Grasustek European Union - Slovenian - EMA (European Medicines Agency)

grasustek

juta pharma gmbh - pegfilgrastim - nevtropenija - immunostimulants, - skrajšanje trajanja nevtropenija in pojavnost vročinskih nevtropenija pri odraslih bolnikih, zdravljenih s citotoksično kemoterapijo za malignosti (razen kronično mieloično levkemijo in mielodisplastični sindrom).

Yescarta European Union - Slovenian - EMA (European Medicines Agency)

yescarta

kite pharma eu b.v. - axicabtagene ciloleucel - lymphoma, follicular; lymphoma, large b-cell, diffuse - antineoplastična sredstva - yescarta is indicated for the treatment of adult patients with diffuse large b cell lymphoma (dlbcl) and high-grade b-cell lymphoma (hgbl) that relapses within 12 months from completion of, or is refractory to, first-line chemoimmunotherapy. yescarta is indicated for the treatment of adult patients with relapsed or refractory (r/r) dlbcl and primary mediastinal large b cell lymphoma (pmbcl), after two or more lines of systemic therapy. yescarta is indicated for the treatment of adult patients with r/r follicular lymphoma (fl) after three or more lines of systemic therapy.

Yesafili European Union - Slovenian - 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.

Zavesca European Union - Slovenian - EMA (European Medicines Agency)

zavesca

janssen cilag international nv - miglustat - gaucher disease; niemann-pick diseases - drugi zdravljene bolezni prebavil in presnove izdelki, - zdravilo zavesca je indicirano za oralno zdravljenje odraslih bolnikov z blago do zmerno gaucherjevo boleznijo tipa 1. zdravilo zavesca se lahko uporablja le pri zdravljenju bolnikov, pri katerih je nadomestno zdravljenje z encimi nezadostno. zavesca je primerna za zdravljenje progresivne nevrološke manifestacije pri odraslih bolnikih in pediatričnih bolnikih z niemann-pick tip-c bolezen.

Ablavar (previously Vasovist) European Union - Slovenian - EMA (European Medicines Agency)

ablavar (previously vasovist)

tmc pharma services ltd. - gadofosveset trisodium - angiografija magnetne resonance - kontrastni mediji - to zdravilo je samo za diagnostično uporabo. ablavar je označen za kontrast, podkrepljeno z magnetno resonanco angiography (ce-mra) za vizualizacijo v trebuhu ali telo plovil v odrasli samo s sumi ali ve žilne bolezni,.

Flexyess 0,02 mg/3 mg filmsko obložene tablete Slovenia - Slovenian - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

flexyess 0,02 mg/3 mg filmsko obložene tablete

bayer d.o.o. - drospirenon; etinilestradiol - filmsko obložena tableta - drospirenon 3 mg / 1 tableta  etinilestradiol0,02 mg / 1 tableta; etinilestradiol 0,02 mg / 1 tableta - drospirenon in etinilestradiol

Flexyess 0,02 mg/3 mg filmsko obložene tablete Slovenia - Slovenian - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

flexyess 0,02 mg/3 mg filmsko obložene tablete

bayer d.o.o. - drospirenon; etinilestradiol - filmsko obložena tableta - drospirenon 3 mg / 1 tableta  etinilestradiol0,02 mg / 1 tableta; etinilestradiol 0,02 mg / 1 tableta - drospirenon in etinilestradiol

Ceprotin European Union - Slovenian - EMA (European Medicines Agency)

ceprotin

takeda manufacturing austria ag - človeški protein c - purpura fulminans; protein c deficiency - antitrombotična sredstva - ceprotin is indicated for prophylaxis and treatment of  purpura fulminans  coumarin-induced skin necrosis and venous thrombotic events in patients with severe congenital protein c deficiency.

Nonafact European Union - Slovenian - EMA (European Medicines Agency)

nonafact

sanquin plasma products b.v. - človeški koagulacijski faktor ix - hemofilija b - antihemoragije - zdravljenje in profilaksa krvavitve pri bolnikih s hemofilijo b (prirojene pomanjkljivosti faktorja ix).

Strimvelis European Union - Slovenian - EMA (European Medicines Agency)

strimvelis

fondazione telethon ets - avtologni cd34 + obogaten del celice, ki vsebuje cd34 + celice transduced retrovirusni vektor, ki kodira za ljudi adenozin deaminase (ada) zaporedje cdna iz človeške krvotvornih matičnih/matičnih (cd34 +) celic - huda kombinirana imunska pomanjkljivost - immunostimulants, - strimvelis je indicirano za zdravljenje bolnikov z huda kombinirane imunske pomanjkljivosti zaradi pomanjkanja adenozin deaminase (ada-hu), za katere ni primeren človeških levkocitov antigenov (hla)-ujema povezanih izvornih celic darovalca je na voljo (glej oddelek 4. 2 in oddelek 4.