Drug Guide

Generic Name

Atorvastatin Calcium

Brand Names Lipitor, Atorvaliq

Classification

Therapeutic: Lipid-lowering agent, HMG-CoA reductase inhibitor

Pharmacological: Statin

FDA Approved Indications

  • Hypercholesterolemia
  • Prevention of cardiovascular disease

Mechanism of Action

Inhibits HMG-CoA reductase, an enzyme involved in hepatic cholesterol synthesis, leading to decreased LDL cholesterol and total cholesterol levels.

Dosage and Administration

Adult: Start with 10-20 mg once daily, titrate up to 80 mg as needed.

Pediatric: Not typically recommended for children under 10 years; dosing for adolescents and older children to be determined by healthcare provider.

Geriatric: Adjust dose considering potential increased risk of adverse effects; start at lower end of dosage range.

Renal Impairment: Use with caution; no specific dosage adjustment necessary but monitor renal function.

Hepatic Impairment: Contraindicated in active liver disease; use with caution and monitor liver function.

Pharmacokinetics

Absorption: Well absorbed from gastrointestinal tract.

Distribution: Extensively protein-bound (~98%).

Metabolism: Primarily metabolized by CYP3A4 enzyme.

Excretion: Excreted mainly in feces; urine accounts for a small proportion.

Half Life: About 14 hours.

Contraindications

  • Active liver disease
  • Unexplained persistent elevations of serum transaminases
  • Pregnancy and breastfeeding

Precautions

  • History of liver enzyme abnormalities
  • Muscle pain or weakness during therapy, indicating potential myopathy

Adverse Reactions - Common

  • Muscle pain, weakness (Often)
  • Diarrhea, nausea (Common)
  • Elevations in liver enzymes (Uncommon)

Adverse Reactions - Serious

  • Rhabdomyolysis (Rare)
  • Hepatotoxicity (Rare)

Drug-Drug Interactions

  • Cyclosporine, Gemfibrozil, other strong CYP3A4 inhibitors, certain antibiotics and antifungals

Drug-Food Interactions

  • Large quantities of grapefruit juice may increase plasma levels.

Drug-Herb Interactions

N/A

Nursing Implications

Assessment: Monitor lipid profile, liver enzymes, and muscle enzymes periodically.

Diagnoses:

  • Risk for decreased tissue perfusion related to altered lipid levels
  • Risk for muscle damage

Implementation: Administer once daily; monitor for symptoms of myopathy and liver dysfunction.

Evaluation: Assess lipid levels periodically to determine efficacy and adjust dose accordingly.

Patient/Family Teaching

  • Take medication as prescribed, at any time of day, with or without food.
  • Report unexplained muscle pain, tenderness, weakness, or liver-related symptoms.
  • Maintain a healthy diet and exercise regimen.
  • Limit alcohol consumption.

Special Considerations

Black Box Warnings:

  • Increased risk of diabetes mellitus

Genetic Factors: Genetic variations can influence drug metabolism and response.

Lab Test Interference: May slightly elevate liver transaminases and creatine kinase.

Overdose Management

Signs/Symptoms: Severe muscle pain, weakness, or signs of liver injury.

Treatment: Supportive care; no specific antidote. Hospitalize for monitoring and supportive therapy as needed.

Storage and Handling

Storage: Store at room temperature away from moisture and heat.

Stability: Stable under recommended storage conditions.

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