The Medical Letter on Drugs and Therapeutics
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1237
Transdermal Methylphenidates (Daytrana) for ADHD
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A transdermal patch formulation of methylphenidate (Daytrana – Noven/Shire) has been approved by the FDA for treatment of attention-deficit/hyperactivity disorder (ADHD) in patients ≥6 years old. Like other methylphenidate products, the patch is a schedule II controlled substance. According to the manufacturer, it will be available in pharmacies by the end of June.

PHARMACOKINETICS — After application of the patch, methylphenidate is not detected in plasma for about 3 hours (range 1-6 hours). Plasma concentrations of the more pharmacologically active d-enantiomer (d-MPH) peak after about 7-9 hours. In children, following a single transdermal methylphenidate application of about 9 hours, plasma concentrations were similar to those found with equivalent doses of long-acting oral methylphenidate (Concerta), but after repeat daily dosing, concentrations were almost double those of the ... more      

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Title: Transdermal Methylphenidates (Daytrana) for ADHD
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