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2 days ago · Today, the U.S. Food and Drug Administration approved Journavx (suzetrigine) 50 milligram oral tablets, a first-in-class non-opioid analgesic, to treat moderate to severe acute pain in adults.

2 days ago · The U.S. Food and Drug Administration said it approved Vertex Pharmaceuticals’ Journavx for short-term pain that often follows surgery or injuries. It’s the first new pharmaceutical approach to treating pain in more than 20 years, offering an alternative to both opioids and over-the-counter medications like ibuprofen and acetaminophen.

Jan 22, 2025 · The pause is in effect through Feb. 1, the memo said. Agencies subject to the HHS directive include the CDC, the National Institutes of Health and the Food and Drug Administration — entities that fight epidemics, protect the nation’s food supply and search for cures to diseases.

Oct 2, 2024 · The latest news and events at the U.S. Food and Drug Administration (FDA) and resources for journalists.

The Food and Drug Administration on Thursday approved a new type of nonopioid painkiller from Vertex Pharmaceuticals. The drug, Journavx, or suzetrigine, was approved to treat moderate to severe ...

Jan 24, 2025 · The Food and Drug Administration, a federal agency of the HHS, usually releases updates on probes of outbreaks linked to contaminated food every Wednesday, but the agency did not release them this ...

Jan 23, 2025 · According to NBC News, Fink sent a memo to leaders of the Centers for Disease Control and Prevention (CDC), the U.S. Food and Drug Administration (FDA), and the National Institutes of Health to ...

3 days ago · The Vertex drug is a milestone after a long history of unsuccessful efforts to develop painkillers without the addictive potential of opioids.

Jan 16, 2025 · Companies say they are working to update their products to comply with the Food and Drug Administration's decision Wednesday to ban the artificial food dye Red 3, after the agency said...