Aceon and Dyspepsia aggravated - a phase IV clinical study of FDA data

Summary:

Dyspepsia aggravated is reported as a side effect among people who take Aceon (perindopril erbumine), especially for people who are female, 60+ old, have been taking the drug for < 1 month also take Vicodin, and have Back pain.

The phase IV clinical study analyzes which people have Dyspepsia aggravated when taking Aceon. It is created by eHealthMe based on reports of 1,743 people who have side effects when taking Aceon from the FDA, and is updated regularly.

What is Aceon?

Aceon has active ingredients of perindopril erbumine. It is often used in high blood pressure. eHealthMe is studying from 1,785 Aceon users. Check the latest studies of Aceon.

What is Dyspepsia aggravated?

Dyspepsia aggravated (indigestion) is found to be associated with 1,926 drugs and 514 conditions by eHealthMe. Check the latest studies of Dyspepsia aggravated.

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

1,743 people reported to have side effects when taking Aceon.
Among them, 17 people (0.98%) have Dyspepsia aggravated.

Among these 17 people:

How long have people been on Aceon when they have Dyspepsia aggravated? *

What is the gender of people who have Dyspepsia aggravated when taking Aceon? *

female: 58.82 %
male: 41.18 %

What is the age of people who have Dyspepsia aggravated when taking Aceon? *

What are other drugs people take besides Aceon? *

What are other side effects people have besides Dyspepsia aggravated? *

Nausea (feeling of having an urge to vomit): 9 people, 52.94%
Weakness: 8 people, 47.06%
Headache (pain in head): 6 people, 35.29%
Hyperhidrosis (abnormally increased sweating): 4 people, 23.53%
Colonic Polyp (extra part of colon tissue grow in intestine): 4 people, 23.53%
Chills (felling of cold): 4 people, 23.53%
Bone Marrow Disorder: 4 people, 23.53%
Rashes (redness): 4 people, 23.53%
Red Blood Cell Count Decreased: 4 people, 23.53%
White Blood Cell Count Decreased: 4 people, 23.53%

What are the existing conditions these people have? *

Back Pain: 4 people, 23.53%
Type 2 Diabetes: 3 people, 17.65%
Stable Angina (a constant chest pain): 1 person, 5.88%
Depression: 1 person, 5.88%
Bipolar Disorder (mood disorder): 1 person, 5.88%

* Approximation only. Some reports may have incomplete information.

Do you take Aceon and have Dyspepsia aggravated?

- Check whether Dyspepsia aggravated 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 Aceon:

Aceon (1,785 reports)

Browse all side effects of Aceon:

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 Dyspepsia aggravated:

Dyspepsia aggravated (1,926 drugs)

Browse all the conditions that are associated with Dyspepsia aggravated:

Dyspepsia aggravated (514 conditions)

Related publications that referenced our studies

Krishnan K, Krishnasamy K, "Evaluation of anaphylactic reaction as an adverse event for perindopril erbumine tablets", International Current Pharmaceutical Journal, 2014 Mar .
Krishnan K, Krishnasamy K, "Evaluation of anaphylactic reaction as an adverse event for perindopril erbumine tablets", International Current Pharmaceutical Journal, 2014 Mar .

How the study uses the data?

The study uses data from the FDA. It is based on perindopril erbumine (the active ingredients of Aceon) and Aceon (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.