Adenosine and Ejection fraction decreased - a phase IV clinical study of FDA data

Summary:

Ejection fraction decreased is reported as a side effect among people who take Adenosine (adenosine), especially for people who are 30-39 old, have been taking the drug for < 1 month also take Digoxin, and have Heart rate irregular.

The phase IV clinical study analyzes which people have Ejection fraction decreased when taking Adenosine. It is created by eHealthMe based on reports of 2,699 people who have side effects when taking Adenosine from the FDA, and is updated regularly.

What is Adenosine?

Adenosine has active ingredients of adenosine. eHealthMe is studying from 2,711 Adenosine users. Check the latest studies of Adenosine.

What is Ejection fraction decreased?

Ejection fraction decreased (systolic heart failure) is found to be associated with 1,066 drugs and 1,252 conditions by eHealthMe. Check the latest studies of Ejection fraction decreased.

On Jul, 09, 2026

2,699 people reported to have side effects when taking Adenosine.
Among them, 12 people (0.44%) have Ejection fraction decreased.

$Could Adenosine cause Ejection fraction decreased?$

Among these 12 people:

How long have people been on Adenosine when they have Ejection fraction decreased? *

What is the age of people who have Ejection fraction decreased when taking Adenosine? *

What are other drugs people take besides Adenosine? *

What are other side effects people have besides Ejection fraction decreased? *

Hypotension (abnormally low blood pressure): 6 people, 50.00%
Tricuspid Valve Incompetence (inefficient heart valve): 5 people, 41.67%
Dyspnea (difficult or laboured breathing): 4 people, 33.33%
Drug Ineffective: 4 people, 33.33%
Arrhythmias (irregular heartbeat): 4 people, 33.33%
Left Ventricular Hypertrophy (the thickening of the myocardium (muscle) of the left ventricle of the heart): 3 people, 25.00%
Blood Creatinine Increased: 3 people, 25.00%
Mitral Valve Incompetence (inefficient heart valve): 3 people, 25.00%
Maternal Exposure During Pregnancy (use of substance during pregnancy): 3 people, 25.00%
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): 3 people, 25.00%

What are the existing conditions these people have? *

High Blood Pressure: 2 people, 16.67%
Heart Rate Irregular: 2 people, 16.67%
High Blood Cholesterol: 1 person, 8.33%
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): 1 person, 8.33%
Blood Testosterone Increased: 1 person, 8.33%
Bowel Movement Irregularity: 1 person, 8.33%
Cardiomyopathy (weakening of the heart muscle): 1 person, 8.33%
Chronic Obstructive Pulmonary Disease (a progressive disease that makes it hard to breathe): 1 person, 8.33%
Furuncle (infection of the hair follicle): 1 person, 8.33%
Virilism (development or possession of male secondary sex characters in a female or prepubertal male): 1 person, 8.33%

* Approximation only. Some reports may have incomplete information.

Do you take Adenosine and have Ejection fraction decreased?

- Check whether Ejection fraction decreased is associated with a drug or a condition
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Related studies:

Effectiveness of, long term effects of, and alternative drugs to Adenosine:

Adenosine (2,711 reports)

Browse all side effects of Adenosine:

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Browse all the drugs that are associated with Ejection fraction decreased:

Ejection fraction decreased (1,066 drugs)

Browse all the conditions that are associated with Ejection fraction decreased:

Ejection fraction decreased (1,252 conditions)

How the study uses the data?

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