Pulmozyme and Tracleer drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Pulmozyme (dornase alfa) and Tracleer (bosentan). Common drug interactions include disease progression among females and dyspnoea among males.
The phase IV clinical study analyzes what interactions people have when they take Pulmozyme and Tracleer. It is created by eHealthMe based on reports of 17 people who take the same drugs from the FDA, and is updated regularly.
What is Pulmozyme?
Pulmozyme has active ingredients of dornase alfa. It is often used in cystic fibrosis. eHealthMe is studying from 20,012 Pulmozyme users. Check the latest studies of Pulmozyme.
What is Tracleer?
Tracleer has active ingredients of bosentan. It is often used in primary pulmonary hypertension. eHealthMe is studying from 55,125 Tracleer users. Check the latest studies of Tracleer.
17 people who take Pulmozyme and Tracleer together, and have interactions are studied.

What are the common drug interactions of Pulmozyme and Tracleer, by gender? *:
female:
- Disease progression
- Enterococcal sepsis
- Fungaemia (fungi circulate in the blood)
- Hypomagnesaemia (electrolyte disturbance in which there is an abnormally low level of magnesium in the blood)
- Nasopharyngitis (inflammation of the nasopharynx)
- Right ventricular failure (right half of the heart fails to work)
- Supraventricular tachycardia (rapid heart rhythm originating at or above the atrioventricular node)
- Fatigue (feeling of tiredness)
- Dyspnoea (difficult or laboured respiration)
- Blood urea increased
male:
- Dyspnoea (difficult or laboured respiration)
- Nausea (feeling of having an urge to vomit)
- Aspartate aminotransferase increased
- Blood sodium decreased
- Cardiac failure
- Cardiomegaly (increased size of heart than normal)
- Generalised oedema (swelling all over the body)
- Hypokalaemia (low potassium)
- Pericardial effusion (fluid around the heart)
- Pleural effusion (water on the lungs)
What are the common drug interactions of Pulmozyme and Tracleer, by age (0-1 to 60+)? *:
0-1:
- Bronchial secretion retention
- Electrolyte imbalance
- Gastroenteritis norovirus (inflammation of stomach and intestine caused by norovirus infection)
- Respiratory distress (difficulty in breathing)
- Tracheostomy malfunction (a surgical opening of trachea not working normally)
- Hospitalisation
2-9:
- Adverse drug reaction
- Bacterial infection
- Blood urea increased
- Catheter site discharge
- Catheter site erythema (redness of skin at catheter site)
- Catheter site pain
- Diarrhoea
- Fatigue (feeling of tiredness)
- Haemoglobin increased
- Heart rate decreased
10-19:
- Ascites (accumulation of fluid in the abdominal cavity)
- Aspartate aminotransferase increased
- Cardiomegaly (increased size of heart than normal)
- Generalised oedema (swelling all over the body)
- Hypokalaemia (low potassium)
- Pericardial effusion (fluid around the heart)
- Weight increased
- Dyspnoea (difficult or laboured respiration)
- Pleural effusion (water on the lungs)
- Pyrexia (fever)
20-29:
- Dyspnoea (difficult or laboured respiration)
- Fatigue (feeling of tiredness)
- Fluid retention (an abnormal accumulation of fluid in the blood)
- General physical health deterioration (weak health status)
- Oxygen saturation decreased
- Pulmonary function test decreased
- Concomitant disease progression (progress in accompanying disease)
- Disease progression
- Right ventricular failure (right half of the heart fails to work)
- Cardiac failure
30-39:
- Atrial tachycardia (rhythm disturbance that arises in the atria)
- Blood magnesium decreased
- Catheter related complication
- Deep vein thrombosis (blood clot in a major vein that usually develops in the legs and/or pelvis)
- Dyspnoea (difficult or laboured respiration)
- Enterococcal sepsis
- Fungaemia (fungi circulate in the blood)
- Hypomagnesaemia (electrolyte disturbance in which there is an abnormally low level of magnesium in the blood)
- Supraventricular tachycardia (rapid heart rhythm originating at or above the atrioventricular node)
40-49:
n/a
50-59:
n/a
60+:
n/a
What are the existing conditions these people have? *
- Pulmonary Hypertension (increase in blood pressure in the lung artery): 5 people, 29.41%
- Pulmonary Hypertension Secondary (increase in blood pressure in the lung artery): 2 people, 11.76%
* Approximation only. Some reports may have incomplete information.
Do you take Pulmozyme and Tracleer?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Pulmozyme and Tracleer:
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 Pulmozyme:
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 Tracleer:
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 Pulmozyme 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 Tracleer 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 dornase alfa and bosentan (the active ingredients of Pulmozyme and Tracleer, respectively), and Pulmozyme and Tracleer (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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