Glimepiride and Post procedural haemorrhage - a phase IV clinical study of FDA data

Summary:

Post procedural haemorrhage is reported as a side effect among people who take Glimepiride (glimepiride), especially for people who are male, 60+ old, also take Metformin, and have Atrial fibrillation/flutter.

The phase IV clinical study analyzes which people have Post procedural haemorrhage when taking Glimepiride. It is created by eHealthMe based on reports of 45,086 people who have side effects when taking Glimepiride from the FDA, and is updated regularly.

What is Glimepiride?

Glimepiride has active ingredients of glimepiride. It is often used in diabetes. eHealthMe is studying from 45,909 Glimepiride users. Check the latest studies of Glimepiride.

What is Post procedural haemorrhage?

Post procedural haemorrhage (post procedural bleeding) is found to be associated with 664 drugs and 854 conditions by eHealthMe. Check the latest studies of Post procedural haemorrhage.

On Jul, 12, 2026

45,086 people reported to have side effects when taking Glimepiride.
Among them, 30 people (0.07%) have Post procedural haemorrhage.

Could Glimepiride cause Post procedural haemorrhage?

Among these 30 people:

What is the gender of people who have Post procedural haemorrhage when taking Glimepiride? *

female: 29.63 %
male: 70.37 %

What is the age of people who have Post procedural haemorrhage when taking Glimepiride? *

What are other drugs people take besides Glimepiride? *

What are other side effects people have besides Post procedural haemorrhage? *

Haemorrhage (bleeding): 7 people, 23.33%
Dyspnea (difficult or laboured breathing): 7 people, 23.33%
Haematoma (collection of blood outside the blood vessels): 5 people, 16.67%
Diarrhea: 5 people, 16.67%
Nausea And Vomiting: 4 people, 13.33%
Hypotension (abnormally low blood pressure): 4 people, 13.33%
Hypovolaemic Shock (shock caused by severe blood or fluid loss): 4 people, 13.33%
Lactic Acidosis (low ph in body tissues): 3 people, 10.00%
Swelling: 3 people, 10.00%
Fatigue (feeling of tiredness): 3 people, 10.00%

What are the existing conditions these people have? *

Atrial Fibrillation/flutter (atrial fibrillation and flutter are abnormal heart rhythms in which the atria, or upper chambers of the heart, are out of sync with the ventricles): 9 people, 30.00%
High Blood Pressure: 8 people, 26.67%
Stroke (sudden death of a portion of the brain cells due to a lack of oxygen): 6 people, 20.00%
High Blood Cholesterol: 4 people, 13.33%
Sick Sinus Syndrome (a collection of heart rhythm disorders): 2 people, 6.67%
Thyroid Diseases: 2 people, 6.67%
Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 2 people, 6.67%
Pain: 2 people, 6.67%
Gout (uric acid crystals building up in the body): 2 people, 6.67%
Crohn's Disease (a condition that causes inflammation of the gastrointestinal tract): 2 people, 6.67%

* Approximation only. Some reports may have incomplete information.

Do you take Glimepiride and have Post procedural haemorrhage?

- Check whether Post procedural haemorrhage 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 Glimepiride:

Glimepiride (45,909 reports)

Browse all side effects of Glimepiride:

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 procedural haemorrhage:

Post procedural haemorrhage (664 drugs)

Browse all the conditions that are associated with Post procedural haemorrhage:

Post procedural haemorrhage (854 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on glimepiride (the active ingredients of Glimepiride) and Glimepiride (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.