Gonzalez J P, Todd P A
ADIS Drug Information Service, Manchester.
Drugs. 1987 Sep;34(3):289-310. doi: 10.2165/00003495-198734030-00001.
Tenoxicam is a new non-steroidal anti-inflammatory and analgesic agent of the oxicam class, and therefore closely related to piroxicam. It possesses a long half-life which enables it to be administered once daily. Clinical trials in patients with rheumatoid arthritis, osteoarthritis, ankylosing spondylitis, gout and non-articular rheumatism suggest that tenoxicam 20mg daily is an equally effective anti-inflammatory and analgesic agent compared with piroxicam 20mg daily, and that it is at least as well tolerated. Additionally, a few small studies in rheumatoid arthritis and osteoarthritis suggest that tenoxicam 20mg daily is as effective and as well tolerated as usual therapeutic dosages of diclofenac, ibuprofen, indomethacin and naproxen. Transient mild or moderate gastrointestinal symptoms, in 8% of patients at a dosage of 20mg daily, are the most frequently reported side effects. If further studies confirm the initially favourable efficacy and tolerability findings, particularly the relatively low incidence of adverse effects, tenoxicam can be considered a useful new agent for the symptomatic treatment of rheumatic and inflammatory diseases, and a worthwhile alternative to other non-steroidal anti-inflammatory drugs.
替诺昔康是一种新型的昔康类非甾体抗炎镇痛药,因此与吡罗昔康密切相关。它具有较长的半衰期,使得每日给药一次成为可能。针对类风湿性关节炎、骨关节炎、强直性脊柱炎、痛风及非关节性风湿病患者的临床试验表明,每日服用20mg替诺昔康与每日服用20mg吡罗昔康相比,抗炎和镇痛效果相当,且耐受性至少相同。此外,一些针对类风湿性关节炎和骨关节炎的小型研究表明,每日服用20mg替诺昔康与双氯芬酸、布洛芬、吲哚美辛和萘普生的常规治疗剂量效果相同,耐受性也相当。每日剂量为20mg时,8%的患者会出现短暂的轻度或中度胃肠道症状,这是最常报告的副作用。如果进一步的研究证实了最初良好的疗效和耐受性结果,特别是不良反应的发生率相对较低,那么替诺昔康可被视为一种用于风湿性和炎性疾病症状治疗的有用新药,以及其他非甾体抗炎药的一个有价值的替代品。