Xylazine
tranq · veterinary sedative
What is currently changing about this drug in the UK?
NRS recorded four Scottish drug use deaths implicating xylazine in 2025; routine testing began in 2024, limiting comparison. ACMD identified multifaceted evidence of UK detection, but coverage is incomplete and does not support a national prevalence estimate. Naloxone only treats any opioid component.
Overview
Identity, legal classification, form and pharmacological context
- Drug category
- Depressants · Synthetic drugs
- Common names
- tranq, veterinary sedative
- Typical forms
- Detected in UK drug samples, including mixtures with opioids; it may be an undeclared adulterant rather than a product people intended to obtain
- Routes
- Exposure may be unintentional through the route used for another drug; no single routine chosen route should be assumed
- UK legal classification
- Class CControlled from January 2025 and placed in Schedule 4 Part 1 to preserve legitimate veterinary use.Check government source ↗
- Concise pharmacology
- Reduces central nervous system activity through substance-specific sedative mechanisms.
Main harms
Concise clinical and polydrug picture
Marked sedation, reduced consciousness, slow heart rate and low blood pressure; mixed opioid exposure can stop breathing.
Repeated exposure has been associated with severe skin and soft-tissue injury; the UK scale is uncertain.
International evidence describes clinically significant withdrawal after sustained exposure; UK evidence remains limited.
Opioids and other sedatives compound reduced-consciousness and breathing risks.
Unknown concentration and unintended exposure make dose difficult to assess. Injecting a contaminated product adds infection and tissue-damage risks; wounds may occur beyond injection sites.
Current intelligence status
Assessment, confidence and direction
Signals justify continued monitoring, but current evidence does not support a formal escalation assessment.
Operational implications
Evidence-supported prompts for professional response
Combine opioid-overdose response with airway support, urgent clinical assessment, wound pathways and rapid analytical reporting.
Record substance, sold identity, route, frequency and combinations; review overdose and withdrawal needs.
Use symptom-led assessment and escalate reduced consciousness, seizures, overheating, chest pain or severe agitation.
Send unexpected products or incidents through agreed testing and alert routes; distinguish confirmed results from preliminary reports.
Related intelligence
Continue into connected platform evidence
Sources & limitations
Direct evidence links, reference periods and status
Drug-related deaths in Scotland, 2025
Published23 Sep 2026Reference period2025 registrations
NRS calls this series drug use deaths. Substance implication overlaps and does not prove sole causation. Nitazene testing expanded, including etonitazene in May 2025; 2025 versus 2024 rate difference is not statistically significant.Use and harms of xylazine
Published16 Feb 2024Reference periodUpdated publication collection · Jan 2026
UK detections remain incomplete; international harms cannot be assumed to occur at the same scale in the UK.Welsh Emerging Drugs and Identification of Novel Substances
PublishedContinuousReference periodSubmitted samples
Submitted samples confirm their own contents but cannot estimate prevalence or represent the wider drug supply.