Pfizer oral COVID-19 pill gets U.S. authorization for at-home use
231 Articles
231 Articles
FDA authorizes second antiviral pill to treat COVID-19 - Local News 8
By Jamie Gumbrecht, Amanda Sealy and Jacqueline Howard, CNNThe US Food and Drug Administration on Thursday authorized Merck’s antiviral pill, molnupiravir, to treat COVID-19 “for the treatment of mild-to-moderate coronavirus disease (COVID-19) in adults with positive results of direct SARS-CoV-2 viral testing, and who are at high risk for progression to severe COVID-19, including hospitalization or death, and for whom alternative COVID-19 treatm…
Merck’s at-home antiviral COVID-19 pill gets US authorization
Author: ReutersID: 1640277240159278300Thu, 2021-12-23 19:39 DUBAI: The US on Thursday authorized Merck & Co’s antiviral pill for COVID-19 for certain high-risk adult patients, a day after giving the go-ahead to a similar but more effective treatment from Pfizer Inc. Merck’s drug, molnupiravir, developed with Ridgeback Biotherapeutics, was shown to reduce hospitalizations and deaths by around 30 percent in a clinical trial of high-risk individu…
FDA authorizes second antiviral pill to treat Covid-19
By Jamie Gumbrecht, Amanda Sealy and Jacqueline Howard | CNNThe US Food and Drug Administration on Thursday authorized Merck’s antiviral pill, molnupiravir, to treat Covid-19 “for the treatment of mild-to-moderate coronavirus disease (COVID-19) in adults with positive results of direct SARS-CoV-2 viral testing, and who are at high risk for progression to severe COVID-19, including hospitalization or death, and for whom alternative COVID-19 treat…
FDA Authorizes First Oral Antiviral for Treatment Of COVID-19
On Wednesday, the U.S. Food and Drug Administration issued an emergency use authorization (EUA) for Pfizer’s Paxlovid, nirmatrelvir tablets,… FDA Authorizes First Oral Antiviral for Treatment Of COVID-19
US health regulator authorizes Pfizer's Covid pill as Omicron surges
The United States on Wednesday authorized Pfizer's anti-Covid pill for high-risk people aged 12 and up, as a surge of cases driven by the highly infectious Omicron variant threatened holiday plans and Americans struggled to find tests.Paxlovid, which comprises two types of tablet, was granted an emergency use authorization by the Food and Drug Administration (FDA) after a clinical trial showed it to reduce the risk of hospitalizations and deaths…
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