Pulmicort and Total lung capacity increased - a phase IV clinical study of FDA data

Summary:

Total lung capacity increased is reported as a side effect among people who take Pulmicort (budesonide), especially for people who are female, 40-49 old, also take Advair Hfa, and have Otitis.

The phase IV clinical study analyzes which people have Total lung capacity increased when taking Pulmicort. It is created by eHealthMe based on reports of 34,552 people who have side effects when taking Pulmicort from the FDA, and is updated regularly.

What is Pulmicort?

Pulmicort has active ingredients of budesonide. It is often used in asthma. eHealthMe is studying from 34,980 Pulmicort users. Check the latest studies of Pulmicort.

What is Total lung capacity increased?

Total lung capacity increased is found to be associated with 68 drugs and 26 conditions by eHealthMe. Check the latest studies of Total lung capacity increased.

On Aug, 01, 2026

34,552 people reported to have side effects when taking Pulmicort.
Among them, 11 people (0.03%) have Total lung capacity increased.

Could Pulmicort cause Total lung capacity increased?

Among these 11 people:

What is the gender of people who have Total lung capacity increased when taking Pulmicort? *

female: 100 %
male: 0.0 %

What is the age of people who have Total lung capacity increased when taking Pulmicort? *

What are other drugs people take besides Pulmicort? *

Symbicort: 10 people, 90.91%
Advair Hfa: 10 people, 90.91%
Prednisone: 2 people, 18.18%
Methotrexate: 2 people, 18.18%
Folic Acid: 2 people, 18.18%
Ciprofloxacin: 2 people, 18.18%
Albuterol Sulfate: 2 people, 18.18%
Ciprofloxacin Hydrochloride: 1 person, 9.09%
Amoxicillin And Clavulanate Potassium: 1 person, 9.09%
Albuterol: 1 person, 9.09%

What are other side effects people have besides Total lung capacity increased? *

Throat Irritation: 11 people, 100.00%
Papilloma (small, noncancerous (benign) tumour): 11 people, 100.00%
Obstructive Airways Disorder (a progressive disease that makes it hard to breathe): 11 people, 100.00%
Feeling Abnormal: 11 people, 100.00%
Excessive Granulation Tissue (excessive collagen-rich tissue which forms at the site of an injury): 11 people, 100.00%
Eosinophilia (eosinophil count in the peripheral blood exceeds): 11 people, 100.00%
Dyspnea Exertional: 11 people, 100.00%
Dyspnea (difficult or laboured breathing): 11 people, 100.00%
Drug Intolerance (drug sensitivity): 11 people, 100.00%
Drug Ineffective: 11 people, 100.00%

What are the existing conditions these people have? *

Otitis (ear infection): 11 people, 100.00%

* Approximation only. Some reports may have incomplete information.

Do you take Pulmicort and have Total lung capacity increased?

- Check whether Total lung capacity increased 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 Pulmicort:

Pulmicort (34,980 reports)

Browse all side effects of Pulmicort:

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 Total lung capacity increased:

Total lung capacity increased (68 drugs)

Browse all the conditions that are associated with Total lung capacity increased:

Total lung capacity increased (26 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on budesonide (the active ingredients of Pulmicort) and Pulmicort (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.