Federal Register14d
Food and Drug Administration
The Food and Drug Administration (FDA or Agency) is denying a request for a hearing submitted by Yong Sheng Jiao, also known as Yongsheng Jiao and Wilson Jiao (Jiao), and is issuing an order under the ...
USA Today17d
FDA: Costco eggs recalled over salmonella fears now classified as highest risk level
The Food and Drug Administration has classified a recall of eggs sold at Costco caused by potential salmonella contamination as the highest risk level for infection. The FDA defines a Class I ...
Medical News Today17d
Topamax (topiramate) dosing schedule and details
To treat seizures, the typical starting dosage is 50 mg per day. Topamax is a brand-name drug approved by the Food and Drug Administration (FDA) to help prevent migraine headaches in adults and ...
CNN17d
There’s still no generic Ozempic, but a lower-priced daily injected GLP-1 is coming
The US Food and Drug Administration on Monday approved a generic version of the daily injectable GLP-1 medicine liraglutide for people with type 2 diabetes, opening the door for lower-priced ...
The Laconia Daily Sun18d
GLP-1 Zepbound Is Approved As First Drug For Sleep Apnea
MONDAY, Dec. 23, 2024 (HealthDay News) -- The U.S. Food and Drug Administration (FDA) has approved the first prescription medication specifically for treating obstructive sleep apnea (OSA): the weight ...
New Atlas20d
"100% successful" cancer drug gets landmark FDA approval
Hugely promising cancer drug dostarlimab is one step closer to being widely available, after the Food and Drug Administration ... 30-40% of requests have been approved. Dostarlimab has been ...
FiercePharma21d
A 'pivotal moment': Ionis enters next phase of commercial evolution with Tryngolza's FDA approval
With an FDA approval for Tryngolza (olezarsen) to treat the rare genetic disorder familial chylomicronemia syndrome (FCS), Ionis Pharmaceuticals enters a new era. While Ionis has gained several ...
Yahoo Finance21d
U.S. FDA Approves Pfizer’s BRAFTOVI® Combination Regimen as First-Line Treatment of BRAF V600E-Mutant Metastatic Colorectal Cancer
NEW YORK, December 20, 2024--(BUSINESS WIRE)--Pfizer Inc. (NYSE: PFE) today announced that the U.S. Food and Drug Administration (FDA) has approved BRAFTOVI ® (encorafenib) in combination with ...
CNN22d
Which foods are ‘healthy’? FDA has new requirements for food labels
“It’s critical for the future of our country that food be a vehicle for wellness. Improving access to nutrition information is an important public health effort the FDA can undertake to help ...
STAT22d
Ionis wins FDA approval for a rare disease therapy that lowers triglycerides
Ionis Pharmaceuticals on Thursday won Food and Drug Administration approval of a therapy for patients with a rare and deadly genetic disease that impedes the body’s ability to break down fats ...
JD Supra22d
Three Overhauls to Accelerated Drug Approval You Need to Know About: Novel Endpoints, Confirmatory Trials, and Expedited Withdrawal of Approvals
Earlier this month, the US Food and Drug Administration (FDA) issued new draft guidance regarding their accelerated approval pathway for new drugs and biologics, an expedited program designed to ...