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

Summary:

Device dislocation is reported as a side effect among people who take Actos (pioglitazone hydrochloride), especially for people who are female, 60+ old, also take Actonel, and have Allergic rhinitis.

The phase IV clinical study analyzes which people have Device dislocation when taking Actos. It is created by eHealthMe based on reports of 49,087 people who have side effects when taking Actos from the FDA, and is updated regularly.

What is Actos?

Actos has active ingredients of pioglitazone hydrochloride. It is often used in diabetes. eHealthMe is studying from 49,754 Actos users. Check the latest studies of Actos.

What is Device dislocation?

Device dislocation is found to be associated with 719 drugs and 706 conditions by eHealthMe. Check the latest studies of Device dislocation.

On May, 04, 2026

49,087 people reported to have side effects when taking Actos.
Among them, 13 people (0.03%) have Device dislocation.

Among these 13 people:

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

female: 100 %
male: 0.0 %

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

What are other drugs people take besides Actos? *

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

Osteoarthritis (a joint disease caused by cartilage loss in a joint): 8 people, 61.54%
Fall: 7 people, 53.85%
Hypoaesthesia (reduced sense of touch or sensation): 7 people, 53.85%
Spinal Column Stenosis (narrowing of spinal column): 7 people, 53.85%
Pain: 7 people, 53.85%
High Blood Pressure: 6 people, 46.15%
Paraesthesia (sensation of tingling, tickling, prickling, pricking, or burning of a person's skin with no apparent long-term physical effect): 6 people, 46.15%
Arthritis (form of joint disorder that involves inflammation of one or more joints): 6 people, 46.15%
Blood Urea Increased: 6 people, 46.15%
Cataract (clouding of the lens inside the eye): 6 people, 46.15%

What are the existing conditions these people have? *

Ventricular Extrasystoles (premature cardiac contraction): 6 people, 46.15%
Osteoporosis (bones weak and more likely to break): 6 people, 46.15%
Osteopenia (a condition where bone mineral density is lower than normal): 6 people, 46.15%
Allergic Rhinitis: 6 people, 46.15%
Diabetic Retinopathy (damage to the retina caused by complications of diabetes): 2 people, 15.38%
Diabetic Retinal Oedema (excessive build-up of fluid in the retina due to diabetes): 2 people, 15.38%
Pain: 1 person, 7.69%
Narcolepsy (brain's inability to regulate sleep-wake cycles normally): 1 person, 7.69%
Muscle Spasticity (tight or stiff muscles and an inability to control those muscles): 1 person, 7.69%
Muscle Spasms (muscle contraction): 1 person, 7.69%

* Approximation only. Some reports may have incomplete information.

Do you take Actos 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 Actos:

Actos (49,754 reports)

Browse all side effects of Actos:

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 (719 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 pioglitazone hydrochloride (the active ingredients of Actos) and Actos (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.