Giant platelet disease
Giant platelet disease is an inherited disorder characterized by thrombocytopenia, giant platelets, prolonged bleeding time, and impaired prothrombin consumption.
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Site of disease:
Blood vessels -
Infectious :
Not contagious -
Frequent population:
All groups -
Related symptoms:
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Concurrent disease:
Related Drugs
Recombinant Human Coagulation Factor VIIa for Injection
Indication: It is used for the following patient groups to treat bleeding episodes and prevent bleeding during surgical procedures or invasive procedures. 1. Congenital hemophilia patients with inhibitors of coagulation factor VIII or IX > 5BU; 2. Congenital hemophilia patients who are expected to have a high memory response to injection of coagulation factor VIII or coagulation factor IX; 3. Acquired hemophilia patients; 4. Congenital FVII deficiency patients; 5. Thrombasthenia patients with GPⅡb-Ⅲa and/or HLA antibodies and who have been or are currently ineffective or poorly responsive to platelet transfusions.