The present study aimed to characterize the seizures produced of HAL, CPZ, and FXT increased onset latencies of GTCS (p<0.01) while HAL (1.5 mg/kg), CPZ (2 mg/kg), and FXT (1 and 2 mg/kg) also increased onset latencies of PMS (p<0.05). Our study validated TSC-induced seizures in rats as a dose-dependent model of PMS, GTCS, and SE.