bortezomib pharmaswiss 3,5 mg pulveris injekciju šķīduma pagatavošanai
pharmaswiss ceska republika s.r.o., czech republic - bortezomibs - pulveris injekciju šķīduma pagatavošanai - 3,5 mg
bortezomib ebewe 3,5 mg pulveris injekciju šķīduma pagatavošanai
sandoz d.d., slovenia - bortezomibs - pulveris injekciju šķīduma pagatavošanai - 3,5 mg
bortezomib sandoz 3,5 mg pulveris injekciju šķīduma pagatavošanai
sandoz d.d., slovenia - bortezomibs - pulveris injekciju šķīduma pagatavošanai - 3,5 mg
vortemyel 3,5 mg pulveris injekciju šķīduma pagatavošanai
alvogen ipco s.a.r.l, luxembourg - bortezomibs - pulveris injekciju šķīduma pagatavošanai - 3,5 mg
bortezomib teva 3,5 mg pulveris injekciju šķīduma pagatavošanai
teva b.v., netherlands - bortezomibs - pulveris injekciju šķīduma pagatavošanai - 3,5 mg
bortezomib actavis 3,5 mg pulveris injekciju šķīduma pagatavošanai
actavis group ptc ehf., iceland - bortezomibs - pulveris injekciju šķīduma pagatavošanai - 3,5 mg
blincyto
amgen europe b.v. - blinatumomab - prekursoru šūnu limfoblastiska leikēmija-limfoma - antineoplastiski līdzekļi - 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.
ferant 250 mikrogrami šķīdums injekcijām
medochemie ltd., cyprus - palonosetrons - Šķīdums injekcijām - 250 µg
palonosetron sandoz 250 mikrogramu šķīdums injekcijām
sandoz d.d., slovenia - palonosetrons - Šķīdums injekcijām - 250 µg