Dupuytren's contracture and drugs of ingredients of divalproex sodium - a phase IV clinical study of FDA data
Dupuytren's contracture is found among people who take drugs with ingredients of divalproex sodium, especially for people who are male, 60+ old , have been taking the drugs for 5 - 10 years. This phase IV clinical study is created by eHealthMe based on reports of 62,415 people who have side effects when taking drugs with ingredients of divalproex sodium from the FDA, and is updated regularly.
Drug(s) considered in the study (i.e. both brand name and generic drugs): Depakote, Depakote cp, Depakote er, Divalproex, Divalproex sodium, Epival.
Phase IV trials are used to detect adverse drug outcomes and monitor drug effectiveness in the real world. With medical big data and AI algorithms, eHealthMe is running millions of phase IV trials and makes the results available to the public. Our original studies have been referenced on 600+ medical publications including The Lancet, Mayo Clinic Proceedings, and Nature.
62,415 people reported to have side effects when taking drugs with ingredients of divalproex sodium.
Among them, 6 people (0.01%) have Dupuytren's contracture
What is Dupuytren's contracture?
Dupuytren's contracture (thickening of the fibrous tissue layer underneath the skin of the palm and fingers) is found to be associated with 459 drugs and 212 conditions by eHealthMe.
Number of reports submitted per year:
Time on drugs with ingredients of divalproex sodium when people have Dupuytren's contracture *:
- < 1 month: 0.0 %
- 1 - 6 months: 0.0 %
- 6 - 12 months: 0.0 %
- 1 - 2 years: 0.0 %
- 2 - 5 years: 0.0 %
- 5 - 10 years: 100 %
- 10+ years: 0.0 %
Gender of people who have Dupuytren's contracture when taking drugs with ingredients of divalproex sodium *:
- female: 50 %
- male: 50 %
Age of people who have Dupuytren's contracture when taking drugs with ingredients of divalproex sodium *:
- 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: 40 %
- 60+: 60 %
Conditions people have *:
- Depression: 2 people, 33.33%
- Tremor (trembling or shaking movements in one or more parts of your body): 1 person, 16.67%
- Adjustment Disorder: 1 person, 16.67%
Other drugs people take *:
- Zoloft: 2 people, 33.33%
- Vitamin D3: 2 people, 33.33%
- Depakene: 2 people, 33.33%
- Wellbutrin Sr: 1 person, 16.67%
- Venlafaxine Hydrochloride: 1 person, 16.67%
- Sertraline: 1 person, 16.67%
- Seroquel: 1 person, 16.67%
- Pramipexole Dihydrochloride: 1 person, 16.67%
- Fish Oil: 1 person, 16.67%
- Ergocalciferol: 1 person, 16.67%
Other side effects people have besides Dupuytren's contracture *:
- Weight Increased: 3 people, 50.00%
- Tremor (trembling or shaking movements in one or more parts of your body): 3 people, 50.00%
- Weakness: 3 people, 50.00%
- Anger: 2 people, 33.33%
- Fall: 2 people, 33.33%
- Insomnia (sleeplessness): 2 people, 33.33%
- High Blood Pressure: 2 people, 33.33%
- Hearing Loss: 2 people, 33.33%
- Gingival Bleeding (bleeding gums): 2 people, 33.33%
- Gait Disturbance: 2 people, 33.33%
* Approximation only. Some reports may have incomplete information.
How to use the study?
You can discuss the study with your doctor, to ensure that all drug risks and benefits are fully discussed and understood.
Drugs with ingredients of divalproex sodium, their effectiveness, alternatives and more:
How the study uses the data?
The study uses data from the FDA. It is based on divalproex sodium. All drugs that have the same active ingredients (e.g. brand name and generic drugs) are considered. Dosage of drugs is not considered in the study.
Who is eHealthMe?
With medical big data and proven AI 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 600+ 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
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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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