Tremfya Eiropas Savienība - maltiešu - EMA (European Medicines Agency)

tremfya

janssen-cilag international nv - guselkumab - psorajiżi - immunosoppressanti - plaque psoriasis tremfya is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. psoriatic arthritis tremfya, alone or in combination with methotrexate (mtx), is indicated for the treatment of active psoriatic arthritis in adult patients who have had an inadequate response or who have been intolerant to a prior disease-modifying antirheumatic drug (dmard) therapy (see section 5.

Crysvita Eiropas Savienība - maltiešu - EMA (European Medicines Agency)

crysvita

kyowa kirin holdings b.v. - burosumab - hypophosphatemia, familial; hypophosphatemic rickets, x-linked dominant; osteomalacia - drogi għat-trattament ta 'mard tal-għadam - crysvita is indicated for the treatment of x-linked hypophosphataemia, in children and adolescents aged 1 to 17 years with radiographic evidence of bone disease, and in adults. crysvita is indicated for the treatment of fgf23-related hypophosphataemia in tumour-induced osteomalacia associated with phosphaturic mesenchymal tumours that cannot be curatively resected or localised in children and adolescents aged 1 to 17 years and in adults.

Hemlibra Eiropas Savienība - maltiešu - EMA (European Medicines Agency)

hemlibra

roche registration limited - emicizumab - hemofilja a - sustanzi kontra l-emorraġija - hemlibra is indicated for routine prophylaxis of bleeding episodes in patients with haemophilia a (congenital factor viii deficiency):with factor viii inhibitorswithout factor viii inhibitors who have:severe disease (fviii < 1%)moderate disease (fviii ≥ 1% and ≤ 5%) with severe bleeding phenotype. hemlibra jistgħu jintużaw fil-gruppi kollha tal-età.

Lamzede Eiropas Savienība - maltiešu - EMA (European Medicines Agency)

lamzede

chiesi farmaceutici s.p.a. - velmanase alfa - alfa-mannosidosis - oħra tal-passaġġ alimentari u tal-metaboliżmu-prodotti, - il-kura ta ' manifestazzjonijiet mhux newroloġiċi f'pazjenti b'indeboliment ħafif għal moderat alfa-mannosidosis.

Takhzyro Eiropas Savienība - maltiešu - EMA (European Medicines Agency)

takhzyro

takeda pharmaceuticals international ag ireland branch - lanadelumab - angioedemas, ereditarji - other hematological agents - takhzyro is indicated for routine prevention of recurrent attacks of hereditary angioedema (hae) in patients aged 2 years and older.

Zessly Eiropas Savienība - maltiešu - EMA (European Medicines Agency)

zessly

sandoz gmbh - infliximab - arthritis, psoriatic; psoriasis; crohn disease; arthritis, rheumatoid; colitis, ulcerative; spondylitis, ankylosing - immunosoppressanti - it-trattament ta 'l-artrite rewmatika, il-marda ta' crohn, kolite ulċerattiva, spondilite ankilożanti, artrite psorjatika u psorjasi.

Ilumetri Eiropas Savienība - maltiešu - EMA (European Medicines Agency)

ilumetri

almirall s.a - tildrakizumab - psorajiżi - immunosoppressanti, impedituri ta ' interlukin, - ilumetri huwa indikat għat-trattament ta ' adulti b'indeboliment moderat jew sever tal-psorjasi tal-plakka li huma kandidati għat-terapija sistemika.

Aimovig Eiropas Savienība - maltiešu - EMA (European Medicines Agency)

aimovig

novartis europharm limited - erenumab - disturbi fl-emigranja - analġeżiċi - aimovig huwa indikat għall-profilassi ta ' l-emigranja fl-adulti li jkollhom mill-anqas 4-emigranja jiem kull xahar meta tinbeda l-kura b'aimovig.

Shingrix Eiropas Savienība - maltiešu - EMA (European Medicines Agency)

shingrix

glaxosmithkline biologicals sa - recombinant varicella zoster virus glycoprotein e - herpes zoster - vaċċini - shingrix is indicated for prevention of herpes zoster (hz) and post-herpetic neuralgia (phn), in:adults 50 years of age or older;adults 18 years of age or older at increased risk of hz. l-użu ta shingrix għandha tkun skond ir-rakkomandazzjonijiet uffiċjali.

Veyvondi Eiropas Savienība - maltiešu - EMA (European Medicines Agency)

veyvondi

baxalta innovations gmbh - vonicog alfa - mard von willebrand - sustanzi kontra l-emorraġija - veyvondi huwa indikat fl-adulti (età ta '18-il sena u akbar) bl-mard ta' von willebrand (vwd), meta desmopressin (ddavp) il-kura waħdu huwa ineffettivi jew mhux indikat għal - kura ta 'emorraġija u kirurġija ta' fsada - prevenzjoni tal-kirurġika emorraġija. veyvondi m'għandux jintuża fil-kura ta'l-emofilja a.