Federal regulators say the newly identified products were flagged after state partners detected significant lead transfer ...

The request comes after a two-year review into reported links between GLP-1RAs and psychiatric adverse events.

Agency cites increased risk of febrile seizure risk in postmarking studies ...

Numerous recalls have been initiated in the past year because of the potential for foodborne illness and bacteria.

I’m a 70-year-old woman who has suffered with vaginal dryness ever since I went through menopause. My doctor has prescribed a ...

But, under anti-vaccine Health Secretary Robert F. Kennedy Jr.—who has numerous ties to the wellness industry—that FDA ...

The US Food and Drug Administration found no increased risk of suicidal behavior or ideation linked to popular weight-loss drugs, the regulator said in a letter Tuesday, and asked companies to remove ...

Federal regulators are telling drugmakers to remove label warnings about potential suicidal thoughts and behaviors from their ...

More changes are coming from the Food and Drug Administration as officials move to get rid of warning labels on some medications.Just last month, the administration announced it will remove black box ...

FDA commissioner Marty Makary said it would be “magical” for consumers to see prescription drugs on pharmacy shelves instead ...

Novo Nordisk, which has stumbled through a bit of a manufacturing hangover at a former Catalent production site it picked up a year ago, was hit with a warning letter from the FDA last month. The ...

The post “A Godsend”: ProPublica’s Rx Inspector Tool Is Helping People Find Critical Safety Information on Generic Drugs ...