Long‐term study of lisdexamfetamine dimesylate in Japanese children and adolescents with attention‐deficit/hyperactivity disorder

Abstract Aims As an extension of a phase 2/3 study evaluating the efficacy and safety of lisdexamfetamine dimesylate (LDX) 30, 50, or 70 mg/d for 4 weeks in Japanese patients aged 6‐17 years with attention‐deficit/hyperactivity disorder (ADHD), this study evaluated its long‐term safety and efficacy....

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Váldodahkkit: Hironobu Ichikawa (Dahkki), Tasuku Miyajima (Dahkki), Yushiro Yamashita (Dahkki), Masakazu Fujiwara (Dahkki), Akimasa Fukushi (Dahkki), Kazuhiko Saito (Dahkki)
Materiálatiipa: Girji
Almmustuhtton: Wiley, 2020-03-01T00:00:00Z.
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3rd Floor Main Library

oažžasuvvan: 3rd Floor Main Library
Hildobáiki: A1234.567
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