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Evolution of the NBOMes: 25C- and 25B- Sold as 25I-NBOMe

Larissa K. Laskowski, Faesal Elbakoush, Jessica Calvo, Gina Exantus-Bernard, Jane Fong, Justin L. Poklis, Alphonse Poklis, Lewis S. Nelson

Journal of Medical Toxicology November 12, 2014 DOI: 10.1007/s13181-014-0445-9 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Case report Peer reviewed
Sample size 2
Population Adolescents with NBOMe intoxication
Intervention Benzodiazepines
Keywords Anesthesia Pharmacology
Citations 39
Key findings Two adolescents who reported using 25I-NBOMe were confirmed by mass spectrometry to have ingested 25C-NBOMe and 25B-NBOMe, respectively. Both presented with seizures and muscle rigidity, with one case showing extreme CPK elevation. The authors propose that laboratory confirmation can reveal unexpected NBOMe variants and contribute to epidemiological data.

Abstract

IntroductionThe NBOMes (N-benzyl-oxy-methyl derivatives of known 2C phenylethylamines) are a new and growing class of potent synthetic stimulants. Case reports provide the bulk of available safety and clinical data for clinicians. We report two cases of NBOMe intoxication with 25C-NBOMe (the first lab-confirmed US case) and 25B-NBOMe, respectively, both confirmed via triple quadrapole mass spectrometry.Case reportsCase 1: A 16-year-old girl had a generalized seizure after reported use of 25I-NBOMe. She presented with altered mental status, lower extremity rigidity, and elevated CPK (6042 U/L). Despite treatment with benzodiazepines, her lower extremity rigidity persisted and CPK peaked at 47,906 U/L. She was discharged on hospital day 8. Serum and urine specimens confirmed presence of 25C-NBOMe. Case 2: A 15-year-old boy developed bizarre behavior after reported use of 25I-NBOMe. In the ED, he had two generalized seizures and persistent muscle rigidity. CPK peaked at 429 U/L. Seizures were managed with benzodiazepines, and he was discharged within 24 h. Serum specimens revealed 25B-NBOMe.DiscussionNBOMes are amphetamine derivatives and highly potent 5-HT(2A) receptor agonists. Clinical manifestations are a product of enhanced central sympathetic and serotonergic tone. We report two cases of NBOMe intoxication in patients who believed they used 25I-NBOME, while lab confirmation proved otherwise. Whether unique clinical manifestations are specific to the NBOMe variant, dose, route of administration, or other factors is unknown. Laboratory confirmation may play a role in identifying unexpected NBOMe variants, while contributing to the epidemiologic data on these novel substances.

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