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CARDIOVASCULAR SYSTEM › ANTIHYPERTENSIVES › ANTIHYPERTENSIVES AND DIURETICS IN COMBINATION › Imidazoline receptor agonists in combination with diuretics
clonidine and diuretics
C02LC01
Forms & Strengths
- Clonidine 0.1-0.3 mg, Hydrochlorothiazide 25 mg tablets
- Clonidine 0.1-0.3 mg, Chlorthalidone 15-30 mg tablets
- Oral capsules and extended-release formulations
Adult Dosing
- Initial dose: Clonidine 0.1 mg, Hydrochlorothiazide 25 mg orally twice daily
- Titrate to 0.2-0.3 mg Clonidine and 25-50 mg Hydrochlorothiazide as needed
- Maximum dose: Clonidine 2.4 mg, Hydrochlorothiazide 100 mg per day
Pediatric Dosing
- Safety and efficacy not established in children under 12 years
- For hypertensive children over 12 years, start with 0.1 mg Clonidine, 12.5 mg Hydrochlorothiazide orally twice daily
- Titrate with caution, not exceeding adult maximum doses
Indications
- Hypertension in patients who are not adequately controlled with single-agent therapy
- Treatment of resistant hypertension
- Management of hypertension in patients with renal impairment
Mechanism of Action
- Clonidine stimulates alpha-2 adrenergic receptors, reducing sympathetic nervous system activity and blood pressure
- Diuretic component (e.g. Hydrochlorothiazide) increases sodium and water excretion, reducing blood volume and pressure
Contraindications
- Hypersensitivity to Clonidine, Hydrochlorothiazide, or sulfonamide-derived diuretics
- Anuria, severe renal impairment, or patients on hemodialysis
- Concomitant use of MAO inhibitors
Adverse Reactions
- Drowsiness, dizziness, fatigue, dry mouth, and constipation from Clonidine
- Hypokalemia, hyperglycemia, and increased uric acid levels from diuretic component
- Rebound hypertension with abrupt Clonidine withdrawal
Drug Interactions
- Enhanced hypotensive effects with other antihypertensives, especially beta-blockers
- Potentiation of sedative effects by CNS depressants, such as opioids and sedatives
- Increased risk of lithium toxicity with diuretic-induced sodium depletion
Curated Content: Needs Vetting Before Put to Clinical Use