Pfizer and BioNTech announced Thursday that they had submitted an emergency request to the U.S. Food and Drug Administration for authorization of the companies' two-dose Covid-19 vaccine in children ...

Thirty percent of unvaccinated American adults say they’re waiting for the COVID-19 vaccines currently authorized for emergency use to be officially approved by the U.S. Food and Drug Administration.

(INDIANAPOLIS) – The three COVID vaccines approved in the U.S. have what’s called an emergency use authorization. That doesn’t mean they’re not safe. Opponents of vaccines or vaccine requirements have ...

LANCASTER, Pa. (WHTM) — In the midst of a coronavirus surge initiated by the delta variant, Pfizer’s COVID-19 vaccine received full FDA approval on Monday. The process for a vaccine to receive full ...

INDIANAPOLIS, April 16, 2021 /PRNewswire/ -- Eli Lilly and Company (NYSE: LLY) has requested the U.S. Food and Drug Administration (FDA) revoke the Emergency Use Authorization (EUA) for bamlanivimab ...

More than 110 million Americans have yet to receive their first booster shot. Novavax has submitted an application to the Food and Drug Administration for Emergency Use Authorization of its COVID-19 ...

Pfizer is asking federal regulators to authorize its experimental COVID-19 pill, which the drugmaker says can protect people from the most severe symptoms of the disease. Pfizer on Tuesday said it is ...

Pfizer-BioNTech submitted an application to the U.S. Food and Drug Administration Tuesday, for children ages 5 through 11-years-old to receive the COVID-19 vaccine booster, the company announced. In a ...

The Food and Drug Administration denied an emergency use authorization for fluvoxamine as a SARS-CoV-2 antiviral. Fluvoxamine was proposed as a possible antiviral in 2021 due to its mechanisms of ...

Indonesia has become the first country in the world to greenlight Novavax’s Covid-19 vaccine, the Maryland-based biotech announced Monday, a possible game changer in the fight against the pandemic and ...

Thirty percent of unvaccinated American adults say they’re waiting for the COVID-19 vaccines currently authorized for emergency use to be officially approved by the U.S. Food and Drug Administration.