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FDA MedWatch Report for Product Case ID 23055040 (Multiple Reactions, US)
FDA MedWatch Report for Product Case ID 23055040 (Multiple Reactions, US)
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Original Request: • Request for MedWatch Report for Product Case ID 23055040 • Suspect Product: Medrol; Jakafi; Lupkynis • Reaction: Still's Disease; Constipation; Diarrhoea; Hypersensitivity; Mental Status Changes; Sinus Disorder; Therapeutic Product Effect Variable; Condition Aggravated; Emotional Disorder; Haemophagocytic Lymphohistiocytosis; Dizziness; Pollakiuria; Nausea; Dyspnoea Exertional; Off Label Use; Stress; Vomiting; Fatigue; Hallucination; Depression • unspecified sex and age • Country of occurrence: US • Manufacturer Control Number: US-INCYTE CORPORATION-2023IN010280
Tags: Pharma, MedWatch, 2025
Tags: Pharma, MedWatch, 2025
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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