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Prescription medication · Sulfonamide Antibiotic Combination

sulfamethoxazole/trimethoprim

Also sold as Bactrim, Septra. This medicine can treat urinary tract infections, ear infections, bronchitis, and traveler's diarrhea.

Data updated 2026-05-15

43,818
FDA reports
Rx
Availability

sulfamethoxazole/trimethoprim (Bactrim) is a prescription Sulfonamide Antibiotic Combination. This medicine can treat urinary tract infections, ear infections, bronchitis, and traveler's diarrhea.

Sulfamethoxazole and trimethoprim is a combination antibiotic. It is used to treat bacterial infections.

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What it does

This medicine can treat urinary tract infections, ear infections, bronchitis, and traveler's diarrhea.

Common side effects

Nausea, Vomiting, Loss of appetite

Key warnings

Rarely, this medicine has caused severe reactions, including Stevens-Johnson syndrome and liver damage, which can be deadly.

The sections below are summarized in plain English from sulfamethoxazole/trimethoprim's FDA-approved prescribing information. They describe what the official label says, and are not personal medical advice.

How It Works

This medicine contains two drugs that work together to kill bacteria. Sulfamethoxazole and trimethoprim both stop bacteria from making folic acid. Bacteria need folic acid to grow and multiply.

How to Take It

Take this medicine exactly as your doctor tells you. Adults usually take 1 double strength tablet or 2 regular tablets every 12 hours. Children's doses are based on weight. You can take it with or without food.

This is a plain-language summary of sulfamethoxazole/trimethoprim's FDA labeling, not individualized dosing advice. Ask a pharmacist or prescriber before changing how you take this medication.

Pregnancy & Breastfeeding

Tell your doctor if you are pregnant or plan to become pregnant. This medicine may not be safe for your baby. Talk to your doctor about breastfeeding while taking this medicine.

This is a plain-language summary of sulfamethoxazole/trimethoprim's FDA labeling, not individualized advice. Ask a pharmacist or prescriber about pregnancy or breastfeeding on this medication.

Missed Dose

If you miss a dose, take it as soon as you remember. If it is almost time for your next dose, skip the missed dose and continue with your regular schedule.

This is a plain-language summary of sulfamethoxazole/trimethoprim's FDA labeling, not individualized advice. Ask a pharmacist or prescriber what to do about your specific missed dose.

Storage

Store at room temperature, away from light and moisture.

Side Effects (from patient reports)

Based on 43,818 FDA adverse event reports.

Most-reported reactions

Adverse reactions in FAERS for sulfamethoxazole/trimethoprim, by number of reports

reports

What this shows Bars show how often each reaction was reported, not how likely it is to happen, a report records a temporal association, never proof that the drug caused it.

Source FDA Adverse Event Reporting System (FAERS)

Serious Warnings

Rarely, this medicine has caused severe reactions, including Stevens-Johnson syndrome and liver damage, which can be deadly. Tell your doctor right away if you have a fever, rash, blisters, mouth sores, or yellowing of your skin or eyes.

Common Questions

Can I drink alcohol while taking this medicine?
Ask your doctor or pharmacist. Alcohol may worsen some side effects.
How long should I take this medicine?
Take this medicine for the full number of days that your doctor prescribes it. Do not stop early, even if you feel better.
What should I do if I have diarrhea?
Tell your doctor if you have diarrhea, especially if it is severe or bloody. This medicine can sometimes cause a serious type of diarrhea.
Can this medicine interact with other medicines I am taking?
Yes, this medicine can interact with other medicines. Tell your doctor about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.
What if I am allergic to sulfa drugs?
Tell your doctor if you are allergic to sulfa drugs. This medicine contains a sulfa drug, so you should not take it if you are allergic.
Can this medicine cause sun sensitivity?
Yes, this medicine can make your skin more sensitive to the sun. Wear protective clothing and sunscreen when you are outside.
Is it okay to drive while taking this medication?
This medicine can cause dizziness or drowsiness. Do not drive or operate machinery until you know how this medicine affects you.
What if I feel worse after starting this medicine?
Tell your doctor if your symptoms get worse or if you develop new symptoms.
Can I take this medication if I have kidney problems?
Tell your doctor if you have kidney problems. Your dose may need to be adjusted.
Can this medication be used for a viral infection?
No, this medicine is an antibiotic and only works for bacterial infections. It will not work for viral infections like the common cold or flu.
What are the common side effects of sulfamethoxazole/trimethoprim?
The most commonly reported side effects of sulfamethoxazole/trimethoprim include Nausea, Vomiting, Loss of appetite, Skin rash. Based on 43,818 FDA adverse event reports. Always consult your healthcare provider about potential side effects.
What drug class is sulfamethoxazole/trimethoprim?
sulfamethoxazole/trimethoprim belongs to the Sulfonamide Antibiotic Combination drug class. It requires a prescription (Rx). This medicine can treat urinary tract infections, ear infections, bronchitis, and traveler's diarrhea.
Is sulfamethoxazole/trimethoprim safe during pregnancy?
Tell your doctor if you are pregnant or plan to become pregnant. This medicine may not be safe for your baby. Always consult your healthcare provider before using any medication during pregnancy or breastfeeding.

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What the FDA Data Shows for sulfamethoxazole/trimethoprim

The FDA label for sulfamethoxazole/trimethoprim (sold under brand names such as Bactrim, Septra) classifies it as a prescription-only medication in the Sulfonamide Antibiotic Combination class. This medicine can treat urinary tract infections, ear infections, bronchitis, and traveler's diarrhea. Official labeling lists 4 commonly reported side effects, including Nausea, Vomiting, Loss of appetite.

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 43,818 voluntary reports. Interaction data is drawn directly from FDA-approved prescribing information. Acquisition-cost data is surveyed weekly by CMS and updated as manufacturers report changes.

Report counts do not establish causation, a FAERS entry documents a temporal association, not proof that the drug produced the outcome. Widely prescribed medications naturally accumulate more reports than niche therapies, so raw totals must be interpreted alongside total exposure. Shortage status, recall history, and patent information further shape supply and switching decisions. This page summarizes public FDA data for educational purposes only and is not a substitute for professional medical advice, always consult a licensed healthcare provider before starting, stopping, or changing any medication.

Data Sources

Drug labeling: FDA Drug Labels (SPL/DailyMed). Adverse events: FDA Adverse Event Reporting System (FAERS).

FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. Always consult a healthcare professional before making medication decisions.

Last updated: October 9, 2022

Data currency: FDA FAERS adverse-event reports through 2025, CMS NADAC acquisition-cost pricing effective December 2024, compiled and last refreshed May 2026. See our methodology for per-source dates and refresh cadence. Spot a figure that looks wrong? Report a correction.

All federal data sources used on this page