Pemetrexed Pfizer (previously known as Pemetrexed Hospira UK Limited) Unia Europejska - chorwacki - EMA (European Medicines Agency)

pemetrexed pfizer (previously known as pemetrexed hospira uk limited)

pfizer europe ma eeig - пеметрексед ditromethamine - carcinoma, non-small-cell lung; mesothelioma - analozi folne kiseline, антиметаболиты - kancerogen плевральный mesotheliomapemetrexed završetak deflacije podržali velika britanija ograničeni u kombinaciji s цисплатином indiciran za liječenje naivne kemoterapije u bolesnika s operirati raka mesothelioma плевры. Немелкоклеточного pluća cancerpemetrexed završetak deflacije podržali wk društva u kombinaciji s цисплатином indiciran za prva linija terapije u bolesnika s lokalno-uobičajena ili metastatskih немелкоклеточным raka pluća od drugih pretežno плоскоклеточного гистологии (vidi Смпц 5. Пеметрексед završetak deflacije podržali wk društva je prikazan u monoterapiji za liječenje местнораспространенного ili метастатического немелкоклеточного raka pluća, druge, nego pretežno плоскоклеточного гистологии kod pacijenata, bolest kojoj se ne прогрессировало odmah nakon платиносодержащей kemoterapije (vidi Смпц 5. Пеметрексед završetak deflacije podržali velika britanija društva je prikazan u monoterapiji za drugu liniju liječenja bolesnika s lokalno-uobičajena ili metastatskih немелкоклеточным raka pluća od drugih pretežno плоскоклеточного гистологии (vidi Смпц 5.

Zaltrap Unia Europejska - chorwacki - EMA (European Medicines Agency)

zaltrap

sanofi winthrop industrie - aflibercept - kolorektalne neoplazme - antineoplastična sredstva - liječenje metastaziranog kolorektalnog karcinoma (mcrc).

KOGENATEBAYER 250i.j./2.5ml Prašak i rastvarač za rastvor za injekciju Czarnogóra - chorwacki - CInMED-Institut za ljekove i medicinska sredstva Crne Gore

kogenatebayer 250i.j./2.5ml prašak i rastvarač za rastvor za injekciju

društvo za trgovinu, promet i usluge "farmegra" d.o.o. podgorica - koagulacioni faktor viii, rekombinantni (oktokog alfa) - prašak i rastvarač za rastvor za injekciju - 250i.j./2.5ml

KOGENATEBAYER 500i.j./2.5ml Prašak i rastvarač za rastvor za injekciju Czarnogóra - chorwacki - CInMED-Institut za ljekove i medicinska sredstva Crne Gore

kogenatebayer 500i.j./2.5ml prašak i rastvarač za rastvor za injekciju

društvo za trgovinu, promet i usluge "farmegra" d.o.o. podgorica - koagulacioni faktor viii, rekombinantni (oktokog alfa) - prašak i rastvarač za rastvor za injekciju - 500i.j./2.5ml

KOGENATEBAYER 1000i.j./2.5ml Prašak i rastvarač za rastvor za injekciju Czarnogóra - chorwacki - CInMED-Institut za ljekove i medicinska sredstva Crne Gore

kogenatebayer 1000i.j./2.5ml prašak i rastvarač za rastvor za injekciju

društvo za trgovinu, promet i usluge "farmegra" d.o.o. podgorica - koagulacioni faktor viii, rekombinantni (oktokog alfa) - prašak i rastvarač za rastvor za injekciju - 1000i.j./2.5ml

COTELLIC 20mg Film tableta Czarnogóra - chorwacki - CInMED-Institut za ljekove i medicinska sredstva Crne Gore

cotellic 20mg film tableta

"hoffmann-la roche ltd" d.s.d. podgorica - kobimetinib - film tableta - 20mg

Blincyto Unia Europejska - chorwacki - EMA (European Medicines Agency)

blincyto

amgen europe b.v. - blinatumomab - prekursorska stanica limfoblastične leukemije-limfom - 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.

Lynparza Unia Europejska - chorwacki - EMA (European Medicines Agency)

lynparza

astrazeneca ab - olaparib - neoplazme jajnika - antineoplastična sredstva - jajnika cancerlynparza prikazan kao monoterapija za:podržava liječenje odraslih bolesnika s поздними (figo faze iii i iv) u genima brca1/2-mutirani (зародышевой linije i/ili somatskih) brzorezni epitela jajnika, masterbatch cijevi ili primarni перитонеальный rak, koji u odgovor (potpuno ili djelomično) nakon završetka prve linije na bazi platine kemoterapije. maintenance treatment of adult patients with platinum sensitive relapsed high grade epithelial ovarian, fallopian tube, or primary peritoneal cancer who are in response (complete or partial) to platinum based chemotherapy. lynparza in combination with bevacizumab is indicated for the:maintenance treatment of adult patients with advanced (figo stages iii and iv) high-grade epithelial ovarian, fallopian tube or primary peritoneal cancer who are in response (complete or partial) following completion of first-line platinum-based chemotherapy in combination with bevacizumab and whose cancer is associated with homologous recombination deficiency (hrd) positive status defined by either a brca1/2 mutation and/or genomic instability (see section 5. breast cancerlynparza is indicated as:monotherapy or in combination with endocrine therapy for the adjuvant treatment of adult patients with germline brca1/2-mutations who have her2-negative, high risk early breast cancer previously treated with neoadjuvant or adjuvant chemotherapy (see sections 4. 2 i 5. monotherapy for the treatment of adult patients with germline brca1/2-mutations, who have her2 negative locally advanced or metastatic breast cancer. pacijenti moraju prethodno bile tretirane s антрациклина i таксана u (neo)adjuvantne ili метастатический, ako pacijenti nisu prikladni za tih postupaka (vidi odjeljak 5. pacijenti s receptore hormona (h)-pozitivnog raka dojke treba također razvili ili nakon pre-hormonska terapija, ili se smatraju neprikladnim za endokrine terapije. adenocarcinoma of the pancreaslynparza is indicated as:monotherapy for the maintenance treatment of adult patients with germline brca1/2-mutations who have metastatic adenocarcinoma of the pancreas and have not progressed after a minimum of 16 weeks of platinum treatment within a first-line chemotherapy regimen. prostate cancerlynparza is indicated as:monotherapy for the treatment of adult patients with metastatic castration-resistant prostate cancer (mcrpc) and brca1/2-mutations (germline and/or somatic) who have progressed following prior therapy that included a new hormonal agent. in combination with abiraterone and prednisone or prednisolone for the treatment of adult patients with mcrpc in whom chemotherapy is not clinically indicated (see section 5.

Calquence Unia Europejska - chorwacki - EMA (European Medicines Agency)

calquence

astrazeneca ab - acalabrutinib - leukemija, limfocitna, kronična, b-stanica - antineoplastic agents, protein kinase inhibitors, - calquence as monotherapy or in combination with obinutuzumab is indicated for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia (cll). calquence as monotherapy is indicated for the treatment of adult patients with chronic lymphocytic leukaemia (cll) who have received at least one prior therapy.

SYNAGIS 50 mg/0,5 ml Rastvor za injekciju Czarnogóra - chorwacki - CInMED-Institut za ljekove i medicinska sredstva Crne Gore

synagis 50 mg/0,5 ml rastvor za injekciju

druŠtvo za trgovinu na veliko farmaceutskim proizvodima "glosarij" d.o.o.-podgorica - palivizumab - rastvor za injekciju - 50 mg/0,5 ml