ADHD medication use and risk of self-harm: a multinational self-controlled case series study
Self-harm risk peaked before ADHD medicine started, not after.
*Multinational self-controlled case series; Level 3 (OCEBM).
Citation
Chan AYL, Beyene K, Park S, et al. BMJ Mental Health. 2026;29:1-9. doi:10.1136/bmjment-2026-302819
Background
Prior studies have disagreed on whether attention-deficit/hyperactivity disorder (ADHD) medicines raise self-harm risk. This large multinational study tested timing of self-harm before and after starting treatment.
Patients
People aged 6 years or older from Hong Kong, New Zealand, South Korea, Taiwan, and the United Kingdom who received ADHD medicine and had a first recorded self-harm event from 2001 to 2020. Exclusions included self-harm before the study period, missing age or sex, and cancer diagnosis.
Intervention
ADHD medicines, including stimulant and non-stimulant medicines.
Control
Unexposed time periods within the same person.
Outcome
First recorded self-harm, meaning intentional self-injury or self-poisoning, regardless of intent.
Follow-up Period
Individual observation between January 2001 and December 2020.
Results
Among 461,024 people prescribed ADHD medicine, 6,847 had incident self-harm and were included in the case-series analysis.
| Risk period | Adjusted rate ratio for self-harm | Meaning |
|---|---|---|
| 90 days before starting medicine | 2.58 (95% CI 2.12 to 3.13) | Highest risk |
| First 90 days of medicine use | 1.78 (95% CI 1.23 to 2.57) | Risk lower than before treatment |
| Later medicine use | 1.27 (95% CI 1.01 to 1.60) | Small remaining elevation |
ADHD, attention-deficit/hyperactivity disorder; CI, confidence interval.
Analyses compared each person with themselves and adjusted for age, season, and other psychiatric medicines. The control was not another treatment.
Limitations
Administrative records may miss self-harm that never reached medical care. Prescriptions do not prove medicine was taken. Time-changing factors, such as worsening symptoms, family stress, or new depression, may still confound results. The study cannot prove protection or harm, only timing patterns.
Funding
Public research grants; several authors reported industry relationships.
Clinical Application
Do not delay indicated ADHD medication for self-harm fears; assess and monitor self-harm risk before starting and during early treatment.
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