Avrupa Birliği - Maltaca - EMA (European Medicines Agency)

novo nordisk a/s - insulin aspart - diabetes mellitus - drogi użati fid-dijabete - trattament tad-dijabete mellitus.

Avrupa Birliği - Maltaca - EMA (European Medicines Agency)

ipsen pharma - somatropin - turner syndrome; dwarfism, pituitary - ormoni u analogi pitwitarji u ipotalamiċi - trattament fuq medda twila ta 'tfal bi ħsara fit-tkabbir minħabba sekrezzjoni inadegwata ta' l-ormon tat-tkabbir endoġenu. -kura fit-tul ta 'falliment tat-tkabbir assoċjat mas-sindromu ta' turner. it-trattament ta 'qabel il-puberta tfal b'falliment tat-tkabbir assoċjat ma' insuffiċjenza kronika tal-kliewi sa l-żmien tat-trapjant renali. is-sostituzzjoni tal-ormon tat-tkabbir endoġenu f'adulti b'defiċjenza tal-ormon tat-tkabbir ta ' jew fit-tfulija jew adulti bidu etjoloġija. ormon tat-tkabbir għandu jiġi kkonfermat kif suppost qabel it-trattament.

Avrupa Birliği - Maltaca - EMA (European Medicines Agency)

sanofi-aventis deutschland gmbh - insulina glargine - diabetes mellitus - drogi użati fid-dijabete - it-trattament tad-dijabete mellitus fl-adulti, l-adoloxxenti u t-tfal mill-età ta ' 6 snin.

Avrupa Birliği - Maltaca - EMA (European Medicines Agency)

teva b.v. - raloxifene hydrochloride - l-osteoporożi, il-menopawża - - ormoni tas-sess u modulaturi ta ' l-ġenitali-sistema, - raloxifene huwa indikat għat-trattament u l-prevenzjoni ta 'l-osteoporożi f'nisa wara l-menopawża. Ġie muri tnaqqis sinifikanti fl-inċidenza ta 'ksur vertebrali, iżda mhux tal-ġenbejn. meta jiddeterminaw l-għażla ta ' raloxifene jew terapiji oħra, inklużi l-estroġeni, għall-individwu mara wara l-menopawża, għandha tingħata konsiderazzjoni lill-sintomi tal-menopawsa, l-effetti fuq l-utru u tas-sider-tessuti, u kardjovaskulari ir-riskji u l-benefiċċji.

Avrupa Birliği - Maltaca - EMA (European Medicines Agency)

novo nordisk a/s - insulin human - diabetes mellitus - drogi użati fid-dijabete - trattament tad-dijabete mellitus.

Avrupa Birliği - Maltaca - EMA (European Medicines Agency)

viatris limited - insulina glargine - diabetes mellitus - drogi użati fid-dijabete - trattament tad-dijabete mellitus f'adulti, adolexxenti u tfal ta 'sentejn u aktar.

Avrupa Birliği - Maltaca - EMA (European Medicines Agency)

sanofi winthrop industrie - insulin aspart - diabetes mellitus - drogi użati fid-dijabete - truvelog mix 30 is indicated for treatment of diabetes mellitus in adults, adolescents and children aged 10 years and above.

Avrupa Birliği - Maltaca - EMA (European Medicines Agency)

eli lilly nederland b.v. - tirzepatide - diabetes mellitus, tip 2 - drogi użati fid-dijabete - mounjaro is indicated for the treatment of adults with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exercise- as monotherapy when metformin is considered inappropriate due to intolerance or contraindications- in addition to other medicinal products for the treatment of diabetes. for study results with respect to combinations, effects on glycaemic control and the populations studied, see sections 4. 4, 4. 5 u 5.

Avrupa Birliği - Maltaca - EMA (European Medicines Agency)

novo nordisk a/s - insulin aspart - diabetes mellitus - drugs used in diabetes, insulins and analogues for injection, fast-acting - trattament tad-dijabete mellitus f'adulti, adolexxenti u tfal ta 'sena u aktar.

Avrupa Birliği - Maltaca - EMA (European Medicines Agency)

nordic group b.v. - methotrexate - arthritis, psoriatic; psoriasis; arthritis, juvenile rheumatoid; arthritis, rheumatoid - aġenti antineoplastiċi - nordimet is indicated for the treatment of:active rheumatoid arthritis in adult patients,polyarthritic forms of severe, active juvenile idiopathic arthritis (jia), when the response to nonsteroidal anti-inflammatory drugs (nsaids) has been inadequate,moderate to severe plaque psoriasis in adults who are candidates for systemic therapy, and severe psoriatic arthritis in adult patients, induction of remission in moderate steroid-dependent crohn's disease in adult patients, in combination with corticosteroids and for maintenance of remission, as monotherapy, in patients who have responded to methotrexate.