Icosapent ethyl side effects by duration, gender and age - a phase IV clinical study of FDA data
Summary:
Side effects are reported by people who take Icosapent ethyl. Common side effects include drug ineffective among females, and cerebrovascular accident among males.
The phase IV clinical study is created by eHealthMe based on 524 reports from the FDA, and is updated regularly. You can use the study as a second opinion to make health care decisions.
Phase IV trials are used to detect adverse drug outcomes and monitor drug effectiveness in the real world. With medical big data and AI algorithms, eHealthMe is running millions of phase IV trials and makes the results available to the public. Our original studies have been referenced on 700+ medical publications including The Lancet, Mayo Clinic Proceedings, and Nature.
524 people who take Icosapent Ethyl and have side effects are studied.
What is Icosapent Ethyl?
Icosapent ethyl has active ingredients of icosapent ethyl. Currently, eHealthMe is studying from 535 Icosapent ethyl users.
Number of Icosapent ethyl reports submitted per year:
Icosapent ethyl side effects by time on the drug *:
Icosapent ethyl side effects by gender *:
Icosapent ethyl side effects by age *:
* Approximation only. Some reports may have incomplete information.
Do you take Icosapent ethyl?
Personalize this study to your gender and ageHow to use the study?
You can discuss the study with your doctor, to ensure that all drug risks and benefits are fully discussed and understood.
How the study uses the data?
The study is based on icosapent ethyl (the active ingredients of Icosapent ethyl) and Icosapent ethyl (the brand name). Other drugs that have the same active ingredients (e.g. generic drugs) are not considered.
Related studies
Alternative drugs to, pros and cons of Icosapent ethyl:
- Icosapent ethyl (535 reports)
All Icosapent ethyl side effects 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 zWho is eHealthMe?
With medical big data and proven AI 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 700+ 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).
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