The Food and Drug Administration’s (FDA) Psychopharmacologic Drugs Advisory Committee (PDAC) voted 10-1 against the approval of brexpiprazole in combination with sertraline for the treatment of adults ...

A recall of bread amid fears it contains undeclared hazelnuts—a potentially deadly allergen to some—was classified as a ...

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

Replimune shares collapsed on Tuesday after the U.S. Food and Drug Administration rejected the clinical-stage biotechnology company's proposed advanced melanoma treatment. Shares of the Woburn, Mass., ...

Sarepta Therapeutics reversed course and agreed to halt all shipments of Elevidys, its gene therapy for Duchenne muscular ...

Pennsylvania-based A.P. Deauville, LLC is recalling several types of its Power Stick deodorant, due to a process issue.

Curcumin, the active ingredient in the spice turmeric, hasn’t been clinically proven to slow disease progression in people with dementia or Alzheimer’s disease, but researchers believe it has some ...

The US Food and Drug Administration has announced a plan to revoke 52 food standards after concluding they are "obsolete and unnecessary." ...

U.S. Food & Drug Administration (FDA) warning letter to a prominent wellness product and services company offers a blunt reminder ...

Pennsylvania-based A.P. Deauville, LLC is recalling several types of its Power Stick deodorant, due to a process issue.

The FDA has granted marketing authorization to JUUL Labs, allowing the sale of the JUUL System, a closed, cartridge-based nicotine vapor product, in the US.

Xanthan gum is a common additive that helps in thickening and stabilizing various products. Let's find out more about its ...