1
/
of
0
FDA MedWatch Report for Lupkynis Adverse Reactions – Case ID 24376423: Lupus Nephritis, Polyarthritis, Dermatitis Bullous, Autoimmune Haemolytic Anaemia.
FDA MedWatch Report for Lupkynis Adverse Reactions – Case ID 24376423: Lupus Nephritis, Polyarthritis, Dermatitis Bullous, Autoimmune Haemolytic Anaemia.
Regular price
$89.00 USD
Regular price
Sale price
$89.00 USD
Unit price
/
per
Original Request: • 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
Couldn't load pickup availability
- 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.
View full details