1,783 reports of this reaction
1.4% of all LAMOTIRIGINE reports
#20 most reported adverse reaction
EPILEPSY is the #20 most commonly reported adverse reaction for LAMOTIRIGINE, manufactured by Actavis Pharma, Inc.. There are 1,783 FDA adverse event reports linking LAMOTIRIGINE to EPILEPSY. This represents approximately 1.4% of all 130,106 adverse event reports for this drug.
Patients taking LAMOTIRIGINE who experience epilepsy should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
EPILEPSY is a less commonly reported adverse event for LAMOTIRIGINE, but still significant enough to appear in the safety profile.
In addition to epilepsy, the following adverse reactions have been reported for LAMOTIRIGINE:
The following drugs have also been linked to epilepsy in FDA adverse event reports:
EPILEPSY has been reported as an adverse event in 1,783 FDA reports for LAMOTIRIGINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
EPILEPSY accounts for approximately 1.4% of all adverse event reports for LAMOTIRIGINE, making it a notable side effect.
If you experience epilepsy while taking LAMOTIRIGINE, contact your healthcare provider. They can evaluate whether the symptom is related to your medication and discuss potential adjustments to your treatment plan. Do not stop taking prescribed medication without consulting your doctor.