Exforge and Device dislocation - a phase IV clinical study of FDA data

Summary:

Device dislocation is reported as a side effect among people who take Exforge (amlodipine besylate; valsartan), especially for people who are male, 60+ old, also take Eylea, and have Parkinson's disease.

The phase IV clinical study analyzes which people have Device dislocation when taking Exforge. It is created by eHealthMe based on reports of 12,942 people who have side effects when taking Exforge from the FDA, and is updated regularly.

What is Exforge?

Exforge has active ingredients of amlodipine besylate; valsartan. It is often used in high blood pressure. eHealthMe is studying from 13,350 Exforge users. Check the latest studies of Exforge.

What is Device dislocation?

Device dislocation is found to be associated with 737 drugs and 706 conditions by eHealthMe. Check the latest studies of Device dislocation.

On Jan, 22, 2026

12,942 people reported to have side effects when taking Exforge.
Among them, 12 people (0.09%) have Device dislocation.

Among these 12 people:

What is the gender of people who have Device dislocation when taking Exforge? *

female: 33.33 %
male: 66.67 %

What is the age of people who have Device dislocation when taking Exforge? *

What are other drugs people take besides Exforge? *

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

Agitation (state of anxiety or nervous excitement): 3 people, 25.00%
Device Occlusion: 3 people, 25.00%
Fainting (loss of consciousness and postural tone): 3 people, 25.00%
Fall: 3 people, 25.00%
Orthostatic Hypotension (a medical condition consisting of a sudden decrease in blood pressure when a person stands up): 3 people, 25.00%
Photophobia (extreme sensitivity to light): 2 people, 16.67%
Cataract (clouding of the lens inside the eye): 2 people, 16.67%
Dyspnea (difficult or laboured breathing): 2 people, 16.67%
Eye Swelling: 2 people, 16.67%
Fibula Fracture: 2 people, 16.67%

What are the existing conditions these people have? *

Parkinson's Disease: 4 people, 33.33%
Diabetes: 3 people, 25.00%
Diabetic Retinal Oedema (excessive build-up of fluid in the retina due to diabetes): 2 people, 16.67%
Osteoporosis (bones weak and more likely to break): 1 person, 8.33%
Osteopenia (a condition where bone mineral density is lower than normal): 1 person, 8.33%
High Blood Cholesterol: 1 person, 8.33%
Enlarged Prostate: 1 person, 8.33%
Blood Glucose Abnormal: 1 person, 8.33%
Birth Control: 1 person, 8.33%

* Approximation only. Some reports may have incomplete information.

Do you take Exforge and have Device dislocation?

- Check whether Device 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 Exforge:

Exforge (13,350 reports)

Device dislocation treatments and more:

Device dislocation (43,936 reports)

How severe was Device dislocation and when was it recovered:

Device dislocation in Exforge

Expand to all the drugs that have ingredients of amlodipine besylate; valsartan:

Device dislocation and drugs with ingredients of amlodipine besylate; valsartan

Sub-studies by gender and age:

Female: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+

Male: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+

Browse all side effects of Exforge:

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 Device dislocation:

Device dislocation (737 drugs)

Browse all the conditions that are associated with Device dislocation:

Device dislocation (706 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on amlodipine besylate; valsartan (the active ingredients of Exforge) and Exforge (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.