Drug Guide

Generic Name

Levamlodipine Maleate

Brand Names Conjupri

Classification

Therapeutic: Antihypertensive

Pharmacological: Calcium Channel Blocker

FDA Approved Indications

Mechanism of Action

Levamlodipine maleate is a racemic mixture, with the pharmacologically active S-isomer inhibiting calcium influx into vascular smooth muscle and cardiac muscle, leading to vasodilation and decreased blood pressure.

Dosage and Administration

Adult: Typically, 2.5 to 10 mg once daily, adjusted based on response.

Pediatric: Not commonly used in pediatrics; consult specific guidelines.

Geriatric: Start at lower doses due to increased sensitivity and comorbidities, monitor closely.

Renal Impairment: Adjust doses cautiously; no specific dosage adjustment, but monitor blood pressure and renal function.

Hepatic Impairment: Use with caution; start at lower doses due to reduced metabolism.

Pharmacokinetics

Absorption: Well absorbed orally, with peak plasma levels in about 6-12 hours.

Distribution: Extensively protein-bound (~97%), distributed widely.

Metabolism: Primarily hepatic via CYP3A4 to inactive metabolites.

Excretion: Excreted mainly in urine (about 60%) and feces.

Half Life: Approximately 30-50 hours, allowing for once-daily dosing.

Contraindications

Precautions

Adverse Reactions - Common

Adverse Reactions - Serious

Drug-Drug Interactions

Drug-Food Interactions

Drug-Herb Interactions

N/A

Nursing Implications

Assessment: Monitor blood pressure and heart rate regularly. Assess for signs of edema, dizziness, or adverse cardiovascular effects.

Diagnoses:

  • Ineffective tissue perfusion related to vasodilation leading to hypotension.
  • Risk for falls due to dizziness or hypotension.

Implementation: Administer consistently at the same time each day. Educate patient on monitoring blood pressure at home.

Evaluation: Evaluate reduction in blood pressure and monitor for adverse effects; adjust dosage as necessary.

Patient/Family Teaching

Special Considerations

Black Box Warnings:

Genetic Factors: None currently known.

Lab Test Interference: May affect laboratory assessments of liver function or kidney function.

Overdose Management

Signs/Symptoms: Severe hypotension, tachycardia or bradycardia, dizziness, and possibly shock.

Treatment: Supportive care, intravenous fluids, vasopressors for hypotension, occasionally calcium administration if indicated.

Storage and Handling

Storage: Store at room temperature, 20°C to 25°C (68°F to 77°F).

Stability: Stable under recommended storage conditions for the duration of the shelf life.

This guide is for educational purposes only and is not intended for clinical use.