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 ...
Nature

Gastrointestinal adverse events associated with Lenvatinib versus Lenvatinib plus Pembrolizumab: A pharmacovigilance study in FDA adverse event reporting system

This study aimed to empirically analyze gastrointestinal adverse events associated with Lenvatinib monotherapy and its combination with Pembrolizumab using FDA FAERS data (January 2015-December 2023), ...
Nature

Triptorelin associated adverse events evaluated using FAERS pharmacovigilance data

Triptorelin, a gonadotropin-releasing hormone(GnRH) agonist, is approved by the US Food and Drug Administration(FDA) for treating advanced prostate cancer ...
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 ...
FiercePharma

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

A new FDA adverse events monitoring system combines seven different databases across the spread of the agency's sectors, which together has cost the FDA $37 million yearly to operate. (Stock Photo ) ...
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 ...
TCTMD

‘Sobering’ Adverse Event Rate With Evoque Seen in Real-world Use

The number of adverse events reported with the Evoque transcatheter tricuspid valve replacement (TTVR) system (Edwards Lifesciences) during the first year of commercial use should put operators on ...
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 ...

Pfizer didn't say hantavirus is side effect of its COVID-19 vaccine, contrary to online claims

Those eager to discredit Pfizer's mRNA vaccine, which is safe and effective, exploited the cruise ship outbreak.
UUHC Health Feed

How to Recover from Adverse Events

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