DepoCyte Den europeiske union - norsk - EMA (European Medicines Agency)

depocyte

pacira limited - cytarabin - meningeal neoplasmer - antineoplastiske midler - intratekal behandling av lymfomatøs meningitt. i de fleste pasienter vil slike behandling være en del av symptomatisk palliation av sykdommen.

Bonviva 3 mg Norge - norsk - Statens legemiddelverk

bonviva 3 mg

2care4 aps - ibandronatnatriummonohydrat - injeksjonsvæske, oppløsning - 3 mg

Adrenalin Martindale Pharma 0.1 mg/ ml Norge - norsk - Statens legemiddelverk

adrenalin martindale pharma 0.1 mg/ ml

ethypharm (1) - adrenalintartrat - injeksjonsvæske, oppløsning - 0.1 mg/ ml

Lipogen Duo vet - Norge - norsk - Statens legemiddelverk

lipogen duo vet -

elanco europe ltd - aeromonas salmonicida subspesie salmonicida, inaktivert / vibrio anguillarum serotype o1, inaktivert - injeksjonsvæske, emulsjon

Pentium Forte Plus vet Norge - norsk - Statens legemiddelverk

pentium forte plus vet

elanco gmbh - aeromonas salmonicida, hel, inaktivert / vibrio anguillarum, serotype o1, inaktivert / vibrio anguillarum, serotype o2a, inaktivert / aliivibrio salmonicida, inaktivert / moritella viscosa, inaktivert / pankreasnekrosevirus, infeksiøs, inaktivert - injeksjonsvæske, emulsjon

Toradol 30 mg/ ml Norge - norsk - Statens legemiddelverk

toradol 30 mg/ ml

atnahs pharma netherlands b.v. - ketorolaktrometamol - injeksjonsvæske, oppløsning - 30 mg/ ml

Glycopyrronium bromide Martindale 200 mikrog/ ml Norge - norsk - Statens legemiddelverk

glycopyrronium bromide martindale 200 mikrog/ ml

ethypharm (2) - glykopyrroniumbromid - injeksjonsvæske, oppløsning - 200 mikrog/ ml

Suxamethonium chloride dihydrate Ethypharm 50 mg/ ml Norge - norsk - Statens legemiddelverk

suxamethonium chloride dihydrate ethypharm 50 mg/ ml

ethypharm (1) - suksametoniumkloriddihydrat - injeksjons-/infusjonsvæske, oppløsning - 50 mg/ ml

Adrenalin Ethypharm 1 mg/ ml Norge - norsk - Statens legemiddelverk

adrenalin ethypharm 1 mg/ ml

ethypharm (1) - adrenalintartrat - injeksjonsvæske, oppløsning - 1 mg/ ml

Blincyto Den europeiske union - norsk - EMA (European Medicines Agency)

blincyto

amgen europe b.v. - blinatumomab - forløpercellelymfoblastisk leukemi-lymfom - antineoplastiske midler - blincyto is indicated as monotherapy for the treatment of adults with cd19 positive relapsed or refractory b precursor acute lymphoblastic leukaemia (all). patients with philadelphia chromosome positive b-precursor all should have failed treatment with at least 2 tyrosine kinase inhibitors (tkis) and have no alternative treatment options. blincyto is indicated as monotherapy for the treatment of adults with philadelphia chromosome negative cd19 positive b-precursor all in first or second complete remission with minimal residual disease (mrd) greater than or equal to 0. blincyto is indicated as monotherapy for the treatment of paediatric patients aged 1 year or older with philadelphia chromosome negative cd19 positive b precursor all which is refractory or in relapse after receiving at least two prior therapies or in relapse after receiving prior allogeneic haematopoietic stem cell transplantation. blincyto is indicated as monotherapy for the treatment of paediatric patients aged 1 year or older with high-risk first relapsed philadelphia chromosome negative cd19 positive b-precursor all as part of the consolidation therapy (see section 4.