Propofol and Autonomic dysreflexia - a phase IV clinical study of FDA data

Summary:

Autonomic dysreflexia is reported as a side effect among people who take Propofol (propofol), especially for people who are female, 40-49 old, also take Baclofen, and have Hypertonic bladder.

The phase IV clinical study analyzes which people have Autonomic dysreflexia when taking Propofol. It is created by eHealthMe based on reports of 37,986 people who have side effects when taking Propofol from the FDA, and is updated regularly.

What is Propofol?

Propofol has active ingredients of propofol. It is often used in colonoscopy abnormal. eHealthMe is studying from 38,225 Propofol users. Check the latest studies of Propofol.

What is Autonomic dysreflexia?

Autonomic dysreflexia (state that is unique to patients after spinal cord injury at a t-5 level and above) is found to be associated with 28 drugs and 98 conditions by eHealthMe. Check the latest studies of Autonomic dysreflexia.

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, 30, 2026

37,986 people reported to have side effects when taking Propofol.
Among them, 12 people (0.03%) have Autonomic dysreflexia.

Could Propofol cause Autonomic dysreflexia?

Among these 12 people:

What is the gender of people who have Autonomic dysreflexia when taking Propofol? *

female: 100 %
male: 0.0 %

What is the age of people who have Autonomic dysreflexia when taking Propofol? *

What are other drugs people take besides Propofol? *

What are other side effects people have besides Autonomic dysreflexia? *

Visual Impairment: 11 people, 91.67%
Skin Blushing/flushing (a sudden reddening of the face, neck): 11 people, 91.67%
Rashes (redness): 11 people, 91.67%
High Blood Pressure: 11 people, 91.67%
Heart Rate Decreased: 11 people, 91.67%
Headache (pain in head): 11 people, 91.67%
Dry Mouth: 11 people, 91.67%
Bradycardia (abnormally slow heart action): 11 people, 91.67%

What are the existing conditions these people have? *

Hypertonic Bladder (bladder-storage function that causes a sudden urge to urinate): 12 people, 100.00%
Bradycardia (abnormally slow heart action): 9 people, 75.00%

* Approximation only. Some reports may have incomplete information.

Do you take Propofol and have Autonomic dysreflexia?

- Check whether Autonomic dysreflexia 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 Propofol:

Propofol (38,225 reports)

Browse all side effects of Propofol:

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 Autonomic dysreflexia:

Autonomic dysreflexia (28 drugs)

Browse all the conditions that are associated with Autonomic dysreflexia:

Autonomic dysreflexia (98 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on propofol (the active ingredients of Propofol) and Propofol (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.