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WinRho [Rho(D) Immune Globulin Intravenous (Human)] has been manufactured by Cangene Corporation since it was first introduced in 1995, but until recently other companies distributed WinRho. We are proud to announce that Cangene bioPharma, Inc. has now taken over the distribution of
WinRho SDF
.

Over the next few months, we will be updating this site to provide comprehensive information on acute and chronic immune thrombocytopenic purpura (ITP), as well as its treatment. Please check back periodically for updates.


WinRho SDF Liquid is Bioequivalent to WinRho SDF Lyophilized1

In two comparative pharmacokinetic studies (n=101), the formulations were bioequivalent following IV administration based on the area under the curve to 84 days and had comparable pharmacokinetics following IM administration. Both formulations also had similar elimination half-lives. WinRho SDF must be administered via the intravenous route for the treatment of ITP.

WARNING: INTRAVASCULAR HEMOLYSIS (IVH) Intravascular hemolysis (IVH) leading to death has been reported in patients treated for immune thrombocytopenic purpura (ITP) with WinRho SDF.

IVH can lead to clinically compromising anemia and multi-system organ failure including acute respiratory distress syndrome (ARDS).

Serious complications including severe anemia, acute renal insufficiency, renal failure and disseminated intravascular coagulation (DIC) have also been reported.

Closely monitor patients treated with WinRho® SDF for ITP in a healthcare setting for at least eight hours after administration. Perform a dipstick urinalysis at baseline, 2 hours and 4 hours after administration and prior to the end of the monitoring period. Alert patients and monitor the signs and symptoms of IVH including back pain, shaking chills, fever, and discolored urine or hematuria. Absence of these signs and/or symptoms of IVH within eight hours do not indicate IVH cannot occur subsequently. If signs and/or symptoms of IVH are present or suspected after WinRho administration post-treatment laboratory tests should be performed including plasma hemoglobin, haptoglobin, LDH and plasma bilirubin (direct and indirect).

WinRho® SDF [Rho(D) Immune Globulin Intravenous (Human)]must be administered via the intravenous route when used in clinical situations requiring an increase in platelet count to prevent excessive hemorrhage in the treatment of non-splenectomized, Rho(D)-positive:

• children with chronic or acute ITP,

• adults with chronic ITP, or

• children and adults with ITP secondary to HIV infection

The safety and efficacy of WinRho SDF has not been evaluated in clinical trials for patients with non-ITP causes of thrombocytopenia or in previously splenectomized patients or in patients who are Rho(D)-negative.

Please see full Important Risk Information for more detailed risk information
Please see WinRho SDF Prescribing Information for full prescribing details

Reference: 1. WinRho SDF Prescribing Information, March 2010.