| If this is not your name, click here. | | |
| | Contact Us | Order Now | Journals | Bookstore | Register a colleague | | |
| | | ![]() FDA Update on Intravascular Haemolysis Risk With Immune Globulin Intravenous (Human) ROCKVILLE, Md -- March 10, 2010 -- The US Food and Drug Administration (FDA), Baxter, and Cangene, are notifying healthcare professionals that cases of intravascular haemolysis (IVH) and its complications, including fatalities, have been reported in patients treated for immune thrombocytopenic purpura (ITP) with human intravenous immune globulin (WinRho SDF). Intravascular haemolysis can lead to clinically compromising anaemia and multi-system organ failure including acute respiratory distress syndrome. Serious complications including severe anaemia, acute renal insufficiency, renal failure, and disseminated intravascular coagulation have also been reported. Fatal outcomes associated with IVH and its complications have occurred most frequently in patients of advanced age (> 65 years) with co-morbid conditions. The Boxed Warning informs healthcare professionals that: More information can be found here: http://www.fda.gov/downloads/BiologicsBloodVaccines/BloodBloodProducts/ApprovedProducts/LicensedProductsBLAs/FractionatedPlasmaProducts/UCM198725.pdf http://www.fda.gov/downloads/BiologicsBloodVaccines/BloodBloodProducts/ApprovedProducts/LicensedProductsBLAs/FractionatedPlasmaProducts/UCM198717.pdf
SOURCE: US Food and Drug Administration
|