Earlier this month, the FDA backed off on a pause in shipments of the chikungunya vaccine Ixchiq to older adults. Now, the ...

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

The FDA Adverse Event Reporting System, which Commissioner Marty Makary called “clunky,” previously published updates on a ...

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

SCA slowdown, with FDA review set for Q4 2025 and no advisory meeting required. Find out why BHVN stock is a strong buy.

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

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

Shares of Axogen fell more than 15% in premarket trading Monday after the U.S. Food and Drug Administration extended by three months its review of the proposed transition of the company's Avance nerve ...

Kennedy, a skeptic of weight-loss drugs, has advocated for dietary and behavioral changes over GLP-1s to reverse the most ...

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

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

Some packages of Great Value frozen shrimp sold at Walmart are at risk for potential for Cesium-137 contamination, the FDA ...