Diltiazem hydrochloride is a slow calcium channel blocker that blocks calcium ion influx during depolarization of cardiac and vascular smooth muscle. It decreases peripheral vascular resistance and causes relaxation of the vascular smooth muscle resulting in a decrease of both systolic and diastolic blood pressure
藥動學
Bioavailability: approximately 93% to greater than 95%
Vd: 305 L to 391 L
Metabolism: Hepatic; cytochrome P450, extensive, deacetylation, N-demethylation, O-demethylation, and conjugation
Excretion: Renal; 2% to 4% unchanged; not dialyzable
Elimination Half Life: 4 h to 9.5 h
禁忌症
1. Acute MI with pulmonary congestion on x-ray
2. Administration of IV beta-blockers within a few hours of IV diltiazem
3. Atrial fibrillation or flutter associated with an accessory bypass tract (Wolff-Parkinson-White or short PR syndromes); risk of potentially fatal heart rate fluctuations
4. Cardiogenic shock
5. Heart block, second or third-degree atrioventricular without a functioning ventricular pacemaker
6. Hypersensitivity to diltiazem
7. Newborns; some IV injections contain benzyl alcohol
8. Sick sinus syndrome without a functioning ventricular pacemaker
9. Symptomatic hypotension, systolic blood pressure 90 mmHg or less
10. Ventricular tachycardia; may lead to hemodynamic deterioration and ventricular fibrillation
懷孕分類
C(FDA) (AUS)
哺乳分類
Maternal medication usually compatible with breastfeeding.(AAP)
WHO documentation states insufficient data.
Infant risk is minimal.(MDX)
Hypertension:
Initial, 120 to 240 mg orally once daily; usual dose, 240 to 360 mg orally once daily, up to 480 mg/day Chronic stable angina:
Initial, 120 to 180 mg orally once daily up to 480 mg once daily
小兒調整劑量
Safety and effectiveness not established in children