Palonosetron Fresenius Kabi 250 mikrogramov raztopina za injiciranje Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

palonosetron fresenius kabi 250 mikrogramov raztopina za injiciranje

fresenius kabi deutschland gmbh - palonosetron - raztopina za injiciranje - palonosetron 250 µg / 1 viala - palonosetron

Blincyto Evropska unija - slovenščina - EMA (European Medicines Agency)

blincyto

amgen europe b.v. - blinatumomab - predkroglomerna limfoblastna levkemija limfoma - antineoplastična sredstva - 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.

Palonosetron Accord Evropska unija - slovenščina - EMA (European Medicines Agency)

palonosetron accord

accord healthcare s.l.u. - palonosetron - vomiting; nausea; cancer - antiemetics in antinauseants, - palonosetron soglasju je navedeno v odraslih za:preprečevanje akutne slabosti in bruhanja, povezanih z močno emetogenic rak, kemoterapija,preprečevanje slabosti in bruhanja, povezanih z zmerno emetogenic kemoterapijo raka. palonosetron soglasju je navedeno v pediatričnih bolnikih od 1 meseca starosti in starejših za:preprečevanje akutne slabosti in bruhanja, povezanih z močno emetogenic rak, kemoterapija in preprečevanje slabosti in bruhanja, povezanih z zmerno emetogenic kemoterapijo raka.

Palonosetron Hospira Evropska unija - slovenščina - EMA (European Medicines Agency)

palonosetron hospira

pfizer europe ma eeig - palonosetronijev hidroklorid - nausea; vomiting; cancer - antiemetics in antinauseants, - palonosetron hospira je navedeno v odraslih za:preprečevanje akutne slabosti in bruhanja, povezanih z močno emetogenic raka kemoterapijo;preprečevanje slabosti in bruhanja, povezanih z zmerno emetogenic kemoterapijo raka. palonosetron hospira je navedeno v pediatričnih bolnikih od 1 meseca starosti in starejših za:preprečevanje akutne slabosti in bruhanja, povezanih z močno emetogenic rak, kemoterapija in preprečevanje slabosti in bruhanja, povezanih z zmerno emetogenic kemoterapijo raka.

Nibix 100 mg trde kapsule Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

nibix 100 mg trde kapsule

adamed sp. z.o.o - imatinib - kapsula, trda - imatinib 100 mg / 1 kapsula - imatinib