CSL Behring announced that Corifact (factor XIII concentrate [human] injection) has been approved for the routine prophylactic treatment of congenital factor XIII deficiency. Corifact is a ...
CSL Behring announced that the FDA has approved an expansion of the indication for Corifact (Factor XIII concentrate [human]) infusion, to include the peri-operative management of surgical bleeding in ...
First and only factor XIII concentrate approved in U.S. to treat extremely rare and potentially life-threatening bleeding disorder Congenital FXIII deficiency, also known as fibrin-stabilizing factor ...
Please provide your email address to receive an email when new articles are posted on . The first product to prevent bleeding in people with congenital Factor XIII deficiency has been approved by the ...
SILVER SPRING, Md. — The Food and Drug Administration has approved a treatment for a rare bleeding disorder. The FDA announced the approval of Corifact, used to prevent bleeding in people with the ...
SILVER SPRING, Md., Feb. 17, 2011 /PRNewswire-USNewswire/ -- The U.S. Food and Drug Administration today approved Corifact, the first product intended to prevent bleeding in people with the rare ...
Label broadened to include the peri-operative management of surgical bleeding in adult and pediatric patients with congenital factor XIII deficiency Congenital FXIII deficiency is a rare and ...
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