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 ...

Drug safety relates to the potential for adverse effects related to the administration of drugs. Efforts to establish the safely profile of drugs begin early in their development, with in vitro ...

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 ...

Something to crow about is coming up Saturday at the Chicken Farm Art Center in San Angelo. The First Saturday Mad Spring Art Market will offer a range of art, food, fun for the family, music and ...

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 ...

FDA plans to rehire around 300 recently fired ... swiftly to cut wasteful spending and non-critical government jobs. Reporting by Patrick Wingrove and Michael Erman in New York and Rachael Levy ...

according to a Thursday report from The Partnership for Safe Medicines. Separately, a bipartisan coalition of state attorney generals have urged acting FDA Commissioner Sara Brenner to act on scammers ...

Gray cautioned that the results are not to be taken as a reason to stop overseas production of generic drugs. The US Food and Drug Authority (FDA) makes adverse event reports available on the 'FDA ...