Beovu and Intraocular pressure increased - a phase IV clinical study of FDA data
Summary:
Intraocular pressure increased is reported as a side effect among people who take Beovu (brolucizumab-dbll), especially for people who are female, 60+ old, have been taking the drug for < 1 month also take Eylea, and have Age-related macular degeneration.
The phase IV clinical study analyzes which people have Intraocular pressure increased when taking Beovu. It is created by eHealthMe based on reports of 3,872 people who have side effects when taking Beovu from the FDA, and is updated regularly.
What is Beovu?
Beovu has active ingredients of brolucizumab-dbll. eHealthMe is studying from 3,872 Beovu users. Check the latest studies of Beovu.
What is Intraocular pressure increased?
Intraocular pressure increased is found to be associated with 722 drugs and 953 conditions by eHealthMe. Check the latest studies of Intraocular pressure increased.
3,872 people reported to have side effects when taking Beovu.
Among them, 126 people (3.25%) have Intraocular pressure increased.
Among these 126 people:
How long have people been on Beovu when they have Intraocular pressure increased? *
What is the gender of people who have Intraocular pressure increased when taking Beovu? *
What is the age of people who have Intraocular pressure increased when taking Beovu? *
What are other drugs people take besides Beovu? *
What are other side effects people have besides Intraocular pressure increased? *
What are the existing conditions these people have? *
* Approximation only. Some reports may have incomplete information.
Do you take Beovu and have Intraocular pressure increased?
- Check whether Intraocular pressure increased 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 Beovu:
- Beovu (3,872 reports)
Intraocular pressure increased treatments and more:
- Intraocular pressure increased (19,280 reports)
How severe was Intraocular pressure increased and when was it recovered:
Expand to all the drugs that have ingredients of brolucizumab-dbll:
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 Beovu:
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 Intraocular pressure increased:
- Intraocular pressure increased (722 drugs)
Browse all the conditions that are associated with Intraocular pressure increased:
- Intraocular pressure increased (953 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on brolucizumab-dbll (the active ingredients of Beovu) and Beovu (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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