Buspar and Post procedural infection - a phase IV clinical study of FDA data

Summary:

Post procedural infection is reported as a side effect among people who take Buspar (buspirone hydrochloride), especially for people who are female, 50-59 old, also take Oxycontin, and have Narcolepsy.

The phase IV clinical study analyzes which people have Post procedural infection 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 20,462 Buspar users. Check the latest studies of Buspar.

What is Post procedural infection?

Post procedural infection is found to be associated with 582 drugs and 564 conditions by eHealthMe. Check the latest studies of Post procedural infection.

On Jul, 11, 2026

17,598 people reported to have side effects when taking Buspar.
Among them, 11 people (0.06%) have Post procedural infection.

Could Buspar cause Post procedural infection?

Among these 11 people:

What is the gender of people who have Post procedural infection when taking Buspar? *

female: 90.91 %
male: 9.09 %

What is the age of people who have Post procedural infection when taking Buspar? *

What are other drugs people take besides Buspar? *

What are other side effects people have besides Post procedural infection? *

Joint Swelling: 5 people, 45.45%
Head Injury: 5 people, 45.45%
Tendon Rupture (tear of tendon): 4 people, 36.36%
Fall: 4 people, 36.36%
Gastrointestinal Disorder (functional problems of gastrointestinal tract): 4 people, 36.36%
Joint Injury: 4 people, 36.36%
Chronic Hepatitis (long lasting inflammation of liver): 2 people, 18.18%
Drug Dependence: 2 people, 18.18%
Drug Abuse: 2 people, 18.18%
Essential Hypertension (primary hypertension): 2 people, 18.18%

What are the existing conditions these people have? *

Narcolepsy (brain's inability to regulate sleep-wake cycles normally): 4 people, 36.36%
Pain: 3 people, 27.27%
Short-Bowel Syndrome (a condition in which the body cannot absorb enough fluids and nutrients because part of the small intestine is missing): 1 person, 9.09%
Psoriatic Arthropathy (inflammation of the skin and joints with kin condition which typically causes patches (plaques) of red, scaly skin to develop): 1 person, 9.09%
High Blood Cholesterol: 1 person, 9.09%
Crohn's Disease (a condition that causes inflammation of the gastrointestinal tract): 1 person, 9.09%
Constipation: 1 person, 9.09%
Blood Pressure Abnormal: 1 person, 9.09%
Attention Deficit Hyperactivity Disorder (a chronic condition including attention difficulty, hyperactivity, and impulsiveness): 1 person, 9.09%

* Approximation only. Some reports may have incomplete information.

Do you take Buspar and have Post procedural infection?

- Check whether Post procedural infection 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 Buspar:

Buspar (20,462 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 Post procedural infection:

Post procedural infection (582 drugs)

Browse all the conditions that are associated with Post procedural infection:

Post procedural infection (564 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.