Revenue segments as reported by the company.

Pharmaceutical

Animal Health

Other Revenues

Revenue Segments

Gross Profit, Operating Income, and Net Income as a percentage of Revenue

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Margins

An operating expense is an expense a business incurs through its normal business operations. Often abbreviated as OPEX.

Selling, general and administrative

Research and development

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Operating Expenses

Year over year growth in Revenue and Operating Expenses.

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OpEx Y/Y

Growth

Shares outstanding refer to a company's stock currently held by all its shareholders, including share blocks held by institutional investors and restricted shares owned by the company's officers and insiders.

Outstanding Shares

Market Cap

Also known as Price/Sales Ratio. Calculated using Average market cap for the quarter / Annualized quarterly revenue.

Revenue Multiple

Merck

Merck & Co., Inc. engages in the provision of health solutions through its prescription medicines, vaccines, biologic therapies, animal health, and consumer care products. It operates through the following segments: Pharmaceutical, Animal Health, and Other. The Pharmaceutical segment includes human health pharmaceutical and vaccine products. The Animal Health segment discovers, develops, manufactures, and markets animal health products, such as pharmaceutical and vaccine products, for the prevention, treatment and control of disease in livestock and companion animal species. The Other segment consists of sales for the non-reportable segments of healthcare services. The company was founded in 1891 and is headquartered in Kenilworth, NJ.

Earnings data Q1 2021

Earnings data Q2 2021

Earnings data Q3 2021

Earnings data Q4 2021

Earnings data Q1 2022

Earnings data Q2 2022

Earnings data Q3 2022

Earnings data Q4 2022

Earnings data Q1 2023

Earnings data Q2 2023

Earnings data Q3 2023

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Earnings data Q1 2024

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Earnings data Q3 2024

Earnings data Q4 2024

Merck reports robust Q4 earnings, eyes growth through innovation

Merck's Q4 2022 performance reflects strong revenue growth and strategic advancements across key therapeutic areas, positioning the company for future success.
While facing challenges such as patent estate concerns and competitive pressures, Merck's focus on innovation and partnerships presents opportunities for sustained growth.
Analyst inquiries and executive responses during the earnings call highlight the company's commitment to transparency, patient outcomes, and shareholder value.

Merck reports robust Q1 earnings, eyes growth in oncology and vaccines

Merck's Q1 performance reflects strong revenue growth driven by oncology and vaccines, with a raised full-year guidance and focus on pipeline advancements.
The company's strategic strengths lie in its focus on compelling science, value alignment in business decisions, and commitment to innovation.
Challenges include potential impacts of EU legislation, post-KEYTRUDA LOE growth strategies, and navigating regulatory complexities for new treatments.
Opportunities in expansion in China, revenue diversification, innovative combination therapies, and protective treatment strategies position Merck for future growth.

Merck reports robust Q2 earnings, focuses on growth opportunities

Merck's Q2 performance showcased strong earnings driven by Oncology and Vaccines growth
Despite challenges like regulatory concerns and price pressures, the company remains focused on innovation
Opportunities lie in expanding KEYTRUDA's reach in cancer indications and advancing in immunology
Overall, Merck's strategic acquisitions and commitment to growth position it well for the future

Merck reports robust Q3 earnings, eyes growth in precision medicine

Merck's Q3 2023 Earnings Call highlighted strong revenue growth, pipeline advancements, and increased full-year revenue guidance. The company's strategic focus on key therapeutic areas and precision medicine approaches positions it for continued success and innovation.

Merck reports robust Q4 earnings, eyes growth through strategic investments

Merck's strong Q4 performance was driven by KEYTRUDA and Vaccines, with positive revenue guidance for 2024. The company remains focused on R&D advancements, strategic investments, and shareholder value. Challenges include managing expenses and maximizing market opportunities.

Merck reports robust Q1 earnings, eyes growth in innovative treatments

Merck's Q1 performance reflects strong revenue growth, operational efficiency, and a positive outlook for future earnings.
The company's focus on innovation, strategic investments, and commitment to patient access position it well for long-term success.
Challenges in pipeline differentiation and market competition require continued strategic planning and differentiation strategies.
Opportunities in new treatment areas, market expansion, and upcoming events offer avenues for sustained growth and market leadership.

Merck reports robust Q2 earnings, eyes future drug launches

Merck's Q2 earnings call highlighted strong financial performance, innovative product launches, and confidence in future growth. The company addressed analyst inquiries, emphasizing long-term pipeline growth and short-term financial guidance while expressing gratitude for investor support.

Merck reports solid Q3 earnings, eyes growth through diversification

Merck's Q3 2024 performance reflects revenue growth driven by key products and clinical advancements, despite regional sales variations and inventory challenges.
The company's strengths in diversification, clinical progress, and strategic investments position it well for future growth and competitive edge in the market.
While facing challenges in specific product sales and clinical trials, Merck has opportunities to capitalize on its strengths, expand offerings, and drive sustained growth.

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Merck & Co., Inc. is a health care company, which engages in the provision of health solutions through its prescription medicines, vaccines, biologic therapies, animal health, and consumer care products. It operates through the following segments: Pharmaceutical, Animal Health, and Other. The Pharmaceutical segment includes human health pharmaceutical and vaccine products. The Animal Health segment discovers, develops, manufactures, and markets animal health products, such as pharmaceutical and vaccine products, for the prevention, treatment and control of disease in livestock, and companion animal species. The Other segment consists of sales for the non-reportable segments of healthcare services. The company was founded in 1891 and is headquartered in Rahway, NJ.

Bristol-Myers

The FDA has accepted for review Bristol Myers Squibb Co's (NYSE: BMY) supplemental application seeking approval for Reblozyl (luspatercept-aamt) in adults with non-transfusion dependent (NTD) beta-thalassemia. The FDA has set a Prescription Drug User Fee Act goal date of March 27, 2022.

Bristol Myers - Merck's Thalassemia Candidate Under FDA Priority Review

The treatment window for COVID is very narrow; this limits the value of even effective treatments. Molnupiravir effectiveness ~30%; Paxlovid seems more effective in trials, but the real world awaits.

Early Stage COVID Treatments: Merck's Molnupiravir Struggles

Novartis

As 2021 winds down, investors may want to keep an eye on several drug companies that hope to get key approvals from the Food and Drug Administration before the year is out. Among the pharmas hoping to get their treatments green-lighted are Argenx SE ( ARGX , Financial), Calliditas Therapeutics AB ( CALT , Financial), Merck & Co. Inc. ( MRK , Financial) and Novartis ( NVS , Financial).

Merck, Novartis in Line for Key FDA Approvals This Month

Merck (MRK) is seeking label expansion for Vaxneuvance for use in pediatric patients aged six weeks through 17 years for the prevention of invasive pneumococcal disease. A decision is expected by on Apr 1, 2022.

Merck (MRK) Vaxneuvance sBLA for Pediatrics Gets Priority Review

Merck & Co., Inc. (MRK) Management on 4th Annual Evercore ISI HealthCONx Virtual Conference (Transcript)

Just a few days back we discussed that the stock price of Merck is being weighed down due to concerns around its Covid-19 antiviral pill - Molnupiravir - which has an efficacy of 30% against hospitalization and death in high-risk patients. Yesterday, a panel of advisors to the U.S. FDA voted in.

What's Next For Merck Stock After FDA Advisors Back Its Covid-19 Pill?

AbbVie

Members of U.S. Congress are free to buy and sell stocks as long as the moves are disclosed within 45 days of the transaction. This practice has been controversial over the years, with members of Congress who make decisions on key policies and department spending often having an inside line on companies that could benefit.

2 Biotech Stocks A Congressman Is Betting On With Omicron Variant Emerging

An FDA committee voted 13-0 to recommend authorization of Merck's (MRK) antiviral pill to treat COVID-19.

Merck (MRK) Up as COVID Pill Gets FDA Panel's Positive Vote

AstraZeneca

FDA grants priority review to AstraZeneca (AZN) and Merck's (MRK) sNDA for Lynparza for BRCA-mutated HER2-negative high-risk early breast cancer.

AstraZeneca, Merck's Lynparza sNDA Gets FDA Priority Tag

Johnson & Johnson

Novavax

Pfizer

Vir Biotechnology

Could biotech stocks be top buys as the world battles a new Covid-19 variant?

5 Biotech Stocks For Your December 2021 Watchlist

It's likely that Merck's COVID-19 pill will be authorized in the U.S. this month even though Wall Street's interest has cooled and physicians have raised questions about the drug's efficacy and safety profile, particularly among people who are pregnant.

After high hopes for Merck's COVID-19 pill, Wall Street now expects a ‘tepid' authorization

The FDA has accepted for priority review Merck & Co Inc's (NYSE: MRK) supplemental application seeking approval for Vaxneuvance (Pneumococcal 15-valent Conjugate Vaccine) for the prevention of invasive pneumococcal disease in children six weeks through 17 years of age.  The FDA set a Prescription Drug User Fee Act (PDUFA), or target action date, of April 1, 2022.

Merck's Pneumococcal 15-valent Conjugate Vaccine Under Priority FDA Review For Use In Kids

KENILWORTH, N.J.--(BUSINESS WIRE)---- $MRK #MRK--U.S. FDA Accepts for Priority Review the Supplemental Biologics License Application for Merck's VAXNEUVANCE™ for Use in Infants and Children

U.S. FDA Accepts for Priority Review the Supplemental Biologics License Application for Merck's VAXNEUVANCE™ (Pneumococcal 15-valent Conjugate Vaccine) for Use in Infants and Children

The FDA's Antimicrobial Drugs Advisory Committee voted 13 to 10 to recommend emergency authorization of Merck & Co Inc's (NYSE: MRK) molnupiravir, antiviral pill to treat COVID-19. Molnupiravir, developed with Ridgeback Biotherapeutics, targets part of the virus called the RNA polymerase that has not been changed much by mutations in the Omicron variant.

AdComm Narrowly Backs Merck's COVID-19 Pill, Despite Efficacy Questions

A pill that could reduce severe Covid symptoms has gained the narrow backing of US health regulators. Merck & Co Inc (NYSE:MRK)'s antiviral treatment molnupiravir was cleared for use by a panel of experts from the Food & Drug Administration, which voted 13 to 10 in favour of the new drug.

Merck's new Covid pill gets the US regulatory green light - but only just

The financial ratios that tend to lead price action show good things for MRK's stock price. Treating MRK as a value stock and considering its fundamentals and pipeline, we can expect upward momentum sometime in the near future.

Merck Is A Buy Now

Merck continues to impress with strong growth in its key franchises. It maintains a very strong balance sheet, and just increased its dividend, which remains well-covered by earnings.

Bargain Alert: Merck Is A Strong Buy On The Drop

The FDA still needs to officially authorize molnupiravir for people at high risk of severe COVID-19.

FDA panel narrowly moves to authorize Merck's COVID treatment pill

KENILWORTH, N.J. & MIAMI--(BUSINESS WIRE)---- $MRK #MRK--Merck and Ridgeback Statement on Positive FDA Vote for Oral Antiviral Molnupiravir for Treatment of Mild to Moderate COVID-19 in High Risk Adults

Merck and Ridgeback Statement on Positive FDA Advisory Committee Vote for Investigational Oral Antiviral Molnupiravir for Treatment of Mild to Moderate COVID-19 in High Risk Adults

A COVID-19 pill could prevent infected people from getting seriously sick. But the FDA panel expressed concerns over the safety of Merck's antiviral.

An FDA expert panel narrowly supports the first COVID-19 pill but suggests restrictions on its use driven by safety concerns

The FDA's Antimicrobial Drugs Advisory Committee voted 13 to 10 to recommend emergency authorization of molnupiravir.

FDA advisory panel narrowly endorses Merck's oral Covid treatment pill, despite reduced efficacy and safety questions

Merck's pill is the first oral medication to be endorsed for authorization in the United States.

FDA Panel Recommends Merck's Covid-19 Antiviral Pill For Emergency Use Authorization

On Monday, Merck & Co Inc. (NYSE:MRK) shares plunged by more than 5% amid concerns about the efficacy of its molnupiravir drug as a treatment for covid-19. The pill is poised for authorisation by the US Food and Drug Administration (FDA), but analysts fear its efficacy could hamper use.

Is Merck stock a buy or sell as covid pill efficacy concerns send shares crushing?

KENILWORTH, N.J.--(BUSINESS WIRE)---- $MRK #MRK--Merck Announces First-Quarter 2022 Dividend

Merck Announces First-Quarter 2022 Dividend

Merck's (MRK) Keytruda, in combination with Eisai's Lenvima, gets approval for treating first-line renal cell carcinoma and recurrent endometrial carcinoma in Europe.

News for Merck Stock (MRK)