Bivalirudin and Brilinta drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Bivalirudin (bivalirudin) and Brilinta (ticagrelor). Common drug interactions include subarachnoid haemorrhage among females and acute myocardial infarction among males.
The phase IV clinical study analyzes what interactions people have when they take Bivalirudin and Brilinta. It is created by eHealthMe based on reports of 14 people who take the same drugs from the FDA, and is updated regularly.
What is Bivalirudin?
Bivalirudin has active ingredients of bivalirudin. eHealthMe is studying from 908 Bivalirudin users. Check the latest studies of Bivalirudin.
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.
14 people who take Bivalirudin and Brilinta together, and have interactions are studied.

What are the common drug interactions of Bivalirudin and Brilinta, by gender? *:
female:
- Subarachnoid haemorrhage (blood leaks into the space between two membranes that surround the brain)
male:
- Acute myocardial infarction (acute heart attack)
- Thrombosis (formation of a blood clot inside a blood vessel)
- Electrocardiogram st segment elevation
- Nephropathy (damage to or disease of a kidney)
- Nephropathy toxic (damage to kidney due to toxins)
- Pulmonary fibrosis (formation or development of excess fibrous connective tissue (fibrosis) in the lungs)
- Renal failure acute (rapid kidney dysfunction)
- Renal tubular necrosis (death of kidney tubules)
- Ventricular asystole (cardiac arrest rhythm in which there is no discernible electrical activity on the ecg monitor)
- Vomiting
What are the common drug interactions of Bivalirudin and Brilinta, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
- Vomiting
40-49:
n/a
50-59:
- Acute myocardial infarction (acute heart attack)
- Coronary artery thrombosis (clot formation in coronary artery)
60+:
- Acute myocardial infarction (acute heart attack)
- Subarachnoid haemorrhage (blood leaks into the space between two membranes that surround the brain)
- Pulmonary fibrosis (formation or development of excess fibrous connective tissue (fibrosis) in the lungs)
- Renal failure acute (rapid kidney dysfunction)
- Renal tubular necrosis (death of kidney tubules)
- Thrombosis (formation of a blood clot inside a blood vessel)
- Ventricular asystole (cardiac arrest rhythm in which there is no discernible electrical activity on the ecg monitor)
- Acute respiratory distress syndrome
- Atrioventricular block (heart block)
- Atrioventricular block complete (heart block complete)
What are the existing conditions these people have? *
- Percutaneous Coronary Intervention: 6 people, 42.86%
- Acute Coronary Syndrome (acute chest pain and other symptoms that happen because the heart does not get blood): 5 people, 35.71%
- Electrocardiogram St Segment Elevation: 1 person, 7.14%
- Coal Worker's Pneumoconiosis (lung disease of coal worker affects upper part of lung): 1 person, 7.14%
- Acute Myocardial Infarction (acute heart attack): 1 person, 7.14%
* Approximation only. Some reports may have incomplete information.
Do you take Bivalirudin and Brilinta?
- Personalize this study to your gender, age, symptoms and drugs
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously
Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
- Bivalirudin (908 reports)
- Brilinta (22,469 reports)
Browse all drug interactions of Bivalirudin and 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 zSub-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 Bivalirudin:
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 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 interactions between Bivalirudin and drugs from A to Z:
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 interactions between Brilinta and drugs from A to Z:
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 zHow the study uses the data?
The study uses data from the FDA. It is based on bivalirudin and ticagrelor (the active ingredients of Bivalirudin and Brilinta, respectively), and Bivalirudin and Brilinta (the brand names). 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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