New Product - Obizur
Obizur (susoctocog alfa (bhk)) is a recombinant analogue of porcine coagulation factor VIII, with the B domain deleted. Patients with acquired haemophilia A have normal factor VIII genes but develop autoantibodies against their own factor VIII (i.e. inhibitors), creating a functional deficiency of this procoagulant protein. Obizur is indicated for the treatment of bleeding episodes in adults with acquired haemophilia A. Safety and efficacy of Obizur have not been established in patients with baseline antiporcine factor VIII inhibitor titre greater than 20 BU. Obizur is not indicated for the treatment of congenital haemophilia A or von Willebrand disease. Obizur 500 unit single use vials are available in packs of 1, 5 and 10.
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