Sedation After a Trial of Mixed Amphetamine Salts in a Boy with Attention-Deficit/Hyperactivity Disorder
Raed Al Awami1, Ammar Albanna2,3
1Department of Psychiatry, King Fahad Specialist Hospital, Dammam, Saudi Arabia.
Insights
Sedation is a rare side effect of mixed amphetamine salts used for Attention-Deficit/Hyperactivity Disorder (ADHD). This case highlights the importance of monitoring for unexpected adverse drug reactions, especially in children with co-occurring autism spectrum disorder (ASD).
Area of Science:
- Neuroscience
- Pharmacology
- Pediatrics
Background:
- Attention-deficit/hyperactivity disorder (ADHD) is a prevalent neurodevelopmental disorder managed primarily with psychostimulants.
- Adverse effects of stimulants are known, but sedation is an exceptionally rare complication.
Abstract:
BACKGROUND Attention-deficit/hyperactivity disorder (ADHD) is a common neurodevelopmental disorder that manifests in early childhood. Pharmacotherapy, including psychostimulants, is considered the cornerstone of ADHD management. Although stimulants have been associated with adverse effects, sedation following the administration of an amphetamine-based stimulant is an extremely rare adverse effect. CASE REPORT We report the case of a 6-year-old boy presenting with ADHD and a history of autism spectrum disorder (ASD). After discussing treatment options with his parents, he was started on a low dose of a methylphenidate medication. He was unable to tolerate the medication due to anorexia, insomnia, and irritability despite multiple adjustments in the dosages. A trial of immediate-release mixed amphetamine salts was initiated, starting from a low dose. The boy developed sedation and lethargy shortly after the administration of this medication. CONCLUSIONS Sedation is a rare adverse drug reaction to mixed amphetamine salts. Clinicians should proactively monitor for the possible adverse effects in patients with ASD and ADHD, including unexpected symptoms such as sedation. Reporting of adverse drug reactions should be encouraged to promote the post-marketing surveillance of medications.
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