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In the guéridone and listings that follow, MedDRA terminology ha been used to classify reported adverse reactions.
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The primary efficacy outcome was troc in Masse Ordre from baseline to endpoint in investigator ratings nous the ADHD Rating Scale (ADHD-RS), a measure of the core symptoms of ADHD. Endpoint was defined as the last post-randomization treatment week (i.e. Weeks 1 through 4) conscience which a valid score was obtained. All Vyvanse dose groups were superior to placebo in the primary efficacy outcome.
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