Propofol and Haemothorax - a phase IV clinical study of FDA data

Summary:

Haemothorax is reported as a side effect among people who take Propofol (propofol), especially for people who are 50-59 old, also take Fentanyl, and have Sedation.

The phase IV clinical study analyzes which people have Haemothorax 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 Haemothorax?

Haemothorax (collection of blood in the pleural space (the space between the lungs and the walls of the chest)) is found to be associated with 406 drugs and 531 conditions by eHealthMe. Check the latest studies of Haemothorax.

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 Sep, 02, 2026

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

Among these 12 people:

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

What are other drugs people take besides Propofol? *

What are other side effects people have besides Haemothorax? *

Bleeding Disorders: 5 people, 41.67%
Hypotension (abnormally low blood pressure): 5 people, 41.67%
Brain Stem Infarction (brainstem stroke): 4 people, 33.33%
Grand Mal Convulsion (a type of generalized seizure that affects the entire brain): 4 people, 33.33%
Metabolic Encephalopathy (disorder or disease of the brain due to the body's disability to use energy): 4 people, 33.33%
Drowsiness: 4 people, 33.33%
Rib Fracture: 3 people, 25.00%
Pneumonia: 3 people, 25.00%
Hyporeflexia (a condition of below normal or absent reflexes): 3 people, 25.00%
Neurotoxicity (when the exposure to natural or artificial toxic substances, which are called neurotoxins, alters the normal activity of the nervous system): 3 people, 25.00%

What are the existing conditions these people have? *

Sedation: 3 people, 25.00%
Immunodeficiency Disorders: 2 people, 16.67%
Traumatic Haemorrhage (a bleeding due to trauma): 1 person, 8.33%
Rickets (softening of bones): 1 person, 8.33%
Pain: 1 person, 8.33%
Nephrogenic Anaemia (anaemia due to kidney disease): 1 person, 8.33%
Hepatitis C: 1 person, 8.33%
Gastric Ulcer (stomach ulcer): 1 person, 8.33%
Fluid Retention (an abnormal accumulation of fluid in the blood): 1 person, 8.33%
Cytomegalovirus Infection: 1 person, 8.33%

* Approximation only. Some reports may have incomplete information.

Do you take Propofol and have Haemothorax?

- Check whether Haemothorax 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)

Haemothorax treatments and more:

Haemothorax (3,670 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 Haemothorax:

Haemothorax (406 drugs)

Browse all the conditions that are associated with Haemothorax:

Haemothorax (531 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.