COVID pill Paxlovid gets full FDA approval after more than a year of emergency use
U.S. health regulators have given full approval to Pfizer’s COVID-19 pill Paxlovid
WASHINGTON (AP) — Pfizer received full approval on Thursday for its COVID-19 pill Paxlovid that's been the go-to treatment against the coronavirus.
More than 11 million prescriptions for Paxlovid have been dispensed since the Food and Drug Administration allowed emergency use in late 2021. The emergency status was based on early studies and was intended to be temporary pending follow-up research.
The FDA granted full approval for adults with COVID-19 who face high risks of severe disease, which can lead to hospitalization or death. That group typically includes older adults and those with common medical conditions like diabetes, asthma and obesity.
The decision allows Pfizer's drug to remain on the market indefinitely and to be marketed similarly to other drugs.
