Danjou P, Hackett D
CNS Group, Wyeth-Ayerst European Clinical Research and Development, Paris, France.
Int Clin Psychopharmacol. 1995 Mar;10 Suppl 2:15-20. doi: 10.1097/00004850-199503002-00004.
Venlafaxine has been shown in clinical trials to be safe and well tolerated in patients with major depression. Data were pooled from 19 studies in which 2181 patients were given venlafaxine, 451 were given placebo and 591 were given a reference antidepressant (imipramine, trazodone, clomipramine, maprotiline, dothiepin or amineptine). Long-term safety was evaluated in 422 patients who were given venlafaxine for at least 1 year; as well, a total of 229 elderly patients have been treated with venlafaxine, including 66 who were given it for at least 1 year. The adverse events that occurred during short-term treatment in > or = 10% of patients were nausea, headache, insomnia, somnolence, dry mouth, dizziness, constipation, asthenia, sweating and nervousness. In comparator-controlled trials, the frequency of anticholinergic events with the reference agents was approximately twice that with venlafaxine. The safety profile and patient acceptability of venlafaxine are comparable to those of third-generation antidepressants, and possibly better than those of first-generation agents.
临床试验表明,文拉法辛对于重度抑郁症患者安全且耐受性良好。数据汇总自19项研究,其中2181例患者服用文拉法辛,451例服用安慰剂,591例服用对照抗抑郁药(丙咪嗪、曲唑酮、氯米帕明、马普替林、多塞平或阿米替林)。对422例服用文拉法辛至少1年的患者进行了长期安全性评估;此外,共有229例老年患者接受了文拉法辛治疗,其中66例服用至少1年。在短期治疗期间,≥10%的患者出现的不良事件有恶心、头痛、失眠、嗜睡、口干、头晕、便秘、乏力、出汗和紧张。在对照试验中,对照药物的抗胆碱能事件发生率约为文拉法辛的两倍。文拉法辛的安全性和患者可接受性与第三代抗抑郁药相当,可能优于第一代药物。