Nature

Drug Safety and Adverse Event Analysis in Clinical Trials

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 ...
FiercePharma

FDA rolls out daily updates to adverse event dashboard, plans to further 'streamline' system

As Department of Health and Human Services (HHS) and FDA leadership continue to look for ways to boost transparency and reshape the U.S' healthcare infrastructure, the U.S. drug regulator has unveiled ...
STAT

FDA says it will publish reports of adverse events tied to drugs on daily basis

Lizzy Lawrence leads STAT’s coverage of the Food and Drug Administration. She was previously a medical devices reporter. You can reach Lizzy on Signal at lizzylaw.53. WASHINGTON — The Food and Drug ...
CNN

With about 5,000 adverse events related to cosmetics reported to the FDA each year, the agency is updating its oversight

The US Food and Drug Administration receives about 5,000 reports each year about health problems related to the use of cosmetic products, and under a new law, the agency has issued updated ...
UPI

FDA to provide daily updates on adverse events

The U.S. Food and Drug Administration is now providing real-time, daily publication updates on adverse event data from its reporting system. In an effort to modernize and provide transparency on ...
MedPage Today on MSN

Adverse Event Risks Vary Among Asthma Biologics, FDA Data Show

C HICAGO -- Adverse event risks varied across biologics used by asthma patients, an analysis of data submitted to the FDA ...