COVID-19 Pill Paxlovid Moves Closer To Full FDA Approval

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COVID-19 Pill Paxlovid Moves Closer To Full FDA Approval
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U.S. health advisers are backing the continued use of Pfizer’s COVID-19 pill Paxlovid, saying it remains an important option for adults at high risk of severe illness.

WASHINGTON — Pfizer’s COVID-19 pill Paxlovid won another vote of confidence from U.S. health advisers Thursday, clearing the way for its full regulatory approval by the Food and Drug Administration.in late 2021. The agency has the final say on giving Pfizer’s drug full approval and is expected to decide by May.

“We still have many groups that stand to benefit from Paxlovid, including unvaccinated persons, under-vaccinated persons, the elderly and the immuno-compromised,” said Dr. Richard Murphy of the Department of Veterans Affairs. The FDA said using Paxlovid in high-risk patients could prevent 1,500 COVID-19 deaths and 13,000 hospitalizations per week.

The panel’s positive vote was widely expected, given that Paxlovid has been the go-to treatment against COVID-19, especially since an entire group ofThe U.S. continues reporting about 4,000 deaths and 35,000 hospitalizations weekly, the FDA noted. Doses of the anti-viral drug Paxlovid are displayed in New York, on Aug. 1, 2022. The COVID-19 medication won another vote of confidence from U.S. health advisors on March 16, 2023, clearing the way for its full regulatory approval after being used by millions of Americans under emergency use.

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