Bisoprolol fumarate and Coma scale abnormal - a phase IV clinical study of FDA data

Summary:

Coma scale abnormal is reported as a side effect among people who take Bisoprolol fumarate (bisoprolol fumarate), especially for people who are male, 60+ old, have been taking the drug for < 1 month also take Acetaminophen, and have Lung neoplasm malignant.

The phase IV clinical study analyzes which people have Coma scale abnormal when taking Bisoprolol fumarate. It is created by eHealthMe based on reports of 39,019 people who have side effects when taking Bisoprolol fumarate from the FDA, and is updated regularly.

What is Bisoprolol fumarate?

Bisoprolol fumarate has active ingredients of bisoprolol fumarate. It is often used in high blood pressure. eHealthMe is studying from 40,828 Bisoprolol fumarate users. Check the latest studies of Bisoprolol fumarate.

What is Coma scale abnormal?

Coma scale abnormal is found to be associated with 265 drugs and 359 conditions by eHealthMe. Check the latest studies of Coma scale abnormal.

On Jul, 07, 2026

39,019 people reported to have side effects when taking Bisoprolol fumarate.
Among them, 59 people (0.15%) have Coma scale abnormal.

Could Bisoprolol fumarate cause Coma scale abnormal?

Among these 59 people:

How long have people been on Bisoprolol fumarate when they have Coma scale abnormal? *

What is the gender of people who have Coma scale abnormal when taking Bisoprolol fumarate? *

female: 40 %
male: 60 %

What is the age of people who have Coma scale abnormal when taking Bisoprolol fumarate? *

What are other drugs people take besides Bisoprolol fumarate? *

What are other side effects people have besides Coma scale abnormal? *

Hypotension (abnormally low blood pressure): 39 people, 66.10%
Consciousness - Decreased: 22 people, 37.29%
Bradycardia (abnormally slow heart action): 21 people, 35.59%
Confusional State: 21 people, 35.59%
Weakness: 20 people, 33.90%
Hypoglycemia (low blood sugar): 20 people, 33.90%
Dehydration (dryness resulting from the removal of water): 18 people, 30.51%
Mental Status Changes (general changes in brain function, such as confusion, amnesia (memory loss), loss of alertness, loss of orientation): 16 people, 27.12%
Appetite - Decreased (decreased appetite occurs when you have a reduced desire to eat): 16 people, 27.12%
Haemoglobin Decreased: 16 people, 27.12%

What are the existing conditions these people have? *

Lung Neoplasm Malignant (cancer tumour of lung): 15 people, 25.42%
Pneumonia: 7 people, 11.86%
Indigestion: 4 people, 6.78%
Schizophrenia (a mental disorder characterized by a breakdown of thought processes): 3 people, 5.08%
Gastritis (inflammation of stomach): 3 people, 5.08%
Headache (pain in head): 2 people, 3.39%
Back Pain: 2 people, 3.39%
Stroke (sudden death of a portion of the brain cells due to a lack of oxygen): 2 people, 3.39%
Type 2 Diabetes: 1 person, 1.69%
Breast Cancer: 1 person, 1.69%

* Approximation only. Some reports may have incomplete information.

Do you take Bisoprolol fumarate and have Coma scale abnormal?

- Check whether Coma scale abnormal 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 Bisoprolol fumarate:

Bisoprolol fumarate (40,828 reports)

Browse all side effects of Bisoprolol fumarate:

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 Coma scale abnormal:

Coma scale abnormal (265 drugs)

Browse all the conditions that are associated with Coma scale abnormal:

Coma scale abnormal (359 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on bisoprolol fumarate (the active ingredients of Bisoprolol fumarate) and Bisoprolol fumarate (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.