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 ...

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 ...

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 ...

Moderna has submitted a request to the Food and Drug Administration (FDA) to authorize booster doses of its coronavirus vaccine for all adults, seeking to expand the number of people eligible for a ...

Since the start of the pandemic, the Food and Drug Administration has signed off on 430 COVID-19 tests through its emergency use authorization powers — rules that let the agency push tests and drugs ...

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.