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.

Briviact 25 mg Norge - norsk - Statens legemiddelverk

briviact 25 mg

2care4 aps - brivaracetam - tablett, filmdrasjert - 25 mg

Briviact 50 mg Norge - norsk - Statens legemiddelverk

briviact 50 mg

2care4 aps - brivaracetam - tablett, filmdrasjert - 50 mg

Briviact 75 mg Norge - norsk - Statens legemiddelverk

briviact 75 mg

2care4 aps - brivaracetam - tablett, filmdrasjert - 75 mg

Briviact 100 mg Norge - norsk - Statens legemiddelverk

briviact 100 mg

2care4 aps - brivaracetam - tablett, filmdrasjert - 100 mg

Palladon 50 mg/ ml Norge - norsk - Statens legemiddelverk

palladon 50 mg/ ml

mundipharma as - hydromorfonhydroklorid - injeksjons-/infusjonsvæske, oppløsning - 50 mg/ ml

Palladon 4 mg Norge - norsk - Statens legemiddelverk

palladon 4 mg

mundipharma as - hydromorfonhydroklorid - depotkapsel, hard - 4 mg

Palladon 16 mg Norge - norsk - Statens legemiddelverk

palladon 16 mg

mundipharma as - hydromorfonhydroklorid - depotkapsel, hard - 16 mg

Palladon 2 mg/ ml Norge - norsk - Statens legemiddelverk

palladon 2 mg/ ml

mundipharma as - hydromorfonhydroklorid - injeksjons-/infusjonsvæske, oppløsning - 2 mg/ ml

Palladon 10 mg/ ml Norge - norsk - Statens legemiddelverk

palladon 10 mg/ ml

mundipharma as - hydromorfonhydroklorid - injeksjons-/infusjonsvæske, oppløsning - 10 mg/ ml