Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

novartis pharma schweiz ag - secukinumabum - soluzione iniettabile in siringa preriempita - secukinumabum 75 mg, trehalosum dihydricum, histidinum, histidini hydrochloridum monohydricum, methioninum, polysorbatum 80, aqua ad iniectabile q.s. ad solutionem pro 0.5 ml. - plaque psoriasis bei erwachsenen und kindern ab 6 jahren, ankylosierende spondylarthritis, psoriatische arthritis, nicht-röntgenologische axiale spondyloarthritis; hidradenitis suppurativa - biotechnologika

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

novartis pharma schweiz ag - secukinumabum - soluzione iniettabile in penna preriempita - secukinumabum 300.0 mg, trehalosum dihydricum, histidinum, histidini hydrochloridum monohydricum, methioninum, polysorbatum 80, aqua ad iniectabile q.s. ad solutionem pro 2 ml. - plaque psoriasis bei erwachsenen, psoriatische arthritis, hidradenitis suppurativa - biotechnologika

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

almirall ag - tildrakizumabum - soluzione iniettabile - tildrakizumabum 200 mg, histidinum, histidini hydrochloridum monohydricum, polysorbatum 80, saccharum, aqua ad iniectabile q.s. ad solutionem pro 2 ml. - placca psoriasi nell'adulto - biotechnologika

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

boehringer ingelheim (schweiz) gmbh - spesolimabum - concentrato per soluzione per infusione - spesolimabum 450 mg, natrii acetas trihydricus, acidum aceticum glaciale, saccharum 386 mg, arginini hydrochloridum, polysorbatum 20, aqua ad iniectabile ad solutionem pro 7.5 ml, natrium 6.8 mg. - generalisierte pustulöse psoriasis - biotechnologika

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

abbvie ag - risankizumabum - injektionslösung in einer patrone für ein dosiergerät - risankizumabum 360 mg, natrii acetas trihydricus corresp. natrium 0.5 mg, acidum aceticum glaciale, trehalosum dihydricum, polysorbatum 20, aqua ad iniectabile q.s. ad solutionem pro 2.4 ml. - morbus crohn bei erwachsenen - biotechnologika

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

abbvie ag - risankizumabum - concentrato per soluzione per infusione - risankizumabum 600 mg, natrii acetas trihydricus corresp. natrium 2.09 mg, acidum aceticum glaciale, trehalosum dihydricum, polysorbatum 20, aqua ad iniectabile q.s. ad solutionem pro 10 ml. - morbus crohn bei erwachsenen - biotechnologika

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

almirall ag - tildrakizumabum - 100 mg/1 ml, injektionslösung im fertigpen - tildrakizumabum 100 mg, histidinum, histidini hydrochloridum monohydricum, polysorbatum 80, saccharum, aqua ad iniectabile q.s. ad solutionem pro 1 ml. - placca psoriasi nell'adulto - biotechnologika

Unione Europea - italiano - EMA (European Medicines Agency)

fresenius kabi deutschland gmbh - tocilizumab - arthritis, rheumatoid; cytokine release syndrome; arthritis, juvenile rheumatoid; covid-19 virus infection; giant cell arteritis - immunosoppressori - tyenne, in combination with methotrexate (mtx), is indicated for- the treatment of severe, active and progressive rheumatoid arthritis (ra) in adults not previously treated with mtx. - the treatment of moderate to severe active ra in adult patients who have either responded inadequately to, or who were intolerant to, previous therapy with one or more disease-modifying anti-rheumatic drugs (dmards) or tumour necrosis factor (tnf) antagonists. in these patients, tyenne can be given as monotherapy in case of intolerance to mtx or where continued treatment with mtx is inappropriate. tocilizumab has been shown to reduce the rate of progression of joint damage as measured by x-ray and to improve physical function when given in combination with methotrexate. tyenne is indicated for the treatment of coronavirus disease 2019 (covid-19) in adults who are receiving systemic corticosteroids and require supplemental oxygen or mechanical ventilation. tyenne is indicated for the treatment of active systemic juvenile idiopathic arthritis (sjia) in patients 1 year of age and older, who have responded inadequately to previous therapy with nsaids and systemic corticosteroids. tyenne can be given as monotherapy (in case of intolerance to mtx or where treatment with mtx is inappropriate) or in combination with mtx. tyenne in combination with methotrexate (mtx) is indicated for the treatment of juvenile idiopathic polyarthritis (pjia; rheumatoid factor positive or negative and extended oligoarthritis) in patients 2 years of age and older, who have responded inadequately to previous therapy with mtx. tyenne can be given as monotherapy in case of intolerance to mtx or where continued treatment with mtx is inappropriate. tyenne is indicated for the treatment of chimeric antigen receptor (car) t cell-induced severe or life-threatening cytokine release syndrome (crs) in adults and paediatric patients 2 years of age and older. tyenne is indicated for the treatment of giant cell arteritis (gca) in adult patients.

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

eli lilly (suisse) sa - mirikizumabum - soluzione per infusione - mirikizumabum 300 mg, natrii citras dihydricus, acidum citricum, natrii chloridum, polysorbatum 80, aqua ad iniectabile q.s. ad solutionem pro 15 ml corresp. natrium 60.02 mg. - la colite ulcerosa - biotechnologika

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

eli lilly (suisse) sa - mirikizumabum - soluzione iniettabile en seringue préremplie - mirikizumabum 100 mg, natrii citras dihydricus, acidum citricum, natrii chloridum, polysorbatum 80, aqua ad iniectabile q.s. ad solutionem pro 1 ml corresp. natrium 4.001 mg. - la colite ulcerosa - biotechnologika