(Reuters) -Elanco Animal Health said on Friday it had received an emergency use authorization from the U.S. Food and Drug Administration for its flea and tick drug to treat dogs infected with a ...

The Food and Drug Administration (FDA) had rescinded emergency use authorizations (EUAs) for COVID-19 vaccines, Health and Human Services Secretary Robert F. Kennedy Jr. announced Wednesday, saying ...

The US Food and Drug Administration said Monday it had issued an emergency use authorization for Eli Lilly and Co's monoclonal antibody therapy to treat mild to moderate coronavirus infections in ...

The Food and Drug Administration on Monday revoked emergency use authorization for giving the malaria drug hydroxychloroquine, and a related drug chloroquine, for COVID-19. The drugs were heavily ...

Pfizer/BioNTech has initiated its application to the US Food and Drug Administration for full FDA approval of its Covid-19 vaccine for people ages 16 and older, the companies said Friday. This is the ...

The Food and Drug Administration gave emergency approval to a coronavirus antibody test that has 100% accuracy, according to its Swiss manufacturer. According to drugmaker Roche, the antibody test has ...

The U.S. Food and Drug Administration has approved emergency use authorization for a booster shot of the Pfizer-BioNTech vaccine to be given at least six months after completion of the second dose for ...

The United States continues to set new pandemic records – on Thursday, the country reported more than 225,000 new coronavirus cases and 3,100 deaths, according to a tally by NBC News. The nationwide ...

De Novo clearance for urinary incontinence wearable. The FDA has granted De Novo clearance to Atlantic Therapeutics’ Innovo therapy device, an externally worn electrical muscle stimulator for the ...

On Tuesday, September 23, 2025, FDA published guidance titled “Consideration of Enforcement Policies for In Vitro Diagnostic Tests During a Section 564 Declared Emergency.” The guidance, a draft of ...