Medication | United States trade name (generic availability) | Description of release and duration of action | Initial dose* | Dose advancement | Maximum dose (per day) |
Methylphenidate | |||||
Methylphenidate ER chewable tablets
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Methylphenidate XR-ODT
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Methylphenidate ER (OROS)
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Methylphenidate LA
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Methylphenidate CD
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Methylphenidate XR
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Methylphenidate XR oral suspension
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Methylphenidate delayed and extended release capsules
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Methylphenidate transdermal patch¥
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Dexmethylphenidate | |||||
Dexmethylphenidate XR
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Serdexmethylphenidate-dexmethylphenidate
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Amphetamines | |||||
Dextroamphetamine-amphetamine ER
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Dextroamphetamine-amphetamine ER
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Amphetamine ER
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Amphetamine ER
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Dextroamphetamine SR
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Dextroamphetamine transdermal patch¥
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Lisdexamfetamine
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Nonstimulants | |||||
Selective norepinephrine reuptake inhibitors | |||||
Atomoxetine
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Viloxazine ER
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Alpha-2 adrenergic agonists | |||||
Guanfacine ER¶¶
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Clonidine ER tablets¶¶
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Clonidine ER oral suspension¶¶
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CD: controlled dispense; ER: extended release; LA: long-acting; ODT: orally disintegrating tablet; OROS: osmotic controlled release formulation; SR: sustained release; XR: extended release.
* Suggested doses for initiating treatment with long-acting stimulant medications for treatment of children aged ≥6 years.
¶ Cotempla XR-ODT strengths are expressed by the manufacturer as methylphenidate base. Most other methylphenidate product doses are expressed as methylphenidate hydrochloride salt. Cotempla XR-ODT dose needs to be converted to methylphenidate hydrochloride for comparison with other methylphenidate products.
Δ Although the prescribing information indicates that Cotempla XR-ODT should be taken consistently with or without food, we suggest that it be taken consistently with food – given the general stimulant effect of appetite suppression.
◊ Generic (ie, nonproprietary) products are available, however they are not therapeutic equivalents to Concerta or Relexxii. Only Relexxii is available as 45, 63, and 72 mg tablets.
§ This maximum dose exceeds the US Food and Drug Administration (FDA)-approved maximum dose; careful monitoring for adverse effects is warranted.
¥ Patch is applied 2 hours before needed effect and worn for a total of 9 hours. Doses for the methylphenidate and dextroamphetamine patches are not equivalent to those for the oral preparations.
‡ Amphetamine ER oral suspension, tablet, and ODT strengths reflect milligrams of amphetamine base, whereas dextroamphetamine-amphetamine ER capsule strengths reflect milligrams of dextroamphetamine-amphetamine salts. These cannot be substituted on an mg-per-mg basis. Refer to UpToDate content related to dose equivalents of stimulants for attention deficit hyperactivity disorder in children.
† Doses above 40 mg per day total are rarely necessary and warrant close monitoring.
** Mydayis is not approved by the FDA for children <13 years.
¶¶ Different formulations (eg, immediate-release tablets, extended-release tablets, extended-release oral suspension) may not be substituted on a mg-for-mg basis due to pharmacokinetic differences. Discontinuation requires dose tapering to prevent rebound increase in blood pressure.
ΔΔ The typical maximum dose for this age group is 4 mg/day; a maximum dose of 7 mg/day may be used for adolescents >12 years who weigh >58.5 kg (120 pounds), but the 7 mg dose may be associated with somnolence.