Clonidine (Kapvay)
Mechanism of ActionClonidine is an alpha-2 adrenergic receptor agonist. It works by stimulating these receptors in the central nervous system, particularly in the brainstem. This stimulation reduces the release of norepinephrine, leading to a decrease in sympathetic nerve signals. As a result, clonidine calms hyperactivity and impulsivity and promotes focus by regulating the overactive noradrenergic system commonly seen in ADHD.
Clinical Benefits
Dosage Clonidine is available in both immediate-release and extended-release formulations. Kapvay (Extended-Release): Specifically approved for ADHD. Starting Dose: 0.1 mg at bedtime. Titration: Increase by 0.1 mg weekly, divided into morning and bedtime doses. Maintenance Dose: Typically 0.2–0.4 mg/day in divided doses. Maximum Dose: 0.4 mg/day. Dosage adjustments are necessary for individuals with renal impairment or sensitivity to sedation. |
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- Common Side Effects (10-30%):
- Fatigue or drowsiness
- Dry mouth
- Dizziness
- Irritability
- Less Common Side Effects (1-10%):
- Low blood pressure (hypotension)
- Bradycardia (slow heart rate)
- Constipation
- Rare but Serious Side Effects (<1%):
- Syncope (fainting)
- Rebound hypertension upon abrupt discontinuation
- Depression or mood changes
- Clonidine is particularly effective for ADHD patients who struggle with emotional dysregulation, sleep issues, or cannot tolerate stimulants.
- The extended-release formulation (Kapvay) provides steady symptom control and minimizes peaks and troughs.
- Its non-stimulant nature eliminates the risk of abuse, making it a safe choice for long-term use.
Sources:
- Prescribing Information for Kapvay (Clonidine Extended-Release), Concordia Pharmaceuticals.
- Connor DF, et al. "Clonidine for ADHD management: Clinical evidence and considerations." CNS Drugs.
- Wilens TE, et al. "The role of alpha-2 adrenergic agonists in ADHD treatment." Journal of the American Academy of Child & Adolescent Psychiatry.
- FDA Drug Database: Kapvay