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

Summary:

Bradyphrenia is reported as a side effect among people who take Proair hfa (albuterol sulfate), especially for people who are male, 40-49 old, have been taking the drug for 1 - 6 months also take Effexor, and have Narcolepsy.

The phase IV clinical study analyzes which people have Bradyphrenia 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 Bradyphrenia?

Bradyphrenia (neurological term referring to the slowness of thought common to many disorders of the brain) is found to be associated with 535 drugs and 693 conditions by eHealthMe. Check the latest studies of Bradyphrenia.

On Jul, 06, 2026

52,628 people reported to have side effects when taking Proair hfa.
Among them, 23 people (0.04%) have Bradyphrenia.

Among these 23 people:

How long have people been on Proair hfa when they have Bradyphrenia? *

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

female: 47.83 %
male: 52.17 %

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

What are other drugs people take besides Proair hfa? *

What are other side effects people have besides Bradyphrenia? *

Headache (pain in head): 14 people, 60.87%
Drug Ineffective: 10 people, 43.48%
Drowsiness: 10 people, 43.48%
Dizziness: 9 people, 39.13%
Dizziness Postural: 8 people, 34.78%
Bipolar I Disorder (mood disorder that is characterized by at least one manic or mixed episode): 8 people, 34.78%
Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 8 people, 34.78%
Tachyphrenia (abnormally rapid mental activity): 8 people, 34.78%
Nausea (feeling of having an urge to vomit): 8 people, 34.78%
Respiratory Acidosis (respiratory failure or ventilatory failure, causes the ph of blood and other bodily fluids to decrease): 8 people, 34.78%

What are the existing conditions these people have? *

Narcolepsy (brain's inability to regulate sleep-wake cycles normally): 7 people, 30.43%
Cataplexy (loss of muscle tone accompanied by full conscious awareness): 5 people, 21.74%
Lactose Intolerance (inability to digest lactose): 3 people, 13.04%
Migraine (headache): 3 people, 13.04%
Hypothyroidism (abnormally low activity of the thyroid gland, resulting in retardation of growth and mental development): 3 people, 13.04%
Impaired Gastric Emptying: 3 people, 13.04%
Joint Pain: 3 people, 13.04%
Trigeminal Neuralgia (a painful condition of the nerve responsible for most facial sensation): 3 people, 13.04%
Anaphylaxis (serious allergic reaction that is rapid in onset and may cause death): 3 people, 13.04%
Muscle Spasms (muscle contraction): 3 people, 13.04%

* Approximation only. Some reports may have incomplete information.

Do you take Proair hfa and have Bradyphrenia?

- Check whether Bradyphrenia 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)

Bradyphrenia treatments and more:

Bradyphrenia (7,508 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 Bradyphrenia:

Bradyphrenia (535 drugs)

Browse all the conditions that are associated with Bradyphrenia:

Bradyphrenia (693 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.