Suboxone and Fainting - a phase IV clinical study of FDA data
Summary:
Fainting is reported as a side effect among people who take Suboxone (buprenorphine hydrochloride; naloxone hydrochloride), especially for people who are female, 20-29 old, have been taking the drug for < 1 month also take Cymbalta, and have Drug dependence.
The phase IV clinical study analyzes which people have Fainting when taking Suboxone. It is created by eHealthMe based on reports of 28,308 people who have side effects when taking Suboxone from the FDA, and is updated regularly.
What is Suboxone?
Suboxone has active ingredients of buprenorphine hydrochloride; naloxone hydrochloride. It is often used in opiate withdrawal. eHealthMe is studying from 31,249 Suboxone users. Check the latest studies of Suboxone.
What is Fainting?
Fainting (loss of consciousness and postural tone) is found to be associated with 2,456 drugs and 3,547 conditions by eHealthMe. Check the latest studies of Fainting.
28,308 people reported to have side effects when taking Suboxone.
Among them, 108 people (0.38%) have Fainting.

Among these 108 people:
How long have people been on Suboxone when they have Fainting? *
What is the gender of people who have Fainting when taking Suboxone? *
What is the age of people who have Fainting when taking Suboxone? *
What are other drugs people take besides Suboxone? *
What are other side effects people have besides Fainting? *
What are the existing conditions these people have? *
* Approximation only. Some reports may have incomplete information.
Do you take Suboxone and have Fainting?
- Check whether Fainting 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 Suboxone:
- Suboxone (31,249 reports)
Fainting treatments and more:
- Fainting (131,321 reports)
How severe was Fainting and when was it recovered:
Expand to all the drugs that have ingredients of buprenorphine hydrochloride; naloxone hydrochloride:
- Fainting and drugs with ingredients of buprenorphine hydrochloride; naloxone hydrochloride (128 reports)
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 Suboxone:
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 Fainting:
- Fainting (2,456 drugs)
Browse all the conditions that are associated with Fainting:
- Fainting (3,547 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on buprenorphine hydrochloride; naloxone hydrochloride (the active ingredients of Suboxone) and Suboxone (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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