Advair diskus 100/50 and Procedural complication - a phase IV clinical study of FDA data
Summary:
Procedural complication 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, also take Albuterol, and have Osteoporosis.
The phase IV clinical study analyzes which people have Procedural complication 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 Procedural complication?
Procedural complication is found to be associated with 644 drugs and 915 conditions by eHealthMe. Check the latest studies of Procedural complication.
eHealthMe: drug outcomes in the real world
eHealthMe runs one of the largest post-marketing drug safety studies in the world. We study millions of patients and 5,000 more each day. Our data-driven phase IV clinical trials have been referenced on 800+ peer-reviewed medical publications including The Lancet, Mayo Clinic Proceedings, and Nature. Tools to study our phase IV findings are available to the public, anonymous and free >>>.
38,800 people reported to have side effects when taking Advair diskus 100/50.
Among them, 22 people (0.06%) have Procedural complication.

Among these 22 people:
What is the gender of people who have Procedural complication when taking Advair diskus 100/50? *
- female: 77.27 %
- male: 22.73 %
What is the age of people who have Procedural complication when taking Advair diskus 100/50? *
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 0.0 %
- 30-39: 0.0 %
- 40-49: 23.53 %
- 50-59: 17.65 %
- 60+: 58.82 %
What are other drugs people take besides Advair diskus 100/50? *
- Albuterol: 8 people, 36.36%
- Crestor: 6 people, 27.27%
- Synthroid: 5 people, 22.73%
- Folic Acid: 4 people, 18.18%
- Nexium: 4 people, 18.18%
- Spiriva: 3 people, 13.64%
- Forteo: 3 people, 13.64%
- Vitamin E: 3 people, 13.64%
- Aspirin: 3 people, 13.64%
- Omeprazole: 3 people, 13.64%
What are other side effects people have besides Procedural complication? *
- Weight Decreased: 4 people, 18.18%
- Fever: 4 people, 18.18%
- Fatigue (feeling of tiredness): 4 people, 18.18%
- Nasal Discharge (discharge from nose): 3 people, 13.64%
- Diarrhea: 3 people, 13.64%
- Headache (pain in head): 3 people, 13.64%
- Sinus Disorder (disease of sinus): 3 people, 13.64%
- Nausea (feeling of having an urge to vomit): 3 people, 13.64%
- Dyspnea (difficult or laboured breathing): 3 people, 13.64%
- Dizziness: 3 people, 13.64%
What are the existing conditions these people have? *
- Osteoporosis (bones weak and more likely to break): 4 people, 18.18%
- High Blood Cholesterol: 2 people, 9.09%
- Paroxysmal Nocturnal Haemoglobinuria (haemoglobin in the urine): 2 people, 9.09%
- Lung Cancer - Non-Small Cell (lung cancer): 2 people, 9.09%
- Hypothyroidism (abnormally low activity of the thyroid gland, resulting in retardation of growth and mental development): 2 people, 9.09%
- Stress And Anxiety: 1 person, 4.55%
- Bradycardia (abnormally slow heart action): 1 person, 4.55%
- Bronchospasm (spasm of bronchial smooth muscle producing narrowing of the bronchi): 1 person, 4.55%
- Depression: 1 person, 4.55%
- Diabetes: 1 person, 4.55%
* Approximation only. Some reports may have incomplete information.
Do you take Advair diskus 100/50 and have Procedural complication?
- Check whether Procedural complication 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)
Procedural complication treatments and more:
- Procedural complication (9,426 reports)
How severe was Procedural complication and when was it recovered:
Expand to all the drugs that have ingredients of fluticasone propionate; salmeterol xinafoate:
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 zBrowse all the drugs that are associated with Procedural complication:
- Procedural complication (644 drugs)
Browse all the conditions that are associated with Procedural complication:
- Procedural complication (915 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.
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