Abstract Aim Atomoxetine (ATX) is a non‐central stimulant and a standard treatment for adult attention‐deficit/hyperactivity disorder (ADHD). The long‐term efficacy of Atomoxetine is about 40% at 6 months. The variability in efficacy between individuals is thought to be related to patient‐specific factors, but no detailed research has been conducted. In this retrospective cohort study, we aimed to identify the factors associated with Atomoxetine efficacy. Methods A total of 147 patients with attention‐deficit/hyperactivity disorder aged ≥18 years who were using Atomoxetine for the first time were included in this study. The outcome was treatment success (treatment maintained for at least 6 months and improvement in symptoms). Symptom assess...
Objective: To assess the effect of atomoxetine on ADHD-related executive functions over a 6-month pe...
Atomoxetine was first licensed to treat attention-deficit/hyperactivity disorder (ADHD) in children ...
OBJECTIVE. In this study we examined the effectiveness of atomoxetine for the treatment of oppositio...
Abstract Background The objective of this study was to evaluate the efficacy of atomoxetine, a new a...
Background: Responses to atomoxetine vary for individual patients with attention-deficit/hyperactivi...
Background: While atomoxetine is an established treatment for attention-deficit/hyperactivity disord...
Background: While atomoxetine is an established treatment for attention-deficit/hyperactivity disord...
(ADHD) has been less studied in adults than in children, and the treatment studies reported to date ...
To evaluate the effect of atomoxetine treatment on executive functions in young adults with attentio...
Atomoxetine is a non-stimulant medication with sustained benefit throughout the day, and is a useful...
PubMed ID: 23737214The DSM-IV-TR (Diagnostic and Statistical Manual of Mental Disorders, 1994, Ameri...
Objective: Intra-individual variability in reaction time (IIV-RT) is common in individuals with atte...
Atomoxetine was first licensed to treat attention-deficit/hyperactivity disorder (ADHD) in children ...
Objective: To assess the effect of atomoxetine on ADHD-related executive functions over a 6-month pe...
Atomoxetine was first licensed to treat attention-deficit/hyperactivity disorder (ADHD) in children ...
OBJECTIVE. In this study we examined the effectiveness of atomoxetine for the treatment of oppositio...
Abstract Background The objective of this study was to evaluate the efficacy of atomoxetine, a new a...
Background: Responses to atomoxetine vary for individual patients with attention-deficit/hyperactivi...
Background: While atomoxetine is an established treatment for attention-deficit/hyperactivity disord...
Background: While atomoxetine is an established treatment for attention-deficit/hyperactivity disord...
(ADHD) has been less studied in adults than in children, and the treatment studies reported to date ...
To evaluate the effect of atomoxetine treatment on executive functions in young adults with attentio...
Atomoxetine is a non-stimulant medication with sustained benefit throughout the day, and is a useful...
PubMed ID: 23737214The DSM-IV-TR (Diagnostic and Statistical Manual of Mental Disorders, 1994, Ameri...
Objective: Intra-individual variability in reaction time (IIV-RT) is common in individuals with atte...
Atomoxetine was first licensed to treat attention-deficit/hyperactivity disorder (ADHD) in children ...
Objective: To assess the effect of atomoxetine on ADHD-related executive functions over a 6-month pe...
Atomoxetine was first licensed to treat attention-deficit/hyperactivity disorder (ADHD) in children ...
OBJECTIVE. In this study we examined the effectiveness of atomoxetine for the treatment of oppositio...