VELCADE bortezomib 3.0mg powder for injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

velcade bortezomib 3.0mg powder for injection vial

janssen-cilag pty ltd - bortezomib, quantity: 3 mg - injection, powder for - excipient ingredients: mannitol; nitrogen - - velcade, in combination with melphalan and prednisone is indicated for the treatment of patients with previously untreated multiple myeloma who are not candidates for high dose chemotherapy. - velcade, as part of combination therapy, is indicated for induction therapy prior to high dose chemotherapy with autologous stem cell rescue for patients under 65 years of age with previously untreated multiple myeloma. - velcade is also indicated for the treatment of multiple myeloma patients who have received at least one prior therapy, and who have progressive disease. - velcade in combination with rituximab, cyclophosphamide, doxorubicin and prednisone is indicated for the treatment of adult patients with previously untreated mantle cell lymphoma.

AZACITIDINE JUNO azacitidine 100 mg powder for injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

azacitidine juno azacitidine 100 mg powder for injection vial

dr reddys laboratories australia pty ltd - azacitidine, quantity: 100 mg - injection, powder for - excipient ingredients: mannitol - azacitidine juno is indicated for the treatment of patients with intermediate-2 and high-risk myelodysplastic syndromes (mds) according to the international prognostic scoring system (ipss), chronic myelomonocytic leukemia (cmmol (10-29 percent marrow blasts without myeloproliferative disorder)), acute myeloid leukemia (aml) with 20-30 percent blasts and multi-lineage dysplasia, according to world health organisation classification (who), in whom allogenic stem cell transplantation is not indicated.

AZADINE azacitidine 100 mg powder for injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

azadine azacitidine 100 mg powder for injection vial

dr reddys laboratories australia pty ltd - azacitidine, quantity: 100 mg - injection, powder for - excipient ingredients: mannitol - azadine is indicated for the treatment of patients with intermediate-2 and high-risk myelodysplastic syndromes (mds) according to the international prognostic scoring system (ipss), chronic myelomonocytic leukemia (cmmol (10-29 percent marrow blasts without myeloproliferative disorder)), acute myeloid leukemia (aml) with 20-30 percent blasts and multi-lineage dysplasia, according to world health organisation classification (who), in whom allogenic stem cell transplantation is not indicated.

BUSULFEX busulfan 60mg/10mL injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

busulfex busulfan 60mg/10ml injection vial

otsuka australia pharmaceutical pty ltd - busulfan, quantity: 60 mg - injection - excipient ingredients: dimethylacetamide; macrogol 400 - busulfex is indicated for use in combination with cyclophosphamide, melphalan or fludarabine in conditioning prior to haematopoietic stem cell transplantation.

VELCADE bortezomib 1mg powder for injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

velcade bortezomib 1mg powder for injection vial

janssen-cilag pty ltd - bortezomib, quantity: 1 mg - injection, powder for - excipient ingredients: mannitol; nitrogen - - velcade, in combination with melphalan and prednisone is indicated for the treatment of patients with previously untreated multiple myeloma who are not candidates for high dose chemotherapy. - velcade, as part of combination therapy, is indicated for induction therapy prior to high dose chemotherapy with autologous stem cell rescue for patients under 65 years of age with previously untreated multiple myeloma. - velcade is also indicated for the treatment of multiple myeloma patients who have received at least one prior therapy, and who have progressive disease. - velcade in combination with rituximab, cyclophosphamide, doxorubicin and prednisone is indicated for the treatment of adult patients with previously untreated mantle cell lymphoma.

ERAXIS anidulafungin 100 mg powder for injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

eraxis anidulafungin 100 mg powder for injection vial

pfizer australia pty ltd - anidulafungin, quantity: 100 mg - injection, powder for - excipient ingredients: tartaric acid; mannitol; fructose; polysorbate 80 - treatment of invasive candidiasis, including candidaemia in adult and in paediatric patients one month and older (see section 5.1)

VELCADE bortezomib 3.5 mg powder for injection Australia - English - Department of Health (Therapeutic Goods Administration)

velcade bortezomib 3.5 mg powder for injection

janssen-cilag pty ltd - bortezomib, quantity: 3.5 mg - injection, powder for - excipient ingredients: mannitol; nitrogen - - velcade, in combination with melphalan and prednisone is indicated for the treatment of patients with previously untreated multiple myeloma who are not candidates for high dose chemotherapy. - velcade, as part of combination therapy, is indicated for induction therapy prior to high dose chemotherapy with autologous stem cell rescue for patients under 65 years of age with previously untreated multiple myeloma. - velcade is also indicated for the treatment of multiple myeloma patients who have received at least one prior therapy, and who have progressive disease. - velcade in combination with rituximab, cyclophosphamide, doxorubicin and prednisone is indicated for the treatment of adult patients with previously untreated mantle cell lymphoma.

EPILIM IV sodium valproate 400 mg powder for injection with diluent Australia - English - Department of Health (Therapeutic Goods Administration)

epilim iv sodium valproate 400 mg powder for injection with diluent

sanofi-aventis australia pty ltd - sodium valproate, quantity: 400 mg - injection, powder for - excipient ingredients: - epilim iv is used for the treatment of patients with epilepsy or mania, who would normally be maintained on oral sodium valproate, and for whom oral therapy is temporarily not possible.