The Institute for Healthcare Improvement offers a free, downloadable checklist to help healthcare organizations manage adverse events. The checklist, Respectful Management of Serious Clinical Adverse ...

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 ...

The FDA has launched a new adverse event reporting system that will consolidate several systems it has for reporting different types of adverse events, the agency announced Wednesday. The new system, ...

Health care workers face adverse events daily. These events include secondary trauma, occupational trauma, unexpected death or injury, moral injury, medical error and ...

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 ...

Although adverse event rates within 30 days after surveillance colonoscopy increase with age, peaking among patients aged 76-85 years, they remain infrequent, occurring in < 1% of procedures.

The FDA has launched a single public platform for adverse event reports related to drugs, biologics, vaccines, cosmetics and animal food. The Adverse Event Monitoring System will publish reports in ...

When safety concerns emerged for an FDA-regulated product, the suspected problem could be reported to one of seven online databases. The agency is now consolidating this reporting into a single online ...

ROCHESTER — The number of adverse health events reported in Minnesota's hospitals has increased slightly, the smallest increase since the start of the COVID-19 pandemic, according to the Minnesota ...

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, ...