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  2. The Janssen COVID‑19 vaccine is used to provide protection against infection by the SARS-CoV-2 virus in order to prevent COVID‑19 in people aged eighteen years and older. [37] [1] The vaccine is given by intramuscular injection into the deltoid muscle. The initial course consists of a single dose.

  3. Feb 27, 2021 · | February 27, 2021. Johnson & Johnson J&J Innovative Medicine COVID-19 Vaccines Supply Chain Ebola. Discover 8 facts and things to know about Johnson & Johnson's Janssen COVID-19 vaccine, including how it works and how it might be manufactured and distributed.

    • Overview
    • Reporting of Vaccine Adverse Events
    • References

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    Table 1

    FDA requires that immunization providers report vaccine administration errors, serious adverse events, cases of multisystem inflammatory syndrome, and cases of COVID-19 that result in hospitalization or death after administration of COVID-19 vaccine under an EUA.***** Adverse events that occur after receipt of any COVID-19 vaccine should be reporte...

    1.Food and Drug Administration. Janssen COVID-19 vaccine emergency use authorization. Silver Spring, MD: US Department of Health and Human Services, Food and Drug Administration; 2021. https://www.fda.gov/emergency-preparedness-and-response/coronavirus-disease-2019-covid-19/Janssen-covid-19-vaccineexternal icon

    2.Oliver SE, Gargano JW, Scobie H, et al. The Advisory Committee on Immunization Practices’ interim recommendation for use of Janssen COVID-19 vaccine—United States, February 2021. MMWR Morb Mortal Wkly Rep 2021;70:329–32. https://doi.org/10.15585/mmwr.mm7009e4external icon PMID:33661860external icon

    3.MacNeil JR, Su JR, Broder KR, et al. Updated recommendations from the Advisory Committee on Immunization Practices for use of the Janssen (Johnson & Johnson) COVID-19 vaccine after reports of thrombosis with thrombocytopenia syndrome among vaccine recipients—United States, April 2021. MMWR Morb Mortal Wkly Rep 2021;70:651–6. https://doi.org/10.15585/mmwr.mm7017e4external icon PMID:33914723external icon

    4.Gargano JW, Wallace M, Hadler SC, et al. Use of mRNA COVID-19 vaccine after reports of myocarditis among vaccine recipients: update from the Advisory Committee on Immunization Practices—United States, June 2021. MMWR Morb Mortal Wkly Rep 2021;70:977–82. https://doi.org/10.15585/mmwr.mm7027e2external icon PMID:34237049external icon

    5.Rosenblum HG, Hadler SC, Moulia D, et al. Use of COVID-19 vaccines after reports of adverse events among adult recipients of Janssen (Johnson & Johnson) and mRNA COVID-19 vaccines (Pfizer-BioNTech and Moderna): update from the Advisory Committee on Immunization Practices—United States, July 2021. MMWR Morb Mortal Wkly Rep 2021;70:1094–9. https://doi.org/10.15585/mmwr.mm7032e4external icon PMID:34383735external icon

    6.Greinacher A, Thiele T, Warkentin TE, Weisser K, Kyrle PA, Eichinger S. Thrombotic thrombocytopenia after ChAdOx1 nCov-19 vaccination. N Engl J Med 2021;384:2092–101. https://doi.org/10.1056/NEJMoa2104840external icon PMID:33835769external icon

  4. Jun 6, 2022 · Русский. Español. Updated 6 June 2022, pursuant to updated interim recommendations. The WHO Strategic Advisory Group of Experts on Immunization (SAGE) has issued interim recommendations for the use of the Janssen Ad26.COV2.S COVID-19 vaccine against COVID-19. Here is what you need to know.

  5. May 5, 2022 · The Janssen COVID-19 Vaccine is authorized for use under an Emergency Use Authorization (EUA) for active immunization to prevent Coronavirus Disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in individuals 18 years of age and older for whom other FDA-authorized or approved COVID-19 vaccines are not ac...

  6. The Janssen COVID-19 vaccine has not been approved or licensed by the U.S. Food and Drug Administration (FDA), but has been authorized by FDA through an Emergency Use Authorization (EUA) for active immunization to prevent Coronavirus Disease 2019 (COVID-19) in individuals 18 years of age and older.

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