Buspar and Depression suicidal - a phase IV clinical study of FDA data

Summary:

Depression suicidal is reported as a side effect among people who take Buspar (buspirone hydrochloride), especially for people who are female, 60+ old, have been taking the drug for < 1 month also take Remeron, and have High blood pressure.

The phase IV clinical study analyzes which people have Depression suicidal when taking Buspar. It is created by eHealthMe based on reports of 17,598 people who have side effects when taking Buspar from the FDA, and is updated regularly.

What is Buspar?

Buspar has active ingredients of buspirone hydrochloride. It is often used in stress and anxiety. eHealthMe is studying from 20,464 Buspar users. Check the latest studies of Buspar.

What is Depression suicidal?

Depression suicidal (suicide depressive disorder) is found to be associated with 314 drugs and 474 conditions by eHealthMe. Check the latest studies of Depression suicidal.

eHealthMe: drug outcomes in the real world

eHealthMe runs one of the largest post-marketing drug safety studies in the world. We study millions of patients and 5,000 more each day. Our data-driven phase IV clinical trials have been referenced on 800+ peer-reviewed medical publications including The Lancet, Mayo Clinic Proceedings, and Nature. Tools to study our phase IV findings are available to the public, anonymous and free >>>.

On Aug, 31, 2026

17,598 people reported to have side effects when taking Buspar.
Among them, 14 people (0.08%) have Depression suicidal.

Among these 14 people:

How long have people been on Buspar when they have Depression suicidal? *

What is the gender of people who have Depression suicidal when taking Buspar? *

female: 57.14 %
male: 42.86 %

What is the age of people who have Depression suicidal when taking Buspar? *

What are other drugs people take besides Buspar? *

What are other side effects people have besides Depression suicidal? *

Fatigue (feeling of tiredness): 5 people, 35.71%
Drug Ineffective: 4 people, 28.57%
Suicide Attempt: 4 people, 28.57%
Feeling Abnormal: 3 people, 21.43%
Pain: 3 people, 21.43%
Insomnia (sleeplessness): 3 people, 21.43%
Memory Loss: 3 people, 21.43%
Drug Effect Decreased: 3 people, 21.43%
Nausea (feeling of having an urge to vomit): 3 people, 21.43%
Diarrhea: 3 people, 21.43%

What are the existing conditions these people have? *

Multiple Sclerosis (a nervous system disease that affects your brain and spinal cord. it damages the myelin sheath): 3 people, 21.43%
High Blood Pressure: 3 people, 21.43%
Rheumatoid Arthritis (a chronic progressive disease causing inflammation in the joints): 2 people, 14.29%
Pain: 2 people, 14.29%
Irritable Bowel Syndrome: 2 people, 14.29%
Inflammation: 2 people, 14.29%
Indigestion: 2 people, 14.29%
Bipolar Ii Disorder (characterized by at least one episode of hypomania and at least one episode of major depression): 2 people, 14.29%
Back Pain: 2 people, 14.29%
Major Depression (a mood state that goes well beyond temporarily feeling sad or blue. it is a serious medical illness that affects one's thoughts, feelings): 1 person, 7.14%

* Approximation only. Some reports may have incomplete information.

Do you take Buspar and have Depression suicidal?

- Check whether Depression suicidal is associated with a drug or a condition
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Related studies:

Effectiveness of, long term effects of, and alternative drugs to Buspar:

Buspar (20,464 reports)

Browse all side effects of Buspar:

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 Depression suicidal:

Depression suicidal (314 drugs)

Browse all the conditions that are associated with Depression suicidal:

Depression suicidal (474 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on buspirone hydrochloride (the active ingredients of Buspar) and Buspar (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.