Ursodiol and Letairis drug interactions - a phase IV clinical study of FDA data

Summary:

Drug interactions are reported among people who take Ursodiol (ursodiol) and Letairis (ambrisentan). Common drug interactions include atrial fibrillation among females and dyspnoea among males.

The phase IV clinical study analyzes what interactions people have when they take Ursodiol and Letairis. It is created by eHealthMe based on reports of 76 people who take the same drugs from the FDA, and is updated regularly.

What is Ursodiol?

Ursodiol has active ingredients of ursodiol. It is often used in primary biliary cirrhosis. eHealthMe is studying from 19,061 Ursodiol users. Check the latest studies of Ursodiol.

What is Letairis?

Letairis has active ingredients of ambrisentan. It is often used in pulmonary hypertension. eHealthMe is studying from 94,041 Letairis users. Check the latest studies of Letairis.



On Jul, 18, 2026

76 people who take Ursodiol and Letairis together, and have interactions are studied.

Ursodiol and Letairis drug interactions.

What are the common drug interactions of Ursodiol and Letairis, by gender? *:

female:

  1. Atrial fibrillation (fibrillation of the muscles of the atria of the heart)
  2. Bone pain
  3. Brain natriuretic peptide increased
  4. Cardiac failure
  5. Cardiomegaly (increased size of heart than normal)
  6. Contusion (a type of hematoma of tissue in which capillaries)
  7. Decreased appetite
  8. Depression
  9. Dilatation ventricular
  10. Dysphagia (a condition in which swallowing is difficult or painful)

male:

  1. Dyspnoea (difficult or laboured respiration)
  2. Cough
  3. Gastric haemorrhage (bleeding stomach)
  4. Gastritis (inflammation of stomach)
  5. Gastroduodenitis (an inflammation of the mucous membrane of the stomach and duodenum)
  6. Haemoptysis (blood-stained sputum from the bronchi, larynx, trachea, or lungs)
  7. Haemorrhoids (a swollen vein or group of veins in the region of the anus)
  8. Iron deficiency anaemia
  9. Leukaemia recurrent (repeat cancer of bone marrow or blood cells)
  10. Lung transplant

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

0-1:

n/a

2-9:

n/a

10-19:

n/a

20-29:

  1. Acute respiratory failure
  2. Brain natriuretic peptide increased
  3. Cardiomegaly (increased size of heart than normal)
  4. Chest discomfort
  5. Death
  6. Dilatation ventricular
  7. Dyspnoea (difficult or laboured respiration)
  8. Fluid overload (too much fluid in the blood)
  9. Fluid retention (an abnormal accumulation of fluid in the blood)
  10. Gastrointestinal haemorrhage (bleeding gastrointestinal tract)

30-39:

n/a

40-49:

  1. Haemorrhage (bleeding)
  2. Headache (pain in head)
  3. Oedema (fluid collection in tissue)
  4. Anaemia (lack of blood)

50-59:

  1. Throat irritation
  2. Weight decreased
  3. Cardiac failure
  4. Death
  5. Diarrhoea
  6. Fall
  7. Influenza
  8. Localised oedema (fluid retention in a particular part of the body)
  9. Nausea (feeling of having an urge to vomit)
  10. Oedema (fluid collection in tissue)

60+:

  1. Dyspnoea (difficult or laboured respiration)
  2. Cough
  3. Death
  4. Headache (pain in head)
  5. Nasopharyngitis (inflammation of the nasopharynx)
  6. Peripheral swelling
  7. Pneumonia
  8. Renal failure acute (rapid kidney dysfunction)
  9. Asthenia (weakness)
  10. Chest discomfort

What are the existing conditions these people have? *

  1. Primary Pulmonary Hypertension (primary high blood pressure that affects the arteries in the lungs and the right side of your heart): 47 people, 61.84%
  2. Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 4 people, 5.26%
  3. Gallstones (stone formation by bile component): 4 people, 5.26%

* Approximation only. Some reports may have incomplete information.

Do you take Ursodiol and Letairis?

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Related studies:

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

Browse all drug interactions of Ursodiol and Letairis:

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 Ursodiol:

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 Letairis:

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 Ursodiol 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 Letairis 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 ursodiol and ambrisentan (the active ingredients of Ursodiol and Letairis, respectively), and Ursodiol and Letairis (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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