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

nubeqa

bayer ag - darolutamide - tumori prostate, Кастраци-uporan - endokrinska terapija - nubeqa is indicated for the treatment of adult men with- non metastatic castration resistant prostate cancer (nmcrpc) who are at high risk of developing metastatic disease (see section 5. - metastatic hormone sensitive prostate cancer (mhspc) in combination with docetaxel and androgen deprivation therapy (see section 5.

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

verquvo

bayer ag - vericiguat - zastoj srca - srčana terapija - treatment of symptomatic chronic heart failure.

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

byooviz

samsung bioepis nl b.v. - ranibizumab - wet macular degeneration; macular edema; diabetic retinopathy; myopia, degenerative - ophthalmologicals - byooviz is indicated in adults for:the treatment of neovascular (wet) age-related macular degeneration (amd)the treatment of visual impairment due to diabetic macular oedema (dme)the treatment of proliferative diabetic retinopathy (pdr)the treatment of visual impairment due to macular oedema secondary to retinal vein occlusion (branch rvo or central rvo)the treatment of visual impairment due to choroidal neovascularisation (cnv).

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

vumerity

biogen netherlands b.v. - diroximel fumarate (biib098) - multipla skleroza, Рецидивно-Ремиттирующее - imunosupresivi - vumerity is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis (see section 5. 1 for important information on the populations for which efficacy has been established).

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

kerendia

bayer ag - finerenone - renal insufficiency, chronic; diabetes mellitus, type 2 - sredstva koja djeluju na sustav renin-angiotenzina - kerendia is indicated for the treatment of chronic kidney disease (stage 3 and 4 with albuminuria) associated with type 2 diabetes in adults.

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

abrysvo

pfizer europe ma eeig - respiratory syncytial virus, subgroup a, stabilized prefusion f protein / respiratory syncytial virus, subgroup b, stabilized prefusion f protein - infekcije respiratornih sincicijskih virusa - cjepiva - abrysvo is indicated for:passive protection against lower respiratory tract disease caused by respiratory syncytial virus (rsv) in infants from birth through 6 months of age following maternal immunisation during pregnancy. pogledajte odjeljke 4. 2 i 5. active immunisation of individuals 60 years of age and older for the prevention of lower respiratory tract disease caused by rsv. korištenje ovog cjepiva mora se provoditi u skladu sa službenim preporukama.

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

bosulif

pfizer europe ma eeig - bosutinib (kao monohidrat) - leukemija, mieloid - antineoplastic agents, protein kinase inhibitors - bosulif indiciran za liječenje odraslih bolesnika s prvi put prijavljene kronične faze (cp) kromosoma-pozitivnim philadelphia kronične миелогенной leukemije (ph+ kml). srijeda, ubrzana faza (ap), i бластном (bp) ph+ kml, prethodno liječenih jedan ili više inhibitora тирозинкиназы(s) [тки(e)] i za koga imatinib, nilotinib i dasatinib ne uzeti u obzir odgovarajuće mogućnosti liječenja .

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

conbriza

pfizer europe ma eeig - bazedoxifene - osteoporoza, postmenopauzalna - spolni hormoni i modulatori genitalnog sustava, - conbriza je indiciran za liječenje osteoporoze u postmenopauzi kod žena s povećanim rizikom od prijeloma. značajno smanjenje incidencije fraktura kralješaka je dokazano; djelotvornost na prijelome kuka nije utvrđena. pri određivanju izbor conbriza ili druge vrste terapije, uključujući i estrogena za određenu žene u postmenopauzi, treba uzeti u obzir simptome menopauze, utjecaj na maternice i tkiva dojke i kardiovaskularne rizike i koristi.

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

ibrance

pfizer europe ma eeig  - palbociclib - neoplazme dojki - antineoplastična sredstva - ibrance indiciran za liječenje hormonalnih receptora (op) je pozitivan, людское эпидермическое ako uređaj primatelja 2 faktor rasta (her2 i) negativne lokalno-uobičajena ili metastatskih tumora dojke:u kombinaciji s inhibitor aromataze, u kombinaciji s fulvestrant kod žena koje su dobili preliminarne hormonsko nadomjesno liječenje. u pre - ili perimenopauzi, endokrini terapija mora biti u kombinaciji s luteinizirajućeg hormona releasing hormon (lhrh) agonist.

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

inlyta

pfizer europe ma eeig  - axitinib - karcinom, stanice bubrega - inhibitori протеинкиназы - inlyta is indicated for the treatment of adult patients with advanced renal cell carcinoma (rcc) after failure of prior treatment with sunitinib or a cytokine.