Unjoni Ewropea - Malti - EMA (European Medicines Agency)

sanofi-aventis groupe - clopidogrel, acetylsalicylic acid - acute coronary syndrome; myocardial infarction - aġenti antitrombotiċi - koronarju akut syndromemyocardial mijokardijaku.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

pharmathen s.a. - levetiracetam - epilessija - anti-epilettiċi, - matever huwa indikat bħala monoterapija fit-trattament ta 'attakki ta' bidu parzjali b'ġeneralizzazzjoni sekondarja jew mingħajrha f'pazjenti minn 16-il sena b'epilessija li għadha kif ġiet iddijanjostikata. matever huwa indikat bħala terapija aġġuntiva:fil-kura ta 'aċċessjonijiet ta' bidu parzjali bi jew mingħajr ġeneralizzazzjoni sekondarja f'adulti, tfal u trabi mill-età ta'xahar bl-epilessija;fit-trattament ta ' aċċessjonijiet mijokloniċi f'adulti u addoloxxenti minn 12 il-sena tal-minorenni b'epilessija mijoklonika;fit-trattament ta seizures tonic-clonic ġeneralizzati fl-adulti u addoloxxenti minn 12 il-sena b'epilessija ġeneralizzata idjopatika.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

n.v. organon - nomegestrol acetate, estradiol - kontraċezzjoni - - ormoni tas-sess u modulaturi ta ' l-ġenitali-sistema, - kontraċezzjoni orali.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

rad neurim pharmaceuticals eec sarl - melatonin - sleep inizjattiva u maintenance disorders - psikolettiċi - circadin huwa indikat bħala monoterapija għat-trattament għal żmien qasir ta 'nuqqas ta' rqad primarju kkaratterizzat minn kwalità fqira ta 'rqad f'pazjenti li għandhom 55 sena jew aktar.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

takeda pharmaceuticals international ag ireland - prucalopride succinate - stitikezza - mediċini oħra għal stitikezza - resolor huwa indikat għal kura sintomatika ta 'stitikezza kronika f'adulti li fihom il-lassattivi jonqsu milli jipprovdu eżenzjoni adegwata.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

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).

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

otsuka pharmaceutical netherlands b.v. - tolvaptan - kliewi poliċistiku, autosomal dominanti - id-dijuretiċi, - jinarc huwa indikat biex tnaqqas il-progressjoni tal-iżvilupp tal-Ġlata u insuffiċjenza renali tal-marda tal-kliewi polycystic dominanti autosomal (adpkd) fl-adulti b ' ckd stadju 1 sa 3 fil-bidu tat-trattament bi prova tal-marda malajr jipprogressa b ' mod.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

glaxosmithkline trading services - mepolizumab - ażma - mediċini għall-imblokkar tal-passaġġ tan-nifs mard, - severe eosinophilic asthmanucala is indicated as an add-on treatment for severe refractory eosinophilic asthma in adults, adolescents and children aged 6 years and older. chronic rhinosinusitis with nasal polyps (crswnp)nucala is indicated as an add-on therapy with intranasal corticosteroids for the treatment of adult patients with severe crswnp for whom therapy with systemic corticosteroids and/or surgery do not provide adequate control. eosinophilic granulomatosis with polyangiitis (egpa)nucala is indicated as an add-on treatment for patients aged 6 years and older with relapsing-remitting or refractory eosinophilic granulomatosis with polyangiitis (egpa). hypereosinophilic syndrome (hes)nucala is indicated as an add-on treatment for adult patients with inadequately controlled hypereosinophilic syndrome without an identifiable non-haematologic secondary cause.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

otsuka pharmaceutical netherlands b.v. - brexpiprazole - skizofrenija - psikolettiċi - il-kura ta ' skizofrenja.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

glaxosmithkline trading services limited - sotrovimab - covid-19 virus infection - sera immuni u immunoglobulini, - xevudy is indicated for the treatment of adults and adolescents (aged 12 years and over and weighing at least 40 kg) with coronavirus disease 2019 (covid-19) who do not require oxygen supplementation and who are at increased risk of progressing to severe covid-19.