For 35 years, the FDA has placed onerous restrictions on the only drug it has ever approved for treatment-resistant ...
Advocates and clinicians say that patients are still having trouble getting refills, even though the FDA has lifted REMS for ...
7don MSN
President Donald Trump’s pick to lead the US Food and Drug Administration told senators in a tense confirmation hearing ...
Marty Makary wouldn't commit to maintaining current access to mifepristone during his Senate confirmation hearing on Thursday ...
Dr. Marty Makary, President Trump's pick to run the Food and Drug Administration, faced questions from the Senate HELP ...
"Although the risk of severe neutropenia with clozapine still exists, FDA has determined that the REMS program for clozapine ...
Dr. Marty Makary, nominee to be commissioner of the U.S. Food and Drug Administration (FDA), appears before the Senate Health ...
The Muscular Dystrophy Association (MDA) welcomes the U.S. Food and Drug Administration (FDA) approval of the expanded indication of Alexion/AstraZeneca’s eculizumab (Soliris) for pediatric patients ...
If confirmed as FDA commissioner, Makary will report to ... which is required to be collected as a part of the REMS program, the Risk Evaluation and Mitigation Strategy,” Makary said in the ...
FDA Makes Access to Clozapine Easier for Patients With Schizophrenia By Stephanie Brown HealthDay Reporter FRIDAY, Feb. 28, 2025 (HealthDay News) -- The U.S. Food and Drug Administration has ...
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