Combivent and Eye discharge - a phase IV clinical study of FDA data

Summary:

Eye discharge is reported as a side effect among people who take Combivent (albuterol sulfate; ipratropium bromide), especially for people who are female, 50-59 old, also take Vicodin, and have Bone density abnormal.

The phase IV clinical study analyzes which people have Eye discharge when taking Combivent. It is created by eHealthMe based on reports of 35,104 people who have side effects when taking Combivent from the FDA, and is updated regularly.

What is Combivent?

Combivent has active ingredients of albuterol sulfate; ipratropium bromide. It is often used in asthma. eHealthMe is studying from 35,341 Combivent users. Check the latest studies of Combivent.

What is Eye discharge?

Eye discharge is found to be associated with 690 drugs and 802 conditions by eHealthMe. Check the latest studies of Eye discharge.

On Jul, 14, 2026

35,104 people reported to have side effects when taking Combivent.
Among them, 30 people (0.09%) have Eye discharge.

Among these 30 people:

What is the gender of people who have Eye discharge when taking Combivent? *

female: 79.31 %
male: 20.69 %

What is the age of people who have Eye discharge when taking Combivent? *

What are other drugs people take besides Combivent? *

What are other side effects people have besides Eye discharge? *

Pain: 20 people, 66.67%
Stress And Anxiety: 19 people, 63.33%
Oedema Peripheral (superficial swelling): 19 people, 63.33%
Gait Disturbance: 18 people, 60.00%
Faecal Incontinence (a lack of control over passing stool): 18 people, 60.00%
Retching (strong involuntary effort to vomit): 18 people, 60.00%
Fall: 18 people, 60.00%
Fibula Fracture: 18 people, 60.00%
Foot Deformity (functional disability of foot): 18 people, 60.00%
Foot Fracture: 18 people, 60.00%

What are the existing conditions these people have? *

Bone Density Abnormal: 16 people, 53.33%
Osteoporosis (bones weak and more likely to break): 5 people, 16.67%
Lung Neoplasm Malignant (cancer tumour of lung): 2 people, 6.67%
Schizophrenia (a mental disorder characterized by a breakdown of thought processes): 1 person, 3.33%
High Blood Pressure: 1 person, 3.33%
Cardiac Disorder: 1 person, 3.33%
Diabetes: 1 person, 3.33%
Fluid Retention (an abnormal accumulation of fluid in the blood): 1 person, 3.33%
Heart Rate Irregular: 1 person, 3.33%
High Blood Cholesterol: 1 person, 3.33%

* Approximation only. Some reports may have incomplete information.

Do you take Combivent and have Eye discharge?

- Check whether Eye discharge 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 Combivent:

Combivent (35,341 reports)

Eye discharge treatments and more:

Eye discharge (10,525 reports)

How severe was Eye discharge and when was it recovered:

Eye discharge in Combivent

Expand to all the drugs that have ingredients of albuterol sulfate; ipratropium bromide:

Eye discharge and drugs with ingredients of albuterol sulfate; ipratropium bromide

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 Combivent:

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 Eye discharge:

Eye discharge (690 drugs)

Browse all the conditions that are associated with Eye discharge:

Eye discharge (802 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on albuterol sulfate; ipratropium bromide (the active ingredients of Combivent) and Combivent (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.