How long after infantile epilepsy drinks medicine won't irritable

summary

summary Childhood is a high incidence of epilepsy in children, epilepsy symptoms are usually manifested as muscle twitch and disturbance of consciousness, recurrent seizures, there will also be sensory, emotional, behavioral or autonomic nervous function abnormalities, the cause of epilepsy in children is complex, easy to recurrent seizures, so the following is a specific introduction of how long children epilepsy after drinking medicine will not be irritable this problem, hope to help some people. Drug 1: aminohexenoic acid. It is highly water-soluble, has high oral bioavailability, and is not affected by food. The peak time is 1-4 hours. Most of it does not bind to protein. The half-life is 5-7 hours. It is not metabolized by liver. The original form is excreted by kidney. It has no liver enzyme induction and inhibition. It can slightly reduce the concentration of phenytoin sodium, phenobarbital and deoxyphenobarbital, There was no interaction with most antiepileptic drugs. Drug 2: lamotrigine. Oral absorption is fast, the bioavailability is more than half, not affected by food, the peak time is 2-3 hours, the protein binding rate is very high, the half-life is 19-30 hours, most of them are excreted by urine, no liver enzyme induction. Sodium valproate inhibited its metabolism, while carbamazepine, phenobarbital and phenytoin accelerated its excretion. Clinically, it is mainly used for adjuvant treatment of refractory atypical absence seizures, myoclonic seizures, atonic seizures and tonic seizures. Drug 3: non amino ester. Oral absorption is not affected by food and anti acid drugs. The bioavailability reaches the peak at 1-3.5 hours. The protein binding rate is very low, with a half-life of 14-21 hours. About half of the drug is excreted in urine after liver metabolism and the other half.

How long after infantile epilepsy drinks medicine won't irritable

Oral absorption is not affected by food and anti acid drugs. The bioavailability reaches the peak at 1-3.5 hours. The protein binding rate is very low, with a half-life of 14-21 hours. About half of the drug is excreted in urine after liver metabolism and the other half.

药物二：拉莫三嗪。口服吸收快，生物利用度在将近一半以上，不受食物影响，达峰时间2至3小时，蛋白结合率很高，半衰期19至30小时，大部分由尿 排泄，无肝酶诱导作用。丙戊酸钠抑制其代谢，而卡马西平、苯巴比妥及苯妥英钠可加速其排泄。临床上主要用于辅助治疗难治性不典型失神发作、肌阵挛发作、失张力发作及强直发作。

药物三：非氨酯。口服吸收不受食物及抗酸药物的影响，生物利用度达顶峰，达峰时间为1至3.5小时，蛋白结合率很低，半衰期为 14至21小时，约一半由肝代谢后与另一半母药由尿排泄。

注意事项

关于小儿癫痫喝药后多久才不会烦躁的信息就说到这了，还要提醒大家的是，家长朋友要积极配合医生的治疗，给孩子更多的关爱和照顾，合理安排生活和学习，避免去一些危险的地方玩耍，要定期到医院进行复查，以便随时了解病情。