Treatment with acetaminophen/paracetamol or ibuprofen alleviates post-dose symptoms related to intravenous infusion with zoledronic acid 5 mg

被引:77
作者
Wark, J. D. [1 ,2 ]
Bensen, W. [3 ]
Recknor, C. [4 ]
Ryabitseva, O. [5 ]
Chiodo, J., III [6 ]
Mesenbrink, P. [7 ]
de Villiers, T. J. [8 ,9 ]
机构
[1] Univ Melbourne, Royal Melbourne Hosp, Dept Med, Melbourne, Vic 3050, Australia
[2] Univ Melbourne, Royal Melbourne Hosp, Bone & Mineral Serv, Melbourne, Vic 3050, Australia
[3] McMaster Univ, St Josephs Hosp, Hamilton, ON, Canada
[4] United Osteoporosis Ctr, Gainesville, GA USA
[5] Reg Hosp 1, Ekaterinburg, Russia
[6] Otsuka Amer Pharmaceut Inc, Princeton, NJ USA
[7] Novartis Pharmaceut, E Hanover, NJ USA
[8] Panorama MediClin, Cape Town, South Africa
[9] Univ Stellenbosch, Cape Town, South Africa
基金
澳大利亚国家健康与医学研究理事会; 澳大利亚研究理事会;
关键词
Acetaminophen; Ibuprofen; Paracetamol; Zoledronic acid; OSTEOPOROSIS; FRACTURES;
D O I
10.1007/s00198-011-1563-8
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Patients treated with intravenous zoledronic acid 5 mg for osteoporosis may experience post-dose influenza-like symptoms. Oral acetaminophen/paracetamol or ibuprofen administered 4 h post-infusion reduced the proportion of patients with increased oral temperature and worsening post-infusion symptom scores vs. placebo, thus providing an effective strategy for the treatment of such symptoms. Once-yearly intravenous zoledronic acid 5 mg is a safe and effective treatment for postmenopausal osteoporosis. This study assessed whether transient influenza-like post-dose symptoms associated with intravenous infusion of zoledronic acid can be reduced by post-dose administration of acetaminophen/paracetamol or ibuprofen. In an international, multicenter, randomized, double-blind, double-dummy parallel-group study, bisphosphonate-na < ve postmenopausal women with osteopenia (n = 481) were randomized to receive zoledronic acid 5 mg + acetaminophen/paracetamol (n = 135), ibuprofen (n = 137) or placebo (n = 137), or placebo + placebo (n = 72). Acetaminophen/paracetamol and ibuprofen were administered every 6 h for 3 days beginning 4 h post-infusion. The proportion of patients with increased oral temperature (a parts per thousand yen1A degrees C above 37.5A degrees C) and with worsening post-infusion symptom scores over 3 days was significantly lower in patients receiving ibuprofen (36.8% and 48.5%) or acetaminophen/paracetamol (37.3% and 46.3%) vs. those receiving placebo (63.5% and 75.9%, respectively; all p < 0.0001) compared with background rates of 11.1% and 16.7%, respectively, in the absence of any active treatment. Overall incidence of adverse events was comparable for patients receiving acetaminophen/paracetamol or ibuprofen. Oral acetaminophen/paracetamol or ibuprofen effectively managed the transient influenza-like symptoms associated with zoledronic acid 5 mg.
引用
收藏
页码:503 / 512
页数:10
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