Browne T R
Arch Neurol. 1976 May;33(5):326-32. doi: 10.1001/archneur.1976.00500050012003.
Clonazepam is a new benzodiazepine anticonvulsant recently approved by the Food and Drug Administration for the treatment of typical absence, infantile myoclonic, atypical absence, myoclonic, and akinetic seizures. It is rapidly absorbed by the oral route and appears to pass quickly from blood to brain. Preliminary results indicate a biological half-life of 22 to 32 hours and a therapeutic serum concentration of 5 to 50 ng/ml. Many studies report tolerance to the anticonvulsant effects with chronic administration. Major side effects of the drug are drowsiness, ataxia, and behavior changes. They tend to be dose related, occur early in the course of therapy, and may subside with chronic administration. Accordingly, the dosage is begun at a low level and increased slowly.
氯硝西泮是一种新型苯二氮䓬类抗惊厥药,最近被美国食品药品监督管理局批准用于治疗典型失神发作、婴儿肌阵挛性发作、非典型失神发作、肌阵挛发作和失张力发作。它经口服迅速吸收,似乎能迅速从血液进入大脑。初步结果表明其生物半衰期为22至32小时,治疗性血清浓度为5至50纳克/毫升。许多研究报告称长期服用会产生抗惊厥作用耐受性。该药物的主要副作用是嗜睡、共济失调和行为改变。这些副作用往往与剂量相关,在治疗初期出现,长期服用可能会减轻。因此,用药剂量从低水平开始,缓慢增加。