Proair hfa and Cerebellar atrophy - a phase IV clinical study of FDA data

Summary:

Cerebellar atrophy is reported as a side effect among people who take Proair hfa (albuterol sulfate), especially for people who are male, 60+ old, also take Dilantin, and have Seizures.

The phase IV clinical study analyzes which people have Cerebellar atrophy when taking Proair hfa. It is created by eHealthMe based on reports of 52,628 people who have side effects when taking Proair hfa from the FDA, and is updated regularly.

What is Proair hfa?

Proair hfa has active ingredients of albuterol sulfate. It is often used in asthma. eHealthMe is studying from 53,227 Proair hfa users. Check the latest studies of Proair hfa.

What is Cerebellar atrophy?

Cerebellar atrophy (degeneration of the section of the brain responsible for balance, voluntary muscle movements) is found to be associated with 260 drugs and 102 conditions by eHealthMe. Check the latest studies of Cerebellar atrophy.

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 >>>.

On Aug, 30, 2026

52,628 people reported to have side effects when taking Proair hfa.
Among them, 16 people (0.03%) have Cerebellar atrophy.

Could Proair hfa cause Cerebellar atrophy?

Among these 16 people:

What is the gender of people who have Cerebellar atrophy when taking Proair hfa? *

female: 37.5 %
male: 62.5 %

What is the age of people who have Cerebellar atrophy when taking Proair hfa? *

What are other drugs people take besides Proair hfa? *

What are other side effects people have besides Cerebellar atrophy? *

Memory Loss: 14 people, 87.50%
Tremor (trembling or shaking movements in one or more parts of your body): 14 people, 87.50%
Balance Disorder: 13 people, 81.25%
Weakness: 13 people, 81.25%
Fall: 12 people, 75.00%
Neuropathy Peripheral (surface nerve damage): 12 people, 75.00%
Coordination Abnormal (abnormal movement): 10 people, 62.50%
Speech Impairment (Adult) (inability to speak (adult)): 9 people, 56.25%
Gait Disturbance: 9 people, 56.25%
Hand Fracture: 9 people, 56.25%

What are the existing conditions these people have? *

Seizures (abnormal excessive or synchronous neuronal activity in the brain): 16 people, 100.00%
Depression: 10 people, 62.50%
Wheezing (a high-pitched whistling sound made while you breath): 7 people, 43.75%
Cough: 7 people, 43.75%
Pain: 6 people, 37.50%
Epilepsy (common and diverse set of chronic neurological disorders characterized by seizures): 6 people, 37.50%
Headache (pain in head): 6 people, 37.50%
Sleep Disorder: 5 people, 31.25%
Gastric Disorder (disease of stomach): 5 people, 31.25%
Cardiac Disorder: 4 people, 25.00%

* Approximation only. Some reports may have incomplete information.

Do you take Proair hfa and have Cerebellar atrophy?

- Check whether Cerebellar atrophy 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 Proair hfa:

Proair hfa (53,227 reports)

Browse all side effects of Proair 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 Cerebellar atrophy:

Cerebellar atrophy (260 drugs)

Browse all the conditions that are associated with Cerebellar atrophy:

Cerebellar atrophy (102 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on albuterol sulfate (the active ingredients of Proair hfa) and Proair 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.