Müller F O, Middle M V, Schall R, Terblanché J, Hundt H K, Groenewoud G
FARMOVS Research Centre for Clinical Pharmacology and Drug Development, Department of Pharmacology, University of the Orange Free State, Bloemfontein, South Africa.
Br J Clin Pharmacol. 1997 Oct;44(4):393-8. doi: 10.1046/j.1365-2125.1997.t01-1-00586.x.
To evaluate the interaction of meloxicam with frusemide in patients with compensated cardiac failure.
Nineteen patients with Grade II or III compensated chronic cardiac failure completed this randomized, double-blind, cross-over study. The patients received 40 mg frusemide day(-1) for 7 days. Thereafter, patients received either 15 mg meloxicam plus 40 mg frusemide day(-1), or one placebo tablet plus 40 mg frusemide day(-1) for 7 days. After a washout period of 7 days during which patients received 40 mg frusemide day(-1) for 7 days, the patients were crossed over to the alternate treatment. The effect of concomitant ingestion of meloxicam and frusemide on frusemide-induced diuresis, urine and serum electrolytes, urinary frusemide excretion, and plasma frusemide pharmacokinetics was also determined.
The estimate (90% confidence interval) of the '(frusemide + meloxicam)/(frusemide alone)' mean ratio of the variables Cmax, AUC(SS) and Cmax/AUC(SS) for plasma frusemide were 121% (101% to 145%), 106% (96.4% to 117%), and 114% (98.3% to 132%), respectively. Similarly, the estimate (90% confidence interval) of the '(frusemide + meloxicam)/(frusemide alone)' of the mean ratio of the variable cumulative urinary frusemide excretion after multiple doses of frusemide were 123% (101% to 150%) for the period 0-8 h, and 122% (105% to 142%) for the period 0-24 h after drug administration on day 7. The estimate (90% confidence interval) of the '(frusemide + meloxicam)/(frusemide alone)' mean ratio of the pharmacodynamic variables cumulative sodium excretion was 105% (95.2% to 116%) for the period 0-8 h and 108% (96.5% to 121%) for the period 0-24 h after drug administration on day 7.
Meloxicam may lead to slightly increased maximum concentrations of frusemide in plasma, as well as to slightly increased urinary excretion of frusemide, without affecting the pharmacodynamics of frusemide. Thus there is no clinically significant pharmacokinetic or pharmacodynamic interaction of meloxicam with frusemide following repeated co-administration of meloxicam and frusemide to patients with compensated chronic cardiac failure.
评估美洛昔康与呋塞米在代偿性心力衰竭患者中的相互作用。
19例II级或III级代偿性慢性心力衰竭患者完成了这项随机、双盲、交叉研究。患者每天服用40mg呋塞米,共7天。此后,患者接受15mg美洛昔康加40mg呋塞米,或一片安慰剂加40mg呋塞米,均为每日一次,持续7天。在为期7天的洗脱期内,患者每天服用40mg呋塞米,之后进行交叉接受另一种治疗。还测定了美洛昔康与呋塞米同时服用对呋塞米诱导的利尿作用、尿液和血清电解质、尿中呋塞米排泄以及血浆呋塞米药代动力学的影响。
血浆呋塞米的Cmax、AUC(SS)和Cmax/AUC(SS)变量的‘(呋塞米+美洛昔康)/(单独使用呋塞米)’平均比值的估计值(90%置信区间)分别为121%(101%至145%)、106%(96.4%至117%)和114%(98.3%至132%)。同样,多次服用呋塞米后,在第7天给药后0-8小时期间,累积尿呋塞米排泄变量的‘(呋塞米+美洛昔康)/(单独使用呋塞米)’平均比值的估计值(90%置信区间)为123%(101%至150%),0-24小时期间为122%(105%至142%)。在第7天给药后0-8小时期间,药效学变量累积钠排泄的‘(呋塞米+美洛昔康)/(单独使用呋塞米)’平均比值的估计值(90%置信区间)为105%(95.2%至116%),0-24小时期间为108%(9