Related Experiment Video
Updated: Jan 9, 2026

Assessing Changes in Volatile General Anesthetic Sensitivity of Mice after Local or Systemic Pharmacological Intervention
Published on: October 16, 2013
Lemborexant overdose presenting with mild sedation despite high plasma levels: A case report
Makoto Suzuki1, Daisuke Usuda1, Hiroki Takami1
1Department of Emergency and Critical Care Medicine, Juntendo University Nerima Hospital, 3-1-10, Takanodai, Nerima-city, Tokyo 177-8521, Japan.
Introduction:
Lemborexant is a dual orexin receptor antagonist (DORA) with a favorable safety profile at therapeutic doses. However, clinical data regarding its toxic effects in overdose scenarios are limited. This is the first published case report of serially measured plasma concentrations of lemborexant in a patient who survived following acute overdose.
Case Report:
A 33-year-old woman presented to the emergency department four hours after ingesting an estimated 720 mg of lemborexant and 78 mg of eszopiclone. She exhibited mild central nervous system depression (Glasgow Coma Scale score 11) but was hemodynamically stable. With supportive care alone, the patient's consciousness spontaneously improved. Retrospective analysis revealed that her plasma lemborexant concentration increased from 0.144 µg/mL at four hours to a peak of 1.410 µg/mL at nine hours post-ingestion, despite undergoing clinical recovery.
Discussions:
This case suggests that massive lemborexant overdoses may not cause life-threatening toxicity even when plasma levels approach those reported in fatal cases. This case provides preliminary but clinically important data and highlights the need for further research to better characterize the clinical implications and management of lemborexant overdoses.
More Related Videos
06:58Non-restraining EEG Radiotelemetry: Epidural and Deep Intracerebral Stereotaxic EEG Electrode Placement
Published on: June 25, 2016
07:54Drug-Induced Sleep Endoscopy DISE with Target Controlled Infusion TCI and Bispectral Analysis in Obstructive Sleep Apnea
Published on: December 6, 2016
Related Concept Videos
Sedatives and Hypnotics Drugs: Miscellaneous Agents
Melatonin congeners like ramelteon (Rozerem) and tasimelteon (Hetlioz) selectively bind to melatonin receptors (MT1 and MT2) and thus mimic the actions of melatonin, a hormone that regulates sleep-wake cycles. Tasimelteon is primarily used for non-24-hour sleep-wake disorder, common in blind patients. They are also used to treat conditions like insomnia...
Sedatives and Hypnotics Drugs: Barbiturates
Anticholinesterase Agents: Poisoning and Treatment
Irreversible agents form a strong bond with the cholinesterase enzyme, making it inactive. The breakdown of the phosphorylated enzyme is...
Sedatives and Hypnotics: Overview
Sedative-hypnotics are categorized into barbiturates, benzodiazepines (BZDs), and non-benzodiazepines or Z-drugs. These drugs work by suppressing central nervous system activity, and this suppression is dose-dependent. Older sedative medications, like barbiturates, follow a linear curve in...
Sedatives and Hypnotics Drugs: Benzodiazepines
Benzodiazepines work by enhancing the effects of the inhibitory neurotransmitter GABA. They bind to the GABAA receptor, increasing its affinity for GABA, which opens chloride...
Skeletal Muscle Relaxants: Adverse Effects
Unlike...