Dexmethylphenidate
Dexmethylphenidate (Focalin) is the pharmacologically active d-threo enantiomer of methylphenidate, approved for ADHD. Delivering the active isomer alone allows roughly half the milligram dose for comparable effect, with a large clinical evidence base inherited from decades of methylphenidate research.
01 Overview
Racemic methylphenidate contains d- and l-threo enantiomers, but nearly all central activity resides in the d-isomer. Dexmethylphenidate isolates that isomer, marketed as immediate-release Focalin and extended-release Focalin XR.
It is a Schedule II stimulant with efficacy and a side-effect profile essentially matching methylphenidate on a milligram-equivalent basis (about 2:1 potency). Abuse and diversion potential are those of any prescription psychostimulant.
02 Mechanism
Blocks the dopamine and norepinephrine transporters (DAT/NET), increasing synaptic catecholamines in striatal and prefrontal circuits; the d-threo isomer carries the transporter affinity.
03 Dosing
| Tier | Dose | Route | Notes |
|---|---|---|---|
| IR | 5–20 mg/day | Oral | Immediate-release, typically split BID; start 2.5 mg twice daily. |
04 Effects
| Effect | Magnitude | Evidence | |
|---|---|---|---|
| Improved attentionReduced inattention and impulsivity in ADHD, comparable to racemic methylphenidate at half the dose. | n/a | Clinical | |
| Increased alertnessHeightened wakefulness and task persistence. | n/a | Clinical |
05 Side effects
| Effect | Severity | Frequency | Evidence | Countermeasures |
|---|---|---|---|---|
| Appetite suppressionReduced appetite that can affect growth in children. | Mild | Very common | Clinical | |
| InsomniaDifficulty sleeping with late dosing. | Mild | Common | Clinical | |
| Cardiovascular stimulationIncreased heart rate and blood pressure. | Moderate | Common | Clinical |