Швейцария - немски - Swissmedic (Swiss Agency for Therapeutic Products)

janssen-cilag ag - guselkumabum - injektionslösung im fertigpen - guselkumabum 100 mg, saccharum, histidinum, histidini hydrochloridum monohydricum, polysorbatum 80, aqua ad iniectabile q.s. ad solutionem pro 1 ml. - plaque psoriasis, psoriasis-arthritis - biotechnologika

Швейцария - немски - Swissmedic (Swiss Agency for Therapeutic Products)

pfizer ag - tofacitinibum - filmtabletten - tofacitinibum 5 mg zu tofacitinibi citras, excipiens pro compresso dunst. - selektives immunsuppressivum - synthetika

Швейцария - немски - Swissmedic (Swiss Agency for Therapeutic Products)

pfizer ag - tofacitinibum - filmtabletten - tofacitinibum 10 mg zu tofacitinibi citras, color.: e 132, e 133, excipiens pro compresso dunst. - selektives immunsuppressivum - synthetika

Германия - немски - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

clinigen healthcare b.v. (8181225) - aldesleukin - pulver zur herstellung einer injektions- bzw. infusionslösung - aldesleukin (23971) 1 milligramm

Швейцария - немски - Swissmedic (Swiss Agency for Therapeutic Products)

pierre fabre pharma sa - encorafenibum - hartkapseln - encorafenibum 50 mg, excipiens pro kapsel. - melanom mit braf-v600-mutation in kombination mit binimetinib,; metastasiertes kolorektalkarzinom (crc) mit einer braf-v600e-mutation in kombination mit cetuximab - synthetika

Швейцария - немски - Swissmedic (Swiss Agency for Therapeutic Products)

pierre fabre pharma sa - encorafenibum - hartkapseln - encorafenibum 75 mg, excipiens pro kapsel. - melanom mit braf-v600-mutation in kombination mit binimetinib,; metastasiertes kolorektalkarzinom (crc) mit einer braf-v600e-mutation in kombination mit cetuximab - synthetika

Швейцария - немски - Swissmedic (Swiss Agency for Therapeutic Products)

pierre fabre pharma sa - binimetinibum - filmtabletten - binimetinibum 15 mg, excipiens pro compresso obducto. - melanom mit braf-v600-mutation in kombination mit encorafenib - synthetika

Швейцария - немски - Swissmedic (Swiss Agency for Therapeutic Products)

ucb-pharma sa - bimekizumabum - solution injectable en seringue préremplie - bimekizumabum 160 mg, glycinum, natrii acetas trihydricus, acidum aceticum glaciale, polysorbatum 80, aqua ad iniectabile, ad solutionem pro 1.0 ml corresp., natrium 0.45 mg. - psoriasis en plaques chez l'adulte - biotechnologika

Швейцария - немски - Swissmedic (Swiss Agency for Therapeutic Products)

ucb-pharma sa - bimekizumabum - injektionslösung in einem fertigpen - bimekizumabum 160 mg, glycinum, natrii acetas trihydricus, acidum aceticum glaciale, polysorbatum 80, aqua ad iniectabile, ad solutionem pro 1.0 ml corresp., natrium 0.45 mg. - psoriasis en plaques chez l'adulte - biotechnologika

Европейски съюз - немски - EMA (European Medicines Agency)

pfizer europe ma eeig - tofacitinib - arthritis, rheumatoide - immunsuppressiva - rheumatoid arthritistofacitinib in combination with methotrexate (mtx) is indicated for the treatment of moderate to severe active rheumatoid arthritis (ra) in adult patients who have responded inadequately to, or who are intolerant to one or more disease-modifying antirheumatic drugs (dmards) (see section 5. tofacitinib can be given as monotherapy in case of intolerance to mtx or when treatment with mtx is inappropriate (see sections 4. 4 und 4. psoriatic arthritistofacitinib in combination with mtx is indicated for the treatment of active psoriatic arthritis (psa) 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. ulcerative colitistofacitinib is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis (uc) who have had an inadequate response, lost response, or were intolerant to either conventional therapy or a biologic agent (see section 5. tofacitinib is indicated for the treatment of active polyarticular juvenile idiopathic arthritis (rheumatoid factor positive [rf+] or negative [rf-] polyarthritis and extended oligoarthritis), and juvenile psoriatic arthritis (psa) in patients 2 years of age and older, who have responded inadequately to previous therapy with disease modifying antirheumatic drugs (dmards). tofacitinib can be given in combination with methotrexate (mtx) or as monotherapy in case of intolerance to mtx or where continued treatment with mtx is inappropriate. ankylosing spondylitistofacitinib is indicated for the treatment of adult patients with active ankylosing spondylitis (as) who have responded inadequately to conventional therapy.