Opioid Crisis
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Etodesnitazene
Etodesnitazene Sample Type: Biological Fluid Latest Revision: February 23, 2021 Date of Report: February 23, 2021 1. GENERAL INFORMATION IUPAC Name: 2-[2-[(4-ethoxyphenyl)methyl]benzimidazol-1-yl]-N,N-diethyl- ethanamine InChI String: InChI=1S/C22H29N3O/c1-4-24(5-2)15-16-25-21-10-8-7-9-20(21)23- 22(25)17-18-11-13-19(14-12-18)26-6-3/h7-14H,4-6,15-17H2,1-3H3 CFR: Not Scheduled (02/2021) CAS# Not available Synonyms: Etazene, Desnitroetonitazene, Etazen, Etazone Source: Oregon State Police Forensic Laboratory Important Notes: All identifications were made based on evaluation of analytical data (LC-QTOF-MS) in comparison to analysis of acquired reference material. This drug was also confirmed via LC-MS/MS. Prepared By: Janet Schultz, PhD; Sailee Raje; Sara Short, MS, D-ABFT-FT; Michele Stauffenberg, MD; Alex J. Krotulski, PhD; Melissa F. Fogarty, MSFS, D-ABFT-FT; and Barry K. Logan, PhD, F-ABFT 2. CHEMICAL DATA Chemical Molecular Molecular Exact Mass Analyte Formula Weight Ion [M+] [M+H]+ Etodesnitazene C22H29N3O 351.5 351 352.2383 3. SAMPLE HISTORY Etodesnitazene has been identified in one case since December 2020. The geographical and demographical breakdown is below: Geographical Location: Oregon (n=1) Biological Sample: Subclavian Blood (n=1) Date of First Receipt: December 2020 Other Notable Findings: Etizolam, Methamphetamine, Mitragynine 4. BRIEF DESCRIPTION Etodesnitazene is classified as a novel opioid of the benzimidazole sub-class and is structurally dissimilar from fentanyl. Novel opioids have been reported to cause psychoactive effects similar to heroin, fentanyl, and other opioids. -
DEPARTMENT of JUSTICE Drug Enforcement
This document is scheduled to be published in the Federal Register on 08/03/2021 and available online at DEPARTMENT OF JUSTICEfederalregister.gov/d/2021-16499, and on govinfo.gov Drug Enforcement Administration Bulk Manufacturer of Controlled Substances Application: Cerilliant Corporation [Docket No. DEA-873] AGENCY: Drug Enforcement Administration, Justice. ACTION: Notice of application. SUMMARY: Cerilliant Corporation has applied to be registered as a bulk manufacturer of basic class(es) of controlled substance(s). Refer to Supplemental Information listed below for further drug information. DATES: Registered bulk manufacturers of the affected basic class(es), and applicants therefore, may file written comments on or objections to the issuance of the proposed registration on or before [INSERT DATE 60 DAYS AFTER DATE OF PUBLICATION IN THE FEDERAL REGISTER]. Such persons may also file a written request for a hearing on the application on or before [INSERT DATE 60 DAYS AFTER DATE OF PUBLICATION IN THE FEDERAL REGISTER]. ADDRESS: Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/DPW, 8701 Morrissette Drive, Springfield, Virginia 22152. SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.33(a), this is notice that on June, 24, 2021, Cerilliant Corporation, 811 Paloma Drive, Suite A, Round Rock, Texas 78665-2402, applied to be registered as a bulk manufacturer of the following basic class(es) of controlled substance(s): Controlled Substance Drug Code Schedule 3-Fluoro-N-methylcathinone -
Communicationfile-132886.Pdf
From: Nazlee Maghsoudi To: Board of Health Cc: Werb, Daniel; Hayley Thompson; Karen McDonald Subject: BOH June 14, 2021 - CDPE Comments on HL29.2 Date: June 13, 2021 6:52:20 PM Attachments: 2021-06-14_CDPE Comments to BOH_Toronto Overdose Action Plan Status Report 2021.pdf To the Members of the Board of Health, Please find attached comments from the Centre on Drug Policy Evaluation (CDPE) regarding agenda item HL29.2 (Toronto Overdose Action Plan: Status Report 2021) to be considered at the Board of Health meeting on Monday, June 14. We would greatly appreciate if you could please confirm receipt. Thanks so much, Nazlee Maghsoudi, BComm, MGA Doctoral Candidate, Health Services Research | Institute of Health Policy, Management and Evaluation, University of Toronto Manager, Policy Impact Unit | Centre on Drug Policy Evaluation (CDPE) Chairperson, Executive Committee | New York NGO Committee on Drugs (NYNGOC) Strategic Advisor | Canadian Students for Sensible Drug Policy (CSSDP) (647) 702-7825 Pronouns: She/Her Submission from Nazlee Maghsoudi, Centre on Drug Policy Evaluation Toronto's Dru·g Checking Service Coordinated by the Centre on Drug Policy Evaluation > i" Comments for Board of Health Consideration of “Toronto Overdose Action Plan: Status Report 2021” June 14, 2021 What does Toronto’s drug checking service do? • Offers people who use drugs timely and detailed information on the contents of their drugs, helping them to make more informed decisions • Shares information on Toronto’s unregulated drug supply to help harm reduction workers and clinicians tailor the care they provide to people who use drugs • Advocates for services and safer alternatives for people who use drugs 2 Free and anonymous drug checking is now available! What you give .. -
Recommended Methods for the Identification and Analysis of Fentanyl and Its Analogues in Biological Specimens
Recommended methods for the Identification and Analysis of Fentanyl and its Analogues in Biological Specimens MANUAL FOR USE BY NATIONAL DRUG ANALYSIS LABORATORIES Laboratory and Scientific Section UNITED NATIONS OFFICE ON DRUGS AND CRIME Vienna Recommended Methods for the Identification and Analysis of Fentanyl and its Analogues in Biological Specimens MANUAL FOR USE BY NATIONAL DRUG ANALYSIS LABORATORIES UNITED NATIONS Vienna, 2017 Note Operating and experimental conditions are reproduced from the original reference materials, including unpublished methods, validated and used in selected national laboratories as per the list of references. A number of alternative conditions and substitution of named commercial products may provide comparable results in many cases. However, any modification has to be validated before it is integrated into laboratory routines. ST/NAR/53 Original language: English © United Nations, November 2017. All rights reserved. The designations employed and the presentation of material in this publication do not imply the expression of any opinion whatsoever on the part of the Secretariat of the United Nations concerning the legal status of any country, territory, city or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. Mention of names of firms and commercial products does not imply the endorse- ment of the United Nations. This publication has not been formally edited. Publishing production: English, Publishing and Library Section, United Nations Office at Vienna. Acknowledgements The Laboratory and Scientific Section of the UNODC (LSS, headed by Dr. Justice Tettey) wishes to express its appreciation and thanks to Dr. Barry Logan, Center for Forensic Science Research and Education, at the Fredric Rieders Family Founda- tion and NMS Labs, United States; Amanda L.A. -
WHO Expert Committee on Drug Dependence
WHO Technical Report Series 1034 This report presents the recommendations of the forty-third Expert Committee on Drug Dependence (ECDD). The ECDD is responsible for the assessment of psychoactive substances for possible scheduling under the International Drug Control Conventions. The ECDD reviews the therapeutic usefulness, the liability for abuse and dependence, and the public health and social harm of each substance. The ECDD advises the Director-General of WHO to reschedule or to amend the scheduling status of a substance. The Director-General will, as appropriate, communicate the recommendations to the Secretary-General of the United Nations, who will in turn communicate the advice to the Commission on Narcotic Drugs. This report summarizes the findings of the forty-third meeting at which the Committee reviewed 11 psychoactive substances: – 5-Methoxy-N,N-diallyltryptamine (5-MeO-DALT) WHO Expert Committee – 3-Fluorophenmetrazine (3-FPM) – 3-Methoxyphencyclidine (3-MeO-PCP) on Drug Dependence – Diphenidine – 2-Methoxydiphenidine (2-MeO-DIPHENIDINE) Forty-third report – Isotonitazene – MDMB-4en-PINACA – CUMYL-PEGACLONE – Flubromazolam – Clonazolam – Diclazepam The report also contains the critical review documents that informed recommendations made by the ECDD regarding international control of those substances. The World Health Organization was established in 1948 as a specialized agency of the United Nations serving as the directing and coordinating authority for international health matters and public health. One of WHO’s constitutional functions is to provide objective, reliable information and advice in the field of human health, a responsibility that it fulfils in part through its extensive programme of publications. The Organization seeks through its publications to support national health strategies and address the most pressing public health concerns of populations around the world. -
Toxicology Report Division of Toxicology Daniel D
Franklin County Forensic Science Center Office of the Coroner Anahi M. Ortiz, M.D. 2090 Frank Road Columbus, Ohio 43223 Toxicology Report Division of Toxicology Daniel D. Baker, Chief Toxicologist Casey Goodson Case # LAB-20-5315 Date report completed: January 28, 2021 A systematic toxicological analysis has been performed and the following agents were detected. Postmortem Blood: Gray Top Thoracic ELISA Screen Acetaminophen Not Detected ELISA Screen Barbiturates Not Detected ELISA Screen Benzodiazepines Not Detected ELISA Screen Benzoylecgonine Not Detected ELISA Screen Buprenorphine Not Detected ELISA Screen Cannabinoids See Confirmation ELISA Screen Fentanyl Not Detected ELISA Screen Methamphetamine Not Detected ELISA Screen Naltrexone/Naloxone Not Detected ELISA Screen Opiates Not Detected ELISA Screen Oxycodone/Oxymorphone Not Detected ELISA Screen Salicylates Not Detected ELISA Screen Tricyclics Not Detected Page 1 of 4 Casey Goodson Case # LAB-20-5315 GC/FID Ethanol Not Detected GC/MS Acidic/Neutral Drugs None Detected GC/MS Nicotine Positive GC/MS Cotinine Positive Reference Lab Delta-9-THC 13 ng/mL Reference Lab 11-Hydroxy-Delta-9-THC 1.2 ng/mL Reference Lab 11-Nor-9-Carboxy-Delta-9-THC 15 ng/mL Postmortem Urine: Gray Top Urine GC/MS Cotinine Positive This report has been verified as accurate and complete by ______________________________________ Daniel D. Baker, M.S., F-ABFT Cannabinoid quantitations in blood were performed by NMS Labs, Horsham, PA. Page 2 of 4 Casey Goodson Case # LAB-20-5315 Postmortem Toxicology Scope of Analysis Franklin County Coroner’s Office Division of Toxicology Enzyme Linked Immunosorbant Assay (ELISA) Blood Screen: Qualitative Presumptive Compounds/Classes: Acetaminophen (cut-off 10 µg/mL), Benzodiazepines (cut-off 20 ng/mL), Benzoylecgonine (cut-off 50 ng/mL), Cannabinoids (cut-off 40 ng/mL), Fentanyl (cut-off 1 ng/mL), Methamphetamine/MDMA (cut-off 50 ng/mL), Opiates (cut-off 40 ng/mL), Oxycodone/Oxymorphone (cut-off 40 ng/mL), Salicylates (50 µg/mL). -
Benzimidazole-Opioids June 2021
Drug Enforcement Administration Diversion Control Division Drug & Chemical Evaluation Section Benzimidazole-Opioids June 2021 Introduction: metonitazene, metodesnitazene, and protonitazene involved interaction with β-arrestin-2. Mu-opioid receptor and β-arrestin-2 Recently, several synthetic substances of benzimidazole interaction has been implicated in adverse health effects of many structural class are being trafficked and abused for their opioid- opioid analgesics. It is well established that mu-opioid receptor like effects. In the late 1950s, the pharmaceutical research agonists have a high potential for addiction and can produce dose- laboratories of the Swiss chemical company CIBA dependent respiratory depression and arrest. Abuse of these Aktiengesellschaft synthesized numerous benzimidazole- benzimidazole-opioids has led to their positive identification in opioids to include butonitazene, etodesnitazene, flunitazene, several toxicological cases in the United States. Specifically, metonitazene, metodesnitazene, and protonitazene. Since metonitazene has been identified in twenty post-mortem cases. 2019, the abuse of benzimidazole-opioids as evidenced by their identification in toxicology cases, similar to other synthetic opioids, has resulted in adverse health effects including deaths. User Population: As the United States continues to experience an unprecedented The population likely to abuse benzimidazole-opioids appears to be epidemic of opioid misuse and abuse, the continued evolution the same as those abusing prescription opioid analgesics, heroin, and increased trafficking and popularity of new and deadly and other synthetic opioid substances. This is evidenced by the synthetic opioids including benzimidazole-opioids with no types of other drugs co-identified in isotonitazene seizures and in approved medical use are of public health concern. fatal overdose cases. Toxicology analyses co-identified some of these benzimidazole-opioids with other opioids, stimulants, and Chemistry: benzodiazepines. -
(SEOW) Meeting Minutes, October 21, 2020
MINUTE RECORD MICHIGAN DEPARTMENT OF HEALTH AND HUMAN SERVICES (MDHHS) OFFICE OF RECOVERY ORIENTED SYSTEMS OF CARE (OROSC) State Epidemiological Outcomes Workgroup (SEOW) WORKGROUP NAME State Epidemiological Outcomes Workgroup (SEOW) Core Team DATE Wednesday, October 21, 2020 TIME 1:00 p.m. – 2:00 p.m. LOCATION Virtual Meeting CHAIRPERSON Joel Hoepfner RECORDER BlueJeans System ATTENDEES PHONE: Prashanti Boinapally, Lisa Coleman, Jane Goerge, Choua Gonzalez- Medina, Alicia Goodman, David Havens, Joel Hoepfner, Brandon Hool, Rich Isaacson, Rita Seith, Thomas Largo, Stephanie Larocco, Patricia McKane, Mary Miller, Janelle Murray, Hannah Napolillo, Su Min Oh, Dawn Radzioch, Brooke Rodriguez, Samantha Jones, Christy Sanborn, Larry Scott, Gabrielle Stroh-Steiner ABSENT: Liz Agius, Bret Bielawski, Sandra Bullard, Joe Coyle, Seth Eckle, Kimberly Fox, Brian Hartl, Denise Herbert, Patrick Hindman, Rachel Jantz, Jeanne Kapenga, Haley Kehus, Scott Josephs, Alia Lucas, Mary Ludtke, Jamie Meister, Logan O’Neill, Annette Perrino, Eva Petoskey, Sarah Rockhill, Kelsey Schell, Angie Smith-Butterwick, Ricki Torsch, Stephanie VanDerKooi, Danielle Walsh SUMMARY OF KEY POINTS Introductions, Welcome, and Approval of Agenda/Minutes – Su Min Oh Agenda reviewed and added heroin emerging issues and trends is now approved. If anyone has any items for future agendas, please contact Larry Scott ([email protected]), Angie Smith-Butterwick ([email protected]), Su Min Oh ([email protected]), Lisa Coleman ([email protected], or Joel Hoepfner at [email protected]. -
Metonitazene Begins Proliferation As Newest Synthetic Opioid Among Latest Cycle of Non-Fentanyl Related Drugs
January 2021 Metonitazene Begins Proliferation as Newest Synthetic Opioid Among Latest Cycle of Non-Fentanyl Related Drugs Purpose: The objective of this announcement is to notify public health and safety, law enforcement, first responders, clinicians, medical examiners and coroners, forensic and clinical laboratory personnel, and all other related Demographics communities about new information surrounding the emergent synthetic opioid metonitazene. Case Type: • Postmortem (n=8) Background: Synthetic opioids are chemically manufactured drugs, often accompanied with unknown potency and adverse effects or health risks. New synthetic opioids may be mixed with more traditional opioids, creating additional Age: • Range: 30s to 50s risk and danger for recreational drug users. Synthetic opioids may be distributed in powder or tablet form. In the United States (U.S.), an alarming increase in the number of deaths linked to synthetic opioid use has been reported. Date of Collection: • Aug. to Dec. 2020 The primary adverse effect associated with synthetic opioid use is respiratory depression, often leading to death. Other Notable Findings: Summary: Metonitazene is a potent synthetic opioid bearing structural resemblance to etonitazene, a synthetic opioid • Fentanyl (n=6) that is nationally and internationally controlled. Metonitazene is dissimilar in structure to other synthetic opioids • Cocaine (n=4) typically encountered in forensic casework (e.g. fentanyl analogues). Metonitazene and similar analogues (e.g. • Methamphetamine (n=4) etonitazene, isotonitazene) were first synthesized and reported in the literature in the 1950s. Pharmacological data suggest that this group of synthetic opioids have potency similar to or greater than fentanyl. Metonitazene was first reported by NPS Discovery after detection in a seized drug powder in July 2020. -
NFLIS-Drug Selected Substance List
2017-2020 NFLIS-Drug Substance List (Sorted by Date) Date Added NFLIS Substance Name Synonyms Chemical Name Structure InChI Formula to NFLIS- Drug InChI=1S/C16H20BrN/ c17-14-1-3-15(4-2-14)18-16-12-6-10-5-11 Bromantane ladasten N-(4-bromophenyl)adamantan-2-amine C16H20BrN 12/7/20 (8-12)9-13(16)7-10/h1-4,10-13,16,18H, 5-9H2 InChI=1S/C21H29FN2O3/ c1-4-27-21(26)19(15(2)3)23-20(25)17-14- ethyl 2-(1-(5-fluoropentyl)-1H-indole-3-carboxamido)-3- 5F-EMB-PICA EMB-2201; 5-fluoro-EMB-PICA 24(13-9-5-8-12-22)18-11-7-6-10-16(17)18 C21H29FN2O3 11/12/20 methylbutanoate /h6-7,10-11,14-15,19H, 4-5,8-9,12-13H2,1-3H3,(H,23,25) InChI=1S/C20H27FN2O3/ c1-20(2,3)17(19(25)26-4)22-18(24)15-13- methyl 2-(1-(4-fluorobutyl)-1H-indole-3- 4F-MDMB-BUTICA 4-fluoro-MDMB-BUTICA; 4F-MDMB-BICA 23(12-8-7-11-21)16-10-6-5-9-14(15)16/ C20H27FN2O3 10/23/20 carboxamido)-3,3-dimethylbutanoate h5-6,9-10,13,17H,7-8,11-12H2,1-4H3,(H, 22,24) InChI=1S/C10H14BrNO2/ 4-methoxy-6-[(1E)-2-phenylethenyl]-5,6-dihydro-2H- 2Br-4,5-Dimethoxyphenethylamine 2-bromo-4,5-dimethoxyphenethylamine c1-13-9-5-7(3-4-12)8(11)6-10(9)14-2/ C10H14BrNO2 10/2/20 pyran-2-one h5-6H,3-4,12H2,1-2H3 InChI=1S/C16H22FNO/ 4-fluoro-3-methyl-alpha-PVP; 4F-3-methyl-alpha- c1-3-6-15(18-9-4-5-10-18)16(19)13-7-8-1 4F-3-Methyl-alpha-PVP 4-fluoro-3-methyl-alpha-pyrrolidinopentiophenone C16H22FNO 10/2/20 pyrrolidinovalerophenone 4(17)12(2)11-13/h7-8,11,15H, 3-6,9-10H2,1-2H3 InChI=1S/C21H26N4O3/ N,N-diethyl-2-[2-(4-methoxybenzyl)-5-nitro-1H- c1-4-23(5-2)12-13-24-20-11-8-17(25(26)2 Metonitazene C21H26N4O3 9/15/20 benzimidazol-1-yl]ethanamine -
NPS Discovery Toolkit » Metonitazene
NPS Discovery Toolkit » Metonitazene 1 JULY ● 2021 Acknowledgements: This report was prepared by Alex J. Krotulski, PhD; Sara E. Walton, BS; Melissa F. Fogarty, MSFS, D-ABFT-FT; Donna M. Papsun, MS, D-ABFT; and Barry K. Logan, PhD, F-ABFT. Funding was received from the National Institute of Justice (NIJ) of the U.S. Department of Justice (DOJ) (Award Number 2020-DQ-BX-0007). The opinions, findings, and conclusions or recommendations expressed in this publication are those of the authors and do not necessarily reflect those of the Department of Justice. Recommended Citation: NPS Discovery (2021), NPS Discovery Toolkit: Metonitazene, Center for Forensic Science Research and Education, United States of America. Contact Information: Email: [email protected] Webpage: www.npsdiscovery.org 2 © 2021 The Center for Forensic Science Research & Education TABLE OF CONTENTS Purpose: The NPS Discovery Toolkit is a consolidation of our program outcomes into a comprehensive document detailing relevant Public Alert: Metonitazene Begins information about the characterization of a Proliferation as Newest Synthetic Opioid specified novel psychoactive substance (NPS). Page 4 This toolkit includes basic drug information, Among Latest Cycle of Non-Fentanyl date of first appearance, prevalence, temporal Related Drugs (January 2021) trends, geographical trends, demographics, poly-drug combinations (including with other NPS), metabolism, methods for identification and confirmation, reference concentration Trend Plots for Metonitazene and Page 5 ranges, and much more. This toolkit is NPS Opioids (up to Q2 2021) designed to serve as a one-stop resource for scientists and interested individuals looking for all-inclusive information about a new drug. Quarterly Trend Reports (Q3 2020 Page 6 through Q2 2021) About Us: The Center for Forensic Science Research and Education (CFSRE, Willow Drug Monograph: Metonitazene Grove, PA) is a non-profit organization that Page 8 operates a state-of-the-art laboratory with a (July 30, 2020) mission to advance forensic science testing and knowledge. -
Phar-Mon Plus
Phar-Mon plus Der Konsum etablierter sowie neuer psychoaktiver Substanzen in unterschiedlichen Risikopopulationen Ergebnisse des Projekts Phar-Mon plus aus dem Jahr 2020 Dr. Kirsten Lochbühler, Regina Kühnl, Simona Maspero, Darya Aydin & Mark Hulm IFT Institut für Therapieforschung DANKSAGUNG Unser herzlicher Dank gilt denjenigen, die uns bei der Erstellung des Berichts unterstützt haben: unserem Kooperationspartner Karsten Tögel-Lins von Basis e. V., unseren Kolleginnen Renate Schlüter, Julia Heck, Monika Rossa, Katharina Schoder und Selina Moser sowie unseren Praktikantinnen und Praktikanten Helena Faust, Elena Schauer, Anna Hodges, Olivia Hoppe, Jan Kustermann, Anna Preitenwieser, Tim Sedelmaier, Lisa Pfefferseder und Magdalena Wimmer. Darüber hinaus möchten wir all unseren engagierten Kooperationspartnerinnen und -partnern danken: den Partyprojekten, den Suchthilfeeinrichtungen, dem HaLT-Projekt der BAS, dem GIZ- Nord und der JVA Wittlich, die uns seit Jahren bei der Rekrutierung von Studienteilnehmerinnen und -teilnehmern unterstützen bzw. uns Daten aus ihren Projekten/Einrichtungen zur Verfügung stellen. Außerdem möchten wir uns bei allen Personen, die sich für ein Interview bereit erklärt haben, ganz herzlich bedanken. Ein besonderer Dank geht auch an alle Teilnehmerinnen und Teilnehmer, die Fragebögen ausgefüllt haben und uns somit einen wertvollen Einblick in ihr Konsumverhalten erlauben. 3 INHALT Inhalt Teil 1: Auswirkungen der COVID-19-Pandemie auf den Konsum psychoaktiver Substanzen und das Suchthilfesystem ............................................................