New Zealand - English - Medsafe (Medicines Safety Authority)

asta medica australasia pty (nz) limited - cyclophosphamide monohydrate 1000mg - powder for injection - 1000 mg - active: cyclophosphamide monohydrate 1000mg

New Zealand - English - Medsafe (Medicines Safety Authority)

asta medica australasia pty (nz) limited - cyclophosphamide monohydrate 100mg - powder for injection - 100 mg - active: cyclophosphamide monohydrate 100mg

New Zealand - English - Medsafe (Medicines Safety Authority)

asta medica australasia pty (nz) limited - cyclophosphamide monohydrate 200mg - powder for injection - 200 mg - active: cyclophosphamide monohydrate 200mg

New Zealand - English - Medsafe (Medicines Safety Authority)

asta medica australasia pty (nz) limited - cyclophosphamide monohydrate 500mg - powder for injection - 500 mg - active: cyclophosphamide monohydrate 500mg

Malta - English - Medicines Authority

1 a pharma gmbh keltenring 1+3, 82041 oberhaching, germany - cyclophosphamide - powder for solution for injection/infusion - cyclophosphamide 500 mg - antineoplastic agents

Malta - English - Medicines Authority

1 a pharma gmbh keltenring 1+3, 82041 oberhaching, germany - cyclophosphamide - powder for solution for injection/infusion - cyclophosphamide 1000 mg - antineoplastic agents

New Zealand - English - Medsafe (Medicines Safety Authority)

baxter healthcare ltd - cyclophosphamide monohydrate 534.5mg equivalent to cyclophosphamide anhydrous 500 mg;   - powder for injection - 500 mg - active: cyclophosphamide monohydrate 534.5mg equivalent to cyclophosphamide anhydrous 500 mg   - the proper use of cyclophosphamide requires accurate diagnosis, careful assessment of the anatomic extent of the disease, knowledge of the type and effects of any previous therapy, and continued evaluation of the patient's general and haematologic status. it is essential that adequate clinical and laboratory facilities be available for proper monitoring of patients during treatment with cyclophosphamide. the clinical course of the disease should be recorded in objective terms before treatment is begun and thereafter at regular intervals. careful management of patients receiving cyclophosphamide will help achieve maximum benefit with minimum risk. antineoplastic properties: patients with neoplasms that might preferably be treated by surgical and/or irradiation procedures should ordinarily not be treated by chemotherapy alone.

Australia - English - Department of Health (Therapeutic Goods Administration)

reach pharmaceuticals pty ltd - cyclophosphamide monohydrate, quantity: 1069 mg (equivalent: cyclophosphamide, qty 1000 mg) - injection, powder for - excipient ingredients: mannitol - the proper use of cyclophosphamide requires accurate diagnosis, careful assessment of the anatomic extent of the disease, knowledge of the type and effects of any previous therapy, and continued evaluation of the patient?s general and haematologic status. it is essential that adequate clinical and laboratory facilities be available for proper monitoring of patients during treatment with cyclophosphamide.,the clinical course of the disease should be recorded in objective terms before treatment is begun and thereafter at regular intervals. careful management of patients receiving cyclophosphamide will help achieve maximum benefit with minimum risk.,antineoplastic properties,patients with neoplasms that might preferably be treated by surgical and/or irradiation procedures should ordinarily not be treated by chemotherapy alone.,the following classification is a guide to the various neoplastic conditions in which benefit may be derived from chemotherapy with cyclophosphamide:,frequently responsive myeloproliferative and lymphoproliferative disorders:,malignant lymphomas including hodgkins (stages iii and iv, peter?s staging system*) and non- hodgkins lymphomas; multiple myeloma; leukaemias; mycosis fungoides (advanced disease).,stage i: disease limited to one anatomic region (stage i) or two contiguous anatomic regions (stage i2) on the same side of the diaphragm.,stage ii: disease in more than two anatomic regions or two contiguous regions on the same side of the diaphragm.,stage iii: disease on both sides of the diaphragm, but not extending beyond the involvement of lymph nodes, spleen, and/or waldeyer?s ring.,stage iv: involvement of the bone marrow, lung parenchyma, pleura, liver, bone, skin, kidneys, gastrointestinal tract, or in any tissue or organ in addition to lymph nodes, spleen or waldeyer?s ring.,all stages are subclassified as a or b to indicate the absence or presence, respectively, of systemic symptoms.,frequently responsive solid malignancies:,neuroblastoma (patients with disseminated disease); adenocarcinoma of the ovary, retinoblastoma.,infrequently responsive malignancies:,carcinoma of the breast; malignant neoplasms of the lung.,immunosuppressive properties,cyclophosphamide has also been used in the treatment of autoimmune diseases and immunopathies of unspecified type (ie wegener?s granulomatosis) when these diseases have been resistant to conventional first and second line of treatment, and for the prevention of transplant rejection. cyclophosphamide can be recommended for use in treatment of nonmalignancies only when in the opinion of the physician the benefits to the patient outweigh the risk of treatment with cyclophosphamide.,* modified as the international staging classification for hodgkin?s disease in ?report of the committee on the staging of hodgkin?s disease?. cancer res 26:1310, 1966.

Australia - English - Department of Health (Therapeutic Goods Administration)

reach pharmaceuticals pty ltd - cyclophosphamide monohydrate, quantity: 534.5 mg (equivalent: cyclophosphamide, qty 500 mg) - injection, powder for - excipient ingredients: mannitol - the proper use of cyclophosphamide requires accurate diagnosis, careful assessment of the anatomic extent of the disease, knowledge of the type and effects of any previous therapy, and continued evaluation of the patient?s general and haematologic status. it is essential that adequate clinical and laboratory facilities be available for proper monitoring of patients during treatment with cyclophosphamide.,the clinical course of the disease should be recorded in objective terms before treatment is begun and thereafter at regular intervals. careful management of patients receiving cyclophosphamide will help achieve maximum benefit with minimum risk.,antineoplastic properties,patients with neoplasms that might preferably be treated by surgical and/or irradiation procedures should ordinarily not be treated by chemotherapy alone.,the following classification is a guide to the various neoplastic conditions in which benefit may be derived from chemotherapy with cyclophosphamide:,frequently responsive myeloproliferative and lymphoproliferative disorders:,malignant lymphomas including hodgkins (stages iii and iv, peter?s staging system*) and non- hodgkins lymphomas; multiple myeloma; leukaemias; mycosis fungoides (advanced disease).,stage i: disease limited to one anatomic region (stage i) or two contiguous anatomic regions (stage i2) on the same side of the diaphragm.,stage ii: disease in more than two anatomic regions or two contiguous regions on the same side of the diaphragm.,stage iii: disease on both sides of the diaphragm, but not extending beyond the involvement of lymph nodes, spleen, and/or waldeyer?s ring.,stage iv: involvement of the bone marrow, lung parenchyma, pleura, liver, bone, skin, kidneys, gastrointestinal tract, or in any tissue or organ in addition to lymph nodes, spleen or waldeyer?s ring.,all stages are subclassified as a or b to indicate the absence or presence, respectively, of systemic symptoms.,frequently responsive solid malignancies:,neuroblastoma (patients with disseminated disease); adenocarcinoma of the ovary, retinoblastoma.,infrequently responsive malignancies:,carcinoma of the breast; malignant neoplasms of the lung.,immunosuppressive properties,cyclophosphamide has also been used in the treatment of autoimmune diseases and immunopathies of unspecified type (ie wegener?s granulomatosis) when these diseases have been resistant to conventional first and second line of treatment, and for the prevention of transplant rejection. cyclophosphamide can be recommended for use in treatment of nonmalignancies only when in the opinion of the physician the benefits to the patient outweigh the risk of treatment with cyclophosphamide.,* modified as the international staging classification for hodgkin?s disease in ?report of the committee on the staging of hodgkin?s disease?. cancer res 26:1310, 1966.

Belgium - English - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

accord healthcare b.v. - cyclophosphamide monohydrate 1069 mg - eq. cyclophosphamide 1000 mg - powder for solution for injection/infusion - 1000 mg - cyclophosphamide monohydrate 1069 mg - cyclophosphamide