Bowden Charles L, Asnis Gregory M, Ginsberg Lawrence D, Bentley Beth, Leadbetter Robert, White Robin
Department of Psychiatry, University of Texas Health Science Center at San Antonio, San Antonio, Texas 78229-3900, USA.
Drug Saf. 2004;27(3):173-84. doi: 10.2165/00002018-200427030-00002.
Tolerability and safety are important considerations in optimising pharmacotherapy for bipolar disorder. This paper reviews the tolerability and safety of lamotrigine, an anticonvulsant recommended in the 2002 American Psychiatric Association guidelines as a first-line treatment for acute depression in bipolar disorder and one of several options for maintenance therapy. This paper reviews the tolerability and safety of lamotrigine using data available from a large programme of eight placebo-controlled clinical trials of lamotrigine enrolling a total of nearly 1800 patients with bipolar disorder. This review is the first to collate all the safety information from these clinical trials, including data from four unpublished studies. The results these trials in which 827 patients with bipolar disorder were given lamotrigine as monotherapy or adjunctive therapy for up to 18 months for a total of 280 patient-years of exposure demonstrated that lamotrigine is well-tolerated with an adverse-event profile generally comparable with that of placebo. The most common adverse event with lamotrigine was headache. Lamotrigine did not appear to destabilise mood and was not associated with sexual adverse effects, weight gain, or withdrawal symptoms. Few patients experienced serious adverse events with lamotrigine, and the incidence of withdrawals because of adverse events was low. Serious rash occurred rarely (0.1% incidence) in the clinical development programme including both controlled and uncontrolled clinical trials. These findings - considered in the context of data showing lamotrigine to be effective for bipolar depression - establish lamotrigine as a well-tolerated addition to the psychotropic armamentarium.
耐受性和安全性是优化双相情感障碍药物治疗时的重要考量因素。本文回顾了拉莫三嗪的耐受性和安全性,拉莫三嗪作为一种抗惊厥药,在2002年美国精神病学协会指南中被推荐为双相情感障碍急性抑郁的一线治疗药物以及维持治疗的几种选择之一。本文利用一项大型项目中的数据回顾了拉莫三嗪的耐受性和安全性,该项目包括八项拉莫三嗪安慰剂对照临床试验,共纳入了近1800例双相情感障碍患者。本综述首次整理了这些临床试验的所有安全信息,包括四项未发表研究的数据。这些试验中,827例双相情感障碍患者接受了拉莫三嗪单药治疗或辅助治疗长达18个月,累计暴露患者年数达280年,结果表明拉莫三嗪耐受性良好,不良事件谱总体与安慰剂相当。拉莫三嗪最常见的不良事件是头痛。拉莫三嗪似乎不会使情绪不稳定,也与性方面的不良反应、体重增加或撤药症状无关。很少有患者因拉莫三嗪出现严重不良事件,因不良事件而停药的发生率很低。在包括对照和非对照临床试验在内的临床研发项目中,严重皮疹很少发生(发生率为0.1%)。这些发现在显示拉莫三嗪对双相抑郁有效的数据背景下,确立了拉莫三嗪是一种耐受性良好的精神药物。