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Azathioprine Sodium

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

Azathioprine Sodium is an immunosuppressive medication that works by inhibiting the synthesis of DNA and RNA in rapidly dividing cells, thereby suppressing immune system activity. It is primarily used to prevent organ rejection in transplant patients and to treat various autoimmune conditions such as rheumatoid arthritis, lupus, and inflammatory bowel disease.

Quick summary

Azathioprine Sodium is an immunosuppressant used to prevent transplant rejection and treat autoimmune disorders by suppressing cell division and immune function.

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

Key facts at a glance

RxNorm
267476
Generic
Azathioprine Sodium
Class
pin-variant
Brands
—
Availability
rx
Lactation
unknown
Routes
—
Forms
—
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 dose that may cause serious toxicity including bone marrow suppression and gastrointestinal effects
Chronic overdose: Prolonged use leading to cumulative bone marrow suppression, particularly in patients with thiopurine methyltransferase (TPMT) deficiency
Immediate actions
Gastric decontamination if ingestion within 1-2 hours, supportive care, intravenous fluids, monitoring of blood counts and liver function
Antidote
No specific antidote available(Supportive care only - no specific antidote exists)
Poison Control: 1-800-222-1222

Special Populations

7 groups
✗

pregnancy

first trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks; consider discontinuation before planned pregnancy

Monitor

regular fetal monitoring

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

⚠

pregnancy

second third trimester
caution
FDA Category
C
Dose Adjustment

maintain lowest effective dose

Key Recommendations

continue only if benefits outweigh risks; close monitoring of maternal and fetal status

Monitor

regular fetal growth monitoring, ultrasound assessments

Use with caution and monitor for adverse effects.

⚠

lactation

breastfeeding
caution
FDA Category
N
Dose Adjustment

no specific adjustment

Key Recommendations

considered compatible with breastfeeding per AAP; monitor infant for unusual symptoms

Monitor

observe infant for signs of infection or bone marrow suppression

Use with caution and monitor for adverse effects.

⚠

pediatric_age

children 2 17 years
caution
FDA Category
C
Dose Adjustment

weight-based dosing starting at 1-2 mg/kg/day

Key Recommendations

use with caution; monitor CBC regularly; adjust dose based on response and tolerability

Monitor

complete blood count weekly initially, then monthly

Use with caution and monitor for adverse effects.

⚠

geriatric

elderly over 65
caution
FDA Category
C
Dose Adjustment

start at lower end of dosing range, 1-1.5 mg/kg/day

Key Recommendations

use with caution due to increased susceptibility to infections and myelosuppression

Monitor

frequent CBC monitoring, renal and hepatic function assessment

Use with caution and monitor for adverse effects.

⚠

renal_impairment

moderate severe
caution
FDA Category
C
Dose Adjustment

reduce dose by 25-50% in moderate impairment; 50-75% reduction in severe impairment

Key Recommendations

use with caution; metabolites accumulate in renal impairment

Monitor

monitor CBC, renal function, adjust dose based on hematologic response

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

moderate severe
caution
FDA Category
C
Dose Adjustment

reduce dose by 25-50% in moderate impairment; avoid in severe impairment if possible

Key Recommendations

use with caution; drug is metabolized in liver

Monitor

monitor CBC, liver function tests, adjust dose based on response

Use with caution and monitor for adverse effects.

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:1968

Initial FDA approval for azathioprine

drug_classWHO
2023

Drug class

Value:Immunosuppressant (antimetabolite)

WHO ATC code L04AX01

usageMedical guidelines
2023

Common uses

Value:Organ transplant rejection prevention, autoimmune diseases (rheumatoid arthritis, lupus, Crohn's disease)

Primary therapeutic applications

mechanismPharmacology databases
2023

Mechanism of action

Value:Purine analog that interferes with DNA synthesis in rapidly dividing cells

Molecular mechanism of immunosuppression

Prevention of organ transplant rejection (kidney, liver, heart); treatment of rheumatoid arthritis, systemic lupus erythematosus, inflammatory bowel disease (Crohn's disease, ulcerative colitis), and certain hematologic conditions such as immune thrombocytopenia and autoimmune hemolytic anemia.

Azathioprine is a prodrug that is converted to 6-mercaptopurine (6-MP) in the body. It inhibits purine synthesis, which disrupts DNA and RNA production. This prevents rapid proliferation of immune cells (particularly T-cells and B-cells), thereby suppressing the immune response that would otherwise attack transplanted organs or cause autoimmune inflammation.

Requires regular blood monitoring to check blood counts due to risk of bone marrow suppression. Increases susceptibility to infections and certain cancers. Should not be used during pregnancy unless clearly needed. May interact with allopurinol (requires dose reduction) and other immunosuppressants. Patients should avoid live vaccines while taking this medication.

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

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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