Perindopril erbumine vs. Spironolactone and hydrochlorothiazide: side effect and effectiveness comparison (a real world drug study)
Summary:
We compare the side effects and drug effectiveness of Perindopril erbumine and Spironolactone and hydrochlorothiazide. The phase IV clinical study is created by eHealthMe based on reports (from sources including the FDA) of 43,271 people who take Perindopril erbumine and Spironolactone and hydrochlorothiazide, and is updated regularly.
What is Perindopril erbumine?
Perindopril erbumine has active ingredients of perindopril erbumine. It is often used in high blood pressure. eHealthMe is studying from 8,958 Perindopril erbumine users. Check the latest studies of Perindopril erbumine.
What is Spironolactone and hydrochlorothiazide?
Spironolactone and hydrochlorothiazide has active ingredients of hydrochlorothiazide; spironolactone. It is often used in high blood pressure. eHealthMe is studying from 567 Spironolactone and hydrochlorothiazide users. Check the latest studies of Spironolactone and hydrochlorothiazide.
43,271 people who take Perindopril erbumine and Spironolactone and hydrochlorothiazide are studied.
Drugs being compared in this study:
- Perindopril Erbumine (perindopril erbumine)
- Spironolactone And Hydrochlorothiazide (hydrochlorothiazide; spironolactone)
Most common side effects of the drugs, overall:
Most common side effects of the drugs, in long term (1+ years) use:
Drug effectiveness:
Perindopril Erbumine:
- not at all: 2.5 %
- somewhat: 10.62 %
- moderate: 37.92 %
- high: 38.33 %
- very high: 10.62 %
Spironolactone And Hydrochlorothiazide:
- not at all: 2.04 %
- somewhat: 18.37 %
- moderate: 34.69 %
- high: 38.78 %
- very high: 6.12 %
Want to compare Perindopril erbumine with Spironolactone and hydrochlorothiazide?
- Personalize this study to your gender and age (0-99+)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.
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 .
Related studies
Alternative drugs to, pros and cons of:
- Perindopril erbumine (8,308 reports)
- Spironolactone and hydrochlorothiazide (548 reports)
Browse all side effects of Perindopril erbumine:
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 zBrowse all side effects of Spironolactone and hydrochlorothiazide:
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 zHow the study uses the data?
The study is based on perindopril erbumine and hydrochlorothiazide; spironolactone (the active ingredients of Perindopril erbumine and Spironolactone and hydrochlorothiazide, respectively). Other drugs that have the same active ingredients (e.g. generic drugs or brand names) are also considered. Dosage of drugs is not considered in the study.
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.
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