Amisulpride and Tardive dyskinesia - a phase IV clinical study of FDA data
Summary:
Tardive dyskinesia is reported as a side effect among people who take Amisulpride (amisulpride), especially for people who are female, 60+ old, have been taking the drug for 6 - 12 months also take Risperidone, and have Schizophrenia.
The phase IV clinical study analyzes which people have Tardive dyskinesia when taking Amisulpride. It is created by eHealthMe based on reports of 6,364 people who have side effects when taking Amisulpride from the FDA, and is updated regularly.
What is Amisulpride?
Amisulpride has active ingredients of amisulpride. eHealthMe is studying from 6,389 Amisulpride users. Check the latest studies of Amisulpride.
What is Tardive dyskinesia?
Tardive dyskinesia (a disorder that involves involuntary movements) is found to be associated with 774 drugs and 1,319 conditions by eHealthMe. Check the latest studies of Tardive dyskinesia.
6,364 people reported to have side effects when taking Amisulpride.
Among them, 61 people (0.96%) have Tardive dyskinesia.
Among these 61 people:
How long have people been on Amisulpride when they have Tardive dyskinesia? *
What is the gender of people who have Tardive dyskinesia when taking Amisulpride? *
What is the age of people who have Tardive dyskinesia when taking Amisulpride? *
What are other drugs people take besides Amisulpride? *
What are other side effects people have besides Tardive dyskinesia? *
What are the existing conditions these people have? *
* Approximation only. Some reports may have incomplete information.
Do you take Amisulpride and have Tardive dyskinesia?
- Check whether Tardive dyskinesia 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 Amisulpride:
- Amisulpride (6,389 reports)
Tardive dyskinesia treatments and more:
- Tardive dyskinesia (50,883 reports)
How severe was Tardive dyskinesia and when was it recovered:
Expand to all the drugs that have ingredients of amisulpride:
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 Amisulpride:
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 Tardive dyskinesia:
- Tardive dyskinesia (774 drugs)
Browse all the conditions that are associated with Tardive dyskinesia:
- Tardive dyskinesia (1,319 conditions)
Related publications that referenced our studies
- Manjunatha N, Ganjekar S, Mahendra JV, Kilara N, Srinivasa R, "Tardive Dyskinesia Associated With Anastrozole", The Journal of neuropsychiatry and clinical neurosciences, 2013 Jan .
- Manjunatha N, Ganjekar S, Mahendra JV, Kilara N, Srinivasa R, "Tardive Dyskinesia Associated With Anastrozole", The Journal of neuropsychiatry and clinical neurosciences, 2013 Jan .
How the study uses the data?
The study uses data from the FDA. It is based on amisulpride (the active ingredients of Amisulpride) and Amisulpride (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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