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

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 ...

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, ...

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

Pevnick, M.D., M.S.H.S., discusses medications and the risk of an adverse drug event among older people after they get discharged from the hospital. Adverse drug events are common in the days 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, ...

Patients with adrenal insufficiency had significant improvements in bone and metabolic markers on a once-daily, low-dose ...

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.