Tao G K, Harada D T, Kootsikas M E, Gordon M N, Brinkman J H
Drug Intell Clin Pharm. 1985 Jul-Aug;19(7-8):548-9. doi: 10.1177/106002808501900707.
A case report of amoxapine-induced tardive dyskinesia following discontinuation of amoxapine therapy is reported. During 68 weeks of therapy, the patient received a maximum of amoxapine 400 mg/d. Six months after amoxapine discontinuation, the patient continued to have symptoms of tardive dyskinesia. These symptoms correlate with the dopamine receptor-blocking property of amoxapine and its metabolites. We propose that amoxapine therapy be monitored for the long-term as well as the short-term adverse effects of dopamine receptor-blockade.
本文报告了1例停用阿莫沙平治疗后出现阿莫沙平所致迟发性运动障碍的病例。在68周的治疗期间,该患者接受的阿莫沙平最大剂量为400mg/d。停用阿莫沙平6个月后,患者仍有迟发性运动障碍症状。这些症状与阿莫沙平及其代谢产物的多巴胺受体阻断特性相关。我们建议对阿莫沙平治疗进行长期监测,以观察多巴胺受体阻断的短期和长期不良反应。