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First-of-its-kind COVID-19 antibody treatment: FDA authorization requested

Key FDA advisory panel votes on Pfizer and BioNTech’s application | GMA

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First-of-its-kind COVID-19 antibody treatment: FDA authorization requested

First-of-its-kind COVID-19 antibody treatment: FDA authorization requested

First-of-its-kind COVID-19 antibody treatment: FDA authorization requested

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First-of-its-kind COVID-19 antibody treatment: FDA authorization requested

TENSE DECISION MAKING BETWEEN CDC AND FDA

Key FDA advisory panel votes on Pfizer and BioNTech’s application | GMA

TVNET3 November 2, 2021 3:48 pm

The panel deciding not to recommend boosters for everyone 16 and up but approving them for those 65 and over or those at high risk. SUBSCRIBE to GMA’s YouTube page: https://bit.ly/2Zq0dU5 VISIT GMA’s homepage: https://www.goodmorningamerica.com SIGN UP to get the daily GMA Wake-Up Newsletter: https://gma.abc/2Vzcd5j FOLLOW GMA: TikTok: https://tiktok.com/@gma Facebook: https://facebook.com/GoodMorningAmerica Twitter: https://twitter.com/gma Instagram: https://instagram.com/GoodMorningAmerica #GMA #FDAAdvisoryPanel #Pfizer #BioNTech #Boosters #HighRisk

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