Unione Europea - italiano - EMA (European Medicines Agency)

gilead sciences ireland uc - sofosbuvir - epatite c, cronica - antivirali per uso sistemico - sovaldi is indicated in combination with other medicinal products for the treatment of chronic hepatitis c (chc) in adult and paediatric patients aged 3 years and above (see sections 4. 2, 4. 4 e 5. per il virus dell'epatite c (hcv) di genotipo specifico di attività, vedere sezioni 4. 4 e 5. sovaldi is indicated in combination with other medicinal products for the treatment of chronic hepatitis c (chc) in adults and paediatric patients aged 3 years and above (see sections 4. 2, 4. 4 e 5. per il virus dell'epatite c (hcv) di genotipo specifico di attività, vedere sezioni 4. 4 e 5.

Unione Europea - italiano - EMA (European Medicines Agency)

samsung bioepis nl b.v. - adalimumab - spondylitis, ankylosing; arthritis, rheumatoid; uveitis; colitis, ulcerative; psoriasis; arthritis, psoriatic; crohn disease; hidradenitis suppurativa; arthritis - immunosoppressori - reumatoide arthritisimraldi in combinazione con metotressato è indicato per:il trattamento di moderata a grave artrite reumatoide attiva in pazienti adulti quando la risposta ai modificanti la malattia farmaci anti-reumatici, incluso il metotressato è stata inadeguata. il trattamento di grave, attiva e progressiva artrite reumatoide negli adulti non precedentemente trattati con metotressato. imraldi può essere somministrato come monoterapia in caso di intolleranza al metotressato o quando il trattamento continuato con metotressato è inappropriato. adalimumab ha dimostrato di ridurre il tasso di progressione del danno articolare misurato da x-ray e di migliorare la funzione fisica, quando somministrato in combinazione con metotressato. juvenile idiopathic arthritispolyarticular juvenile idiopathic arthritisimraldi in combination with methotrexate is indicated for the treatment of active polyarticular juvenile idiopathic arthritis, in patients from the age of 2 years who have had an inadequate response to one or more disease-modifying anti-rheumatic drugs (dmards). imraldi can be given as monotherapy in case of intolerance to methotrexate or when continued treatment with methotrexate is inappropriate (for the efficacy in monotherapy see section 5. adalimumab non è stato studiato in pazienti di età inferiore a 2 anni. enthesitis-related arthritisimraldi is indicated for the treatment of active enthesitis-related arthritis in patients, 6 years of age and older, who have had an inadequate response to, or who are intolerant of, conventional therapy (see section 5. axial spondyloarthritisankylosing spondylitis (as)imraldi is indicated for the treatment of adults with severe active ankylosing spondylitis who have had an inadequate response to conventional therapy. axial spondyloarthritis without radiographic evidence of asimraldi is indicated for the treatment of adults with severe axial spondyloarthritis without radiographic evidence of as but with objective signs of inflammation by elevated crp and / or mri, who have had an inadequate response to, or are intolerant to non-steroidal anti-inflammatory drugs (nsaids). psoriasica arthritisimraldi è indicato per il trattamento di attiva e progressiva artrite psoriasica negli adulti, quando la risposta alla precedente la malattia (disease modifying anti-rheumatic drug therapy è stata inadeguata. adalimumab has been shown to reduce the rate of progression of peripheral joint damage as measured by x-ray in patients with polyarticular symmetrical subtypes of the disease (see section 5. 1) e di migliorare la funzione fisica. psoriasisimraldi è indicato per il trattamento di moderata a grave psoriasi a placche cronica in pazienti adulti che non sono candidati per la terapia sistemica. pediatrica placca psoriasisimraldi è indicato per il trattamento di una grave psoriasi a placche cronica nei bambini e negli adolescenti a partire dai 4 anni di età che hanno avuto una risposta inadeguata o sono inadeguati, i candidati per la terapia attuale e phototherapies. hidradenitis suppurativa (hs)imraldi is indicated for the treatment of active moderate to severe hidradenitis suppurativa (acne inversa) in adults and adolescents from 12 years of age with an inadequate response to conventional systemic hs therapy (see sections 5. 1 e 5. il morbo di crohn diseaseimraldi è indicato per il trattamento di moderata a grave malattia di crohn attiva grave, in pazienti adulti che non abbiano risposto nonostante un completo e adeguato corso di terapia con corticosteroidi e/o immunosoppressori; o che sono intolleranti o hanno controindicazioni mediche per tali terapie. paediatric crohn's diseaseimraldi is indicated for the treatment of moderately to severely active crohn's disease in paediatric patients (from 6 years of age) who have had an inadequate response to conventional therapy including primary nutrition therapy and a corticosteroid and/or an immunomodulator, or who are intolerant to or haveulcerative colitisimraldi is indicated for treatment of moderately to severely active ulcerative colitis in adult patients who have had an inadequate response to conventional therapy including corticosteroids and mercaptopurine (6-mp) or azathioprine (aza), or who are intolerant to or have medical contraindications for such therapies. paediatric ulcerative colitisimraldi is indicated for the treatment of moderately to severely active ulcerative colitis in paediatric patients (from 6 years of age) who have had an inadequate response to conventional therapy including corticosteroids and/or 6-mercaptopurine (6-mp) or azathioprine (aza), or who are intolerant to or have medical contraindications for such therapies. uveitisimraldi is indicated for the treatment of non-infectious intermediate, posterior and panuveitis in adult patients who have had an inadequate response to corticosteroids, in patients in need of corticosteroidsparing, or in whomcorticosteroid treatment is inappropriate. paediatric uveitisimraldi is indicated for the treatment of paediatric chronic non-infectious anterior uveitis in patients from 2 years of age who have had an inadequate response to or are intolerant to conventional therapy, or in whom conventional therapy is inappropriate.

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

tillotts pharma ag - mesalazinum - suppositorien - mesalazinum 0.5 g, adeps solidus, pro suppositorio. - proktitis ulcerosa - synthetika

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

tillotts pharma ag - mesalazinum - suppositorien - mesalazinum 1 g, adeps solidus, pro suppositorio. - proktitis ulcerosa - synthetika

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

gilead sciences switzerland sàrl - sofosbuvirum - compresse rivestite con film - sofosbuvirum 400 mg, mannitolum, cellulosum microcristallinum, carmellosum natricum solo tenuti insieme corrisp. sodio 5.702 mg, silice colloidalis anhydrica, magnesio stearas, Überzug: poli(alcole vinylicus), e 171, macrogolum 3350, talco, e 172 (giallo), per compresso haze. - chronische epatite c - synthetika

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

tillotts pharma ag - mesalazinum - compressa gastroresistente - mesalazinum 400 mg, lactosum monohydricum 76.4 mg, carboxymethylamylum natricum a corresp. natrium 0.768 mg, magnesii stearas, talcum, povidonum k 25, Überzug: acidi methacrylici et methylis methacrylatis polymerisatum 1:2, talcum, triethylis citras, macrogolum 6000, e 172, pro compresso obducto. - la colite ulcerosa - synthetika

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

tillotts pharma ag - mesalazinum - magensaftesistente compressa - mesalazinum 800 mg, lactosum monohydricum 153 mg, carboxymethylamylum natricum a corresp. natrium 1.537 mg, magnesii stearas, talcum, povidonum k 25, Überzug: acidi methacrylici et methylis methacrylatis polymerisatum 1:2, talcum, triethylis citras, macrogolum 6000, e 172, pro compresso obducto. - la colite ulcerosa - synthetika

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

tillotts pharma ag - mesalazinum - compressa gastroresistente - mesalazinum 1600 mg, cellulosum microcristallinum, carboxymethylamylum natricum a corresp. natrium 2.268 mg, hypromellosum, silica colloidalis, magnesii stearas, Überzug: hypromellosum, macrogolum 6000, acidi methacrylici et methylis methacrylatis polymerisatum 1:2, triethylis citras, glyceroli monostearas 40-55, polysorbatum 80, kalii dihydrogenophosphas, maydis amylum, e 172, pro compresso obducto. - la colite ulcerosa - synthetika

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

samsung bioepis ch gmbh - adalimumabum - soluzione iniettabile in siringa preriempita - lösung: adalimumabum 40 mg, natrii citras dihydricus, acidum citricum monohydricum, histidinum, histidini hydrochloridum monohydricum, sorbitolum 20 mg, polysorbatum 20, aqua ad iniectabile q.s. ad solutionem pro 0.8 ml corresp. natrium 375 µg. - l'artrite reumatoide, poliarticolare artrite idiopatica giovanile, artrite psoriasica; spondilite anchilosante malattia di bechterew), malattia di crohn negli adulti; colite ulcerosa, psoriasi a placche in adulti, hidradenitis suppurativa - biotechnologika

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

samsung bioepis ch gmbh - adalimumabum - soluzione iniettabile in penna preriempita - lösung: adalimumabum 40 mg, natrii citras dihydricus, acidum citricum monohydricum, histidinum, histidini hydrochloridum monohydricum, sorbitolum 20 mg, polysorbatum 20, aqua ad iniectabile q.s. ad solutionem pro 0.8 ml corresp. natrium 375 µg. - l'artrite reumatoide, poliarticolare artrite idiopatica giovanile, artrite psoriasica; spondilite anchilosante malattia di bechterew), malattia di crohn negli adulti; colite ulcerosa, psoriasi a placche in adulti, hidradenitis suppurativa - biotechnologika