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Bayer HealthCare Marks 20th Anniversary of World Hemophilia Day With Euro 250,000 Contribution to the World Federation of Hemophilia
Date:4/17/2009

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  • Supporting the Bayer Hemophilia Awards Program (BHAP), one of the largest and oldest programs of its kind in the industry. Since 2002, BHAP has funded novel hemophilia research and education projects around the world.

    • Bayer has a long history of advocating for and supporting the global hemophilia community. Over the years, Bayer has donated more than 30 million international units of product to countries with limited access to hemophilia treatment and, just recently, provided critical support to develop hemophilia treatment centers throughout China, where approximately one quarter of the world's hemophilia population lives (between 70,000 and 100,000 people).

    About Hemophilia A

    Hemophilia A, also known as factor VIII deficiency or classic hemophilia, is largely an inherited bleeding disorder in which one of the proteins needed to form blood clots in the body is missing or reduced. Hemophilia A is the most common type of hemophilia and is characterized by prolonged or spontaneous bleeding, especially into the muscles, joints, or internal organs. Approximately 400,000 people around the world have hemophilia A.

    About Kogenate(R) FS

    Kogenate(R) FS (Antihemophilic Factor [Recombinant]) is a recombinant factor VIII treatment indicated for the control and prevention of bleeding episodes and perioperative management in adults and children (0-16 years) with hemophilia A. Kogenate(R) FS is indicated for routine prophylaxis to reduce the frequency of bleeding episodes and the risk of joint damage in children with hemophilia A with no preexisting joint damage.

    The most serious adverse reactions are systemic hypersensitivity reactions and the development of high-titer inhibitors. The most frequently reported adverse events were local injection site reactions, dizziness and rash. Known intolerance or allergic reactions
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    SOURCE Bayer HealthCare
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