Levetiracetam and Limb reduction defect - a phase IV clinical study of FDA data
Summary:
Limb reduction defect is reported as a side effect among people who take Levetiracetam (levetiracetam), especially for people who are male, 0-1 old, have been taking the drug for 1 - 6 months also take Folic Acid, and have Foetal exposure during pregnancy.
The phase IV clinical study analyzes which people have Limb reduction defect when taking Levetiracetam. It is created by eHealthMe based on reports of 74,747 people who have side effects when taking Levetiracetam from the FDA, and is updated regularly.
What is Levetiracetam?
Levetiracetam has active ingredients of levetiracetam. It is often used in epilepsy. eHealthMe is studying from 75,292 Levetiracetam users. Check the latest studies of Levetiracetam.
What is Limb reduction defect?
Limb reduction defect (a birth defect in which all or some of the limbs of a foetus do not completely form while in utero) is found to be associated with 62 drugs and 134 conditions by eHealthMe. Check the latest studies of Limb reduction defect.
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 >>>.
74,747 people reported to have side effects when taking Levetiracetam.
Among them, 26 people (0.03%) have Limb reduction defect.

Among these 26 people:
How long have people been on Levetiracetam when they have Limb reduction defect? *
- < 1 month: 0.0 %
- 1 - 6 months: 66.67 %
- 6 - 12 months: 0.0 %
- 1 - 2 years: 33.33 %
- 2 - 5 years: 0.0 %
- 5 - 10 years: 0.0 %
- 10+ years: 0.0 %
What is the gender of people who have Limb reduction defect when taking Levetiracetam? *
- female: 6.25 %
- male: 93.75 %
What is the age of people who have Limb reduction defect when taking Levetiracetam? *
- 0-1: 100 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 0.0 %
- 30-39: 0.0 %
- 40-49: 0.0 %
- 50-59: 0.0 %
- 60+: 0.0 %
What are other drugs people take besides Levetiracetam? *
- Folic Acid: 11 people, 42.31%
- Lamotrigine: 8 people, 30.77%
- Vigabatrin: 1 person, 3.85%
- Topiramate: 1 person, 3.85%
- Primidone: 1 person, 3.85%
- Pregabalin: 1 person, 3.85%
- Phenytoin: 1 person, 3.85%
- Oxcarbazepine: 1 person, 3.85%
- Lorazepam: 1 person, 3.85%
- Gabapentin: 1 person, 3.85%
What are other side effects people have besides Limb reduction defect? *
- Foetal Exposure During Pregnancy (exposing your unborn child to contraindicated in pregnancy leads birth defect): 19 people, 73.08%
- Maternal Exposure During Pregnancy (use of substance during pregnancy): 6 people, 23.08%
- Potter's Syndrome: 2 people, 7.69%
- Caudal Regression Syndrome (disorder that impairs the development of the lower (caudal) half of the body): 2 people, 7.69%
- Premature Baby: 1 person, 3.85%
- Oligohydramnios (a condition in pregnancy characterized by a deficiency of amniotic fluid): 1 person, 3.85%
- Low Birth Weight Baby: 1 person, 3.85%
- Klinefelter's Syndrome (a chromosomal abnormality (xxy)weaker muscles and reduced strength): 1 person, 3.85%
- Foetal Growth Restriction (poor growth of a baby while in the mother's womb during pregnancy): 1 person, 3.85%
- Bone Development Abnormal: 1 person, 3.85%
What are the existing conditions these people have? *
- Foetal Exposure During Pregnancy (exposing your unborn child to contraindicated in pregnancy leads birth defect): 3 people, 11.54%
* Approximation only. Some reports may have incomplete information.
Do you take Levetiracetam and have Limb reduction defect?
- Check whether Limb reduction defect 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 Levetiracetam:
- Levetiracetam (75,292 reports)
Limb reduction defect treatments and more:
- Limb reduction defect (807 reports)
How severe was Limb reduction defect and when was it recovered:
Expand to all the drugs that have ingredients of levetiracetam:
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 Levetiracetam:
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 Limb reduction defect:
- Limb reduction defect (62 drugs)
Browse all the conditions that are associated with Limb reduction defect:
- Limb reduction defect (134 conditions)
Related publications that referenced our studies
- Schattner A, Al-Bewerat A, "Levetiracetam (Keppra), urinary retention and literature search", A fatty cause of renal failure; what is your diagnosis?, 2016 Oct .
- Spengler DC, Montouris GD, Hohler AD, "Levetiracetam as a possible contributor to acute kidney injury", Clinical therapeutics, 2014 Aug .
- Almeida DM, Jean MR, Chystsiakova A, Monahan E, Oliveira SB, Monteiro IM, "Levetiracetam-associated acute pancreatitis in an adolescent with autism: a case report", Pancreas, 2013 Jan .
- Schattner A, Al-Bewerat A, "Levetiracetam (Keppra), urinary retention and literature search", A fatty cause of renal failure; what is your diagnosis?, 2016 Oct .
- Spengler DC, Montouris GD, Hohler AD, "Levetiracetam as a possible contributor to acute kidney injury", Clinical therapeutics, 2014 Aug .
- Almeida DM, Jean MR, Chystsiakova A, Monahan E, Oliveira SB, Monteiro IM, "Levetiracetam-associated acute pancreatitis in an adolescent with autism: a case report", Pancreas, 2013 Jan .
How the study uses the data?
The study uses data from the FDA. It is based on levetiracetam (the active ingredients of Levetiracetam) and Levetiracetam (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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