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These studies suggest atomoxetine is an effective and well-tolerated treatment for ADHD in children, adolescents, and adults, and may also help with binge-eating disorder and ADHD symptoms in individuals with autism spectrum disorder.
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Atomoxetine, a selective norepinephrine reuptake inhibitor, has been extensively studied for its efficacy in treating attention-deficit/hyperactivity disorder (ADHD) in children and adolescents. Research indicates that atomoxetine significantly reduces core ADHD symptoms, including both inattentive and hyperactive/impulsive behaviors, compared to placebo . Studies have shown that atomoxetine can be administered once daily, providing continuous symptom relief throughout the day and into the evening and morning hours.
The effectiveness of atomoxetine appears to follow a graded dose-response relationship. Higher doses (1.2 mg/kg/day and 1.8 mg/kg/day) have been associated with superior outcomes in symptom reduction compared to lower doses (0.5 mg/kg/day) and placebo. This suggests that a dose of 1.2 mg/kg/day is likely to be an appropriate initial target for most patients.
Atomoxetine is generally well tolerated in children and adolescents, with discontinuation rates due to adverse events being less than 5% . Common side effects include decreased appetite, somnolence, and fatigue. Long-term studies indicate that while atomoxetine may cause modest increases in heart rate and blood pressure, these effects are typically not clinically significant.
Atomoxetine has also been shown to be effective in treating ADHD in adults. In well-controlled trials, adults receiving atomoxetine demonstrated significant improvements in ADHD symptoms compared to those receiving placebo. The medication can be administered once or twice daily and is not associated with abuse or diversion, making it a valuable option for adults, particularly those at risk for substance abuse.
In adults with ADHD and comorbid alcohol use disorders, atomoxetine has been found to significantly improve ADHD symptoms. However, its effects on reducing heavy drinking days are inconsistent. This suggests that while atomoxetine can be beneficial for managing ADHD symptoms in this population, additional interventions may be needed to address alcohol use.
Atomoxetine has been prescribed to children with autism spectrum disorder (ASD) who also exhibit ADHD symptoms. Meta-analyses indicate that atomoxetine can improve hyperactivity and inattention in this population, although the magnitude of these effects is uncertain. The medication is associated with non-serious adverse effects such as nausea, vomiting, decreased sleep, and decreased appetite.
Atomoxetine has been investigated for treating depressive symptoms in patients with Parkinson's disease. While it did not show significant efficacy in reducing depression, it was associated with improvements in global cognitive performance and daytime sleepiness. This suggests potential benefits in addressing cognitive and wakefulness issues in this population.
In a study on binge-eating disorder (BED), atomoxetine was found to significantly reduce the frequency of binge-eating episodes and associated symptoms such as weight and body mass index. This indicates that atomoxetine may be a useful treatment option for BED, particularly in patients who are also managing obesity.
Atomoxetine is a versatile medication primarily used for treating ADHD in both children and adults. It is effective in reducing core ADHD symptoms and is generally well tolerated. Additionally, atomoxetine shows promise in treating ADHD symptoms in children with ASD and managing binge-eating disorder. While its efficacy in treating depressive symptoms in Parkinson's disease is limited, it may offer cognitive and wakefulness benefits. Overall, atomoxetine is a valuable treatment option with a broad range of applications in neuropsychiatric disorders.
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