Pet Food Recall Prompts Warning in Eight States
The U.S. Food and Drug Administration (FDA) is warning dog owners in eight states after some Blue Ridge Beef raw dog food was ...
US FDA approves Axsome Therapeutics' migraine drug
The U.S. Food and Drug Administration has approved Axsome Therapeutics' migraine treatment, the company said on Thursday.
Do food warning labels actually work? Answering your questions.
Readers had a lot to say about my latest column on the Food and Drug Administration’s proposed front-of-package labels. Most ...
FDA Approves the First Non-Opioid Pain Drug in 20 Years
The prescription pills, sold under the brand name Journavx and made by Vertex Pharmaceuticals, are taken twice a day and ...
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US drug agency approves potent painkiller — the first non-opioid in decades
The FDA’s nod for suzetrigine bolsters confidence in the pharmaceutical industry’s strategy to target sodium channels.
The Food Dyes And Additives That Are Banned In The United States vs. Europe, Explained By A Dietitian
Food additives have been a huge topic in the U.S. for years, but really caught fire earlier this month when the U.S. Food and ...
Americans might finally have to face what’s in their food
A front-of-package food label would be a great educational tool. The Trump administration should keep it.
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The FDA banned Red 3 food coloring. A scientist explains the dye’s history and health risks
These risks prompted California to ban its use in food in 2023 and the Food and Drug Administration to ban its use in both ...
More than 5,000 lbs of pet food recalled due to Salmonella risk
CINCINNATI (WKRC) - A pet food manufacturer has issued a recall due to Salmonella contamination. Blue Ridge Beef recalled ...
Food and Drug Administration wants to put nutrition labels front and center on food products
The U.S. Food and Drug Administration wants to put nutrition information front and center on food products to give consumers ...
ConsumerAffairs12h
A new non-opioid pain medication wins Food and Drug Administration approval
The U.S. Food and Drug Administration has approved Journavx (suzetrigine) 50 milligram oral tablets, marking the introduction of a first-in-class non-opioi ...
BioPharma Dive1d
Vertex’s non-opioid pain drug gets FDA approval in milestone for company and research
Despite high demand for an option like Journavx, doctors fear the drug’s price could be a major hangup for insurers, ...