Healio

Transparency or ‘unnecessary alarm’? Explaining FDA’s reporting tool for cosmetic harms

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 ...
clinicaladvisor.com

FDA Now Providing Daily Updates on Adverse Events

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 ...
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 ...
Medscape

Patient-Reported Outcome Data Enhances Reliability of Adverse Event Assessments in Cancer Care

Access to patient-reported outcome (PRO) data significantly improved providers' consistency in assessing adverse events in patients with cancer, with the greatest improvements observed for ...
Everyday Health

FDA Raises Safety Concerns About Compounded GLP-1 Weight Loss Drugs

The FDA has received hundreds of adverse event reports after people used compounded GLP-1 drugs for weight loss. Compounded GLP-1 drugs aren’t reviewed by the FDA for safety or effectiveness. The FDA ...
FiercePharma

FDA rolls out new streamlined adverse event monitoring system, eyes $120M in savings

It’s out with the old, in with the new at the FDA as the agency is unveiling a new adverse events monitoring system that joins several reporting systems into one unified platform, an effort that’s ...
MedPage Today

So Long, MAUDE? FDA Launches New Combined Adverse Event Database

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, ...
RAPS

FDA consolidates adverse events reporting systems

The US Food and Drug Administration (FDA) announced it is unifying its various adverse reporting systems into a single system called the Adverse Event Monitoring System (AEMS). The agency said the ...
Becker's Hospital Review

FDA launches single adverse event platform

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 ...