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 ...

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 ...

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 ...

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 ...