This meta-analysis (2015, n=20) examined the toxicity of the synthetic serotonergic hallucinogen NBOMe reported in publications that described adverse effects in response to analytically confirmed human ingestion. Severe adverse effects included agitation (85.0%), tachycardia (85.0%), and hypertension (65.0%), and seizures (40.0%) among patients.
Abstract
“Objective: A new class of synthetic hallucinogens called NBOMe has emerged as drugs of abuse. Our aim was to conduct a systematic review of published reports of toxicities associated with NBOMe ingestion.
Methods: We searched the PubMed for relevant English language citations that described adverse effects from analytically confirmed human NBOMe ingestion. Demographic and clinical data were extracted.
Results: Ten citations met criteria for inclusion, representing 20 individual patients. 25I-NBOMe was the most common analog identified, followed by 25B-NBOMe and 25C-NBOMe. Fatalities were reported in 3 (15%) cases. Seven (35%) were discharged after a period of observation, while 8 (40.0%) required admission to an intensive care unit. The most common adverse effects were agitation (85.0%), tachycardia (85.0%), and hypertension (65.0%). Seizures were reported in 8 (40.0%) patients. The most common laboratory abnormalities were elevated creatine kinase (45.0%), leukocytosis (25.0%), and hyperglycemia (20.0%).
Conclusion: NBOMe ingestion is associated with severe adverse effects. Clinicians need to have a high index of suspicion for NBOMe ingestion in patients reporting the recent use of hallucinogens.”
Authors: Joji Suzuki, Michael A. Dekker, Erin S. Valenti, Fabiola A. Arbelo Cruz, Ady M. Correa, Justin L. Poklis & Alphonse Poklis
Summary of Toxicities Associated With NBOMe Ingestion—A Novel Class of Potent Hallucinogens: A Review of the Literature
Introduction
NBOMes are N-benzylmethoxy derivatives of the 2C family of hallucinogens, which are phenethylamines with methoxy substitutions at positions 2 and 5 and a substitution at position 4 often consisting of a halogen. They produce effects similar to mescaline, but have a higher affinity at the 5-HT2A receptor.
Methods
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http://dx.doi.org/10.1016/j.psym.2014.11.002
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