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Carmustine Injection
  • Professionals
  • FDA PI

Carmustine Injection

Dosage form: injection
Drug class:Alkylating agents

Medically reviewed by Drugs.com. Last updated on Aug 1, 2021.

BOXED WARNING

WARNING: MYELOSUPPRESSION and PULMONARY TOXICITY

Myelosuppression

Carmustine causes suppression of marrow function (including thrombocytopenia and leukopenia), which may contribute to bleeding and overwhelming infections. [see Warnings and Precautions (5.1) and Adverse Reactions (6)]. Monitor blood counts weekly for at least 6 weeks after each dose. Adjust dosage based on nadir blood counts from the prior dose [see Dosage and Administration (2.1)]. Do not administer a repeat course of carmustine until blood counts recover.

Pulmonary Toxicity

Carmustine causes dose-related pulmonary toxicity. Patients receiving greater than 1400 mg/m2 cumulative dose are at significantly higher risk than those receiving less. Delayed pulmonary toxicity can occur years after treatment, and can result in death, particularly in patients treated in childhood[see Adverse Reactions (6) and Use in Specific Populations (8.4)].

Indications and Usage for Carmustine Injection

Carmustine for injection is indicated as palliative therapy as a single agent or in established combination therapy in the following:

- Brain tumors glioblastoma, brainstem glioma, medulloblastoma, astrocytoma, ependymoma, and metastatic brain tumors.

- Multiple myeloma in combination with prednisone.

- Relapsed or refractory Hodgkin's lymphoma in combination with other approved drugs.

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