A Food and Drug Administration panel has recommended the FDA grant emergency use authorization for Pfizer’s COVID-19 vaccine in the United States.
The advisory panel met virtually on Thursday to scrutinize Pfizer’s data on the vaccine for any red flags. The FDA does not have to follow its panel's recommendation, but the agency is widely expected to do so.
Seventeen people voted yes, four voted no and one abstained.
The panel's decision to recommend the vaccine came down to one question:
Based on the totality of scientific evidence available, do the benefits of the Pfizer vaccine outweigh its risks for use in individuals 16 years of age and older?
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