We did not observe a dose-dependent relationship between lacosamide therapy and the development of adverse effects. Indeed, the patient who received the highest lacosamide dose (20 mg/kg/day) did not experience any adverse effects. Moreover, a very large dose of lacosamide, used in a suicide attempt, did not result in death or permanent injury; complete physical recovery was achieved after several days.[15] Plasma drug levels were not determined in our study, although determination of saliva

drug concentrations is a new alternative that may provide a more objective method of analysis in the near future.[16] As a consequence, this may enable a more rational method of adjusting lacosamide doses. The literature suggests that adverse effects associated with lacosamide therapy are generally see more mild-to-moderate in severity at doses of up to 600 mg/day.[3,4,6] Although adverse effects were observed in 30% of selleck chemicals llc patients in our CRT0066101 ic50 study, these effects led to drug withdrawal in only 10% of the overall study population. Additionally, the series by Gavatha et al.[10] reported a similar incidence of adverse effects (33%). In the study by Chez et al.,[9] adverse effects were observed in 8.6% of cases, which is a slightly lower rate, but lower doses were also used. However, there continues to be doubt concerning the hypothetical relationship

between adverse effects and dose, which we were unable to confirm either way. The marked instability, difficulty walking, and blurred vision that were observed here in ten patients have also been reported previously in a series of adult patients.[17] In five of our cases, symptom intensity remained unchanged, despite an immediate dose decrease, which eventually led to suspension of treatment. Furthermore, these symptoms differed significantly between patients, which prevented determination of a convincing pathophysiological explanation, or the relationship Resveratrol between these symptoms and the use of other AEDs. Further investigation of these effects is required in randomized, controlled trials to fully elucidate any causal factors in this patient

population. No cardiovascular effects were observed in our patients. In contrast, lacosamide has been associated with atrial flutter/atrial fibrillation at doses of 600 mg/day or above in adults with epilepsy.[5] Furthermore, we did not observe any alterations in conventional laboratory tests or significant changes in EEG records. However, we did not have the opportunity to assess favorable effects of lacosamide on photoparoxysmal responses, which have recently been reported.[18] Conclusion In summary, lacosamide appears to be an effective and generally well tolerated AED in children and adolescents with pharmaco-resistant focal epileptic seizures. However, the instability, accompanied by difficulty walking and blurred vision, that was observed in ten patients requires further investigation.