Trelegy ellipta and Fenoterol hydrobromide drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Trelegy ellipta (fluticasone furoate; umeclidinium bromide; vilanterol trifenatate) and Fenoterol hydrobromide (fenoterol hydrobromide). Common drug interactions include arthralgia among females and hyponatraemia among males.
The phase IV clinical study analyzes what interactions people have when they take Trelegy ellipta and Fenoterol hydrobromide. It is created by eHealthMe based on reports of 72 people who take the same drugs from the FDA, and is updated regularly.
What is Trelegy ellipta?
Trelegy ellipta has active ingredients of fluticasone furoate; umeclidinium bromide; vilanterol trifenatate. eHealthMe is studying from 28,101 Trelegy ellipta users. Check the latest studies of Trelegy ellipta.
What is Fenoterol hydrobromide?
Fenoterol hydrobromide has active ingredients of fenoterol hydrobromide. eHealthMe is studying from 1,327 Fenoterol hydrobromide users. Check the latest studies of Fenoterol hydrobromide.
72 people who take Trelegy ellipta and Fenoterol hydrobromide together, and have interactions are studied.

What are the common drug interactions of Trelegy Ellipta and Fenoterol Hydrobromide, by gender? *:
female:
- Arthralgia (joint pain)
- Joint swelling
- Death
- Pneumonia
- Type iii immune complex mediated reaction
male:
- Hyponatraemia (abnormally low level of sodium in the blood; associated with dehydration)
- Abdominal distension
- Drug hypersensitivity
- General physical health deterioration (weak health status)
- Nausea (feeling of having an urge to vomit)
- Hypophosphataemia (electrolyte disturbance in which there is an abnormally low level of phosphate in the blood)
- Abdominal pain
- Appendicitis (inflammation of the appendix)
- Ascites (accumulation of fluid in the abdominal cavity)
- Cardiogenic shock (inadequate circulation of blood)
What are the common drug interactions of Trelegy Ellipta and Fenoterol Hydrobromide, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
n/a
40-49:
- Nightmare (unpleasant dream)
- Arthralgia (joint pain)
- Joint swelling
- Type iii immune complex mediated reaction
50-59:
- Gamma-glutamyltransferase increased
- Plasma cell myeloma (cancer that begins in plasma cells)
- Renal disorder (kidney disease)
- General physical health deterioration (weak health status)
- White blood cell count decreased
- Conjunctivitis (pink eye)
- Escherichia urinary tract infection (urinary tract infection by escherichia coli)
- Pneumonia klebsiella (pneumonia caused by bacteria klebsiella)
- Platelet count decreased
- Stomatitis (inflammation of mucous membrane of mouth)
60+:
- Hyponatraemia (abnormally low level of sodium in the blood; associated with dehydration)
- Abdominal distension
- Drug hypersensitivity
- Hypophosphataemia (electrolyte disturbance in which there is an abnormally low level of phosphate in the blood)
- Abdominal pain
- Appendicitis (inflammation of the appendix)
- Ascites (accumulation of fluid in the abdominal cavity)
- Cardiogenic shock (inadequate circulation of blood)
- Constipation
- General physical health deterioration (weak health status)
What are the existing conditions these people have? *
- Chronic Obstructive Pulmonary Disease (a progressive disease that makes it hard to breathe): 63 people, 87.50%
- Stress And Anxiety: 45 people, 62.50%
- Bacterial Infection: 42 people, 58.33%
- Ventricular Fibrillation (abnormally irregular heart rhythm): 40 people, 55.56%
- Blood Phosphorus Increased: 40 people, 55.56%
- Diabetes: 40 people, 55.56%
- Constipation: 40 people, 55.56%
- High Blood Cholesterol: 40 people, 55.56%
- Hyperphosphataemia (electrolyte disturbance in which there is an abnormally elevated level of phosphate in the blood): 40 people, 55.56%
- Cardiogenic Shock (inadequate circulation of blood): 40 people, 55.56%
* Approximation only. Some reports may have incomplete information.
Do you take Trelegy ellipta and Fenoterol hydrobromide?
- 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:
- Trelegy ellipta (28,101 reports)
- Fenoterol hydrobromide (1,327 reports)
Browse all drug interactions of Trelegy ellipta and Fenoterol hydrobromide:
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 Trelegy ellipta:
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 Fenoterol hydrobromide:
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 Trelegy ellipta 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 Fenoterol hydrobromide 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 fluticasone furoate; umeclidinium bromide; vilanterol trifenatate and fenoterol hydrobromide (the active ingredients of Trelegy ellipta and Fenoterol hydrobromide, respectively), and Trelegy ellipta and Fenoterol hydrobromide (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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