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The Advisory Committee on Immunization Practices’ Interim Recommendation for Use of Janssen COVID-19 Vaccine — United States, February 2021

Sara E. Oliver, MD1; Julia W. Gargano, PhD1; Heather Scobie, PhD1; Megan Wallace, DrPH1,2; Stephen C. Hadler, MD1; Jessica Leung, MPH1; Amy E. Blain, MPH1; Nancy McClung, PhD1; Doug Campos-Outcalt, MD3; Rebecca L. Morgan, PhD4; Sarah Mbaeyi, MD1; Jessica MacNeil, MPH1; José R. Romero, MD5; H. Keipp Talbot, MD6; Grace M. Lee, MD7; Beth P. Bell, MD8; Kathleen Dooling, MD1w
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Resumen

What is already known about this topic?

On February 27, 2021, the Food and Drug Administration issued an Emergency Use Authorization (EUA) for the Janssen COVID-19 vaccine.

What is added by this report?

On February 28, 2021, after a transparent evidence-based review of all available data, the Advisory Committee on Immunization Practices (ACIP) issued an interim recommendation for use of the Janssen COVID-19 vaccine in persons aged ≥18 years for the prevention of COVID-19.

What are the implications for public health practice?

The Janssen COVID-19 vaccine has high efficacy against COVID-19–associated hospitalization and death. Persons may receive any ACIP-recommended COVID-19 vaccine and are encouraged to receive the earliest vaccine available to them. Use of all EUA-authorized COVID-19 vaccines is critical in controlling the pandemic.

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Publicado en el sitio 2021-03-10 16:43:51

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