Evrenzo Unjoni Ewropea - Malti - EMA (European Medicines Agency)

evrenzo

astellas pharma europe b.v. - roxadustat - anemia; kidney failure, chronic - preparazzjonijiet antianemiċi - evrenzo is indicated for treatment of adult patients with symptomatic anaemia associated with chronic kidney disease (ckd).

Celsentri Unjoni Ewropea - Malti - EMA (European Medicines Agency)

celsentri

viiv healthcare b.v. - maraviroc - infezzjonijiet ta 'hiv - antivirali għal użu sistemiku - celsentri, in combination with other antiretroviral medicinal products, is indicated for treatment experienced adults, adolescents and children of 2 years of age and older and weighing at least 10 kg infected with only ccr5-tropic hiv-1 detectable,.

Kisqali Unjoni Ewropea - Malti - EMA (European Medicines Agency)

kisqali

novartis europharm limited - ribociclib succinate - neoplażmi tas-sider - aġenti antineoplastiċi - kisqali huwa indikat għall-kura ta 'nisa bl-ormon tat-riċettur (hr)‑pożittivi, tal-bniedem tar-riċettur tal-fattur tat-tkabbir epidermali 2 (her2) negattivi lokalment avvanzata jew metastatika tal-kanċer tas-sider f'kumbinazzjoni ma' inibitur aromatase jew fulvestrant bħala inizjali endokrinali bbażata fuq it-terapija, jew f'nisa li kienu rċevew qabel terapija endokrinali. fil‑ pre- jew perimenopausal-nisa, l-endokrinali it-terapija għandha tingħata flimkien ma 'ormon ta' lutejniżżazzjoni‑releasing hormone (lhrh) agonist.

Lacosamide Accord Unjoni Ewropea - Malti - EMA (European Medicines Agency)

lacosamide accord

accord healthcare s.l.u. - lacosamide - epilessija - anti-epilettiċi, - lacosamide accord is indicated as monotherapy in the treatment of partial-onset seizures with or without secondary generalisation in adults, adolescents and children from 4 years of age with epilepsy. lacosamide accord is indicated as adjunctive therapy•         in the treatment of partial-onset seizures with or without secondary generalisation in adults, adolescents and children from 4 years of age with epilepsy. •         in the treatment of primary generalised tonic-clonic seizures in adults, adolescents and children from 4 years of age with idiopathic generalised epilepsy.

Lupkynis Unjoni Ewropea - Malti - EMA (European Medicines Agency)

lupkynis

otsuka pharmaceutical netherlands b.v. - voclosporin - lupus nephritis - immunosoppressanti - lupkynis is indicated in combination with mycophenolate mofetil for the treatment of adult patients with active class iii, iv or v (including mixed class iii/v and iv/v) lupus nephritis (ln).

Orgovyx Unjoni Ewropea - Malti - EMA (European Medicines Agency)

orgovyx

accord healthcare s.l.u. - relugolix - neoplasmi prostatiċi - terapija endokrinali - orgovyx is indicated for the treatment of adult patients with advanced hormone-sensitive prostate cancer.

Advagraf Unjoni Ewropea - Malti - EMA (European Medicines Agency)

advagraf

astellas pharma europe bv - tacrolimus - rifjut ta 'graft - immunosoppressanti - profilassi tar-rifjut tat-trapjanti f'riċevituri ta 'l-alloġib tal-kliewi jew tal-fwied adulti. kura ta 'rifjut tal-allograft reżistenti għat-trattament ma' prodotti mediċinali immunosoppressivi oħra f'pazjenti adulti.

Comtess Unjoni Ewropea - Malti - EMA (European Medicines Agency)

comtess

orion corporation - entacapone - marda ta 'parkinson - mediċini kontra l-parkinson - entacapone huwa indikat bħala frozen preparazzjonijiet standard ta ' ticlopidine hydrochloride / benserazide jew ticlopidine hydrochloride / carbidopa għall-użu fil-pazjenti bil-marda ta ' parkinson's u l-tmiem tad-doża oxxillazzjonijiet vetturi bil-mutur, li ma jistax jiġi stabbilizzat fuq dawk l-għaqdiet.

Entacapone Orion Unjoni Ewropea - Malti - EMA (European Medicines Agency)

entacapone orion

orion corporation - entacapone - marda ta 'parkinson - mediċini kontra l-parkinson - entacapone huwa indikat bħala frozen preparazzjonijiet standard ta ' ticlopidine hydrochloride / benserazide jew ticlopidine hydrochloride / carbidopa għall-użu fil-pazjenti adulti mal-marda ta ' parkinson's u l-tmiem tad-doża oxxillazzjonijiet vetturi bil-mutur, li ma jistax jiġi stabbilizzat fuq dawk l-għaqdiet.

Leflunomide medac Unjoni Ewropea - Malti - EMA (European Medicines Agency)

leflunomide medac

medac gesellschaft für klinische spezialpräparate mbh - leflunomide - artrite, rewmatika - immunosuppressanti selettivi - leflunomide huwa indikat għall-kura ta ' pazjenti adulti bil:artrite rewmatika attiva bħala 'mard tal-anti-rewmatiċi li jimmodifikaw il-mediċina' (dmard). riċenti jew fl-istess waqt it-trattament b'tossiku għall-fwied jew haematotoxic dmards (e. methotrexate), tista 'tirriżulta f'żieda fir-riskju ta' reazzjonijiet avversi serji, għalhekk, l-inizjazzjoni tal-kura b'leflunomide għandu jiġi kkunsidrat bir-reqqa dwar dawn il-benefiċċju / riskju aspetti. barra minn hekk, il-qlib minn leflunomide għal dmard ieħor, mingħajr wara l-proċedura tat-tneħħija jistgħu wkoll iżidu r-riskju ta ' reazzjonijiet avversi serji anke għal żmien twil wara l-qlib tal -.