GHB
G · liquid ecstasy
What does current UK evidence show?
GBL is widely encountered in UK chemsex and sexualised drug-use settings and is rapidly converted to GHB in the body. GHB is also reported, and many UK datasets group GHB and GBL together, so the precise substance used or sold is not always distinguishable.
Overview
Identity, legal classification, form and pharmacological context
- Drug category
- Depressants
- Common names
- G, liquid ecstasy
- Typical forms
- Usually a clear liquid; GHB may also occur as powder or capsules
- Routes
- Usually swallowed, commonly as a measured or unmeasured liquid dose
- UK legal classification
- Class BReclassified from Class C to Class B in April 2022.Check government source ↗
- Concise pharmacology
- Reduces central nervous system activity through substance-specific sedative mechanisms.
Main harms
Concise clinical and polydrug picture
Impaired coordination, reduced consciousness, vomiting and breathing problems, especially in combinations.
Cognitive, physical and mental-health harms vary by substance and pattern of use.
Withdrawal after frequent dependent use can develop rapidly and be severe; urgent specialist clinical assessment is needed.
Alcohol, opioids, benzodiazepines and other depressants substantially increase severe-sedation and breathing risks.
Small differences in liquid dose or concentration can cause rapid loss of consciousness. Product identity and strength may be uncertain.
Current intelligence status
Assessment, confidence and direction
GBL is widely encountered in UK chemsex and sexualised drug-use settings and is rapidly converted to GHB in the body. GHB is also reported, and many UK datasets group GHB and GBL together, so the precise substance used or sold is not always distinguishable.
Reason: Credible but partial sources support a constrained assessment; the direction or reach cannot be generalised across the UK.
Principal source limits: Deaths are counted by registration year; 62.7% of the 2025 registrations concern earlier deaths. Substance mentions overlap and do not prove sole causation. Treatment contact reflects recorded service need and access in England, not population prevalence.
Geography and reference periods are given in each linked source card below. The rating is an editorial evidence judgement, not a probability, clinical risk score or TD priority.The assessment reflects the latest linked evidence and is not a universal severity rating.
Operational implications
Evidence-supported prompts for professional response
Join GBL/GHB overdose, withdrawal, consent, sexual-health and safeguarding responses; severe dependence can require specialist clinical management.
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.
Triangulate treatment, mortality, testing, hospital and frontline evidence before assigning a local trend.
Related intelligence
Continue into connected platform evidence
Sources & limitations
Direct evidence links, reference periods and status
Deaths related to drug poisoning in England and Wales: 2025 registrations
Published4 Nov 2026Reference period2025 registrations; 2024 occurrences
Deaths are counted by registration year; 62.7% of the 2025 registrations concern earlier deaths. Substance mentions overlap and do not prove sole causation.Adult substance misuse treatment statistics
Published04 Dec 2025Reference periodEngland · 2024–25
Treatment contact reflects recorded service need and access in England, not population prevalence.Drug misuse and dependence: UK clinical management guidelines
Published2017; landing page updated 13 Aug 2026Reference periodClinical guidance
Use current local clinical protocols alongside this guidance.Assessment of GHB, GBL and related compounds
Published20 Nov 2020Reference periodClinical and social harms
Evidence often combines GHB and GBL; selected-use settings do not establish population prevalence.