Regional Centre for Pharmacovigilance and Pharmacoepidemiology, Reims University Teaching Hospitals, Avenue du General Koenig, 51092 Reims, France.
Drug Saf. 2013 Jul;36(7):515-9. doi: 10.1007/s40264-013-0069-z.
Depressive disorders and use of antidepressants are associated with adverse effects on sexual function. In pharmacoepidemiological studies, sexual disorders are reported by more than 50 % of patients taking serotonin reuptake inhibitors (SRIs).
The aim of this study was to determine the reporting rate of sexual disorders in association with SRIs, and to investigate the association between reported cases and the use of SRIs.
All cases of adverse drug reactions (ADRs) involving sexual disorders, spontaneously reported to the French Pharmacovigilance Database from 1 January 1985 to December 2009, were reviewed. Cases of sexual disorders in SRI users were described. We calculated the rate of reported sexual disorders as a percentage of the total ADRs reported for each drug. The association between reported cases and the use of SRIs was assessed using reporting odds ratios (ROR) with 95 % confidence intervals (CIs).
A total of 11,863 ADRs in association with SRIs were collected, of which 98 (0.83 %) were spontaneous reports of sexual disorders. Subjects were, on average, 45.0 ± 10.6 years of age and mainly male. Sexual disorders were associated with the use of SRI antidepressants (ROR 4.47; 95 % CI 3.61-5.53), milnacipran (ROR 11.72; 95 % CI 5.79-23.72), fluvoxamine (ROR 6.91; 95 % CI 3.79-12.58), paroxetine (ROR 5.54; 95 % CI 3.92-7.83), venlafaxine (ROR 3.50; 95 % CI 1.93-6.36), fluoxetine (ROR 3.46; 95 % CI 2.26-5.29), citalopram (ROR 2.69; 95 % CI 1.28-5.67) and sertraline (ROR 2.49; 95 % CI 1.03-6.01).
It is likely that there are instances of underreporting, particularly for ADRs that are embarrassing to talk about spontaneously. Despite the likely underreporting of this well-described adverse effect, this case/non-case study performed in a large national pharmacovigilance database confirms the existence of the risk of sexual disorders associated with SRIs, and is an example of the lack of sensitivity of spontaneous notification to measure ADRs. Minimization of antidepressant-induced sexual dysfunction could be an important factor to avoid unsuccessful treatment. Physicians should advise their patients on the possible sexual adverse effects.
抑郁障碍和抗抑郁药的使用与性功能障碍的不良影响有关。在药物流行病学研究中,超过 50%的服用 5-羟色胺再摄取抑制剂(SSRIs)的患者报告有性功能障碍。
本研究旨在确定 SSRIs 相关的性功能障碍报告率,并探讨报告病例与 SSRIs 使用之间的关系。
从 1985 年 1 月 1 日至 2009 年 12 月,检索法国药物警戒数据库中自发报告的与 SSRIs 相关的所有不良药物反应(ADR)的不良药物反应(ADR)病例。描述了 SSRIs 使用者的性功能障碍病例。我们计算了每种药物报告的性功能障碍病例占总 ADR 报告的百分比。使用报告比值比(ROR)和 95%置信区间(CI)评估报告病例与 SSRIs 使用之间的关系。
共收集到 11863 例 SSRIs 相关 ADR,其中 98 例(0.83%)为自发性性功能障碍报告。患者平均年龄为 45.0±10.6 岁,主要为男性。性功能障碍与 SSRIs 抗抑郁药(ROR 4.47;95%CI 3.61-5.53)、米那普仑(ROR 11.72;95%CI 5.79-23.72)、氟伏沙明(ROR 6.91;95%CI 3.79-12.58)、帕罗西汀(ROR 5.54;95%CI 3.92-7.83)、文拉法辛(ROR 3.50;95%CI 1.93-6.36)、氟西汀(ROR 3.46;95%CI 2.26-5.29)、西酞普兰(ROR 2.69;95%CI 1.28-5.67)和舍曲林(ROR 2.49;95%CI 1.03-6.01)有关。
很可能存在报告不足的情况,特别是对于那些难以自发报告的不良反应。尽管这种不良反应描述得很好,但在大型国家药物警戒数据库中进行的病例/非病例研究证实了 SSRIs 相关性功能障碍的风险的存在,这是自发报告在衡量不良反应的敏感性方面不足的一个例子。减少抗抑郁药引起的性功能障碍可能是避免治疗失败的一个重要因素。医生应告知患者可能出现的性不良反应。