The U.S. Food and Drug Administration has denied approval for PTC Therapeutics' oral medication for a rare genetic disorder ...

A series of panels convened by the Food and Drug Administration is raising concerns that the agency is skirting federal rules ...

The Food and Drug Administration (FDA) became authorized Tuesday to allow the use of animal drugs to treat or prevent ...

The FDA urged consumers not to use the foam-style products because they may not be effective in protecting the skin from the sun's harmful UV rays.

The U.S. Department of Health and Human Services (HHS) issued a declaration on Aug. 19 allowing the U.S. Food and Drug Administration (FDA) to issue Emergency Use Authorizations (EUAs) for animal ...

The U.S. Food and Drug Administration has declined to approve PTC Therapeutics' drug to treat a rare genetic disorder with ...

More than 5,000 pounds of cheese products made by Middlefield Original Cheese Co‑op are being voluntarily recalled after the ...

The biotech, which cut jobs following the rejection in May of its Barth syndrome therapy, claimed it has addressed the agency ...

Families concerned about color additives in school lunches, at grocery stores and at fast-food counters can now reference a ...

Lead is toxic to people of any age or health status and higher exposure levels can lead to neurological changes ...

Some experts worry that patient groups’ growing influence is leading to the approval of drugs that may not work and could sometimes be dangerous.

The 5th Circuit ruled on Aug. 16 that it would limit access to mifepristone, finding that the Food and Drug Administration overstepped its authority with a series of actions that made it easier ...