324 reports of this reaction
2.2% of all PERAMPANEL reports
#8 most reported adverse reaction
STATUS EPILEPTICUS is the #8 most commonly reported adverse reaction for PERAMPANEL, manufactured by Catalyst Pharmaceuticals, Inc.. There are 324 FDA adverse event reports linking PERAMPANEL to STATUS EPILEPTICUS. This represents approximately 2.2% of all 14,467 adverse event reports for this drug.
Patients taking PERAMPANEL who experience status epilepticus should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
STATUS EPILEPTICUS is a less commonly reported adverse event for PERAMPANEL, but still significant enough to appear in the safety profile.
In addition to status epilepticus, the following adverse reactions have been reported for PERAMPANEL:
The following drugs have also been linked to status epilepticus in FDA adverse event reports:
STATUS EPILEPTICUS has been reported as an adverse event in 324 FDA reports for PERAMPANEL. This does not prove causation, but indicates an association observed in post-market surveillance data.
STATUS EPILEPTICUS accounts for approximately 2.2% of all adverse event reports for PERAMPANEL, making it a notable side effect.
If you experience status epilepticus 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.