Vanilla planifolia (Pot.-Angaben) - Meklēšanas rezultāti

Eiropas Savienība - īslandiešu - EMA (European Medicines Agency)

evalon

laboratorios hipra, s.a. - bóluefni gegn hníslalyfjum í kjúklingum - lifandi sníkjudýra bóluefni, Ónæmislyf fyrir aves - kjúklingur - fyrir virk bólusetningar kjúklinga frá 1 dag aldri til að draga úr klínískum merki (niðurgangur), þarma sár og eaablöðrur framleiðsla tengslum við hníslasótt af völdum eimeria acervulina, eimeria brunetti, eimeria maxima, eimeria necatrix og eimeria tenella.

Eiropas Savienība - īslandiešu - 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.

Eiropas Savienība - īslandiešu - EMA (European Medicines Agency)

pergoveris

merck europe b.v. - follitropin alfa, lutropin alfa - Ófrjósemi, kvenkyns - hormón kynlíf og stillum kynfæri - voru er ætlað fyrir örvun tíðahvörf þróun í konur með alvarlega gulbúsörvandi-hormón (ace) og anti-örvandi-hormón skort. Í klínískum rannsóknum, þessar sjúklinga sem voru skilgreind af innræn blóðvatn ace stigi < 1. 2 ae / l.

Eiropas Savienība - īslandiešu - EMA (European Medicines Agency)

veltassa

vifor fresenius medical care renal pharma france - kalsíumhýdrat sorbítak - blóðkalíumlækkun - lyf til meðferð kalíum og blóðfosfathækkun - veltassa er ætlað til meðferðar við blóðkalíumhækkun hjá fullorðnum.