Advair hfa and Blood test abnormal - a phase IV clinical study of FDA data

Summary:

Blood test abnormal is reported as a side effect among people who take Advair hfa (fluticasone propionate; salmeterol xinafoate), especially for people who are female, 60+ old, also take Spiriva, and have Gastroesophageal reflux disease.

The phase IV clinical study analyzes which people have Blood test abnormal when taking Advair hfa. It is created by eHealthMe based on reports of 69,236 people who have side effects when taking Advair hfa from the FDA, and is updated regularly.

What is Advair hfa?

Advair hfa has active ingredients of fluticasone propionate; salmeterol xinafoate. It is often used in asthma. eHealthMe is studying from 69,790 Advair hfa users. Check the latest studies of Advair hfa.

What is Blood test abnormal?

Blood test abnormal is found to be associated with 836 drugs and 724 conditions by eHealthMe. Check the latest studies of Blood test abnormal.

On Aug, 12, 2026

69,236 people reported to have side effects when taking Advair hfa.
Among them, 150 people (0.22%) have Blood test abnormal.

Could Advair hfa cause Blood test abnormal?

Among these 150 people:

What is the gender of people who have Blood test abnormal when taking Advair hfa? *

Click here to view

What is the age of people who have Blood test abnormal when taking Advair hfa? *

Click here to view more results

* Approximation only. Some reports may have incomplete information.

Do you take Advair hfa and have Blood test abnormal?

- Check whether Blood test abnormal 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 hfa:

Advair hfa (69,790 reports)

Blood test abnormal treatments and more:

Blood test abnormal (15,862 reports)

How severe was Blood test abnormal and when was it recovered:

Blood test abnormal in Advair hfa

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

Blood test abnormal and drugs with ingredients of fluticasone propionate; salmeterol xinafoate (306 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 hfa:

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 Blood test abnormal:

Blood test abnormal (836 drugs)

Browse all the conditions that are associated with Blood test abnormal:

Blood test abnormal (724 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 hfa) and Advair hfa (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.