Trade Names:Cleviprex- Injection, emulsion 0.5 mg/mL
Mediates the influx of calcium during depolarization in arterial smooth muscle.
Plasma protein binding is greater than 99.5%. Steady-state Vd is 0.17 L/kg.
Rapidly metabolized by hydrolysis, primarily by esterases in the blood and extravascular tissues to inactive metabolites.
Cl of the primary dihydropyridine metabolite is 0.03 L/h/kg and terminal half-life is 9 h. Major fraction excreted is 63% to 74% in the urine and 7% to 22% in the feces.
2 to 4 min.
No data available.Hepatic Function Impairment
No data available.
Reduction of BP.
Allergies to soybeans, soy products, eggs, or egg products; patients with defective lipid metabolism such as pathologic hyperlipemia, lipoid nephrosis, or acute pancreatitis if it is accompanied by hyperlipidemia; patients with severe aortic stenosis.
IV Titrate drug to achieve the desired BP reduction. Individualize the dose depending on the BP to be obtained and the response of the patient. Start with 1 to 2 mg/h. The dose may be doubled at 90-sec intervals, initially. As the BP approaches goal, the increase in dose should be less than doubling and the time between dose adjustments should be lengthened to every 5 to 10 min. Approximately a 1 to 2 mg/h increase will generally produce an additional 2 to 4 mm Hg decrease in systolic BP. The desired therapeutic response for most patients occurs at doses of 4 to 6 mg/h. No more than 1,000 mL or an average of 21 mg/h is recommended per 24-h period.
Store in refrigerator at 36° to 46°F. Do not freeze. Vials in cartons may be transferred to 77°F for a period not to exceed 2 months. Once the stopper is punctured, use within 4 h and discard unused portion, including product being infused.
None well documented.
None well documented.
Atrial fibrillation (21%).
Nausea (21%); vomiting (3%).
Acute renal failure (9%).
Monitor heart rate and BP continually during infusion, and then until vital signs are stable; monitor for possible rebound hypertension for at least 8 h after infusion is stopped in patients who receive clevidipine infusions and who are not transitioned to other antihypertensive therapies. Carefully monitor heart failure patients.
Category C .
Safety and efficacy not established.
Use with caution, usually starting at the low end of the dosage range, because of the greater frequency of decreased hepatic, renal, or cardiac function, and concomitant diseases or other drug therapy.
Discontinue beta-blocker by gradually reducing the dose.
Can preclude negative inotropic effects and exacerbate heart failure.
May occur, requiring dosage reduction.
Clevidipine contains approximately 0.2 g of lipid per mL. In some patients with disorders in lipid metabolism, a reduction in the quantity of concomitantly consumed lipids may be necessary to compensate for the amount of lipid in clevidipine.
Expected effect is hypotension with reflex tachycardia.
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