Clinical Toxicology and General Medicine, Guy's and St Thomas' NHS Foundation Trust and King's Health Partners, London, UK.
LGC ASSURE, Fordham, Cambridgeshire, UK.
J Med Toxicol. 2024 Oct;20(4):422-426. doi: 10.1007/s13181-024-01027-8. Epub 2024 Aug 6.
Vortioxetine is an antidepressant with a multimodal mechanism of action. It is used as a treatment option for patients with major depressive episodes. There have only been two previously reported non-fatal overdoses of vortioxetine; neither of these were analytically confirmed There has also been one case of serotonin syndrome potentially related to vortioxetine and two deaths where vortioxetine was detected. We report here a non-fatal analytically confirmed case of vortioxetine overdose.
A 32-year-old male presented to the emergency department (ED) 12-13 h after oral ingestion of 1,260 mg of vortioxetine and 350 mg of diazepam. A family member reported that he had been drowsy after the overdose, but his level of consciousness and observations (heart rate, blood pressure and temperature) were normal on review by the pre-hospital emergency services and on arrival to the ED. During a period of observation, he did not develop any features of serotonin syndrome or any other significant toxicity. Toxicological analysis of a blood sample taken in the ED detected vortioxetine (plasma concentration 457 ng/mL 10 h after ingestion) and sub-therapeutic concentrations of diazepam and pregabalin.
Despite having a plasma vortioxetine concentration nearly 15-times therapeutic vortioxetine concentrations, this patient did not develop any significant toxicity. In particular he did not develop any clinical or biochemical features of serotonin toxicity that would be expected with this class of antidepressant. Additional reporting of analytically confirmed vortioxetine overdoses will allow clinicians and licensing authorities to further understand the safety of this medication in overdose.
文拉法辛是一种具有多种作用机制的抗抑郁药。它被用作治疗重性抑郁发作患者的选择。此前仅有两例文拉法辛非致命性过量的报告;这两者均未进行分析确认。也有一例可能与文拉法辛相关的 5-羟色胺综合征和两例检测到文拉法辛的死亡报告。我们在此报告一例非致命性经分析确认的文拉法辛过量。
一名 32 岁男性在口服文拉法辛 1260mg 和地西泮 350mg 后 12-13 小时到急诊就诊。一名家属报告称,他在过量后一直嗜睡,但他的意识水平和观察结果(心率、血压和体温)在院前急救服务和到达急诊时都正常。在观察期间,他没有出现任何 5-羟色胺综合征或其他明显毒性的特征。在急诊采集的血样毒理学分析检测到文拉法辛(摄入后 10 小时的血浆浓度为 457ng/ml)和地西泮及普瑞巴林的治疗性浓度。
尽管该患者的血浆文拉法辛浓度接近治疗性文拉法辛浓度的 15 倍,但他没有出现任何明显的毒性。特别是,他没有出现任何预期的与这类抗抑郁药相关的 5-羟色胺毒性的临床或生化特征。更多经分析确认的文拉法辛过量报告将使临床医生和许可机构能够进一步了解该药物在过量时的安全性。