332 reports of this reaction
2.3% of all PERAMPANEL reports
#7 most reported adverse reaction
EPILEPSY is the #7 most commonly reported adverse reaction for PERAMPANEL, manufactured by Catalyst Pharmaceuticals, Inc.. There are 332 FDA adverse event reports linking PERAMPANEL to EPILEPSY. This represents approximately 2.3% of all 14,467 adverse event reports for this drug.
Patients taking PERAMPANEL 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 PERAMPANEL, but still significant enough to appear in the safety profile.
In addition to epilepsy, the following adverse reactions have been reported for PERAMPANEL:
The following drugs have also been linked to epilepsy in FDA adverse event reports:
EPILEPSY has been reported as an adverse event in 332 FDA reports for PERAMPANEL. This does not prove causation, but indicates an association observed in post-market surveillance data.
EPILEPSY accounts for approximately 2.3% of all adverse event reports for PERAMPANEL, making it a notable side effect.
If you experience epilepsy while taking PERAMPANEL, 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.