The U.S. Food and Drug Administration (FDA) and drug manufacturer Novo Nordisk are warning consumers about “counterfeit” Ozempic found outside the authorized drug supply chain. The contents of ...

The U.S. Food and Drug Administration (FDA) and drug manufacturer Novo Nordisk are warning consumers about “counterfeit” Ozempic found outside the authorized drug supply chain. The contents of ...

The FDA temporarily suspended some milk quality tests due to federal workforce cuts. Testing of Grade A dairy products like milk, cheese, and yogurt has been paused. Experts say consumers should ...

Food and Drug Administration (FDA) Commissioner Marty Makary said he has no plans to change current policy to restrict access to the abortion pill mifepristone, despite a steady pressure campaign ...

Now, the U.S. Food and Drug Administration is warning the public about the risks. The FDA warning is about a topical spray version of finasteride, a drug often sold online by telehealth companies ...

The ongoing recall was made in February but wasn’t announced by the U.S. Food and Drug Administration (FDA) until this week, when it was made a Class II recall in an Enforcement Report from the ...

Many conservatives want the FDA to impose tighter restrictions on mifepristone and misoprostol, which can be delivered by mail. The medication accounted for 63 percent of U.S. abortions in 2023.

Two senior officials at the FDA's drug promotion regulatory office have resigned, leading to speculation that a clampdown on some direct-to-consumer (DTC) advertising of medicines could be on the way.

Martinelli's, famous for its glass-bottled apple juices, has begun recalling certain products, according to the Food and Drug Administration (FDA). The recall pertains to certain four-packs of ...

The pasteurization process cannot rid a product of patulin, either, the FDA says. “For humans, nausea, gastrointestinal disturbances and vomiting have been reported,” WHO writes of those who ...

The terms need to be negotiated before Novavax’s vaccine could be granted full approval, the source said, declining to be named because they weren’t authorized to speak on behalf of the FDA.