Leukeran

— THERAPEUTIC CATEGORIES —
  • Leukemias, lymphomas, and other hematologic cancers

Leukeran Generic Name & Formulations

General Description

Chlorambucil 2mg; tabs.

Pharmacological Class

Alkylating agent.

How Supplied

Tabs—50

Manufacturer

Leukeran Indications

Indications

Palliative treatment of chronic lymphatic (lymphocytic) leukemia and malignant lymphomas (including lymphosarcoma, giant follicular lymphoma, and Hodgkin's disease).

Leukeran Dosage and Administration

Adult

See literature. 0.1–0.2mg/kg per day for 3–6 weeks. Reduce dose if leukocyte or platelet counts fall below normal values and discontinue if more severe depression occurs. Do not give full dose within 4 weeks of radio- or chemotherapy.

Children

Not recommended.

Leukeran Contraindications

Not Applicable

Leukeran Boxed Warnings

Not Applicable

Leukeran Warnings/Precautions

Warnings/Precautions

Compromised bone marrow function. History of seizure disorder or head trauma. Monitor blood weekly (during first 3–6 weeks, do WBC count 3–4 days after each weekly CBC). Discontinue if skin reactions occur. Elderly. Pregnancy (Cat.D), nursing mothers: not recommended.

Leukeran Pharmacokinetics

See Literature

Leukeran Interactions

Interactions

Avoid live vaccines. Myelosuppressives, radiotherapy potentiate antineoplastic effect. Caution with drugs that lower seizure threshold.

Leukeran Adverse Reactions

Adverse Reactions

Bone marrow suppression, seizures, fever, rash, hypersensitivity, urticaria, azoospermia, amenorrhea, sterility, hepato- and pulmonary toxicity, secondary malignancies, GI upset.

Leukeran Clinical Trials

See Literature

Leukeran Note

Not Applicable

Leukeran Patient Counseling

See Literature