Nasacort and Tracleer drug interactions - a phase IV clinical study of FDA data

Summary:

Drug interactions are reported among people who take Nasacort (triamcinolone acetonide) and Tracleer (bosentan). Common drug interactions include weight decreased among females and dysphagia among males.

The phase IV clinical study analyzes what interactions people have when they take Nasacort and Tracleer. It is created by eHealthMe based on reports of 26 people who take the same drugs from the FDA, and is updated regularly.

What is Nasacort?

Nasacort has active ingredients of triamcinolone acetonide. It is often used in allergies. eHealthMe is studying from 13,298 Nasacort users. Check the latest studies of Nasacort.

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.



On Jul, 16, 2026

26 people who take Nasacort and Tracleer together, and have interactions are studied.

Nasacort and Tracleer drug interactions.

What are the common drug interactions of Nasacort and Tracleer, by gender? *:

female:

  1. Weight decreased
  2. Autoimmune hepatitis
  3. Dyspnoea (difficult or laboured respiration)
  4. Diarrhoea
  5. Pruritus (severe itching of the skin)
  6. Anxiety
  7. Dizziness
  8. Fall
  9. Laceration (tearing of soft body tissue)
  10. Asthenia (weakness)

male:

  1. Dysphagia (a condition in which swallowing is difficult or painful)
  2. Dyspnoea (difficult or laboured respiration)
  3. Diastolic dysfunction
  4. Fatigue (feeling of tiredness)
  5. Presyncope
  6. Pulmonary hypertension (increase in blood pressure in the lung artery)
  7. Right ventricular systolic pressure decreased
  8. Syncope (loss of consciousness with an inability to maintain postural tone)
  9. Tricuspid valve incompetence (inefficient heart valve)
  10. Eye oedema (swelling or thickening of the macula, the area of the retina responsible for central vision)

What are the common drug interactions of Nasacort and Tracleer, by age (0-1 to 60+)? *:

0-1:

n/a

2-9:

  1. Immobile (not moving)
  2. Infusion site pain
  3. Diarrhoea
  4. Flushing (the warm, red condition of human skin)

10-19:

  1. Pulmonary hypertension (increase in blood pressure in the lung artery)
  2. Right ventricular systolic pressure decreased
  3. Syncope (loss of consciousness with an inability to maintain postural tone)
  4. Tricuspid valve incompetence (inefficient heart valve)
  5. Petechiae (a small red or purple spot caused by bleeding into the skin)
  6. Purpura (purplish discoloration of the skin)
  7. Bundle branch block right (absence of transmission of electric impulses from the atrioventricular (av) bundle of his to the right ventricle)
  8. Cardiac disorder
  9. Cardiac hypertrophy (thickening of the heart muscle)
  10. Diastolic dysfunction

20-29:

n/a

30-39:

n/a

40-49:

  1. Cough
  2. Stomatitis (inflammation of mucous membrane of mouth)

50-59:

  1. Autoimmune hepatitis
  2. Drug ineffective
  3. Headache (pain in head)
  4. Respiratory failure (inadequate gas exchange by the respiratory system)
  5. Amnesia (deficit in memory caused by brain damage, disease, or psychological trauma)
  6. Anxiety
  7. Cerebral haemorrhage (bleeding within the brain)
  8. Chest pain
  9. Contusion (a type of hematoma of tissue in which capillaries)
  10. Death

60+:

  1. Dyspnoea (difficult or laboured respiration)
  2. Oedema peripheral (superficial swelling)
  3. Rash
  4. Vomiting
  5. Abdominal pain
  6. Abscess limb (limb infection)
  7. Anxiety
  8. Aspartate aminotransferase increased
  9. Blood alkaline phosphatase increased
  10. Blood bilirubin increased

What are the existing conditions these people have? *

  1. Pulmonary Hypertension (increase in blood pressure in the lung artery): 12 people, 46.15%
  2. Pulmonary Hypertension Secondary (increase in blood pressure in the lung artery): 3 people, 11.54%
  3. Insomnia (sleeplessness): 2 people, 7.69%
  4. Discomfort: 2 people, 7.69%

* Approximation only. Some reports may have incomplete information.

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Related studies:

Effectiveness of, side effects of, and alternative drugs to the 2 drugs:

Browse all drug interactions of Nasacort 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 z

Sub-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 Nasacort:

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 z

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 z

Browse all interactions between Nasacort 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 z

Browse 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 z

How the study uses the data?

The study uses data from the FDA. It is based on triamcinolone acetonide and bosentan (the active ingredients of Nasacort and Tracleer, respectively), and Nasacort 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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