FDA revises EUA for COVID-19 treatment Paxlovid
Having first authorized US pharma giant Pfizer’s (NYSE: PFE) Paxlovid (nirmatrelvir and ritonavir) for emergency use in adults and pediatric patients (12 years of age and older weighing at least 40 kg) who are at high risk for progression to severe COVID-19, including hospitalization or death in December 2021, and amended this in May 2023, the US Food and Drug Administration (FDA) is now making another amendment.
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