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. 2017 Mar 3;114(9):149–159. doi: 10.3238/arztebl.2017.0149

Table 3. Approved substances in Germany for the treatment of attention-deficit/hyperactivity disorder.

Substance class Typical dose range Effect
strength
Number
needed
to treat
Adverse effects Remarks
Methylphenidate (MPH) Psychostimulant 0.3–1.0 mg/kg BW 0.8–1.0 ca. 2.5
(e81)
On average. mild increase in blood pressure and heart rate; appetite suppression. weight loss. abdominal pain. headache. difficulty falling asleep. insomnia. emotional irritability. intensification of tic manifestations if already present Drug of first choice; sustained-release preparations are available (e81, e82)
Dexamfetamine Psychostimulant 0.1–0.5 mg/kg BW 0.8–1.0 ca. 2
(e82)
Efficacy and tolerability comparable to that of MPH; approved if MPH is not sufficiently effective (e81, e82)
Lisdexamfetamine Psychostimulant 30–70 mg Ø  1.0 Prodrug with prolonged effect; approved in Germany if the response to MPH is inadequate (e83)
Atomoxetine Selective norepinephrine reuptake inhibitor (SNRI) 1.2 mg/kg BW 0.5–0.7 ca. 4
(e84)
On average. mild increase in blood pressure and heart rate; mild shortening of QTc. dry mouth. appetite suppression. weight loss. gastrointestinal symptoms. dizziness. headache. drowsiness. fatigue. sedation Drug of first choice in the presence of a comorbid tic. anxiety. or substance disorder; otherwise. drug of second choice (e84)
Guanfacine Central
α2-agonist
1–5 mg 0.6 ca. 4
(e85)
Fatigue. sedation. somnolence. mild lowering of blood pressure and heart rate. mild QTc prolongation Sustained-release preparation available as a drug of second choice if MPH is ineffective or poorly tolerated; metabolized by CYP3A4 (e85, e86)

BW. body weight

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