Hemophilia A is a hereditary bleeding disorder caused by a lack of blood clotting factor VIII. Without enough factor VIII, the blood cannot
DRUG INTERACTIONS: A) Avoid simultaneous use of activated prothrombin FACTOR VIII INHIBITORS. DIAGNOSIS OF FACTOR VIII AUTOANTIBODIES. Partial
These non-factor drugs can be given subcutaneously instead of intravenously. The factor VIII procoagulant protein (antihemophilic factor) and the factor
Knowledge on rare diseases and orphan drugs Search for an orphan drug Human coagulation factor VIII (antihemophilic A factor).
Indications and dose: Congenital factor VIII deficiency (haemophilia A), acquired factor VIII deficiency, Von Willebrand's disease for factor VIII fraction
Recombinant antihemophilic factor replaces clotting factor VIII in the blood. Other drugs may affect recombinant antihemophilic factor
by P Giangrande 2024drugs. Drugs that have been implicated in published case reports include Porcine factor VIII: Factor VIII concentrate made from the blood of pigs
drugs. Inoculate. Introduce into an organism a substance that contains the Contains factor VIII (coagulant, 80–120 U), von Willebrand factor VIII
Human blood coagulation factor VIII is an essential blood-clotting protein, also known as anti-haemophilic factor (AHF). Recombinant factor VIII is used for the
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