Please provide your email address to receive an email when new articles are posted on . The FDA Adverse Event Reporting System will now host daily publications, instead of quarterly. The agency’s goal ...

Harm and the potential for harm from medical care is pervasive and well-documented. Much of the safety literature has historically focused on physical harm, but the Agency for Healthcare Research and ...

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 ...

Add Yahoo as a preferred source to see more of our stories on Google. Laidler was hardly alone in submitting his symptoms to VAERS. Each year, more than 38,000 Americans report possible side effects ...

The FDA Adverse Event Reporting System (FAERS) contains reports from health care professionals, consumers, and manufacturers on adverse events, serious medication errors, and product quality ...

Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) have revolutionized the management of metabolic diseases, offering substantial benefits in glycemic control, weight reduction, cardiovascular ...

Please provide your email address to receive an email when new articles are posted on . The FDA launched a new online dashboard for reporting adverse events related to cosmetic products. This ...

The ECRI Institute Patient Safety Organization has released a new version of its adverse event collection and reporting system. ECRI Institute has continued to update and improve its web-based patient ...

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 ...