Tricor and Joint dislocation - a phase IV clinical study of FDA data

Summary:

Joint dislocation is reported as a side effect among people who take Tricor (fenofibrate), especially for people who are male, 60+ old, have been taking the drug for < 1 month also take Lasix, and have Insomnia.

The phase IV clinical study analyzes which people have Joint dislocation when taking Tricor. It is created by eHealthMe based on reports of 21,730 people who have side effects when taking Tricor from the FDA, and is updated regularly.

What is Tricor?

Tricor has active ingredients of fenofibrate. It is often used in high blood cholesterol. eHealthMe is studying from 22,641 Tricor users. Check the latest studies of Tricor.

What is Joint dislocation?

Joint dislocation (a joint position is changed from normal position) is found to be associated with 1,004 drugs and 923 conditions by eHealthMe. Check the latest studies of Joint dislocation.

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, 31, 2026

21,730 people reported to have side effects when taking Tricor.
Among them, 36 people (0.17%) have Joint dislocation.

Among these 36 people:

How long have people been on Tricor when they have Joint dislocation? *

What is the gender of people who have Joint dislocation when taking Tricor? *

female: 47.22 %
male: 52.78 %

What is the age of people who have Joint dislocation when taking Tricor? *

What are other drugs people take besides Tricor? *

What are other side effects people have besides Joint dislocation? *

Fall: 22 people, 61.11%
Back Pain: 17 people, 47.22%
Acute Kidney Failure: 15 people, 41.67%
Joint Injury: 15 people, 41.67%
Intervertebral Disc Protrusion (spinal disc protrusion): 15 people, 41.67%
Sleep Walking (walking during sleep): 15 people, 41.67%
Anaemia (lack of blood): 14 people, 38.89%
Weakness: 14 people, 38.89%
Dizziness: 14 people, 38.89%
Hypoaesthesia (reduced sense of touch or sensation): 13 people, 36.11%

What are the existing conditions these people have? *

Insomnia (sleeplessness): 12 people, 33.33%
Rheumatoid Arthritis (a chronic progressive disease causing inflammation in the joints): 6 people, 16.67%
Pain: 4 people, 11.11%
Dyskinesia (abnormality or impairment of voluntary movement): 3 people, 8.33%
Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 3 people, 8.33%
High Blood Pressure: 3 people, 8.33%
Uveitis (inflammation of the uvea): 2 people, 5.56%
Depression: 2 people, 5.56%
Diabetes: 2 people, 5.56%
Dry Eyes (lack of adequate tears): 2 people, 5.56%

* Approximation only. Some reports may have incomplete information.

Do you take Tricor and have Joint dislocation?

- Check whether Joint dislocation 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 Tricor:

Tricor (22,641 reports)

Browse all side effects of Tricor:

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 Joint dislocation:

Joint dislocation (1,004 drugs)

Browse all the conditions that are associated with Joint dislocation:

Joint dislocation (923 conditions)

How the study uses the data?

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