Fenofibrate and Affect lability - a phase IV clinical study of FDA data

Summary:

Affect lability is reported as a side effect among people who take Fenofibrate (fenofibrate), especially for people who are male, 50-59 old, also take Metformin, and have Schizoaffective disorder.

The phase IV clinical study analyzes which people have Affect lability when taking Fenofibrate. It is created by eHealthMe based on reports of 39,402 people who have side effects when taking Fenofibrate from the FDA, and is updated regularly.

What is Fenofibrate?

Fenofibrate has active ingredients of fenofibrate. It is often used in high blood cholesterol. eHealthMe is studying from 40,457 Fenofibrate users. Check the latest studies of Fenofibrate.

What is Affect lability?

Affect lability (emotional incontinence) is found to be associated with 666 drugs and 830 conditions by eHealthMe. Check the latest studies of Affect lability.

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 Sep, 01, 2026

39,402 people reported to have side effects when taking Fenofibrate.
Among them, 33 people (0.08%) have Affect lability.

Could Fenofibrate cause Affect lability?

Among these 33 people:

What is the gender of people who have Affect lability when taking Fenofibrate? *

female: 48.48 %
male: 51.52 %

What is the age of people who have Affect lability when taking Fenofibrate? *

What are other drugs people take besides Fenofibrate? *

What are other side effects people have besides Affect lability? *

Fall: 14 people, 42.42%
C-Reactive Protein Increased: 12 people, 36.36%
Neutrophil Count Increased (excess than normal number of neutrophil a type of blood cell): 12 people, 36.36%
Delirium (wild excitement): 12 people, 36.36%
Lymphocyte Count Decreased: 12 people, 36.36%
Pneumonia: 12 people, 36.36%
Monocyte Count Increased: 12 people, 36.36%
Dizziness: 11 people, 33.33%
Stress And Anxiety: 10 people, 30.30%
Drug Level Increased: 10 people, 30.30%

What are the existing conditions these people have? *

Schizoaffective Disorder (a mental disorder characterized by disordered thought): 13 people, 39.39%
High Blood Pressure: 6 people, 18.18%
Pain: 5 people, 15.15%
Dizziness: 4 people, 12.12%
Neuropathy Peripheral (surface nerve damage): 4 people, 12.12%
Diabetes: 3 people, 9.09%
Depression: 3 people, 9.09%
Irritable Bowel Syndrome: 3 people, 9.09%
Multiple Sclerosis (a nervous system disease that affects your brain and spinal cord. it damages the myelin sheath): 3 people, 9.09%
Neuralgia (pain in one or more nerves): 3 people, 9.09%

* Approximation only. Some reports may have incomplete information.

Do you take Fenofibrate and have Affect lability?

- Check whether Affect lability 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 Fenofibrate:

Fenofibrate (40,457 reports)

Affect lability treatments and more:

Affect lability (13,491 reports)

Browse all side effects of Fenofibrate:

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 Affect lability:

Affect lability (666 drugs)

Browse all the conditions that are associated with Affect lability:

Affect lability (830 conditions)

How the study uses the data?

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