Haddad Z H, Stumbaugh S, Davis W R
Ann Allergy. 1980 Feb;44(2):86-90.
Terbutaline tablets and oral solution were tested in 16 subjects between the ages of seven and 15 in a double-blind acute cross-over study. Doses of terbutaline were 2.5, 3.75 or 5.0 mg depending upon the weight of each subject. Both formulations produced significant increases in pulmonary function between 15 minutes and five hours after drug administration as measured by FVC and FEV1. The mean maximal increase in FEV1 was 0.60 liters for the tablet and 0.70 liters for the solution. The mean maximal increase in FVC was 0.53 liters for the tablet and 0.67 for the solution. There were significant increases in heart rate following both tablet and solution. The mean increases were statistically significant between two and five hours after drug administration, ranging from two to nine beats/minute for the tablet and eight to 13 beats/minute for the solution. Terbutaline produced no clinically or statistically significant mean changes in systolic or diastolic blood pressure. The responses to tablet and solution did not differ significantly from each other in any parameter. Terbutaline tablet and oral solution were, therefore, bioequivalent.
在一项双盲急性交叉研究中,对16名年龄在7至15岁之间的受试者进行了特布他林片剂和口服溶液的测试。根据每个受试者的体重,特布他林的剂量分别为2.5、3.75或5.0毫克。给药后15分钟至5小时内,通过用力肺活量(FVC)和1秒用力呼气容积(FEV1)测量,两种制剂均使肺功能显著增加。片剂组FEV1的平均最大增加量为0.60升,溶液组为0.70升。片剂组FVC的平均最大增加量为0.53升,溶液组为0.67升。片剂和溶液给药后心率均显著增加。给药后2至5小时内平均增加量具有统计学意义,片剂组为每分钟2至9次心跳,溶液组为每分钟8至13次心跳。特布他林对收缩压或舒张压没有产生临床上或统计学上显著的平均变化。在任何参数方面,片剂和溶液的反应彼此之间没有显著差异。因此,特布他林片剂和口服溶液具有生物等效性。