Actigall and Fainting - a phase IV clinical study of FDA data

Summary:

Fainting is reported as a side effect among people who take Actigall (ursodiol), especially for people who are female, 60+ old, have been taking the drug for 5 - 10 years also take Lasix, and have Nausea and vomiting.

The phase IV clinical study analyzes which people have Fainting when taking Actigall. It is created by eHealthMe based on reports of 2,122 people who have side effects when taking Actigall from the FDA, and is updated regularly.

What is Actigall?

Actigall has active ingredients of ursodiol. It is often used in gallstones. eHealthMe is studying from 2,162 Actigall users. Check the latest studies of Actigall.

What is Fainting?

Fainting (loss of consciousness and postural tone) is found to be associated with 2,455 drugs and 3,548 conditions by eHealthMe. Check the latest studies of Fainting.

On Jul, 27, 2026

2,122 people reported to have side effects when taking Actigall.
Among them, 21 people (0.99%) have Fainting.

Among these 21 people:

How long have people been on Actigall when they have Fainting? *

What is the gender of people who have Fainting when taking Actigall? *

female: 75 %
male: 25 %

What is the age of people who have Fainting when taking Actigall? *

What are other drugs people take besides Actigall? *

What are other side effects people have besides Fainting? *

Weakness: 11 people, 52.38%
Dizziness: 7 people, 33.33%
Nausea (feeling of having an urge to vomit): 7 people, 33.33%
Nausea And Vomiting: 7 people, 33.33%
Dyspnea (difficult or laboured breathing): 5 people, 23.81%
Malaise (a feeling of general discomfort or uneasiness): 5 people, 23.81%
Pain In Extremity: 5 people, 23.81%
Pleural Effusion (water on the lungs): 5 people, 23.81%
Pneumonia: 5 people, 23.81%
Rales (an abnormal respiratory sound characterized by fine crackles): 5 people, 23.81%

What are the existing conditions these people have? *

Nausea (feeling of having an urge to vomit): 4 people, 19.05%
Pain: 4 people, 19.05%
Nausea And Vomiting: 4 people, 19.05%
Swelling: 3 people, 14.29%
Pulmonary Hypertension (increase in blood pressure in the lung artery): 3 people, 14.29%
Richter's Syndrome (hairy cell cancer changes in fast growing b cell cancer tumour): 2 people, 9.52%
Schizophrenia (a mental disorder characterized by a breakdown of thought processes): 2 people, 9.52%
Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 2 people, 9.52%
Gallbladder Disorder: 2 people, 9.52%
Febrile Neutropenia (fever with reduced white blood cells): 2 people, 9.52%

* Approximation only. Some reports may have incomplete information.

Do you take Actigall and have Fainting?

- Check whether Fainting 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 Actigall:

Actigall (2,162 reports)

Fainting treatments and more:

Fainting (131,321 reports)

Browse all side effects of Actigall:

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 Fainting:

Fainting (2,455 drugs)

Browse all the conditions that are associated with Fainting:

Fainting (3,548 conditions)

How the study uses the data?

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