Rifaximin 2care4 550 mg Filmdragerad tablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

rifaximin 2care4 550 mg filmdragerad tablett

2care4 aps - rifaximin - filmdragerad tablett - 550 mg - rifaximin 550 mg aktiv substans; propylenglykol hjälpämne

Rifaximin Orifarm 550 mg Filmdragerad tablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

rifaximin orifarm 550 mg filmdragerad tablett

orifarm ab - rifaximin - filmdragerad tablett - 550 mg - propylenglykol hjälpämne; rifaximin 550 mg aktiv substans

Xifaxan 550 mg Filmdragerad tablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

xifaxan 550 mg filmdragerad tablett

norgine bv - rifaximin - filmdragerad tablett - 550 mg - rifaximin 550 mg aktiv substans; propylenglykol hjälpämne - rifaximin

Tixteller 550 mg Filmdragerad tablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

tixteller 550 mg filmdragerad tablett

alfasigma s.p.a. - rifaximin - filmdragerad tablett - 550 mg - propylenglykol hjälpämne; rifaximin 550 mg aktiv substans - rifaximin

Xifaxan 550 mg Filmdragerad tablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

xifaxan 550 mg filmdragerad tablett

medartuum ab - rifaximin - filmdragerad tablett - 550 mg - rifaximin 550 mg aktiv substans; propylenglykol hjälpämne

Xifaxan 550 mg Filmdragerad tablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

xifaxan 550 mg filmdragerad tablett

ebb medical ab - rifaximin - filmdragerad tablett - 550 mg - propylenglykol hjälpämne; rifaximin 550 mg aktiv substans

Riximyo Europeiska unionen - svenska - EMA (European Medicines Agency)

riximyo

sandoz gmbh - rituximab - lymphoma, non-hodgkin; arthritis, rheumatoid; microscopic polyangiitis; wegener granulomatosis - antineoplastiska medel - riximyo is indicated in adults for the following indications:non-hodgkin’s lymphoma (nhl)riximyo is indicated for the treatment of previously untreated adult patients with stage iii-iv follicular lymphoma in combination with chemotherapy. riximyo maintenance therapy is indicated for the treatment of adult follicular lymphoma patients responding to induction therapy. riximyo monotherapy is indicated for treatment of adult patients with stage iii-iv follicular lymphoma who are chemoresistant or are in their second or subsequent relapse after chemotherapy. riximyo is indicated for the treatment of adult patients with cd20 positive diffuse large b cell non-hodgkin’s lymphoma in combination with chop (cyclophosphamide, doxorubicin, vincristine, prednisolone) chemotherapy. riximyo in combination with chemotherapy is indicated for the treatment of paediatric patients (aged ≥ 6 months to < 18 years old) with previously untreated advanced stage cd20 positive diffuse large b-cell lymphoma (dlbcl), burkitt lymphoma (bl)/burkitt leukaemia (mature b-cell acute leukaemia) (bal) or burkitt-like lymphoma (bll). chronic lymphocytic leukaemia (cll)riximyo in combination with chemotherapy is indicated for the treatment of patients with previously untreated and relapsed/refractory chronic lymphocytic leukaemia. endast begränsade data finns tillgängliga om effekten och säkerheten för patienter som tidigare behandlats med monoklonala antikroppar inklusive rituximab eller patienter med refraktära mot tidigare rituximab plus kemoterapi. se avsnitt 5. 1 för ytterligare information. rheumatoid arthritisriximyo in combination with methotrexate is indicated for the treatment of adult patients with severe active rheumatoid arthritis who have had an inadequate response or intolerance to other disease-modifying anti-rheumatic drugs (dmard) including one or more tumour necrosis factor (tnf) inhibitor therapies. rituximab har visat sig minska risken för progression av ledskador mätt med röntgen och förbättra den fysiska funktionen, när det ges i kombination med metotrexat. granulomatosis with polyangiitis and microscopic polyangiitisriximyo, in combination with glucocorticoids, is indicated for the treatment of adult patients with severe, active granulomatosis with polyangiitis (wegener’s) (gpa) and microscopic polyangiitis (mpa). riximyo, in combination with glucocorticoids, is indicated for the induction of remission in paediatric patients (aged ≥ 2 to < 18 years old) with severe, active gpa (wegener’s) and mpa. pemphigus vulgarisriximyo is indicated for the treatment of patients with moderate to severe pemphigus vulgaris (pv).

Rixathon Europeiska unionen - svenska - EMA (European Medicines Agency)

rixathon

sandoz gmbh - rituximab - lymphoma, non-hodgkin; arthritis, rheumatoid; leukemia, lymphocytic, chronic, b-cell; wegener granulomatosis; microscopic polyangiitis; pemphigus - antineoplastiska medel - rixathon is indicated in adults for the following indications:non-hodgkin’s lymphoma (nhl)rixathon is indicated for the treatment of previously untreated adult patients with stage iii-iv follicular lymphoma in combination with chemotherapy. rixathon maintenance therapy is indicated for the treatment of adult follicular lymphoma patients responding to induction therapy. rixathon monotherapy is indicated for treatment of adult patients with stage iii-iv follicular lymphoma who are chemoresistant or are in their second or subsequent relapse after chemotherapy. rixathon is indicated for the treatment of adult patients with cd20 positive diffuse large b cell non-hodgkin’s lymphoma in combination with chop (cyclophosphamide, doxorubicin, vincristine, prednisolone) chemotherapy. rixathon in combination with chemotherapy is indicated for the treatment of paediatric patients (aged ≥ 6 months to < 18 years old) with previously untreated advanced stage cd20 positive diffuse large b-cell lymphoma (dlbcl), burkitt lymphoma (bl)/burkitt leukaemia (mature b-cell acute leukaemia) (bal) or burkitt-like lymphoma (bll). kronisk lymfatisk leukemi (kll)rixathon i kombination med kemoterapi är indicerat för behandling av patienter med tidigare obehandlat och återfall/refraktär kronisk lymfatisk leukemi. endast begränsade data finns tillgängliga om effekten och säkerheten för patienter som tidigare behandlats med monoklonala antikroppar inklusive rituximab eller patienter med refraktära mot tidigare rituximab plus kemoterapi. se avsnitt 5. 1 för ytterligare information. reumatoid arthritisrixathon i kombination med metotrexat är indicerat för behandling av vuxna patienter med svår aktiv reumatoid artrit som har haft ett otillräckligt svar på eller intolerans mot andra sjukdomsmodifierande antireumatiska läkemedel (dmard), inklusive en eller flera tumor necrosis factor (tnf) - hämmare behandlingar. rituximab har visat sig minska risken för progression av ledskador mätt med röntgen och förbättra den fysiska funktionen, när det ges i kombination med metotrexat. granulomatosis with polyangiitis and microscopic polyangiitisrixathon, in combination with glucocorticoids, is indicated for the treatment of adult patients with severe, active granulomatosis with polyangiitis (wegener’s) (gpa) and microscopic polyangiitis (mpa). rixathon, in combination with glucocorticoids, is indicated for the induction of remission in paediatric patients (aged ≥ 2 to < 18 years old) with severe, active gpa (wegener’s) and mpa. pemphigus vulgarisrixathon is indicated for the treatment of patients with moderate to severe pemphigus vulgaris (pv).

Relafalk 200 mg Tablett med modifierad frisättning Sverige - svenska - Läkemedelsverket (Medical Products Agency)

relafalk 200 mg tablett med modifierad frisättning

adalvo limited - rifamycinnatrium - tablett med modifierad frisättning - 200 mg - rifamycinnatrium 200 mg aktiv substans; mannitol hjälpämne