Bisacodyl and Concomitant disease aggravated - a phase IV clinical study of FDA data

Summary:

Concomitant disease aggravated is reported as a side effect among people who take Bisacodyl (bisacodyl), especially for people who are female, 60+ old, have been taking the drug for < 1 month also take Cordarone, and have High blood pressure.

The phase IV clinical study analyzes which people have Concomitant disease aggravated when taking Bisacodyl. It is created by eHealthMe based on reports of 18,779 people who have side effects when taking Bisacodyl from the FDA, and is updated regularly.

What is Bisacodyl?

Bisacodyl has active ingredients of bisacodyl. It is often used in constipation. eHealthMe is studying from 18,852 Bisacodyl users. Check the latest studies of Bisacodyl.

What is Concomitant disease aggravated?

Concomitant disease aggravated (advanced due to some of accompanying) is found to be associated with 597 drugs and 631 conditions by eHealthMe. Check the latest studies of Concomitant disease aggravated.

On Jul, 07, 2026

18,779 people reported to have side effects when taking Bisacodyl.
Among them, 19 people (0.1%) have Concomitant disease aggravated.

Could Bisacodyl cause Concomitant disease aggravated?

Among these 19 people:

How long have people been on Bisacodyl when they have Concomitant disease aggravated? *

What is the gender of people who have Concomitant disease aggravated when taking Bisacodyl? *

female: 78.95 %
male: 21.05 %

What is the age of people who have Concomitant disease aggravated when taking Bisacodyl? *

What are other drugs people take besides Bisacodyl? *

What are other side effects people have besides Concomitant disease aggravated? *

Nausea (feeling of having an urge to vomit): 12 people, 63.16%
Dizziness: 10 people, 52.63%
Fall: 9 people, 47.37%
High Blood Pressure: 9 people, 47.37%
Weakness: 8 people, 42.11%
Agitation (state of anxiety or nervous excitement): 8 people, 42.11%
Oxygen Saturation Decreased: 7 people, 36.84%
Hypokalemia (low potassium): 7 people, 36.84%
Delirium (wild excitement): 7 people, 36.84%
Listless (lack of interest, energy, or spirit): 7 people, 36.84%

What are the existing conditions these people have? *

Rheumatoid Arthritis (a chronic progressive disease causing inflammation in the joints): 7 people, 36.84%
Post Herpetic Neuralgia (neuralgia caused by the varicella zoster virus): 7 people, 36.84%
Pain: 7 people, 36.84%
Chronic Thyroiditis (long lasting inflammation of thyroid gland): 7 people, 36.84%
High Blood Pressure: 7 people, 36.84%
Atrial Fibrillation/flutter (atrial fibrillation and flutter are abnormal heart rhythms in which the atria, or upper chambers of the heart, are out of sync with the ventricles): 4 people, 21.05%
Encephalopathy (functioning of the brain is affected by some agent or condition): 4 people, 21.05%
Calcium Deficiency (lack of calcium): 4 people, 21.05%
Nausea (feeling of having an urge to vomit): 4 people, 21.05%
Immunodeficiency Disorders: 4 people, 21.05%

* Approximation only. Some reports may have incomplete information.

Do you take Bisacodyl and have Concomitant disease aggravated?

- Check whether Concomitant disease aggravated is associated with a drug or a condition
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Related studies:

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

Bisacodyl (18,852 reports)

Browse all side effects of Bisacodyl:

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 Concomitant disease aggravated:

Concomitant disease aggravated (597 drugs)

Browse all the conditions that are associated with Concomitant disease aggravated:

Concomitant disease aggravated (631 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on bisacodyl (the active ingredients of Bisacodyl) and Bisacodyl (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.