This surveillance's objectives are 1. Unknown adverse reactions 2. Incidences of adverse drug reaction 3. Efficacy during long-term administration 4. Factors considered to have effect to safety and effectiveness 5. Incidences of status epileptics, skin disorders and hyper sensitivity reaction, and central nervous system-related adverse events(ataxia , somnolence and/or dizzy, etc.)
Study Type
OBSERVATIONAL
Enrollment
707
Administration of Inovelon 100mg or 200mg Tablets
Unnamed facility
Osaka, Japan
Unnamed facility
Tokyo, Japan
Investigations on adverse events and adverse drug reactions
Time frame: Up to 2 years
Frequency of attacks
Time frame: 12 weeks and every 6 months up to 2years
Overall assessments of the improvement in the seriousness of seizures
Time frame: 12 weeks and every 6 months up to 2years
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