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Baxter Receives Marketing Authorisation

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Baxter Receives Marketing Authorisation From the European Commission for ADVATE to Treat Haemophilia A; -- First Factor VIII Therapy Available in Europe with Innovative Processing to Help Address Safety Concerns --.
ZURICH, Switzerland, March 3 /PRNewswire/ -- Baxter Healthcare S.A. announced today that the European Commission has issued a Marketing Authorisation for ADVATE (Octocog Alfa Recombinant Coagulation Factor VIII). ADVATE is indicated for the prevention and control of bleeding episodes in people with ...
March 3, 2004; PR Newswire

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