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Could Buspar, Prazosin Hydrochloride together cause Tardive dyskinesia?

Tardive dyskinesia: a disorder that involves involuntary movements.

This is a real world study of Tardive dyskinesia among people who take Buspar, Prazosin Hydrochloride. The study is created by eHealthMe based on 2 reports from FDA and social media.

What are the drugs

Buspar (latest outcomes from 11,041 users) has active ingredients of buspirone hydrochloride. It is often used in stress and anxiety.

Prazosin hydrochloride (latest outcomes from 386 users) has active ingredients of prazosin hydrochloride. It is often used in post-traumatic stress disorder.

On Nov, 1, 2014: 24 people reported to have side effects when taking Buspar, Prazosin Hydrochloride. Among them, 2 people (8.33%) have Tardive Dyskinesia.

Trend of Tardive dyskinesia in Buspar, Prazosin Hydrochloride

Gender of people who have Tardive dyskinesia when taking the drugs * :

FemaleMale
Tardive dyskinesia0%100%

Age of people who have Tardive dyskinesia when taking the drugs * :

0-12-910-1920-2930-3940-4950-5960+
Tardive dyskinesia0%0%0%0%0%100%0%0%

Severity of Tardive dyskinesia when taking the drugs ** :

n/a

How people recovered from Tardive dyskinesia ** :

n/a

* Approximation only. Some reports may have incomplete information.

** Reports from social media are used.

More about the drug combination: Buspar, Prazosin Hydrochloride drug interactions

You can also:

NOTE: The study is based on active ingredients. Other drugs that have the same active ingredients are also considered.

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, and has not been supported by scientific studies or clinical trials unless otherwise stated. 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.

You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).

If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.

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