Tracleer and Soliris drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Tracleer (bosentan) and Soliris (eculizumab). Common drug interactions include haemoglobin decreased among females and alanine aminotransferase increased among males.
The phase IV clinical study analyzes what interactions people have when they take Tracleer and Soliris. It is created by eHealthMe based on reports of 12 people who take the same drugs from the FDA, and is updated regularly.
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.
What is Soliris?
Soliris has active ingredients of eculizumab. It is often used in paroxysmal nocturnal hemoglobinuria (pnh). eHealthMe is studying from 58,821 Soliris users. Check the latest studies of Soliris.
12 people who take Tracleer and Soliris together, and have interactions are studied.

What are the common drug interactions of Tracleer and Soliris, by gender? *:
female:
- Haemoglobin decreased
- Fatigue (feeling of tiredness)
- Asthenia (weakness)
- Back pain
- Jaundice (a yellowish pigmentation of the skin, the conjunctival membranes)
- Migraine (headache)
- Amnesia (deficit in memory caused by brain damage, disease, or psychological trauma)
- Dyspnoea (difficult or laboured respiration)
- Gastric disorder (disease of stomach)
- Haemoglobinuria (the presence of free haemoglobin in the urine)
male:
- Alanine aminotransferase increased
- Aspartate aminotransferase increased
- Viral infection
- Femur fracture
- Platelet count decreased
- Pneumonia
- Pseudomonas infection (pseudomonas infection is caused by a bacterium, pseudomonas aeruginosa)
- Pulmonary hypertension (increase in blood pressure in the lung artery)
- Heart valve replacement
- Blood lactate dehydrogenase increased
What are the common drug interactions of Tracleer and Soliris, by age (0-1 to 60+)? *:
0-1:
- Femur fracture
- Platelet count decreased
- Pneumonia
- Pseudomonas infection (pseudomonas infection is caused by a bacterium, pseudomonas aeruginosa)
- Pulmonary hypertension (increase in blood pressure in the lung artery)
2-9:
n/a
10-19:
- Alanine aminotransferase increased
- Aspartate aminotransferase increased
- Blood lactate dehydrogenase increased
- Chest pain
- Contusion (a type of hematoma of tissue in which capillaries)
- Fatigue (feeling of tiredness)
- Feeling hot
- Haemoglobin decreased
- Headache (pain in head)
- Liver disorder (liver diseases)
20-29:
n/a
30-39:
n/a
40-49:
- Abdominal pain
- Alanine aminotransferase increased
- Aspartate aminotransferase increased
- Blood alkaline phosphatase increased
- Dehydration (dryness resulting from the removal of water)
- Fatigue (feeling of tiredness)
- Gamma-glutamyltransferase increased
- Haemolysis (breaking open of red blood cells and the release of haemoglobin into the surrounding fluid)
50-59:
- Amnesia (deficit in memory caused by brain damage, disease, or psychological trauma)
- Asthenia (weakness)
- Back pain
- Dyspnoea (difficult or laboured respiration)
- Fatigue (feeling of tiredness)
- Gastric disorder (disease of stomach)
- Haemoglobin decreased
- Haemoglobinuria (the presence of free haemoglobin in the urine)
- Headache (pain in head)
- Hepatic enzyme increased
60+:
- Pneumonia
- Haemoglobin decreased
- Back pain
- Blood glucose increased
- Chest discomfort
- Chest pain
- Contusion (a type of hematoma of tissue in which capillaries)
- Fluid retention (an abnormal accumulation of fluid in the blood)
- Hot flush (sudden feelings of heat)
- Jaundice (a yellowish pigmentation of the skin, the conjunctival membranes)
What are the existing conditions these people have? *
- Paroxysmal Nocturnal Haemoglobinuria (haemoglobin in the urine): 6 people, 50.00%
- Haemolytic Uraemic Syndrome (blood clotting disease caused by e. coli infection, birth control pills, pneumonia, medications, and more): 4 people, 33.33%
- High Blood Pressure: 2 people, 16.67%
- Thrombotic Microangiopathy (a pathology that results in thrombosis in capillaries and arterioles, due to an endothelial injury): 1 person, 8.33%
- Seasonal Allergy (allergic condition due to certain season): 1 person, 8.33%
- Renal Impairment (severely reduced kidney function): 1 person, 8.33%
- Graft Versus Host Disease (the donated bone marrow or stem cells view the recipient's body as foreign, and the donated cells/bone marrow attack the body): 1 person, 8.33%
- Cor Pulmonale Chronic (long lasting enlargement of the right ventricle of the heart): 1 person, 8.33%
- Bone Pain: 1 person, 8.33%
- Birth Control: 1 person, 8.33%
* Approximation only. Some reports may have incomplete information.
Do you take Tracleer and Soliris?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Tracleer and Soliris:
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 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 side effects of Soliris:
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 zBrowse all interactions between Soliris 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 bosentan and eculizumab (the active ingredients of Tracleer and Soliris, respectively), and Tracleer and Soliris (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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