Medscape

FDA Puts 16 Drugs on Watch List

April 17, 2012 — The US Food and Drug Administration (FDA) today issued its latest quarterly list of drugs to monitor after having identified potential signs of serious risks or new safety information ...
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 ...
Healio

FDA begins daily reporting of adverse event data

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 ...
Seeking Alpha

FDA starts daily publication of adverse event data

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 ...
Medscape

Violence and Prescription Drugs

Moore and associates extracted from the US Food and Drug Administration's Adverse Event Reporting System (AERS) all serious adverse event reports for drugs with 200 or more cases received from 2004 ...