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  2. New non-opioid painkiller approved by US health agency - AOL

    www.aol.com/non-opioid-painkiller-approved-us...

    A new type of non-opioid painkiller, aimed at treating short-term pain in adults, has been approved by the US Food and Drug Administration (FDA). The drug suzetrigine, known by its brand name ...

  3. FDA approves new pain medication as an alternative to ... - AOL

    www.aol.com/fda-approves-pain-medication...

    For the first time in two decades, the Food and Drug Administration (FDA) has approved a new class of medication that provides an alternative to addictive opioids for patients looking to manage ...

  4. FDA approves opioid-free pain medication with 'no sign of ...

    www.aol.com/fda-approves-opioid-free-pain...

    A new opioid-free pain medication was approved by the U.S. Food and Drug Administration (FDA) on Thursday, marking a non-addictive alternative for patients. Journavx (suzetrigine), made by Vertex ...

  5. Is Vertex Pharmaceuticals a Buy Now That the FDA Approved Its ...

    www.aol.com/vertex-pharmaceuticals-buy-now-fda...

    The U.S. Food and Drug Administration (FDA) approved suzetrigine under the brand name Journavx on Jan. 30, 2025. Journavx is a first-in-class non-opioid painkiller that acts on sodium channels in ...

  6. List of drugs granted breakthrough therapy designation

    en.wikipedia.org/wiki/List_of_drugs_granted...

    In combination with palbociclib and fulvestrant for the treatment of adults with endocrine-resistant, PIK3CA-mutated, hormone receptor (HR)-positive, human epidermal growth-factor receptor 2 (HER2)-negative, locally advanced or metastatic breast cancer, as detected by an FDA-approved test, following recurrence on or after completing adjuvant ...

  7. Daprodustat - Wikipedia

    en.wikipedia.org/wiki/Daprodustat

    Daprodustat was approved for medical use in Japan in June 2020, [5] [6] and in the United States in February 2023. [2] [3] [7] [8] making it the first oral treatment for anemia caused by chronic kidney disease for adults in the US. [3] The US Food and Drug Administration (FDA) considers it to be a first-in-class medication. [9]

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