The U.S. Food and Drug Administration (FDA) is warning dog owners in eight states after some Blue Ridge Beef raw dog food was ...
The U.S. Food and Drug Administration has approved Axsome Therapeutics' migraine treatment, the company said on Thursday.
Readers had a lot to say about my latest column on the Food and Drug Administration’s proposed front-of-package labels. Most ...
The prescription pills, sold under the brand name Journavx and made by Vertex Pharmaceuticals, are taken twice a day and ...
These risks prompted California to ban its use in food in 2023 and the Food and Drug Administration to ban its use in both ...
The U.S. Food and Drug Administration has approved Journavx (suzetrigine) 50 milligram oral tablets, marking the introduction ...
You may have heard in the news that the U.S. Food and Drug Administration will no longer allow the use of FD&C Red Dye No. 3 ...
Despite high demand for an option like Journavx, doctors fear the drug’s price could be a hangup for insurers and limit ...
The FDA just approved a new type of pain medication, and it's a non-opioid called suzetrigine that stops body pain at its ...
The U.S. Food and Drug Administration wants to put nutrition information front and center on food products to give consumers ...
CINCINNATI (WKRC) - A pet food manufacturer has issued a recall due to Salmonella contamination. Blue Ridge Beef recalled ...
On January 16, 2025, the Food and Drug Administration (FDA) issued an order banning FD&C Red No.3 in food and ingested drugs.1 Food and ingested ...