Sverige - svenska - Läkemedelsverket (Medical Products Agency)

ebb medical ab - mykofenolatmofetil - filmdragerad tablett - 500 mg - mykofenolatmofetil 500 mg aktiv substans - mykofenolsyra

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

ebb medical ab - isoniazid; rifampicin - filmdragerad tablett - 150 mg/75 mg - natriumlaurilsulfat hjälpämne; rifampicin 150 mg aktiv substans; isoniazid 75 mg aktiv substans - rifampicin och isoniazid

Europeiska unionen - svenska - EMA (European Medicines Agency)

amgen europe b.v. - adalimumab - arthritis, psoriatic; colitis, ulcerative; arthritis, juvenile rheumatoid; spondylitis, ankylosing; psoriasis; crohn disease; arthritis, rheumatoid - immunsuppressiva - rheumatoid arthritis  amgevita in combination with methotrexate, is indicated for: , the treatment of moderate to severe, active rheumatoid arthritis in adult patients when the response to disease-modifying anti-rheumatic drugs including methotrexate has been inadequate. behandling av svår, aktiv och progredierande reumatoid artrit hos vuxna som inte tidigare behandlats med metotrexat. ,  amgevita can be given as monotherapy in case of intolerance to methotrexate or when continued treatment with methotrexate is inappropriate. amgevita minskar graden av progression av ledskador mätt med röntgen och förbättrar fysisk funktion, när det ges i kombination med metotrexat. juvenile idiopathic arthritis polyarticular juvenile idiopathic arthritis amgevita 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). amgevita kan ges som monoterapi vid intolerans mot metotrexat eller när fortsatt behandling med metotrexat är olämplig (för effekt i monoterapi se avsnitt 5. adalimumab har inte studerats hos patienter yngre än 2 år. enthesitis-related arthritis amgevita 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 spondyloarthritis ankylosing spondylitis (as) amgevita 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 as amgevita 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. psoriatic arthritis amgevita is indicated for the treatment of active and progressive psoriatic arthritis in adults when the response to previous disease-modifying anti-rheumatic drug therapy has been inadequate. amgevita minskar graden av progression av perifer ledskada mätt med röntgen hos patienter med polyartikulär symmetrisk subtyper av sjukdomen (se avsnitt 5. 1) och förbättrar fysisk funktion. psoriasis amgevita is indicated for the treatment of moderate to severe chronic plaque psoriasis in adult patients who are candidates for systemic therapy. paediatric plaque psoriasis amgevita is indicated for the treatment of severe chronic plaque psoriasis in children and adolescents from 4 years of age who have had an inadequate response to or are inappropriate candidates for topical therapy and phototherapies. hidradenitis suppurativa (hs) amgevita 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 och 5. crohn’s disease amgevita is indicated for treatment of moderately to severely active crohn’s disease, in adult patients who have not responded despite a full and adequate course of therapy with a corticosteroid and/or an immunosuppressant; or who are intolerant to or have medical contraindications for such therapies. paediatric crohn's disease amgevita 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 have contraindications for such therapies. ulcerative colitis amgevita 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 6-mercaptopurine (6-mp) or azathioprine (aza), or who are intolerant to or have medical contraindications for such therapies. uveitis amgevita 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 corticosteroid-sparing, or in whom corticosteroid treatment is inappropriate. paediatric uveitis amgevita 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.

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

orion corporation - metotrexatdinatrium - tablett - 10 mg - laktosmonohydrat hjälpämne; metotrexatdinatrium 10,97 mg aktiv substans

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

orion corporation - metotrexatdinatrium - tablett - 2,5 mg - metotrexatdinatrium 2,742 mg aktiv substans; laktosmonohydrat hjälpämne

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

2care4 aps - mykofenolatmofetil - filmdragerad tablett - 500 mg - mykofenolatmofetil 500 mg aktiv substans

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

ebb medical ab - mykofenolatmofetil - filmdragerad tablett - 500 mg - mykofenolatmofetil 500 mg aktiv substans

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

orifarm ab - mykofenolatmofetil - kapsel, hård - 250 mg - natriumlaurilsulfat hjälpämne; propylenglykol hjälpämne; mykofenolatmofetil 250 mg aktiv substans

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

alfrapharma s.r.l. - metotrexat - injektionsvätska, lösning i förfylld injektionspenna - 15 mg - metotrexat 15 mg aktiv substans

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

alfrapharma s.r.l. - metotrexat - injektionsvätska, lösning i förfylld injektionspenna - 10 mg - metotrexat 10 mg aktiv substans