Sugammadex Piramal Avrupa Birliği - Norveççe - EMA (European Medicines Agency)

sugammadex piramal

piramal critical care b.v. - sugammadex sodium - neuromuskulær blokkade - sugammadex - reversal of neuromuscular blockade induced by rocuronium or vecuronium in adults.

Lacosamide Adroiq Avrupa Birliği - Norveççe - EMA (European Medicines Agency)

lacosamide adroiq

extrovis eu ltd. - lakosamid - epilepsi - antiepileptics, - lacosamide adroiq is indicated as monotherapy in the treatment of partial-onset seizures with or without secondary generalisation in adults, adolescents and children from 2 years of age with epilepsy. lacosamide adroiq is indicated as adjunctive therapyin the treatment of partial-onset seizures with or without secondary generalisation in adults, adolescents and children from 2 years of age with epilepsy. in the treatment of primary generalised tonic-clonic seizures in adults, adolescents and children from 4 years of age with idiopathic generalised epilepsy.

Mallozen 3 mg Norveç - Norveççe - Statens legemiddelverk

mallozen 3 mg

medice arzneimittel pütter gmbh & co kg - melatonin - tablett - 3 mg

Mallozen 2 mg Norveç - Norveççe - Statens legemiddelverk

mallozen 2 mg

medice arzneimittel pütter gmbh & co kg - melatonin - tablett - 2 mg

Mallozen 5 mg Norveç - Norveççe - Statens legemiddelverk

mallozen 5 mg

medice arzneimittel pütter gmbh & co kg - melatonin - tablett - 5 mg

Tepkinly Avrupa Birliği - Norveççe - EMA (European Medicines Agency)

tepkinly

abbvie deutschland gmbh & co. kg - epcoritamab - lymphoma, large b-cell, diffuse - antineoplastiske midler - tepkinly as monotherapy is indicated for the treatment of adult patients with relapsed or refractory diffuse large b-cell lymphoma (dlbcl) after two or more lines of systemic therapy.

Eprex 10000 IU/ ml Norveç - Norveççe - Statens legemiddelverk

eprex 10000 iu/ ml

janssen-cilag as - epoetin alfa - injeksjonsvæske, oppløsning i ferdigfylt sprøyte - 10000 iu/ ml

Eprex 40000 IU/ ml Norveç - Norveççe - Statens legemiddelverk

eprex 40000 iu/ ml

janssen-cilag as - epoetin alfa - injeksjonsvæske, oppløsning i ferdigfylt sprøyte - 40000 iu/ ml

Myalepta Avrupa Birliği - Norveççe - EMA (European Medicines Agency)

myalepta

amryt pharmaceuticals dac - metreleptin - lipodystrophy, familiær delvis - andre alimentary tract and metabolism products, - myalepta er indisert som et tillegg til diett som en erstatning terapi for å behandle komplikasjoner av leptin mangel på lipodystrophy (ld) pasienter med bekreftet medfødt generell ld (berardinelli-seip syndrom) eller ervervet generell ld (lawrence syndrom) hos voksne og barn 2 år og abovewith bekreftet familiær delvis ld eller ervervet delvis ld (barraquer-simons syndrom), i voksne og barn 12 år og over som standard behandlinger har mislyktes i å oppnå tilstrekkelig metabolsk kontroll.

Adempas Avrupa Birliği - Norveççe - EMA (European Medicines Agency)

adempas

bayer ag - riociguat - hypertensjon, pulmonal - antihypertensive midler for pulmonal arteriell hypertensjon - chronic thromboembolic pulmonary hypertension (cteph)adempas is indicated for the treatment of adult patients with who functional class (fc) ii to iii withinoperable cteph,persistent or recurrent cteph after surgical treatment,to improve exercise capacity. pulmonary arterial hypertension (pah)adultsadempas, as monotherapy or in combination with endothelin receptor antagonists, is indicated for the treatment of adult patients with pulmonary arterial hypertension (pah) with who functional class (fc) ii to iii to improve exercise capacity. effekten har vært vist i en pah befolkningen, herunder aetiologies av idiopatisk eller heritable pah eller pah assosiert med bindevev sykdom. paediatricsadempas is indicated for the treatment of pah in paediatric patients aged less than 18 years of age and body weight ≥ 50 kg with who functional class (fc) ii to iii in combination with endothelin receptor antagonists.