Skip to content

Cytarabine

Published: July 26, 2026Updated: August 24, 2026

Cytarabine is a chemotherapy medication classified as a pyrimidine analog antimetabolite. It is primarily used in the treatment of various leukemias, including acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL), as well as certain lymphomas. The drug works by interfering with DNA synthesis in rapidly dividing cells, leading to cell death.

Quick summary

Cytarabine is an antimetabolite chemotherapy drug used primarily to treat leukemias by disrupting cancer cell DNA synthesis.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 24, 2026Editorial policy
BOXED WARNING

This medication carries a boxed (black box) warning — the strongest type of FDA warning. Review the full prescribing information before use.

Key facts at a glance

ATC
L01BC01
RxNorm
3041
Generic
Cytarabine
Class
atc-l01
Brands
Vyxeos
Availability
rx
Lactation
unknown
Routes
—
Forms
injection, solution, suspension
Regions
US, EU, CN, JP
Monitoring
—

This page is for informational purposes only.

Do not use this information to diagnose yourself or to replace a physician's advice. Always consult a qualified healthcare provider before starting, stopping, or changing any medication. If you believe you are experiencing a medical emergency, call your local emergency number immediately.

Dosage and administration

adult (standard)tablet
Usual dose
500mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
250mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
400mg daily
Maximum
consult physician
Frequency
once daily
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Single doses above 5g/m2 have been associated with severe toxicity
Chronic overdose: cumulative doses exceeding therapeutic regimens can lead to prolonged myelosuppression
Immediate actions
discontinue drug, supportive care, monitor CBC, hydration, treat infections
Antidote
no specific antidote(supportive care is mainstay of treatment)
Poison Control: 1-800-222-1222

Special Populations

7 groups
✗

pregnancy

first trimester
unsafe
FDA Category
D
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy due to demonstrated fetal toxicity; use only if life-threatening condition where benefits outweigh risks

Monitor

regular fetal monitoring including ultrasound

Use of this medication in this population requires careful consideration of risks and benefits.

⚠

pregnancy

second third trimester
caution
FDA Category
D
Dose Adjustment

use lowest effective dose

Key Recommendations

use only if clearly needed; consider risks versus benefits carefully

Monitor

fetal growth monitoring and ultrasound assessments

Use with caution and monitor for adverse effects.

✗

lactation

breastfeeding
unsafe
FDA Category
N
Dose Adjustment

discontinue breastfeeding

Key Recommendations

do not breastfeed during treatment and for at least 1 week after last dose

Monitor

not applicable

Use of this medication in this population requires careful consideration of risks and benefits.

⚠

pediatric_age

children adolescents
caution
FDA Category
N
Dose Adjustment

weight-based dosing required

Key Recommendations

commonly used in pediatric leukemia protocols; doses vary by indication and regimen

Monitor

close hematologic monitoring; watch for myelosuppression and neurotoxicity

Use with caution and monitor for adverse effects.

⚠

geriatric

elderly
caution
FDA Category
N
Dose Adjustment

consider dose reduction based on comorbidities

Key Recommendations

use with caution; monitor renal and hepatic function; consider performance status

Monitor

frequent hematologic monitoring and organ function assessment

Use with caution and monitor for adverse effects.

⚠

renal_impairment

severe renal impairment
caution
FDA Category
N
Dose Adjustment

dose reduction recommended

Key Recommendations

reduce dose by 20-30% in severe renal impairment; monitor renal function closely

Monitor

frequent renal function monitoring including creatinine clearance

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

severe hepatic impairment
caution
FDA Category
N
Dose Adjustment

dose reduction recommended

Key Recommendations

reduce dose in severe hepatic impairment; monitor liver function tests

Monitor

regular hepatic function monitoring

Use with caution and monitor for adverse effects.

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:2017

Vyxeos (CPX-351) FDA approval date

drug_classWHO
2023

Drug class

Value:Antineoplastic agent/Nucleoside analog

Antimetabolite chemotherapy agent

usageMedical guidelines
2023

Common uses

Value:Acute myeloid leukemia (AML)

Primary therapeutic indication

mechanismFDA
2023

Mechanism of action

Value:DNA synthesis inhibition

Antimetabolite action

Cytarabine is used to treat acute myeloid leukemia (AML), acute lymphoblastic leukemia (ALL), chronic myelogenous leukemia (CML), and non-Hodgkin lymphoma. It may also be administered intrathecally to prevent or treat meningeal leukemia.

As a pyrimidine analog, cytarabine is converted to its active form inside cells where it gets incorporated into DNA during synthesis. This incorporation causes chain termination and inhibits DNA polymerase, ultimately preventing DNA synthesis and triggering cell death in rapidly dividing cancer cells.

Cytarabine is typically administered by injection (intravenously, subcutaneously, or intrathecally) by healthcare professionals. Common side effects include bone marrow suppression, nausea, vomiting, fever, and liver toxicity. It requires careful blood count monitoring and may cause significant immunosuppression. Patients should avoid live vaccines during treatment.

Contraindications

Conditions and patient states where this medication should be avoided or used with caution.

Do not use (1)

ABSOLUTEhypersensitivity

Known allergy to this medication or its components

Use caution (1)

RELATIVEpregnancy

Consult healthcare provider for benefits vs risks assessment

Official drug label

WellAlly may earn a referral fee from linked resources at no extra cost to you. Editorial content is never influenced by commercial relationships.

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 24, 2026. · Read our editorial policy