Adverse drug events are more common in older people with comorbidities, a new study finds. Factors that are independently linked with adverse drug events are being female, taking more drugs daily, ...

A new study has found Twitter contains more than three times as many reports of adverse reactions for 23 commonly used medications than the Food and Drug Administration. For the study, researchers ...

A new study explored the correlation between older, hospitalized women and adverse drug reactions. When hospitalized, 28% of women experienced one or more adverse drug reactions compared to 21% of men ...

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 ...

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

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, ...

The U.S. Food and Drug Administration said that it has begun the daily publication of adverse event reports related to drugs and biological products. This marks a shift from the previous quarterly ...

The evaluation of drug safety in clinical trials is a critical element of the drug development process, ensuring that therapeutic benefits outweigh potential harms. Clinical trials, particularly in ...

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

CHICAGO -- Adverse event risks varied across biologics used by asthma patients, an analysis of data submitted to the FDA Adverse Event Reporting System (FAERS) showed. In comparing relative number of ...

Adverse reactions to prescription drugs (adverse drug events, or ADEs) are quite common and usually do little harm to patients. But in a small percentage of cases, they can have serious consequences ...