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| (GWAHN-uh-benz ASS-uh-TATE) |
| Wytensin |
| Class: Antihypertensive/Antiadrenergic, centrally acting |
Action Appears to stimulate central alpha2-adrenergic receptors, inhibiting sympathetic outflow from brain to peripheral circulation.
Indications Treatment of hypertension alone or with a thiazide diuretic.
Contraindications Standard considerations.
ADULTS: PO 4 mg bid initially; may increase by 4 to 8 mg daily every 1 to 2 wk; maximum dose 32 mg bid.
CNS depressants: Increased sedation.
Lab Test Interferences None well documented.
CV: Chest pain; edema; arrhythmias; palpitations; atrioventricular dysfunction. CNS: Drowsiness; sedation; dizziness; anxiety; ataxia; depression; sleep disturbances. DERM: Rash; pruritus. EENT: Blurred vision; nasal congestion. GI: Dry mouth; constipation; diarrhea; nausea; vomiting; abdominal discomfort. GU: Urinary frequency; disturbances of sexual function. HEPA: Increased liver enzymes. RESP: Dyspnea. OTHER: Gynecomastia; muscle or joint pain; weakness; taste disorders.
Pregnancy: Category C. Lactation: Undetermined. Children: Safety and efficacy in children < 12 yr not established. Special risk patients: Use with caution in patients with severe coronary insufficiency, recent MI, or cerebrovascular disease. Sedation: Occurs in large percentage of patients. Withdrawal: Do not discontinue therapy without consulting health care provider; drug must be withdrawn gradually to avoid rapid rise in BP.
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