck & Co., Inc. $ 3,219 $ 2,915 Average common shares outstanding 2,533 2,585 Common shares issuable (1) 14 18 Average common shares outstanding assuming dilution 2,547 2,603 Basic earnings per common share attributable to Merck & Co., Inc. common shareholders $ 1.27 $ 1.13 Earnings per common share assuming dilution attributable to Merck & Co., Inc. common shareholders $ 1.26 $ 1.12 (1) Issuable primarily under share-based compensation plans. |
Other Comprehensive Income (L_2
Other Comprehensive Income (Loss) (Tables) | 3 Months Ended |
Mar. 31, 2020 | |
Equity [Abstract] | |
Changes in AOCI by Component | Changes in AOCI by component are as follows: Three Months Ended March 31, ($ in millions) Derivatives Investments Employee Benefit Plans Cumulative Translation Adjustment Accumulated Other Comprehensive Income (Loss) Balance January 1, 2019, net of taxes $ 166 $ (78 ) $ (3,556 ) $ (2,077 ) $ (5,545 ) Other comprehensive income (loss) before reclassification adjustments, pretax (13 ) 76 (1 ) 156 218 Tax 3 — 6 (6 ) 3 Other comprehensive income (loss) before reclassification adjustments, net of taxes (10 ) 76 5 150 221 Reclassification adjustments, pretax (48 ) (1) 6 (2) 14 (3) — (28 ) Tax 10 — (4 ) — 6 Reclassification adjustments, net of taxes (38 ) 6 10 — (22 ) Other comprehensive income (loss), net of taxes (48 ) 82 15 150 199 Balance March 31, 2019, net of taxes $ 118 $ 4 $ (3,541 ) $ (1,927 ) $ (5,346 ) Balance January 1, 2020, net of taxes $ 31 $ 18 $ (4,261 ) $ (1,981 ) $ (6,193 ) Other comprehensive income (loss) before reclassification adjustments, pretax 178 3 — (333 ) (152 ) Tax (37 ) — 5 (11 ) (43 ) Other comprehensive income (loss) before reclassification adjustments, net of taxes 141 3 5 (344 ) (195 ) Reclassification adjustments, pretax (47 ) (1) (21 ) (2) 69 (3) — 1 Tax 10 — (14 ) — (4 ) Reclassification adjustments, net of taxes (37 ) (21 ) 55 — (3 ) Other comprehensive income (loss), net of taxes 104 (18 ) 60 (344 ) (198 ) Balance March 31, 2020, net of taxes $ 135 $ — $ (4,201 ) $ (2,325 ) $ (6,391 ) (1) Relates to foreign currency cash flow hedges that were reclassified from AOCI to Sales . (2) Represents net realized (gains) losses on the sales of available-for-sale debt securities that were reclassified from AOCI to Other (income) expense, net . (3) Includes net amortization of prior service cost and actuarial gains and losses included in net periodic benefit cost (see Note 10). |
Segment Reporting (Tables)
Segment Reporting (Tables) | 3 Months Ended |
Mar. 31, 2020 | |
Segment Reporting [Abstract] | |
Sales of Company's products | Sales of the Company’s products were as follows: Three Months Ended March 31, 2020 2019 ($ in millions) U.S. Int’l Total U.S. Int’l Total Pharmaceutical: Oncology Keytruda $ 1,906 $ 1,378 $ 3,284 $ 1,284 $ 985 $ 2,269 Alliance revenue - Lynparza (1) 85 60 145 50 29 79 Alliance revenue - Lenvima (1) 90 38 128 50 24 74 Emend 5 38 43 63 53 117 Vaccines Gardasil/Gardasil 9 461 636 1,097 362 476 838 ProQuad/M-M-R II /Varivax 333 102 435 343 153 496 Pneumovax 23 182 75 256 125 59 185 RotaTeq 140 82 222 154 57 211 Vaqta 30 30 60 29 18 47 Hospital Acute Care Bridion 143 157 299 119 136 255 Noxafil 8 87 94 91 99 190 Invanz 6 59 64 14 58 72 Prevymis 26 33 60 18 14 32 Cancidas 3 52 55 1 60 61 Primaxin — 51 51 — 59 59 Cubicin 15 31 46 42 46 88 Zerbaxa 20 16 37 12 14 26 Immunology Simponi — 215 215 — 208 208 Remicade — 88 88 — 123 123 Neuroscience Belsomra 27 53 79 24 44 67 Virology Isentress/Isentress HD 75 170 245 108 147 255 Zepatier 18 37 55 33 81 114 Cardiovascular Zetia (2 ) 147 145 — 140 140 Vytorin 3 50 53 3 94 97 Atozet — 122 122 — 94 94 Adempas — 56 56 — 48 48 Alliance revenue - Adempas (2) 49 5 53 40 2 42 Diabetes Januvia 355 419 774 384 440 824 Janumet 113 390 503 167 364 530 Women’s Health Implanon/Nexplanon 149 45 195 149 50 199 NuvaRing 26 37 63 185 34 219 Diversified Brands Singulair 5 151 155 5 186 191 Cozaar/Hyzaar 7 95 102 4 99 103 Nasonex 6 65 71 (1 ) 97 96 Arcoxia — 70 70 — 75 75 Follistim AQ 21 21 41 29 28 57 Other pharmaceutical (3) 409 780 1,194 328 754 1,082 Total Pharmaceutical segment sales 4,714 5,941 10,655 4,215 5,448 9,663 Animal Health: Livestock 162 577 739 117 494 611 Companion Animals 222 253 475 177 237 414 Total Animal Health segment sales 384 830 1,214 294 731 1,025 Other segment sales (4) 23 — 23 39 — 39 Total segment sales 5,121 6,771 11,892 4,548 6,179 10,727 Other (5) 16 149 165 7 82 89 $ 5,137 $ 6,920 $ 12,057 $ 4,555 $ 6,261 $ 10,816 U.S. plus international may not equal total due to rounding. (1) Alliance revenue represents Merck’s share of profits, which are product sales net of cost of sales and commercialization costs (see Note 3). (2) Alliance revenue represents Merck’s share of profits from sales in Bayer’s marketing territories, which are product sales net of cost of sales and commercialization costs (see Note 3). (3) Other pharmaceutical primarily reflects sales of other human health pharmaceutical products, including products within the franchises not listed separately. (4) Represents sales for the Healthcare Services segment. All the businesses in the Healthcare Services segment were divested as of March 31, 2020. (5) |
Consolidated revenues by geographic area | Consolidated sales by geographic area where derived are as follows: Three Months Ended ($ in millions) 2020 2019 United States $ 5,137 $ 4,555 Europe, Middle East and Africa 3,534 3,103 China 864 746 Japan 811 799 Asia Pacific (other than China and Japan) 728 745 Latin America 556 561 Other 427 307 $ 12,057 $ 10,816 |
Reconciliation of segment profits to income before taxes | A reconciliation of segment profits to Income before taxes is as follows: Three Months Ended ($ in millions) 2020 2019 Segment profits: Pharmaceutical segment $ 7,477 $ 6,574 Animal Health segment 478 415 Other segment 1 2 Total segment profits 7,956 6,991 Other profits 139 30 Unallocated: Interest income 25 89 Interest expense (212 ) (209 ) Depreciation and amortization (381 ) (359 ) Research and development (2,097 ) (1,843 ) Amortization of purchase accounting adjustments (295 ) (397 ) Restructuring costs (72 ) (153 ) Other unallocated, net (1,225 ) (1,082 ) $ 3,838 $ 3,067 |
Acquisitions, Research Collab_3
Acquisitions, Research Collaborations and License Agreements - Acquisitions (Details) - ArQule $ in Millions | Jan. 16, 2020USD ($) |
Acquisitions Research Collaborations And License Agreements Transactions [Line Items] | |
Payment to acquire business | $ 2,700 |
Share-based compensation payments attributable to precombination service | 138 |
Transaction costs | $ 95 |
Acquisitions, Research Collab_4
Acquisitions, Research Collaborations and License Agreements - Fair Value of Assets Acquired and Liabilities Assumed (Details) $ in Millions | Mar. 31, 2020USD ($) | Jan. 16, 2020USD ($) | Dec. 31, 2019USD ($) |
Acquisitions Research Collaborations And License Agreements Transactions [Line Items] | |||
Goodwill | $ 19,767 | $ 19,425 | |
ArQule | |||
Acquisitions Research Collaborations And License Agreements Transactions [Line Items] | |||
Cash and cash equivalents | $ 145 | ||
Licensing arrangement | 80 | ||
Deferred income tax liabilities | (434) | ||
Other assets and liabilities, net | 35 | ||
Total identifiable net assets | 2,276 | ||
Goodwill | 414 | ||
Consideration transferred | $ 2,690 | ||
Measurement Input, Discount Rate | ArQule | |||
Acquisitions Research Collaborations And License Agreements Transactions [Line Items] | |||
Present value discount rate | 0.125 | ||
IPR&D MK-1026 | ArQule | |||
Acquisitions Research Collaborations And License Agreements Transactions [Line Items] | |||
IPR&D | $ 2,280 | ||
IPR&D MK-7075 | ArQule | |||
Acquisitions Research Collaborations And License Agreements Transactions [Line Items] | |||
IPR&D | $ 170 |
Collaborative Arrangements - Na
Collaborative Arrangements - Narrative (Details) - USD ($) $ in Millions | 1 Months Ended | 3 Months Ended | 12 Months Ended | 21 Months Ended | 29 Months Ended | 37 Months Ended | |||||||
Mar. 31, 2021 | Mar. 31, 2020 | Jan. 31, 2020 | Mar. 31, 2019 | Mar. 31, 2018 | Jul. 31, 2017 | Mar. 31, 2020 | Mar. 31, 2019 | Dec. 31, 2019 | Dec. 31, 2018 | Dec. 31, 2019 | Dec. 31, 2019 | Mar. 31, 2021 | |
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||||||||||||
Research and development | $ 2,209 | $ 1,931 | |||||||||||
Other liabilities, noncurrent | $ 11,550 | 11,550 | $ 11,970 | $ 11,970 | $ 11,970 | ||||||||
Lynparza | Other Assets | |||||||||||||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||||||||||||
Finite-lived intangible assets | 928 | 928 | |||||||||||
Lenvima | Other Assets | |||||||||||||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||||||||||||
Finite-lived intangible assets | 921 | 921 | |||||||||||
Adempas | Other intangible assets | |||||||||||||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||||||||||||
Finite-lived intangible assets | 844 | 844 | |||||||||||
AstraZeneca | |||||||||||||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||||||||||||
Upfront and milestone payments | $ 1,600 | ||||||||||||
License option payment related to collaborative arrangement | $ 750 | ||||||||||||
AstraZeneca | Sales-Based Milestones | |||||||||||||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||||||||||||
Contingent milestone payments collaborative arrangement | 3,100 | ||||||||||||
AstraZeneca | Sales-Based Milestones | Lynparza | |||||||||||||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||||||||||||
Probable contingent payments collaborative arrangement | $ 1,000 | ||||||||||||
Milestone payments made to collaborative partner | $ 250 | 200 | $ 250 | ||||||||||
AstraZeneca | Regulatory Milestones | Lynparza | |||||||||||||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||||||||||||
Milestone payments made to collaborative partner | 60 | 140 | |||||||||||
Contingent milestone payments collaborative arrangement | 1,700 | ||||||||||||
Eisai | |||||||||||||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||||||||||||
Upfront and milestone payments | $ 750 | ||||||||||||
License option payment related to collaborative arrangement | $ 200 | $ 325 | |||||||||||
Eisai | Forecast | |||||||||||||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||||||||||||
License option payment related to collaborative arrangement | $ 125 | $ 650 | |||||||||||
Eisai | Sales-Based Milestones | |||||||||||||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||||||||||||
Contingent milestone payments collaborative arrangement | 3,000 | ||||||||||||
Eisai | Sales-Based Milestones | Lenvima | |||||||||||||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||||||||||||
Probable contingent payments collaborative arrangement | $ 950 | ||||||||||||
Milestone payments made to collaborative partner | 300 | $ 50 | |||||||||||
Eisai | Regulatory Milestones | |||||||||||||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||||||||||||
Contingent milestone payments collaborative arrangement | 135 | ||||||||||||
Eisai | Regulatory Milestones | Lenvima | |||||||||||||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||||||||||||
Milestone payments made to collaborative partner | 250 | ||||||||||||
Bayer AG | Sales-Based Milestones | |||||||||||||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||||||||||||
Probable contingent payments collaborative arrangement | 725 | ||||||||||||
Milestone payments made to collaborative partner | $ 350 | ||||||||||||
Contingent milestone payments collaborative arrangement | $ 400 |
Collaborative Arrangements - Sc
Collaborative Arrangements - Schedule of Transactions (Details) - USD ($) $ in Millions | 3 Months Ended | ||
Mar. 31, 2020 | Mar. 31, 2019 | Dec. 31, 2019 | |
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||
Sales | $ 12,057 | $ 10,816 | |
Cost of sales | 3,312 | 3,052 | |
Selling, general and administrative | 2,555 | 2,425 | |
Research and development | 2,209 | 1,931 | |
Payables, current | 23,483 | $ 22,220 | |
Other current assets | AstraZeneca | Collaborative Arrangement | |||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||
Receivables | 142 | 128 | |
Other current assets | Eisai | Collaborative Arrangement | |||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||
Receivables | 140 | 150 | |
Other current assets | Bayer AG | Collaborative Arrangement | |||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||
Receivables | 50 | 49 | |
Accounts payable and accrued liabilities | AstraZeneca | Collaborative Arrangement | |||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||
Payables, current | 326 | 577 | |
Accounts payable and accrued liabilities | Eisai | Collaborative Arrangement | |||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||
Payables, current | 425 | 700 | |
Other Noncurrent Liabilities | Eisai | Collaborative Arrangement | |||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||
Payables, Noncurrent | 300 | 525 | |
Other Noncurrent Liabilities | Bayer AG | Collaborative Arrangement | |||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||
Payables, Noncurrent | 375 | $ 375 | |
Revenue | AstraZeneca | Collaborative Arrangement | |||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||
Sales | 145 | 79 | |
Revenue | Eisai | Collaborative Arrangement | |||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||
Sales | 128 | 74 | |
Revenue | Bayer AG | Collaborative Arrangement | |||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||
Net sales of Adempas recorded by Merck | 56 | 48 | |
Alliance revenue | 53 | 42 | |
Sales | 109 | 90 | |
Cost of sales | AstraZeneca | Collaborative Arrangement | |||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||
Cost of sales | 28 | 19 | |
Cost of sales | Eisai | Collaborative Arrangement | |||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||
Cost of sales | 35 | 51 | |
Cost of sales | Bayer AG | Collaborative Arrangement | |||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||
Cost of sales | 28 | 29 | |
Selling, general and administrative | AstraZeneca | Collaborative Arrangement | |||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||
Selling, general and administrative | 33 | 27 | |
Selling, general and administrative | Eisai | Collaborative Arrangement | |||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||
Selling, general and administrative | 11 | 19 | |
Selling, general and administrative | Bayer AG | Collaborative Arrangement | |||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||
Selling, general and administrative | 15 | 8 | |
Research and development | AstraZeneca | Collaborative Arrangement | |||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||
Research and development | 36 | 45 | |
Research and development | Eisai | Collaborative Arrangement | |||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||
Research and development | 64 | 47 | |
Research and development | Bayer AG | Collaborative Arrangement | |||
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items] | |||
Research and development | $ 25 | $ 30 |
Restructuring - Narrative (Deta
Restructuring - Narrative (Details) - USD ($) $ in Millions | 3 Months Ended | ||
Mar. 31, 2020 | Mar. 31, 2019 | Dec. 31, 2020 | |
Restructuring Cost and Reserve [Line Items] | |||
Cumulative costs since program inception | $ 1,100 | ||
Estimate of cumulative pre tax costs that will result in cash outlays | 60.00% | ||
Estimate of cumulative pre tax costs that will be noncash | 40.00% | ||
Expected restructuring and related cost | $ 2,500 | ||
Total pretax restructuring costs | $ 168 | $ 187 | |
Forecast | |||
Restructuring Cost and Reserve [Line Items] | |||
Expected restructuring and related cost | $ 800 |
Restructuring - Charges Activit
Restructuring - Charges Activities by Type of Cost (Details) - USD ($) $ in Millions | 3 Months Ended | |
Mar. 31, 2020 | Mar. 31, 2019 | |
Restructuring Cost and Reserve [Line Items] | ||
Total pretax restructuring costs | $ 168 | $ 187 |
Separation Costs | ||
Restructuring Cost and Reserve [Line Items] | ||
Total pretax restructuring costs | 47 | 128 |
Accelerated Depreciation | ||
Restructuring Cost and Reserve [Line Items] | ||
Total pretax restructuring costs | 53 | 34 |
Other | ||
Restructuring Cost and Reserve [Line Items] | ||
Total pretax restructuring costs | 68 | 25 |
Cost of sales | ||
Restructuring Cost and Reserve [Line Items] | ||
Total pretax restructuring costs | 68 | 34 |
Cost of sales | Separation Costs | ||
Restructuring Cost and Reserve [Line Items] | ||
Total pretax restructuring costs | 0 | 0 |
Cost of sales | Accelerated Depreciation | ||
Restructuring Cost and Reserve [Line Items] | ||
Total pretax restructuring costs | 25 | 34 |
Cost of sales | Other | ||
Restructuring Cost and Reserve [Line Items] | ||
Total pretax restructuring costs | 43 | 0 |
Selling, general and administrative | ||
Restructuring Cost and Reserve [Line Items] | ||
Total pretax restructuring costs | 11 | |
Selling, general and administrative | Separation Costs | ||
Restructuring Cost and Reserve [Line Items] | ||
Total pretax restructuring costs | 0 | |
Selling, general and administrative | Accelerated Depreciation | ||
Restructuring Cost and Reserve [Line Items] | ||
Total pretax restructuring costs | 11 | |
Selling, general and administrative | Other | ||
Restructuring Cost and Reserve [Line Items] | ||
Total pretax restructuring costs | 0 | |
Research and development | ||
Restructuring Cost and Reserve [Line Items] | ||
Total pretax restructuring costs | 17 | |
Research and development | Separation Costs | ||
Restructuring Cost and Reserve [Line Items] | ||
Total pretax restructuring costs | 0 | |
Research and development | Accelerated Depreciation | ||
Restructuring Cost and Reserve [Line Items] | ||
Total pretax restructuring costs | 17 | |
Research and development | Other | ||
Restructuring Cost and Reserve [Line Items] | ||
Total pretax restructuring costs | 0 | |
Restructuring costs | ||
Restructuring Cost and Reserve [Line Items] | ||
Total pretax restructuring costs | 72 | 153 |
Restructuring costs | Separation Costs | ||
Restructuring Cost and Reserve [Line Items] | ||
Total pretax restructuring costs | 47 | 128 |
Restructuring costs | Accelerated Depreciation | ||
Restructuring Cost and Reserve [Line Items] | ||
Total pretax restructuring costs | 0 | 0 |
Restructuring costs | Other | ||
Restructuring Cost and Reserve [Line Items] | ||
Total pretax restructuring costs | $ 25 | $ 25 |
Restructuring - Activities by P
Restructuring - Activities by Program (Details) - USD ($) $ in Millions | 3 Months Ended | |
Mar. 31, 2020 | Mar. 31, 2019 | |
Restructuring Reserve [Roll Forward] | ||
Restructuring reserve, beginning balance | $ 759 | |
Expense | 168 | $ 187 |
(Payments) receipts, net | (290) | |
Non-cash activity | (11) | |
Restructuring reserve, ending balance | 626 | |
Separation Costs | ||
Restructuring Reserve [Roll Forward] | ||
Restructuring reserve, beginning balance | 690 | |
Expense | 47 | 128 |
(Payments) receipts, net | (168) | |
Non-cash activity | 0 | |
Restructuring reserve, ending balance | 569 | |
Accelerated Depreciation | ||
Restructuring Reserve [Roll Forward] | ||
Restructuring reserve, beginning balance | 0 | |
Expense | 53 | 34 |
(Payments) receipts, net | 0 | |
Non-cash activity | (53) | |
Restructuring reserve, ending balance | 0 | |
Other | ||
Restructuring Reserve [Roll Forward] | ||
Restructuring reserve, beginning balance | 69 | |
Expense | 68 | $ 25 |
(Payments) receipts, net | (122) | |
Non-cash activity | 42 | |
Restructuring reserve, ending balance | $ 57 |
Financial Instruments - Narrati
Financial Instruments - Narrative (Details) | 3 Months Ended | |||
Mar. 31, 2020USD ($)interest_rate_swap | Dec. 31, 2019USD ($) | Mar. 31, 2019USD ($) | Feb. 29, 2020USD ($) | |
Derivative [Line Items] | ||||
Pretax net unrealized gain on derivatives maturing within next 12 months estimated to be reclassified from AOCI to sales | $ 136,000,000 | |||
Equity investments without readily determinable fair values | 450,000,000 | $ 542,000,000 | ||
Unrealized losses recognized on investments in equity securities without readily determinable fair values | 9,000,000 | |||
Cumulative unrealized gains on investments | 109,000,000 | |||
Cumulative unrealized losses on investments | 21,000,000 | |||
Payments of contingent consideration | 106,000,000 | $ 85,000,000 | ||
Fair value of loans payable and long-term debt, including current portion | 30,600,000,000 | $ 28,800,000,000 | ||
Debt, carrying amount | 28,000,000,000 | 26,300,000,000 | ||
Accounts Receivable, Sale | 1,900,000,000 | 2,700,000,000 | ||
Cash collateral received from counterparties | 216,000,000 | 34,000,000 | ||
Cash collateral advanced to counterparties | 0 | 0 | ||
Total swap notional amount | 27,453,000,000 | 30,666,000,000 | ||
Level 2 | ||||
Derivative [Line Items] | ||||
Cash equivalents | 6,800,000,000 | 8,900,000,000 | ||
Derivatives Designated as Hedging Instruments | ||||
Derivative [Line Items] | ||||
Total swap notional amount | $ 12,749,000,000 | 14,728,000,000 | ||
Derivatives Designated as Hedging Instruments | Maximum | ||||
Derivative [Line Items] | ||||
Maximum average period of maturities of contracts in years (less than) | 2 years | |||
Derivatives Not Designated as Hedging Instruments | ||||
Derivative [Line Items] | ||||
Total swap notional amount | $ 14,704,000,000 | $ 15,938,000,000 | ||
Derivatives Not Designated as Hedging Instruments | Maximum | ||||
Derivative [Line Items] | ||||
Maximum average period of maturities of contracts in years (less than) | 1 year | |||
1.85% Notes Due 2020 | ||||
Derivative [Line Items] | ||||
Face amount of debt | $ 1,250,000,000 | |||
Stated interest rate (as percent) | 1.85% | |||
Interest rate swap contracts | ||||
Derivative [Line Items] | ||||
Number of interest rate swaps held (in interest rate swaps) | 14 | 5 | ||
Total swap notional amount | $ 250,000,000 |
Financial Instruments - Effect
Financial Instruments - Effect of Net Investment Hedges (Details) - USD ($) $ in Millions | 3 Months Ended | |
Mar. 31, 2020 | Mar. 31, 2019 | |
Foreign exchange contracts | ||
Derivative Instruments, Gain (Loss) [Line Items] | ||
Amount of Pretax (Gain) Loss Recognized in Other Comprehensive Income | $ (3) | $ (11) |
Foreign exchange contracts | Other (income) expense, net | ||
Derivative Instruments, Gain (Loss) [Line Items] | ||
Amount of Pretax (Gain) Loss Recognized in Other (income) expense, net for Amounts Excluded from Effectiveness Testing | (8) | (8) |
Euro-denominated notes | ||
Derivative Instruments, Gain (Loss) [Line Items] | ||
Amount of Pretax (Gain) Loss Recognized in Other Comprehensive Income | (51) | (30) |
Euro-denominated notes | Other (income) expense, net | ||
Derivative Instruments, Gain (Loss) [Line Items] | ||
Amount of Pretax (Gain) Loss Recognized in Other (income) expense, net for Amounts Excluded from Effectiveness Testing | $ 0 | $ 0 |
Financial Instruments - Summary
Financial Instruments - Summary of Interest Rate Swaps Held (Details) | Mar. 31, 2020USD ($)interest_rate_swap | Feb. 29, 2020USD ($) | Dec. 31, 2019USD ($) |
Derivative [Line Items] | |||
Total swap notional amount | $ 27,453,000,000 | $ 30,666,000,000 | |
Interest rate swap contracts | |||
Derivative [Line Items] | |||
Number of Interest Rate Swaps Held (in interest rate swaps) | 14 | 5 | |
Total swap notional amount | $ 250,000,000 | ||
3.875% notes due 2021 | Interest rate swap contracts | |||
Derivative [Line Items] | |||
Stated interest rate (as percent) | 3.875% | ||
Par Value of Debt | $ 1,150,000,000 | ||
Number of Interest Rate Swaps Held (in interest rate swaps) | interest_rate_swap | 5 | ||
Total swap notional amount | $ 1,150,000,000 | ||
2.40% notes due 2022 | Interest rate swap contracts | |||
Derivative [Line Items] | |||
Stated interest rate (as percent) | 2.40% | ||
Par Value of Debt | $ 1,000,000,000 | ||
Number of Interest Rate Swaps Held (in interest rate swaps) | interest_rate_swap | 4 | ||
Total swap notional amount | $ 1,000,000,000 | ||
2.35% notes due 2022 | Interest rate swap contracts | |||
Derivative [Line Items] | |||
Stated interest rate (as percent) | 2.35% | ||
Par Value of Debt | $ 1,250,000,000 | ||
Number of Interest Rate Swaps Held (in interest rate swaps) | interest_rate_swap | 5 | ||
Total swap notional amount | $ 1,250,000,000 |
Financial Instruments - Fair Va
Financial Instruments - Fair Value Hedges (Details) - USD ($) $ in Millions | Mar. 31, 2020 | Dec. 31, 2019 |
Loans payable and current portion of long-term debt | ||
Derivative Instruments and Hedging Activities Disclosures [Line Items] | ||
Carrying Amount of Hedged Liabilities | $ 1,160 | $ 1,249 |
Cumulative Amount of Fair Value Hedging Adjustment Increase (Decrease) Included in the Carrying Amount | 11 | (1) |
Long-Term Debt | ||
Derivative Instruments and Hedging Activities Disclosures [Line Items] | ||
Carrying Amount of Hedged Liabilities | 2,315 | 3,409 |
Cumulative Amount of Fair Value Hedging Adjustment Increase (Decrease) Included in the Carrying Amount | $ 69 | $ 14 |
Financial Instruments - Fair _2
Financial Instruments - Fair Value of Derivatives Segregated between those Derivatives that are Designated as Hedging Instruments and those that are Not Designated as Hedging Instruments (Details) - USD ($) $ in Millions | Mar. 31, 2020 | Dec. 31, 2019 |
Derivatives, Fair Value [Line Items] | ||
Fair Value of Derivative, Asset | $ 710 | $ 288 |
Fair Value of Derivative, Liability | 93 | 97 |
U.S Dollar Notional Amount | 27,453 | 30,666 |
Derivatives Designated as Hedging Instruments | ||
Derivatives, Fair Value [Line Items] | ||
Fair Value of Derivative, Asset | 363 | 222 |
Fair Value of Derivative, Liability | 8 | 24 |
U.S Dollar Notional Amount | 12,749 | 14,728 |
Derivatives Not Designated as Hedging Instruments | ||
Derivatives, Fair Value [Line Items] | ||
Fair Value of Derivative, Asset | 347 | 66 |
Fair Value of Derivative, Liability | 85 | 73 |
U.S Dollar Notional Amount | 14,704 | 15,938 |
Interest rate swap contracts | Derivatives Designated as Hedging Instruments | Other current assets | ||
Derivatives, Fair Value [Line Items] | ||
Fair Value of Derivative, Asset | 11 | 0 |
U.S Dollar Notional Amount | 1,150 | 0 |
Interest rate swap contracts | Derivatives Designated as Hedging Instruments | Other Assets | ||
Derivatives, Fair Value [Line Items] | ||
Fair Value of Derivative, Asset | 70 | 15 |
U.S Dollar Notional Amount | 2,250 | 3,400 |
Interest rate swap contracts | Derivatives Designated as Hedging Instruments | Accrued and other current liabilities | ||
Derivatives, Fair Value [Line Items] | ||
Fair Value of Derivative, Liability | 0 | 1 |
U.S Dollar Notional Amount | 0 | 1,250 |
Foreign exchange contracts | Derivatives Designated as Hedging Instruments | Other current assets | ||
Derivatives, Fair Value [Line Items] | ||
Fair Value of Derivative, Asset | 194 | 152 |
U.S Dollar Notional Amount | 6,546 | 6,117 |
Foreign exchange contracts | Derivatives Designated as Hedging Instruments | Other Assets | ||
Derivatives, Fair Value [Line Items] | ||
Fair Value of Derivative, Asset | 88 | 55 |
U.S Dollar Notional Amount | 2,064 | 2,160 |
Foreign exchange contracts | Derivatives Designated as Hedging Instruments | Accrued and other current liabilities | ||
Derivatives, Fair Value [Line Items] | ||
Fair Value of Derivative, Liability | 7 | 22 |
U.S Dollar Notional Amount | 734 | 1,748 |
Foreign exchange contracts | Derivatives Designated as Hedging Instruments | Other Noncurrent Liabilities | ||
Derivatives, Fair Value [Line Items] | ||
Fair Value of Derivative, Liability | 1 | 1 |
U.S Dollar Notional Amount | 5 | 53 |
Foreign exchange contracts | Derivatives Not Designated as Hedging Instruments | Other current assets | ||
Derivatives, Fair Value [Line Items] | ||
Fair Value of Derivative, Asset | 347 | 66 |
U.S Dollar Notional Amount | 10,039 | 7,245 |
Foreign exchange contracts | Derivatives Not Designated as Hedging Instruments | Accrued and other current liabilities | ||
Derivatives, Fair Value [Line Items] | ||
Fair Value of Derivative, Liability | 85 | 73 |
U.S Dollar Notional Amount | $ 4,665 | $ 8,693 |
Financial Instruments - Informa
Financial Instruments - Information on Derivative Positions Subject to Master Netting Arrangements as if they were Presented on a Net Basis (Details) - USD ($) | Mar. 31, 2020 | Dec. 31, 2019 |
Derivative Instruments and Hedging Activities Disclosure [Abstract] | ||
Gross amounts recognized in the consolidated balance sheet, asset | $ 710,000,000 | $ 288,000,000 |
Gross amount subject to offset in master netting arrangements not offset in the condensed balance sheet, asset | (89,000,000) | (84,000,000) |
Cash collateral received, asset | (216,000,000) | (34,000,000) |
Net amounts, asset | 405,000,000 | 170,000,000 |
Gross amounts recognized in the consolidated balance sheet, liability | 93,000,000 | 97,000,000 |
Gross amount subject to offset in master netting arrangements not offset in the condensed balance sheet, liability | (89,000,000) | (84,000,000) |
Cash collateral received, liability | 0 | 0 |
Net amounts, liability | $ 4,000,000 | $ 13,000,000 |
Financial Instruments - Locatio
Financial Instruments - Location and Amount of Pretax (Gains) Losses of Derivatives (Details) - USD ($) $ in Millions | 3 Months Ended | |
Mar. 31, 2020 | Mar. 31, 2019 | |
Derivative Instruments, Gain (Loss) [Line Items] | ||
Sales | $ 12,057 | $ 10,816 |
Other (income) expense, net | 71 | 188 |
Other comprehensive income (loss) | (198) | 199 |
Interest rate swap contracts | ||
Derivative Instruments, Gain (Loss) [Line Items] | ||
Amount of gain (loss) recognized in OCI on derivatives | (1) | (4) |
Interest rate swap contracts | Other (income) expense, net | ||
Derivative Instruments, Gain (Loss) [Line Items] | ||
Hedged items | 67 | 33 |
Derivatives designated as hedging instruments | (67) | (23) |
Amount of gain recognized in Other (income) expense, net on derivatives | (1) | (1) |
Foreign exchange contracts | ||
Derivative Instruments, Gain (Loss) [Line Items] | ||
Amount of gain (loss) recognized in OCI on derivatives | 178 | (13) |
Increase (decrease) in Sales as a result of AOCI reclassifications | (46) | (44) |
Foreign exchange contracts | Reclassification out of Accumulated Other Comprehensive Income | Accumulated Gain (Loss), Cash Flow Hedge, Including Noncontrolling Interest | ||
Derivative Instruments, Gain (Loss) [Line Items] | ||
Sales | $ 46 | $ 44 |
Financial Instruments - Income
Financial Instruments - Income Statement Effects on Derivatives Not Designated as Hedging Instruments (Details) - USD ($) $ in Millions | 3 Months Ended | |
Mar. 31, 2020 | Mar. 31, 2019 | |
Foreign currency | Other (income) expense, net | ||
Derivative Instruments, Gain (Loss) [Line Items] | ||
Amount of Derivative Pretax (Gain) Loss Recognized in Income | $ (180) | $ 118 |
Forecasted transactions | Sales | ||
Derivative Instruments, Gain (Loss) [Line Items] | ||
Amount of Derivative Pretax (Gain) Loss Recognized in Income | $ (7) | $ 10 |
Financial Instruments - Infor_2
Financial Instruments - Information on Available-for-sale Investments (Details) - USD ($) $ in Millions | 3 Months Ended | ||
Mar. 31, 2020 | Mar. 31, 2019 | Dec. 31, 2019 | |
Debt Securities, Available-for-sale [Line Items] | |||
Debt securities, amortized cost | $ 64 | $ 1,768 | |
Debt securities, unrealized gains | 0 | 17 | |
Debt securities, unrealized losses | 0 | 0 | |
Debt securities, fair value | 64 | 1,785 | |
Publicly traded equity securities, fair value | 779 | 838 | |
Total debt and publicly traded equity securities, fair value | 843 | 2,623 | |
Unrealized net losses (gains) | 4 | $ (114) | |
U.S. government and agency securities | |||
Debt Securities, Available-for-sale [Line Items] | |||
Debt securities, amortized cost | 62 | 266 | |
Debt securities, unrealized gains | 0 | 3 | |
Debt securities, unrealized losses | 0 | 0 | |
Debt securities, fair value | 62 | 269 | |
Foreign government bonds | |||
Debt Securities, Available-for-sale [Line Items] | |||
Debt securities, amortized cost | 2 | 0 | |
Debt securities, unrealized gains | 0 | 0 | |
Debt securities, unrealized losses | 0 | 0 | |
Debt securities, fair value | 2 | 0 | |
Commercial paper | |||
Debt Securities, Available-for-sale [Line Items] | |||
Debt securities, amortized cost | 0 | 668 | |
Debt securities, unrealized gains | 0 | 0 | |
Debt securities, unrealized losses | 0 | 0 | |
Debt securities, fair value | 0 | 668 | |
Corporate notes and bonds | |||
Debt Securities, Available-for-sale [Line Items] | |||
Debt securities, amortized cost | 0 | 608 | |
Debt securities, unrealized gains | 0 | 13 | |
Debt securities, unrealized losses | 0 | 0 | |
Debt securities, fair value | 0 | 621 | |
Asset-backed securities | |||
Debt Securities, Available-for-sale [Line Items] | |||
Debt securities, amortized cost | 0 | 226 | |
Debt securities, unrealized gains | 0 | 1 | |
Debt securities, unrealized losses | 0 | 0 | |
Debt securities, fair value | $ 0 | $ 227 |
Financial Instruments - Financi
Financial Instruments - Financial Assets and Liabilities Measured at Fair Value on Recurring Basis (Details) - USD ($) $ in Millions | 3 Months Ended | |||
Mar. 31, 2020 | Dec. 31, 2019 | Mar. 31, 2019 | Dec. 31, 2018 | |
Assets | ||||
Investments | $ 64 | $ 1,785 | ||
Publicly traded equity securities | 779 | 838 | ||
Derivative assets | 710 | 288 | ||
Liabilities | ||||
Contingent consideration | 694 | 767 | $ 667 | $ 788 |
Derivative liabilities | 93 | 97 | ||
Foreign government bonds | ||||
Assets | ||||
Investments | 2 | 0 | ||
Corporate notes and bonds | ||||
Assets | ||||
Investments | 0 | 621 | ||
Commercial paper | ||||
Assets | ||||
Investments | 0 | 668 | ||
Asset-backed securities | ||||
Assets | ||||
Investments | $ 0 | 227 | ||
Liabilities | ||||
Primary weighted average life of collateral | 5 years | |||
U.S. government and agency securities | ||||
Assets | ||||
Investments | $ 62 | 269 | ||
Fair Value, Measurements, Recurring | ||||
Assets | ||||
Investments | 562 | 2,243 | ||
Other assets | 281 | 380 | ||
Derivative assets | 710 | 288 | ||
Total assets | 1,553 | 2,911 | ||
Liabilities | ||||
Contingent consideration | 694 | 767 | ||
Derivative liabilities | 93 | 97 | ||
Total liabilities | 787 | 864 | ||
Fair Value, Measurements, Recurring | Foreign exchange contracts | ||||
Assets | ||||
Derivative assets | 455 | 169 | ||
Liabilities | ||||
Derivative liabilities | 90 | 95 | ||
Fair Value, Measurements, Recurring | Interest rate swap contracts | ||||
Assets | ||||
Derivative assets | 81 | 15 | ||
Fair Value, Measurements, Recurring | Currency options | ||||
Assets | ||||
Derivative assets | 174 | 104 | ||
Liabilities | ||||
Derivative liabilities | 3 | 1 | ||
Fair Value, Measurements, Recurring | Interest rate swap contracts | ||||
Liabilities | ||||
Derivative liabilities | 0 | 1 | ||
Fair Value, Measurements, Recurring | Level 1 | ||||
Assets | ||||
Investments | 560 | 518 | ||
Other assets | 281 | 380 | ||
Derivative assets | 0 | 0 | ||
Total assets | 841 | 898 | ||
Liabilities | ||||
Contingent consideration | 0 | 0 | ||
Derivative liabilities | 0 | 0 | ||
Total liabilities | 0 | 0 | ||
Fair Value, Measurements, Recurring | Level 1 | Foreign exchange contracts | ||||
Assets | ||||
Derivative assets | 0 | 0 | ||
Liabilities | ||||
Derivative liabilities | 0 | 0 | ||
Fair Value, Measurements, Recurring | Level 1 | Interest rate swap contracts | ||||
Assets | ||||
Derivative assets | 0 | 0 | ||
Fair Value, Measurements, Recurring | Level 1 | Currency options | ||||
Assets | ||||
Derivative assets | 0 | 0 | ||
Liabilities | ||||
Derivative liabilities | 0 | 0 | ||
Fair Value, Measurements, Recurring | Level 1 | Interest rate swap contracts | ||||
Liabilities | ||||
Derivative liabilities | 0 | 0 | ||
Fair Value, Measurements, Recurring | Level 2 | ||||
Assets | ||||
Investments | 2 | 1,725 | ||
Other assets | 0 | 0 | ||
Derivative assets | 710 | 288 | ||
Total assets | 712 | 2,013 | ||
Liabilities | ||||
Contingent consideration | 0 | 0 | ||
Derivative liabilities | 93 | 97 | ||
Total liabilities | 93 | 97 | ||
Fair Value, Measurements, Recurring | Level 2 | Foreign exchange contracts | ||||
Assets | ||||
Derivative assets | 455 | 169 | ||
Liabilities | ||||
Derivative liabilities | 90 | 95 | ||
Fair Value, Measurements, Recurring | Level 2 | Interest rate swap contracts | ||||
Assets | ||||
Derivative assets | 81 | 15 | ||
Fair Value, Measurements, Recurring | Level 2 | Currency options | ||||
Assets | ||||
Derivative assets | 174 | 104 | ||
Liabilities | ||||
Derivative liabilities | 3 | 1 | ||
Fair Value, Measurements, Recurring | Level 2 | Interest rate swap contracts | ||||
Liabilities | ||||
Derivative liabilities | 0 | 1 | ||
Fair Value, Measurements, Recurring | Level 3 | ||||
Assets | ||||
Investments | 0 | 0 | ||
Other assets | 0 | 0 | ||
Derivative assets | 0 | 0 | ||
Total assets | 0 | 0 | ||
Liabilities | ||||
Contingent consideration | 694 | 767 | ||
Derivative liabilities | 0 | 0 | ||
Total liabilities | 694 | 767 | ||
Fair Value, Measurements, Recurring | Level 3 | Foreign exchange contracts | ||||
Assets | ||||
Derivative assets | 0 | 0 | ||
Liabilities | ||||
Derivative liabilities | 0 | 0 | ||
Fair Value, Measurements, Recurring | Level 3 | Interest rate swap contracts | ||||
Assets | ||||
Derivative assets | 0 | 0 | ||
Fair Value, Measurements, Recurring | Level 3 | Currency options | ||||
Assets | ||||
Derivative assets | 0 | 0 | ||
Liabilities | ||||
Derivative liabilities | 0 | 0 | ||
Fair Value, Measurements, Recurring | Level 3 | Interest rate swap contracts | ||||
Liabilities | ||||
Derivative liabilities | 0 | 0 | ||
Fair Value, Measurements, Recurring | Foreign government bonds | ||||
Assets | ||||
Investments | 2 | 0 | ||
Fair Value, Measurements, Recurring | Foreign government bonds | Level 1 | ||||
Assets | ||||
Investments | 0 | 0 | ||
Fair Value, Measurements, Recurring | Foreign government bonds | Level 2 | ||||
Assets | ||||
Investments | 2 | 0 | ||
Fair Value, Measurements, Recurring | Foreign government bonds | Level 3 | ||||
Assets | ||||
Investments | 0 | 0 | ||
Fair Value, Measurements, Recurring | Corporate notes and bonds | ||||
Assets | ||||
Investments | 0 | 621 | ||
Fair Value, Measurements, Recurring | Corporate notes and bonds | Level 1 | ||||
Assets | ||||
Investments | 0 | 0 | ||
Fair Value, Measurements, Recurring | Corporate notes and bonds | Level 2 | ||||
Assets | ||||
Investments | 0 | 621 | ||
Fair Value, Measurements, Recurring | Corporate notes and bonds | Level 3 | ||||
Assets | ||||
Investments | 0 | 0 | ||
Fair Value, Measurements, Recurring | Commercial paper | ||||
Assets | ||||
Investments | 0 | 668 | ||
Fair Value, Measurements, Recurring | Commercial paper | Level 1 | ||||
Assets | ||||
Investments | 0 | 0 | ||
Fair Value, Measurements, Recurring | Commercial paper | Level 2 | ||||
Assets | ||||
Investments | 0 | 668 | ||
Fair Value, Measurements, Recurring | Commercial paper | Level 3 | ||||
Assets | ||||
Investments | 0 | 0 | ||
Fair Value, Measurements, Recurring | Asset-backed securities | ||||
Assets | ||||
Investments | 0 | 227 | ||
Fair Value, Measurements, Recurring | Asset-backed securities | Level 1 | ||||
Assets | ||||
Investments | 0 | 0 | ||
Fair Value, Measurements, Recurring | Asset-backed securities | Level 2 | ||||
Assets | ||||
Investments | 0 | 227 | ||
Fair Value, Measurements, Recurring | Asset-backed securities | Level 3 | ||||
Assets | ||||
Investments | 0 | 0 | ||
Fair Value, Measurements, Recurring | U.S. government and agency securities | ||||
Assets | ||||
Investments | 0 | 209 | ||
Other assets | 62 | 60 | ||
Fair Value, Measurements, Recurring | U.S. government and agency securities | Level 1 | ||||
Assets | ||||
Investments | 0 | 0 | ||
Other assets | 62 | 60 | ||
Fair Value, Measurements, Recurring | U.S. government and agency securities | Level 2 | ||||
Assets | ||||
Investments | 0 | 209 | ||
Other assets | 0 | 0 | ||
Fair Value, Measurements, Recurring | U.S. government and agency securities | Level 3 | ||||
Assets | ||||
Investments | 0 | 0 | ||
Other assets | 0 | 0 | ||
Fair Value, Measurements, Recurring | Publicly traded equity securities | ||||
Assets | ||||
Publicly traded equity securities | 560 | 518 | ||
Other assets | 219 | 320 | ||
Fair Value, Measurements, Recurring | Publicly traded equity securities | Level 1 | ||||
Assets | ||||
Publicly traded equity securities | 560 | 518 | ||
Other assets | 219 | 320 | ||
Fair Value, Measurements, Recurring | Publicly traded equity securities | Level 2 | ||||
Assets | ||||
Publicly traded equity securities | 0 | 0 | ||
Other assets | 0 | 0 | ||
Fair Value, Measurements, Recurring | Publicly traded equity securities | Level 3 | ||||
Assets | ||||
Publicly traded equity securities | 0 | 0 | ||
Other assets | $ 0 | $ 0 |
Financial Instruments - Infor_3
Financial Instruments - Information About Changes in Liabilities for Contingent Consideration (Details) $ in Millions | 3 Months Ended | |||
Mar. 31, 2020USD ($) | Mar. 31, 2019USD ($) | Mar. 31, 2020USD ($) | Dec. 31, 2019USD ($) | |
Fair Value, Liabilities Measured on Recurring Basis, Unobservable Input Reconciliation, Calculation [Roll Forward] | ||||
Fair value, beginning balance | $ 767 | $ 788 | ||
Changes in estimated fair value | 33 | (36) | ||
Payments | (106) | (85) | ||
Fair value, ending balance | 694 | 667 | ||
Current liability | $ 119 | |||
Contingent consideration | 694 | $ 667 | 694 | $ 767 |
Sanofi Pasteur | ||||
Fair Value, Liabilities Measured on Recurring Basis, Unobservable Input Reconciliation, Calculation [Roll Forward] | ||||
Fair value, beginning balance | 625 | |||
Fair value, ending balance | 520 | |||
Contingent consideration | $ 625 | $ 520 | $ 625 | |
Contingent consideration, measurement input, discount rate (as percent) | 0.115 | |||
Measurement Input, Discount Rate | Sanofi Pasteur | ||||
Fair Value, Liabilities Measured on Recurring Basis, Unobservable Input Reconciliation, Calculation [Roll Forward] | ||||
Contingent consideration, measurement input, discount rate (as percent) | 0.08 |
Inventories - Inventories (Deta
Inventories - Inventories (Details) - USD ($) $ in Millions | Mar. 31, 2020 | Dec. 31, 2019 |
Inventory Disclosure [Abstract] | ||
Finished goods | $ 1,753 | $ 1,772 |
Raw materials and work in process | 5,629 | 5,650 |
Supplies | 232 | 207 |
Total (approximates current cost) | 7,614 | 7,629 |
Decrease to LIFO cost | (138) | (171) |
Total current and noncurrent inventories | 7,476 | 7,458 |
Recognized as: | ||
Inventories | 5,846 | 5,978 |
Other assets | $ 1,630 | $ 1,480 |
Inventories - Narrative (Detail
Inventories - Narrative (Details) - USD ($) $ in Millions | Mar. 31, 2020 | Dec. 31, 2019 |
Inventory [Line Items] | ||
Inventories classified in Other assets | $ 1,630 | $ 1,480 |
Inventories Not Expected to be Sold Within One Year | ||
Inventory [Line Items] | ||
Inventories classified in Other assets | 1,400 | 1,300 |
Inventories Produced in Preparation for Product Launches | ||
Inventory [Line Items] | ||
Inventories classified in Other assets | $ 258 | $ 168 |
Contingencies - Narrative (Deta
Contingencies - Narrative (Details) $ in Millions | 1 Months Ended | ||
Mar. 31, 2014Case | Mar. 31, 2020USD ($)ClaimCase | Dec. 31, 2019USD ($) | |
Legal Defense Costs | |||
Loss Contingencies [Line Items] | |||
Legal defense costs reserve | $ | $ 255 | $ 240 | |
Fosamax | |||
Loss Contingencies [Line Items] | |||
Loss contingency, pending claims, number (in legal matters) | 3,590 | ||
Fosamax | Femur Fracture Litigation | Federal | |||
Loss Contingencies [Line Items] | |||
Loss contingency, pending claims, number (in legal matters) | 970 | ||
Loss contingency, claims dismissed, number (in legal matters) | 650 | ||
Loss contingency, claims on appeal, number (in legal matters) | 515 | ||
Fosamax | Femur Fracture Litigation | New Jersey state court | |||
Loss Contingencies [Line Items] | |||
Loss contingency, pending claims, number (in legal matters) | 2,345 | ||
Fosamax | Femur Fracture Litigation | California state court | |||
Loss Contingencies [Line Items] | |||
Loss contingency, pending claims, number (in legal matters) | 275 | ||
Fosamax | Femur Fracture Litigation | Other state courts | |||
Loss Contingencies [Line Items] | |||
Loss contingency, pending claims, number (in legal matters) | 4 | ||
Januvia | |||
Loss Contingencies [Line Items] | |||
Loss contingency, pending claims, number (in legal matters) | Claim | 1,410 | ||
Januvia | Other state courts | |||
Loss Contingencies [Line Items] | |||
Loss contingency, pending claims, number (in legal matters) | Claim | 6 | ||
Januvia | Cases Company Agreed To Toll Statute Of Limitations | |||
Loss Contingencies [Line Items] | |||
Loss contingency, pending claims, number (in legal matters) | Claim | 50 |
Equity - Rollforward Reconcilia
Equity - Rollforward Reconciliations (Details) - USD ($) $ / shares in Units, $ in Millions | 3 Months Ended | |
Mar. 31, 2020 | Mar. 31, 2019 | |
Increase (Decrease) in Stockholders' Equity [Roll Forward] | ||
Shares, beginning balance (in shares) | 3,577,103,522 | |
Equity, beginning balance | $ 26,001 | $ 26,882 |
Net income attributable to Merck & Co., Inc. | 3,219 | 2,915 |
Other comprehensive income (loss), net of taxes | (198) | 199 |
Cash dividends declared on common stock | (1,549) | (1,429) |
Treasury stock shares purchased | (1,281) | (1,090) |
Share-based compensation plans and other | 107 | 243 |
Net income (loss) attributable to noncontrolling interests | 0 | (53) |
Noncontrolling interest, changes in ownership interest, other | $ 1 | 3 |
Shares, ending balance (in shares) | 3,577,103,522 | |
Equity, ending balance | $ 26,300 | $ 27,670 |
Cash dividends declared on common stock (in dollars per share) | $ 0.61 | $ 0.55 |
Common Stock | ||
Increase (Decrease) in Stockholders' Equity [Roll Forward] | ||
Shares, beginning balance (in shares) | 3,577,000,000 | 3,577,000,000 |
Equity, beginning balance | $ 1,788 | $ 1,788 |
Shares, ending balance (in shares) | 3,577,000,000 | 3,577,000,000 |
Equity, ending balance | $ 1,788 | $ 1,788 |
Other Paid-In Capital | ||
Increase (Decrease) in Stockholders' Equity [Roll Forward] | ||
Equity, beginning balance | 39,660 | 38,808 |
Share-based compensation plans and other | 37 | (40) |
Equity, ending balance | 39,697 | 38,768 |
Retained Earnings | ||
Increase (Decrease) in Stockholders' Equity [Roll Forward] | ||
Equity, beginning balance | 46,602 | 42,579 |
Net income attributable to Merck & Co., Inc. | 3,219 | 2,915 |
Cash dividends declared on common stock | (1,549) | (1,429) |
Equity, ending balance | 48,272 | 44,065 |
Accumulated Other Comprehensive Loss | ||
Increase (Decrease) in Stockholders' Equity [Roll Forward] | ||
Equity, beginning balance | (6,193) | (5,545) |
Other comprehensive income (loss), net of taxes | (198) | 199 |
Equity, ending balance | $ (6,391) | $ (5,346) |
Treasury Stock | ||
Increase (Decrease) in Stockholders' Equity [Roll Forward] | ||
Shares, beginning balance (in shares) | 1,038,000,000 | 985,000,000 |
Equity, beginning balance | $ (55,950) | $ (50,929) |
Treasury stock shares purchased (in shares) | 16,000,000 | 14,000,000 |
Treasury stock shares purchased | $ (1,281) | $ (1,090) |
Share-based compensation plans and other (in shares) | (1,000,000) | (5,000,000) |
Share-based compensation plans and other | $ 70 | $ 283 |
Shares, ending balance (in shares) | 1,053,000,000 | 994,000,000 |
Equity, ending balance | $ (57,161) | $ (51,736) |
Non- controlling Interests | ||
Increase (Decrease) in Stockholders' Equity [Roll Forward] | ||
Equity, beginning balance | 94 | 181 |
Net income (loss) attributable to noncontrolling interests | (53) | |
Noncontrolling interest, changes in ownership interest, other | 1 | 3 |
Equity, ending balance | $ 95 | $ 131 |
Share-Based Compensation Plan_2
Share-Based Compensation Plans - Expense Allocations (Details) - USD ($) $ in Millions | 3 Months Ended | |
Mar. 31, 2020 | Mar. 31, 2019 | |
Share-based Payment Arrangement [Abstract] | ||
Pretax share-based compensation expense | $ 108 | $ 93 |
Income tax benefit | (15) | (14) |
Total share-based compensation expense, net of taxes | $ 93 | $ 79 |
Share-Based Compensation Plan_3
Share-Based Compensation Plans - Narrative (Details) - USD ($) $ / shares in Units, shares in Thousands, $ in Billions | 3 Months Ended | |
Mar. 31, 2020 | Mar. 31, 2019 | |
Share-based Compensation Arrangement by Share-based Payment Award [Line Items] | ||
Total pretax unrecognized compensation expense related to nonvested stock options, RSU and PSU awards | $ 1.1 | |
Weighted average period in years of recognition for nonvested stock options, RSU and PSU awards | 2 years 4 months 24 days | |
Restricted Stock Units (RSUs) | ||
Share-based Compensation Arrangement by Share-based Payment Award [Line Items] | ||
Shares granted (in shares) | 58 | 70 |
Weighted-average fair value per share granted (in dollars per share) | $ 85.66 | $ 77.39 |
Performance Share Units (PSUs) | ||
Share-based Compensation Arrangement by Share-based Payment Award [Line Items] | ||
Shares granted (in shares) | 770 | 609 |
Weighted-average fair value per share granted (in dollars per share) | $ 75.65 | $ 90.50 |
Pension and Other Postretirem_3
Pension and Other Postretirement Benefit Plans (Details) - USD ($) $ in Millions | 3 Months Ended | |
Mar. 31, 2020 | Mar. 31, 2019 | |
Other Postretirement Benefit Plans | ||
Defined Benefit Plan Disclosure [Line Items] | ||
Service cost | $ 13 | $ 12 |
Interest cost | 14 | 17 |
Expected return on plan assets | (19) | (18) |
Amortization of unrecognized prior service credit | (22) | (21) |
Net periodic benefit cost | (14) | (10) |
U.S. | Pension Plans | ||
Defined Benefit Plan Disclosure [Line Items] | ||
Service cost | 86 | 71 |
Interest cost | 109 | 114 |
Expected return on plan assets | (194) | (206) |
Amortization of unrecognized prior service credit | (12) | (12) |
Net loss amortization | 75 | 35 |
Termination benefits | 3 | 2 |
Curtailments | 2 | 0 |
Net periodic benefit cost | 69 | 4 |
International | Pension Plans | ||
Defined Benefit Plan Disclosure [Line Items] | ||
Service cost | 74 | 60 |
Interest cost | 34 | 45 |
Expected return on plan assets | (103) | (108) |
Amortization of unrecognized prior service credit | (3) | (3) |
Net loss amortization | 31 | 16 |
Termination benefits | 1 | 0 |
Curtailments | (1) | 0 |
Net periodic benefit cost | $ 33 | $ 10 |
Other (Income) Expense, Net (De
Other (Income) Expense, Net (Details) - USD ($) $ in Millions | 3 Months Ended | |
Mar. 31, 2020 | Mar. 31, 2019 | |
Other Income and Expenses [Abstract] | ||
Interest income | $ (25) | $ (89) |
Interest expense | 212 | 209 |
Exchange losses | 54 | 101 |
(Income) loss from investments in equity securities, net (1) | (52) | 25 |
Net periodic defined benefit plan (credit) cost other than service cost | (90) | (141) |
Other, net | (28) | 83 |
Other (income) expense, net | $ 71 | $ 188 |
Other (Income) Expense, Net Oth
Other (Income) Expense, Net Other (Income) Expense, Net - Narrative (Details) - USD ($) $ in Millions | 3 Months Ended | |
Mar. 31, 2020 | Mar. 31, 2019 | |
Component of Other Income / Expense of Nonoperating [Line Items] | ||
Interest paid | $ 250 | $ 195 |
Healthcare Services Segment | ||
Component of Other Income / Expense of Nonoperating [Line Items] | ||
Goodwill, Impairment Loss | $ 84 |
Taxes on Income (Details)
Taxes on Income (Details) - USD ($) $ in Millions | 3 Months Ended | |
Mar. 31, 2020 | Mar. 31, 2019 | |
Income Tax Examination [Line Items] | ||
Effective income tax rate (as percent) | 16.10% | 6.70% |
Internal Revenue Service (IRS) | Domestic Tax Authority | ||
Income Tax Examination [Line Items] | ||
Tax benefit recognized related to settlement | $ 360 | |
Income taxes paid | $ 107 |
Earnings Per Share (Details)
Earnings Per Share (Details) - USD ($) $ / shares in Units, shares in Millions, $ in Millions | 3 Months Ended | |
Mar. 31, 2020 | Mar. 31, 2019 | |
Earnings Per Share [Abstract] | ||
Net income attributable to Merck & Co., Inc. | $ 3,219 | $ 2,915 |
Average common shares outstanding | 2,533 | 2,585 |
Common shares issuable (1) | 14 | 18 |
Average common shares outstanding assuming dilution | 2,547 | 2,603 |
Basic earnings per common share attributable to Merck & Co., Inc. common shareholders | $ 1.27 | $ 1.13 |
Earnings per common share assuming dilution attributable to Merck & Co., Inc. common shareholders | $ 1.26 | $ 1.12 |
Common shares issuable under share-based compensation plans excluded from diluted earnings per common share because the effect would have been antidilutive (in shares) | 2 | 2 |
Other Comprehensive Income (L_3
Other Comprehensive Income (Loss) (Details) - USD ($) $ in Millions | 3 Months Ended | |
Mar. 31, 2020 | Mar. 31, 2019 | |
Accumulated Other Comprehensive Income (Loss) [Roll Forward] | ||
Equity, beginning balance | $ 26,001 | $ 26,882 |
Other comprehensive income (loss) before reclassification adjustments, pretax | (152) | 218 |
Tax | (43) | 3 |
Other comprehensive income (loss) before reclassification adjustments, net of taxes | (195) | 221 |
Reclassification adjustments, pretax | 1 | (28) |
Tax | (4) | 6 |
Reclassification adjustments, net of taxes | (3) | (22) |
Other comprehensive income (loss), net of taxes | (198) | 199 |
Equity, ending balance | 26,300 | 27,670 |
Derivatives | ||
Accumulated Other Comprehensive Income (Loss) [Roll Forward] | ||
Equity, beginning balance | 31 | 166 |
Other comprehensive income (loss) before reclassification adjustments, pretax | 178 | (13) |
Tax | (37) | 3 |
Other comprehensive income (loss) before reclassification adjustments, net of taxes | 141 | (10) |
Reclassification adjustments, pretax | (47) | (48) |
Tax | 10 | 10 |
Reclassification adjustments, net of taxes | (37) | (38) |
Other comprehensive income (loss), net of taxes | 104 | (48) |
Equity, ending balance | 135 | 118 |
Investments | ||
Accumulated Other Comprehensive Income (Loss) [Roll Forward] | ||
Equity, beginning balance | 18 | (78) |
Other comprehensive income (loss) before reclassification adjustments, pretax | 3 | 76 |
Tax | 0 | 0 |
Other comprehensive income (loss) before reclassification adjustments, net of taxes | 3 | 76 |
Reclassification adjustments, pretax | (21) | 6 |
Tax | 0 | 0 |
Reclassification adjustments, net of taxes | (21) | 6 |
Other comprehensive income (loss), net of taxes | (18) | 82 |
Equity, ending balance | 0 | 4 |
Employee Benefit Plans | ||
Accumulated Other Comprehensive Income (Loss) [Roll Forward] | ||
Equity, beginning balance | (4,261) | (3,556) |
Other comprehensive income (loss) before reclassification adjustments, pretax | 0 | (1) |
Tax | 5 | 6 |
Other comprehensive income (loss) before reclassification adjustments, net of taxes | 5 | 5 |
Reclassification adjustments, pretax | 69 | 14 |
Tax | (14) | (4) |
Reclassification adjustments, net of taxes | 55 | 10 |
Other comprehensive income (loss), net of taxes | 60 | 15 |
Equity, ending balance | (4,201) | (3,541) |
Cumulative Translation Adjustment | ||
Accumulated Other Comprehensive Income (Loss) [Roll Forward] | ||
Equity, beginning balance | (1,981) | (2,077) |
Other comprehensive income (loss) before reclassification adjustments, pretax | (333) | 156 |
Tax | (11) | (6) |
Other comprehensive income (loss) before reclassification adjustments, net of taxes | (344) | 150 |
Reclassification adjustments, pretax | 0 | 0 |
Tax | 0 | 0 |
Reclassification adjustments, net of taxes | 0 | 0 |
Other comprehensive income (loss), net of taxes | (344) | 150 |
Equity, ending balance | (2,325) | (1,927) |
Accumulated Other Comprehensive Income (Loss) | ||
Accumulated Other Comprehensive Income (Loss) [Roll Forward] | ||
Equity, beginning balance | (6,193) | (5,545) |
Equity, ending balance | $ (6,391) | $ (5,346) |
Segment Reporting - Narrative (
Segment Reporting - Narrative (Details) $ in Billions | 3 Months Ended | |
Mar. 31, 2020USD ($)segment | Mar. 31, 2019USD ($) | |
Segment Reporting [Abstract] | ||
Number of operating segments | segment | 3 | |
Sales discounts | $ | $ 3.2 | $ 2.6 |
Segment Reporting - Sales of Co
Segment Reporting - Sales of Company's Products (Details) - USD ($) $ in Millions | 3 Months Ended | |
Mar. 31, 2020 | Mar. 31, 2019 | |
Segment Reporting Information [Line Items] | ||
Sales | $ 12,057 | $ 10,816 |
Proceeds from Sale of Intangible Assets | 75 | 15 |
Operating Segments | ||
Segment Reporting Information [Line Items] | ||
Sales | 11,892 | 10,727 |
Other | ||
Segment Reporting Information [Line Items] | ||
Sales | 165 | 89 |
United States | ||
Segment Reporting Information [Line Items] | ||
Sales | 5,137 | 4,555 |
United States | Operating Segments | ||
Segment Reporting Information [Line Items] | ||
Sales | 5,121 | 4,548 |
United States | Other | ||
Segment Reporting Information [Line Items] | ||
Sales | 16 | 7 |
International | ||
Segment Reporting Information [Line Items] | ||
Sales | 6,920 | 6,261 |
International | Operating Segments | ||
Segment Reporting Information [Line Items] | ||
Sales | 6,771 | 6,179 |
International | Other | ||
Segment Reporting Information [Line Items] | ||
Sales | 149 | 82 |
Total Pharmaceutical segment sales | Operating Segments | ||
Segment Reporting Information [Line Items] | ||
Sales | 10,655 | 9,663 |
Total Pharmaceutical segment sales | Operating Segments | Keytruda | ||
Segment Reporting Information [Line Items] | ||
Sales | 3,284 | 2,269 |
Total Pharmaceutical segment sales | Operating Segments | Alliance revenue - Lynparza (1) | ||
Segment Reporting Information [Line Items] | ||
Sales | 145 | 79 |
Total Pharmaceutical segment sales | Operating Segments | Alliance revenue - Lenvima (1) | ||
Segment Reporting Information [Line Items] | ||
Sales | 128 | 74 |
Total Pharmaceutical segment sales | Operating Segments | Emend | ||
Segment Reporting Information [Line Items] | ||
Sales | 43 | 117 |
Total Pharmaceutical segment sales | Operating Segments | Gardasil/Gardasil 9 | ||
Segment Reporting Information [Line Items] | ||
Sales | 1,097 | 838 |
Total Pharmaceutical segment sales | Operating Segments | ProQuad/M-M-R II/Varivax | ||
Segment Reporting Information [Line Items] | ||
Sales | 435 | 496 |
Total Pharmaceutical segment sales | Operating Segments | Pneumovax 23 | ||
Segment Reporting Information [Line Items] | ||
Sales | 256 | 185 |
Total Pharmaceutical segment sales | Operating Segments | RotaTeq | ||
Segment Reporting Information [Line Items] | ||
Sales | 222 | 211 |
Total Pharmaceutical segment sales | Operating Segments | Vaqta | ||
Segment Reporting Information [Line Items] | ||
Sales | 60 | 47 |
Total Pharmaceutical segment sales | Operating Segments | Bridion | ||
Segment Reporting Information [Line Items] | ||
Sales | 299 | 255 |
Total Pharmaceutical segment sales | Operating Segments | Noxafil | ||
Segment Reporting Information [Line Items] | ||
Sales | 94 | 190 |
Total Pharmaceutical segment sales | Operating Segments | Invanz | ||
Segment Reporting Information [Line Items] | ||
Sales | 64 | 72 |
Total Pharmaceutical segment sales | Operating Segments | Prevymis | ||
Segment Reporting Information [Line Items] | ||
Sales | 60 | 32 |
Total Pharmaceutical segment sales | Operating Segments | Cancidas | ||
Segment Reporting Information [Line Items] | ||
Sales | 55 | 61 |
Total Pharmaceutical segment sales | Operating Segments | Primaxin | ||
Segment Reporting Information [Line Items] | ||
Sales | 51 | 59 |
Total Pharmaceutical segment sales | Operating Segments | Cubicin | ||
Segment Reporting Information [Line Items] | ||
Sales | 46 | 88 |
Total Pharmaceutical segment sales | Operating Segments | Zerbaxa | ||
Segment Reporting Information [Line Items] | ||
Sales | 37 | 26 |
Total Pharmaceutical segment sales | Operating Segments | Simponi | ||
Segment Reporting Information [Line Items] | ||
Sales | 215 | 208 |
Total Pharmaceutical segment sales | Operating Segments | Remicade | ||
Segment Reporting Information [Line Items] | ||
Sales | 88 | 123 |
Total Pharmaceutical segment sales | Operating Segments | Belsomra | ||
Segment Reporting Information [Line Items] | ||
Sales | 79 | 67 |
Total Pharmaceutical segment sales | Operating Segments | Isentress/Isentress HD | ||
Segment Reporting Information [Line Items] | ||
Sales | 245 | 255 |
Total Pharmaceutical segment sales | Operating Segments | Zepatier | ||
Segment Reporting Information [Line Items] | ||
Sales | 55 | 114 |
Total Pharmaceutical segment sales | Operating Segments | Zetia | ||
Segment Reporting Information [Line Items] | ||
Sales | 145 | 140 |
Total Pharmaceutical segment sales | Operating Segments | Vytorin | ||
Segment Reporting Information [Line Items] | ||
Sales | 53 | 97 |
Total Pharmaceutical segment sales | Operating Segments | Atozet | ||
Segment Reporting Information [Line Items] | ||
Sales | 122 | 94 |
Total Pharmaceutical segment sales | Operating Segments | Adempas | ||
Segment Reporting Information [Line Items] | ||
Sales | 56 | 48 |
Total Pharmaceutical segment sales | Operating Segments | Alliance revenue - Adempas (2) | ||
Segment Reporting Information [Line Items] | ||
Sales | 53 | 42 |
Total Pharmaceutical segment sales | Operating Segments | Januvia | ||
Segment Reporting Information [Line Items] | ||
Sales | 774 | 824 |
Total Pharmaceutical segment sales | Operating Segments | Janumet | ||
Segment Reporting Information [Line Items] | ||
Sales | 503 | 530 |
Total Pharmaceutical segment sales | Operating Segments | Implanon/Nexplanon | ||
Segment Reporting Information [Line Items] | ||
Sales | 195 | 199 |
Total Pharmaceutical segment sales | Operating Segments | NuvaRing | ||
Segment Reporting Information [Line Items] | ||
Sales | 63 | 219 |
Total Pharmaceutical segment sales | Operating Segments | Singulair | ||
Segment Reporting Information [Line Items] | ||
Sales | 155 | 191 |
Total Pharmaceutical segment sales | Operating Segments | Cozaar/Hyzaar | ||
Segment Reporting Information [Line Items] | ||
Sales | 102 | 103 |
Total Pharmaceutical segment sales | Operating Segments | Nasonex | ||
Segment Reporting Information [Line Items] | ||
Sales | 71 | 96 |
Total Pharmaceutical segment sales | Operating Segments | Arcoxia | ||
Segment Reporting Information [Line Items] | ||
Sales | 70 | 75 |
Total Pharmaceutical segment sales | Operating Segments | Follistim AQ | ||
Segment Reporting Information [Line Items] | ||
Sales | 41 | 57 |
Total Pharmaceutical segment sales | Operating Segments | Other pharmaceutical (3) | ||
Segment Reporting Information [Line Items] | ||
Sales | 1,194 | 1,082 |
Total Pharmaceutical segment sales | United States | Operating Segments | ||
Segment Reporting Information [Line Items] | ||
Sales | 4,714 | 4,215 |
Total Pharmaceutical segment sales | United States | Operating Segments | Keytruda | ||
Segment Reporting Information [Line Items] | ||
Sales | 1,906 | 1,284 |
Total Pharmaceutical segment sales | United States | Operating Segments | Alliance revenue - Lynparza (1) | ||
Segment Reporting Information [Line Items] | ||
Sales | 85 | 50 |
Total Pharmaceutical segment sales | United States | Operating Segments | Alliance revenue - Lenvima (1) | ||
Segment Reporting Information [Line Items] | ||
Sales | 90 | 50 |
Total Pharmaceutical segment sales | United States | Operating Segments | Emend | ||
Segment Reporting Information [Line Items] | ||
Sales | 5 | 63 |
Total Pharmaceutical segment sales | United States | Operating Segments | Gardasil/Gardasil 9 | ||
Segment Reporting Information [Line Items] | ||
Sales | 461 | 362 |
Total Pharmaceutical segment sales | United States | Operating Segments | ProQuad/M-M-R II/Varivax | ||
Segment Reporting Information [Line Items] | ||
Sales | 333 | 343 |
Total Pharmaceutical segment sales | United States | Operating Segments | Pneumovax 23 | ||
Segment Reporting Information [Line Items] | ||
Sales | 182 | 125 |
Total Pharmaceutical segment sales | United States | Operating Segments | RotaTeq | ||
Segment Reporting Information [Line Items] | ||
Sales | 140 | 154 |
Total Pharmaceutical segment sales | United States | Operating Segments | Vaqta | ||
Segment Reporting Information [Line Items] | ||
Sales | 30 | 29 |
Total Pharmaceutical segment sales | United States | Operating Segments | Bridion | ||
Segment Reporting Information [Line Items] | ||
Sales | 143 | 119 |
Total Pharmaceutical segment sales | United States | Operating Segments | Noxafil | ||
Segment Reporting Information [Line Items] | ||
Sales | 8 | 91 |
Total Pharmaceutical segment sales | United States | Operating Segments | Invanz | ||
Segment Reporting Information [Line Items] | ||
Sales | 6 | 14 |
Total Pharmaceutical segment sales | United States | Operating Segments | Prevymis | ||
Segment Reporting Information [Line Items] | ||
Sales | 26 | 18 |
Total Pharmaceutical segment sales | United States | Operating Segments | Cancidas | ||
Segment Reporting Information [Line Items] | ||
Sales | 3 | 1 |
Total Pharmaceutical segment sales | United States | Operating Segments | Primaxin | ||
Segment Reporting Information [Line Items] | ||
Sales | 0 | 0 |
Total Pharmaceutical segment sales | United States | Operating Segments | Cubicin | ||
Segment Reporting Information [Line Items] | ||
Sales | 15 | 42 |
Total Pharmaceutical segment sales | United States | Operating Segments | Zerbaxa | ||
Segment Reporting Information [Line Items] | ||
Sales | 20 | 12 |
Total Pharmaceutical segment sales | United States | Operating Segments | Simponi | ||
Segment Reporting Information [Line Items] | ||
Sales | 0 | 0 |
Total Pharmaceutical segment sales | United States | Operating Segments | Remicade | ||
Segment Reporting Information [Line Items] | ||
Sales | 0 | 0 |
Total Pharmaceutical segment sales | United States | Operating Segments | Belsomra | ||
Segment Reporting Information [Line Items] | ||
Sales | 27 | 24 |
Total Pharmaceutical segment sales | United States | Operating Segments | Isentress/Isentress HD | ||
Segment Reporting Information [Line Items] | ||
Sales | 75 | 108 |
Total Pharmaceutical segment sales | United States | Operating Segments | Zepatier | ||
Segment Reporting Information [Line Items] | ||
Sales | 18 | 33 |
Total Pharmaceutical segment sales | United States | Operating Segments | Zetia | ||
Segment Reporting Information [Line Items] | ||
Sales | (2) | 0 |
Total Pharmaceutical segment sales | United States | Operating Segments | Vytorin | ||
Segment Reporting Information [Line Items] | ||
Sales | 3 | 3 |
Total Pharmaceutical segment sales | United States | Operating Segments | Atozet | ||
Segment Reporting Information [Line Items] | ||
Sales | 0 | 0 |
Total Pharmaceutical segment sales | United States | Operating Segments | Adempas | ||
Segment Reporting Information [Line Items] | ||
Sales | 0 | 0 |
Total Pharmaceutical segment sales | United States | Operating Segments | Alliance revenue - Adempas (2) | ||
Segment Reporting Information [Line Items] | ||
Sales | 49 | 40 |
Total Pharmaceutical segment sales | United States | Operating Segments | Januvia | ||
Segment Reporting Information [Line Items] | ||
Sales | 355 | 384 |
Total Pharmaceutical segment sales | United States | Operating Segments | Janumet | ||
Segment Reporting Information [Line Items] | ||
Sales | 113 | 167 |
Total Pharmaceutical segment sales | United States | Operating Segments | Implanon/Nexplanon | ||
Segment Reporting Information [Line Items] | ||
Sales | 149 | 149 |
Total Pharmaceutical segment sales | United States | Operating Segments | NuvaRing | ||
Segment Reporting Information [Line Items] | ||
Sales | 26 | 185 |
Total Pharmaceutical segment sales | United States | Operating Segments | Singulair | ||
Segment Reporting Information [Line Items] | ||
Sales | 5 | 5 |
Total Pharmaceutical segment sales | United States | Operating Segments | Cozaar/Hyzaar | ||
Segment Reporting Information [Line Items] | ||
Sales | 7 | 4 |
Total Pharmaceutical segment sales | United States | Operating Segments | Nasonex | ||
Segment Reporting Information [Line Items] | ||
Sales | 6 | (1) |
Total Pharmaceutical segment sales | United States | Operating Segments | Arcoxia | ||
Segment Reporting Information [Line Items] | ||
Sales | 0 | 0 |
Total Pharmaceutical segment sales | United States | Operating Segments | Follistim AQ | ||
Segment Reporting Information [Line Items] | ||
Sales | 21 | 29 |
Total Pharmaceutical segment sales | United States | Operating Segments | Other pharmaceutical (3) | ||
Segment Reporting Information [Line Items] | ||
Sales | 409 | 328 |
Total Pharmaceutical segment sales | International | Operating Segments | ||
Segment Reporting Information [Line Items] | ||
Sales | 5,941 | 5,448 |
Total Pharmaceutical segment sales | International | Operating Segments | Keytruda | ||
Segment Reporting Information [Line Items] | ||
Sales | 1,378 | 985 |
Total Pharmaceutical segment sales | International | Operating Segments | Alliance revenue - Lynparza (1) | ||
Segment Reporting Information [Line Items] | ||
Sales | 60 | 29 |
Total Pharmaceutical segment sales | International | Operating Segments | Alliance revenue - Lenvima (1) | ||
Segment Reporting Information [Line Items] | ||
Sales | 38 | 24 |
Total Pharmaceutical segment sales | International | Operating Segments | Emend | ||
Segment Reporting Information [Line Items] | ||
Sales | 38 | 53 |
Total Pharmaceutical segment sales | International | Operating Segments | Gardasil/Gardasil 9 | ||
Segment Reporting Information [Line Items] | ||
Sales | 636 | 476 |
Total Pharmaceutical segment sales | International | Operating Segments | ProQuad/M-M-R II/Varivax | ||
Segment Reporting Information [Line Items] | ||
Sales | 102 | 153 |
Total Pharmaceutical segment sales | International | Operating Segments | Pneumovax 23 | ||
Segment Reporting Information [Line Items] | ||
Sales | 75 | 59 |
Total Pharmaceutical segment sales | International | Operating Segments | RotaTeq | ||
Segment Reporting Information [Line Items] | ||
Sales | 82 | 57 |
Total Pharmaceutical segment sales | International | Operating Segments | Vaqta | ||
Segment Reporting Information [Line Items] | ||
Sales | 30 | 18 |
Total Pharmaceutical segment sales | International | Operating Segments | Bridion | ||
Segment Reporting Information [Line Items] | ||
Sales | 157 | 136 |
Total Pharmaceutical segment sales | International | Operating Segments | Noxafil | ||
Segment Reporting Information [Line Items] | ||
Sales | 87 | 99 |
Total Pharmaceutical segment sales | International | Operating Segments | Invanz | ||
Segment Reporting Information [Line Items] | ||
Sales | 59 | 58 |
Total Pharmaceutical segment sales | International | Operating Segments | Prevymis | ||
Segment Reporting Information [Line Items] | ||
Sales | 33 | 14 |
Total Pharmaceutical segment sales | International | Operating Segments | Cancidas | ||
Segment Reporting Information [Line Items] | ||
Sales | 52 | 60 |
Total Pharmaceutical segment sales | International | Operating Segments | Primaxin | ||
Segment Reporting Information [Line Items] | ||
Sales | 51 | 59 |
Total Pharmaceutical segment sales | International | Operating Segments | Cubicin | ||
Segment Reporting Information [Line Items] | ||
Sales | 31 | 46 |
Total Pharmaceutical segment sales | International | Operating Segments | Zerbaxa | ||
Segment Reporting Information [Line Items] | ||
Sales | 16 | 14 |
Total Pharmaceutical segment sales | International | Operating Segments | Simponi | ||
Segment Reporting Information [Line Items] | ||
Sales | 215 | 208 |
Total Pharmaceutical segment sales | International | Operating Segments | Remicade | ||
Segment Reporting Information [Line Items] | ||
Sales | 88 | 123 |
Total Pharmaceutical segment sales | International | Operating Segments | Belsomra | ||
Segment Reporting Information [Line Items] | ||
Sales | 53 | 44 |
Total Pharmaceutical segment sales | International | Operating Segments | Isentress/Isentress HD | ||
Segment Reporting Information [Line Items] | ||
Sales | 170 | 147 |
Total Pharmaceutical segment sales | International | Operating Segments | Zepatier | ||
Segment Reporting Information [Line Items] | ||
Sales | 37 | 81 |
Total Pharmaceutical segment sales | International | Operating Segments | Zetia | ||
Segment Reporting Information [Line Items] | ||
Sales | 147 | 140 |
Total Pharmaceutical segment sales | International | Operating Segments | Vytorin | ||
Segment Reporting Information [Line Items] | ||
Sales | 50 | 94 |
Total Pharmaceutical segment sales | International | Operating Segments | Atozet | ||
Segment Reporting Information [Line Items] | ||
Sales | 122 | 94 |
Total Pharmaceutical segment sales | International | Operating Segments | Adempas | ||
Segment Reporting Information [Line Items] | ||
Sales | 56 | 48 |
Total Pharmaceutical segment sales | International | Operating Segments | Alliance revenue - Adempas (2) | ||
Segment Reporting Information [Line Items] | ||
Sales | 5 | 2 |
Total Pharmaceutical segment sales | International | Operating Segments | Januvia | ||
Segment Reporting Information [Line Items] | ||
Sales | 419 | 440 |
Total Pharmaceutical segment sales | International | Operating Segments | Janumet | ||
Segment Reporting Information [Line Items] | ||
Sales | 390 | 364 |
Total Pharmaceutical segment sales | International | Operating Segments | Implanon/Nexplanon | ||
Segment Reporting Information [Line Items] | ||
Sales | 45 | 50 |
Total Pharmaceutical segment sales | International | Operating Segments | NuvaRing | ||
Segment Reporting Information [Line Items] | ||
Sales | 37 | 34 |
Total Pharmaceutical segment sales | International | Operating Segments | Singulair | ||
Segment Reporting Information [Line Items] | ||
Sales | 151 | 186 |
Total Pharmaceutical segment sales | International | Operating Segments | Cozaar/Hyzaar | ||
Segment Reporting Information [Line Items] | ||
Sales | 95 | 99 |
Total Pharmaceutical segment sales | International | Operating Segments | Nasonex | ||
Segment Reporting Information [Line Items] | ||
Sales | 65 | 97 |
Total Pharmaceutical segment sales | International | Operating Segments | Arcoxia | ||
Segment Reporting Information [Line Items] | ||
Sales | 70 | 75 |
Total Pharmaceutical segment sales | International | Operating Segments | Follistim AQ | ||
Segment Reporting Information [Line Items] | ||
Sales | 21 | 28 |
Total Pharmaceutical segment sales | International | Operating Segments | Other pharmaceutical (3) | ||
Segment Reporting Information [Line Items] | ||
Sales | 780 | 754 |
Total Animal Health segment sales | Operating Segments | ||
Segment Reporting Information [Line Items] | ||
Sales | 1,214 | 1,025 |
Total Animal Health segment sales | Operating Segments | Livestock | ||
Segment Reporting Information [Line Items] | ||
Sales | 739 | 611 |
Total Animal Health segment sales | Operating Segments | Companion Animals | ||
Segment Reporting Information [Line Items] | ||
Sales | 475 | 414 |
Total Animal Health segment sales | United States | Operating Segments | ||
Segment Reporting Information [Line Items] | ||
Sales | 384 | 294 |
Total Animal Health segment sales | United States | Operating Segments | Livestock | ||
Segment Reporting Information [Line Items] | ||
Sales | 162 | 117 |
Total Animal Health segment sales | United States | Operating Segments | Companion Animals | ||
Segment Reporting Information [Line Items] | ||
Sales | 222 | 177 |
Total Animal Health segment sales | International | Operating Segments | ||
Segment Reporting Information [Line Items] | ||
Sales | 830 | 731 |
Total Animal Health segment sales | International | Operating Segments | Livestock | ||
Segment Reporting Information [Line Items] | ||
Sales | 577 | 494 |
Total Animal Health segment sales | International | Operating Segments | Companion Animals | ||
Segment Reporting Information [Line Items] | ||
Sales | 253 | 237 |
Other segment sales (4) | Operating Segments | ||
Segment Reporting Information [Line Items] | ||
Sales | 23 | 39 |
Other segment sales (4) | United States | Operating Segments | ||
Segment Reporting Information [Line Items] | ||
Sales | 23 | 39 |
Other segment sales (4) | International | Operating Segments | ||
Segment Reporting Information [Line Items] | ||
Sales | $ 0 | $ 0 |
Segment Reporting - Revenues by
Segment Reporting - Revenues by Geographic Area (Details) - USD ($) $ in Millions | 3 Months Ended | |
Mar. 31, 2020 | Mar. 31, 2019 | |
Revenue from External Customer [Line Items] | ||
Sales | $ 12,057 | $ 10,816 |
United States | ||
Revenue from External Customer [Line Items] | ||
Sales | 5,137 | 4,555 |
Europe, Middle East and Africa | ||
Revenue from External Customer [Line Items] | ||
Sales | 3,534 | 3,103 |
China | ||
Revenue from External Customer [Line Items] | ||
Sales | 864 | 746 |
Japan | ||
Revenue from External Customer [Line Items] | ||
Sales | 811 | 799 |
Asia Pacific (other than China and Japan) | ||
Revenue from External Customer [Line Items] | ||
Sales | 728 | 745 |
Latin America | ||
Revenue from External Customer [Line Items] | ||
Sales | 556 | 561 |
Other | ||
Revenue from External Customer [Line Items] | ||
Sales | $ 427 | $ 307 |
Segment Reporting - Profits to
Segment Reporting - Profits to Income Before Taxes (Details) - USD ($) $ in Millions | 3 Months Ended | |
Mar. 31, 2020 | Mar. 31, 2019 | |
Segment Reporting Information [Line Items] | ||
Profits | $ 3,838 | $ 3,067 |
Interest income | 25 | 89 |
Interest expense | (212) | (209) |
Depreciation and amortization | (821) | (898) |
Research and development | (2,209) | (1,931) |
Restructuring costs | (72) | (153) |
Total segment profits | ||
Segment Reporting Information [Line Items] | ||
Profits | 7,956 | 6,991 |
Total segment profits | Pharmaceutical segment | ||
Segment Reporting Information [Line Items] | ||
Profits | 7,477 | 6,574 |
Total segment profits | Animal Health segment | ||
Segment Reporting Information [Line Items] | ||
Profits | 478 | 415 |
Total segment profits | Other segment | ||
Segment Reporting Information [Line Items] | ||
Profits | 1 | 2 |
Other profits | ||
Segment Reporting Information [Line Items] | ||
Profits | 139 | 30 |
Unallocated | ||
Segment Reporting Information [Line Items] | ||
Interest income | 25 | 89 |
Interest expense | (212) | (209) |
Depreciation and amortization | (381) | (359) |
Research and development | (2,097) | (1,843) |
Amortization of purchase accounting adjustments | (295) | (397) |
Restructuring costs | (72) | (153) |
Other unallocated, net | $ (1,225) | $ (1,082) |