Luvox and Pradaxa drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Luvox (fluvoxamine maleate) and Pradaxa (dabigatran etexilate mesylate). Common drug interactions include weight increased among females and vomiting among males.
The phase IV clinical study analyzes what interactions people have when they take Luvox and Pradaxa. It is created by eHealthMe based on reports of 18 people who take the same drugs from the FDA, and is updated regularly.
What is Luvox?
Luvox has active ingredients of fluvoxamine maleate. It is often used in obsessive-compulsive disorder. eHealthMe is studying from 13,439 Luvox users. Check the latest studies of Luvox.
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.
18 people who take Luvox and Pradaxa together, and have interactions are studied.

What are the common drug interactions of Luvox and Pradaxa, by gender? *:
female:
- Weight increased
- Suicidal ideation
- Dyspnoea (difficult or laboured respiration)
- Dyskinesia (abnormality or impairment of voluntary movement)
- Dyspepsia (indigestion)
- Musculoskeletal discomfort (discomfort in the body's muscles, joints, tendons, ligaments and nerves)
- Periodic limb movement disorder
- Thrombosis (formation of a blood clot inside a blood vessel)
- Hospitalisation
- Pulmonary embolism (blockage of the main artery of the lung)
male:
- Vomiting
- Abasia (inability to walk)
- Chronic kidney disease
- Conjunctival haemorrhage (bleeding underneath the conjunctiva)
- Constipation
- Drug clearance decreased
- Drug hypersensitivity
- Drug ineffective
- Dysgraphia (impaired ability to learn to write)
- Dyspnoea (difficult or laboured respiration)
What are the common drug interactions of Luvox and Pradaxa, 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:
- Aphasia (damage to the parts of the brain that control language)
- Dysgraphia (impaired ability to learn to write)
- Transient ischaemic attack (a transient episode of neurologic dysfunction caused by ischemia (loss of blood flow))
- Visual impairment
60+:
- Dyspnoea (difficult or laboured respiration)
- Abdominal discomfort
- Erosive oesophagitis (acid reflux disease can cause tissue damage in the oesophagus over time)
- Gastrointestinal haemorrhage (bleeding gastrointestinal tract)
- Haematemesis (vomiting of blood)
- Hiatus hernia (hernia resulting from the protrusion of part of the stomach through the diaphragm)
- Loss of consciousness
- Oxygen saturation decreased
- Upper gastrointestinal haemorrhage (upper gastrointestinal bleeding)
- Vomiting
What are the existing conditions these people have? *
- Narcolepsy (brain's inability to regulate sleep-wake cycles normally): 6 people, 33.33%
- Pain: 3 people, 16.67%
- High Blood Pressure: 2 people, 11.11%
- Primary Pulmonary Hypertension (primary high blood pressure that affects the arteries in the lungs and the right side of your heart): 2 people, 11.11%
- Neuralgia (pain in one or more nerves): 2 people, 11.11%
- High Blood Cholesterol: 2 people, 11.11%
- Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 1 person, 5.56%
- Adverse Event: 1 person, 5.56%
- Back Pain: 1 person, 5.56%
- Bladder Spasm: 1 person, 5.56%
* Approximation only. Some reports may have incomplete information.
Do you take Luvox and Pradaxa?
- 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 Luvox and 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 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 Luvox:
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 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 interactions between Luvox 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 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 zRelated publications that referenced our studies
- Pang, T., & Gudi, A., "Chest pain following the use of fluvoxamine in depression", Proceedings of Singapore Healthcare, 2018 Jan .
- Pang, T., & Gudi, A., "Chest pain following the use of fluvoxamine in depression", Proceedings of Singapore Healthcare, 2018 Jan .
How the study uses the data?
The study uses data from the FDA. It is based on fluvoxamine maleate and dabigatran etexilate mesylate (the active ingredients of Luvox and Pradaxa, respectively), and Luvox and Pradaxa (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.
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