How effective is Lotrel for Essential Hypertension? (a real world drug study)
Summary:
Overall ratings: 3.6/5 Long term ratings: 3.6/5
This is a phase IV clinical study of how effective Lotrel (amlodipine besylate; benazepril hydrochloride) is for Essential hypertension and for what kind of people. The study is created by eHealthMe from 7 Lotrel users and is updated continuously.
What is Lotrel?
Lotrel has active ingredients of amlodipine besylate; benazepril hydrochloride. It is often used in high blood pressure. eHealthMe is studying from 13,571 Lotrel users. Check the latest studies of Lotrel.
What is Essential hypertension?
Essential hypertension (primary hypertension) is found to be associated with 661 drugs and 652 conditions by eHealthMe. Check the latest studies of Essential hypertension.
7 people are studied for taking Lotrel in Essential hypertension
Overall effectiveness (number of people):

Long term (1+ years) effectiveness (number of people):

Lotrel effectiveness for Essential hypertension (number of people):
Overall:
- not at all: 0
- somewhat: 0
- moderate: 4
- high: 2
- very high: 1
Long Term:
- not at all: 0
- somewhat: 0
- moderate: 4
- high: 2
- very high: 1
Gender of people who take Lotrel for Essential hypertension *:
- female: 42.86 %
- male: 57.14 %
Age of people who take Lotrel for Essential hypertension *:
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 0.0 %
- 30-39: 0.0 %
- 40-49: 0.0 %
- 50-59: 28.57 %
- 60+: 71.43 %
Who find Lotrel more effective for Essential Hypertension?
Gender of people who take Lotrel for Essential hypertension *:
- female: 33.33 %
- male: 66.67 %
Age of people who take Lotrel for Essential hypertension *:
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 0.0 %
- 30-39: 0.0 %
- 40-49: 0.0 %
- 50-59: 66.67 %
- 60+: 33.33 %
* Approximation only. Some reports may have incomplete information.
Do you take Lotrel?
- You can start a phase IV clinical trial to monitor Lotrel safety and effectiveness.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 studies
Alternative drugs to, pros and cons of:
- Lotrel (13,571 reports)
Treatments, associated drugs and conditions:
- Essential hypertension (15,964 reports)
How the study uses the data?
The study is based on amlodipine besylate; benazepril hydrochloride (the active ingredients of Lotrel) and Lotrel (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 neither.
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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