Pradaxa and Silodosin drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Pradaxa (dabigatran etexilate mesylate) and Silodosin (silodosin). Common drug interactions include dizziness among males.
The phase IV clinical study analyzes what interactions people have when they take Pradaxa and Silodosin. It is created by eHealthMe based on reports of 37 people who take the same drugs from the FDA, and is updated regularly.
What is Pradaxa?
Pradaxa has active ingredients of dabigatran etexilate mesylate. It is often used in atrial fibrillation/flutter. eHealthMe is studying from 86,906 Pradaxa users. Check the latest studies of Pradaxa.
What is Silodosin?
Silodosin has active ingredients of silodosin. eHealthMe is studying from 3,839 Silodosin users. Check the latest studies of Silodosin.
37 people who take Pradaxa and Silodosin together, and have interactions are studied.

What are the common drug interactions of Pradaxa and Silodosin, by gender? *:
female:
n/a
male:
- Dizziness
- Bradycardia (abnormally slow heart action)
- Mucosal dryness (dryness of mucous membrane)
- Oedema peripheral (superficial swelling)
- Presyncope
- Pulmonary congestion (congestion in the lungs)
- Renal disorder (kidney disease)
- Skin disorder (skin disease)
- Syncope (loss of consciousness with an inability to maintain postural tone)
- Anaemia (lack of blood)
What are the common drug interactions of Pradaxa and Silodosin, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
n/a
40-49:
n/a
50-59:
n/a
60+:
- Bradycardia (abnormally slow heart action)
- Dizziness
- Mucosal dryness (dryness of mucous membrane)
- Oedema peripheral (superficial swelling)
- Presyncope
- Pulmonary congestion (congestion in the lungs)
- Renal disorder (kidney disease)
- Skin disorder (skin disease)
- Syncope (loss of consciousness with an inability to maintain postural tone)
- Anaemia (lack of blood)
What are the existing conditions these people have? *
- High Blood Pressure: 10 people, 27.03%
- Type 2 Diabetes: 7 people, 18.92%
- Cardiac Failure: 6 people, 16.22%
- High Blood Cholesterol: 4 people, 10.81%
- Enlarged Prostate: 4 people, 10.81%
- Stroke (sudden death of a portion of the brain cells due to a lack of oxygen): 3 people, 8.11%
- Prostatomegaly (enlargement of the prostate): 3 people, 8.11%
- Lung Adenocarcinoma Stage Iv (the cancer has spread to other organs of the body, such as the other lung, brain, or liver): 3 people, 8.11%
- Idiopathic Pulmonary Fibrosis (chronic lung disease): 3 people, 8.11%
- Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 3 people, 8.11%
* Approximation only. Some reports may have incomplete information.
Do you take Pradaxa and Silodosin?
- Personalize this study to your gender, age, symptoms and drugs
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously
Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Pradaxa and Silodosin:
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 zSub-studies by gender and age:
Female: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+
Male: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+
Browse all side effects of Pradaxa:
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 zBrowse all side effects of Silodosin:
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 zBrowse all interactions between Pradaxa and drugs from A to Z:
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 zBrowse all interactions between Silodosin and drugs from A to Z:
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 zHow the study uses the data?
The study uses data from the FDA. It is based on dabigatran etexilate mesylate and silodosin (the active ingredients of Pradaxa and Silodosin, respectively), and Pradaxa and Silodosin (the brand names). 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.
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