{"product_id":"fda-medwatch-report-for-myfortic-adverse-reactions-case-id-24237687-gastrointestinal-disorder-proteinuria-renal-failure-streptococcal-bacteraemia","title":"FDA MedWatch Report for Myfortic Adverse Reactions – Case ID 24237687: Gastrointestinal Disorder, Proteinuria, Renal Failure, Streptococcal Bacteraemia.","description":"\u003cb\u003eOriginal Request:\u003c\/b\u003e  • Request for MedWatch Report for Product Case ID 24237687 • Suspect Product: Myfortic • Reaction: Gastrointestinal Disorder; Proteinuria; Renal Failure; Streptococcal Bacteraemia; Urine Protein\/Creatinine Ratio Increased; Cellulitis; Oedema • 68-Year-old male • Country of occurrence: US • Manufacturer Control Number: NVSC2024US165672","brand":"FDA","offers":[{"title":"Default Title","offer_id":50860941508772,"sku":"FDAFT814","price":89.0,"currency_code":"USD","in_stock":true}],"url":"https:\/\/foiadocs.com\/products\/fda-medwatch-report-for-myfortic-adverse-reactions-case-id-24237687-gastrointestinal-disorder-proteinuria-renal-failure-streptococcal-bacteraemia","provider":"FOIA Document Source","version":"1.0","type":"link"}