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| (ter-AZE-oh-sin) |
| Hytrin |
| Class: Antihypertensive/Antiadrenergic, peripherally acting |
Action Selectively blocks post-synaptic alpha1-adrenergic receptors, resulting in dilation of arterioles and veins.
Indications Management of hypertension and symptomatic benign prostatic hyperplasia.
Contraindications Hypersensitivity to doxazosin or prazosin.
Hypertension
ADULTS: PO Initial: 1 mg at bedtime. (Do not exceed this as initial dose to avoid severe hypotensive effects; reinstitute at this dose if drug is discontinued for several days). Maintenance: 1–5 mg q day; may consider bid dosing (maximum 20 mg/day).
Benign Prostatic Hyperplasia
ADULTS: PO Initial: 1 mg at bedtime. (Do not exceed this as initial dose); increase dose in stepwise fashion. Usual maintenance: 10 mg q day for minimum of 4–6 wk (maximum 20 mg/day).
Interactions None well documented.
Lab Test Interferences None well documented.
CV: Palpitations; orthostatic hypotension; hypotension; tachycardia; arrhythmias; vasodilation. CNS: Dizziness; nervousness; paresthesia; somnolence; anxiety; headache; insomnia; weakness; drowsiness. DERM: Pruritus; rash; sweating. EENT: Blurred or abnormal vision; conjunctivitis; tinnitus; nasal congestion; sinusitis; epistaxis; pharyngitis. GI: Nausea; vomiting; dry mouth; diarrhea; constipation; abdominal discomfort or pain; flatulence. GU: Impotence; urinary frequency; urinary tract infection. RESP: Dyspnea; bronchitis; bronchospasm; flu symptoms; increased cough. OTHER: Shoulder; neck; back or extremity pain; arthralgia; edema; fever; weight gain.
Pregnancy: Category C. Lactation: Undetermined. Children: Safety and efficacy not established. BPH complications: Long-term effects on incidence of surgery, acute urinary obstruction or other complications of BPH have not been determined. First-dose effect: May cause marked hypotension (especially orthostatic) and syncope at 15–90 min after first few doses, after reintroduction, with rapid increase in dosing, or after addition of another anti-hypertensive; to avoid, initiate dosing with low dose and gradually increase after 2 weeks; monitor patients carefully. Hemodilution: Small decreases in hematocrit, hemoglobin, WBCs, total protein and albumin may occur, possibly because of hemodilution.
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