União Europeia - alemão - EMA (European Medicines Agency)

sandoz gmbh - rituximab - lymphoma, non-hodgkin; arthritis, rheumatoid; leukemia, lymphocytic, chronic, b-cell; wegener granulomatosis; microscopic polyangiitis; pemphigus - antineoplastische mittel - 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). chronische lymphatische leukämie (cll)rixathon in kombination mit einer chemotherapie ist indiziert für die behandlung von patienten mit zuvor unbehandeltem und rezidivierter/refraktärer chronischer lymphatischer leukämie. nur begrenzte daten verfügbar sind, auf wirksamkeit und sicherheit für die patienten behandelt, die zuvor mit monoklonalen antikörpern einschließlich rituximab oder patienten, die refraktär auf vorherige rituximab plus chemotherapie. siehe abschnitt 5. 1 für weitere informationen. rheumatoide arthritisrixathon in kombination mit methotrexat ist indiziert für die behandlung erwachsener patienten mit schwerer aktiver rheumatoider arthritis, die hatten eine unzureichende reaktion oder unverträglichkeit der anderen krankheitsmodifizierenden antirheumatika (dmard) einschliesslich einer oder mehrerer therapien mit tumornekrosefaktor (tnf) - hemmern. rituximab hat sich gezeigt, zur verringerung der rate des fortschreitens von gelenkschäden, wie gemessen, durch die x-ray und für die verbesserung der physischen funktion, wenn sie in kombination mit methotrexat. 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).

União Europeia - alemão - EMA (European Medicines Agency)

sandoz gmbh - rituximab - lymphoma, non-hodgkin; arthritis, rheumatoid; microscopic polyangiitis; wegener granulomatosis - antineoplastische mittel - 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. nur begrenzte daten verfügbar sind, auf wirksamkeit und sicherheit für die patienten behandelt, die zuvor mit monoklonalen antikörpern einschließlich rituximab oder patienten, die refraktär auf vorherige rituximab plus chemotherapie. siehe abschnitt 5. 1 für weitere informationen. 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 hat sich gezeigt, zur verringerung der rate des fortschreitens von gelenkschäden, wie gemessen, durch die x-ray und für die verbesserung der physischen funktion, wenn sie in kombination mit methotrexat. 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).

Suíça - alemão - Swissmedic (Swiss Agency for Therapeutic Products)

roche pharma (schweiz) ag - rituximabum - konzentrat zur herstellung einer infusionslösung - rituximabum 100 mg, natrii citras dihydricus, polysorbatum 80, natrii chloridum, acidum hydrochloridum aut natrii hydroxidum, aqua ad iniectabile q.s. ad solutionem pro 10 ml corresp. natrium 52.6 mg. - non-hodgkin-lymphom, rheumatoide arthritis, anca-assoziierte vaskulitis - biotechnologika

Suíça - alemão - Swissmedic (Swiss Agency for Therapeutic Products)

roche pharma (schweiz) ag - rituximabum - konzentrat zur herstellung einer infusionslösung - rituximabum 500 mg, natrii citras dihydricus, polysorbatum 80, natrii chloridum, acidum hydrochloridum aut natrii hydroxidum, aqua ad iniectabile q.s. ad solutionem pro 50 ml corresp. natrium 263.2 mg. - non-hodgkin-lymphom, rheumatoide arthritis, anca-assoziierte vaskulitis - biotechnologika

Suíça - alemão - Swissmedic (Swiss Agency for Therapeutic Products)

future health pharma gmbh - aliskirenum, hydrochlorothiazidum - filmtabletten - aliskirenum 150 mg bis aliskireni hemifumaras, hydrochlorothiazidum 12.5 mg, excipiens pro compresso dunst. - hypertonie - synthetika

Suíça - alemão - Swissmedic (Swiss Agency for Therapeutic Products)

future health pharma gmbh - aliskirenum, hydrochlorothiazidum - filmtabletten - aliskirenum 150 mg bis aliskireni hemifumaras, hydrochlorothiazidum 25 mg, excipiens pro compresso dunst. - hypertonie - synthetika

Suíça - alemão - Swissmedic (Swiss Agency for Therapeutic Products)

future health pharma gmbh - aliskirenum, hydrochlorothiazidum - filmtabletten - aliskirenum 300 mg bis aliskireni hemifumaras, hydrochlorothiazidum 12.5 mg, excipiens pro compresso dunst. - hypertonie - synthetika

Suíça - alemão - Swissmedic (Swiss Agency for Therapeutic Products)

future health pharma gmbh - aliskirenum, hydrochlorothiazidum - filmtabletten - aliskirenum 300 mg bis aliskireni hemifumaras, hydrochlorothiazidum 25 mg, excipiens pro compresso dunst. - hypertonie - synthetika

Suíça - alemão - Swissmedic (Swiss Agency for Therapeutic Products)

roche pharma (schweiz) ag - rituximabum - lösung zur subkutanen injektion - rituximabum 1400 mg, hyaluronidasum humanum adnr, histidinum, histidini hydrochloridum monohydricum, trehalosum dihydricum, methioninum, polysorbatum 80, aqua ad iniectabile q.s. ad solutionem pro 11.7 ml. - non-hodgkin-lymphome - biotechnologika

Suíça - alemão - Swissmedic (Swiss Agency for Therapeutic Products)

takeda pharma ag - immunoglobulinum humanum normale - injektionslösung - solvens (i.m.): immunoglobulinum humanum normale 200 mg, glycinum, aqua ad iniectabile q.s. ad solutionem pro 1 ml. - substitutionstherapie bei primären immunmangelkrankheiten, substitutionstherapie bei multiplem myelom, chronisch-lymphatischer leukämie oder nach allogener hämatopoetischer stammzellentransplantation mit sekundärer hypogammaglobulinämie - blutprodukte