Notes from the Field: Nitazene-Related Deaths…

Nitazenes are a novel group of powerful illicit synthetic opioids derived from 2-benzylbenzimidazole that have been linked to overdose deaths in several states (1). Nitazenes were created as a potential pain reliever medication nearly 60 years ago but have never been approved for use in the United States (2). Laboratory test results indicate that the potency of certain nitazene analogs (e.g., isotonitazene, protonitazene, and etonitazene) greatly exceeds that of fentanyl, whereas the potency of the analog metonitazene is similar to fentanyl (3,4). Naloxone has been effective in reversing nitazene-involved overdoses, but multiple doses might be needed (3,4). The prevalence of nitazene deaths in the United States is unknown and the frequency of nitazene involvement in overdose deaths in Tennessee has not yet been assessed. However, of concern is that nitazenes are increasingly recorded in toxicology reports and death certificate cause-of-death fields. Given their potency, raising awareness about nitazenes and implementing strategies to reduce harm through increased testing, surveillance, and linkage to treatment for substance use disorders are of vital importance.

The Office of Informatics and Analytics at the Tennessee Department of Health conducts routine surveillance of fatal drug overdoses using the Tennessee State Unintentional Drug Overdose Reporting System (TN SUDORS). The surveillance system collects sociodemographic information and circumstances associated with overdose deaths, including death scene information, autopsy reports, and toxicology reports for drug overdose deaths of unintentional and undetermined intent. For this analysis, nitazene-involved deaths were identified using a text search for the term “nitazene” (and common misspellings) in death certificate cause-of-death fields and in toxicology reports for deaths that occurred during January 1, 2019–December 31, 2021, with data available as of June 10, 2022. TN SUDORS data were examined for demographic characteristics and circumstances surrounding deaths. Tennessee death certificate data for 2021 are provisional, as are SUDORS data for July–December 2021. This analysis was determined to be exempt from review by the Tennessee Department of Health’s Institutional Review Board and was reviewed by CDC and conducted consistent with applicable federal law and CDC policy.*

During 2019–2021, a total of 52 nitazene-involved fatal drug overdoses were identified using TN SUDORS data, including no cases in 2019, 10 in 2020, and 42 in 2021 (Table). In 2020, most of nitazene-involved deaths were attributed to isotonitazene, but in 2021, most were attributed to metonitazene. Among the 10 nitazene-involved overdose deaths identified in 2020, the average decedent age was 40.6 years, and nine (90.0%) decedents were White males. In 2021, the average decedent age was similar (42.6 years); a smaller percentage of the 42 decedents were male (66.7%) and White (88.1%). Whereas nitazene-involved deaths increased in 2021, 85.7% were attributed to metonitazene, which has a lower potency compared with other nitazenes. All nitazene-involved overdoses involved multiple substances. During both 2020 and 2021, the most frequent route of administration was injection (18; 34.6%). Other routes of administration were smoking, snorting, and ingestion. In addition to fentanyl (59.6%), other co-occurring substances included methamphetamine (46.2%), amphetamine (25.0%), and flualprazolam (13.5%).

Most nitazene-involved deaths in Tennessee were identified in Knox County. This apparent high prevalence is most likely because Knox County’s Regional Forensic Center sends blood samples for secondary laboratory testing to the Drug Enforcement Agency (DEA) (5); traditional laboratory panels do not always capture nitazenes. Therefore, nitazene-involved deaths that occur in other counties of Tennessee are likely to be undercounted. DEA provides laboratory testing as a free resource and encourages state and national forensic centers to submit their samples for additional testing to assist in the accurate counting of deaths and to better guide drug overdose prevention efforts.

Naloxone was only administered to 12 (23%) persons with nitazene-involved fatal overdoses. Given naloxone’s effectiveness in preventing fatal overdoses, more frequent administration of naloxone by first responders, bystanders, and clinicians is important. Implementing naloxone training and distribution efforts throughout all states is also necessary. As with fentanyl, multiple naloxone doses might be required because of the potency of nitazene^† and can be safely administered. In addition, contacting emergency services is necessary to provide immediate medical attention to persons who might be overdosing.

Four times as many nitazene-involved overdoses were identified in Tennessee in 2021 than in 2020, and this number could be underestimated because of low testing frequency. Nitazenes are an emerging group of highly potent psychoactive substances, tests for which are often not included in standard toxicology panels. Given their potency, raising awareness about nitazenes and implementing strategies to reduce harm through increased testing, surveillance, and linkage to treatment for substance use disorders are of vital importance. More data are required to better understand this emerging group of psychoactive substances in the United States.

MMWR and Morbidity and Mortality Weekly Report are service marks of the U.S. Department of Health and Human Services.

Use of trade names and commercial sources is for identification only and does not imply endorsement by the U.S. Department of
Health and Human Services.
References to non-CDC sites on the Internet are
provided as a service to MMWR readers and do not constitute or imply
endorsement of these organizations or their programs by CDC or the U.S.
Department of Health and Human Services. CDC is not responsible for the content
of pages found at these sites. URL addresses listed in MMWR were current as of
the date of publication.

All HTML versions of MMWR articles are generated from final proofs through an automated process.
This conversion might result in character translation or format errors in the HTML version.
Users are referred to the electronic PDF version (https://www.cdc.gov/mmwr)
and/or the original MMWR paper copy for printable versions of official text, figures, and tables.

Questions or messages regarding errors in formatting should be addressed to
mmwrq@cdc.gov.