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  • FDA Approves Uzedy Once-Monthly Extended Release Injectable Suspension . . .
    Teva Pharmaceuticals recently announced that the US Food and Drug Administration (FDA) has approved Uzedy (risperidone) as a once-monthly extended-release injectable suspension as monotherapy or as adjunctive therapy to lithium or valproate for the maintenance treatment of adults with bipolar I disorder (BD-I) 1 Uzedy is the first subcutaneous, long-acting formulation of risperidone that
  • FDA Approves Expanded Indication for UZEDY® (risperidone) Extended . . .
    FDA approves UZEDY ® (risperidone) extended-release injectable suspension for subcutaneous use as monotherapy or as adjunctive therapy to lithium or valproate for the maintenance treatment of bipolar I disorder in adults 1 UZEDY (risperidone) extended-release injectable suspension for subcutaneous use is indicated for use every one or two months for the treatment of schizophrenia in adults
  • In Brief: A New Indication for Uzedy | The Medical Letter Inc.
    Valproate, lamotrigine, and carbamazepine are alternatives Second-generation antipsychotic drugs are effective in preventing recurrences of manic and depressive episodes, especially when taken in combination with a mood stabilizer (lithium or valproate); they may be more effective in preventing hypomania than depression
  • Uzedy: FDA Approves Once-a-Month Subcutaneous Injectable . . . - WebMD
    The FDA has approved Uzedy, a long-acting form of risperidone, to treat adults with bipolar I disorder The shot is given under the skin, and the medicine is released slowly and steadily over time
  • FDA Approves Uzedy Injectable for Bipolar 1 Disorder| bpHope. com
    Uzedy is the first under-the-skin, long-acting risperidone injection for adults with bipolar 1 disorder, designed to help maintain stability
  • Teva Pharmaceuticals Announces FDA Approval of UZEDY® (risperidone) for . . .
    UZEDY, also approved for schizophrenia in adults, utilizes Medincell's proprietary technology to ensure a controlled release of the medication The approval is supported by existing evidence demonstrating the safety and efficacy of risperidone formulations, alongside findings specific to UZEDY from pivotal clinical studies
  • FDA Approves Expanded Indication for Risperidone Extended-Release . . .
    FDA approves Uzedy, an extended-release injectable formulation of risperidone, enhancing treatment options for adults with bipolar I disorder
  • FDA approves Teva and Medincell’s bipolar I disorder treatment
    Teva Pharmaceuticals and Medincell have gained approval from the US Food and Drug Administration (FDA) for Uzedy (risperidone), a once-a-month extended-release injectable suspension to treat adult patients with bipolar I disorder (BD-I) The medication has been approved for use as a standalone treatment or as an addition to lithium or valproate therapies for maintenance treatment of the disorder
  • UZEDY® Administration Guide Injection Techniques | UZEDY®
    Learn proper UZEDY® (risperidone) extended-release injectable suspension preparation and administration techniques with step-by-step guidance and instructional video demonstrations See full Prescribing Information, including Boxed WARNING
  • Official Patient Site | UZEDY®
    UZEDY® IS NOW APPROVED AS MONOTHERAPY OR AS ADJUNCTIVE THERAPY TO LITHIUM OR VALPROATE FOR THE MAINTENANCE TREATMENT OF BIPOLAR I DISORDER IN ADULTS The efficacy of UZEDY is based on the established effectiveness of another risperidone long-acting injection (LAI) that was administered into the muscle UZEDY offers the same medication, but it's injected just under the skin





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