Lyrica and Post procedural infection - a phase IV clinical study of FDA data
Summary:
Post procedural infection is reported as a side effect among people who take Lyrica (pregabalin), especially for people who are female, 60+ old, have been taking the drug for 6 - 12 months also take Celebrex, and have Rheumatoid arthritis.
The phase IV clinical study analyzes which people have Post procedural infection when taking Lyrica. It is created by eHealthMe based on reports of 255,839 people who have side effects when taking Lyrica from the FDA, and is updated regularly.
What is Lyrica?
Lyrica has active ingredients of pregabalin. It is often used in fibromyalgia. eHealthMe is studying from 261,646 Lyrica users. Check the latest studies of Lyrica.
What is Post procedural infection?
Post procedural infection is found to be associated with 583 drugs and 565 conditions by eHealthMe. Check the latest studies of Post procedural infection.
255,839 people reported to have side effects when taking Lyrica.
Among them, 157 people (0.06%) have Post procedural infection.
Among these 157 people:
How long have people been on Lyrica when they have Post procedural infection? *
What is the gender of people who have Post procedural infection when taking Lyrica? *
What is the age of people who have Post procedural infection when taking Lyrica? *
What are other drugs people take besides Lyrica? *
What are other side effects people have besides Post procedural infection? *
What are the existing conditions these people have? *
* Approximation only. Some reports may have incomplete information.
Do you take Lyrica and have Post procedural infection?
- Check whether Post procedural infection 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 Lyrica:
- Lyrica (261,646 reports)
Post procedural infection treatments and more:
- Post procedural infection (10,700 reports)
How severe was Post procedural infection and when was it recovered:
Expand to all the drugs that have ingredients of pregabalin:
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 Lyrica:
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 infection:
- Post procedural infection (583 drugs)
Browse all the conditions that are associated with Post procedural infection:
- Post procedural infection (565 conditions)
Related publications that referenced our studies
- de Landaluce, L. O., Carbonell, P., Asensio, C., Escoda, N., López, P., & Laporte, J. R. , "Gabapentin and Pregabalin and Risk of Atrial Fibrillation in the Elderly: A Population-Based Cohort Study in an Electronic Prescription Database", Drug safety, 2018 Jan .
- Bonnet U, Taazimi B, Grabbe HD, "Pregabalin-Related Hypertriglyceridemia", Psychosomatics, 2014 Nov .
- de Landaluce, L. O., Carbonell, P., Asensio, C., Escoda, N., López, P., & Laporte, J. R. , "Gabapentin and Pregabalin and Risk of Atrial Fibrillation in the Elderly: A Population-Based Cohort Study in an Electronic Prescription Database", Drug safety, 2018 Jan .
- Bonnet U, Taazimi B, Grabbe HD, "Pregabalin-Related Hypertriglyceridemia", Psychosomatics, 2014 Nov .
How the study uses the data?
The study uses data from the FDA. It is based on pregabalin (the active ingredients of Lyrica) and Lyrica (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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