Gleevec and Letairis drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Gleevec (imatinib mesylate) and Letairis (ambrisentan). Common drug interactions include death among females and infection among males.
The phase IV clinical study analyzes what interactions people have when they take Gleevec and Letairis. It is created by eHealthMe based on reports of 19 people who take the same drugs from the FDA, and is updated regularly.
What is Gleevec?
Gleevec has active ingredients of imatinib mesylate. It is often used in chronic myelogenous leukemia (cml). eHealthMe is studying from 35,415 Gleevec users. Check the latest studies of Gleevec.
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.
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 >>>.
19 people who take Gleevec and Letairis together, and have interactions are studied.

What are the common drug interactions of Gleevec and Letairis, by gender? *:
female:
- Death
- Dyspnoea (difficult or laboured respiration)
- Cerebrovascular accident (sudden death of some brain cells due to lack of oxygen when the blood flow to the brain is impaired by blockage or rupture)
- Fluid retention (an abnormal accumulation of fluid in the blood)
- Hemiplegia (paralysis of one side of the body)
- Malignant melanoma (skin cancer rises from melancytes)
- Neoplasm malignant (cancer tumour)
- Speech disorder
- Syncope (loss of consciousness with an inability to maintain postural tone)
- White blood cell count decreased
male:
- Infection
- Bronchitis (inflammation of the mucous membrane in the bronchial tubes)
- Swelling face
- Vomiting
- Hospitalisation
- Influenza
- Medical device complication
- Pyrexia (fever)
- Surgery
- Dyspnoea (difficult or laboured respiration)
What are the common drug interactions of Gleevec and Letairis, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
- Hospitalisation
- Infection
- Influenza
- Medical device complication
- Pyrexia (fever)
- Surgery
20-29:
n/a
30-39:
n/a
40-49:
- Cardiac failure congestive
- Renal failure (kidney dysfunction)
- Sepsis (a severe blood infection that can lead to organ failure and death)
- Syncope (loss of consciousness with an inability to maintain postural tone)
50-59:
- Brain abscess
- Cardio-respiratory arrest (sudden dysfunction of heart and lungs)
- Death
- Meningitis (inflammation of the protective membranes covering the brain and spinal cord, known collectively as the meninges)
- Mental status changes (general changes in brain function, such as confusion, amnesia (memory loss), loss of alertness, loss of orientation)
60+:
- Death
- Dyspnoea (difficult or laboured respiration)
- Neoplasm malignant (cancer tumour)
- Pulmonary oedema (fluid accumulation in the lungs)
- Right ventricular failure (right half of the heart fails to work)
- White blood cell count decreased
- Cerebrovascular accident (sudden death of some brain cells due to lack of oxygen when the blood flow to the brain is impaired by blockage or rupture)
- Fluid retention (an abnormal accumulation of fluid in the blood)
- Hemiplegia (paralysis of one side of the body)
- Speech disorder
What are the existing conditions these people have? *
- Primary Pulmonary Hypertension (primary high blood pressure that affects the arteries in the lungs and the right side of your heart): 11 people, 57.89%
- Systemic Sclerosis (an autoimmune or connective tissue disease. it is characterized by thickening of the skin): 1 person, 5.26%
- Gastric Cancer (stomach cancer): 1 person, 5.26%
- Cor Pulmonale Chronic (long lasting enlargement of the right ventricle of the heart): 1 person, 5.26%
- Chronic Myeloid Leukaemia (long lasting type of cancer that starts in the blood-forming cells of the bone marrow and invades the blood): 1 person, 5.26%
* Approximation only. Some reports may have incomplete information.
Do you take Gleevec and Letairis?
- 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 Gleevec 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 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 Gleevec:
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 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 zBrowse all interactions between Gleevec 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 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 zRelated publications that referenced our studies
- O'rafferty C, McElligott F, Storey L, O'marcaigh A, Smith O, "Pneumatosis intestinalis and imatinib mesylate", Annals of hematology, 2014 Oct .
- O'rafferty C, McElligott F, Storey L, O'marcaigh A, Smith O, "Pneumatosis intestinalis and imatinib mesylate", Annals of hematology, 2014 Oct .
How the study uses the data?
The study uses data from the FDA. It is based on imatinib mesylate and ambrisentan (the active ingredients of Gleevec and Letairis, respectively), and Gleevec 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.
If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.
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