FDA officer-in-charge Oscar Gutierrez said the drug regulator has approved the application of the Department of Health for a special permit for the institutional use of Bexovid, the first generic version of Pfizer’s Paxlovid.
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The treatment is said to reduce the risk of hospitalization or death by 89% if given within three days of the onset of symptoms and by 88% if given within five days. “Ito ay talagang makakabigay ng medyo pagasa sa ating 2022 lalong lalo na itong pagharap natin sa COVID-19. At least meron na tayong mga gamot aside sa vaccination that we are pursuing,” Vega said.
Medicines (File photo / MANILA BULLETIN) The Food and Drug Administration (FDA) has granted a compassionate special permit (CSP) for coronavirus disease (COVID-19) drug Bexovid, which is the generic version of Pfizer’s COVID-19 pill Paxlovid. “Mr. President, na-approve po ng FDA ang application ng