Illicitly Manufactured Fentanyl–Involved Overdose Deaths with Detected Xylazine — United States, January 2019–June 2022

In 2022, provisional data indicated that more than two thirds (68%) of the reported 107,081 drug overdose deaths in the United States involved synthetic opioids other than methadone, principally illicitly manufactured fentanyls (IMFs) (1). Xylazine, a nonopioid sedative not approved for human use and with no known antidote, has been increasingly detected in IMF products in the U.S. drug supply* and in IMF-involved overdose deaths (2). Limited studies suggest xylazine can cause central nervous system depression, respiratory depression, bradycardia, and hypotension in humans (3,4); chronic use might lead to severe withdrawal symptoms^† as well as skin ulcerations (4). This report uses data from CDC’s State Unintentional Drug Overdose Reporting System (SUDORS) to describe IMF-involved^§ overdose deaths with and without xylazine detected that occurred during January 2019–June 2022. Among 21 jurisdictions, which included 20 states and the District of Columbia, the monthly percentage of IMF-involved deaths with xylazine detected increased 276%, from 2.9% to 10.9%. Among IMF-involved deaths during January 2021–June 2022 in 32 jurisdictions, xylazine was detected in a higher percentage of jurisdictions in the Northeast U.S. Census Bureau region; listing detected xylazine as a cause of death varied across jurisdictions. Expanded postmortem and illicit drug product testing for xylazine is needed to clarify prevalence in drug supplies; further investigation of xylazine’s effects on humans is necessary to characterize morbidity and overdose risk. It is important for overdose prevention and response messages to highlight the potential presence of xylazine in IMF products and emphasize the need for respiratory and cardiovascular support to address the sedative effects of xylazine.

Jurisdictions entered information on drug overdose deaths that were unintentional or of undetermined intent into SUDORS using death certificates, medical examiner and coroner reports (including information about circumstances of the overdose from scene evidence and witness reports), and toxicology reports. Monthly counts of IMF-involved deaths^¶ with xylazine detected and co-involved as a cause of death, and proportions of IMF-involved deaths with xylazine detected were examined in 21 jurisdictions** for January 2019–June 2022. The most recent 18 months of data (January 2021–June 2022) were further examined among 32 jurisdictions.^†† The number and percentage of IMF-involved deaths with xylazine detected, and the proportion of those with xylazine detected for which xylazine was listed as a cause of death, were calculated for each jurisdiction. The number and percentage of IMF-involved deaths with and without xylazine detected were calculated, stratified by decedent demographics, U.S. Census Bureau region,^§§ co-involved drugs, and overdose circumstances (e.g., route of drug use, decedent drug use history, and overdose response efforts). Jurisdictions were included in analyses if toxicology reports were available for ≥75% of deaths for the relevant study periods, resulting in variation in the number of states included in each analysis; analyses were restricted to deaths with toxicology reports or with xylazine listed as a cause of death on the death certificate. Analyses were performed using SAS (version 9.4; SAS Institute). This activity was reviewed by CDC and conducted consistent with applicable federal law and CDC policy.^¶¶

Among 21 jurisdictions, the monthly proportion of IMF-involved deaths with xylazine detected increased 276% from January 2019 (2.9%) to June 2022 (10.9%) (Figure 1). The monthly number of IMF-involved deaths with xylazine co-involved increased from 12 in January 2019 to 188 in June 2022. During January 2021–June 2022, among 32 jurisdictions, xylazine was detected in 9.0% (4,859) of 53,969 IMF-involved deaths (Table) and co-involved in 6.9% (3,735). Xylazine detection varied by jurisdiction (Figure 2). The highest percentages and numbers of IMF-involved deaths with xylazine detected were in Maryland (27.7%; 923 deaths), Connecticut (26.4%; 507), and Pennsylvania (23.3%; 1,285). The proportion of IMF-involved deaths with xylazine detected in which xylazine was determined to be a cause of death ranged from none to ≥90% across jurisdictions. Although jurisdictions that did not submit toxicology reports to SUDORS for ≥75% of deaths were excluded from analyses, death certificate data provided to SUDORS indicated that xylazine was co-involved in IMF-involved deaths in several excluded states, including New York, which recorded 735 such deaths.***

During January 2021–June 2022, decedent demographics, overdose circumstances, and other drug co-involvement were largely similar in comparisons of IMF-involved deaths with and without xylazine detected (Table). However, compared with IMF-involved deaths without xylazine, a lower percentage of those with xylazine detected had evidence of no pulse when first responders arrived (53.3% versus 62.2%) and a higher percentage had evidence of injection drug use^††† (28.6% versus 19.5%). Compared with IMF-involved deaths without xylazine, a higher proportion of IMF-involved deaths with xylazine detected were in the Northeast U.S. Census Bureau region (49.9% versus 28.5%) and a lower proportion were in the West (1.1% versus 16.5%).

Acknowledgments

Jurisdictions participating in CDC’s Overdose Data to Action (OD2A) program and providing data to the State Unintentional Drug Overdose Reporting System, including state and jurisdictional health departments, vital registrar offices, and coroner and medical examiner offices; CDC OD2A team; Lauren Tanz, Division of Overdose Prevention, National Center for Injury Prevention and Control, CDC.

Corresponding author: Mbabazi Kariisa, mkariisa@cdc.gov.

¹Division of Overdose Prevention, National Center for Injury Prevention and Control, CDC; ²Forensic Medicine Division, Department of Pathology, Immunology and Laboratory Medicine, College of Medicine, University of Florida, Gainesville, Florida.

References

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FIGURE 1. Number and percentage of drug overdose deaths involving* illicitly manufactured fentanyls,^† by month and xylazine detection or co-involvement — State Unintentional Drug Overdose Reporting System, 21 jurisdictions,^§ January 2019–June 2022

Abbreviations: IMF = illicitly manufactured fentanyl; SUDORS = State Unintentional Drug Overdose Reporting System.

* A drug was considered involved or co-involved if it was listed as a cause of death on the death certificate or medical examiner or coroner report.

^† Fentanyl was classified as likely illicitly manufactured using toxicology, scene, and witness evidence. For the 8% of deaths involving fentanyl that had insufficient evidence for classification as illicit or prescription, fentanyl was classified as illicit because the vast majority of fentanyl overdose deaths involve illicit fentanyl. All fentanyl analogs except alfentanil, remifentanil, and sufentanil, which have legitimate human medical use, were included as IMFs.

^§ Connecticut, Delaware, District of Columbia, Georgia, Illinois, Maine, Massachusetts, Minnesota, Nevada, New Hampshire, New Jersey, New Mexico, Ohio, Oklahoma, Pennsylvania, Rhode Island, Utah, Vermont, Virginia, Washington, and West Virginia. Illinois, Pennsylvania, and Washington reported deaths from counties that accounted for ≥75% of drug overdose deaths in the state in 2017 per SUDORS funding requirements; all other jurisdictions reported deaths from the full jurisdiction. Jurisdictions were included if data were available for each 6-month period (January–June 2019, July–December 2019, January–June 2020, July–December 2020, January–June 2021, July–December 2021, and January–June 2022), and toxicology reports were available for ≥75% of deaths in the included period or periods. Analysis was restricted to decedents with an available toxicology report or with xylazine listed as a cause of death on the death certificate.

Abbreviations: IMF = illicitly manufactured fentanyl; SUDORS = State Unintentional Drug Overdose Reporting System.
* Fentanyl was classified as likely illicitly manufactured using toxicology, scene, and witness evidence. For the 8% of deaths involving fentanyl that had insufficient evidence for classification as illicit or prescription, fentanyl was classified as illicit because the vast majority of fentanyl overdose deaths involve illicit fentanyl. All fentanyl analogs except alfentanil, remifentanil, and sufentanil, which have legitimate human medical use, were included as IMFs.
^† Arizona, Arkansas, Colorado, Connecticut, Delaware, District of Columbia, Georgia, Illinois, Iowa, Kansas, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Dakota, Utah, Vermont, Virginia, Washington, and West Virginia. Illinois, Louisiana, Pennsylvania, and Washington reported deaths from counties that accounted for ≥75% of drug overdose deaths in the state in 2017, per SUDORS funding requirements; all other jurisdictions reported deaths from the full jurisdiction. Jurisdictions were included if data were available for the full period of January 2021–June 2022, including toxicology reports for ≥75% of deaths. Analysis was restricted to decedents with an available toxicology report; or, if no toxicology report was available, deaths were also included if xylazine was listed as part of the cause of death on the death certificate. Analysis of overdose circumstances was further restricted to jurisdictions with coroner or medical examiner report data for ≥75% of deaths during January 2021–June 2022 (resulting in the same 32 jurisdictions), and to deaths with a coroner or medical examiner report.
^§ Missing values were excluded from calculations of percentages. Percentages might not sum to 100% because of rounding.
^¶ Northeast: Connecticut, Maine, Massachusetts, New Hampshire, New Jersey, Pennsylvania, Rhode Island, and Vermont; Midwest: Illinois, Iowa, Kansas, Michigan, Minnesota, Nebraska, Ohio, and South Dakota; South: Arkansas, Delaware, District of Columbia, Georgia, Louisiana, Maryland, Oklahoma, Virginia, and West Virginia; West: Arizona, Colorado, Nevada, New Mexico, Oregon, Utah, and Washington.
** A drug was considered involved or co-involved if it was listed as a cause of death on the death certificate or in the medical examiner or coroner report. Percentages sum to >100% because drug categories are not mutually exclusive.
^†† Drug entries coded as heroin were heroin and 6-acetylmorphine. In addition, morphine was coded as heroin if detected along with 6-acetylmorphine or if scene, toxicology, or witness evidence indicated presence of known heroin adulterants or impurities (including quinine, procaine, xylazine, noscapine, papaverine, thebaine, or acetylcodeine), injection, illicit drug use, or a history of heroin use.
^§§ Drug entries coded as prescription opioids were alfentanil, buprenorphine, butorphanol, codeine, dextrorphan, dihydrocodeine, hydrocodone, hydromorphone, levorphanol, meperidine, methadone, morphine, nalbuphine, noscapine, oxycodone, oxymorphone, pentazocine, prescription fentanyl, propoxyphene, sufentanil, tapentadol, and tramadol. Also included as prescription opioids were brand names and metabolites (e.g., nortramadol) of these drugs and combinations of these drugs and nonopioids (e.g., acetaminophen-oxycodone). Morphine was included as prescription only if scene or witness evidence did not indicate likely heroin use and if 6-acetylmorphine was not also detected. Fentanyl was coded as a prescription opioid based on scene, toxicology, or witness evidence.
^¶¶ For SUDORS, a potential bystander is defined as a person aged ≥11 years who was physically nearby either during or shortly preceding a drug overdose and potentially had an opportunity to intervene or respond to the overdose. This includes any persons in the same structure (e.g., same room or same building, but different room) as the decedent during that time; a family member who was in another room during the fatal incident would be considered a potential bystander if they might have had an opportunity to provide lifesaving measures (e.g., naloxone administration), if adequate resources were available, and if they were aware that an overdose event could occur. Persons in different self-contained parts of larger buildings (e.g., a different apartment in the same apartment building) would not be considered potential bystanders.
*** Evidence of injection, smoking, snorting, ingestion, and other route of drug use are not mutually exclusive; a death could have evidence of more than one of these routes. Routes of use cannot be linked to a specific drug or type of drug.
^††† Other routes of drug use were buccal, sublingual, transdermal, and suppository.

FIGURE 2. Number and percentage of drug overdose deaths involving* illicitly manufactured fentanyls,^† by xylazine detection or co-involvement — State Unintentional Drug Overdose Reporting System, 31 states and District of Columbia,^§ January 2021–June 2022

Abbreviations: DC = District of Columbia; IMF = illicitly manufactured fentanyl; SUDORS = State Unintentional Drug Overdose Reporting System.

* A drug was considered involved or co-involved if it was listed as a cause of death on the death certificate or in the medical examiner or coroner report.

^† Fentanyl was classified as likely illicitly manufactured using toxicology, scene, and witness evidence. For the 8% of deaths involving fentanyl that had insufficient evidence for classification as illicit or prescription, fentanyl was classified as illicit because the vast majority of fentanyl overdose deaths involve illicit fentanyl. All fentanyl analogs except alfentanil, remifentanil, and sufentanil, which have legitimate human medical use, were included as IMFs.

^§ Arizona, Arkansas, Colorado, Connecticut, Delaware, District of Columbia, Georgia, Illinois, Iowa, Kansas, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Dakota, Utah, Vermont, Virginia, Washington, and West Virginia. Illinois, Louisiana, Pennsylvania, and Washington reported deaths from counties that accounted for ≥75% of drug overdose deaths in the state in 2017, per SUDORS funding requirements; all other jurisdictions reported deaths from the full jurisdiction. Jurisdictions were included if data were available for the full period of January 2021–June 2022, including toxicology reports for ≥75% of deaths. Analysis was restricted to decedents with an available toxicology report; or, if no toxicology report was available, deaths were also included if xylazine was listed as part of the cause of death on the death certificate. Four funded states were excluded from analyses because they were known to have not tested for xylazine during the analysis period. Toxicology report data were not available for ≥75% of all deaths in eight states with complete death certificate data for January 2021–June 2022, and they were therefore excluded from analyses, but death certificate data identified IMF-involved deaths with xylazine co-involved: Alabama (46 deaths), Florida (261), Indiana (82), Mississippi (10), Missouri (93), New York (735), South Carolina (178), and Tennessee (167).