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.

Blincyto 38.5 mikrog Norge - norsk - Statens legemiddelverk

blincyto 38.5 mikrog

orifarm as - blinatumomab - pulver til konsentrat og oppløsning til infusjonsvæske, oppløsning - 38.5 mikrog

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

unituxin

united therapeutics europe ltd - dinutuximab - neuroblastom - antineoplastiske midler - unituxin er indisert for behandling av høy risiko neuroblastom hos pasienter i alderen 12 måneder til 17years, som tidligere har mottatt induksjon kjemoterapi og oppnås minst delvis svar, etterfulgt av myeloablative terapi og autologous stilk cellen transplantasjon (asct). det administreres i kombinasjon med granulocyt-makrofag kolonistimulerende faktor (gm-csf), interleukin-2 (il-2) og isotretinoin.

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

elzonris

stemline therapeutics b.v. - tagraxofusp - lymphoma - antineoplastiske midler - elzonris is indicated as monotherapy for the first-line treatment of adult patients with blastic plasmacytoid dendritic cell neoplasm (bpdcn).

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

inbrija

acorda therapeutics ireland limited - levodopa - parkinsonsykdom - anti-parkinson medisiner - inbrija er indikert for intermitterende behandling av episodisk motoriske fluktuasjoner (av episoder) hos voksne pasienter med parkinsons sykdom (pd) behandlet med levodopa/dopa-decarboxylase inhibitor.

Omeprazol Bluefish 20 mg Norge - norsk - Statens legemiddelverk

omeprazol bluefish 20 mg

bluefish pharmaceuticals ab - omeprazol - enterokapsel, hard - 20 mg

Omeprazol Bluefish 10 mg Norge - norsk - Statens legemiddelverk

omeprazol bluefish 10 mg

bluefish pharmaceuticals ab - omeprazol - enterokapsel, hard - 10 mg

Losec Mups 10 mg Norge - norsk - Statens legemiddelverk

losec mups 10 mg

cheplapharm arzneimittel gmbh - omeprazolmagnesium - enterotablett - 10 mg

Losec Mups 20 mg Norge - norsk - Statens legemiddelverk

losec mups 20 mg

cheplapharm arzneimittel gmbh - omeprazolmagnesium - enterotablett - 20 mg

Omeprazol Medical Valley 10 mg Norge - norsk - Statens legemiddelverk

omeprazol medical valley 10 mg

medical valley invest ab - omeprazol - enterokapsel, hard - 10 mg