Vlok G J, van Vuren J P
Department of Orthopaedic Surgery, University of Stellenbosch, Parowvallei, CP.
S Afr Med J. 1987 Oct 17;Suppl:1, 4-6.
Twenty-eight patients with osteoarthritis participated in a prospective, double-blind, cross-over study to compare the safety and efficacy of a new combination analgesic containing ibuprofen 200 mg, paracetamol 250 mg and codeine phosphate 10 mg per tablet (Myprodol; Rio Ethicals) with a standard treatment regimen (ibuprofen 200 mg per tablet). The combination tablet was found to provide significantly better pain relief than ibuprofen alone (P less than 0.05). Analysis of the results of haematological, hepatic and renal function tests showed no statistically significant differences between treatments. No serious side-effects or clinically important changes were encountered with either drug.
28名骨关节炎患者参与了一项前瞻性、双盲、交叉研究,以比较每片含200毫克布洛芬、250毫克对乙酰氨基酚和10毫克磷酸可待因的新型复方镇痛药(Myprodol;Rio Ethicals)与标准治疗方案(每片200毫克布洛芬)的安全性和疗效。结果发现,复方片剂的止痛效果明显优于单独使用布洛芬(P小于0.05)。血液学、肝功能和肾功能测试结果分析显示,各治疗组之间无统计学显著差异。两种药物均未出现严重副作用或具有临床意义的变化。