Sarepta Therapeutics, FDA and gene
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The Food and Drug Administration (FDA) has been busy lately with various recalls. One involved Power Stick deodorant and another involved various ice cream bars across 23 states. Now, a new recall was announced on Monday by the FDA,
Thursday’s authorization, following a multiyear FDA review, has come under scrutiny, including from Yolanda Richardson, president and CEO of Campaign for Tobacco-Free Kids, who called it a “big step” backward for preventing youth e-cigarette use.
The U.S. Food and Drug Administration ( FDA) has placed an immediate clinical hold on Sarepta Therapeutics' investigational gene therapy trials for limb girdle muscular dystrophy following three patient deaths potentially linked to the company's treatments.
A Food and Drug Administration expert panel has reignited a debate over whether hormone therapy should be used to treat menopause. The 12-person panel encouraged the use of the
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Health and Me on MSN"Obsolete And Unnecessary": FDA Set To Revoke 52 Nutrition And Labeling RulesThe FDA plans to revoke 52 outdated nutrition and labeling regulations to streamline food industry standards, citing them as obsolete and no longer necessary for modern practices.
US Food and Drug Administration Commissioner Marty Makary signaled Thursday that he is open to revising strict warning labels on Hormone Replacement Therapy.
Recent actions by the Food and Drug Administration (FDA or Agency) reflect a sharpened scrutiny in areas where public health and safety may
WASHINGTON (AP) — The Food and Drug Administration is allowing vaping brand Juul to keep its e-cigarettes on the market. Copyright © 2025 The Associated Press. All rights reserved. This material may not be published, broadcast, written or redistributed.