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  2. May 5, 2022 · Following the update to the Fact Sheet, the Johnson & Johnson COVID-19 vaccine is now authorized in the U.S. for use in individuals 18 years of age and older for whom other FDA-authorized or approved COVID-19 vaccines are not accessible or clinically appropriate, as well as for individuals 18 years of age and older who elect to receive the ...

    • 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

  3. Apr 13, 2021 · Español. As of April 12, more than 6.8 million doses of the Johnson & Johnson (Janssen) vaccine have been administered in the U.S. CDC and FDA are reviewing data involving six reported U.S. cases ...

  4. Mar 5, 2021 · The mRNA vaccines from Pfizer and Moderna were both found to be about 95% effective against preventing symptomatic COVID-19 after the second dose. The Johnson & Johnson vaccine, by contrast, was ...

  5. Mar 20, 2022 · The US public and even some health experts may have underestimated the Covid-19 vaccine made by Janssen, a division of Johnson & Johnson, new data shows. And there’s emerging evidence that it ...

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