Asa and Adverse event - a phase IV clinical study of FDA data

Summary:

Adverse event is reported as a side effect among people who take Asa (aspirin), especially for people who are female, 60+ old, also take Nexium, and have High blood cholesterol.

The phase IV clinical study analyzes which people have Adverse event when taking Asa. It is created by eHealthMe based on reports of 32,003 people who have side effects when taking Asa from the FDA, and is updated regularly.

What is Asa?

Asa has active ingredients of aspirin. It is often used in blood clots. eHealthMe is studying from 32,557 Asa users. Check the latest studies of Asa.

What is Adverse event?

Adverse event is found to be associated with 1,688 drugs and 1,665 conditions by eHealthMe. Check the latest studies of Adverse event.

On Jul, 13, 2026

32,003 people reported to have side effects when taking Asa.
Among them, 66 people (0.21%) have Adverse event.

Among these 66 people:

What is the gender of people who have Adverse event when taking Asa? *

female: 62.3 %
male: 37.7 %

What is the age of people who have Adverse event when taking Asa? *

What are other drugs people take besides Asa? *

What are other side effects people have besides Adverse event? *

Malaise (a feeling of general discomfort or uneasiness): 12 people, 18.18%
Fatigue (feeling of tiredness): 11 people, 16.67%
Feeling Abnormal: 9 people, 13.64%
Drug Ineffective: 9 people, 13.64%
Fall: 9 people, 13.64%
Back Pain: 8 people, 12.12%
Nausea (feeling of having an urge to vomit): 8 people, 12.12%
Weakness: 8 people, 12.12%
Dyspnea (difficult or laboured breathing): 8 people, 12.12%
Head Injury: 8 people, 12.12%

What are the existing conditions these people have? *

High Blood Cholesterol: 13 people, 19.70%
Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 7 people, 10.61%
Parkinson's Disease: 6 people, 9.09%
Pain: 6 people, 9.09%
Asthma: 6 people, 9.09%
Osteoporosis (bones weak and more likely to break): 5 people, 7.58%
Cardiac Disorder: 5 people, 7.58%
Rheumatoid Arthritis (a chronic progressive disease causing inflammation in the joints): 4 people, 6.06%
Chronic Obstructive Pulmonary Disease (a progressive disease that makes it hard to breathe): 4 people, 6.06%
Diabetes: 4 people, 6.06%

* Approximation only. Some reports may have incomplete information.

Do you take Asa and have Adverse event?

- Check whether Adverse event 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 Asa:

Asa (32,557 reports)

Adverse event treatments and more:

Adverse event (100,133 reports)

Browse all side effects of Asa:

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 Adverse event:

Adverse event (1,688 drugs)

Browse all the conditions that are associated with Adverse event:

Adverse event (1,665 conditions)

Related publications that referenced our studies

Alokaily FA, Alghamdi M, Almalki AS, Alhussaini H, "Aspirin induced leukocytoclastic vasculitis, lower gastrointestinal hemorrhage and acute renal failure (mimicking systemic vasculitis)", Saudi medical journal, 2013 Apr .
Alokaily FA, Alghamdi M, Almalki AS, Alhussaini H, "Aspirin induced leukocytoclastic vasculitis, lower gastrointestinal hemorrhage and acute renal failure (mimicking systemic vasculitis)", Saudi medical journal, 2013 Apr .

How the study uses the data?

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