Avandia and Mental disability - a phase IV clinical study of FDA data
Summary:
Mental disability is reported as a side effect among people who take Avandia (rosiglitazone maleate), especially for people who are female, 60+ old, have been taking the drug for 1 - 2 years also take Kadian, and have Cataplexy.
The phase IV clinical study analyzes which people have Mental disability when taking Avandia. It is created by eHealthMe based on reports of 141,991 people who have side effects when taking Avandia from the FDA, and is updated regularly.
What is Avandia?
Avandia has active ingredients of rosiglitazone maleate. It is often used in diabetes. eHealthMe is studying from 142,155 Avandia users. Check the latest studies of Avandia.
What is Mental disability?
Mental disability is found to be associated with 87 drugs and 182 conditions by eHealthMe. Check the latest studies of Mental disability.
141,991 people reported to have side effects when taking Avandia.
Among them, 30 people (0.02%) have Mental disability.

Among these 30 people:
How long have people been on Avandia when they have Mental disability? *
- < 1 month: 0.0 %
- 1 - 6 months: 25 %
- 6 - 12 months: 0.0 %
- 1 - 2 years: 75 %
- 2 - 5 years: 0.0 %
- 5 - 10 years: 0.0 %
- 10+ years: 0.0 %
What is the gender of people who have Mental disability when taking Avandia? *
- female: 60 %
- male: 40 %
What is the age of people who have Mental disability when taking Avandia? *
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 0.0 %
- 30-39: 0.0 %
- 40-49: 0.0 %
- 50-59: 50 %
- 60+: 50 %
What are other drugs people take besides Avandia? *
- Zyrtec: 1 person, 3.33%
- Hyzaar: 1 person, 3.33%
- Adderall: 1 person, 3.33%
- Amaryl: 1 person, 3.33%
- Ambien: 1 person, 3.33%
- Breo Ellipta: 1 person, 3.33%
- Dilaudid: 1 person, 3.33%
- Effexor: 1 person, 3.33%
- Glucophage: 1 person, 3.33%
- Kadian: 1 person, 3.33%
What are other side effects people have besides Mental disability? *
- Stroke (sudden death of a portion of the brain cells due to a lack of oxygen): 11 people, 36.67%
- Cardiac Failure Congestive: 11 people, 36.67%
- Myocardial Ischaemia (the blood flow through one or more of the blood vessels that lead to heart (coronary arteries) is decreased): 6 people, 20.00%
- Cardiac Disorder: 5 people, 16.67%
- Broken Bone: 3 people, 10.00%
- Death: 3 people, 10.00%
- Generalised Oedema (swelling all over the body): 2 people, 6.67%
- Dyspnea (difficult or laboured breathing): 2 people, 6.67%
- Liver Injury: 2 people, 6.67%
- Heart Disease: 1 person, 3.33%
What are the existing conditions these people have? *
- Narcolepsy (brain's inability to regulate sleep-wake cycles normally): 1 person, 3.33%
- Cataplexy (loss of muscle tone accompanied by full conscious awareness): 1 person, 3.33%
* Approximation only. Some reports may have incomplete information.
Do you take Avandia and have Mental disability?
- Check whether Mental disability 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 Avandia:
- Avandia (142,155 reports)
Mental disability treatments and more:
- Mental disability (786 reports)
How severe was Mental disability and when was it recovered:
Expand to all the drugs that have ingredients of rosiglitazone maleate:
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 Avandia:
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 zBrowse all the drugs that are associated with Mental disability:
- Mental disability (87 drugs)
Browse all the conditions that are associated with Mental disability:
- Mental disability (182 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on rosiglitazone maleate (the active ingredients of Avandia) and Avandia (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.
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