Evidence map›Paper›PMID 39107657›Full record

ArticleJournal of medical toxicology : official journal of the American College of Medical Toxicology2024

Analytically Confirmed Intentional Overdose of the Antidepressant Vortioxetine.

Adam Daneshmend, Allon Gould, Simon Hudson, John Robert Howard Archer, Paul Ivor Dargan, David Michael Wood

Abstract readCase Reports
In one paragraph

Article in Journal of medical toxicology : official journal of the American College of Medical Toxicology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Adam DaneshmendClinical Toxicology and General Medicine, Guy's and St Thomas' NHS Foundation Trust and King's Health Partners, London, UK.
Allon GouldClinical Toxicology and General Medicine, Guy's and St Thomas' NHS Foundation Trust and King's Health Partners, London, UK.
Simon HudsonLGC ASSURE, Fordham, Cambridgeshire, UK.
John Robert Howard ArcherClinical Toxicology and General Medicine, Guy's and St Thomas' NHS Foundation Trust and King's Health Partners, London, UK.
Paul Ivor DarganClinical Toxicology and General Medicine, Guy's and St Thomas' NHS Foundation Trust and King's Health Partners, London, UK.
David Michael WoodClinical Toxicology and General Medicine, Guy's and St Thomas' NHS Foundation Trust and King's Health Partners, London, UK. David.Wood@gstt.nhs.uk.ORCID 0000-0002-7826-7237

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionVortioxetine 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. CASE REPORT: 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. DISCUSSION: 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.

Indexed as

Antidepressive AgentsDrug OverdoseVortioxetineAdultDiazepamHumansMalePiperazinesSelective Serotonin Reuptake InhibitorsAntidepressive AgentsDiazepamPiperazinesSelective Serotonin Reuptake InhibitorsVortioxetineAnalysisOverdoseToxicityVortioxetine

Identifiers

PMID39107657
PMCPMC11436597

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.