Ursodiol and Lacrimation increased - a phase IV clinical study of FDA data

Summary:

Lacrimation increased is reported as a side effect among people who take Ursodiol (ursodiol), especially for people who are female, 30-39 old, also take Vitamin D3, and have Cystic fibrosis.

The phase IV clinical study analyzes which people have Lacrimation increased when taking Ursodiol. It is created by eHealthMe based on reports of 18,820 people who have side effects when taking Ursodiol from the FDA, and is updated regularly.

What is Ursodiol?

Ursodiol has active ingredients of ursodiol. It is often used in primary biliary cirrhosis. eHealthMe is studying from 19,061 Ursodiol users. Check the latest studies of Ursodiol.

What is Lacrimation increased?

Lacrimation increased is found to be associated with 1,351 drugs and 1,791 conditions by eHealthMe. Check the latest studies of Lacrimation increased.

On Jul, 08, 2026

18,820 people reported to have side effects when taking Ursodiol.
Among them, 22 people (0.12%) have Lacrimation increased.

Could Ursodiol cause Lacrimation increased?

Among these 22 people:

What is the gender of people who have Lacrimation increased when taking Ursodiol? *

female: 90 %
male: 10 %

What is the age of people who have Lacrimation increased when taking Ursodiol? *

What are other drugs people take besides Ursodiol? *

What are other side effects people have besides Lacrimation increased? *

Visual Impairment: 8 people, 36.36%
Headache (pain in head): 7 people, 31.82%
Sneezing: 7 people, 31.82%
Psoriasis (immune-mediated disease that affects the skin): 6 people, 27.27%
Hypersensitivity: 6 people, 27.27%
Ear Pruritus (pruritus or itching is ""the unpleasant skin sensation that frequently provokes scratching"" in ear): 6 people, 27.27%
Urticaria (rash of round, red welts on the skin that itch intensely): 6 people, 27.27%
Muscle Spasms (muscle contraction): 6 people, 27.27%
Arthritis (form of joint disorder that involves inflammation of one or more joints): 5 people, 22.73%
Blood Glucose Increased: 5 people, 22.73%

What are the existing conditions these people have? *

Cystic Fibrosis (disease of the secretary glands): 6 people, 27.27%
Neurotrophic Keratopathy (decreased corneal sensitivity and poor corneal healing): 4 people, 18.18%
Dermatitis Atopic (inflammatory, chronically relapsing, non-contagious and pruritic skin disorder): 3 people, 13.64%
Thrombophlebitis Migrans (development of recurrent (i.e. migratory) superficial thrombophlebitis): 2 people, 9.09%
Multiple Myeloma (cancer of the plasma cells): 2 people, 9.09%
Graft Versus Host Disease (the donated bone marrow or stem cells view the recipient's body as foreign, and the donated cells/bone marrow attack the body): 1 person, 4.55%
Blood Insulin Abnormal: 1 person, 4.55%
Bone Disorder: 1 person, 4.55%
Bone Marrow Conditioning Regimen: 1 person, 4.55%
Cellulitis (infection under the skin): 1 person, 4.55%

* Approximation only. Some reports may have incomplete information.

Do you take Ursodiol and have Lacrimation increased?

- Check whether Lacrimation increased 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 Ursodiol:

Ursodiol (19,061 reports)

Browse all side effects of Ursodiol:

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 Lacrimation increased:

Lacrimation increased (1,351 drugs)

Browse all the conditions that are associated with Lacrimation increased:

Lacrimation increased (1,791 conditions)

How the study uses the data?

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