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The FDA Adverse Event Reporting System, which Commissioner Marty Makary called “clunky,” previously published updates on a ...
The US Food and Drug Administration on Friday revealed it has begun daily publication of adverse event data from the FDA ...
As Department of Health and Human Services (HHS) and FDA leadership continue to look for ways to boost transparency and ...
The FDA said it has begun publishing reports of adverse events concerning drugs on a daily basis, instead of quarterly, as it ...
The FDA has started reporting real-time data about adverse events through the FDA Adverse Event Reporting System, improving ...
The U.S. Food and Drug Administration said that it has begun the daily publication of adverse event reports related to drugs ...
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Tampa Free Press on MSNFDA Adverse Event Data Reveals Disturbing Links Between SSRIs And Violent Behavior
A new commission will investigate the prevalence of SSRI antidepressants as adverse event reports document hundreds of cases ...
What makes this method of AE reporting more exciting is that it is happening in more-or-less real time and can capture AEs after the trial period has ended.
The U.S. Food and Drug Administration has started "real-time reporting of adverse event data," according to an annoucement ...
The FDA announced it has commenced daily publication of adverse event data from the FDA Adverse Event Reporting System (FAERS ...
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