Seafood Recall Update As FDA Sets Risk Level
The seafood salad may be of particular risk to those customers who have an allergy or severe sensitivity to soy, the FDA has ...
The FDA Can’t Decide Whether Zepbound Is in Shortage. It’s Good News for Hims & Hers Stock.
The Food and Drug Administration told a federal judge Thursday that it needs more time to reconsider whether Eli Lilly’s ...
Cape Cod Times1d
Eaten any cucumbers slices lately? There's a recall in 26 states, including Mass.
Cucumbers are being recalled again in 26 states and five Canadian provinces for possible salmonella contamination, and yes, ...
BioSpace8d
FDA Still Undecided About Shortage Status of Lilly’s Tirzepatide
Pending the FDA’s decision, compounding pharmacies will remain free to make and market versions of the blockbuster ...
FDA probes blood cancer risk from bluebird's gene therapy, weighs regulatory action
The U.S. Food and Drug Administration is weighing the need for a regulatory action on bluebird bio's gene therapy for a rare ...
pharmaphorum2d
FDA probing cancer cases with Bluebird's CALD gene therapy
The FDA is scrutinising reports of haematological cancers in patients treated with bluebird bio's gene therapy for the rare ...
Drinking Water Recall Update as FDA Changes Status
One drinking water recall issued earlier this year by the U.S. Food and Drug Administration was terminated last week.
Exclusive: US FDA finds widely used asthma drug impacts the brain
U.S. government researchers have found that a widely prescribed asthma drug originally sold by Merck & Co may be linked to ...
Targeted Oncology10d
FDA Updates Fludarabine Labeling Under Project Renewal Initiative
The FDA updated the fludarabine phosphate injection labeling under Project Renewal, clarifying the dosage for combination ...
The American Journal of Managed Care5d
FDA Advised to Update Labels on GLP-1 Weight-Loss Drugs
In the US, liraglutide, semaglutide, and tirzepatide are currently under investigation for their ability to stimulate weight ...
Business Insider12d
PharmaTher Announces Update on FDA New Drug Application for Ketamine
FDA granted a post-complete letter clarification meeting scheduled ... and Company is not obligated to update or revise any forward-looking information, whether as a result of new information, future ...
Soup Recall Update as FDA Sets Highest Risk Level
A soup mix recall issued this month has been updated by the U.S. Food and Drug Administration (FDA) as a Class I risk, the ...