{"product_id":"fda-medwatch-report-for-lupkynis-adverse-reactions-case-id-24376423-lupus-nephritis-polyarthritis-dermatitis-bullous-autoimmune-haemolytic-anaemia","title":"FDA MedWatch Report for Lupkynis Adverse Reactions – Case ID 24376423: Lupus Nephritis, Polyarthritis, Dermatitis Bullous, Autoimmune Haemolytic Anaemia.","description":"\u003cb\u003eOriginal Request:\u003c\/b\u003e  • Request for MedWatch Report for Product Case ID 24376423 • Suspect Product: Lupkynis • Reaction: Lupus Nephritis; Polyarthritis; Dermatitis Bullous; Autoimmune Haemolytic Anaemia • Unspecified age and sex • Country of occurrence: DE • Manufacturer Control Number: DE-GSK-DE2024GSK118961","brand":"FDA","offers":[{"title":"Default Title","offer_id":50860941443236,"sku":"FDAFT812","price":89.0,"currency_code":"USD","in_stock":true}],"url":"https:\/\/foiadocs.com\/products\/fda-medwatch-report-for-lupkynis-adverse-reactions-case-id-24376423-lupus-nephritis-polyarthritis-dermatitis-bullous-autoimmune-haemolytic-anaemia","provider":"FOIA Document Source","version":"1.0","type":"link"}