Monograph Details

Neoplasms > Alkylating agents
ALKERAN FOR INJECTION
Manufacturer
GlaxoSmithKline Pharmaceuticals
Legal Classification
Rx
Pharmacological Class
Nitrogen mustard derivative.
Generic Name
Melphalan HCl 50mg/vial; pwd for IV infusion after reconstitution and dilution.
Also
ALKERAN
Indications
Palliative treatment of multiple myeloma when oral therapy is not appropriate.
Children
Not recommended.
Adults
Give by IV infusion over 15–20 minutes. 16mg/m2 every 2 weeks for a total of 4 doses, then at 4-week intervals. Continue treatment as hematological recovery permits. Renal insufficiency (BUN≥30mg/dL): consider reducing dose by 50%.
Contraindications
Prior resistance to melphalan.
Precautions
Prior irradiation or chemotherapy. Bone marrow suppression. Azotemia. Monitor platelets, hemoglobin, WBC and differential at start of therapy and prior to each course; discontinue if WBC <3,000cells/µL or platelets <100,000cells/µL. Moderate to severe renal impairment. Elderly. Pregnancy (Cat.D), nursing mothers: not recommended.
Interactions
Radiotherapy potentiates antineoplastic effect. For IV: caution with cyclosporine, cisplatin, BCNU, nalidixic acid.
Adverse Reactions
Bone marrow suppression, GI upset, hepatic dysfunction, anemia, blood dyscrasias, secondary malignancies (eg, nonlymphocytic leukemia), rash, alopecia, pulmonary fibrosis, interstitial pneumonitis, gonadal toxicity (amenorrhea, infertility); hypersensitivity reactions, cardiac arrest (rare).
How Supplied
Tabs—50
Single-use vial—1 (w. diluent)
Additional Resources
Related Prescribing Note