Advair diskus 100/50 and Swelling - a phase IV clinical study of FDA data

Summary:

Swelling is reported as a side effect among people who take Advair diskus 100/50 (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 Multiple myeloma.

The phase IV clinical study analyzes which people have Swelling when taking Advair diskus 100/50. It is created by eHealthMe based on reports of 38,800 people who have side effects when taking Advair diskus 100/50 from the FDA, and is updated regularly.

What is Advair diskus 100/50?

Advair diskus 100/50 has active ingredients of fluticasone propionate; salmeterol xinafoate. It is often used in asthma. eHealthMe is studying from 39,246 Advair diskus 100/50 users. Check the latest studies of Advair diskus 100/50.

What is Swelling?

Swelling is found to be associated with 2,300 drugs and 2,891 conditions by eHealthMe. Check the latest studies of Swelling.

On Jul, 11, 2026

38,800 people reported to have side effects when taking Advair diskus 100/50.
Among them, 346 people (0.89%) have Swelling.

Could Advair diskus 100/50 cause Swelling?

Among these 346 people:

How long have people been on Advair diskus 100/50 when they have Swelling? *

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What is the gender of people who have Swelling when taking Advair diskus 100/50? *

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* Approximation only. Some reports may have incomplete information.

Do you take Advair diskus 100/50 and have Swelling?

- Check whether Swelling 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 Advair diskus 100/50:

Advair diskus 100/50 (39,246 reports)

Swelling treatments and more:

Swelling (115,742 reports)

How severe was Swelling and when was it recovered:

Swelling in Advair diskus 100/50

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

Swelling and drugs with ingredients of fluticasone propionate; salmeterol xinafoate (1,332 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 Advair diskus 100/50:

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 Swelling:

Swelling (2,300 drugs)

Browse all the conditions that are associated with Swelling:

Swelling (2,891 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 Advair diskus 100/50) and Advair diskus 100/50 (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.