Propulsid and Central auditory processing disorder - a phase IV clinical study of FDA data

Summary:

We study 8,234 people who take Propulsid (cisapride monohydrate) or have Central auditory processing disorder. No report of Central auditory processing disorder is found in people who take Propulsid.

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

What is Propulsid?

Propulsid has active ingredients of cisapride monohydrate. It is often used in gastroesophageal reflux disease. eHealthMe is studying from 8,130 Propulsid users. Check the latest studies of Propulsid.

What is Central Auditory Processing Disorder?

Central auditory processing disorder (cannot process the information they hear in the same way as others do) is found to be associated with 6 drugs and 49 conditions by eHealthMe. Check the latest studies of Central auditory processing disorder.

On Oct, 12, 2025

No report is found.

Do you take Propulsid and have Central auditory processing disorder?

- Check whether Central auditory processing disorder is associated with a drug or a condition
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Related studies:

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

Propulsid (8,130 reports)

Browse all side effects of Propulsid:

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 Central auditory processing disorder:

Central auditory processing disorder

Browse all the conditions that are associated with Central auditory processing disorder:

Central auditory processing disorder

Drugs similar to Propulsid and Central auditory processing disorder :

How the study uses the data?

The study uses data from the FDA. It is based on cisapride monohydrate (the active ingredients of Propulsid) and Propulsid (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.