Hemlibra Euroopan unioni - suomi - EMA (European Medicines Agency)

hemlibra

roche registration limited - emicizumab - hemofilia a - hemostaatit - hemlibra is indicated for routine prophylaxis of bleeding episodes in patients with haemophilia a (congenital factor viii deficiency):with factor viii inhibitorswithout factor viii inhibitors who have:severe disease (fviii < 1%)moderate disease (fviii ≥ 1% and ≤ 5%) with severe bleeding phenotype. hemlibra voidaan käyttää kaikissa ikäryhmissä.