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MITOXANTRONA

MITOXANTRONE · by ATCO

ANTINEOPLASTICS DNA-reactive cytotoxic antibiotic ATCO

Composition

inf/Inj 20 mg:Mitoxantrone HCI 20 mg; solutionn in vial.

Indications & Dosage

Metastatic breast cancer, Non-Hodgkins lymphoma, Adult acute non-lymphocytic leukaemia, Non-resectable primary hepatocellular carcinoma, ovarian carcinoma: BY IV INF: Adult: 12 mg/m2 every 3 months.

Administration

Mitoxantrone HCI is administered by slow IV infusion after dilution to at least 50 ml in D5W or NS over 15 to 30 min through the tubing of a freely running IV solution or by continuous IV infusion over 24 hours. It should not be given over less than three min.

Compatibility

Stable in D5NS, D5W, NS. Incompatible with amphotericin B cholesteryl sulphate complex, aztreonam, cefepime, doxorubicin liposome, paclitaxel, piperacillin/ tazobactam, propofol Y-site administration: Incompatible with heparin when admixed.

Stability

Store intact vials at 15C-25C (59F-77F). Do not freeze. Opened vials may be stored under refrigeration for up to 7 days or at room temperature for 14 days. Solutions diluted for administration are stable for 7 days at room tem-perature or under refrigeration.

Precautions

Patients with pancytopenia or severe infections, severe hepatic and/or renal insufficiency, severe heart disease (avoid) and those previously treated with anthracyclines and/or irradiated on mediasti-num. Monitor hematological blood parameters before each application as well as at least once during each treatment cycle. Caution is necessary with concomitant use of cardiotoxic drugs, or drugs that reduce cardiac contractility. Cardiac function should be monitored closely

Interactions

Anti-neoplastic drugs.

Pregnancy

Positive evidence of risk: Avoid

Lactation

Contraindicated. Discontinue breast-feeding

Side Effects

Abdominal pain, alopecia, amenorrhoea, Anorexia, anxiety, blue discoloration of nails and skin, bone-marrow suppression, confusion, constipation, diarrhoea, cardiotoxicity, drowsiness, dyspnea, extravasation, GI bleeding, hyperuricaemia, myelosuppression, nausea, oral mucositis, paraesthesia, thromboembolism, transient blue-green discoloration of urine, tumourlysis syndrome, vomiting