FDA Definition- Any adverse event associated with the use of drugs in humans whether or not considered drug related including the following: ·an adverse event occurring in the course of the ...

Generic drugs manufactured in India are linked to significantly more "severe adverse events" for patients who use them than equivalent drugs produced in the United States, a new study finds.

S hares of Zoetis (NYSE:ZTS) traded lower on Tuesday after the U.S. FDA notified veterinarians about adverse events linked to the company’s pain therapy, Librela (bedinvetmab injection ...