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FDA Appoints Biotech Exec

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· 22h · on MSN

FDA names former pharmaceutical company executive to oversee US drug program

The Food and Drug Administration named a longtime pharmaceutical executive to run the agency’s drug program. Dr.

· 21h · on MSN

Biotech exec George Tidmarsh picked as FDA's chief drug regulator

· 21h

FDA appoints biotech veteran George Tidmarsh to lead drug evaluation division

FDA recalls Power Stick

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· 19h · on MSN

The FDA just recalled 67,000 cases of deodorant — here’s what you need to know

But one thing we’re confident about is that nobody wants to use a deodorant that has been recalled, which is why we are sharing this news: The Food and Drug Administration has issued a recall on 67,000 cases of Power Stick antiperspirant deodorant.

· 1d · on MSN

FDA recalls over 67,000 cases of Power Stick deodorant due to manufacturing violations

· 1h

FDA recalls Power Stick; what to know about deodorant recall 2025

11mon MSN

Sarepta shares slide again as drugmaker bows to FDA pressure to pause gene therapy

Sarepta Therapeutics is pausing shipments of its gene therapy for muscular dystrophy following several patient deaths that ...

23hon MSN

FDA Issues Highest Risk Warning For Mushroom Recall

Mushrooms sold across two states have been recalled over fears they could be harboring listeria, a bug that "can cause ...

4hon MSN

FDA commissioner stirs debate over hormone therapy for menopause

A Food and Drug Administration expert panel has reignited a debate over whether hormone therapy should be used to treat ...

Healio2h

FDA grants orphan drug designation to taladegib for IPF

The FDA granted an orphan drug designation to novel hedgehog pathway inhibitor taladegib, also known as ENV-101, for treating ...

1don MSN

FDA Suspends Muscular Dystrophy Drug After 3 Patient Deaths

The U.S. Food and Drug Administration ( FDA) has placed an immediate clinical hold on Sarepta Therapeutics' investigational ...

17h

FDA Approves Prefilled Syringe Presentation for Shingles Vaccine

Prefilled syringe eliminates the need to reconstitute separate vials prior to administration and simplifies the vaccine ...

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Food and Drug Administration

FDA Panel Rejects Brexpiprazole-Sertraline Combo for PTSD

An FDA advisory panel concludes that the efficacy of brexpiprazole, when started concurrently with sertraline, has not been ...

15hon MSN

FDA Announces Massive Ice Cream Recall in 23 States

The Food and Drug Administration (FDA) makes sure to stay on top and notify people whenever a recall is put into place.

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