Loraz and Post procedural haemorrhage - a phase IV clinical study of FDA data
Summary:
Post procedural haemorrhage is reported as a side effect among people who take Loraz (lorazepam), especially for people who are female, 60+ old, have been taking the drug for < 1 month also take Lipitor, and have Pain.
The phase IV clinical study analyzes which people have Post procedural haemorrhage when taking Loraz. It is created by eHealthMe based on reports of 161,700 people who have side effects when taking Loraz from the FDA, and is updated regularly.
What is Loraz?
Loraz has active ingredients of lorazepam. It is often used in stress and anxiety. eHealthMe is studying from 165,694 Loraz users. Check the latest studies of Loraz.
What is Post procedural haemorrhage?
Post procedural haemorrhage (post procedural bleeding) is found to be associated with 664 drugs and 854 conditions by eHealthMe. Check the latest studies of Post procedural haemorrhage.
161,700 people reported to have side effects when taking Loraz.
Among them, 102 people (0.06%) have Post procedural haemorrhage.
Among these 102 people:
How long have people been on Loraz when they have Post procedural haemorrhage? *
What is the gender of people who have Post procedural haemorrhage when taking Loraz? *
What is the age of people who have Post procedural haemorrhage when taking Loraz? *
What are other drugs people take besides Loraz? *
What are other side effects people have besides Post procedural haemorrhage? *
What are the existing conditions these people have? *
* Approximation only. Some reports may have incomplete information.
Do you take Loraz and have Post procedural haemorrhage?
- Check whether Post procedural haemorrhage 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 Loraz:
- Loraz (165,694 reports)
Post procedural haemorrhage treatments and more:
- Post procedural haemorrhage (14,222 reports)
How severe was Post procedural haemorrhage and when was it recovered:
Expand to all the drugs that have ingredients of lorazepam:
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 Loraz:
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 Post procedural haemorrhage:
- Post procedural haemorrhage (664 drugs)
Browse all the conditions that are associated with Post procedural haemorrhage:
- Post procedural haemorrhage (854 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on lorazepam (the active ingredients of Loraz) and Loraz (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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