Den europeiske union - kroatisk - EMA (European Medicines Agency)

stemline therapeutics b.v. - selinexor - multipli mijelom - antineoplastična sredstva - nexpovio is indicatedin combination with bortezomib and dexamethasone for the treatment of adult patients with multiple myeloma who have received at least one prior therapy. in combination with dexamethasone for the treatment of multiple myeloma in adult patients who have received at least four prior therapies and whose disease is refractory to at least two proteasome inhibitors, two immunomodulatory agents and an anti-cd38 monoclonal antibody, and who have demonstrated disease progression on the last therapy.

Den europeiske union - kroatisk - EMA (European Medicines Agency)

amgen europe b.v. - carfilzomib - multipli mijelom - antineoplastična sredstva - kyprolis in combination with daratumumab and dexamethasone, with lenalidomide and dexamethasone, or with dexamethasone alone is indicated for the treatment of adult patients with multiple myeloma who have received at least one prior therapy.

Den europeiske union - kroatisk - EMA (European Medicines Agency)

cheplapharm arzneimittel gmbh - kapecitabin - colonic neoplasms; breast neoplasms; colorectal neoplasms; stomach neoplasms - antineoplastična sredstva - Кселода propisan za адъювантного liječenje bolesnika nakon operacije iii faze (dukes faza c) rak debelog crijeva . Кселода propisan za liječenje метастатического raka debelog crijeva . Кселода propisan za prva linija terapije popularnog raka želuca u kombinaciji s platinum temelju stanja. Кселода u kombinaciju sa docetaxel indiciran za liječenje bolesnika s lokalno-uobičajena ili metastatskih tumora dojke neučinkovitosti цитотоксической kemoterapije. prethodna terapija mora sadržavati антрациклиновый. Кселода je također indiciran u monoterapiji za liječenje bolesnika s lokalno-uobičajena ili metastatskih tumora dojke neučinkovitosti Таксанов i антрациклин sadrže načina kemoterapije ili za koje antikancerogena terapija nije naveden.

Den europeiske union - kroatisk - EMA (European Medicines Agency)

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

Kroatia - kroatisk - HALMED (Agencija za lijekove i medicinske proizvode)

glaxosmithkline d.o.o., ulica damira tomljanovića gavrana 15, zagreb - fluticasonum - prašak inhalata - 100 µg - urbroj: jedna inhalacijska doza sadržava 100 µg flutikazonpropionata

Kroatia - kroatisk - HALMED (Agencija za lijekove i medicinske proizvode)

glaxosmithkline d.o.o., ulica damira tomljanovića gavrana 15, zagreb - fluticasonum - prašak inhalata - 250 µg - urbroj: jedna inhalacijska doza sadržava 250 µg flutikazonpropionata

Den europeiske union - kroatisk - EMA (European Medicines Agency)

janssen-cilag international nv - ciltacabtagene autoleucel - multipli mijelom - carvykti is indicated for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least three prior therapies, including an immunomodulatory agent, a proteasome inhibitor and an anti-cd38 antibody and have demonstrated disease progression on the last therapy.

Den europeiske union - kroatisk - EMA (European Medicines Agency)

roche registration gmbh  - glofitamab - lymphoma, large b-cell, diffuse - antineoplastična sredstva - columvi as monotherapy is indicated for the treatment of adult patients with relapsed or refractory diffuse large b cell lymphoma (dlbcl), after two or more lines of systemic therapy.

Den europeiske union - kroatisk - EMA (European Medicines Agency)

gilead sciences ireland uc - idelalisib - lymphoma, non-hodgkin; leukemia, lymphocytic, chronic, b-cell - antineoplastic agents, other antineoplastic agents - zydelig is indicated in combination with an anti‑cd20 monoclonal antibody (rituximab or ofatumumab) for the treatment of adult patients with chronic lymphocytic leukaemia (cll):who have received at least one prior therapy, oras first line treatment in the presence of 17p deletion or tp53 mutation in patients who are not eligible for any other therapies. zydelig is indicated as monotherapy for the treatment of adult patients with follicular lymphoma (fl) that is refractory to two prior lines of treatment.

Den europeiske union - kroatisk - EMA (European Medicines Agency)

roche registration gmbh  - пертузумаб - neoplazme dojki - antineoplastic agents, monoclonal antibodies - Метастатический rak dojke:perjeta indiciran za primjenu u kombinaciji s трастузумабом i docetaxel u odraslih bolesnika s her2 pozitivnim metastaze ili lokalno-najčešći нерезектабельным raka dojke, koji nisu primili prethodne anti-her2 terapije ili kemoterapije za метастатической bolesti. Неоадъювантного liječenje raka dojke perjeta indiciran za primjenu u kombinaciji s трастузумабом i kemoterapije za неоадъювантного liječenje odraslih bolesnika s her2 pozitivnim, lokalno, upalne ili ranog raka dojke s visokim rizikom od recidiva.