This brand name is authorized in Austria, Brazil, Croatia, Cyprus, Estonia, Finland, Hong Kong SAR China, Lithuania, Malta, Poland, Romania, South Africa, Tunisia, Turkey.
The drug IMMUNATE contains one active pharmaceutical ingredient (API):
1
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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 | |
|---|---|---|
| B02BD04 | Coagulation factor IX | B Blood and blood forming organs → B02 Antihemorrhagics → B02B Vitamin K and other hemostatics → B02BD Blood coagulation factors |
| 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 | 501121010034417, 501121010034517, 501121010034617 |
| EE | Ravimiamet | 1038079, 1038091, 1349232 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 541183 |
| HK | Department of Health Drug Office | 57835, 58390 |
| HR | Agencija za lijekove i medicinske proizvode | HR-H-927359696 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1004579, 1004580, 1004581 |
| MT | Medicines Authority | MA162/00701, MA162/00702, MA162/00703 |
| PL | Rejestru Produktów Leczniczych | 100160309, 100160315, 100160338 |
| RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | W62886001, W62887001, W62888001 |
| TN | Direction de la Pharmacie et du Médicament | 10623021H, 10623022H |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8681429550134, 8681429550141 |
| ZA | Health Products Regulatory Authority | A40/30.3/0215, A40/30.3/0216, A40/30.3/0217 |
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