Budesonide and Prothrombin level decreased - a phase IV clinical study of FDA data

Summary:

Prothrombin level decreased is reported as a side effect among people who take Budesonide (budesonide), especially for people who are male, 60+ old, also take Ketek, and have Atrial fibrillation/flutter.

The phase IV clinical study analyzes which people have Prothrombin level decreased when taking Budesonide. It is created by eHealthMe based on reports of 42,490 people who have side effects when taking Budesonide from the FDA, and is updated regularly.

What is Budesonide?

Budesonide has active ingredients of budesonide. It is often used in asthma. eHealthMe is studying from 42,933 Budesonide users. Check the latest studies of Budesonide.

What is Prothrombin level decreased?

Prothrombin level decreased is found to be associated with 203 drugs and 465 conditions by eHealthMe. Check the latest studies of Prothrombin level decreased.

On Jul, 28, 2026

42,490 people reported to have side effects when taking Budesonide.
Among them, 12 people (0.03%) have Prothrombin level decreased.

Could Budesonide cause Prothrombin level decreased?

Among these 12 people:

What is the gender of people who have Prothrombin level decreased when taking Budesonide? *

female: 20 %
male: 80 %

What is the age of people who have Prothrombin level decreased when taking Budesonide? *

What are other drugs people take besides Budesonide? *

What are other side effects people have besides Prothrombin level decreased? *

International Normalised Ratio Increased: 10 people, 83.33%
Coughing Up Blood: 9 people, 75.00%
Bronchitis (inflammation of the mucous membrane in the bronchial tubes): 9 people, 75.00%
Overdose: 8 people, 66.67%
Thrombocytopenia (decrease of platelets in blood): 2 people, 16.67%
Gastrointestinal Haemorrhage (bleeding gastrointestinal tract): 1 person, 8.33%
Escherichia Sepsis (bacterial infection by escherichia coli): 1 person, 8.33%
Erection Problems: 1 person, 8.33%
Epididymitis (pain in the scrotum or testicle): 1 person, 8.33%
Drug Toxicity: 1 person, 8.33%

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): 10 people, 83.33%
Tachyarrhythmia (disturbance of the heart rhythm in which the heart rate is abnormally increased): 9 people, 75.00%
Bronchitis (inflammation of the mucous membrane in the bronchial tubes): 9 people, 75.00%
Coughing Up Blood: 6 people, 50.00%

* Approximation only. Some reports may have incomplete information.

Do you take Budesonide and have Prothrombin level decreased?

- Check whether Prothrombin level decreased 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 Budesonide:

Budesonide (42,933 reports)

Browse all side effects of Budesonide:

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 Prothrombin level decreased:

Prothrombin level decreased (203 drugs)

Browse all the conditions that are associated with Prothrombin level decreased:

Prothrombin level decreased (465 conditions)

How the study uses the data?

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