Rapid Action Drug Alerts and Response (RADAR) quarterly report
January 2025
Management information
- Published
- 28 January 2025 (Latest release)
- Type
- Statistical report
- Author
- Public Health Scotland
About this release
Our quarterly report
The Drugs Team at Public Health Scotland (PHS) has compiled this RADAR quarterly report of drug-related indicators.
The objective of this report is to monitor drug-related harms, service usage and toxicology data, in order to provide an early warning of emerging drug trends and identify actions to reduce and prevent drug harms and deaths.
View a printable version of this report.
Acknowledgements
This report reflects the collective efforts of different organisations and hundreds of people in frontline and supporting roles who record, organise, analyse and interpret information from a range of sources and services.
We gratefully acknowledge the continued commitment and effort of all those involved.
Data and reporting period
RADAR's emphasis is on reporting drug-related information as rapidly as possible, for the purpose of public health surveillance. This means that data may not be fully validated and may be subject to change. Further analysis of these data will be made available in our Accredited official statistics publications on substance use.
Observed changes in indicators may reflect genuine trends in behaviours but may also be influenced by factors such as the configuration of services, or data quality and completeness issues.
Different time periods may be reported across the different indicators. In all cases, the most recently available data are used. Most charts show Scotland-level data based upon a two-year time series. Location and time series can be customised in the RADAR dashboard (external website).
The next release of this publication will be 29 April 2025.
Dashboard
Data for most of the harm and service indicators in this report are published in our RADAR dashboard (external website).
In the dashboard, the time series can be adjusted and the data can be filtered by NHS board.
This dashboard supersedes the substance use section of the COVID-19 wider impacts dashboard (external website), which has now been decommissioned.
For optimal viewing and interaction, we recommend accessing the dashboard using a computer with a large screen. Accessing via a mobile phone may reduce the functionality.
Main points
Drug-related harms decreased during the most recent quarter (September to November 2024). However, intelligence suggests the drug supply remains highly toxic and unpredictable, requiring ongoing vigilance and a heightened response. Significant disruptions and adaptations in the heroin and benzodiazepine markets, appear to be influencing levels and patterns of harm.
Key points
- Benzodiazepines: A decrease in bromazolam detections was observed in post-mortem and seizure toxicology sources. There was a slight increase in emergent benzodiazepines detected during this period including clonazolam and desalkylgidazepam.
- Heroin: Adulteration of heroin with synthetic substances, including nitazenes and xylazine, continued to be reported through RADAR reports and WEDINOS. These adulterants increase the risk of overdose and adverse effects and were associated with unpredictable reactions, including rapid onset overdose and difficulty reversing overdoses with naloxone.
- Cocaine: Cocaine remained the most frequently identified substance in both post-mortem toxicology and the ASSIST project, highlighting its leading role in harms.
Data update
The following changes were observed compared to the previous reporting period (reported in quarterly report 9 – October 2024).
For harm indicators:
- naloxone administration incidents (September to November 24): 30% decrease
- emergency department attendances (September to November 24): 10% decrease
- suspected drug deaths (September to November 24): 10% decrease
- drug-related hospital admissions (July to September 24): 8% decrease
For service indicators:
- drug treatment referrals (August and November 24): stable
- injecting equipment provision (July to September 24): 2% increase in transactions, 2% increase in number of needles and syringes distributed
- opioid substitution therapy (July to September 24): 2% decrease
Alerts
- The legal status section in our public health alerts were updated in January 2025 to reflect changes to the Misuse of Drugs Act (1971) (external website).
Harm indicators
- Between September and November 2024, the number of Scottish Ambulance Service naloxone administration incidents was 30% lower than the previous quarter. Incidents were 24% lower than the same period in 2022 and 34% lower than in 2023.
- Between September and November 2024, drug-related attendances at emergency departments were 10% lower than the previous quarter. Attendances were 14% lower than the same period in 2022 and 16% lower than in 2023.
- Between July and September 2024, drug-related hospital admissions were 8% lower than the previous quarter. Admissions were similar to the same period in 2022 and 20% lower than in 2023.
- Between September and November 2024, there were 215 suspected drug deaths. The number of deaths was 10% lower than the previous quarter (238), 20% lower than the same period in 2022 (268) and 15% lower than in 2023 (254).
Toxicology indicators
- Between September and November 2024, the most frequently detected drug in the ASSIST hospital toxicology project was cocaine (13%), followed by desmethyldiazepam (12%) and temazepam (10%). N-desethyl etonitazene was detected for the first time in the study.
- Between July and September 2024, the most common drug types detected in post-mortem toxicology were opioids (73%) and benzodiazepines (54%). Cocaine continued to be the most commonly detected individual drug (34%), followed by heroin/morphine (31%), diazepam (23%) and methadone (23%). Nitazenes increased slightly, being detected in 4% of deaths (25). Nitazenes have been detected in a total of 105 deaths (to 30 September 2024).
- Synthetic cannabinoids continue to be the most prevalent drug type detected in the Scottish Prisons Non-Judicial Drug Monitoring Project.
Service indicators
- Between August and November 2024, the average weekly number of referrals to specialist drug treatment services was relatively stable. The total number of referrals recorded (6,578) was 7% higher than the same period in 2022 (6,166) and 5% lower than in 2023 (6,910).
- Between July and September 2024, opioid substitution therapy doses supplied per month was 7% lower than the same period in 2022 and similar to 2023. The average monthly number of methadone doses supplied continued to decrease while injectable buprenorphine doses increased over time.
- Between July and September 2024, the average weekly number of injecting equipment provision transactions was similar (2% higher) to the previous quarter, similar to the same period in 2022 and 6% lower than 2023. The number of needles and syringes distributed was similar (2% higher) to the previous quarter, 6% lower than the same period in 2022 and 7% lower than in 2023.
Reporting trends
- Between 5 October 2024 and 4 January 2025, 97 trend reports were received by RADAR.
- The majority of reports related to heroin and benzodiazepines.
- Trend reports can be viewed on our dashboard (external website).
Implications
- The harm caused by drugs is a significant public health issue for Scotland and there is a high likelihood of sudden, localised spikes of drug-related harms. For information on responding to a drug harm incident see: Guidance on the management of clusters of drug related harms.
- Contamination of illicit drugs with toxic substances is both common and widespread across drug types. There remains an urgent need for hospital toxicology and accessible drug checking services across the country.
- The changes in the types of benzodiazepines detected, specifically the reduction in bromazolam and the emergence of novel benzodiazepines, followed international control.
- In 2024, bromazolam was included in the Convention on Psychotropic Substances (1971). These measures are likely to contribute to disruptions in the availability and accessibility of bromazolam.
- Given the dominance of bromazolam within the Scottish drug supply over the past 18 months, a reduction in availability is of concern. There is a risk that previously unseen and highly toxic benzodiazepines may emerge to dominate the supply in the near future.
- There remains an urgent need for evidence-based benzodiazepine harm reduction and polysubstance treatment support interventions.
- Toxicology services and Public Health Scotland should continue to collaborate to support timely identification and risk assessment of the health impact of emergent ‘street benzos’.
- There is a mixed picture of availability and widespread contamination of the heroin supply with both nitazenes and xylazine. It is unclear whether these changes are because of global supply changes or market adaptation.
- Cocaine continued to play a leading role in drug harms. Further work is needed to deliver harm reduction and treatment support. Injecting cocaine carries the highest risk of harm. Scaling up access to evidence-based interventions, including access to safer consumption facilities and provision of inhalation devices should be considered across Scotland.
- People use drugs in different ways and for different reasons, understanding the specific context and nature of drug use amongst people at risk or affected is critical to an effective response. The risk of harm is increased in the context of stigma and exclusion and these factors should be considered when preventing or responding to a drug harm incident.
- There is a risk that as the availability or perceived quality of substances changes, the types of drugs that contribute to harms changes. There is an urgent need for coordination to improve Scotland's ability and agility in responding to polysubstance use and a continually evolving drug market. A focus is needed on development, implementation and evaluation of measures to prevent and reduce the harms of polysubstance use.
- A system-wide approach that prevents drug harms and supports people affected to access treatment, care and recovery remains critical.
Alerts
Current alerts
Nitazenes
A public health alert about nitazene-type opioids was published in January 2023. It was updated in July 2024, due to increasing detections in drugs mis-sold as heroin and diazepam. The legal status section was updated in January 2025 to highlight the introduction of generic nitazene controls under the Misuse of Drugs Act (1971).
Xylazine
A public health alert about xylazine was published in May 2024, due to increasing detections in drugs mis-sold as heroin. The legal status section was updated in January 2025 to highlight the control of xylazine as a class C drug under the Misuse of Drugs Act (1971).
Bromazolam
A public health alert about new benzodiazepines was published in July 2023. Bromazolam is the most common drug detected in ‘street benzos’. The legal status section was updated in January 2025 to highlight the control of new benzodiazepines (including gidazepam and desalkylgidazepam) as class C drugs under the Misuse of Drugs Act (1971).
Trends
Redirect
Police drug trends bulletin
The purposes of the Police Scotland’s Statement of Opinion (STOP) bulletin are to raise awareness of drug trends and to demonstrate some of the substances present in Scotland's drugs market. This edition describes the diversification in the supply of cannabinoids.
Synthetic cannabinoid receptor agonists (SCRAs)
Officers from the STOP Unit West attended an address that was being used in the production of synthetic cannabinoid receptor agonists (SCRAs, also known as synthetic cannabinoids or ‘spice’), namely MDMB-4en-PINACA and ADB-INACA. This is the first known site attended by the STOP Unit in Scotland. The operation was notable for its highly sophisticated setup.
SCRAs are primarily associated with use in prisons, where they are consumed in various forms, including vapes, paper and powder. More information on drug use in prisons, can be found in the indicator: Drug seizures in Scottish prisons.
They have also been identified in community settings, appearing in products such as vapes, edibles or sprayed onto resin and plant material (commonly referred to as ‘bud’). Although less common, SCRAs have occasionally been detected in tablet form as well.
Most synthetic cannabinoids are deemed class B drugs under the Misuse of Drugs Act 1971. Newer ones are covered by the Psychoactive Substances Act 2016.
Semi-synthetic cannabinoids
STOP Unit West have recently seen a recovery of a drug that appeared to be cannabis resin. Laboratory analysis revealed the presence of the SCRA, MDMB-4en-PINACA, as well as hexahydrocannabinol (HHC). While the detection of a SCRA on cannabis resin is not unusual, the presence of HHC is uncommon.
HHC is a semi-synthetic cannabinoid, a compound that is derived from naturally occurring cannabinoids but is modified to enhance or alter the effects. It is controlled by the Psychoactive Substances Act 2016.
Tetrahydrocannabinol
Tetrahydrocannabinol (THC) is a class B drug under the Misuse of Drugs Act 1971. It is most commonly found in herbal form as one of the main cannabinoids in cannabis. It has also been detected in vape oils and in crystal form. Below is an image of a recent recovery of THC crystals.
Cannabidiol
STOP Unit West have seen a recent increase in the recovery of cannabis extracts being recovered containing cannabidiol (CBD) only (no THC). These have taken the form of crystals, similar to but larger than the THC crystals shown above, or as yellow/brown material with similar appearance to ‘shatter’.
CBD is a cannabinoid, but it is non-intoxicating and non-euphoric, meaning it is not psychoactive and does not produce a ‘high’. Unlike other cannabinoids, it is not controlled by the Misuse of Drugs Act or Psychoactive Substances Act. It is commonly sold as a food supplement and is advertised as helping with conditions such as inflammation, pain, nausea, migraines, seizures and anxiety, although further research is needed to establish a firmer evidence base for its use as a treatment for such conditions.
RADAR intelligence and reports
97 reports were validated by RADAR between 5 October 2024 and 4 January 2025.
RADAR has received over 450 reports of drug-related information and harms. Our sincere thanks to everyone who has contributed.
These reports have been invaluable in identifying early changes to trends and supply, enabling more rapid responses to emerging threats. This has been especially important as we currently navigate significant disruptions to several key drug markets. Anyone can make a report through the reporting form and mailbox.
Summary
A summary of key trends is shown below. Intelligence reports to RADAR can be filtered by drug type and region on the dashboard (external website).
Please note, many of these reports have not been confirmed by toxicology and should be considered anecdotal.
Trends by primary drug type
Quarterly dates are shown on the chart below. In the latest period (QR10; 5 October 2024 to 4 January 2025):
- The majority of submissions report polydrug use – the use of more than one substance at a time.
- Most concerns were related to adverse effects (seizures, wounds and confusion), overdose (collapse, unconsciousness) and death.
- The most common primary drugs or drug types reported were heroin and benzodiazepines.
- Heroin was the most commonly reported drug of concern, accounting for 19% of drugs reported. This was stable compared to the previous quarter, but reports have increased throughout the time series, from 5% in QR1.
- Benzodiazepines (benzos) accounted for 16% of all drugs reported. Between QR1 and QR5, benzos accounted for 34% of drugs reported, before decreasing to an average of 20% between QR6 and QR8 and increasing in QR9 (26%).
- Synthetic opioids (nitazene/fentanyl-type drugs) accounted for 13% of drugs reported, similar to the previous five quarters (average 11%). Nitazenes continue to be the most common novel synthetic opioid detected in toxicology but several submissions reported drugs sold as ‘fentanyl’.
- Cocaine accounted for 15% of drugs reported, similar to the 18% average between QR1 and QR8 and an increase from 8% in QR9. Reports of crack cocaine were more frequent than powder cocaine for the first time.
- The most common drugs reported in the ‘other’ category were ketamine, MDMA, pregabalin, alcohol and zopiclone.
- In the last quarter, RADAR received reports from all mainland NHS boards concerning changes to the heroin supply.
- These reports include adverse effects, overdoses and deaths. Reports also concern heroin having a different appearance (colour, texture, smell) than expected, with several noting the heroin turned green when prepared for injection.
- In the last quarter, several reports were received concerning benzo supply shortages. Reports were received from Tayside, Highland and Greater Glasgow and Clyde (GGC).
- Other reports varied, including changes in quality and toxicity, with some reporting lower quality supply, whilst others report suggested increase in adverse or unusual effects (commonly memory loss or ‘losing days’), and people experiencing reduced tolerance (e.g. taking less than normal but experiencing more of an effect).
- Multiple street benzo samples tested by WEDINOS from over the UK including Lothian, Tayside, GGC and Grampian have found paracetamol, sometimes on its own, or with bromazolam, lorazepam or etizolam.
In the last quarter, we received several reports from independent sources about people having seizures following drug consumption. These reports have been received from across Scotland.
Drugs reported during these incidents include cocaine, benzodiazepines, alcohol, ketamine, pregabalin, heroin and synthetic cannabinoids, with several incidents reporting polydrug use.
Seizures can result from drug intoxication (from taking drugs such as MDMA and cocaine) or withdrawal (from suddenly stopping drugs such as benzos and alcohol).
Signs of a seizure
- collapse
- stiff body
- sudden jerky or uncontrolled body movements
- loss of bowel or bladder control
Learn first aid for seizures
If someone is having a seizure:
- Prevent injury by clearing the area of objects that could cause harm.
- Protect their head using a blanket or cushion.
- Do not restrain them.
- Time how long the seizure lasts.
- After seizure ends, check to see if person is breathing normally. Help the person to rest on their side with their head tilted back.
- The person needs urgent medical attention if:
- it is their first seizure
- they are unresponsive for more than 10 minutes after the seizure
- the seizure lasts longer than five minutes
- they have repeated seizures
- they are not breathing normally
- they have hurt themselves
- drugs are suspected to be involved
- you are unsure as to the cause.
- Call 999 and ask for an ambulance:
- tell them your location and what’s happened
- be open about the substances taken.
Learn more about how to respond to an overdose:
WEDINOS
WEDINOS (external website) is a harm reduction project, providing an anonymous testing service, to show trends in substance use.
Between September and November 2024, 142 samples from Scotland were tested by WEDINOS. Seven samples contained no active components.
Among the 135 samples testing positive for a controlled drug:
- There were 235 detections of 135 individual substances.
- The average number of substances detected per sample was two, with the number of substances ranging from one to eight per sample.
- Over half did not test positive for the intended purchase.
The following controlled drugs were the most common:
- bromazolam: 15 (6% of detections, 11% of samples)
- diazepam: 14 (6% of detections, 10% of samples)
- cocaine: 12 (5% of detections, 9% of samples)
- 6-MAM: 11 (5% of detections, 8% of samples)
- heroin: 10 (4% of detections, 7% of samples)
Scottish Drugs Forum (SDF) drug trends
SDF are funded by the Scottish Government to develop regional Living Experience Engagement Groups - safe spaces for those with living experience to express their views and share information about drug trends and harms. These groups typically meet weekly and are facilitated by staff with lived experience from the SDF Living Experience Engagement Team and local partner agencies.
Several groups are operational or in development across Scotland. Regional group members have the opportunity to contribute to a national group, which engages with strategic bodies, stakeholders and policymakers, such as the Scottish Government's National Collaborative. While the groups operate independently, they can provide valuable input to local Lived Experience Panels or Alcohol and Drug Partnership subgroups through member representation.
Each group sets its meeting agenda, ensuring a safe space to discuss their needs, opinions and the issues affecting them. An important part of this is learning and sharing information about current trends and the related risks and harms. SDF publishes regular trend bulletins based on group insights. Read the latest report at Resources - Scottish Drugs Forum (external website).
Reporting drug harms
Please encourage people and services in your area to share information on trends, incidents and harms related to drugs, such as:
- adverse effects including overdose and wounds
- routes of administration
- new substances or patterns of use
- testing data.
The information in the regional breakdown can be used by local areas for their own drug trend surveillance.
Anyone can make a report by using our reporting form (external website) or by emailing phs.drugsradar@phs.scot.
Harm indicators
Redirect
Naloxone administration by Scottish Ambulance Service
The average weekly number of naloxone administration incidents decreased between September (61) and November 2024 (47). The total number of naloxone administration incidents (700) was 30% lower than the previous quarter (998). This was 24% lower than the same period in 2022 (917) and 34% lower than in 2023 (1,058).
Background
Naloxone is a medicine used to prevent fatal opioid overdoses. These data relate to the number of incidents in which naloxone was administered by Scottish Ambulance Service (SAS) clinicians.
While these data count multiple overdose patients at the same incident separately, multiple naloxone administrations to the same patient at the same incident are not counted separately.
The chart below shows the weekly number of SAS naloxone administration incidents in Scotland from 22 August 2022 to 24 November 2024.
An interactive version of this chart can be found in the RADAR dashboard (external website). The dashboard also allows users to download the data and filter by NHS board.
Summary
Historic trend
- The average weekly number of naloxone incidents was broadly stable, at 77 per week between August and November 2022. The average number of weekly incidents decreased to 66 per week in December 2022.
- During 2023, the normal seasonal pattern of lower numbers during winter months and higher numbers during summer months was observed, with an increasing trend in the average weekly number from January (67) to May 2023 (86).
- Between June and August 2023, incidents remained broadly stable at around 103 per week, after which there was a decreasing trend to January 2024.
- Between January and April 2024, the average number of weekly incidents fluctuated within a lower range of 47 to 86.
- Following a sharp increase in early May, the average number of weekly incidents remained stable at a higher level (90) between May and July 2024.
- During August 2024, a decreasing trend in the average weekly number of incidents was observed (76).
National update
For the most recent period (2 September to 24 November 2024):
- 700 SAS naloxone incidents were recorded, at an average of 58 per week. Average weekly numbers decreased between September (61) and November 2024 (47).
- The number of incidents was 30% lower than the previous 12-week period (10 June to 1 September 2024) when 998 incidents were recorded, at an average of 83 per week.
- The number of incidents was 24% lower than the same period in 2022 (917, weekly average 76) and 34% lower than in 2023 (1058, weekly average 88).
Local update
Comparing the most recent period (2 September to 24 November 2024) to the previous quarter, decreases in incidents were observed in all mainland NHS boards:
- NHS Lanarkshire (16%), NHS Lothian (21%), NHS Borders (25%), NHS Ayrshire and Arran (29%), NHS Greater Glasgow and Clyde (31%), NHS Grampian (35%), NHS Highland (35%), NHS Tayside (35%), NHS Forth Valley (36%), NHS Fife (44%) and NHS Dumfries and Galloway (53%).
To analyse these data further, please visit the RADAR dashboard (external website).
Additional information
PHS was provided with these data by SAS.
Scotland-level data for 1 January 2018 to 24 November 2024 are available on the RADAR dashboard (external website).
Information on the carriage of naloxone by Police Scotland officers can be found on Police Scotland’s website.
Information on take-home naloxone distribution can be found in the National Naloxone Programme Scotland Quarterly Monitoring Bulletin, published by PHS.
Scotland's Take-Home Naloxone Programme
The national Take-Home Naloxone Programme was launched by the Scottish Government in 2011 to prevent fatal opioid overdoses.
Naloxone is a medicine that can temporarily reverse the effects of an opioid overdose. It can be given to anyone who is non-responsive and displaying the signs of an overdose (such as unconsciousness, shallow breathing, snoring, blue lips, pale skin and pin-point pupils).
Anyone in Scotland can carry naloxone. It can be accessed through most local drug services or pharmacies, and it can also be delivered to your home through the charity Scottish Families Affected by Alcohol and Drugs (external website).
Naloxone is very easy to administer. You can learn more about administering naloxone in a free e-learning module 'Overdose Prevention, Intervention and Naloxone (external website)' created by the Scottish Drugs Forum.
Drug-related attendances at emergency departments
Between September and November 2024, the number of drug-related attendances at emergency departments (977) was 10% lower than the previous quarter (1,090). This was 14% lower than the same period in 2022 (1,130) and 16% lower than in 2023 (1,162).
Background
A drug-related emergency department (ED) attendance is an attendance for a drug intoxication or overdose, either alone or combined with alcohol intoxication.
The chart below shows the weekly number of drug-related ED attendances in Scotland between 29 August 2022 and 1 December 2024.
An interactive version of this chart can be found in the RADAR dashboard (external website). The dashboard also allows users to download the data and filter by NHS Board.
Summary
Historic trend
- The number of drug-related ED attendances per week was broadly stable between September 2022 until March 2023 (weekly average 84). Attendances generally increased between April and June 2023, with the highest weekly level in the series observed in June 2023 (144).
- From June 2023 to October 2024, despite variations in the number of attendances per week, an overall decreasing trend was observed, from an average of 106 in June 2023, to 91 in October 2023.
- From November 2023 to August 2024, the number of attendances has been broadly stable in the range of 60 to 100 attendances per week.
National update
For the most recent 13-week period (2 September to 1 December 2024):
- 977 emergency department attendances were recorded, at an average of 75 per week. This was 10% lower than the previous 13-week period (3 June to 1 September 2024, 1,090 attendances, weekly average 84).
- Attendances were 14% lower than the same period in 2022 (1,130 attendances, weekly average 87) and 16% lower than in 2023 (1,162 attendances, weekly average 89).
Local update
Comparing the most recent period (2 September to 1 December 2024) to the previous quarter, the key changes observed across mainland NHS boards were:
- Attendances increased in six areas: NHS Forth Valley (8%), NHS Dumfries and Galloway (10%), NHS Borders (21%), NHS Highland (21%), NHS Grampian (35%) and NHS Ayrshire and Arran (75%).
- Attendances decreased in four areas: NHS Lanarkshire (16%), NHS Tayside (22%), NHS Lothian (23%) and NHS Fife (24%).
- Attendances were broadly stable in NHS Greater Glasgow and Clyde.
To analyse further, please visit the RADAR dashboard (external website).
Additional information
These data are taken from our Accident and Emergency Activity Data.
Due to the quality of the data available, it is not possible to accurately report total attendances for specific conditions using the national Accident and Emergency dataset. The diagnosis or reason for attendance can be recorded in a variety of ways, including in free text fields and not all NHS boards submit this information. The numbers presented in this report are based on an experimental definition of drug-related ED attendances and have not been subject to extensive quality assurance. Therefore, they are provisional and may be subject to change in future releases. Further details can be found in the metadata and the Accident and Emergency Activity Data.
Drug-related acute hospital admissions
Between July and September 2024, 2,071 drug-related hospital admissions were recorded, 8% lower than the previous quarter (2,253). Admissions were similar to the same period in 2022 (2,024) and 20% lower than in 2023 (2,577).
Background
The data used in these statistics relate to all inpatient and day-case admissions to general acute hospitals (excluding maternity, neonatal, geriatric long stay and admissions to psychiatric hospitals) where drug use was recorded as a diagnosis at some point during the patient’s hospital stay. Data are presented by date of admission.
The chart below shows the weekly number of drug-related admissions to Scotland’s general acute hospitals from 27 June 2022 to 29 September 2024. Data are taken from Scottish Morbidity Record (SMR) records held by Public Health Scotland (PHS). PHS expects to receive complete SMR data six weeks after the end of the month of discharge/clinic date. Therefore, the period presented here differs from our other harm indicators - this should be taken into consideration when interpreting trends. Data for the most recent quarter are provisional and may change in future publications. For further information, see the data management section on our website.
An interactive version of this chart can be found in the RADAR dashboard (external website). The dashboard also allows users to download the data and filter by NHS board.
A further chart showing the top five drug types associated with admissions is available on the RADAR dashboard (external website).
Summary
Historic trend
- Between July 2022 and March 2023, admissions remained broadly stable averaging 147 per week, with a seasonal decrease during December and January.
- Admissions then increased until July 2023 (averaging 203 per week), remaining relatively stable until September 2023, followed by a decrease in October 2023.
- Between October 2023 and June 2024, admissions were roughly stable averaging 167 admissions per week.
- Opioids were the most common drug category recorded. The percentage of admissions where opioids were recorded remained relatively stable until the end of 2023 (average 47% between July 2022 and December 2023), before following a decreasing trend to 40% in June 2024.
- The second most common drug type was cocaine, with admissions gradually increasing from 17% in July to September 2022, to 20% in April to June 2024.
National update
For the most recent period (1 July to 29 September 2024):
- 2,071 drug-related hospital admissions were recorded, at an average of 159 per week. This was 8% lower than the previous 13-week period (2,253, weekly average 173).
- The total number of admissions was similar to the same period in 2022 (2,024, weekly average 156) and 20% lower than in 2023 (2,577, weekly average 198).
- Opioids continued to be the most common drug type. These were recorded in an average of 41% of admissions per month, a decrease from 43% in the previous quarter. Admissions for cocaine increased to 23%, from 20% in the previous quarter.
Local update
Comparing the most recent period (1 July to 29 September 2024) to the previous quarter, the key changes observed across mainland NHS boards were:
- Admissions increased in three areas: NHS Borders (11%), NHS Forth Valley (11%) and NHS Greater Glasgow and Clyde (11%).
- Admissions decreased in three areas: NHS Lanarkshire (11%), NHS Dumfries and Galloway (22%) and NHS Highland (22%).
- Admissions were broadly stable in three areas: NHS Ayrshire and Arran, NHS Lothian and NHS Tayside.
Due to completeness levels for the most recent period being below 90%, NHS Fife and NHS Grampian have been excluded from this local update. The data can be found on our dashboard. Caution is advised when interpreting local trends for these boards and comparing to other areas.
To analyse further, please visit the RADAR dashboard (external website).
Additional information
These data have been extracted from our Scottish Morbidity Records (SMR01 acute).
The data presented on drug type are based on ICD-10 diagnostic codes and are not confirmed by toxicology analysis, therefore patterns in substance type should be interpreted with caution.
The most recent accredited official statistics on drug-related hospital care, includes a range of further information on drug types and patient demographics. For details, see our information on drug-related hospital statistics (DRHS). Please note, our DRHS dashboard presents data by date of discharge, so figures will differ to those shown above.
Suspected drug deaths
In the latest period (2 September to 24 November 2024), the total number of suspected drug deaths was 215, averaging 18 per week. The average weekly number of deaths decreased between September (21) and November 2024 (14). The total number of deaths was 10% lower than the previous quarter (238), 20% lower than the same period in 2022 (268) and 15% lower than in 2023 (254).
Background
A suspected drug death is a death where controlled drugs are suspected of being involved. Suspected drug death figures are based on reports, observations and initial enquiries from police officers attending scenes of death.
The details of these events are recorded by Police Scotland and shared with Public Health Scotland (PHS).
Following further investigation, these suspected drug deaths are either confirmed as a ‘drug-related death’ or determined ‘not to be a drug death’. This can take several months.
Suspected drug-death figures are used to provide a timely indication of trends and to detect any potential recent changes or clusters of harm to inform prevention activity. These figures are different to those published by the National Records of Scotland (NRS: external website) and do not provide a robust indication of the numbers of drug-related deaths occurring each year.
The chart below shows the weekly number of suspected drug deaths in Scotland from 22 August 2022 to 24 November 2024.
An interactive version of this chart can be found in the RADAR dashboard (external website). The dashboard also allows users to download the data.
Summary
Historic trend
- Between September 2022 and August 2024, the average weekly number of suspected drug deaths fluctuated considerably but generally remained within the range of 18 to 28 deaths per week.
Update
For the most recent complete months (1 September to 30 November 2024):
- There were 237 suspected drug deaths, 92 in September, 84 in October and 61 in November.
For the most recent 12-week period (2 September to 24 November 2024):
- There were 215 suspected drug deaths, 10% lower than in the previous 12-week period (238). This was 20% lower than the same period in 2022 (268) and 15% lower than in 2023 (254).
- The average weekly number of deaths decreased from September (21) to October (18) and decreased further in the first three weeks of November 2024 (14).
- An average of 18 deaths were recorded per week. This was 10% lower than in the previous period (20), 18% lower than in the same period in 2022 (22) and 14% lower than in 2023 (21).
To analyse these data further, please visit the RADAR dashboard (external website).
Additional information
Data on suspected drug deaths are provided by Police Scotland.
The Scottish Government produce a quarterly report (Suspected drug deaths in Scotland) that presents Police Scotland data on suspected drug deaths and describes the age, sex and geographical location of deaths in each quarter. The analysis in this RADAR release is provided for the purpose of real-time detection and prevention of harms and is not comparable with the Scottish Government publication.
The information above is management information and not subject to the same validation and quality assurance as accredited official statistics. The data provided in this release should not be viewed as indicative of the annual deaths reported by NRS.
Accredited official statistics on drug-related deaths are published annually by the NRS during the summer and provide information broken down by age, sex, substance implicated and geographical area. The latest NRS publication (external website) reported that there were 1,172 drug-related deaths in Scotland in 2023. This was a 12% increase compared to 2022 (1,051).
Detailed information on drug-related deaths is presented in the National Drug-Related Deaths Database, which is published by PHS every two years. The latest PHS drug-related deaths report describes deaths that registered in 2019 and 2020, with trend data from 2012.
Toxicology indicators
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Emergency department toxicology: ASSIST
Between September and November 2024, the ‘A Surveillance Study of Illicit Substance Toxicity’ (ASSIST) emergency department project made 212 detections of 39 different illicit drugs, in samples from 48 patients. The most commonly detected drug category was depressants (58% of detections), followed by opioids (20%). The most commonly detected individual drug was cocaine (14%), followed by desmethyldiazepam (12%) and temazepam (10%).
Background
The ASSIST study is conducted by the emergency department (ED) at the Queen Elizabeth University Hospital (QEUH) in NHS Greater Glasgow and Clyde (GGC). This project has been funded by the Scottish Government since August 2022.
The aim of the study is to monitor drug trends and associated clinical features through the use of prospective surveillance of ED attendances due to acute illicit drug toxicity. For the most unwell patients, the study performs full toxicological analysis through the biorepository-approved surplus sampling.
The study allows drug profiling and the identification of emerging drugs or changing trends to inform appropriate harm reduction measures and public health responses.
Data collection
The study collects anonymised data through the analysis of standard-of-care clinical data and surplus serum sample toxicology testing for patients attending QEUH ED due to illicit drug toxicity. Surplus serum samples are leftover blood samples, which were taken as part of usual care.
Each ED attendance is counted once in these data. If the same person presented more than once, each attendance would be a separate data point.
Drug detections presented here are of ‘illicit drugs’ only and were not prescribed to the individual.
Illicit drug definition
The use of the term ‘illicit drug’ encompasses any substance that is controlled. It excludes:
- legal substances, such as alcohol, nicotine, caffeine and paracetamol
- medications recently prescribed to the individual (g. if methadone is detected for an individual prescribed methadone, it will not be included)
- drugs administered to the individual as part of treatment (by ambulance staff or in hospital)
Toxicology analysis of surplus serum samples
- Detections presented are for the substance only. If a metabolite (compound produced when a drug breaks down in the body) is detected, it will be presented as the substance only.
- If the metabolite and substance are detected, it will also be presented as the substance only.
- However, if a drug and a metabolite are both detected and the metabolite could also be a drug, the metabolite is included as it is not possible to say which has been used, if not both.
- Data from the study are presented in quarters, based on the date of ED presentation, and are provided in the table below.
Quarter | Dates |
---|---|
Quarter 1 (Q1) | 17/08/2022 to 16/11/2022 |
Quarter 2 (Q2) | 17/11/2022 to 16/02/2023 |
Quarter 3 (Q3) | 17/02/2023 to 16/05/2023 |
Quarter 4 (Q4) | 17/05/2023 to 16/08/2023 |
Quarter 5 (Q5) | 17/08/2023 to 16/11/2023 |
Quarter 6 (Q6) | 17/11/2023 to 16/02/2024 |
Quarter 7 (Q7) | 17/02/2024 to 16/05/2024 |
Quarter 8 (Q8) | 17/05/2024 to 16/08/2024 |
Quarter 9 (Q9) | 23/09/2024 to 16/11/2024* |
*Due to a temporary pause in the study while funding was being confirmed, the start of Q9 was delayed. Recruitment was suspended from 17 August to 22 September 2024. Consequently, Q9 consists of only 55 study days, compared to the usual 90-92 days, resulting in fewer samples being tested. This discrepancy should be considered when interpreting the data and trends for the most recent quarter.
Results
The first chart shows the most common drug categories detected in toxicology analysis of surplus serum samples between 17 August 2022 and 16 November 2024 (Q1 to Q9).
The results are shown as the total number of detections. They are broken down by the top five drug categories and presented by study quarter.
Summary
Historic trend
Between 17 August 2022 and 16 August 2024:
- The most commonly detected drug type was depressants, making up 62% of all detections, followed by opioids (16%). The most commonly detected individual drug was cocaine (13%).
- 73% of attendances were male and 27% were female.
- 76% of attendances were aged 44 and under. The most common age category was 35 to 44 years (29%), followed by 25 to 34 (27%) and 16 to 24 (19%).
- The most common outcomes were discharged to home (39%), ward (30%) and police custody (11%).
Update
For the most recent period (23 September to 16 November 2024):
- 155 individual ED attendances related to illicit drug use were identified.
- 48 surplus serum samples were analysed for toxicology (as they were categorised as having a higher clinical severity of toxicity as per research inclusion criteria).
Drug type and category
Among the 48 samples analysed:
- There were 212 detections of 39 individual substances (found through the biological detection of the drug or its metabolite).
- The average number of drugs detected per sample was six.
Of the 215 detections, the following drugs were the most common:
- cocaine: 29 (14% of detections, 60% of samples)
- desmethyldiazepam: 25 (12% of detections, 52% of samples)
- temazepam: 22 (10% of detections, 46% of samples)
- oxazepam: 16 (8% of detections, 33% of samples)
- diazepam: 12 (5% of detections, 23% of samples)
- morphine: 11 (5% of detections, 23% of samples)
- bromazolam: 10 (5% of detections, 21% of samples)
- codeine: 9 (4% of detections, 19% of samples)
- etizolam: 9 (4% of detections, 19% of samples)
- pregabalin: 8 (4% of detections, 17% of samples)
- clonazolam: 6 (3% of detections, 13% of samples)
Please note: desmethyldiazepam, temazepam and oxazepam are all benzodiazepine drugs but can also be found as a metabolite of diazepam and other benzodiazepines.
The chart below shows the most common depressant drug detected in toxicology analysis of surplus serum samples between 17 August 2022 and 16 November 2024 (Q1 to Q9). The percentages are of all detections.
Depressants were the most common drug category, making up 58% of detections (125).
- Benzodiazepines were detected 113 times (53% of all detections):
- In total, 14 different types of benzodiazepines were detected, including desmethyldiazepam (12%), temazepam (10%), oxazepam (7%), diazepam (6%) and etizolam (4%).
- Bromazolam made up 5% of all detections, a decrease from 8% in Q8 and the lowest levels observed since Q1.
- Gidazepam/desalkylgidazepam made up 4% of detections and clonazolam made up 3%, similar to Q8.
- Gabapentinoids were detected 10 times (5% of all detections, similar to Q8). Pregabalin was the most common gabapentinoid detected.
- There were less than five detections of xylazine, an increase from no detections in the last quarter.
The chart below provides an indication of specific opioids detected in toxicology analysis of surplus serum samples between 17 August 2022 and 16 November 2024 (Q1 to Q9). The percentages are of all detections.
Opioids were the second most common drug category, making up 21% of detections (44).
- There were 11 detections of heroin/morphine (5%; stable compared to Q8) and 9 of codeine (4%; from 3% in Q8).
- There were less than five detections of nitazenes, similar to the previous quarter. N-desethyl etonitazene was detected for the first time in the study.
Stimulants were the third most common drug category, making up 15% of detections (32).
- The most common stimulant was cocaine, making up 14% of detections (29); stable compared to Q8.
Further findings
Complete clinical data were available for 155 attendances for the most recent period (23 September to 16 November 2024):
- 72% of attendees were male (112) and 28% were female (43).
- 71% of attendances were aged 44 and under. The most common age category was 25 to 34 years (28%, 43 attendees), 26% (40) were aged 35 to 44 years and 17% (27) were aged 16 to 24.
- 29% of attendees were aged 45 years and over, with 17% (26) aged 45 to 54 and 12% (19) aged 55 years or older.
ED outcome records show:
- 72 patients (46%) were discharged home
- 35 patients (23%) were admitted to a ward
- 16 patients (10%) were taken into police custody
- 11 patients (7%) self-discharged
- 19 were recorded as ‘unknown’ or ‘other’
- less than five patients were admitted to an intensive care unit, high-dependency unit, critical care unit or died.
Clinical severity outcome (after 28 days) recorded:
- 139 (90%) patients were discharged following the attendance
- six patients either died or remained an inpatient following the attendance.
Additional information
Public Health Scotland (PHS) was provided with these data by QEUH, NHS GGC.
The ASSIST trial is registered with Clinical Trials UK (ID: NCT05329142).
Ethical approval has been granted by the West of Scotland Research Ethics Service (IRAS ref: 313616, REC ref: 22/WS/0047) and surplus sampling methodology through Biorepository Ethics (ref: 22/WS/0020).
The West of Scotland Safe Haven research database hosts the electronic clinical data under IRAS ref: 321198 or REC ref: 22/WS/0163.
This study is sponsored by NHS GGC Research and Innovation and is funded by the Scottish Government. A temporary pause in funding led to suspension of recruitment to the study from 17 August to 22 September 2024.
The testing has been carried out by the LGC group (external website). LGC analyse pseudonymised samples using mass spectrometry and screen against a database of over 3,500 analytes. This testing can detect drugs and metabolites, but this analysis does not imply that specific drugs were implicated in harms.
Further information on the study can be found at Clinical Trials (external website).
Post-mortem toxicology testing for controlled substances
In Q3 of 2024, the most common drug types detected in post-mortem toxicology were opioids (73%) and benzodiazepines (54%). Cocaine continued to be the most commonly detected drug (34%), followed by heroin/morphine (31%), diazepam (23%) and methadone (23%).
Background
All sudden or unexpected deaths in Scotland are subject to investigation by the Crown Office and Procurator Fiscal Service (COPFS) to determine the cause of death and the need for criminal proceedings. In order to inform these decisions, the COPFS commissions post-mortem toxicology and pathology services.
This analysis is based on data from toxicology testing conducted at post-mortem for sudden and unexplained deaths, or where there was suspicion of involvement of controlled drugs.
Post-mortem toxicology testing is carried out by two services in Scotland:
- The Scottish Police Authority Forensic Services (SPA FS) covers deaths occurring in the west, east and parts of the north of Scotland.
- The Department of Clinical Biochemistry at NHS Grampian covers deaths in the far north and north-east of Scotland.
This report presents data on deaths covering the whole of Scotland, which became available from January 2022. It includes new data for the period from 1 July to 30 September 2024, representing Q3 of 2024.
The range of substances routinely analysed is extensive and includes the detection of alcohol, prescribed medicines and controlled drugs. The data within this report will develop further as other new or emerging drugs are added to toxicology screening.
The charts below show the prevalence of controlled substances detected in deaths which were subject to post-mortem toxicology screening. Drug detections were assigned to specific time periods based on the calendar year quarter of death. Throughout the series, the sum of the percentages for each quarter exceeds 100%, due to the widespread detection of multiple substances in deaths.
The first chart provides an indication of controlled drugs detected at post-mortem, in deaths occurring between 1 January 2022 and 30 September 2024.
The following charts provide an indication of specific opioids and benzodiazepines detected at post-mortem, in deaths occurring between 1 January 2022 and 30 September 2024.
Summary
- The most commonly detected drug types throughout the series were opioids, followed by benzodiazepines. Both have remained relatively stable averaging 71% and 56% respectively between Q1 of 2022 to Q3 of 2024.
- The most commonly detected individual drug was cocaine (averaging 36% between Q2 of 2023 and Q3 of 2024). Before Q2 of 2023, the most common individual drug was heroin/morphine.
- Multiple controlled drugs were detected in 540 of 574 deaths (94%) in Q3 of 2024. This was similar to previous quarters.
- The following drugs/drug types were the most commonly detected in deaths in Q3 of 2024:
- opioids: 418 (73%)
- benzodiazepines: 308 (54%)
- cocaine: 197 (34%)
- heroin/morphine: 180 (31%)
- gabapentin or pregabalin: 165 (29%)
- diazepam: 132 (23%)
- methadone: 132 (23%)
Stimulants
- For the sixth quarter in a row, the most commonly detected drug was cocaine (34% in Q3 of 2024).
- The percentage of deaths where cocaine was detected was relatively stable until Q1 of 2023 (averaging 29%). Detections increased in Q2 of 2023 to 36% and have remained relatively stable (averaging 36%) since.
Opioids
- The percentage of deaths where opioids were detected has remained relatively stable throughout the time series, averaging 71%.
- Heroin/morphine detections have been gradually decreasing, from 36% in Q1 of 2022 to 31% in Q3 of 2024.
- Methadone was detected in 32% of deaths in Q1 of 2022 and has since generally fluctuated within a range of 23% to 29% of deaths.
- Buprenorphine detections remained low and stable throughout the series, detected in an average of 6% of deaths.
- Detections of fentanyl/alfentanil have gradually increased, from 1% in Q1 of 2022 to 8% in Q3 of 2024. Fentanyl-type opioids are commonly used as medicines for pain relief.
- Nitazene-type opioids were first detected in Q1 of 2022 and have increased slightly, being detected in 4% of deaths (25) in Q3 of 2024.
- Two nitazenes were detected in six of the 25 deaths.
- In Q3 of 2024, protonitazene was the most common nitazene detected, overtaking metonitazene which had been the most prevalent since Q2 of 2023.
- Nitazenes have been detected in a total of 105 deaths (to 30 September 2024).
Depressants
- Benzodiazepines have remained broadly stable throughout the series, detected in an average of 56% of deaths.
- Diazepam has been the most commonly detected benzodiazepine since Q2 of 2022, with detections fluctuating between 23% and 35%.
- Detections of bromazolam increased sharply between Q3 of 2022 and Q3 of 2023, replacing etizolam as the most commonly detected ‘street benzo’ from Q1 of 2023 onwards. Since Q3 of 2023, detections of bromazolam have been decreasing, detected in 14% of deaths in Q3 of 2024.
- Etizolam was the most common benzodiazepine detected in Q1 of 2022. Since then, detections have followed a decreasing trend to 7% of deaths in Q3 of 2023 and have remained stable (averaging 7%) since.
- Clonazolam detections remained low and stable throughout the series, detected in an average of 1% of deaths.
- Gidazepam/desalkylgidazepam was first detected in Q4 of 2022 and has gradually increased, being detected in 2% of deaths (14) in Q3 of 2024.
- The percentage of deaths involving gabapentin or pregabalin has been relatively stable throughout the time series, averaging 30%.
- Xylazine (detected for the first time in Q3 of 2023) detections remained stable compared to the previous quarter at 1% of deaths (4). Xylazine has been detected in a total of 27 deaths (to 30 September 2024).
More detailed descriptions of historical changes can be found within our previous reports.
Additional information
PHS was provided with post-mortem toxicology testing data for deaths occurring in the west, east and parts of the north of Scotland by Forensic Medicine and Science at the University of Glasgow and SPA FS.
In late 2022, post-mortem toxicology services for the west, east and parts of the north of Scotland were transferred from the University of Glasgow to the Scottish Police Authority Forensic Services (SPA FS). During the period of transition, tests were completed by other laboratory testing sites in the UK. Although testing has now been moved to SPA FS, these testing sites continued to provide support in 2023 and data from both SPA FS and outsourced sites have been included in this report.
Data on deaths occurring in the far north and north-east of Scotland, was supplied by the Department of Clinical Biochemistry at NHS Grampian.
The total number of deaths testing positive for controlled substances, for each calendar year and quarter, are provided in table 1.
Calendar year | Q1 | Q2 | Q3 | Q4 |
---|---|---|---|---|
2022 | 566 | 631 | 536 | 710 |
2023 | 710 | 680 | 619 | 663 |
2024 | 691 | 599 | 574 |
A number of drugs were detected for the first time when screening was expanded or testing was outsourced to other laboratories. Table 2 provides information on the initial screening period new or emerging substances, from which limited testing data was available, and also when testing is considered to have become routine across Scotland.
Substance | Initial testing (limited data available) | Routine testing (data across Scotland) |
---|---|---|
Nitazenes | Q1 of 2022 | Q1 of 2023 |
Bromazolam | Q1 of 2022 | Q1 of 2023 |
Deschloroetizolam | Q1 of 2023 | Q1 of 2023 |
Xylazine | Q2 of 2023 | - |
'-' denotes information is not available.
Note that these drugs may have been present before this time but were not being tested for, as they have only recently emerged in drug markets. These data will develop further as new or emerging drugs are added to routine toxicology screening by the SPA FS and NHS Grampian.
Detailed interpretation of the levels of drugs found present, drug interactions, co-morbidities, or other factors relating to death, are outside the scope of this analysis. This analysis does not imply that specific drugs were implicated in deaths nor that deaths were classified as ‘drug-related’, and it does not include consideration of wider causes of death.
It should be noted that increases observed in specific substances within this report may be due to differences in toxicology test approaches (e.g. detection of concentration levels of a particular drug) between outsourced laboratories and previous screening. This may result in increases in substance detection. Further data will be required and monitored to determine the impact of any differences in toxicology screening across laboratories.
Additionally, it is important to note that small numbers of detections for specific substances may result in large percentage differences between quarters. Where it is felt that data should be interpreted with caution due to small numbers, the number of detections has also been provided for context.
As some of the data received from other laboratory testing sites did not include date of death, other date variables have been used as a proxy to improve data completeness and enable the inclusion of these deaths within this report. Two separate date variables have been used to approximate date of death information, where this information was unavailable:
- Date of the case being received or sent to other labs for toxicology testing.
- Date of toxicology test being completed.
Similarly, as date of death was unavailable for those tests conducted by the Department of Clinical Biochemistry at NHS Grampian, the date when the case was received from the Crown Office and Procurator Fiscal Service has been used instead.
These dates listed above have been used in the analysis as they are considered to provide a close approximation to the month and year of death. It is anticipated that missing information on date of death will be improved over time, as further information becomes available.
Drug seizures in Scottish prisons
Synthetic cannabinoids continue to be the most prevalent drug type detected in the Scottish Prisons Non-Judicial Drug Monitoring Project.
Background
The Leverhulme Research Centre for Forensic Science (LRCFS) is currently undertaking research with the Scottish Prison Service (SPS). The Scottish Prisons Non-Judicial Drug Monitoring Project tests non-attributable seizures (drugs that cannot be linked to a person or source) made across the Scottish prison estate in order to understand the changing characteristics of synthetic drugs, including synthetic cannabinoids, often referred to as ‘spice’.
The chart shows the number and type of non-attributable samples seized in Scottish prisons between 1 June 2021 and 31 July 2024.
The chart below shows the five most detected drug types from seizures in Scottish prisons between 1 June 2021 and 30 June 2024. This is based on the percentage of samples tested each month and uses 3-month moving average figures.
Summary
Historic trend
- The number of seizures analysed varied widely between June and December 2021, ranging from a low of 23 in June, to a high of 134 in September. In 2022, the monthly average remained relatively stable at 35. During 2023, numbers varied, ranging from a high of 60 in January to a low of 18 in December, with a monthly average of 43.
- Sample-type data were highly variable over time. Changes were observed in detections during 2022 and 2023:
- Paper and card detections decreased, from a monthly average of 72% in 2021, to 23% in 2022, to 6% in 2023. This is due to changes to prison rules that mean prisoners now receive photocopied correspondence rather than original items.
- There were low numbers of e-cigarette samples until late 2022. Detections increased from a monthly average of 1% in 2021, to 18% in 2022, to 28% in 2023.
- Powder samples were low throughout 2021 (monthly average 5%), before increasing and remaining relatively stable at approximately 20% per month throughout 2022, increasing to 29% in 2023.
- The transition from synthetic cannabinoids in paper form to e-cigarette, powder or wax forms has introduced new methods of consumption. This variation in form and purity can make it challenging to achieve consistent dosing, potentially leading to unpredictable effects.
- Drug-type seizure data were highly variable over time, so the following narrative is based on 3-month moving averages:
- Synthetic cannabinoids were the most common substances detected. In 2021, seizures testing positive for synthetic cannabinoids averaged 43% per month. Percentages varied throughout 2022 and 2023, averaging 33% per month in 2022 and 35% in 2023, with higher percentages observed during the summer months.
- Benzodiazepine seizures fluctuated throughout 2021 (monthly average 39%), before decreasing and remaining relatively stable in 2022 (monthly average 26%). In 2023, detections followed an uneven decreasing trend (monthly average 13%).
- Opioid seizures increased in late 2023 (average 33% in December), however sample numbers were small.
Update
Data has been provided from January to July 2024 but may be subject to change, so caution is advised when interpreting. We anticipate complete data will be available for the next release in April 2025.
PHS has received data for 123 samples seized between 1 January and 31 July 2024:
- The average number of samples per month varied widely – from four in May 2024 to 44 in April 2024.
- Synthetic cannabinoids were the most prevalent drug type. They were detected in 52 samples (42%), with 43 samples (35%) containing two cannabinoids.
- MDMB-4en-PINACA was the most common synthetic cannabinoid (41 detections), followed by MDMB-INACA (35).
- 18 samples (15%) contained a benzodiazepine: nine contained bromazolam, five etizolam, three diazepam and one alprazolam.
- 63 samples (51%) were powder, 22 were tablets (18%) and 20 were e-cigarettes (16%).
Further information
In September 2023, this drug analysis project detected hexahydrocannabinol (HHC), for the first time in prisons in Scotland. HHC is a semi-synthetic cannabinoid, a compound that is derived from naturally occurring cannabinoids but is modified to enhance or alter the effects.
- HHC has now been detected ten times between September 2023 and July 2024.
Additional information
PHS was provided with these data by the SPS and the LRCFS.
The Scottish Prisons Non-Judicial Drug Monitoring Project is a collaboration between the SPS and the LRCFS at the University of Dundee.
An initial pilot project ran between September 2018 and January 2021. The project has been funded directly by the SPS since February 2021.
Service indicators
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Specialist drug treatment referrals
Between August and November 2024, the average weekly number of referrals to specialist drug treatment services was relatively stable. A total of 6,578 referrals were recorded, similar to the previous quarter (6,605). This was 7% higher than the same period in 2022 (6,166) and 5% lower than in 2023 (6,910).
Background
Specialist drug treatment referrals occur when a person comes into contact with services designed to support their recovery from problematic drug use.
Figures shown are for referrals relating to either drug use or co-dependency (people seeking help for both drug and alcohol use). Figures include new referrals for treatment and referrals between services.
The chart below shows the weekly number of referrals to drug treatment services in Scotland between 22 August 2022 and 17 November 2024.
An interactive version of this chart can be found in the RADAR dashboard (external website). The dashboard also allows users to download the data and filter by NHS board.
Summary
Historic trend
- From September to November 2022, the weekly average number of referrals was 473.
- Following the seasonal reduction in December 2022, referrals returned to a weekly average of 534 per week in January 2023.
- Though there was considerable variation over time, a broadly stable trend was evident in 2023 and 2024, with average referrals ranging between 466 and 572 per week between January 2023 and May 2024.
- This was followed by a slight decrease and a period with less variation, with the average ranging from 481 to 552 from May to August 2024.
National update
For the most recent 13-week period (19 August to 17 November 2024):
- The weekly number of referrals ranged from 426 to 594 per week.
- 6,578 specialist drug treatment referrals were recorded, at an average of 506 per week, similar to the previous quarter (20 May to 18 August 2024) when 6,605 referrals were recorded, at an average of 508 per week.
- The number of referrals was 7% higher than the same period in 2022 (6,166) and 5% lower than in 2023 (6,910).
Local update
Comparing the most recent period (19 August to 17 November 2024) to the previous quarter, the key changes observed across mainland NHS boards were:
- Referrals increased in two areas: NHS Highland (5%) and NHS Fife (25%).
- Referrals decreased in four areas: NHS Lanarkshire (5%), NHS Forth Valley (6%), NHS Grampian (8%) and NHS Dumfries and Galloway (19%).
- Referrals were broadly stable in five areas: NHS Ayrshire and Arran, NHS Borders, NHS Greater Glasgow and Clyde, NHS Lothian and NHS Tayside.
To analyse these data further, please visit the RADAR dashboard (external website).
Additional information
These data are taken from the Drug and Alcohol Information System (DAISy) and its predecessor, the Drug and Alcohol Treatment Waiting Times (DATWT) database.
DAISy is a dynamic source of data, which means the information above is a snapshot of the data that are on the system at the time of extraction. As such, data for previous quarters may not be the same as that in previous publications for the same period. Similarly, data for the most recent quarter are provisional and may change in future publications.
PHS publishes further information on waiting times for people accessing specialist drug and alcohol treatment services. The latest data can be viewed in our National drug and alcohol treatment waiting times report which also includes a new interactive drug and alcohol treatment waiting times dashboard (external website).
PHS has published a report (external website) summarising the responses to the recent customer survey on drug and alcohol treatment waiting times outputs. PHS’s proposal to discontinue production of the report element of the publication was broadly supported by respondents. The report also provides details of planned publication developments and timescales.
For more information on initial assessments for specialist drug and alcohol treatment services in Scotland, please see: Drug and Alcohol Information System (DAISy): Overview of initial assessments for specialist drug and alcohol treatment 2023/24.
For details of drug treatment services in your area, visit the Scottish Drug Services Directory (external website).
The Medication Assisted Treatment (MAT) standards (external website) is an improvement programme to strengthen access, choice and support within the drug treatment system in Scotland.
Opioid substitution therapy
From July to September 2024, the average number of opioid substitution therapy (OST) doses supplied per month was similar to the previous quarter, 7% lower than the same period in 2022, and similar to 2023. The average monthly number of methadone doses supplied continued to decrease while the number of injectable buprenorphine doses increased over time.
Background
The data used in these statistics relate to the number of average daily quantity (ADQ) doses for OST drugs dispensed in the community in Scotland. OST drugs include methadone, oral buprenorphine and injectable buprenorphine. Methadone and oral buprenorphine are usually taken once every day. Injectable buprenorphine is long-acting and is administered once every week or month (depending on the formulation).
The chart below uses 3-month moving average figures to show the average total monthly number of ADQ doses supplied for OST medications in the community, between 1 July 2022 and 30 September 2024.
The chart below shows trends in the monthly number of ADQ doses for specific OST medications dispensed in the community between 1 July 2022 and 30 September 2024.
Summary
Historic trend
- There was a gradual decrease in the average monthly total number of OST doses supplied. This was due to the decrease in the average monthly number of methadone doses supplied, which reduced by 16%, from 564,800 between July and September 2022, to 475,400 between April and June 2024.
- The average total number of injectable buprenorphine doses supplied has increased steadily since it was first licensed for use in Scotland in early 2020. The average monthly number of doses supplied increased steadily, from 71,500 between July and September 2022, to 126,100 between April and June 2024. Dispensing of injectable buprenorphine has been more common than oral buprenorphine since August 2023.
- The average monthly number of oral buprenorphine doses supplied remained broadly stable between July and September 2022 (118,300) and April and June 2024 (114,100).
Update
For the most recent period (1 July to 30 September 2024):
- The average total monthly number of OST doses supplied was approximately 702,100. This was similar to the previous quarter (April to June 2024; 715,500 doses), 7% lower than the same period in 2022 and similar to 2023.
- The average monthly number of methadone doses supplied was approximately 456,700. This was similar to the previous quarter, 19% lower than the same period in 2022 and 10% lower than in 2023.
- The average monthly number of injectable buprenorphine doses supplied was approximately 132,300. This was slighter higher (5%) compared to the previous quarter, 85% higher than the same period in 2022 and 16% higher than in 2023.
- The average monthly number of oral buprenorphine doses supplied was approximately 113,100. This was similar to the previous quarter and the same periods in 2022 and 2023.
Additional information
These data have been extracted from the Prescribing Information System (PIS) (external website) and the Hospital Medicines Utilisation Data Manual (HMUD) (external website).
The data shown on methadone and oral buprenorphine, and the majority of injectable buprenorphine data, relate to prescriptions dispensed to individuals from a community pharmacy in Scotland, where a request for reimbursement of costs was processed. The time period reflects the month for which reimbursement was claimed. This is regarded as the most comprehensive and reliable way of reporting community prescribing data. There can be a lag of approximately three months from a prescription being written to reimbursement data becoming available.
As a consequence of the direct administration of injectable buprenorphine within clinics, some NHS boards do not request the reimbursement of costs for all of the OST treatments they provide. Data for approximately 28% of injectable buprenorphine doses supplied in Scotland are held in the HMUD and have been combined with the community prescribing data to provide a comprehensive account of OST supply over time.
To analyse information on methadone and oral buprenorphine dispensing by NHS board, visit the RADAR dashboard (external website).
What is average daily quantity (ADQ)?
When comparing use between medicines and over time, it is common to use World Health Organization (WHO) defined daily doses (DDDs). The DDD is defined as the usual average daily maintenance dose used in adults for the main therapeutic use of the medicine.
The WHO DDD is a global average and may not be representative of the doses used in clinical practice at a more local level. This is the case in Scotland, where the WHO DDD of 25 milligrams (mg) daily for methadone is between one-half and one-third of the normal maintenance dose used.
We have therefore replaced DDDs with ADQs, which are more representative of the daily maintenance doses used within Scotland. These values have been developed through a combination of prescription analyses and by consultation with the Specialist Pharmacists in Substance Management group. The ADQs agreed are:
- methadone (oral): 65 mg
- buprenorphine (oral): 13 mg
- buprenorphine (injection): 3.4 mg
Glossary
For detailed definitions on the terms used above, visit the RADAR dashboard (external website).
Injecting equipment provision
Between July and September 2024, the average weekly number of injecting equipment provision (IEP) transactions and the number of needles and syringes, remained stable compared to the previous quarter. The number of transactions was similar to the same period in 2022 and 6% lower than in 2023. The number of needles and syringes distributed was 6% lower than the same period in 2022 and 7% lower than in 2023.
Background
IEP is a form of harm reduction that helps to reduce the transmission of blood-borne viruses among people who inject drugs. These data relate to the number of needle and syringe transactions at IEP sites and the total number of needles and syringes distributed.
Information on the ratio of needles and syringes per transaction is also presented. This provides the number of needles and syringes distributed per visit which can be an indication of the number of injecting episodes.
The chart below shows the weekly number of IEP transactions from 27 June 2022 to 29 September 2024.
An interactive version of this chart can be found in the RADAR dashboard (external website). The dashboard also allows users to download the data and filter by NHS board.
Further charts showing the weekly number of needles and syringes distributed, and the ratio of needles and syringes per transaction, are available on the RADAR dashboard (external website).
Summary
Historic trend
- The average weekly number of transactions (approximately 2,900) remained broadly stable from July 2022 to February 2024, with seasonal fluctuations in December and January and again in March and April each year. Transactions increased following April 2024 and remained stable to June (approximately 2,850).
- The average weekly number of needles and syringes distributed (approximately 41,250) remained broadly stable between July 2022 to February 2024, with seasonal fluctuations in December and January and again in March and April each year. Following April 2024, the number of needles and syringes increased and remained stable to June (approximately 39,750).
- The ratio of needles and syringes distributed between July 2022 and June 2024 was broadly stable, generally between 13 and 16 needles and syringes per transaction.
National update
For the most recent period (1 July to 29 September 2024):
IEP transactions
- 36,950 transactions were recorded, at an average of 2,842 per week.
- This was similar to the previous quarter (1 April to 30 June 2024) when a total of 36,112 transactions were recorded (weekly average 2,778).
- The number of transactions was similar to the same period in 2022 (38,644, weekly average 2,973) and 6% lower than in 2023 (39,376, weekly average 3,029).
Needles and syringes distributed
- 514,795 needles and syringes were distributed, at an average of 39,600 per week.
- This was similar to the previous quarter when a total of 506,850 needles and syringes were distributed, at an average of 38,988 per week.
- The number of needles and syringes distributed was 6% lower than the same period in 2022 (548,969, weekly average 42,228) and 7% lower than in 2023 (551,469, weekly average 42,421).
Ratio of needles and syringes distributed
- There was a weekly average of 13.9 needles and syringes distributed per transaction.
- This was similar to the previous quarter (14.0) and similar to the same period in 2022 (14.2) and 2023 (14.0).
Local update
Comparing the ratio of needles and syringes distributed in the most recent period (1 July to 29 September 2024) to the previous quarter, the key changes observed across mainland NHS boards were:
- The ratio increased in three areas: NHS Tayside (7%; ratio 16.7), NHS Dumfries and Galloway (9%; ratio 7.2) and NHS Borders (17%; ratio 17.3).
- The ratio decreased in two areas: NHS Fife (6%; ratio 12.8) and NHS Lanarkshire (18%; ratio 11.0).
- The ratio was stable in five areas: NHS Greater Glasgow and Clyde (9.9), NHS Ayrshire and Arran (15.5), NHS Forth Valley (16.6), NHS Lothian (23.7) and NHS Grampian (24.5)
To analyse these data further, please visit the RADAR dashboard (external website).
Additional information
These data are taken from the Needle Exchange Online 360 database (neo360).
The 11 mainland NHS boards use neo360 routinely, but due to missing data for part of the period presented, NHS Highland is excluded from the transaction and needle and syringe data and the ratio figures.
For details of injecting equipment providers in your area, visit the Scottish Needle Exchange Directory (external website).
Contact
General enquiries
If you have an enquiry relating to this publication, please email:
- Nicole Jarvie | Principal Information Analyst | phs.drugsteam@phs.scot
- Vicki Craik | Public Health Intelligence Adviser | phs.drugsradar@phs.scot
Reporting a drug harm
To make a report to RADAR and share information such as trends, incidents and harms related to drugs you can either:
Media enquiries
If you have a media enquiry relating to this publication, please contact the Communications and Engagement team.
Requesting other formats and reporting issues
If you require publications or documents in other formats, please email phs.otherformats@phs.scot.
To report any issues with a publication, please email phs.generalpublications@phs.scot.
Further information
RADAR
Find out more about RADAR – Scotland's drugs early warning system.
Data and intelligence
View our wider drug data and intelligence.
Public health information
Visit Scottish Public Health Observatory (ScotPHO) for further drug-related public health information.
Metadata
- Publication title
Rapid Action Drug Alerts and Response (RADAR) quarterly report – January 2025
- Theme
Substance use surveillance
- Topic
Drugs
- Format
HTML
- Release date
28 January 2025
- Frequency
Quarterly
- Relevance and key uses of the statistics
Data are collected as part of public health surveillance on substance use in Scotland.
The most up-to-date data available are published in this report to provide a timely indicator of drug trends as part of RADAR, Scotland’s Drugs Early Warning System.- Revisions statement
Data are provisional and may be revised as a result of planned quality improvements or to reflect data quality and completeness issues.
There are no planned revisions. The data shown in the most recent quarterly update supersede data shown in previous reports.
- Revisions relevant to this publication
N/A
- Comparability
Data are not comparable outwith Scotland.
- Accuracy
The data are considered accurate.
Data are validated locally by data suppliers, partnerships and sources, and then checked by PHS.
Where relevant, data quality and completeness issues are described in the text associated with each indicator.
The Code of Practice for Statistics has been followed to ensure a high standard of data value, trustworthiness and quality.
- Accessibility
It is the policy of PHS to make its websites and products accessible according to our accessibility statement. Graphs and tables have been assessed against PHS accessibility standards.
Accessibility of the report and findings are of continuous consideration throughout the report development.
- Coherence and clarity
The report is available as HTML web pages.
Wherever possible, plain English descriptions have been used within the narrative and any technical words or phrases explained.
- Disclosure
Our Statistical Disclosure Protocol has been followed.
- Official Statistics designation
Management information report
- UK Statistics Authority Assessment
N/A
- Last published
29 October 2024
- Next published
25 April 2025
- Date of first publication
11 October 2022
- Help email
The remaining metadata for this document has been split into sections as there are some differences between the indicators.
Description
This indicator provides a summary of the drug trend bulletin from the Police Scotland Statement of Opinion (STOP) Unit.
Data source(s)
Police Scotland STOP Unit
Date that data were acquired
7 January 2025
Timeframe of data and timeliness
This section includes the most notable drug trends in recent months.
Continuity of data
The Police Scotland drug-trend bulletins are designed to provide drug-trend information, highlighting some of the current trends identified by the police in Scotland and other parts of the UK. The bulletin has and will evolve through time to provide timely distribution of drug-related information.
Concepts and definitions
Cannabinoids are compounds that interact with the endocannabinoid system. They are found in the cannabis plant or can be produced synthetically in a laboratory.
Completeness
The Police Scotland drug trend bulletin highlights some of the current trends identified by the police in Scotland and other parts of the UK.
Value type and unit of measurement
Police seizures positive for controlled substances displayed as drug type.
Description
This indicator provides a summary of the drug reports received by RADAR.
Data source(s)
Public Health Scotland
Date that data were acquired
Various between 5 October 2024 and 4 January 2025. Data were collated on 10 January 2025.
Timeframe of data and timeliness
This section includes the most notable drug trends in recent months.
Continuity of data
Since July 2022, data in this indicator have been collected consistently using reporting forms and email. The indicator has and will continue to evolve through time to provide timely distribution of drug-related information.
- QR1 (Jul – Sep 22) - Number of reports 8; number of primary drugs reported 9
- QR2 (Oct – Dec 22) - Number of reports 18; number of primary drugs reported 20
- QR3 (Jan – Mar 23) - Number of reports 23; number of primary drugs reported 24
- QR4 (Apr – Jun 23) - Number of reports 24; number of primary drugs reported 24
- QR5 (Jul – Sep 23) - Number of reports 36; number of primary drugs reported 38
- QR6 (Oct – Dec 23) - Number of reports 53; number of primary drugs reported 64
- QR7 (Jan – Mar 24) - Number of reports 43; number of primary drugs reported 57
- QR8 (Apr – Jun 24) - Number of reports 85; number of primary drugs reported 128
- QR9 (Jul – Sep 24) - Number of reports 69; number of primary drugs reported 85
- QR10 (Oct – Dec 24) - Number of reports 97; number of primary drugs reported 143
Accuracy
Analysis on the reports received (such as number and type) are considered to be accurate. The individual reports have been validated to check their credibility and likelihood. Reports that we were unable to validate are not shown in this indicator.
Reports accurately represent the individual submissions made, although they have been summarised to ensure anonymity. Unless otherwise specified, these reports have not been confirmed by toxicology and should be considered anecdotal.
Concepts and definitions
Cocaine is a short-lasting stimulant drug. Cocaine powder and crack cocaine are two different forms of the same drug.
Benzodiazepines are depressant drugs with sedative and anxiolytic (anti-anxiety) effects. They are also known as tranquilisers.
Nitazenes are a group of potent synthetic opioids.
Heroin is an opioid drug usually found as a brown powder.
Xylazine is a depressant drug used in veterinary medicine with sedative, analgesic and muscle relaxant properties.
Cannabinoids are substances that interact with the endocannabinoid system, which is involved in regulating processes including movement, motor skills, mood, appetite and pain.
Other: The most common drugs reported in the ‘other’ category were ketamine, MDMA, pregabalin, alcohol, lean and zopiclone.
WEDINOS (The Welsh Emerging Drugs and Identification of Novel Substances) project is a harm reduction project, providing an anonymous drug testing service to members of the public, along with information about substance use. This service is provided to all residents of the UK who would like to receive further information about the substances they are in possession of. WEDINOS results are based on substances submitted by people who may have experienced harms or unusual effects from substances they have taken. As such, they provide useful information about emerging substances in circulation in Scotland but may not be representative of all the substances used or harms experienced by the wider population of people who use drugs.
Completeness
The indicator highlights report by area: National, North Scotland, East Scotland and West Scotland. Reports received are not representative of the level of harms in an area.
Value type and unit of measurement
Report number, type of report, drug appearance and report summary are displayed by NHS Board or local authority area.
Description
This indicator provides information on emergency naloxone administration by Scottish Ambulance Service (SAS) clinicians in Scotland.
Data source(s)
Scottish Ambulance Service
Date that data were acquired
17 December 2024
Timeframe of data and timeliness
22 August 2022 to 24 November 2024, approximately two months in arrears.
Continuity of data
SAS clinicians have been administering naloxone directly to patients experiencing symptoms of an opioid overdose since around 1998. There have been no changes in the guidance given to SAS clinicians regarding the administration of naloxone over the time series shown in the analysis. From April 2024, a new clinical IT system used for recording administration of naloxone started to be rolled out across Scotland.
Scotland's National Naloxone Programme has been operational since 2011 and continues to facilitate the supply of take-home naloxone to people at risk of opioid overdose, members of the public, service workers and professionals (PHS quarterly monitoring bulletin on naloxone). Since August 2023, all Police Scotland officers below the rank of Inspector have carried naloxone. Naloxone kits are also available on all emergency vehicles operated by the Scottish Fire & Rescue Service (SFRS).
This overall increase in the supply of naloxone kits in community settings should be taken into consideration when interpreting figures on the administration of naloxone by SAS clinicians. However, it cannot be assumed that changes in the amount of naloxone supplied to members of the public or other emergency services will result in comparable changes in the amount of naloxone administered by those individuals (kits obtained in case an opioid overdose is witnessed may remain unused). Data on the use of naloxone by Police Scotland officers are available on the Police Scotland website. Currently, no national data are available on naloxone administration by members of the public or SFRS staff.
As overdose awareness training guidelines clearly state that SAS clinicians should be called to opioid overdoses regardless of whether naloxone has already been administered by a third party, it cannot be assumed that the prior administration of naloxone will influence the likelihood of SAS clinicians attending an overdose or administering a further dose of naloxone. While it cannot be assumed that the SAS naloxone administration figures presented here provide a complete count of all opioid overdoses, the number of opioid overdoses not attended by SAS was unknown.
Concepts and definitions
Naloxone is a medicine used to prevent fatal opioid overdoses. Opioid overdoses are commonly associated with drug-related deaths. These data on the numbers of incidents in which naloxone was administered by SAS clinicians provide an indication of numbers of suspected opioid overdoses.
A small percentage of these administrations will have been due to circumstances other than an illicit opioid overdose (for example, some may relate to prescribed opioid overdoses or to adverse reactions associated with medications administered in the course of emergency treatment).
Also, in a small number of cases, naloxone may be administered to someone who is unconscious for unconfirmed reasons, which may be confirmed at a later point not to have been an opioid overdose.
While these data count multiple overdose patients at the same incident separately, multiple naloxone administrations to the same patient at the same incident are not counted separately.
Under some circumstances, naloxone administration will not successfully reverse an opioid overdose (for example, if administered too late) and these statistics should not be interpreted as equating to numbers of lives saved.
Completeness
SAS data on numbers of naloxone incidents are collated from data entered by ambulance clinicians recording medications administered to patients via an electronic tablet in the vehicle. Data recording is typically completed within 30 minutes of the end of an incident.
Value type and unit of measurement
Number of incidents in which naloxone was administered by SAS clinicians and moving averages.
Description
This indicator provides information on drug overdose or intoxication attendances at emergency departments in Scotland.
Data source(s)
Public Health Scotland – Accident & Emergency Datamart
Date that data were acquired
9 December 2024
Timeframe of data and timeliness
29 August 2022 and 1 December 2024, approximately two months in arrears.
Continuity of data
There have been no changes in the national recording mechanisms or processes over the time series shown in the analysis.
Concepts and definitions
A drug–related emergency department (ED) attendance is an attendance for a drug intoxication or overdose, either alone, or combined with alcohol intoxication.
Completeness
It is not possible to accurately report total attendances for specific conditions using the national A&E dataset, due to the quality of the data available. The diagnosis or reason for attendance can be recorded in a variety of ways, including in free text fields and not all NHS Boards submit this information. The numbers presented in this report therefore only give a high–level indication of attendances over time. Further details can be found in the Accident and Emergency Activity Data.
Value type and unit of measurement
Number of drug overdose or intoxication attendances at emergency departments and moving averages.
Description
This indicator provides information on drug-related acute hospital admissions in Scotland.
Data source(s)
Public Health Scotland – Scottish Morbidity Record – general, acute inpatient and day case records (SMR01)
Date that data were acquired
7 January 2025
Timeframe of data and timeliness
27 June 2022 to 29 September 2024, approximately three months in arrears.
Continuity of data
There have been no changes in the recording mechanisms or processes over the time series shown in the analysis. Further detail can be found in the 'Drug-related hospital statistics' publication background information.
Concepts and definitions
Opioids
Opioid drugs act on opioid receptors to produce sedative and painkilling effects. They are respiratory depressants (reduce heart rate and breathing). Opioids include synthetic (lab-made) drugs such as methadone and buprenorphine, as well as opiates (drugs made from opium) such as heroin and morphine.
Cannabinoids
Cannabinoids are compounds that interact with the endocannabinoid system. They are found in the cannabis plant (such as THC) or can be produced synthetically in a laboratory (synthetic cannabinoids).
Cocaine
Cocaine is a short-lasting stimulant drug that increases heart rate and breathing. This group includes powder cocaine and crack cocaine.
Sedatives and hypnotics
Sedatives and hypnotics are drugs that induce sedation and depress the central nervous system, which also decreases heart rate and breathing. They are also known as depressants. This group of drugs includes 'prescribable' benzodiazepines (drugs such as diazepam), 'street' benzodiazepines (such as etizolam and alprazolam) and z-hypnotics (such as zopiclone).
Multiple/other
The 'multiple/other' drugs category includes volatile solvents (such as glue, gases or aerosols) and multiple drug use. This category may also be used to indicate multiple drug use when individual substances are not known or cannot be coded using existing diagnosis codes (International Classification of Diseases 10th Revision – ICD10).
Completeness
The data is routinely drawn from hospital administrative systems and ICD10 diagnosis codes used to identify admissions related to drug use. Some caution is necessary when using these data as drug use may only be suspected and may not always be recorded by the hospital. Further details can be found in the PHS drug-related hospital statistics report, and information on hospital administrative systems (Scottish Morbidity Records – SMR) data completeness can be found on the 'SMR completeness' webpage.
Completeness levels for NHS Fife and NHS Grampian were below 90% as of 12 December 2024 for the most recent time period (July – September 2024), therefore caution is advised when interpreting trends in these areas on the dashboard.
Value type and unit of measurement
Number of inpatient and day case admissions to general acute hospitals (excluding maternity, neonatal, geriatric long stay and admissions to psychiatric hospitals), presented by month of admission with moving averages.
Description
This indicator provides information on suspected drug deaths in Scotland.
Data source(s)
Police Scotland
Date that data were acquired
16 December 2024
Timeframe of data and timeliness
22 August 2022 to 24 November 2024, approximately two months in arrears.
Continuity of data
There have been no changes in the national Police Scotland recording mechanisms or processes over the time series shown in the analysis.
Concepts and definitions
Drug-related death
A drug-related death (also referred to as drug-misuse death) is a death where the underlying cause was confirmed to be drug poisoning and where any of the substances which were implicated, or potentially contributed to death, are controlled in the UK. National Statistics on drug-related deaths are published by the National Records of Scotland (NRS).
Suspected drug death
A suspected drug death is a death where controlled drugs are suspected of being involved. This operational measure used by Police Scotland is based on the reports, observations and initial enquiries of officers attending the scene of death.
Completeness
This indicator includes data on suspected drug deaths as recorded by all Police Scotland Divisions across Scotland.
Value type and unit of measurement
Numbers of suspected drug deaths in Scotland and moving averages.
Description
This indicator provides information on the number of attendances, length of stay and toxicology of presentations due to acute illicit drug toxicity at the Queen Elizabeth University Hospital (QEUH) emergency department (ED), Glasgow, Scotland. This study assesses the feasibility of prospective surveillance of ED presentations due to acute illicit drug toxicity.
Data source(s)
QEUH, NHS Greater Glasgow and Clyde
Date that data were acquired
20 January 2025
Timeframe of data and timeliness
17 August 2022 to 16 November 2024, approximately two months in arrears.
Continuity of data
'ASSIST: A Surveillance Study of Illicit Substance Toxicity' is a study by the ED at the QEUH.
QEUH will provide Public Health Scotland with toxicology screening data on a quarterly and ad-hoc basis for the purposes of public health surveillance.
Because the sample size is small, some of the variables are combined in a different way to the data shared in previous releases of the RADAR quarterly report, to ensure the information are not disclosive. Categories may be revised in future as sample size increases.
Concepts and definitions
Unique ED attendances
Each separate attendance is a count of one. If the same person presented more than once, each attendance was counted.
Illicit drug
'Illicit drug' encompasses any substance that is a controlled drug as per the Misuse of Drugs Act 1971 and Misuse of Drugs Regulations 2001. It excludes legal substances such as alcohol, nicotine, caffeine and paracetamol, as well as medications recently prescribed to the individual or drugs administered to the individual as part of treatment (by ambulance or hospital).
Benzodiazepines
Benzodiazepines are a group of drugs with depressant and anxiolytic (anti-anxiety) effects. They are also known as tranquilisers.
Metabolite
A drug metabolite is a compound produced when a drug breaks down in the body.
In this study, if either a drug or metabolite are detected, this will only be included as one substance – the drug. For example, if both diazepam and its metabolite desmethyldiazepam are detected, only diazepam is recorded.
Due to this we are unable to ascertain the source of some substances, for example, oxazepam is a benzodiazepine, but it is also a metabolite of a range of other benzodiazepines, so we cannot determine whether oxazepam or another benzodiazepine was consumed.
Cocaine
Cocaine is a short-lasting stimulant drug that increases heart rate and breathing.
Gabapentinoids
Gabapentinoids are a group of drugs with depressant and painkilling effects.
Opioids
Opioid drugs act on opioid receptors to produce sedative and painkilling effects. They are respiratory depressants (reduce heart rate and breathing).
Cannabinoids
Cannabinoids are compounds that interact with the endocannabinoid system. They are found in the cannabis plant (such as THC) or can be produced synthetically in a laboratory (synthetic cannabinoids).
Other stimulants
Other stimulants are stimulant drugs apart from cocaine. They increase heart rate, breathing and energy.
Completeness
Not all data identified for all ED attendances is available for analysis, due to the time required to send and receive toxicology results and to link patient and clinical data. A differing proportion of the total attendances recruited for this study are available for each of the data sources:
- completed clinical notes made by research nurses (Castor)
- completed electronic clinical records (West of Scotland Safe Haven)
- toxicology results
- toxicology results with corresponding clinical (Castor) notes
Toxicology testing has been carried out by the LGC Group, formerly the Laboratory of the Government Chemist. LGC screen against a database of over 3,500 chemical substances including illicit drugs, novel psychoactive substances, synthetic cannabinoid receptor agonists, benzodiazepines and medications. This analysis does not, however, imply that specific drugs were implicated in harms.
This study includes patients aged 16 or over attending QEUH adult ED directly related to acute illicit drug use. It excludes patients where the condition is more likely due to a cause other than acute illicit drug use, due to withdrawal, primarily related to alcohol use or where the attendance is due to a complication of previous drug use, i.e. infected injection site.
Due to a temporary pause in the study while funding was being confirmed, the start of Q9 was delayed. Recruitment was suspended from 17 August to 22 September 2024. Consequently, Q9 consists of only 55 study days, compared to the usual 90-92 days, resulting in fewer samples being tested. This discrepancy should be considered when interpreting the data and trends for the most recent quarter.
Value type and unit of measurement
Number of ED attendances related to illicit drug use, destination on discharge from the ED, number of hours in the ED, number of hours in hospital, toxicology results of surplus serum sampling by drug type and drug category.
Description
This indicator provides information on forensic toxicology testing for controlled substances completed at post-mortem in Scotland.
Data source(s)
Forensic Toxicology Service within Forensic Medicine and Science (FMS), University of Glasgow, on behalf of the Crown Office and Procurator Fiscal Service (COPFS).
Other laboratory testing sites in the United Kingdom, outsourced by the Scottish Police Authority (SPA) Forensic Services.
The Department of Clinical Biochemistry at NHS Grampian, on behalf of the Crown Office and Procurator Fiscal Service (COPFS).
Date that data were acquired
20 November 2024
Timeframe of data and timeliness
Between 1 January 2022 and 30 September 2024, approximately three months in arrears.
Continuity of data
PHS was provided with post-mortem toxicology testing data for deaths occurring in the west, east and parts of the north of Scotland by Forensic Medicine and Science at the University of Glasgow and SPA FS.
In late 2022, post-mortem toxicology services for the west, east and parts of the north of Scotland were transferred from the University of Glasgow to the Scottish Police Authority Forensic Services (SPA FS). During the period of transition, tests were completed by other laboratory testing sites in the UK. Although testing has now been moved to SPA FS, these testing sites continued to provide support in 2023 and data from both SPA FS and outsourced sites have been included in this report.
Data on deaths occurring in the far north and north-east of Scotland from January 2022 onwards, was supplied by the Department of Clinical Biochemistry at NHS Grampian.
Concepts and definitions
Post-mortem toxicology testing where controlled drugs (as defined in the Misuse of Drugs Act 1971 - external website) were detected is carried out, on behalf of the COPFS, by two services in Scotland:
- The Scottish Police Authority Forensic Services (SPA FS) covers deaths occurring in the west, east and parts of the north of Scotland.
- The Department of Clinical Biochemistry at NHS Grampian covers deaths in the far north and north-east of Scotland.
Detailed interpretation of the levels of drugs found present, drug interactions, co–morbidities or other factors relating to death are outside the scope of this analysis.
This analysis does not imply that specific drugs were implicated in deaths nor that deaths were classified as 'drug–related' and does not include consideration of wider causes of death.
As some of the data received from other laboratory testing sites did not include date of death, other date variables have been used as a proxy to improve data completeness and enable the inclusion of these deaths within this report. Two separate date variables have been used to approximate date of death information, where this information was unavailable:
- Date of the case being received or sent to other labs for toxicology testing.
- Date of toxicology test being completed.
Similarly, as date of death was unavailable for those tests conducted by the Department of Clinical Biochemistry at NHS Grampian, the date when the case was received from the Crown Office and Procurator Fiscal Service has been used instead.
Benzodiazepines
Benzodiazepines are a group of drugs with depressant and anxiolytic (anti-anxiety) effects. They are also known as tranquilisers. Diazepam is a ‘prescribable benzodiazepine’. Etizolam, clonazolam, gidazepam and bromazolam are ‘street benzos’, benzodiazepines that are not licensed for prescription in the UK.
Cocaine
Cocaine is a short-lasting stimulant drug that increases heart rate and breathing. This group includes powder cocaine and crack cocaine.
Gabapentin and pregabalin
Gabapentin and pregabalin are gabapentinoids, a group of drugs with depressant and painkilling effects.
Opioids
Opioid drugs act on opioid receptors to produce sedative and painkilling effects. They are respiratory depressants (reduce heart rate and breathing). This category includes buprenorphine, fentanyl, heroin/morphine, methadone and nitazenes.
Completeness
The inclusion of data on deaths in the far north and north-east of Scotland (the areas covered by NHS Grampian) from January 2022 onwards, means that the figures presented after that point cover the whole of Scotland and are different from those shown in previous publications.
Value type and unit of measurement
Number and percentage of forensic toxicology cases testing positive for controlled substances by drug type.
Description
This indicator provides information on drug types most commonly detected in drug seizures in Scottish prisons.
Data source(s)
Scottish Prison Service (SPS) and the Leverhulme Research Centre for Forensic Science (LRCFS), University of Dundee.
Date that data were acquired
2 December 2024
Timeframe of data and timeliness
1 June 2021 and 31 July 2024, approximately four months in arrears.
Continuity of data
There have been no changes in the seizures recording mechanisms or processes over the time series shown in the analysis.
Data is available for samples for the latest period (1 January 2024 to 31 July 2024). Analysis is available within the report. Analysis of the drug seizures in Scottish prisons from August 2024 is still ongoing and not all data can be included in this report. We anticipate the updated data will be available for the next release in April 2025.
Concepts and definitions
Benzodiazepines
Benzodiazepines are a group of drugs with depressant and anxiolytic (anti-anxiety) effects. They are also known as tranquilisers. Benzodiazepines detected in this project include etizolam, flubromazepam, bromazolam, diazepam and flualprazolam.
Cocaine
Cocaine is a short-lasting stimulant drug that increases heart rate and breathing. This group includes powder cocaine and crack cocaine.
Gabapentinoids
Gabapentinoids are a group of drugs with depressant and painkilling effects.
Opioids
Opioid drugs act on opioid receptors to produce sedative and painkilling effects. They are respiratory depressants (reduce heart rate and breathing). Opioids include synthetic (lab-made) drugs such as methadone and opiates (drugs made from opium) such as heroin. Opioids detected in this project include buprenorphine, heroin, tramadol, codeine, dihydrocodeine, metonitazene, oxycodone and methadone.
Synthetic cannabinoids
'Synthetic cannabinoids' is a term used to describe over 200 lab-made drugs that interact with the endocannabinoid system.
Completeness
Data is provided to PHS by the LCRFS. LCRFS does not analyse all seizures from the SPS. However, LCRFS data is a sizeable subset of all national prison seizures.
Value type and unit of measurement
Percentage of drug seizures analysed by the LRCFS by drug type and sample type (card, paper, powder or tablet).
Description
This indicator provides information on specialist drug treatment referrals in Scotland.
Data source(s)
Public Health Scotland – Drug and Alcohol Information System (DAISy) and Drug and Alcohol Treatment Waiting Times (DATWT) database
Date that data were acquired
10 December 2024
Timeframe of data and timeliness
22 August 2022 to 17 November 2024, approximately two months in arrears.
Continuity of data
These data have been extracted from the Drug and Alcohol Information System (DAISy) and its predecessor, the Drug and Alcohol Treatment Waiting Times (DATWT) database. DAISy was available in all NHS boards from April 2021.
DAISy introduced a new way of recording referrals, a continuation of care process which affects how referrals are recorded when people have started treatment and move from one service to another without a break or change in their treatment (for instance, when moving between community-based and prison-based services). The number of referrals remain comparable between DATWT and DAISy, but how waits are recorded against the initial and receiving services has changed for referrals transferred by the continuation of care process. These data report on the number of referrals rather than waits so the new continuation of care process should not impact the number of referrals.
DAISy introduced an additional 'co-dependency' service user type, where the referral relates to treatment for both drug and alcohol use. Co-dependency has only been recorded since the introduction of DAISy (April 2021) so is not available as a separate client type in the DATWT database. These data report the number of referrals where the service user type is recorded as either 'drugs' or 'co-dependency' in DAISy and as 'drugs' in DATWT.
Concepts and definitions
These data relate to the number of referrals to specialist drug and alcohol treatment services in Scotland delivering tier 3 and 4 interventions (community-based specialised drug assessment and co-ordinated care-planned treatment, and residential specialised drug treatment). These data are for community-based drug and alcohol treatment services and exclude prison-based and hospital-based services.
Completeness
Drug and alcohol treatment services are required to submit accurate and up-to-date waiting times information to PHS. These referrals data are management information and includes all services that enter data on DAISy and its predecessor, the DATWT database. This contrasts with the figures reported in the 'National drug and alcohol treatment waiting times' statistics release for Scotland where data from services that were unable to confirm their data were accurate and up-to-date within specified timescales are excluded. Further details can be found in the data quality section of the Drug and Alcohol Treatment Waiting Times dashboard.
Value type and unit of measurement
Number of specialist drug treatment referrals and moving averages.
Description
This indicator provides information on opioid substitution therapy prescribing in Scotland.
Data source(s)
Public Health Scotland – Prescribing Information System (PIS) and Hospital Medicines Utilisation Database (HMUD)
Date that data were acquired
13 December 2024
Timeframe of data and timeliness
1 July 2024 to 30 September 2024.
Data from the PIS are available approximately three months in arrears.
HMUD data availability can vary by NHS board. However, the injectable buprenorphine data shown in this release are considered complete.
Continuity of data
The data shown are considered to provide a comprehensive account of OST prescribing for the time series presented, including data from GP and hospital prescribing systems.
Concepts and definitions
Defined daily dose
When comparing use between medicines and over time it is common to use World Health Organization (WHO) defined daily doses (DDDs). The DDD is defined as the usual average daily maintenance dose used in adults for the main therapeutic use of the medicine. The WHO DDD is a global average and may not be representative of the doses used in clinical practice at a more local level.
Average daily quantity
Due to differences between the average OST doses used in Scotland and the rest of the world, the analysis presented here is based on average daily quantities (ADQs). These are more representative of the daily maintenance doses used within Scotland and were developed via analysis of prescriptions and by consultation with the Specialist Pharmacists in Substance Misuse group. The ADQs agreed are:
- methadone (oral): 65 mg
- buprenorphine (oral): 13 mg
- buprenorphine (injection): 3.4 mg
Buprenorphine
Buprenorphine is a synthetic partial opioid agonist used to treat acute pain, chronic pain and opioid dependence. Prescribed for daily use (oral) or weekly or monthly prolonged release (injectable), buprenorphine relieves opioid cravings and withdrawal symptoms and blocks the effects of other opioids. As with other opioids, buprenorphine can result in sedation, respiratory depression and death. These statistics relate to the prescribing of oral (2 mg, 8 mg and 16 mg buprenorphine or buprenorphine and naloxone tablets) and injectable buprenorphine (various strengths) for the treatment of opioid dependence.
Opioids
Opioid drugs act on opioid receptors to produce sedative and painkilling effects. They are respiratory depressants (reduce heart rate and breathing). Opioids include synthetic (lab-made) drugs such as methadone and buprenorphine, as well as opiates (drugs made from opium) such as heroin and morphine.
Methadone
Methadone is a synthetic opioid agonist used to treat chronic pain and opioid dependence. Prescribed for daily use, methadone relieves opioid cravings and withdrawal symptoms. As with other opioids, methadone can result in sedation, respiratory depression and death. These statistics include data on the prescribing of methadone 1mg/1ml solution for the treatment of opioid dependence.
Accuracy
There are differences between community prescribing data from the Prescribing Information System (PIS) and hospital prescribing data from the Hospital Medicines Utilisation Database (HMUD) in the way that dates are allocated to medications supplied. The basis for date allocation in PIS data is the month in which the costs associated with dispensing medication were reimbursed. The basis for date allocation in HMUD data is the month in which medications were supplied to the NHS Board for onward administration to patients. While useful to note, these differences are not thought to have a significant impact on the reliability of this analysis.
For the 2022/23 Q3 and Q4 reports, there were revisions to the injectable buprenorphine data, which means that the number of ADQ doses associated with that medication from April 2022 onwards was slightly higher than shown in previous reports. These changes were associated with the addition of data on Buvidal 160mg/0.45ml prolonged release injections to the PIS data extract in 2022/23 Q3 and to the HMUD data extract in 2022/23 Q4.
For the 2024/25 Q1 reports, there were revisions to the methadone and oral buprenorphine data, which means that the number of ADQ doses associated with these medications from February 2018 onwards was slightly higher than shown in previous reports. These changes were associated with the addition of data on the doses outlined in the table below to the PIS data extract.
Methadone
- methadone 10mg/ml oral solution sugar free
Buprenorphine
- buprenorphine 5.7mg / naloxone 1.4mg sublingual tablets sugar free
- buprenorphine 8.6mg / naloxone 2.1mg sublingual tablets sugar free
- buprenorphine 11.4mg / naloxone 2.9mg sublingual tablets sugar free
- buprenorphine 16mg / naloxone 4mg sublingual tablets sugar free
- buprenorphine 400microgram sublingual tablets sugar free
- buprenorphine 1mg sublingual tablets sugar free
- buprenorphine 4mg sublingual tablets sugar free
- buprenorphine 6mg sublingual tablets sugar free
Completeness
The data shown are considered to provide a comprehensive account of OST prescribing for the time series presented, including data from GP and hospital prescribing systems.
Value type and unit of measurement
Total number of ADQ doses of methadone, oral buprenorphine and injectable buprenorphine supplied in Scotland, based on community and hospital prescribing data.
Description
This indicator provides information on injecting equipment provision (IEP) in Scotland.
Data source(s)
Needle Exchange Online (neo360)
Date that data were acquired
2 December 2024
Timeframe of data and timeliness
27 June 2022 to 29 September 2024, approximately three months in arrears.
Continuity of data
Caution is recommended when interpreting these statistics. Service provision in some areas has changed over time. Some outlets will have closed, and others will have opened.
The methods used by areas to count or estimate some of the figures may also have changed.
Concepts and definitions
Transactions
A transaction is an episode in which a client received equipment relating to an injecting episode (i.e. a barrel and/or fixed needle and syringe). People who inject drugs may attend IEP outlets at any time, whether or not they are undertaking specialist treatment for problematic drug use.
Further details can be found in the PHS Injecting Equipment Provision in Scotland report.
Completeness
This indicator includes data on transactions and needle and syringe distribution by injecting equipment providers in mainland Scotland NHS Boards.
It does not include data for NHS Shetland, NHS Orkney and NHS Western Isles.
The 11 mainland NHS boards use neo360 routinely, but due to missing data for part of the period presented, NHS Highland is excluded from the transaction and needle and syringe data and the ratio figures.
Value type and unit of measurement
Number of IEP transactions, number of needles and syringes distributed, the ratio of the number of needles and syringes per IEP transaction and moving averages.