A pro-drug which has to be activated in the body to active metabolites. Acts on cells at any stage of the cell cycle but the cycle is blocked at G2 (premitotic) stage. This arrest of cell division is brought about by alkylation of the DNA in a dose-dependent manner. Also exerts immunosuppressive effects possibly due to a cytotoxic effect on lymphocytes.
Leukaemias, lymphogranulomatosis, lymphosarcoma, reticulum cell sarcoma. Hodgkin's disease, multiple myeloma, retinoblastoma, carcinoma of the breast, adenocarcinoma of the ovary. Inoperable solid malignancies. Combination with surgery, radiation and other therapeutic measures. Minimal change nephrotic syndrome in children.
After oral administration it is well absorbed. It is metabolised in liver to active metabolites.
Bladder haemorrhage, acute urinary tract infection, myelosuppression.
Nausea, vomiting, visual blurring, facial burning with I.V. administration, teratogenic effect, haemorrhagic cystitis, bone marrow depression, hyponatraemia, sterility, inappropriate secretion of ADH. Alopecia and increased skin pigmentation.
Diabetes, elderly, hepatic, cardiac or renal impairment, acute systemic or urinary infections. to stop the drug if leucocyte count is less than 3000/cu.mm. Carcinogenic potential, infection, adequate contraception, previous X-Ray or cytotoxic therapy.
Minimal change nephrotic syndrome : 2.5-3mg / kg daily orally.
Maximal beneficial effects not felt for upto 6 weeks.
upto several weeks.
250mg,
500mg, 1g
Injection (single vial per box),
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