Derby Michael A, Zhang Lu, Chappell Jill C, Gonzales Celedon R, Callaghan J T, Leibowitz Mark, Ereshefsky Larry, Hoelscher David, Leese Philip T, Mitchell Malcolm I
Eli Lilly and Company, Indianapolis, IN, USA.
J Cardiovasc Pharmacol. 2007 Jun;49(6):384-93. doi: 10.1097/FJC.0b013e31804d1cce.
The effects of supratherapeutic dosages of duloxetine, a serotonin and norepinephrine reuptake inhibitor, on blood pressure and pulse rate were assessed in a multicenter, double-blind, randomized, placebo-controlled, crossover study in 117 healthy women aged 19 to 74 years. Dosages were escalated from 60 mg twice daily (BID) to 200 mg BID over 16 days. Vital signs were monitored at baseline, before morning dosing, and sequentially at steady state. Duloxetine produced increases in supine systolic and diastolic blood pressures, which reached maximums of approximately 12 mm Hg and approximately 7 mm Hg above baseline, respectively, during dosing at 120 mg BID and then stabilized. Supine pulse rate increased gradually with dose, reaching 10 to 12 bpm above baseline after 4 days of dosing at 200 mg BID. Duloxetine caused changes in orthostatic blood pressures and pulse rate that reached plateau values after 3 to 4 days of dosing at 160 mg BID and were generally not associated with subjectively reported orthostatic-related adverse events. All vital signs normalized by 1 to 2 days after study drug discontinuation. Prehypertensive subjects may become hypertensive upon initial duloxetine dosing, but this can be predicted from predose blood pressure. Short-term supratherapeutic duloxetine dosages up to 200 mg BID are not well tolerated but are generally not associated with severe, clinically important adverse events. Overall, the types of adverse events reported in this study were similar to those in other studies of duloxetine in healthy subjects.
在一项针对117名年龄在19至74岁的健康女性的多中心、双盲、随机、安慰剂对照、交叉研究中,评估了超治疗剂量的度洛西汀(一种5-羟色胺和去甲肾上腺素再摄取抑制剂)对血压和脉搏率的影响。剂量在16天内从每日两次60毫克逐步增至每日两次200毫克。在基线、晨服前以及稳态时依次监测生命体征。度洛西汀使仰卧位收缩压和舒张压升高,在每日两次服用120毫克给药期间,收缩压和舒张压分别比基线最高升高约12毫米汞柱和约7毫米汞柱,然后趋于稳定。仰卧位脉搏率随剂量逐渐增加,在每日两次服用200毫克给药4天后比基线升高10至12次/分钟。度洛西汀引起体位性血压和脉搏率变化,在每日两次服用160毫克给药3至4天后达到平稳值,且一般与受试者主观报告的体位性相关不良事件无关。在停用研究药物后1至2天,所有生命体征恢复正常。高血压前期受试者在开始服用度洛西汀时可能会变成高血压患者,但这可以根据给药前血压预测。每日两次高达200毫克的短期超治疗剂量度洛西汀耐受性不佳,但一般与严重的、具有临床重要性的不良事件无关。总体而言,本研究中报告的不良事件类型与其他关于度洛西汀在健康受试者中的研究相似。