This brand name is authorized in Austria, Brazil, Croatia, Cyprus, Estonia, Finland, Israel, Netherlands, Poland, Romania, Spain, Tunisia, Turkey.
The drug HAEMATE contains a combination of these active pharmaceutical ingredients (APIs):
1
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UNII
ZE22NE22F1 - VON WILLEBRAND FACTOR HUMAN
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Administration of von Willebrand factor allows correction of the haemostatic abnormalities exhibited by patients who suffer from von Willebrand factor deficiency. |
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2
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UNII
5T6B772R4Q - HUMAN COAGULATION FACTOR VIII/VON WILLEBRAND FACTOR COMPLEX
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Activated factor VIII acts as a cofactor for activated factor IX, accelerating the conversion of factor X to activated factor X (factor Xa). Haemophilia A is a sex-linked hereditary disorder of blood coagulation due to decreased levels of factor VIII:C. By replacement therapy the plasma levels of factor VIII are increased, thereby enabling a temporary correction of the factor deficiency and correction of the bleeding tendencies. |
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This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| B02BD06 | Von Willebrand factor and coagulation factor VIII in combination | B Blood and blood forming organs → B02 Antihemorrhagics → B02B Vitamin K and other hemostatics → B02BD Blood coagulation factors |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| BR | Câmara de Regulação do Mercado de Medicamentos | 502600904154413, 502612020005803, 502612020005903, 502612020006003, 502621070010907, 502621070011007, 502621070011107 |
| EE | Ravimiamet | 1843095, 1843107, 1843118 |
| ES | Centro de información online de medicamentos de la AEMPS | 56867, 56868 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 149005, 149013, 149120 |
| HR | Agencija za lijekove i medicinske proizvode | HR-H-533693582 |
| IL | מִשְׂרַד הַבְּרִיאוּת | 7003, 8317 |
| NL | Z-Index G-Standaard | 14198193, 14198207, 14198215 |
| NL | Z-Index G-Standaard, PRK | 101788, 101796, 101818 |
| PL | Rejestru Produktów Leczniczych | 100092329, 100092335, 100092341 |
| RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | W13379001, W52389001, W52390001 |
| TN | Direction de la Pharmacie et du Médicament | 8143101H, 8143102H, 8143103H |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8681624980064, 8681624980071 |
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