MORPHINUM- morphine pellet United States - English - NLM (National Library of Medicine)

morphinum- morphine pellet

remedy makers - abt-925 anhydrous free base (unii: e6cki5c54o) (abt-925 anhydrous free base - unii:e6cki5c54o) -

MORPHINUM- morphine pellet United States - English - NLM (National Library of Medicine)

morphinum- morphine pellet

remedy makers - abt-925 anhydrous free base (unii: e6cki5c54o) (abt-925 anhydrous free base - unii:e6cki5c54o) -

MORPHINUM- morphine pellet United States - English - NLM (National Library of Medicine)

morphinum- morphine pellet

remedy makers - abt-925 anhydrous free base (unii: e6cki5c54o) (abt-925 anhydrous free base - unii:e6cki5c54o) -

MORPHINUM- morphine pellet United States - English - NLM (National Library of Medicine)

morphinum- morphine pellet

remedy makers - abt-925 anhydrous free base (unii: e6cki5c54o) (abt-925 anhydrous free base - unii:e6cki5c54o) - pain, nausea, diarrhean neuritis, or other indications

MORPHINUM- morphine pellet United States - English - NLM (National Library of Medicine)

morphinum- morphine pellet

remedy makers - abt-925 anhydrous free base (unii: e6cki5c54o) (abt-925 anhydrous free base - unii:e6cki5c54o) -

MABTHERA SC rituximab (rch) 1600 mg/13.4 mL solution for injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

mabthera sc rituximab (rch) 1600 mg/13.4 ml solution for injection vial

roche products pty ltd - rituximab, quantity: 1600 mg - injection - excipient ingredients: vorhyaluronidase alfa; histidine; histidine hydrochloride; trehalose dihydrate; methionine; polysorbate 80; water for injections - mabthera sc 1600 mg is indicated for the treatment of patients with cd20 positive chronic lymphocytic leukaemia (cll) in combination with chemotherapy.

MABTHERA SC rituximab (rch) 1400 mg/11.7 mL solution for injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

mabthera sc rituximab (rch) 1400 mg/11.7 ml solution for injection vial

roche products pty ltd - rituximab, quantity: 1400 mg - injection - excipient ingredients: vorhyaluronidase alfa; histidine; histidine hydrochloride; trehalose dihydrate; methionine; polysorbate 80; water for injections - mabthera sc is indicated for treatment of patients with: - cd20 positive, previously untreated, stage iii/iv follicular, b-cell non-hodgkin's lymphoma, - cd20 positive, relapsed or refractory low grade or follicular, b-cell non-hodgkin's lymphoma, - cd 20 positive, diffuse large b-cell non-hodgkin's lymphoma, in combination with chemotherapy.

MABTHERA rituximab 500mg/50mL injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

mabthera rituximab 500mg/50ml injection vial

roche products pty ltd - rituximab, quantity: 10 mg/ml - injection, concentrated - excipient ingredients: polysorbate 80; sodium chloride; water for injections; sodium hydroxide; hydrochloric acid; citric acid; sodium citrate dihydrate - non-hodgkin's lymphoma: mabthera is indicated for treatment of patients with: cd20 positive, previously untreated, stage iii/iv follicular, b-cell non-hodgkin's lymphoma. cd20 positive, relapsed or refractory low grade or follicular, b-cell non-hodgkin's lymphoma, cd20 positive, diffuse large b-cell non-hodgkin's lymphoma, in combination with chemotherapy. chronic lymphocytic leukaemia: mabthera is indicated for the treatment of patients with cd20 positive chronic lymphocytic leukaemia (cll) in combination with chemotherapy. rheumatoid arthritis: mabthera (rituximab) 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 at least one tumour necrosis factor (tnf) inhibitor therapy. mabthera has been shown to reduce the rate of progression of joint damage as measured by x-ray when given in combination with methotrexate. granulomatosis with polyangiitis (wegener's ) (gpa) and microscopic poly

MABTHERA rituximab 100mg/10mL injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

mabthera rituximab 100mg/10ml injection vial

roche products pty ltd - rituximab, quantity: 10 mg/ml - injection, concentrated - excipient ingredients: sodium chloride; water for injections; citric acid; polysorbate 80; hydrochloric acid; sodium citrate dihydrate; sodium hydroxide - non-hodgkin's lymphoma: mabthera is indicated for treatment of patients with: cd20 positive, previously untreated, stage iii/iv follicular, b-cell non-hodgkin's lymphoma. cd20 positive, relapsed or refractory low grade or follicular, b-cell non-hodgkin's lymphoma, cd20 positive, diffuse large b-cell non-hodgkin's lymphoma, in combination with chemotherapy. chronic lymphocytic leukaemia: mabthera is indicated for the treatment of patients with cd20 positive chronic lymphocytic leukaemia (cll) in combination with chemotherapy. rheumatoid arthritis: mabthera (rituximab) 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 at least one tumour necrosis factor (tnf) inhibitor therapy. mabthera has been shown to reduce the rate of progression of joint damage as measured by x-ray when given in combination with methotrexate. granulomatosis with polyangiitis (wegener's ) (gpa) and microscopic poly

SIMABTRA trastuzumab (rch) 150 mg powder for injection for intravenous infusion vial Australia - English - Department of Health (Therapeutic Goods Administration)

simabtra trastuzumab (rch) 150 mg powder for injection for intravenous infusion vial

celltrion healthcare australia pty ltd - trastuzumab, quantity: 150 mg - injection, powder for - excipient ingredients: histidine hydrochloride; polysorbate 20; histidine; trehalose dihydrate - early breast cancer,indicated for the treatment of her2-positive early breast cancer following surgery, and in association with chemotherapy and, if applicable, radiotherapy.,locally advanced breast cancer,indicated for the treatment of her2-positive locally advanced breast cancer in combination with neoadjuvant chemotherapy followed by adjuvant therapy.,metastatic breast cancer,indicated for the treatment of patients with metastatic breast cancer who have tumours that overexpress her2:,a) as monotherapy for the treatment of those patients who have received one or more chemotherapy regimens for their metastatic disease;,b) in combination with taxanes for the treatment of those patients who have not received chemotherapy for their metastatic disease; or,c) in combination with an aromatase inhibitor for the treatment of post-menopausal patients with hormone-receptor positive metastatic breast cancer.,advanced gastric cancer,indicated in combination with cisplatin and either capecitabine or 5-fu for the treatmen