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Methotrexate: Uses, Side Effects, and Safe Use

Published: July 22, 2026Updated: July 22, 2026

Methotrexate is a prescription medicine that reduces inflammation and slows immune activity. It is used for conditions such as rheumatoid arthritis and psoriasis, and certain forms of methotrexate are used in cancer treatment. It is available as tablets and as an injection, and the dosing schedule differs by condition and formulation.

Quick summary

Methotrexate can help control inflammatory diseases, but it may affect blood counts, liver function, and the lungs. Take it exactly as prescribed, usually once weekly for inflammatory arthritis, and ask your doctor or pharmacist if you have any questions.

Medically reviewed by WellAlly Editorial TeamLast reviewed July 22, 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
L04AX03
Generic
Methotrexate
Class
dmard
Brands
Rheumatrex, Trexall
Availability
rx
Pregnancy
X
Lactation
unsafe
Half-life (h)
8
Routes
oral, sc, im, iv
Forms
tablet, injection
Regions
CN, US, EU, JP
Monitoring
liver-function, blood-count, renal-function

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
15mg once weekly
Maximum
consult physician
Frequency
once weekly
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
0.3mg per kg once weekly
Maximum
consult physician
Frequency
once weekly
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
7.5mg once weekly
Maximum
consult physician
Frequency
once weekly
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Single dose that may cause serious toxicity
Chronic overdose: Cumulative daily dosing leading to bone marrow suppression and organ damage
Immediate actions
Gastric lavage if within 1-2 hours, activated charcoal, discontinue drug, begin leucovorin rescue, supportive care
Antidote
Leucovorin calcium (folinic acid)(Highly effective when given promptly to neutralize methotrexate and rescue healthy cells)
Poison Control: 1-800-222-1222

Special Populations

8 groups
✗

pregnancy

first trimester
contraindicated
FDA Category
X
Dose Adjustment

avoid use

Key Recommendations

contraindicated during pregnancy due to high risk of fetal malformations and embryotoxicity

Monitor

discontinue before conception if possible, fetal ultrasound monitoring if exposed

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

✗

pregnancy

second third trimester
contraindicated
FDA Category
X
Dose Adjustment

avoid use

Key Recommendations

contraindicated throughout pregnancy due to risk of fetal toxicity and growth restriction

Monitor

regular fetal growth monitoring, ultrasound assessments

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

✗

lactation

n a
contraindicated
FDA Category
N
Dose Adjustment

discontinue breastfeeding

Key Recommendations

methotrexate passes into breast milk and can cause serious toxicity in infants

Monitor

not applicable - breastfeeding should be discontinued

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

⚠

geriatric

elderly
caution
FDA Category
N
Dose Adjustment

reduce starting dose

Key Recommendations

start at lower doses and titrate slowly, increased risk of renal impairment and myelosuppression in elderly

Monitor

close monitoring of renal function, CBC, and liver enzymes more frequently

Use with caution and monitor for adverse effects.

⚠

pediatric_age

children adolescents
caution
FDA Category
N
Dose Adjustment

weight-based dosing

Key Recommendations

used for juvenile idiopathic arthritis and certain pediatric malignancies at reduced doses

Monitor

regular CBC, renal function, and liver function tests, growth monitoring

Use with caution and monitor for adverse effects.

⚠

renal_impairment

mild moderate
caution
FDA Category
N
Dose Adjustment

reduce dose by 25-50%

Key Recommendations

methotrexate is primarily renally eliminated; dose reduction required based on creatinine clearance

Monitor

monitor renal function and methotrexate levels closely

Use with caution and monitor for adverse effects.

✗

renal_impairment

severe
contraindicated
FDA Category
N
Dose Adjustment

avoid use

Key Recommendations

contraindicated in patients with severe renal impairment (CrCl < 30 mL/min)

Monitor

regular monitoring of renal function and methotrexate serum levels

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

⚠

hepatic_impairment

mild moderate
caution
FDA Category
N
Dose Adjustment

use with caution

Key Recommendations

avoid in significant hepatic impairment; hepatotoxicity is a known risk

Monitor

frequent liver function tests, liver biopsy if long-term use anticipated

Use with caution and monitor for adverse effects.

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:1953

Original FDA approval for Methotrexate

drug_classWHO
2023

Drug class

Value:Antimetabolite / Antifolate

Pharmacological classification

usageFDA
2023

Primary indications

Value:Oncology, Rheumatoid arthritis, Psoriasis, Ectopic pregnancy

Therapeutic indications

mechanismFDA
2023

Mechanism of action

Value:Dihydrofolate reductase inhibitor

Pharmacological mechanism

Drug interactions

1 documented interaction(s) with other medications in this knowledge base.

CelecoxibMODERATE

NSAIDs(包括COX-2抑制剂)可通过抑制前列腺素减少肾血流量/GFR,并竞争肾小管分泌,从而降低甲氨蝶呤肾清除率,升高其血药浓度并增加毒性风险(骨髓抑制、黏膜炎、肝肾毒性)。Celecoxib对低剂量MTX的药代动力学影响相对较小,但仍属同类风险。

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 July 22, 2026. · Read our editorial policy