Clonidine Hydrochloride
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Check Drug InteractionsClonidine Hydrochloride Prescribing Information
Clonidine hydrochloride extended-release tablets are indicated for the treatment of attention deficit hyperactivity disorder (ADHD) as monotherapy and as adjunctive therapy to stimulant medications
[see Clinical Studies (14)].
- Start with one 0.1 mg tablet at bedtime for one week. Increase daily dosage in increments of 0.1 mg/day at weekly intervals until the desired response is achieved. Take twice a day, with either an equal or higher split dosage being given at bedtime, as depicted below
Total Daily Dose | Morning Dose | Bedtime Dose |
| 0.1 mg/day | 0.1 mg | |
| 0.2 mg/day | 0.1 mg | 0.1 mg |
| 0.3 mg/day | 0.1 mg | 0.2 mg |
| 0.4 mg/day | 0.2 mg | 0.2 mg |
- Do not crush, chew or break tablet before swallowing.
- Do not substitute for other clonidine products on a mg-per-mg basis, because of differing pharmacokinetic profiles.
- When discontinuing, taper the dose in decrements of no more than 0.1 mg every 3 to 7 days to avoid rebound hypertension.
Clonidine hydrochloride extended-release tablets are available in a 0.1 mg strength formulation. The 0.1 mg tablets are white to off-white round, biconvex tablets with debossing: "U" on one side and "77" on the other side. Clonidine hydrochloride extended-release tablets must be swallowed whole and never crushed, cut or chewed.
- Renal Impairment: The dosage of clonidine hydrochloride extended-release tablets must be adjusted according to the degree of impairment, and patients should be carefully monitored.
Clonidine hydrochloride extended-release tablets are contraindicated in patients with a history of a hypersensitivity reaction to clonidine. Reactions have included generalized rash, urticaria, and angioedema
[see Adverse Reactions (6)].
- Hypotension/bradycardia/syncope: Titrate slowly and monitor vital signs frequently in patients at risk for hypotension, heart block, bradycardia, syncope, cardiovascular disease, vascular disease, cerebrovascular disease or chronic renal failure. Measure heart rate and blood pressure prior to initiation of therapy, following dose increases, and periodically while on therapy. Avoid concomitant use of drugs with additive effects unless clinically indicated. Advise patients to avoid becoming dehydrated or overheated.
- Somnolence/Sedation: Has been observed with clonidine hydrochloride extended-release tablets. Consider the potential for additive sedative effects with CNS depressant drugs. Caution patients against operating heavy equipment or driving until they know how they respond to clonidine hydrochloride extended-release tablets.
- Cardiac Conduction Abnormalities: May worsen sinus node dysfunction and atrioventricular (AV) block, especially in patients taking other sympatholytic drugs. Titrate slowly and monitor vital signs frequently.
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