Skip to content

Trimethoprim-Sulfamethoxazole (TMP-SMX): Patient Guide

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

Trimethoprim-sulfamethoxazole is a combination antibiotic used to treat certain bacterial infections, including urinary tract, skin, intestinal, lung, and bone infections. It is also used to treat or prevent Pneumocystis jirovecii pneumonia in people with weakened immune systems.

Quick summary

Take this antibiotic exactly as prescribed and complete the full course unless a doctor tells you to stop. Contact a doctor or pharmacist before starting it if you are pregnant, have kidney or liver disease, or take other medicines.

Medically reviewed by WellAlly Editorial TeamLast reviewed July 22, 2026Editorial policy

Key facts at a glance

ATC
J01EE01
Generic
Trimethoprim-Sulfamethoxazole
Class
sulfonamide-combination
Brands
Bactrim, Septra
Availability
rx
Pregnancy
D
Lactation
unsafe
Half-life (h)
10
Onset (min)
60
Duration (h)
12
Routes
oral, iv
Forms
tablet, injection
Regions
CN, US, EU, JP
Monitoring
renal-function, photosensitivity

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 of 10g or more of the combined drug may cause serious toxicity
Chronic overdose: Prolonged use at high doses can lead to bone marrow suppression, liver toxicity, and kidney damage
Immediate actions
Gastric lavage if within 1-2 hours of ingestion, activated charcoal, supportive care including intravenous fluids, monitoring of renal and hepatic function
Antidote
No specific antidote exists; N-acetylcysteine may be used for hepatoprotection in cases of significant liver involvement(Supportive care is the mainstay of treatment; N-acetylcysteine may provide some benefit for liver protection but is not curative)
Poison Control: 1-800-222-1222

Special Populations

8 groups
✗

pregnancy

first trimester
unsafe
FDA Category
C
Dose Adjustment

avoid use

Key Recommendations

avoid use during first trimester due to teratogenic risk; folic acid antagonism may increase risk of neural tube defects, cardiovascular malformations, and cleft lip/palate

Monitor

regular fetal monitoring including ultrasound for fetal anatomy

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

✗

pregnancy

third trimester
unsafe
FDA Category
C
Dose Adjustment

avoid use

Key Recommendations

avoid use near term (within 3 weeks of delivery) due to risk of kernicterus in newborns; sulfa displaces bilirubin from albumin

Monitor

monitor newborn for signs of kernicterus

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

✗

lactation

breastfeeding
unsafe
FDA Category
C
Dose Adjustment

contraindicated

Key Recommendations

both trimethoprim and sulfamethoxazole pass into breast milk; contraindicated in breastfeeding due to risk of kernicterus in newborns and hemolytic anemia in G6PD-deficient infants

Monitor

monitor infant for signs of jaundice, hemolytic anemia, and kernicterus

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

✗

pediatric_age

neonates and infants
unsafe
FDA Category
C
Dose Adjustment

contraindicated in infants less than 2 months

Key Recommendations

contraindicated in neonates and infants under 2 months of age due to risk of kernicterus; immature hepatic glucuronidation pathways and bilirubin displacement

Monitor

monitor for signs of kernicterus including jaundice, lethargy, and poor feeding

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

⚠

pediatric_age

children 2 months and older
caution
FDA Category
C
Dose Adjustment

weight-based dosing required

Key Recommendations

use with caution in children 2 months and older; contraindicated in children with G6PD deficiency; monitor for rash and hematologic adverse effects

Monitor

monitor CBC periodically, watch for signs of rash, Stevens-Johnson syndrome

Use with caution and monitor for adverse effects.

⚠

geriatric

elderly
caution
FDA Category
C
Dose Adjustment

adjust based on renal function

Key Recommendations

use with caution in elderly patients; increased risk of adverse effects including bone marrow suppression, hyperkalemia, and renal impairment; increased mortality observed in some studies for trimethoprim component

Monitor

monitor renal function (CrCl), serum potassium, and CBC regularly

Use with caution and monitor for adverse effects.

⚠

renal_impairment

mild to moderate
caution
FDA Category
C
Dose Adjustment

reduce dose; use with caution in CrCl 30-50 mL/min

Key Recommendations

dose adjustment required; reduce dose by 50% for CrCl 15-30 mL/min; avoid use or use with extreme caution for CrCl <15 mL/min due to accumulation and toxicity risk

Monitor

monitor renal function, serum electrolytes (especially potassium), and CBC

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

moderate to severe
caution
FDA Category
C
Dose Adjustment

use with caution

Key Recommendations

use with caution in hepatic impairment; trimethoprim is partially metabolized in liver; monitor liver function tests; avoid in severe hepatic impairment if possible

Monitor

monitor liver function tests (ALT, AST, bilirubin) and clinical status

Use with caution and monitor for adverse effects.

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:1973

Initial FDA approval for Trimethoprim-Sulfamethoxazole

drug_classWHO
2023

Drug class

Value:Antibiotic (Sulfonamide + Dihydrofolate reductase inhibitor)

Antimicrobial agent classification

usageCDC
2023

Common uses

Value:Urinary tract infections, respiratory infections, Pneumocystis pneumonia prophylaxis, traveler's diarrhea

Primary therapeutic indications

formulationFDA
2023

Formulation type

Value:Fixed-dose combination oral tablet

Pharmaceutical formulation

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 July 22, 2026. · Read our editorial policy