FDA Drug Safety Suspensions

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gene therapy, FDA and Sarepta

FDA opens probe into mysterious death linked to gene therapy

The Food & Drug Administration is investigating the death of an 8‑year‑old following Elevidys gene therapy for Duchenne muscular dystrophy. U.S. distribution has been paused amid safety concerns.

· 8d · on MSN

Sarepta Refused FDA’s Request to Halt Elevidys Shipments

· 1d

FDA Probes Death of Patient on Sarepta's Elevidys, Partner Roche Says Death Unrelated to Therapy

BioSpace4d

Sarepta Concedes to FDA Request, Suspends US Shipments of Elevidys

After initially refusing to suspend Elevidys distribution after two deaths, Sarepta has now given in to the FDA’s request, ...

Makary ally named to key FDA drug post

Dr. George Tidmarsh, a Stanford pediatrics adjunct professor and former pharmaceutical executive, is FDA Commissioner Marty ...

5don MSN

FDA names former pharmaceutical company executive to oversee US drug program

FDA Commissioner Marty Makary announced that Dr. George Tidmarsh, a cancer and pediatric specialist, will direct the agency’s ...

Yahoo2mon

How the FDA's Milk Testing Pause Affects Your Child's Safety

By now, you have likely heard that the Food and Drug Administration (FDA) has suspended its testing procedures for milk in the U.S. But the information that has been dispersed online about this ...

ConsumerAffairs8d

FDA greenlights Juul’s e-cigarettes

FDA authorizes Juul’s tobacco- and menthol-flavored e-cigarettes to stay on U.S. shelves, reversing a previous ban due to new ...

15hon MSN

Zepto & Blinkit On The Radar Of The Maharashtra Food & Drug Administration For Inspection Of Dark Stores

Zepto and Eternal's quick-commerce arm Blinkit are on the radar of the Maharashtra Food and Drug Administration (FDA) for ...

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