Case series: toxicity from 25B-NBOMe--a cluster of N-bomb cases.
Paul Gee, Leo J. Schep, Berit P Jensen, Grant Moore, Stuart Barrington
Clinical Toxicology 2016 DOI: 10.3109/15563650.2015.1115056 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Observational case series Case report Peer reviewed |
|---|---|
| Sample size | 10 |
| Population | Patients who suffered adverse effects from 25B-NBOMe |
| Keywords | 25b-nbome N-bomb Novel psychoactive substances Substituted phenylethylamines |
| Key findings | Adverse effects from 25B-NBOMe included hallucinations, violent agitation, and serotonergic/stimulant signs, with most patients requiring sedation with benzodiazepines. |
Abstract
Background: A new class of hallucinogens called NBOMes has emerged. This class includes analogues 25I-NBOMe, 25C-NBOMe and 25B-NBOMe. Case reports and judicial seizures indicate that 25I-NBOMe and 25C-NBOMe are more prevalently abused. There have been a few confirmed reports of 25B-NBOMe use or toxicity. Report Observational case series. This report describes a series of 10 patients who suffered adverse effects from 25B-NBOMe. Hallucinations and violent agitation predominate along with serotonergic/stimulant signs such as mydriasis, tachycardia, hypertension and hyperthermia. The majority (7/10) required sedation with benzodiazepines. Analytical method 25B-NBOMe concentrations in plasma and urine were quantified in all patients using a validated liquid chromatography-tandem mass spectrometry (LC-MS/MS) method. Peak plasma levels were measured between 0.7-10.1 ng/ml.
Discussion: The NBOMes are desired by users because of their hallucinogenic and stimulant effects. They are often sold as LSD or synthetic LSD. Reported cases of 25B- NBOMe toxicity are reviewed and compared to our series. Seizures and one pharmacological death have been described but neither were observed in our series. Based on our experience with cases of mild to moderate toxicity, we suggest that management should be supportive and focused on preventing further (self) harm. High doses of benzodiazepines may be required to control agitation. Patients who develop significant hyperthermia need to be actively managed.
Conclusions: Effects from 25B-NBOMe in our series were similar to previous individual case reports. The clinical features were also similar to effects from other analogues in the class (25I-NBOMe, 25C-NBOMe). Violent agitation frequently present along with signs of serotonergic stimulation. Hyperthermia, rhabdomyolysis and kidney injury were also observed.
Citations in the library
Cited by 22
- Pharmacology and Toxicology of N-Benzylphenethylamine ("NBOMe") Hallucinogens. Current Topics in Behavioral Neurosciences 2017
- NBOMes–Highly Potent and Toxic Alternatives of LSD Frontiers in Neuroscience February 26, 2020
- Effect fingerprinting of new psychoactive substances (NPS): What can we learn from in vitro data? Pharmacology & Therapeutics February 1, 2018
- DARK Classics in Chemical Neuroscience: NBOMes ACS Chemical Neuroscience October 28, 2019
- Hallucinogen-Like Action of the Novel Designer Drug 25I-NBOMe and Its Effect on Cortical Neurotransmitters in Rats Neurotoxicity Research April 15, 2019
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Cites 15
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- Serotonin 2A Receptor Agonist Binding in the Human Brain with [11C]Cimbi-36 Journal of Cerebral Blood Flow & Metabolism April 30, 2014
- Two cases of severe intoxication associated with analytically confirmed use of the novel psychoactive substances 25B-NBOMe and 25C-NBOMe Clinical Toxicology 2014
- 2-(4-Iodo-2,5-dimethoxyphenyl)-N-[(2-methoxyphenyl)methyl]ethanamine (25I-NBOMe): clinical case with unique confirmatory testing. Journal of Medical Toxicology March 1, 2014
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and 10 more in the library