Vasodilatation and drugs of ingredients of allopurinol (a real world drug study)
Summary:
Vasodilatation is found among people who take drugs with ingredients of allopurinol, especially for people who are male, 60+ old . This phase IV clinical study is created by eHealthMe based on reports of 193,129 people who have side effects when taking drugs with ingredients of allopurinol from the FDA, and is updated regularly.
Drug(s) considered in the study (i.e. both brand name and generic drugs): Allopurinol, Lopurin, Zyloprim.
eHealthMe: drug outcomes in the real world
eHealthMe runs one of the largest post-marketing drug safety studies in the world. We study millions of patients and 5,000 more each day. Our data-driven phase IV clinical trials have been referenced on 800+ peer-reviewed medical publications including The Lancet, Mayo Clinic Proceedings, and Nature. Tools to study our phase IV findings are available to the public, anonymous and free >>>.
193,129 people reported to have side effects when taking drugs with ingredients of allopurinol.
Among them, 62 people (0.03%) have Vasodilatation
What is Vasodilatation?
Vasodilatation (widening of blood vessels resulting from relaxation of smooth muscle cells within the vessel walls) is found to be associated with 541 drugs and 550 conditions by eHealthMe. Check the latest studies of Vasodilatation.
Number of reports submitted per year:
Gender of people who have Vasodilatation when taking drugs with ingredients of allopurinol *:
- female: 47.46 %
- male: 52.54 %
Age of people who have Vasodilatation when taking drugs with ingredients of allopurinol *:
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 1.92 %
- 20-29: 0.0 %
- 30-39: 0.0 %
- 40-49: 1.92 %
- 50-59: 15.38 %
- 60+: 80.77 %
Conditions people have *:
You may use this to check any potential undetected conditions.
Other drugs people take *:
You may use this to check any potential interacting drugs.
Other side effects people have besides Vasodilatation *:
You may use this to check any potential undetected side effects.
* Approximation only. Some reports may have incomplete information.
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.
Related studies
Drugs with ingredients of allopurinol, their effectiveness, alternatives and more:
How the study uses the data?
The study uses data from the FDA. It is based on allopurinol. All drugs that have the same active ingredients (e.g. brand name and generic drugs) are considered. Dosage of drugs is not considered in the study.
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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