2022
DOI: 10.1016/j.pharmthera.2021.107940
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Evidence-based pharmacological treatment options for ADHD in children and adolescents

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Cited by 135 publications
(104 citation statements)
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“…For children and adolescents over 70 kg, the recommended dose is to increase from a daily initiation dose of 40–80 mg, and the maximum total daily dose should not exceed 100 mg in the USA and Europe. It is manufactured in capsules containing 10, 18, 25, 40, 60, 80, or 100 mg of atomoxetine hydrochloride as well as in an oral solution (4 mg/ml) ( 103 ).…”
Section: Clinical Efficacymentioning
confidence: 99%
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“…For children and adolescents over 70 kg, the recommended dose is to increase from a daily initiation dose of 40–80 mg, and the maximum total daily dose should not exceed 100 mg in the USA and Europe. It is manufactured in capsules containing 10, 18, 25, 40, 60, 80, or 100 mg of atomoxetine hydrochloride as well as in an oral solution (4 mg/ml) ( 103 ).…”
Section: Clinical Efficacymentioning
confidence: 99%
“…The most common adverse reactions of atomoxetine in children with ADHD include gastrointestinal symptoms, sleep disturbances (somnolence), cardiovascular adverse reactions and other general disorders (irritability, dizziness, fatigue, headache) ( 103 , 117 ). These four aspects will be described in detail below.…”
Section: Clinical Efficacymentioning
confidence: 99%
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“…However, these and other studies either do not provide data in terms of age periods or subtypes of ADHD presentation (inattentive, hyperactive–impulsive (H–I), or combined), or the sample size was not large enough. In addition, they did not consider factors that may influence the diet, such as socioeconomic level [ 36 ], psychological comorbid (internalizing) problems with ADHD [ 37 , 38 ], sex differences [ 6 ], pharmacological treatment [ 39 ], intelligence quotient [ 40 ], and ASD comorbidity [ 38 ].…”
Section: Introductionmentioning
confidence: 99%