Less than three-quarters of medical device-related adverse events are reported on time by their manufacturers.
The inspection comes after a ProPublica investigation revealed that drugs made at the Glenmark Pharmaceuticals plant ...
I was invited by the Frederick County Health Department to attend the Jan. 22 “Community Health Needs Assessment Public Input Session” and was greatly disappointed. Various “experts” gave ...
The Food and Drug Administration unexpectedly canceled an annual meeting of its advisers to update next season's influenza vaccines, an adviser on the panel and multiple officials tell CBS News ...
Adverse event reports they relied on are available in the FDA Adverse Event Reporting System (FAERS) database. “Using exact matching analyses based on the equivalency criteria established by the US ...
The objective of this study was to evaluate adverse events(AEs) associated with ripretinib using data from the FDA Adverse Event Reporting System (FAERS) database. Methods: Individual case safety ...
WASHINGTON — The Trump administration has started quietly rehiring some of the Food and Drug Administration employees it fired last week, according to nine agency sources, shortly after letting ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results