FDA The Food and Drug Administration (FDA) has granted an emergency use authorization (EUA) to Pfizer's Covid-19 treatment drug Paxlovid. "Masaya kong ibinabalita sa inyo na naaprubahan na po namin ang Paxlovid kahapon (I'm glad to announce that we already approved Paxlovid yesterday)," said FDA...
Safe and effective medications for coronavirus disease (COVID-19) are available in the country and these are “essential” in exiting the pandemic, adult infectious disease specialist Dr. Edsel Maurice Salvaña said on Friday, Feb. 11. In a webinar held by the University of the Philippines (UP),...
The Food and Drug Administration (FDA) said on Monday, Feb. 7 that US Pharmaceutical company Pfizer has already applied for an emergency use authorization (EUA) for its coronavirus disease (COVID-19) pill Paxlovid. AFP/ MANILA BULLETIN FDA-Officer-In-Charge Director-General Oscar Gutierrez reported...
FDA US Pharmaceutical company Pfizer has expressed intention to apply for an emergency use authorization (EUA) for its coronavirus disease (COVID-19) pill Paxlovid, the Philippine Food and Drug Administration (FDA) said. “Mayroon pong intensiyon ang Pfizer na magrehistro po ng produkto nila under...
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...
DOH The Department of Health (DOH) said it is currently in talks with the representatives of US Pharmaceutical company Pfizer for possible procurement of the oral antiviral drug Paxlovid for the treatment of coronavirus disease (COVID-19). "Ang team ng DOH nakipagpulong, nakipag-ugnayan kay...
