The U.S. Food and Drug Administration recalled more than 580,000 bottles of a blood pressure medication. Is your medication ...
(Reuters) -The director of the U.S. Food and Drug Administration's Center for Drug Evaluation and Research, George Tidmarsh, ...
In any review of mifepristone, the FDA will now have to grapple with Judge Otake’s conclusion that the 2023 REMS decision for ...
The Food and Drug Administration (FDA) just announced that over 580,000 bottles of blood pressure medications made by Teva ...
The U.S. Food and Drug Administration (FDA) is warning consumers, patients and health care providers about the potential risk for serious complications from radiofrequency (RF) microneedling ...
It was the latest shockwave to sweep through an agency beset by all kinds of tumult in recent months. In interviews, ...
The approval was based on data from a Phase II trial, two retrospective chart review studies and an expanded access programme.