Famotidine and Cardioversion - a phase IV clinical study of FDA data

Summary:

Cardioversion is reported as a side effect among people who take Famotidine (famotidine), especially for people who are female, 60+ old, also take Allopurinol, and have Atrial fibrillation/flutter.

The phase IV clinical study analyzes which people have Cardioversion when taking Famotidine. It is created by eHealthMe based on reports of 81,914 people who have side effects when taking Famotidine from the FDA, and is updated regularly.

What is Famotidine?

Famotidine has active ingredients of famotidine. It is often used in gastroesophageal reflux disease. eHealthMe is studying from 83,424 Famotidine users. Check the latest studies of Famotidine.

What is Cardioversion?

Cardioversion is found to be associated with 186 drugs and 345 conditions by eHealthMe. Check the latest studies of Cardioversion.

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, 03, 2026

81,914 people reported to have side effects when taking Famotidine.
Among them, 11 people (0.01%) have Cardioversion.

Among these 11 people:

What is the gender of people who have Cardioversion when taking Famotidine? *

female: 80 %
male: 20 %

What is the age of people who have Cardioversion when taking Famotidine? *

What are other drugs people take besides Famotidine? *

What are other side effects people have besides Cardioversion? *

Dyspnea (difficult or laboured breathing): 6 people, 54.55%
Overdose: 4 people, 36.36%
Heart Palpitations (feelings or sensations that your heart is pounding or racing): 3 people, 27.27%
Oedema Peripheral (superficial swelling): 3 people, 27.27%
Malaise (a feeling of general discomfort or uneasiness): 3 people, 27.27%
Atrial Tachycardia (rhythm disturbance that arises in the atria): 3 people, 27.27%
Pneumonia: 3 people, 27.27%
Pleural Effusion (water on the lungs): 3 people, 27.27%
Dyspnea Exertional: 2 people, 18.18%
Hypoacusis (loss of hearing): 2 people, 18.18%

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): 6 people, 54.55%
Gout (uric acid crystals building up in the body): 4 people, 36.36%
High Blood Cholesterol: 3 people, 27.27%
Anaemia (lack of blood): 2 people, 18.18%
Pulmonary Hypertension (increase in blood pressure in the lung artery): 2 people, 18.18%
Blood Pressure Abnormal: 2 people, 18.18%
Cardiac Failure Chronic: 2 people, 18.18%
Gastritis - Chronic (long lasting inflammation of stomach): 2 people, 18.18%
Bone Disorder: 1 person, 9.09%
Cardiac Disorder: 1 person, 9.09%

* Approximation only. Some reports may have incomplete information.

Do you take Famotidine and have Cardioversion?

- Check whether Cardioversion 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 Famotidine:

Famotidine (83,424 reports)

Cardioversion treatments and more:

Cardioversion (2,120 reports)

Browse all side effects of Famotidine:

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 Cardioversion:

Cardioversion (186 drugs)

Browse all the conditions that are associated with Cardioversion:

Cardioversion (345 conditions)

How the study uses the data?

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