Orudis and Heart palpitations - a phase IV clinical study of FDA data

Summary:

Heart palpitations is reported as a side effect among people who take Orudis (ketoprofen), especially for people who are female, 50-59 old, also take Provera, and have Fibromyalgia.

The phase IV clinical study analyzes which people have Heart palpitations when taking Orudis. It is created by eHealthMe based on reports of 928 people who have side effects when taking Orudis from the FDA, and is updated regularly.

What is Orudis?

Orudis has active ingredients of ketoprofen. eHealthMe is studying from 932 Orudis users. Check the latest studies of Orudis.

What is Heart palpitations?

Heart palpitations (feelings or sensations that your heart is pounding or racing) is found to be associated with 2,437 drugs and 3,638 conditions by eHealthMe. Check the latest studies of Heart palpitations.

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 Aug, 31, 2026

928 people reported to have side effects when taking Orudis.
Among them, 19 people (2.05%) have Heart palpitations.

Among these 19 people:

What is the gender of people who have Heart palpitations when taking Orudis? *

female: 66.67 %
male: 33.33 %

What is the age of people who have Heart palpitations when taking Orudis? *

What are other drugs people take besides Orudis? *

What are other side effects people have besides Heart palpitations? *

Arrhythmias (irregular heartbeat): 6 people, 31.58%
Chest Pain: 5 people, 26.32%
Weakness: 4 people, 21.05%
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, 21.05%
Dizziness: 4 people, 21.05%
Hypoaesthesia (reduced sense of touch or sensation): 4 people, 21.05%
Fatigue (feeling of tiredness): 3 people, 15.79%
Nausea (feeling of having an urge to vomit): 3 people, 15.79%
Blood Creatine Phosphokinase Increased: 3 people, 15.79%
Rales (an abnormal respiratory sound characterized by fine crackles): 3 people, 15.79%

What are the existing conditions these people have? *

Neuralgia (pain in one or more nerves): 5 people, 26.32%
Fibromyalgia (a long-term condition which causes pain all over the body): 5 people, 26.32%
Rheumatoid Arthritis (a chronic progressive disease causing inflammation in the joints): 1 person, 5.26%
Nausea (feeling of having an urge to vomit): 1 person, 5.26%
Diabetes: 1 person, 5.26%
Depression: 1 person, 5.26%
Chronic Obstructive Pulmonary Disease (a progressive disease that makes it hard to breathe): 1 person, 5.26%

* Approximation only. Some reports may have incomplete information.

Do you take Orudis and have Heart palpitations?

- Check whether Heart palpitations is associated with a drug or a condition
- Predict drug outcomes for up to one year with AI
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Related studies:

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

Orudis (932 reports)

Browse all side effects of Orudis:

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 Heart palpitations:

Heart palpitations (2,437 drugs)

Browse all the conditions that are associated with Heart palpitations:

Heart palpitations (3,638 conditions)

How the study uses the data?

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