RITALIN
Pronunciation: meth-il-FEN-i-dayt (RIT-a-lin)


What it isDopamine and norepinephrine reuptake inhibitor; ADHD and narcolepsy.
Why this oneIts exceptional formulation range includes short-acting, osmotic-release, liquid, chewable, patch, and bedtime-dosed products.
What limits itAppetite loss, insomnia, and slowed growth can end treatment; monitor blood pressure, heart rate, and misuse.
Read the full label on DailyMed ↗
| FDA dosing | Population | Start | Target | Max |
|---|---|---|---|---|
| ADHD; narcolepsy (general dosing) | Peds ≥6 yr | 5 mg BID (before breakfast & lunch) | Individualized; ↑5–10 mg weekly | 60 mg/day (above not recommended) |
| ADHD; narcolepsy (general dosing) | Adults | 20–30 mg/day in 2–3 divided doses, 30–45 min before meals | 20–30 mg/day average | 60 mg/day |
Titration Peds: increase weekly (5–10 mg increments)
Renal Undefined
Hepatic Undefined
Available strengths
Pregnancy Published data have not identified drug-associated risk of major birth defects/miscarriage; possible CNS-stimulant fetal risks; pregnancy exposure registry available
Lactation Present in milk (infant dose 0.16–0.7% of maternal weight-adjusted dose); no adverse infant reports; monitor infant for agitation, insomnia, anorexia, reduced weight gain
| Strength | #/mo | generic $/unit | CostPlus | |
|---|---|---|---|---|
| 5 mg | tab | per unit | $0.13/ea | not offered |
| 10 mg | tab | per unit | $0.16/ea | not offered |
| 20 mg | tab | per unit | $0.20/ea | not offered |
Other forms: Methylphenidate ER chewable (QUILLICHEW ER) · Methylphenidate ER suspension (QUILLIVANT XR) · Methylphenidate ER (Relexxii) · Methylphenidate LA (RITALIN LA) · Methylphenidate ER (OROS) (CONCERTA) · Methylphenidate XR-ODT (COTEMPLA XR-ODT) · Methylphenidate patch (DAYTRANA) · Methylphenidate ER evening-dosed (JORNAY PM) · Methylphenidate CD (METADATE CD) · Methylphenidate oral solution (METHYLIN SOLUTION)
Generic entry2020
⚠ BOXED WARNING
Legacy pregnancy categoryC
Defining liabilityHypertension, appetite/weight effects, misuse and stimulant-induced psychosis or arrhythmia.
This drug is routinely called serotonergic. By Gillman’s human-effect criteria it does not raise serotonin in the synapse.
No clinically meaningful serotonin-elevating mechanism identified in this first-pass Gillman-based review.
Label contraindicationConcomitant MAOI treatment, or within 14 days of stopping an MAOI (hypertensive crisis risk). The label governs prescribing; Gillman’s point concerns serotonin toxicity only.
Gillman’s four human testsA measurable SERT affinity that fails all four is not clinical serotonicity.
Non-elevating actionNone recorded
Evidence confidenceModerate
Background: what serotonicity is · what is and is not an SRI · what counts as a relevant MAOI.
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