BUSULFAN injection

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

BUSULFAN (UNII: G1LN9045DK) (BUSULFAN - UNII:G1LN9045DK)

Available from:

Pharmascience Inc.

INN (International Name):

BUSULFAN

Composition:

BUSULFAN 6 mg in 1 mL

Administration route:

INTRAVENOUS

Prescription type:

PRESCRIPTION DRUG

Therapeutic indications:

Busulfan Injection is indicated for use in combination with cyclophosphamide as a conditioning regimen prior to allogeneic hematopoietic progenitor cell transplantation for chronic myelogenous leukemia. Busulfan Injection is contraindicated in patients with a history of hypersensitivity to any of its components. Risk Summary Busulfan Injection can cause fetal harm when administered to a pregnant woman based on animal data. Busulfan was teratogenic in mice, rats, and rabbits following administration during organogenesis. The solvent, DMA, may also cause fetal harm when administered to a pregnant woman. In rats, DMA doses of approximately 40% of the daily dose of DMA in the Busulfan Injection dose on a mg/m 2 basis given during organogenesis caused significant developmental anomalies ( see Data) . There are no available human data informing the drug-associated risk. Advise pregnant women of the potential risk to a fetus. The background risk of major birth defects and miscarriage for

Product summary:

Busulfan Injection is packaged as a sterile solution in 10 mL single-dose clear glass vials, NDC 51817-170-01 Busulfan Injection is distributed as a unit carton of eight vials.  NDC 51817-170-01 Unopened vials of Busulfan Injection must be stored under refrigerated conditions between 2°C to 8°C (36°F to 46°F). ). Discard unused portion. Busulfan Injection diluted in 0.9% Sodium Chloride Injection, USP or 5% Dextrose Injection, USP is stable at room temperature (25°C) for up to 8 hours but the infusion must be completed within that time. Busulfan Injection diluted in 0.9% Sodium Chloride Injection, USP is stable at refrigerated conditions (2°C to 8°C) for up to 12 hours but the infusion must be completed within that time. Busulfan Injection is a cytotoxic drug. Follow applicable special handling and disposal procedures 1 .

Authorization status:

Abbreviated New Drug Application

Summary of Product characteristics

BUSULFAN- BUSULFAN INJECTION
PHARMASCIENCE INC.
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HIGHLIGHTS OF PRESCRIBING INFORMATION
THESE HIGHLIGHTS DO NOT INCLUDE ALL THE INFORMATION NEEDED TO USE
BUSULFAN INJECTION
SAFELY AND EFFECTIVELY. SEE FULL PRESCRIBING INFORMATION FOR BUSULFAN
INJECTION.
BUSULFAN INJECTION, FOR INTRAVENOUS USE
INITIAL U.S. APPROVAL: 1999
WARNING: MYELOSUPPRESSION
_ SEE FULL PRESCRIBING INFORMATION FOR COMPLETE_
_BOXED WARNING._
Causes severe and prolonged myelosuppression. ( 5.1)
Hematopoietic progenitor cell transplantation is required to prevent
potentially fatal complications
of the prolonged myelosuppression. ( 5.1)
INDICATIONS AND USAGE
Busulfan Injection is an alkylating drug indicated for:
Use in combination with cyclophosphamide as a conditioning regimen
prior to allogeneic hematopoietic
progenitor cell transplantation for chronic myelogenous leukemia (CML)
( 1)
DOSAGE AND ADMINISTRATION
Pre-medicate with anticonvulsants (e.g. benzodiazepines, phenytoin,
valproic acid or levetiracetam)
and antiemetic ( 2.1, 5.2)
Dilute and administer as intravenous infusion. Do not administer as
intravenous push or bolus ( 2.1,
2.3)
Recommended adult dose: 0.8 mg per kg of ideal body weight or actual
body weight, whichever is lower,
administered intravenously via a central venous catheter as a two-hour
infusion every six hours for four
consecutive days for a total of 16 doses ( 2.1)
DOSAGE FORMS AND STRENGTHS
Injection: 60 mg per 10 mL (6 mg per mL) single-dose vial ( 3)
CONTRAINDICATIONS
Busulfan Injection is contraindicated in patients with a history of
hypersensitivity to any of its
components ( 4)
WARNINGS AND PRECAUTIONS
Seizures: Initiate anticonvulsant prophylactic therapy prior to
treatment with Busulfan Injection. Monitor
patients with history of seizure disorder, head trauma or receiving
epileptogenic drugs ( 5.2)
Hepatic Veno-Occlusive Disease (HVOD): Increased risk of developing
HVOD at AUC greater than 1,500
μM•min. Monitor serum transaminases, alkaline phosphatase and
bilirubin daily ( 5.3)
Embryo-fetal Toxicity: