The pandemic is over (POTUS)
Emergency use authorizations
August 31, 2022
Today, the U.S. Food and Drug Administration amended the emergency use authorizations (EUAs) of the Moderna COVID-19 Vaccine,
and the Pfizer-BioNTech COVID-19 Vaccine,
to authorize bivalent formulations,
for use as a single booster dose
Original strain BA.4 and BA.5 lineages
For each bivalent COVID-19 vaccine, the FDA based its decision on the totality of available evidence,
including extensive safety and effectiveness data for each of the monovalent mRNA COVID-19 vaccines,
safety and immunogenicity data obtained from a clinical study of a bivalent COVID-19 vaccine that contained mRNA from omicron
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