Ozurdex Եվրոպական Միություն - սլովեներեն - EMA (European Medicines Agency)

ozurdex

abbvie deutschland gmbh & co. kg - deksametazon - macular edema; uveitis - ophthalmologicals, other ophthalmologicals - ozurdex je indiciran za zdravljenje odraslih bolnikov z degeneracijo edem naslednje bodisi podružnico mrežnice-vene (brvo) ali centralne mrežnice-vene (crvo). ozurdex je indiciran za zdravljenje odraslih bolnikov z vnetjem zadnji segment očesa, ki predstavljajo, kot noninfectious uveitis. ozurdex je indiciran za zdravljenje odraslih bolnikov s vida zaradi diabetično degeneracija edem (dme), ki so pseudophakic ali, ki so ovrednotena dovolj odziven, ali neprimerne za ne-kortikosteroidne terapije.

Yesafili Եվրոպական Միություն - սլովեներեն - EMA (European Medicines Agency)

yesafili

viatris limited - aflibercept - macular edema; retinal vein occlusion; diabetic retinopathy; myopia, degenerative; diabetes complications - oftalmologi - yesafili is indicated for adults for the treatment ofneovascular (wet) age-related macular degeneration (amd) (see section 5. 1),visual impairment due to macular oedema secondary to retinal vein occlusion (branch rvo or central rvo) (see section 5. 1),visual impairment due to diabetic macular oedema (dme) (see section 5. 1),visual impairment due to myopic choroidal neovascularisation (myopic cnv) (see section 5.

Qarziba (previously Dinutuximab beta EUSA and Dinutuximab beta Apeiron) Եվրոպական Միություն - սլովեներեն - EMA (European Medicines Agency)

qarziba (previously dinutuximab beta eusa and dinutuximab beta apeiron)

recordati netherlands b.v. - dinutuximab beta - neuroblastom - antineoplastična sredstva - qarziba je primerna za zdravljenje visokega tveganja neuroblastoma pri bolnikih, starih od 12 mesecev in več, ki so že prejeli indukcijske kemoterapijo in doseči vsaj delni odgovor, sledi myeloablative terapije in presaditev matičnih celic, kot tudi bolnikov z zgodovino relapsed ali ognjevzdržni neuroblastoma, z ali brez ostanka bolezni. pred zdravljenjem ponovnega nevroblastoma je treba vsako drugo aktivno napredujočo bolezen stabilizirati z drugimi ustreznimi ukrepi. pri bolnikih z anamnezo relapsed/ognjevzdržni bolezni in pri bolnikih, ki niso dosegli popolnega odziva po tem, ko prva linija terapije, qarziba je treba v kombinaciji z interleukin 2 (il 2).

Fortral 30 mg/ml raztopina za injiciranje Սլովենիա - սլովեներեն - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

fortral 30 mg/ml raztopina za injiciranje

krka, d.d., novo mesto - pentazocin - raztopina za injiciranje - pentazocin 30 mg / 1 ml - pentazocin

Fortral 50 mg tablete Սլովենիա - սլովեներեն - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

fortral 50 mg tablete

krka, d.d., novo mesto - pentazocin - tableta - pentazocin 50 mg / 1 tableta - pentazocin

Afstyla Եվրոպական Միություն - սլովեներեն - EMA (European Medicines Agency)

afstyla

csl behring gmbh - lonoktokog alfa - hemofilija a - antihemoragije - zdravljenje in profilaksa krvavitve pri bolnikih s hemofilijo a (prirojeno pomanjkanje faktorja viii). afstyla se lahko uporablja za vse starostne skupine.

Byooviz Եվրոպական Միություն - սլովեներեն - EMA (European Medicines Agency)

byooviz

samsung bioepis nl b.v. - ranibizumab - wet macular degeneration; macular edema; diabetic retinopathy; myopia, degenerative - oftalmologi - 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).

Ximluci Եվրոպական Միություն - սլովեներեն - EMA (European Medicines Agency)

ximluci

stada arzneimittel ag - ranibizumab - wet macular degeneration; macular edema; diabetic retinopathy; diabetes complications - oftalmologi - ximluci 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).

Ranivisio Եվրոպական Միություն - սլովեներեն - EMA (European Medicines Agency)

ranivisio

midas pharma gmbh - ranibizumab - wet macular degeneration; macular edema; diabetic retinopathy; diabetes complications - oftalmologi - ranivisio 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).