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  2. Rufinamide - Wikipedia

    en.wikipedia.org/wiki/Rufinamide

    Rufinamide was approved by the US Food and Drug Administration (FDA) in November 2008, as adjunctive treatment of seizures associated with Lennox-Gastaut syndrome in children four years and older and adults. Its official FDA-approved labeling does not mention use in the treatment of partial seizures inasmuch as clinical trials submitted to the ...

  3. List of antiviral drugs - Wikipedia

    en.wikipedia.org/wiki/List_of_antiviral_drugs

    FDA-licensed in 1998; Withdrawn in EU (2002), US (2006) Fosamprenavir: HIV ViiV Healthcare: Amprenavir pro-drug: 2003 (FDA), 2004 Foscarnet: Herpes: Pyrophosphate analogue DNA polymerase inhibitor: 1991 Ganciclovir (Cytovene) [9] Cytomegalovirus (CMV) [10] Competitive nucleoside analogue dGTP inhibitor 1988 Ibacitabine: Herpes labialis ...

  4. FDA Approves Teva's TREANDA® (bendamustine HCI ... - AOL

    www.aol.com/2013/09/17/fda-approves-tevas...

    FDA Approves Teva's TREANDA ® (bendamustine HCI) Injection, a New Liquid Formulation New Formulation Eliminates Need for Reconstitution JERUSALEM--(BUSINESS WIRE)-- Teva Pharmaceutical Industries ...

  5. Intravenous therapy - Wikipedia

    en.wikipedia.org/wiki/Intravenous_therapy

    Intravenous therapy (abbreviated as IV therapy) is a medical technique that administers fluids, medications and nutrients directly into a person's vein.The intravenous route of administration is commonly used for rehydration or to provide nutrients for those who cannot, or will not—due to reduced mental states or otherwise—consume food or water by mouth.

  6. FDA Approves LEQEMBI® (lecanemab-irmb) IV Maintenance Dosing ...

    lite.aol.com/tech/story/0022/20250126/9347687.htm

    Lecanemab is approved in the U.S., 7 Japan, 8 China, 9 South Korea, 10 Hong Kong, 1 1 Israel, 1 2 the United Arab Emirates, 1 3 the United Kingdom, 1 4 Mexico, 1 5 and Macau. In November 2024, the treatment received a positive opinion from the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA ...

  7. Abbreviated New Drug Application - Wikipedia

    en.wikipedia.org/wiki/Abbreviated_New_Drug...

    An Abbreviated New Drug Application (ANDA) is an application for a U.S. generic drug approval for an existing licensed medication or approved drug. The ANDA is submitted to FDA's Center for Drug Evaluation and Research, Office of Generic Drugs, which provides for the review and ultimate approval of a generic drug product. Once approved, an ...

  8. FDA declares IV fluid shortage in the wake of Helene - AOL

    www.aol.com/news/fda-declares-iv-fluid-shortage...

    The Food and Drug Administration (FDA) on Friday declared shortages of three intravenous drugs produced at a North Carolina plant that has been temporarily shut down due to the devastation from ...

  9. We Investigated the 8 Biggest Wellness Trends to See What ...

    www.aol.com/lifestyle/investigated-8-biggest...

    As of July 2021, the FDA approved the usage of hyperbaric oxygen chambers to treat several issues, including burns and wound healing; they have also become popular in aesthetics to reduce surgery ...

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