Brilinta and Reading disorder - a phase IV clinical study of FDA data
Summary:
Reading disorder is reported as a side effect among people who take Brilinta (ticagrelor), especially for people who are male, 60+ old, also take Prozac, and have High blood cholesterol.
The phase IV clinical study analyzes which people have Reading disorder when taking Brilinta. It is created by eHealthMe based on reports of 22,127 people who have side effects when taking Brilinta from the FDA, and is updated regularly.
What is Brilinta?
Brilinta has active ingredients of ticagrelor. It is often used in stent. eHealthMe is studying from 22,469 Brilinta users. Check the latest studies of Brilinta.
What is Reading disorder?
Reading disorder (problem in areas of the brain that help interpret language) is found to be associated with 299 drugs and 474 conditions by eHealthMe. Check the latest studies of Reading disorder.
22,127 people reported to have side effects when taking Brilinta.
Among them, 11 people (0.05%) have Reading disorder.

Among these 11 people:
What is the gender of people who have Reading disorder when taking Brilinta? *
- female: 45.45 %
- male: 54.55 %
What is the age of people who have Reading disorder when taking Brilinta? *
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 0.0 %
- 30-39: 0.0 %
- 40-49: 0.0 %
- 50-59: 25 %
- 60+: 75 %
What are other drugs people take besides Brilinta? *
- Amlodipine: 3 people, 27.27%
- Prozac: 3 people, 27.27%
- Repatha: 2 people, 18.18%
- Lasix: 2 people, 18.18%
- Lisinopril: 1 person, 9.09%
- Capoten: 1 person, 9.09%
- Coenzyme Q10: 1 person, 9.09%
- Coreg: 1 person, 9.09%
- Diovan Hct: 1 person, 9.09%
- Effient: 1 person, 9.09%
What are other side effects people have besides Reading disorder? *
- Memory Loss: 5 people, 45.45%
- Dyspnea (difficult or laboured breathing): 4 people, 36.36%
- Headache (pain in head): 4 people, 36.36%
- Weight Loss: 3 people, 27.27%
- Aortic Aneurysm (enlargement of an aortic artery caused by a weakening of the artery wall): 3 people, 27.27%
- Arrhythmias (irregular heartbeat): 3 people, 27.27%
- Arthropathy: 3 people, 27.27%
- Blood Pressure Fluctuation: 3 people, 27.27%
- Body Height Decreased: 3 people, 27.27%
- Fainting (loss of consciousness and postural tone): 3 people, 27.27%
What are the existing conditions these people have? *
- High Blood Cholesterol: 4 people, 36.36%
- Abdominal Discomfort: 3 people, 27.27%
- Acute Coronary Syndrome (acute chest pain and other symptoms that happen because the heart does not get blood): 3 people, 27.27%
- Cardiac Disorder: 3 people, 27.27%
- Depression: 3 people, 27.27%
- Blood Pressure Abnormal: 2 people, 18.18%
- Eye Disorder: 1 person, 9.09%
- Chest Pain: 1 person, 9.09%
- Device Occlusion: 1 person, 9.09%
- Sleep Disorder: 1 person, 9.09%
* Approximation only. Some reports may have incomplete information.
Do you take Brilinta and have Reading disorder?
- Check whether Reading disorder 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 Brilinta:
- Brilinta (22,469 reports)
Reading disorder treatments and more:
- Reading disorder (2,811 reports)
How severe was Reading disorder and when was it recovered:
Expand to all the drugs that have ingredients of ticagrelor:
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 Brilinta:
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 zBrowse all the drugs that are associated with Reading disorder:
- Reading disorder (299 drugs)
Browse all the conditions that are associated with Reading disorder:
- Reading disorder (474 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on ticagrelor (the active ingredients of Brilinta) and Brilinta (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.
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