Tracleer and Atacand drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Tracleer (bosentan) and Atacand (candesartan cilexetil). Common drug interactions include diverticulum among females and arrhythmia among males.
The phase IV clinical study analyzes what interactions people have when they take Tracleer and Atacand. It is created by eHealthMe based on reports of 38 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 Atacand?
Atacand has active ingredients of candesartan cilexetil. It is often used in high blood pressure. eHealthMe is studying from 22,473 Atacand users. Check the latest studies of Atacand.
eHealthMe: drug outcomes in the real world
eHealthMe runs one of the largest post-marketing drug safety studies in the world. We study millions of patients and 5,000 more each day. Our data-driven phase IV clinical trials have been referenced on 800+ peer-reviewed medical publications including The Lancet, Mayo Clinic Proceedings, and Nature. Tools to study our phase IV findings are available to the public, anonymous and free >>>.
38 people who take Tracleer and Atacand together, and have interactions are studied.

What are the common drug interactions of Tracleer and Atacand, by gender? *:
female:
- Diverticulum (out pouching of a hollow (or a fluid-filled) structure in the body)
- Dyspnoea exertional (breathlessness or shortness of breath)
- Hepatic congestion (liver congestion)
- Hepatic failure (liver failure)
- Hypotension (abnormally low blood pressure)
- International normalised ratio increased
- Lethargy (tiredness)
- Loss of consciousness
- Mental status changes (general changes in brain function, such as confusion, amnesia (memory loss), loss of alertness, loss of orientation)
- Multi-organ failure (multisystem organ failure)
male:
- Arrhythmia (irregular heartbeat)
- Skin ulcer
- Ascites (accumulation of fluid in the abdominal cavity)
- Cardiac failure congestive
- Diarrhoea
- Enterococcal infection
- Hepatic steatosis (fatty liver disease)
- Hepatomegaly (abnormal enlargement of the liver)
- Pleural effusion (water on the lungs)
- Pseudomonas infection (pseudomonas infection is caused by a bacterium, pseudomonas aeruginosa)
What are the common drug interactions of Tracleer and Atacand, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
- Drug ineffective
- Systemic lupus erythematosus (an autoimmune disease, which means the body's immune system mistakenly, attacks healthy tissue)
40-49:
- Alanine aminotransferase increased
- Arrhythmia (irregular heartbeat)
- Aspartate aminotransferase increased
- Brain death
- Brain hypoxia (reduced supply of oxygen to the brain)
- Bronchopulmonary aspergillosis (lung disorder caused by aspergillus fungi)
- Cardio-respiratory arrest (sudden dysfunction of heart and lungs)
- Cardioversion
- Cerebral hypoperfusion (a condition in which the brain doesn't get enough blood)
- Coma (state of unconsciousness lasting more than six hours)
50-59:
- Gastric disorder (disease of stomach)
- Heart rate increased
- Malaise (a feeling of general discomfort or uneasiness)
- Sinusitis (inflammation of sinus)
- Pulmonary hypertension (increase in blood pressure in the lung artery)
- Cholelithiasis (the presence or formation of gallstones in the gallbladder or bile ducts)
- Diabetes mellitus (diabetes, caused by a deficiency of the pancreatic hormone insulin)
- Gastrointestinal disorder (functional problems of gastrointestinal tract)
- Neuropathy peripheral (surface nerve damage)
- Vitamin b12 deficiency
60+:
- Dyspnoea (difficult or laboured respiration)
- Blood alkaline phosphatase increased
- Pneumonia
- Alanine aminotransferase increased
- Amnesia (deficit in memory caused by brain damage, disease, or psychological trauma)
- Aspartate aminotransferase increased
- Conjunctivitis (pink eye)
- Diarrhoea
- Emotional disorder
- Fatigue (feeling of tiredness)
What are the existing conditions these people have? *
- Pulmonary Hypertension (increase in blood pressure in the lung artery): 20 people, 52.63%
- Systemic Sclerosis (an autoimmune or connective tissue disease. it is characterized by thickening of the skin): 2 people, 5.26%
* Approximation only. Some reports may have incomplete information.
Do you take Tracleer and Atacand?
- 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 Tracleer and Atacand:
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 Atacand:
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 Atacand 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 candesartan cilexetil (the active ingredients of Tracleer and Atacand, respectively), and Tracleer and Atacand (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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