Ipratropium bromide and Subdural haematoma - a phase IV clinical study of FDA data

Summary:

Subdural haematoma is reported as a side effect among people who take Ipratropium bromide (ipratropium bromide), especially for people who are male, 60+ old, also take Furosemide, and have Atrial fibrillation/flutter.

The phase IV clinical study analyzes which people have Subdural haematoma when taking Ipratropium bromide. It is created by eHealthMe based on reports of 17,749 people who have side effects when taking Ipratropium bromide from the FDA, and is updated regularly.

What is Ipratropium bromide?

Ipratropium bromide has active ingredients of ipratropium bromide. It is often used in chronic obstructive pulmonary disease. eHealthMe is studying from 17,965 Ipratropium bromide users. Check the latest studies of Ipratropium bromide.

What is Subdural haematoma?

Subdural haematoma (blood collects between the skull and the surface of the brain) is found to be associated with 999 drugs and 1,084 conditions by eHealthMe. Check the latest studies of Subdural haematoma.

On Jul, 13, 2026

17,749 people reported to have side effects when taking Ipratropium bromide.
Among them, 25 people (0.14%) have Subdural haematoma.

Could Ipratropium bromide cause Subdural haematoma?

Among these 25 people:

What is the gender of people who have Subdural haematoma when taking Ipratropium bromide? *

female: 32 %
male: 68 %

What is the age of people who have Subdural haematoma when taking Ipratropium bromide? *

What are other drugs people take besides Ipratropium bromide? *

What are other side effects people have besides Subdural haematoma? *

Fall: 11 people, 44.00%
Convulsion (muscles contract and relax rapidly and repeatedly, resulting in an uncontrolled shaking of the body): 9 people, 36.00%
Head Injury: 7 people, 28.00%
Pneumonia: 5 people, 20.00%
Cardiac Failure Congestive: 5 people, 20.00%
Dyspnea (difficult or laboured breathing): 5 people, 20.00%
General Physical Health Deterioration (weak health status): 5 people, 20.00%
Nausea And Vomiting: 5 people, 20.00%
Loss Of Consciousness: 5 people, 20.00%
Anaemia (lack of blood): 5 people, 20.00%

What are the existing conditions these people have? *

Atrial Fibrillation/flutter (atrial fibrillation and flutter are abnormal heart rhythms in which the atria, or upper chambers of the heart, are out of sync with the ventricles): 4 people, 16.00%
Multiple Myeloma (cancer of the plasma cells): 3 people, 12.00%
Splenic Marginal Zone Lymphoma (cancer of the lymph nodes spleen): 2 people, 8.00%
Dementia With Lewy Bodies (progressive degenerative disease or syndrome of the brain): 2 people, 8.00%
High Blood Pressure: 2 people, 8.00%
Pain: 2 people, 8.00%
Cough: 1 person, 4.00%
Essential Hypertension (primary hypertension): 1 person, 4.00%
Eczema (patches of skin become rough and inflamed, with itching and bleeding blisters): 1 person, 4.00%
Diarrhea: 1 person, 4.00%

* Approximation only. Some reports may have incomplete information.

Do you take Ipratropium bromide and have Subdural haematoma?

- Check whether Subdural haematoma 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 Ipratropium bromide:

Ipratropium bromide (17,965 reports)

Browse all side effects of Ipratropium bromide:

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 Subdural haematoma:

Subdural haematoma (999 drugs)

Browse all the conditions that are associated with Subdural haematoma:

Subdural haematoma (1,084 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on ipratropium bromide (the active ingredients of Ipratropium bromide) and Ipratropium bromide (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.