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Cyclophosphamide for Injection USP 500mg/1g/2g Taj Pharma 1. NAME OF THE MEDICINAL PRODUCT Cyclophosphamide for Injection USP 500mg Taj Pharma Cyclophosphamide for Injection USP 1g Taj Pharma Cyclophosphamide for Injection USP 2g Taj Pharma 2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
a) Cyclophosphamide for Injection USP 500mg Taj Pharma Each vial contains cyclophosphamide monohydrate USP Equivalent to Cyclophosphamide (anhydrous) 500mg b) Cyclophosphamide for Injection USP 1g Taj Pharma Each vial contains cyclophosphamide monohydrate USP Equivalent to Cyclophosphamide (anhydrous) 1g c) Cyclophosphamide for Injection USP 2g Taj Pharma Each vial contains cyclophosphamide monohydrate USP Equivalent to Cyclophosphamide (anhydrous) 2g When reconstituted for intravenous use, the solution for administration contains 20mg cyclophosphamide per ml.
3. PHARMACEUTICAL FORM
4.1 Therapeutic indications Cyclophosphamide Taj Pharma is a cytotoxic drug for the treatment of malignant disease in adults and children. As a single agent, it has successfully produced an objective remission in a wide range of malignant conditions. Cyclophosphamide Taj Pharma is also frequently used in combination with other cytotoxic drugs, radiotherapy or surgery.
4.2 Posology and method of administration Cyclophosphamide Taj Pharma Injection is for intravenous or oral administration. Cyclophosphamide Taj Pharma should only be used by clinicians experienced in the use of cancer chemotherapy. Cyclophosphamide Taj Pharma should only be administered where there are facilities for regular monitoring of clinical, biochemical and haematological parameters before, during, and after administration and under the direction of a specialist oncology service. Posology Dosage must be individualized. Doses and duration of treatment and/or treatment intervals depend on the therapeutic indication, the scheme of a combination therapy, the patient's general state of health and organ function, and the results of laboratory monitoring (in particular, blood cell monitoring). A guide to the dosage regimens used for most indications is given below. This treatment should be continued until a clear remission or improvement is seen or be interrupted when the extent of leucopenia becomes unacceptable. Conventional:
Powder for solution for injection. A white crystalline powder contained in clear glass injection vials.
4. CLINICAL PARTICULARS
Conventional: High dose:
80-300mg/m2 daily as a single i.v. dose or daily divided oral doses. 300-600mg/m2 as a single i.v. dose weekly. 600 - 1500mg/m2 as a single i.v. dose or short infusion given at 10-20