Newton R E, Marunycz J D, Alderdice M T, Napoliello M J
Am J Med. 1986 Mar 31;80(3B):17-21. doi: 10.1016/0002-9343(86)90327-x.
In 984 patients with generalized anxiety disorder who received buspirone in double-blind studies, the incidence of drowsiness (9 percent) did not differ significantly from that (10 percent) reported in 334 patients who received placebo. A probability value of p less than or equal to 0.10 was the criterion for significance. The incidence of drowsiness in buspirone-treated patients was significantly less than that in each of the groups receiving diazepam (32 percent), clorazepate (26 percent), lorazepam (58 percent), or alprazolam (43 percent). The side effects that did occur significantly more frequently in the buspirone group than in the placebo group were dizziness (9 percent versus 2 percent), headache (7 percent versus 2 percent), nervousness (4 percent versus 1 percent), light-headedness (4 percent versus less than 1 percent), diarrhea (3 percent versus less than 1 percent), paresthesia (2 percent versus less than 1 percent), excitation (2 percent versus less than 1 percent), and sweating/clamminess (1 percent versus 0 percent). The severities of these effects were predominantly rated as only mild or moderate. Fatigue occurred less frequently in buspirone-treated patients than in those receiving any of the benzodiazepines, and weakness occurred more frequently in diazepam-treated patients. Depression occurred less frequently in buspirone-treated patients than in those receiving clorazepate, diazepam, or lorazepam. Impotence occurred only in clorazepate- and lorazepam-treated patients. Decreased libido occurred more frequently in diazepam-treated patients, whereas increased libido was more frequent in clorazepate-treated patients. Nausea was reported more frequently in buspirone-treated patients than in those receiving clorazepate, diazepam, or alprazolam; diarrhea occurred more frequently in the buspirone group than in the diazepam group. The mean daily doses of the various treatments were buspirone, 20 mg; diazepam, 20 mg; clorazepate, 24 mg; lorazepam, 3 mg; and alprazolam, 1.5 mg. In an open-field study in West Germany involving 5,414 patients, gastrointestinal-related complaints were the most frequently reported side effects.
在双盲研究中接受丁螺环酮治疗的984例广泛性焦虑症患者中,嗜睡发生率(9%)与接受安慰剂治疗的334例患者的嗜睡发生率(10%)相比,差异无统计学意义。显著性标准为概率值p小于或等于0.10。丁螺环酮治疗患者的嗜睡发生率显著低于接受地西泮(32%)、氯氮䓬(26%)、劳拉西泮(58%)或阿普唑仑(43%)治疗的各组患者。丁螺环酮组比安慰剂组显著更频繁出现的副作用有头晕(9%对2%)、头痛(7%对2%)、紧张(4%对1%)、头晕目眩(4%对不到1%)、腹泻(3%对不到1%)、感觉异常(2%对不到1%)、兴奋(2%对不到1%)以及出汗/冷汗(1%对0%)。这些效应的严重程度主要评定为仅为轻度或中度。丁螺环酮治疗患者出现疲劳的频率低于接受任何一种苯二氮䓬类药物治疗的患者,地西泮治疗患者出现虚弱的频率更高。丁螺环酮治疗患者出现抑郁的频率低于接受氯氮䓬、地西泮或劳拉西泮治疗的患者。阳痿仅出现在氯氮䓬和劳拉西泮治疗的患者中。地西泮治疗患者性欲减退的发生率更高,而氯氮䓬治疗患者性欲增强的发生率更高。丁螺环酮治疗患者报告恶心的频率高于接受氯氮䓬、地西泮或阿普唑仑治疗的患者;丁螺环酮组腹泻的发生率高于地西泮组。各种治疗的平均日剂量分别为:丁螺环酮20毫克;地西泮20毫克;氯氮䓬24毫克;劳拉西泮3毫克;阿普唑仑1.5毫克。在德国西部一项涉及5414例患者的旷场研究中,胃肠道相关的主诉是最常报告的副作用。