Adverse drug reactions (ADRs) remain a common clinical ... Current regulatory oversight has failed to uncover important adverse effects and there is mounting public concern regarding drug safety.
According to the U.S. Food & Drug Administration, “side effects, also known as adverse events, are unwanted or unexpected events or reactions to a drug.” While some side effects are minor and ...
The agency recommended that the maker of Librela update its label to reflect the possibility of more serious adverse ... side effects, such as urinary tract and skin infections. But since the drug ...
According to the American Kennel Club, side-effects from the drug Librela included a skin reaction at the injection ... expect will reflect post-approval adverse event reporting and be consistent ...
Concerned over the widely used life-saving beta blocker drugs causing adverse drug reactions, the government’s Indian Pharmacopoeia Commission (IPC) has issued an alert about the same.