Gliolan Европска Унија - Словеначки - EMA (European Medicines Agency)

gliolan

photonamic gmbh & co. kg - 5-aminolevulinična kislina hidroklorid - glioma - antineoplastična sredstva - gliolan je indiciran pri odraslih bolnikih za vizualizacijo malignih tkiv med operacijo malignih glioma (iii. in iv. svetovna zdravstvena organizacija).

Virbagen Omega Европска Унија - Словеначки - EMA (European Medicines Agency)

virbagen omega

virbac s.a. - rekombinantni omega interferon mačjega izvora - immunostimulants, - dogs; cats - dogsreduction of mortality and clinical signs of parvovirosis (enteric form) in dogs from one month of age. catstreatment of cats infected with feline leukaemia virus (felv) and / or feline immunodeficiency virus (fiv), in non-terminal clinical stages, from the age of nine weeks. in a field study conducted, it was observed that there was:a reduction of clinical signs during the symptomatic phase (four months);a reduction of mortality:in anaemic cats, mortality rate of about 60% at four, six, nine and 12 months was reduced by approximately 30% following treatment with interferon;in non-anaemic cats, mortality rate of 50% in cats infected by felv was reduced by 20% following treatment with interferon. pri mačkah, okuženih s fiv, je bila smrtnost nizka (5%) in na zdravljenje ni vplivala.

Mycamine Европска Унија - Словеначки - EMA (European Medicines Agency)

mycamine

astellas pharma europe b.v. - mikafungin - kandidoza - antimikotiki za sistemsko uporabo - mycamine je indiciran za:odrasli, mladostniki ≥ 16 let in elderlytreatment za invazivne kandidoze;zdravljenje ezofagealni kandidoze pri bolnikih, za katere intravensko zdravljenje je primerno;preventivo candida okužbe pri bolnikih, ki opravljajo allogeneic haematopoietic stem-cell presaditve ali bolniki, ki se pričakuje, da so neutropenia (absolutno neutrophil štetje < 500 celic/µl) za 10 ali več dni. otroci (vključno z novorojenčkih) in mladostnikih < 16 let agetreatment za invazivne kandidoze. profilaksa candida okužbe pri bolnikih, ki opravljajo allogeneic haematopoietic stem-cell presaditve ali bolniki, ki se pričakuje, da so neutropenia (absolutno neutrophil štetje < 500 celic/µl) za 10 ali več dni. odločitev za uporabo mycamine je treba upoštevati morebitno tveganje za razvoj jetrnih tumorjev. mycamine bi zato lahko uporabljajo le, če druge antifungals niso primerne.

Orphacol Европска Унија - Словеначки - EMA (European Medicines Agency)

orphacol

theravia - holinska kislina - digestive system diseases; metabolism, inborn errors - Žolčnih kislin in derivati - orphacol je indicirano za zdravljenje prirojenih napak v primarni sintezo žolčnih kislin zaradi oxidoreductase 3β-hidroksi-Δ5-c27-steroid pomanjkljivost ali Δ4-3-oxosteroid-5β-reduktazo pomanjkljivost pri dojenčkih, otrocih in mladostnikih v starosti enega meseca do 18 let in odrasli.

Xermelo Европска Унија - Словеначки - EMA (European Medicines Agency)

xermelo

serb sas - telotristat etiprat - carcinoid tumor; neuroendocrine tumors - drugi proizvodi prebavnega trakta in metabolizma - xermelo je indicirano za zdravljenje driska sindrom karcinoid v kombinaciji z somatostatina analogne (ssa) terapija pri odraslih, neustrezno nadzira prp terapijo.

Dectova Европска Унија - Словеначки - EMA (European Medicines Agency)

dectova

glaxosmithkline trading services limited - zanamivir - gripa, človek - antivirusi za sistemsko uporabo - dectova je primerna za zdravljenje zapleteno in potencialno smrtno nevarne gripe a ali b virus okužbe pri odraslih in pediatričnih bolnikih (starih ≥6 mesecev), če:bolnik je virus influence je znano ali se sumi, da odporne proti gripi zdravil, razen zanamivir, in/orother anti-virusni zdravila za zdravljenje gripe, vključno pri vdihavanju zanamivir, niso primerni za posameznega pacienta. dectova je treba uporabljati v skladu z uradnimi smernice.

Xospata Европска Унија - Словеначки - EMA (European Medicines Agency)

xospata

astellas pharma europe b.v. - gilteritinib fumarate - leukemija, myeloid, akutna - antineoplastična sredstva - xospata je označen kot monotherapy za zdravljenje odraslih bolnikov, ki so relapsed ali ognjevzdržni akutno mieloično levkemijo (aml), z flt3 mutacija.

Elzonris Европска Унија - Словеначки - EMA (European Medicines Agency)

elzonris

stemline therapeutics b.v. - tagraxofusp - lymphoma - antineoplastična sredstva - elzonris is indicated as monotherapy for the first-line treatment of adult patients with blastic plasmacytoid dendritic cell neoplasm (bpdcn).

Enhertu Европска Унија - Словеначки - EMA (European Medicines Agency)

enhertu

daiichi sankyo europe gmbh - trastuzumab deruxtecan - neoplazme dojke - antineoplastična sredstva - breast cancerher2-positive breast cancerenhertu as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic her2-positive breast cancer who have received one or more prior anti-her2-based regimens. her2-low breast cancerenhertu as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic her2-low breast cancer who have received prior chemotherapy in the metastatic setting or developed disease recurrence during or within 6 months of completing adjuvant chemotherapy (see section 4. non-small cell lung cancer (nsclc)enhertu as monotherapy is indicated for the treatment of adult patients with advanced nsclc whose tumours have an activating her2 (erbb2) mutation and who require systemic therapy following platinum-based chemotherapy with or without immunotherapy. gastric cancerenhertu as monotherapy is indicated for the treatment of adult patients with advanced her2-positive gastric or gastroesophageal junction (gej) adenocarcinoma who have received a prior trastuzumab-based regimen.