The FDA gave the COVID-19 anti-viral emergency use authorization in 2021 for treating mild to moderate illness in high-risk adults.
- Advisers for the Food and Drug Administration are meeting Thursday to consider full approval for Pfizer’s Paxlovid.
Some users had reported a return of symptoms and a positive COVID-19 test after finishing the five-day course of Paxlovid. However, clinical trial data has concluded that there is no clear association with a COVID-19 rebound.The FDA is expected to complete its review for approval in May.
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