Letairis and Drooling - a phase IV clinical study of FDA data
Summary:
Drooling is reported as a side effect among people who take Letairis (ambrisentan), especially for people who are female, 60+ old, also take Adcirca,.
The phase IV clinical study analyzes which people have Drooling when taking Letairis. It is created by eHealthMe based on reports of 93,991 people who have side effects when taking Letairis from the FDA, and is updated regularly.
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.
What is Drooling?
Drooling (drop saliva uncontrollably from the mouth) is found to be associated with 495 drugs and 941 conditions by eHealthMe. Check the latest studies of Drooling.
93,991 people reported to have side effects when taking Letairis.
Among them, 14 people (0.01%) have Drooling.

Among these 14 people:
What is the gender of people who have Drooling when taking Letairis? *
- female: 100 %
- male: 0.0 %
What is the age of people who have Drooling when taking Letairis? *
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 0.0 %
- 30-39: 0.0 %
- 40-49: 41.67 %
- 50-59: 8.33 %
- 60+: 50.0 %
What are other drugs people take besides Letairis? *
- Adcirca: 5 people, 35.71%
- Tyvaso: 3 people, 21.43%
- Revatio: 3 people, 21.43%
- Coumadin: 3 people, 21.43%
- Adempas: 2 people, 14.29%
- Rituxan: 2 people, 14.29%
- Remodulin: 2 people, 14.29%
- Arava: 2 people, 14.29%
- Benicar: 2 people, 14.29%
- Ventavis: 2 people, 14.29%
What are other side effects people have besides Drooling? *
- Rhinorrhea (watery mucus discharge from the nose): 4 people, 28.57%
- Diarrhea: 3 people, 21.43%
- Headache (pain in head): 3 people, 21.43%
- Dizziness: 3 people, 21.43%
- Salivary Hypersecretion (excess saliva secretion): 3 people, 21.43%
- The Flu (the flu is caused by an influenza virus): 3 people, 21.43%
- Taste - Impaired: 3 people, 21.43%
- Weight Increased: 2 people, 14.29%
- Fatigue (feeling of tiredness): 2 people, 14.29%
- Dyspnea (difficult or laboured breathing): 2 people, 14.29%
* Approximation only. Some reports may have incomplete information.
Do you take Letairis and have Drooling?
- Check whether Drooling is associated with a drug or a condition
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously
Related studies:
Effectiveness of, long term effects of, and alternative drugs to Letairis:
- Letairis (94,041 reports)
Drooling treatments and more:
- Drooling (8,115 reports)
How severe was Drooling and when was it recovered:
Expand to all the drugs that have ingredients of ambrisentan:
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 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 the drugs that are associated with Drooling:
- Drooling (495 drugs)
Browse all the conditions that are associated with Drooling:
- Drooling (941 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on ambrisentan (the active ingredients of Letairis) and Letairis (the brand name). 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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