Mulpleo (previously Lusutrombopag Shionogi) Evrópusambandið - íslenska - EMA (European Medicines Agency)

mulpleo (previously lusutrombopag shionogi)

shionogi b.v. - lusutrombopag - blóðflagnafæð - antihemorrhagics - mulpleo er ætlað fyrir meðferð alvarlega blóðflagnafæð í fullorðinn sjúklinga með langvarandi lifrarsjúkdóm gangast undir inngrip.

Doptelet Evrópusambandið - íslenska - EMA (European Medicines Agency)

doptelet

swedish orphan biovitrum ab (publ) - avatrombopag maleate - blóðflagnafæð - antihemorrhagics - doptelet er ætlað fyrir meðferð alvarlega blóðflagnafæð í fullorðinn sjúklinga með langvarandi lifrarsjúkdóm sem eru áætlað er að gangast undir innrásar aðferð. doptelet is indicated for the treatment of primary chronic immune thrombocytopenia (itp) in adult patients who are refractory to other treatments (e. barkstera, immúnóglóbúlín).

Tavlesse Evrópusambandið - íslenska - EMA (European Medicines Agency)

tavlesse

instituto grifols s.a. - fostamatinib dínatríum - blóðflagnafæð - hinn almenna hemostatics - tavlesse er ætlað fyrir meðferð langvarandi ónæmiskerfið blóðflagnafæð (skammtur) í fullorðinn sjúklingum sem svarar til önnur meðferðir.

Nplate Evrópusambandið - íslenska - EMA (European Medicines Agency)

nplate

amgen europe b.v. - romiplostim - purpura, blóðflagnafæð, blóðflagnafæð - antihemorrhagics - adults:nplate is indicated for the treatment of primary immune thrombocytopenia  (itp) in adult patients who are refractory to other treatments (e. barkstera, immúnóglóbúlín). paediatrics:nplate is indicated for the treatment of chronic primary immune thrombocytopenia (itp) in paediatric patients one year of age and older who are refractory to other treatments (e. barkstera, immúnóglóbúlín).

Revolade Evrópusambandið - íslenska - EMA (European Medicines Agency)

revolade

novartis europharm limited - eltrombopag - purpura, blóðflagnafæð, blóðflagnafæð - other systemic hemostatics, antihemorrhagics - revolade is indicated for the treatment of adult patients with primary immune thrombocytopenia (itp) who are refractory to other treatments (e. corticosteroids, immunoglobulins) (see sections 4. 2 og 5. revolade is indicated for the treatment of paediatric patients aged 1 year and above with primary immune thrombocytopenia (itp) lasting 6 months or longer from diagnosis and who are refractory to other treatments (e. corticosteroids, immunoglobulins) (see sections 4. 2 og 5. revolade is indicated in adult patients with chronic hepatitis c virus (hcv) infection for the treatment of thrombocytopenia, where the degree of thrombocytopenia is the main factor preventing the initiation or limiting the ability to maintain optimal interferon-based therapy (see sections 4. 4 and 5. revolade is indicated in adult patients with acquired severe aplastic anaemia (saa) who were either refractory to prior immunosuppressive therapy or heavily pretreated and are unsuitable for haematopoietic stem cell transplantation (see section 5.

Hemlibra Evrópusambandið - íslenska - EMA (European Medicines Agency)

hemlibra

roche registration limited - emicizumab - hemophilia a - antihemorrhagics - 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 hægt er að nota í öllum aldri tekur.