Unione Europea - italiano - EMA (European Medicines Agency)

almirall s.a - dimetilfumarato - psoriasi - immunosoppressori - skilarence è indicato per il trattamento della psoriasi a placche da moderata a grave negli adulti che necessitano di terapia medicinale sistemica.

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

almirall ag - dimethylis fumaras - compressa gastroresistente - dimethylis fumaras 30 mg, lactosum monohydricum 36 mg, cellulosum microcristallinum, carmellosum natricum conexum, silica colloidalis anhydrica, magnesii stearas, Überzug: acidi methacrylici et ethylis acrylatis polymerisatum 1:1, natrii laurilsulfas, polysorbatum 80, talcum, triethylis citras, simeticonum, e 171, pro compresso obducto corresp. natrium 0.45 mg. - trattamento di hautmanifestationen in pazienti con moderata a grave psoriasi a placche - synthetika

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

almirall ag - dimethylis fumaras - compressa gastroresistente - dimethylis fumaras 120 mg, lactosum monohydricum 144 mg, cellulosum microcristallinum, carmellosum natricum conexum, silica colloidalis anhydrica, magnesii stearas, Überzug: acidi methacrylici et ethylis acrylatis polymerisatum 1:1, natrii laurilsulfas, polysorbatum 80, talcum, triethylis citras, simeticonum, e 132, e 171, natrii hydroxidum, pro compresso obducto corresp. natrium 1.94 mg. - trattamento di hautmanifestationen in pazienti con moderata a grave psoriasi a placche - synthetika

Unione Europea - italiano - EMA (European Medicines Agency)

biogen netherlands b.v. - dimetilfumarato - sclerosi multipla - immunosoppressori - tecfidera is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).

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

biogen switzerland ag - dimethylis fumaras - capsule rigide gastroresistenti - dimethylis fumaras 120 mg, carmellosum natricum conexum, cellulosum microcristallinum, magnesii stearas, talcum, silica colloidalis anhydrica, acidi methacrylici et methylis methacrylatis polymerisatum 1:1, Überzug: acidi methacrylici et ethylis acrylatis polymerisati 1:1 dispersio 30 per centum, polysorbatum 80, natrii laurilsulfas, triethylis citras, talcum, simeticonum, kapselhülle: gelatina, e 171, e 172 (flavum), e 133, drucktinte: lacca, kalii hydroxidum, e 172 (nigrum), pro capsula corresp. natrium 1.37 mg. - multiple sklerose - synthetika

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

biogen switzerland ag - dimethylis fumaras - capsule rigide gastroresistenti - dimethylis fumaras 240 mg, carmellosum natricum conexum, cellulosum microcristallinum, silica colloidalis anhydrica, magnesii stearas, acidi methacrylici et methylis methacrylatis polymerisatum 1:1, Überzug: acidi methacrylici et ethylis acrylatis polymerisati 1:1 dispersio 30 per centum, natrii laurilsulfas, triethylis citras, polysorbatum 80, talcum, simeticonum, kapselhülle: gelatina, e 171, e 172 (flavum), e 133, drucktinte: lacca, kalii hydroxidum, e 172 (nigrum), pro capsula corresp. natrium 1.69 mg. - multiple sklerose - synthetika

Unione Europea - italiano - EMA (European Medicines Agency)

mylan ireland limited - lenalidomide - mieloma multiplo - immunosoppressori - multiple myelomalenalidomide mylan as monotherapy is indicated for the maintenance treatment of adult patients with newly diagnosed multiple myeloma who have undergone autologous stem cell transplantation. lenalidomide mylan as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone is indicated for the treatment of adult patients with previously untreated multiple myeloma who are not eligible for transplant. lenalidomide mylan in combination with dexamethasone is indicated for the treatment of multiple myeloma in adult patients who have received at least one prior therapy. follicular lymphomalenalidomide mylan in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1-3a).

Unione Europea - italiano - EMA (European Medicines Agency)

biogen netherlands b.v. - diroximel fumarate (biib098) - sclerosi multipla recidivante-remittente - immunosoppressori - vumerity is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis (see section 5. 1 for important information on the populations for which efficacy has been established).

Unione Europea - italiano - EMA (European Medicines Agency)

mylan ireland limited - dimetilfumarato - sclerosi multipla recidivante-remittente - immunosoppressori - dimethyl fumarate mylan is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Unione Europea - italiano - EMA (European Medicines Agency)

zaklady farmafarmaceutyczne polpharma s.aceutyczne polpharma s.a. - dimetilfumarato - sclerosi multipla recidivante-remittente - immunosoppressori - dimethyl fumarate polpharma is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.