Food and Drug Administration

FDA Approves 1st Non-Opioid Pain Medicine in 20 Years

FDA approves new pain medication as an alternative to opioids: What to know about Journavx

The FDA on Thursday approved a new class of pain medication that provides an alternative to opioids. It will be sold under the brand name Journavx.

U.S. News & World Report · 2h

FDA Approves First New Non-Opioid Pain Pill in Decades

FRIDAY, Jan. 31, 2025 (HealthDay News) -- The U.S. Food and Drug Administration (FDA) has approved Journavx, a new pain reliever without the risks of addiction or overdose linked to drugs like Vicodin and OxyContin.

CNN on MSN · 13h

FDA approves first new type of pain medication in 25 years

A new pain relief drug, suzetrigine, is a prescription pill that’s taken every 12 hours after a larger starter dose. It will be sold under the brand name Journavx.

FDA upgrades recall of Lay's potato chips

Newsweek on MSN · 2d

Chocolate Recall Update As FDA Sets Highest Risk Level for 9 States

A recall which was issued across nine states has now been given the highest risk classification by the federal agency.

USA Today · 2d

Lay's potato chips recall upgraded to FDA's most serious level. Is Ohio affected?

The FDA elevated Lay's Classic Potato Chips to the highest risk level. Here what to know, and whether the recall impacts Ohio.

Hosted on MSN · 23h

Lay's potato chips recalled over life-threatening risk as FDA issues warning

Lay recall on Lay's Classic Potato Chips across Oregon and Washington was updated to a Class 1 recall by the FDA on Thursday.

2don MSN

FDA approves Ozempic to reduce risks from chronic kidney disease in diabetes patients

Ozempic, the blockbuster GLP-1 drug that was originally approved to treat type 2 diabetes, has now also been approved by the ...

19h

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.

22h

US FDA Identifies Cybersecurity Risks in Certain Patient Monitors

(Reuters) - The U.S. Food and Drug Administration (FDA) said on Thursday it had identified three cybersecurity risks ...

PCMag on MSN56m

Chinese-Made Patient Monitor Contains a Secret Backdoor

The backdoor on Contec CMS8000 patient-monitoring devices could allow an IP address at an unnamed university to remotely ...

36m

Couple indicted for running fraudulent “full-body scan” clinics in Colorado, other states

Mary and Fred Blakley of Arizona allegedly offered veterinary medicines and unproven ultrasound procedures through a national ...

57mon MSN

About half of Americans approve of using weight-loss drugs to treat obesity, AP-NORC poll finds

NORC Center for Public Affairs Research shows about half of U.S. adults believe it is a good thing for adults to use weight-loss drugs like Ozempic, Wegovy and other brands if they are struggling with ...

40mon MSN

Red dye #3, banned for cancer risk, linked to behavioral problems in children

A ThedaCare pediatrician says red dye #3 can cause behaviors associated with ADHD, even in kids who don't have it.

21h

Walmart's Broccoli Recall Now Classified As Potentially Deadly, According To The FDA

In early January it was revealed that Walmart's washed and ready-to-eat 12 oz. Marketside Broccoli Florets were voluntarily ...

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FDA Approves 1st Non-Opioid Pain Medicine in 20 Years

FDA upgrades recall of Lay's potato chips

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