Prempro and Post-menopausal bleeding - a phase IV clinical study of FDA data

Summary:

Post-menopausal bleeding is reported as a side effect among people who take Prempro (estrogens, conjugated; medroxyprogesterone acetate), especially for people who are 50-59 old, also take Coumadin,.

The phase IV clinical study analyzes which people have Post-menopausal bleeding when taking Prempro. It is created by eHealthMe based on reports of 42,607 people who have side effects when taking Prempro from the FDA, and is updated regularly.

What is Prempro?

Prempro has active ingredients of estrogens, conjugated; medroxyprogesterone acetate. It is often used in menopause. eHealthMe is studying from 42,950 Prempro users. Check the latest studies of Prempro.

What is Post-menopausal bleeding?

Post-menopausal bleeding is found to be associated with 7 drugs and 7 conditions by eHealthMe. Check the latest studies of Post-menopausal bleeding.

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, 21, 2026

42,607 people reported to have side effects when taking Prempro.
Among them, 13 people (0.03%) have Post-menopausal bleeding.

Could Prempro cause Post-menopausal bleeding?

Among these 13 people:

What is the age of people who have Post-menopausal bleeding when taking Prempro? *

What are other drugs people take besides Prempro? *

What are other side effects people have besides Post-menopausal bleeding? *

Gallstones (stone formation by bile component): 3 people, 23.08%
Constipation: 3 people, 23.08%
Back Pain: 3 people, 23.08%
Abdominal Pain Lower: 3 people, 23.08%
Ovarian Cysts (fluid filled sacs of the ovary): 2 people, 15.38%
Nausea (feeling of having an urge to vomit): 2 people, 15.38%
Initial Insomnia (feeling of inadequate or poor-quality sleep): 2 people, 15.38%
Abdominal Pain Upper: 2 people, 15.38%
Peripheral Coldness: 1 person, 7.69%
Pancreatic Duct Obstruction: 1 person, 7.69%

* Approximation only. Some reports may have incomplete information.

Do you take Prempro and have Post-menopausal bleeding?

- Check whether Post-menopausal bleeding 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 Prempro:

Prempro (42,950 reports)

Post-menopausal bleeding treatments and more:

Post-menopausal bleeding (245 reports)

How severe was Post-menopausal bleeding and when was it recovered:

Post-menopausal bleeding in Prempro

Expand to all the drugs that have ingredients of estrogens, conjugated; medroxyprogesterone acetate:

Post-menopausal bleeding and drugs with ingredients of estrogens, conjugated; medroxyprogesterone acetate

Sub-studies by age:

0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+

Browse all side effects of Prempro:

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 Post-menopausal bleeding:

Post-menopausal bleeding (7 drugs)

Browse all the conditions that are associated with Post-menopausal bleeding:

Post-menopausal bleeding (7 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on estrogens, conjugated; medroxyprogesterone acetate (the active ingredients of Prempro) and Prempro (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.