Wixela inhub and Insomnia - a phase IV clinical study of FDA data

Summary:

Insomnia is reported as a side effect among people who take Wixela inhub (fluticasone propionate; salmeterol xinafoate), especially for people who are female, 60+ old, have been taking the drug for < 1 month also take Albuterol, and have Chronic obstructive pulmonary disease.

The phase IV clinical study analyzes which people have Insomnia when taking Wixela inhub. It is created by eHealthMe based on reports of 2,900 people who have side effects when taking Wixela inhub from the FDA, and is updated regularly.

What is Wixela inhub?

Wixela inhub has active ingredients of fluticasone propionate; salmeterol xinafoate. eHealthMe is studying from 2,925 Wixela inhub users. Check the latest studies of Wixela inhub.

What is Insomnia?

Insomnia (sleeplessness) is found to be associated with 3,117 drugs and 5,170 conditions by eHealthMe. Check the latest studies of Insomnia.

On Jul, 25, 2026

2,900 people reported to have side effects when taking Wixela inhub.
Among them, 34 people (1.17%) have Insomnia.

Among these 34 people:

How long have people been on Wixela inhub when they have Insomnia? *

What is the gender of people who have Insomnia when taking Wixela inhub? *

female: 71.88 %
male: 28.12 %

What is the age of people who have Insomnia when taking Wixela inhub? *

What are other drugs people take besides Wixela inhub? *

What are other side effects people have besides Insomnia? *

Dizziness: 8 people, 23.53%
Dyspnea (difficult or laboured breathing): 8 people, 23.53%
Drug Ineffective: 6 people, 17.65%
Fatigue (feeling of tiredness): 6 people, 17.65%
Paraesthesia (sensation of tingling, tickling, prickling, pricking, or burning of a person's skin with no apparent long-term physical effect): 6 people, 17.65%
Nausea (feeling of having an urge to vomit): 6 people, 17.65%
Chronic Obstructive Pulmonary Disease (a progressive disease that makes it hard to breathe): 5 people, 14.71%
Hypoaesthesia (reduced sense of touch or sensation): 5 people, 14.71%
Visual Impairment: 5 people, 14.71%
Pulmonary Mass: 5 people, 14.71%

What are the existing conditions these people have? *

Asthma: 11 people, 32.35%
Chronic Obstructive Pulmonary Disease (a progressive disease that makes it hard to breathe): 11 people, 32.35%
Post Laminectomy Syndrome: 2 people, 5.88%
High Blood Pressure: 2 people, 5.88%
Stress And Anxiety: 2 people, 5.88%
Wheezing (a high-pitched whistling sound made while you breath): 1 person, 2.94%
Immunodeficiency: 1 person, 2.94%
Blood Uric Acid Increased: 1 person, 2.94%
Breast Cancer Female: 1 person, 2.94%
Breast Cancer Stage Iv: 1 person, 2.94%

* Approximation only. Some reports may have incomplete information.

Do you take Wixela inhub and have Insomnia?

- Check whether Insomnia 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 Wixela inhub:

Wixela inhub (2,925 reports)

Insomnia treatments and more:

Insomnia (438,078 reports)

How severe was Insomnia and when was it recovered:

Insomnia in Wixela inhub

Expand to all the drugs that have ingredients of fluticasone propionate; salmeterol xinafoate:

Insomnia and drugs with ingredients of fluticasone propionate; salmeterol xinafoate (4,064 reports)

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 Wixela inhub:

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 the drugs that are associated with Insomnia:

Insomnia (3,117 drugs)

Browse all the conditions that are associated with Insomnia:

Insomnia (5,170 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on fluticasone propionate; salmeterol xinafoate (the active ingredients of Wixela inhub) and Wixela inhub (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.