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European Commission Approves Subcutaneous Belimumab for SLE; FDA Safety Alert for Febuxostat

Michele B. Kaufman, PharmD, BCGP  |  November 29, 2017


Michele B. Kaufman, PharmD, BCGP, is a freelance medical writer based in New York City and a pharmacist at New York Presbyterian Lower Manhattan Hospital.

References

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  1. GlaxoSmithKline Plc. News release: GSK receives European marketing authorization for self-injectable formulation of Benlysta for the treatment of systemic lupus erythematosus. 2017 Nov 13.
  2. U.S. Food and Drug Administration. Safety alert: Febuxostat (brand name Uloric): Drug safety communication—FDA to evaluate increased risk of heart-related death. 2017 Nov 15.

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Filed under:ConditionsDrug UpdatesGout and Crystalline Arthritis Tagged with:belimumabcardiovascularEuropean UnionFebuxostatGoutInternationalsystemic lupus erythematosus (SLE)

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