Maxzide-25 and Macular reflex abnormal - a phase IV clinical study of FDA data

Summary:

We study 248 people who take Maxzide-25 (hydrochlorothiazide; triamterene) or have Macular reflex abnormal. No report of Macular reflex abnormal is found in people who take Maxzide-25.

The phase IV clinical study is created by eHealthMe based on reports from the FDA, and is updated regularly.

What is Maxzide-25?

Maxzide-25 has active ingredients of hydrochlorothiazide; triamterene. It is often used in high blood pressure. eHealthMe is studying from 231 Maxzide-25 users. Check the latest studies of Maxzide-25.

What is Macular Reflex Abnormal?

Macular reflex abnormal (abnormal an annular reflection of light surrounding the macula retina) is found to be associated with 5 drugs and 54 conditions by eHealthMe. Check the latest studies of Macular reflex abnormal.

On Jul, 03, 2026

No report is found.

Do you take Maxzide-25 and have Macular reflex abnormal?

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Related studies:

Effectiveness of, long term effects of, and alternative drugs to Maxzide-25:

Maxzide-25 (231 reports)

Macular reflex abnormal treatments and more:

Macular reflex abnormal (17 reports)

How severe was Macular reflex abnormal and when was it recovered:

Macular reflex abnormal in Maxzide-25

Expand to all the drugs that have ingredients of hydrochlorothiazide; triamterene:

Macular reflex abnormal and drugs with ingredients of hydrochlorothiazide; triamterene

Browse all side effects of Maxzide-25:

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Browse all the drugs that are associated with Macular reflex abnormal:

Macular reflex abnormal

Browse all the conditions that are associated with Macular reflex abnormal:

Macular reflex abnormal

How the study uses the data?

The study uses data from the FDA. It is based on hydrochlorothiazide; triamterene (the active ingredients of Maxzide-25) and Maxzide-25 (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.