Bisacodyl and Conjunctivitis - a phase IV clinical study of FDA data

Summary:

Conjunctivitis 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 Tramadol, and have Drowsiness.

The phase IV clinical study analyzes which people have Conjunctivitis 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 Conjunctivitis?

Conjunctivitis (pink eye) is found to be associated with 1,298 drugs and 1,644 conditions by eHealthMe. Check the latest studies of Conjunctivitis.

eHealthMe: drug outcomes in the real world

eHealthMe runs one of the largest post-marketing drug safety studies in the world. We study millions of patients and 5,000 more each day. Our data-driven phase IV clinical trials have been referenced on 800+ peer-reviewed medical publications including The Lancet, Mayo Clinic Proceedings, and Nature. Tools to study our phase IV findings are available to the public, anonymous and free >>>.

On Aug, 30, 2026

18,779 people reported to have side effects when taking Bisacodyl.
Among them, 32 people (0.17%) have Conjunctivitis.

Among these 32 people:

How long have people been on Bisacodyl when they have Conjunctivitis? *

What is the gender of people who have Conjunctivitis when taking Bisacodyl? *

female: 75.86 %
male: 24.14 %

What is the age of people who have Conjunctivitis when taking Bisacodyl? *

What are other drugs people take besides Bisacodyl? *

What are other side effects people have besides Conjunctivitis? *

Fever: 20 people, 62.50%
Itching: 20 people, 62.50%
Pain In Extremity: 19 people, 59.38%
Rashes (redness): 18 people, 56.25%
Urinary Tract Infection: 15 people, 46.88%
Hypersensitivity: 15 people, 46.88%
Insomnia (sleeplessness): 15 people, 46.88%
Weakness: 15 people, 46.88%
Thrombocytopenia (decrease of platelets in blood): 15 people, 46.88%
Pain: 15 people, 46.88%

What are the existing conditions these people have? *

Uterine Fibroids (benign growths of the muscle inside the uterus): 10 people, 31.25%
Drowsiness: 10 people, 31.25%
Pain: 8 people, 25.00%
Infection: 5 people, 15.62%
Multiple Myeloma (cancer of the plasma cells): 5 people, 15.62%
Stress And Anxiety: 5 people, 15.62%
Aseptic Necrosis (the death of bone tissue due to a lack of blood supply): 4 people, 12.50%
Bleeding Disorders: 4 people, 12.50%
Immunodeficiency Disorders: 4 people, 12.50%
Depression: 4 people, 12.50%

* Approximation only. Some reports may have incomplete information.

Do you take Bisacodyl and have Conjunctivitis?

- Check whether Conjunctivitis 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 Bisacodyl:

Bisacodyl (18,852 reports)

Conjunctivitis treatments and more:

Conjunctivitis (22,439 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 Conjunctivitis:

Conjunctivitis (1,298 drugs)

Browse all the conditions that are associated with Conjunctivitis:

Conjunctivitis (1,644 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.