Abstract
Background: Although aripiprazole and risperidone are used widespread in pediatrics, there are still limited pieces of evidence on their actual safety profile. By using the EudraVigilance database, we carried out an analysis to perform a comprehensive overview of reported adverse events among children and adolescents treated with aripiprazole and risperidone.Methods: Descriptive analysis was performed of all individual case safety reports (ISCRs) submitted to EudraVigilance associated with aripiprazole and risperidone and related to the pediatric population from 2016 to 2018.Results: A total of 855 and 2,242 ISCRs for aripiprazole and risperidone, respectively, were recorded for a total of 11,042 suspected adverse drug reactions (2,993 for aripiprazole and 8,049 for risperidone). Most ISCRs were related to male patients (65.0 and 86.3% for aripiprazole and risperidone, respectively) and were serious (81.0 and 94.1% for aripiprazole and risperidone, respectively). Schizophrenia spectrum and other psychotic disorders, such as disruptive, impulse-control, and conduct disorders, and autism spectrum disorder were the top three clinical indications for aripiprazole (19.0, 16.1, and 11.6%, respectively). For risperidone, attention-deficit/hyperactivity disorder (25.4%), disruptive, impulse-control, and conduct disorders (17.1%), and bipolar and related disorders (14.2%) were more commonly reported as clinical indications. Data also showed a high proportion of use for clinical conditions not authorized in children. Psychiatric disorders were the main related adverse events for aripiprazole (20.2%), and among these, suicidal behavior was one of the most reported (14.9%). Reproductive system and breast disorders were the main related adverse events for risperidone (19.8%), and gynecomastia was the most reported event; metabolism and nutrition disorders, mainly reported as weight gain disorders, were more reported in children (3–11 years) than in adolescents (12–17 years).Conclusions: Our results demonstrate that spontaneously reported adverse events associated with aripiprazole and risperidone reflect what is already known in terms of safety profile, although with about 90% of them being serious. This analysis stresses the need for further studies and effective training and information activities to better define the actual benefit/risk ratio of these drugs in pediatric patients.
Highlights
Second-generation antipsychotics (SGAs) are becoming an increasingly integral part of comprehensive treatment programs of psychiatric disorders of childhood and adolescence
All spontaneous cases associated with risperidone and aripiprazole and referred to the pediatric population aged 3–17 years were selected as aggregate data using the public access online tools in the adverse drug reactions (ADRs) website, available as line listing and individual case safety reports (ICSRs) form
From 2016 to 2018 in the European Medicine Agency EV database, a total of 3,097 ICSRs were recorded in pediatric patients (3–17 years), of which 855 were for aripiprazole and 2,242 for risperidone, accounting for a total of 11,042 adverse events (AEs) (2,993 for aripiprazole and 8,049 for risperidone), the apparent discrepancy in the number being because single ICSRs can report more than one AE
Summary
Second-generation antipsychotics (SGAs) are becoming an increasingly integral part of comprehensive treatment programs of psychiatric disorders of childhood and adolescence. Within the class of SGAs, risperidone, and aripiprazole are the most frequently prescribed in children and adolescents across most countries [2]. Risperidone and aripiprazole are frequently prescribed in these populations as treatment of attention-deficit/hyperactivity disorder (ADHD), eating disorders, anxiety, and sleep disorders [4, 5]. Despite such a significant increase in SGA use in children and adolescents, reliable and comprehensive efficacy and safety information from specific clinical studies in pediatric patients are still relatively scant [4,5,6]. By using the EudraVigilance database, we carried out an analysis to perform a comprehensive overview of reported adverse events among children and adolescents treated with aripiprazole and risperidone
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