WASHINGTON - The Food and Drug Administration has launched what it is describing as a "unified dashboard" for identifying and ...

System will replace safety databases monitoring drugs, devices, food, and more ...

Adverse drug events (ADEs)—injuries caused by medications— are estimated to rank among the leading causes of death in the United States and represent a major, often preventable threat to patient ...

FDA launches new AI-powered system to track drug and vaccine side effects in real time, replacing outdated databases and saving $120 million annually.

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

The AI adverse event problem nobody is talking about reveals risks in FDA-cleared surgical devices lacking robust clinical ...

Add Yahoo as a preferred source to see more of our stories on Google. The FDA announced it will now update its Adverse Event Reporting System every day, instead of once per quarter. Photo courtesy FDA ...

Yesterday, the Food and Drug Administration (FDA) announced the launch of the Adverse Event Monitoring System ( AEMS ), a new platform for assessing adverse event reports made to the FDA for drugs, ...

ASH 2025 data emphasize that standardized protocols and strong academic-community communication are essential for safe and consistent management of bispecific antibody adverse events in community ...

A registry study across 14 Japanese clinics analyzed 179 cases of post-COVID-19 vaccination syndrome (PCVS) and identified ...

The Modernization of Cosmetics Regulation Act of 2022 (MoCRA) is bringing sweeping changes to the cosmetics industry. One such change requires a “responsible person” to maintain and submit certain ...

Please provide your email address to receive an email when new articles are posted on . Women with vs. without cancer had similar serious adverse event risk after fertility preservation. Younger age, ...