FDA launches new AI-powered system to track drug and vaccine side effects in real time, replacing outdated databases and saving $120 million annually.

Cream cheese recall upgraded as experts warn of ‘serious adverse health consequences or death’ - Over a dozen flavors of cream cheese have been recalled due to Listeria concerns ...

March 11 (Reuters) - The U.S. Food and Drug Administration said on Wednesday it has introduced a unified platform designed to ...

The reports of the two deaths of a man and a woman were made to the Medicines and Healthcare products Regulatory Agency (MHRA ...

Bengaluru: The U.S. Food and Drug Administration said on Wednesday it has introduced a unified platform designed to ...

FDA replaces seven fragmented adverse event databases with AEMS, enabling real-time safety signal access for pharmaceutical manufacturers and researchers. On March 11, the FDA launched a unified ...

Officials wrote that Novo Nordisk had failed to failed to report ‘serious and unexpected’ adverse drug experiences ...

FDA warns Novo Nordisk for failing to report adverse drug events at its Plainsboro, N.J. site during a 2025 inspection.

A case series reports dysesthesia and allodynia in patients treated with semaglutide and tirzepatide, suggesting a possible dose related to sensory adverse effect.

The U.S. Food and Drug Administration (FDA) has issued a warning to Novo Nordisk over its alleged failure to report adverse side effects, including death, in patients who took its GLP-1 medications, ...

Novo Nordisk has been sent a warning letter from the FDA for a series of violations of postmarketing adverse drug experience (PADE) regulations, including failure to report side effects among patients ...

Drug executives say only their GLP-1 drugs are safe for treating obesity and diabetes as they wage a year-long campaign to ...