How effective is Lamotrigine for Complex Partial Seizures? (a real world drug study)
Summary:
Overall ratings: 3.7/5 Long term ratings: 3.5/5
This is a phase IV clinical study of how effective Lamotrigine (lamotrigine) is for Complex partial seizures and for what kind of people. The study is created by eHealthMe from 3 Lamotrigine users and is updated continuously.
What is Lamotrigine?
Lamotrigine has active ingredients of lamotrigine. It is often used in bipolar disorder. eHealthMe is studying from 76,638 Lamotrigine users. Check the latest studies of Lamotrigine.
What is Complex partial seizures?
Complex partial seizures (epileptic seizure) is found to be associated with 218 drugs and 440 conditions by eHealthMe. Check the latest studies of Complex partial seizures.
3 people are studied for taking Lamotrigine in Complex partial seizures
Overall effectiveness (number of people):

Long term (1+ years) effectiveness (number of people):

Lamotrigine effectiveness for Complex partial seizures (number of people):
Overall:
- not at all: 0
- somewhat: 1
- moderate: 0
- high: 1
- very high: 1
Long Term:
- not at all: 0
- somewhat: 1
- moderate: 0
- high: 0
- very high: 1
Gender of people who take Lamotrigine for Complex partial seizures *:
- female: 66.67 %
- male: 33.33 %
Age of people who take Lamotrigine for Complex partial seizures *:
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 33.33 %
- 20-29: 33.33 %
- 30-39: 0.0 %
- 40-49: 0.0 %
- 50-59: 33.33 %
- 60+: 0.0 %
Who find Lamotrigine more effective for Complex Partial Seizures?
Gender of people who take Lamotrigine for Complex partial seizures *:
- female: 50 %
- male: 50 %
Age of people who take Lamotrigine for Complex partial seizures *:
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 50 %
- 20-29: 0.0 %
- 30-39: 0.0 %
- 40-49: 0.0 %
- 50-59: 50 %
- 60+: 0.0 %
* Approximation only. Some reports may have incomplete information.
Do you take Lamotrigine?
- You can start a phase IV clinical trial to monitor Lamotrigine safety and effectiveness.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
Alternative drugs to, pros and cons of:
- Lamotrigine (76,638 reports)
Treatments, associated drugs and conditions:
- Complex partial seizures (4,639 reports)
How the study uses the data?
The study is based on lamotrigine (the active ingredients of Lamotrigine) and Lamotrigine (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 neither.
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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