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FDA approves 1st new type of pain medication in 25 years

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.

Reuters · 1h

US FDA approves Vertex's non-opioid painkiller

The U.S. Food and Drug Administration has approved Vertex Pharmaceuticals' drug to treat acute pain, the health regulator said on Thursday, offering an alternative to addictive opioid painkillers that have fueled a national crisis.

Business Insider · 13m

Vertex Pharmaceuticals’ non-opioid Journavx approved for pain by FDA

Today, the U.S. Food and Drug Administration approved Journavx (suzetrigine) 50 milligram oral tablets, a first-in-class

Axsome Therapeutics, FDA and migraine

Reuters · 3h

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.

Business Insider · 2h

Axsome Therapeutics announces FDA approval of Symbravo

Axsome Therapeutics (AXSM) announced that the U.S. FDA has approved Symbravo for the acute treatment of migraine with or without aura in

Seeking Alpha on MSN · 1h

Axsome gets FDA approval for Symbravo for migraine

Axsome Therapeutics (NASDAQ:AXSM) has received FDA approval for its drug Symbravo for the acute treatment of migraine with or without aura in adults. Symbravo, a combination of meloxicam and rizatriptan,

Recall raised to highest risk level by FDA. What to know

Newsweek on MSN · 9h

Sunscreen Recalled Nationwide as FDA Sets Risk Level

A voluntary recall was initiated by The W.S. Badger Company due to missing labels on a sunscreen product distributed nationwide.

MLive · 52m

This chocolate recall has been upgraded to FDA’s highest risk level

STATEN ISLAND, N.Y. — A December 2024 chocolate recall has been upgraded to highest risk level by the U.S. Food and Drug Administration (FDA), which says consuming the product could “cause serious adverse health consequences or death.”

New York Daily News · 1h

Lay’s recall increased to highest level, could cause ‘death’: FDA

The oversight could result in “death,” at least for those with a milk allergy or sensitivity, says the FDA. FDA initiated the recall on Dec. 13 and announced three days later that it was recalling the chips due to a potential or undeclared allergen. At present, no allergic reactions have been reported.

type 2 diabetes, chronic kidney disease and FDA

CNN on MSN · 2d

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 US Food and Drug Administration to reduce certain risks associated with chronic kidney disease,

U.S. News & World Report · 1d

FDA Approves Ozempic to Protect Kidneys in Patients With Type 2 Diabetes

Doctors already use Ozempic to manage type 2 diabetes and reduce the risk of heart disease in patients with diabetes. This move, as reported by The Times, was based on research sh

Reuters · 1d

US FDA approves Novo Nordisk's Ozempic to cut risk of diabetic kidney disease progression

The U.S. FDA has approved Novo Nordisk's Ozempic for reducing the risk of kidney failure and disease progression, as well as death due to heart problems in diabetes patients with chronic kidney disease (CKD),

3hon MSN

US FDA identifies cybersecurity risks in certain patient monitors

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

Chocolate Recall Now Classified As Potentially Deadly, According To The FDA

Per the FDA, the recalled Cal Yee’s (or Cal Yee Farm branded) products were packaged in clear plastic zippered pouches in ...

2hOpinion

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 ...

45m

Fact check: Kennedy repeats false and misleading claims in confirmation hearing

In his first Senate confirmation hearing to be secretary of the Department of Health and Human Services, Robert F. Kennedy Jr ...

Scientific American2h

Polio Vaccines Saved America from the Disease. What Happens if We Lose Them?

Polio, a disease that can cause lifelong paralysis, has been eliminated from the U.S. Experts fear a resurgence if lifesaving ...

2hon MSN

The Return of Snake Oil

The Trump administration is poised to supercharge America’s appetite for supplements.

8hon MSNOpinion

The FDA’s new, same-old food labels demand better obesity solutions

All things considered, it’s at least as likely to make health outcomes worse as it is to make most people healthier.

WISH-TV on MSN45m

FDA redefines ‘healthy’ food labels to help consumers make informed choices

The FDA is overhauling food labels to redefine "'healthy," focusing on redefining terms and introducing new front-of-package ...

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FDA approves 1st new type of pain medication in 25 years

Axsome Therapeutics, FDA and migraine

Recall raised to highest risk level by FDA. What to know

type 2 diabetes, chronic kidney disease and FDA

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