Septra and Dysaesthesia - a phase IV clinical study of FDA data

Summary:

We study 14,401 people who take Septra (sulfamethoxazole; trimethoprim) or have Dysaesthesia. No report of Dysaesthesia is found in people who take Septra.

The phase IV clinical study is created by eHealthMe based on reports from the FDA, and is updated regularly.

What is Septra?

Septra has active ingredients of sulfamethoxazole; trimethoprim. It is often used in urinary tract infection. eHealthMe is studying from 10,280 Septra users. Check the latest studies of Septra.

What is Dysaesthesia?

Dysaesthesia (abnormal sensation) is found to be associated with 519 drugs and 584 conditions by eHealthMe. Check the latest studies of Dysaesthesia.

On Jul, 21, 2026

No report is found.

Do you take Septra and have Dysaesthesia?

- Check whether Dysaesthesia is associated with a drug or a condition
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously

Related studies:

Effectiveness of, long term effects of, and alternative drugs to Septra:

Septra (10,280 reports)

Dysaesthesia treatments and more:

Dysaesthesia (4,121 reports)

How severe was Dysaesthesia and when was it recovered:

Dysaesthesia in Septra

Expand to all the drugs that have ingredients of sulfamethoxazole; trimethoprim:

Dysaesthesia and drugs with ingredients of sulfamethoxazole; trimethoprim (70 reports)

Browse all side effects of Septra:

a b c d e f g h i j k l m n o p q r s t u v w x y z

Browse all the drugs that are associated with Dysaesthesia:

Dysaesthesia

Browse all the conditions that are associated with Dysaesthesia:

Dysaesthesia

How the study uses the data?

The study uses data from the FDA. It is based on sulfamethoxazole; trimethoprim (the active ingredients of Septra) and Septra (the brand name). Other drugs that have the same active ingredients (e.g. generic drugs) are not considered. Dosage of drugs is not considered in the study.

How to use the study?

DO NOT STOP MEDICATIONS without first consulting your doctor. If there are any serious or long term adverse effects discovered in the study, discuss the study with your doctor to ensure that proper medication management will be in place if applicable.

Who is eHealthMe?

With medical big data and proven AI/ML algorithms, eHealthMe provides a platform for everyone to run phase IV clinical trials. We study millions of patients and 5,000 more each day. Results of our real-world drug study have been referenced on 800+ peer-reviewed medical publications, including The Lancet, Mayo Clinic Proceedings, and Nature. Our analysis results are available to researchers, health care professionals, patients (testimonials), and software developers (open API).

WARNING, DISCLAIMER, USE FOR PUBLICATION

WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.

DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only. Our phase IV clinical studies alone cannot establish cause-effect relationship. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.

If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.