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US FDA approves AbbVie's drug for a type of lung cancer
The U.S. Food and Drug Administration has approved AbbVie's drug to treat adults with a type of lung cancer who have received ...
FDA Approves Merck's Kidney Cancer Drug For Rare Type Of Neuroendocrine Tumors
The U.S. Food and Drug Administration (FDA) on Wednesday approved Merck & Co. Inc.’s (NYSE:MRK) Welireg (belzutifan) for ...
NIH, FDA to focus on processed foods, US health secretary says
U.S. health secretary Robert F. Kennedy Jr. said on Wednesday that the "central focus" of the National Institutes of Health ...
FDA: Premade Sandwiches Recalled Over Listeria Contamination
Fresh and Ready Foods LLC is recalling 86 different types of ready-to-eat sandwiches due to listeria concerns. Here is a list ...
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FDA Plans Ban on Kids’ Ingestible Fluoride Drugs
The U.S. Food and Drug Administration announced on May 14, 2025, plans to remove concentrated ingestible fluoride ...
In-N-Out to remove red dye No. 3 from its strawberry milkshake and pink lemonade
The popular California-based fast food burger chain is giving some of its drinks and ketchup a new taste after the FDA banned ...
Tomatoes Recalled in 14 States as FDA Sets Highest Risk Level
Healthy persons infected with salmonella often experience fever, diarrhea, nausea, vomiting and abdominal pain.
FDA moves to ban widely used kids’ supplements over brain damage risk
The FDA has initiated the process of banning this kind of supplement for children due to fears that it is a neurotoxin.
FDA to review nutrients in baby formula: 3 things for parents to know
The FDA currently specifies 30 nutrients that must be included in infant formulas. There are minimum amounts for all 30 nutrients and maximum amounts for 10 nutrients, according to the agency. Among ...
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Former FDA head Robert Califf says RFK Jr.’s vaccine rhetoric is ‘doing harm’ to Americans
Ex-FDA chief Robert Califf about HHS Secretary Robert F. Kennedy Jr. — “My primary worry is not the FDA, my worry is the ...
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FDA Approves Use of Optison in Pediatric Patients With Suboptimal Echocardiograms
The Food and Drug Administration (FDA) has approved Optison ™ (perflutren protein-type A microsphere) injectable suspension for use in pediatric patients with suboptimal echocardiograms to opacify the ...
Biohaven Shares Down as FDA Extends PDUFA Data for Troriluzole
Biohaven shares slipped after the Food and Drug Administration extended the Prescription Drug User Fee Act date for the biopharmaceutical company's troriluzole application by three months. The stock ...