The United States Food and Drug Administration (FDA) has suspended the license for Valneva's chikungunya vaccine Ixchiq with ...

System integrates glucose biosensor with an AI-driven platform to show how food, activity, stress, sleep affect the body in ...

The FDA said it has begun publishing reports of adverse events concerning drugs on a daily basis, instead of quarterly, as it ...

FDA recalls 7Up Zero Sugar Tropical Soda for being mislabeled full-sugar soda. The affected cans were sold in 12-packs in ...

The Food and Drug Administration approved Papzimeos (zopapogene imadenovec-drba) for the treatment of adults with recurrent ...

The U.S. FDA has advised the public to not eat, sell, or serve certain imported frozen shrimp from an Indonesian firm as it ...

As part of its enforcement activities, the Food and Drug Administration sends warning letters to entities under its ...

A. The Food and Drug Administration has approved montelukast to treat asthma, exercise-induced bronchoconstriction (trouble ...

When the IND green light flashed, labs across three continents synchronized—inside the trial that could dethrone chemo kings.

The FDA classifies this recall as Class II, which the agency describes as a situation "in which use of or exposure to a ...

The U.S. Food and Drug Administration has started "real-time reporting of adverse event data," according to an annoucement ...

Another seafood company is voluntarily recalling a number of its frozen shrimp products after a potential radioactive ...