Reopro and Heart rate decreased - a phase IV clinical study of FDA data
Summary:
Heart rate decreased is reported as a side effect among people who take Reopro (abciximab), especially for people who are male, 60+ old, have been taking the drug for < 1 month also take Heparin, and have Acute myocardial infarction.
The phase IV clinical study analyzes which people have Heart rate decreased when taking Reopro. It is created by eHealthMe based on reports of 4,780 people who have side effects when taking Reopro from the FDA, and is updated regularly.
What is Reopro?
Reopro has active ingredients of abciximab. eHealthMe is studying from 4,782 Reopro users. Check the latest studies of Reopro.
What is Heart rate decreased?
Heart rate decreased is found to be associated with 1,552 drugs and 1,599 conditions by eHealthMe. Check the latest studies of Heart rate decreased.
4,780 people reported to have side effects when taking Reopro.
Among them, 13 people (0.27%) have Heart rate decreased.

Among these 13 people:
How long have people been on Reopro when they have Heart rate decreased? *
- < 1 month: 100 %
- 1 - 6 months: 0.0 %
- 6 - 12 months: 0.0 %
- 1 - 2 years: 0.0 %
- 2 - 5 years: 0.0 %
- 5 - 10 years: 0.0 %
- 10+ years: 0.0 %
What is the gender of people who have Heart rate decreased when taking Reopro? *
- female: 25 %
- male: 75 %
What is the age of people who have Heart rate decreased when taking Reopro? *
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 0.0 %
- 30-39: 0.0 %
- 40-49: 9.09 %
- 50-59: 27.27 %
- 60+: 63.64 %
What are other drugs people take besides Reopro? *
- Heparin: 8 people, 61.54%
- Nitroglycerin: 3 people, 23.08%
- Heparin Sodium: 2 people, 15.38%
- Lisinopril: 2 people, 15.38%
- Amiodarone Hydrochloride: 1 person, 7.69%
- Aspirin: 1 person, 7.69%
- Atenolol: 1 person, 7.69%
- Clopidogrel: 1 person, 7.69%
- Fentanyl: 1 person, 7.69%
- Furosemide: 1 person, 7.69%
What are other side effects people have besides Heart rate decreased? *
- Hypotension (abnormally low blood pressure): 7 people, 53.85%
- Ventricular Fibrillation (abnormally irregular heart rhythm): 2 people, 15.38%
- Cardiac Arrest: 2 people, 15.38%
- Ejection Fraction Decreased (systolic heart failure): 2 people, 15.38%
- Coronary Artery Stenosis (narrowing of coronary artery): 2 people, 15.38%
- Injection Site Haemorrhage (bleeding from injection site): 2 people, 15.38%
- Chest Pain: 2 people, 15.38%
- Cardiogenic Shock (inadequate circulation of blood): 2 people, 15.38%
- Thrombocytopenia (decrease of platelets in blood): 2 people, 15.38%
- Body Temperature Increased: 1 person, 7.69%
What are the existing conditions these people have? *
- Acute Myocardial Infarction (acute heart attack): 3 people, 23.08%
* Approximation only. Some reports may have incomplete information.
Do you take Reopro and have Heart rate decreased?
- Check whether Heart rate decreased 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 Reopro:
- Reopro (4,782 reports)
Heart rate decreased treatments and more:
- Heart rate decreased (51,896 reports)
How severe was Heart rate decreased and when was it recovered:
Expand to all the drugs that have ingredients of abciximab:
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 Reopro:
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 Heart rate decreased:
- Heart rate decreased (1,552 drugs)
Browse all the conditions that are associated with Heart rate decreased:
- Heart rate decreased (1,599 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on abciximab (the active ingredients of Reopro) and Reopro (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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