Craft T M, Vanden Bussche G, De Cree J, Griffiths J V
Department of Anaesthesia and Intensive Care, Milton Keynes, Bucks, UK.
Hum Toxicol. 1987 Nov;6(6):527-8. doi: 10.1177/096032718700600614.
1 Six healthy volunteers took part in a 2-week haemodynamic safety study of astemizole. 2 They were given 30 mg daily (3 X 10 mg tablets) for the first 3 days and 10 mg daily for the next 12 consecutive days. 3 Heart rate, blood pressure, ECG and systolic time intervals at rest were measured before the start and five times during the day. 4 No changes were observed in any of the parameters measured. The configuration of the ECG was not influenced. 5 Serum concentrations of astemizole plus hydroxylated metabolites measured at the end of the study were 16 times lower than those detected in a patient overdosing on 200 mg astemizole.
六名健康志愿者参与了一项为期两周的阿司咪唑血液动力学安全性研究。
他们在开始的3天里每天服用30毫克(3片10毫克的片剂),随后连续12天每天服用10毫克。
在开始前以及白天五次测量静息时的心率、血压、心电图和收缩期时间间期。
所测量的任何参数均未观察到变化。心电图的形态未受影响。
在研究结束时所测得的阿司咪唑加羟基化代谢产物的血清浓度比一名过量服用200毫克阿司咪唑的患者中检测到的浓度低16倍。