Monograph Details

Central Nervous System > ADHD/narcolepsy
DAYTRANA
Manufacturer
Shire US, Inc.
Legal Classification
CII
Pharmacological Class
CNS stimulant.
Generic Name
Methylphenidate 10mg, 15mg, 20mg, 30mg; delivered over 9 hours; transdermal patches.
Indications
Attention deficit hyperactivity disorder (ADHD).
Children
<6 years: not recommended. 6–12 years: Initial: apply one 10mg patch to hip 2 hours before desired effect, remove 9 hours after application; may remove earlier if shorter duration of effect or late day side effects appear. May titrate dose at 1-week intervals. Reevaluate periodically. Rotate application sites.
Adults
Not applicable.
Contraindications
Marked anxiety, tension, agitation. Glaucoma. Motor tics. History of Tourette's syndrome in patient or family. During or within 14 days of MAOIs.
Precautions
Discontinue if contact sensitization is suspected; may develop systemic sensitization with other MPH formulations (see literature). Avoid exposing patch to direct external heat sources. Structural cardiac abnormalities. Psychosis. Seizure disorders. EEG abnormalities. Hypertension. History of drug dependence or alcoholism. Monitor growth, BP, CBCs, differential, and platelet counts. Pregnancy (Cat.C). Nursing mothers.
Interactions
See Contraindications. May potentiate oral anticoagulants, anticonvulsants (eg, phenobarbital, phenytoin, primidone), tricyclics (eg, imipramine, clomipramine, desipramine), SSRIs. Caution with pressor agents, α2-agonists (eg, clonidine).
Adverse Reactions
Application site reactions (eg, erythema), decreased appetite, insomnia, GI upset, weight loss, anorexia, nasal congestion, affect lability, tics, headache, irritability, nasopharyngitis, blurred vision (follow up if occurs).
How Supplied
Patches—10, 30
Additional Resources
Related Prescribing Note