The effects of supratherapeutic doses of duloxetine on blood pressure and pulse rate

被引:30
作者
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.
机构
[1] Eli Lilly & Co, Lilly Res Ctr, Windlesham GU20 6PH, Surrey, England
[2] Eli Lilly & Co, Indianapolis, IN 46285 USA
[3] Indiana Univ, Sch Med, Indianapolis, IN USA
[4] California Clin Trials, Glendale, CA USA
[5] PPD Dev, Austin, TX USA
[6] Quintiles Phase 1 Serv, Lenexa, KS USA
关键词
duloxetine; vital signs; orthostasis; blood pressure; supratherapeutic dose;
D O I
10.1097/FJC.0b013e31804d1cce
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 16days. 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 similar to 12 mm Hg and similar to 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 I 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.
引用
收藏
页码:384 / 393
页数:10
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