- Attention deficit hyperactivity disorder (ADHD) affects millions worldwide, and many worry that ADHD medication might increase the risk of self-harm
- The team led by Aston University’s Dr Adrienne Chan and Professor Ian Wong analysed data from Hong Kong, New Zealand, South Korea, Taiwan and the UK
- They found that the risk of self-harm is highest before people start ADHD medication.
The risk of self-harm amongst people with attention deficit hyperactivity disorder (ADHD) is highest before people start ADHD medication, rather than after treatment begins, according to new research led by Aston University.
The researchers, led by Dr Adrienne Chan, a pharmacy lecturer, and Regius Professor Ian Wong at Aston Pharmacy School, were seeking to address fears that taking ADHD medication raises the risk of self-harm, following conflicting evidence from previous studies of ADHD medication. Millions of adults and children worldwide have ADHD and these concerns can influence whether people start or continue with treatment, despite more recent studies being more reassuring.
The multinational collaboration saw the Aston University researchers partnering with groups from UCL in the UK, the University of Hong Kong, the University of Auckland in New Zealand, Sungkyunkwan University in South Korea, and National Cheng Kung University in Taiwan. There were also collaborators from the Seoul National University in South Korea, the University of Melbourne in Australia, Rutgers University in the US, the University of Waterloo in Canada, the Chinese University of Hong Kong and Macau University of Science and Technology.
In one of the largest multinational studies of ADHD medication safety, the research team analysed data from more than 460,000 people from the healthcare systems in Hong Kong, New Zealand, South Korea, Taiwan and the UK, who had begun a course of ADHD medication and had a record of self-harm between 2001–2020. They compared three periods of ADHD medication exposure – the 90 days before treatment began, the first 90 days of treatment use and the subsequent treatment period – with periods of non-exposure.
The highest risk of self-harm occurred during the 90 days immediately before starting treatment in all five healthcare systems, with lower, although still elevated, risks after treatment began. These consistent findings do not support ADHD medications as the main driver of self-harm.
The researchers say that the findings highlight the importance of closely monitoring people with ADHD, particularly those whose symptoms are worsening before they start treatment, so that support can be provided before self-harm occurs.
Additionally, the study has established an international research platform that can answer other important questions about medication safety. Future work will examine a wider range of health outcomes, including what happens when people stop or restart treatment, and whether ethnicity and socioeconomic disadvantage contribute to inequalities in ADHD care across different healthcare systems.
Dr Chan said:
“People often worry that ADHD medication itself increases the risk of self-harm. What our findings suggest is that many people are already at their highest risk before treatment even begins. This highlights an important opportunity for earlier intervention. Recognising that vulnerable period could help us provide support earlier, when it may make the greatest difference.”
Professor Wong said:
“At Aston, we are committed to using big data not simply to answer scientific questions, but to generate evidence that helps clinicians, informs policy, and ultimately benefits patients. This study reflects that vision by bringing together expertise from five healthcare systems using a common scientific approach while keeping patient-level data securely within each country. It demonstrates how international collaboration can generate robust evidence to improve patient care while respecting patient privacy and the highest standards of data governance.”
To read the full paper, ‘ADHD medication use and risk of self-harm: a multinational self-controlled case series study’ in BMJ Mental Health, visit https://mentalhealth.bmj.com/content/29/1/e302819.
Journal
BMJ Mental Health
Method of Research
Data/statistical analysis
Subject of Research
People
Article Title
ADHD medication use and risk of self-harm: a multinational self-controlled case series study
Article Publication Date
12-Sep-2026
COI Statement
ICW received research grants from Amgen, Janssen, GSK, Novartis, Pfizer, Bayer and Bristol-Myers Squibb and Takeda, Institute for Health Research in England, European Commission, National Health and Medical Research Council in Australia, The European Union’s Seventh Framework Programme for research, technological development, Research Grants Council Hong Kong and Health and Medical Research Fund Hong Kong; consulting fees from IQVIA and World Health Organization; payment for expert testimony for Appeal Court in Hong Kong; serves on advisory committees for Member of Pharmacy and Poisons Board; is a member of the Expert Committee on Clinical Events Assessment Following COVID-19 Immunization; is a member of the Advisory Panel on COVID-19 Vaccines of the Hong Kong Government; is the non-executive director of Jacobson Pharma Corp. in Hong Kong; and was the founder and director of Therakind Limited (UK) and Asia Medicine Regulatory Affairs (AMERA) Services Limited. He is a director of Advance Data Analytics for Medical Science (ADAMS) Limited (HK) and OCUS Innovation Limited (HK, Ireland and UK). He received honorarium from Takeda as a speaker of continuous professional education study day. CSLC has received grants from the Food and Health Bureau of the Hong Kong Government, Hong Kong Research Grant Council, Hong Kong Innovation and Technology Commission, Pfizer, IQVIA, MSD, and Amgen; CEO of Advance Data Analytics for Medical Science (ADAMS) Limited (HK); and personal fees from Manulife, MSD and PrimeVigilance; outside the submitted work. WCYL reports research grants from Diabetes UK, AIR@InnoHK administered by Innovation and Technology Commission outside the submitted work. KKCM. is the recipient of the CW Maplethorpe Fellowship, reports grants from the European Union Horizon 2020, the UK National Institute of Health Research and the Hong Kong Research Grant Council, Hong Kong Innovation and Technology Commission, and reports personal fees from IQVIA unrelated to the submitted work. YKW received personal fees from Eisai Co., Ltd., for delivering a lecture, and sponsorship from Lundbeck HK Ltd and Aculys Pharma, Inc. ASCY reports grants from NIHR UCLH Biomedical Research Centre PPI Starter Bursary, College of Mental Health Pharmacy Education Bursary and UK Turing Scheme. ECCL received research funding from Amgen, AbbVie, Gilead, GW, IQVIA, J&J, MSD, Novartis, Pfizer, Prospection, Sanofi, and Takeda, outside of the submitted work. AYLC reports grants from the National Institute for Health Research in England, the AIR@innoHK programme of the Hong Kong Innovation and Technology Commission, Hong Kong Research Grants Council, consulting fees from ADHD Europe, outside of the submitted work. XL received research grants or contracts from the Health and Medical Research Fund (HMRF) Main Scheme and HMRF Fellowship Scheme of the Hong Kong Special Administrative Region (SAR), China, and from the Research Grants Council Early Career Scheme, Research Impact Fund (Hong Kong SAR); was former nonexecutive director of Advanced Data Analytics for Medical Science Limited, Hong Kong SAR, China; received commission grants from Department of Health, Government of Hong Kong SAR, China; commission grants from Hospital Authority of Hong Kong SAR, China, internal funding from the University of Hong Kong, Hong Kong SAR, China, and research or education grants from Pfizer, Janssen, Bristol Myers Squibb (BMS), Novartis, Roche, Merck Sharp & Dohme (MSD), and Boehringer Ingelheim (BI); received consultancy fees from Merck Sharp & Dohme, Pfizer, Open Health and The Office of Health Economics; and received honoraria for associate editorship from npj Vaccines.