Fluvastatin

A to Z Drug Facts

Fluvastatin

 Actions
 Indications
 Contraindications
 Route/Dosage
 Interactions
 Lab Test Interferences
 Adverse Reactions
 Precautions
Patient Care Considerations
 Administration/Storage
 Assessment/Interventions
 Patient/Family Education


(FLEW-vah-stat-in)
Lescol
Capsules: 20 mg
Capsules: 40 mg
Class: Antihyperlipidemic
HMG-CoA reductase inhibitor

 Actions Increases rate at which body removes cholesterol from blood and reduces production of cholesterol in body by inhibiting enzyme that catalyzes early rate-limiting step in cholesterol synthesis; increases HDL; reduces LDL, VLDL, and triglycerides.

 Indications

Hypercholesterolemia: Reduction of elevated cholesterol and LDL cholesterol levels. Atherosclerosis: To slow the progression of coronary atherosclerosis.

 Contraindications Active liver disease or unexplained persistent elevations of LFTs; pregnancy; lactation.

 Route/Dosage

ADULTS: PO 20 to 80 mg qd.

 Interactions

Azole antifungal agents (eg, fluconazole), cyclosporine, gemfibrozil, macrolide antibiotics (eg, erythromycin), niacin: Severe myopathy or rhabdomyolysis may occur with coadministration. Cholestyramine: Reduced absorption of fluvastatin if taken with or up to 4 hr after cholestyramine. Cimetidine, ranitidine, omeprazole: Fluvastatin serum levels may be increased. Digoxin: Digoxin serum levels may be increased. Rifampicin: Fluvastatin serum levels may be reduced.

 Lab Test Interferences None well documented.

 Adverse Reactions

RESPIRATORY: Upper respiratory tract infection; cough; bronchitis. CNS: Headache; dizziness; insomnia; fatigue. EENT: Rhinitis; sinusitis; pharyngitis. GI: Nausea; vomiting; diarrhea; abdominal pain/cramps; constipation; flatulence; dyspepsia. DERMATOLOGIC: Rash; pruritis. OTHER: Muscle cramps/pain; back pain; arthropathy.

 Precautions

Pregnancy: Category X. Lactation: Excreted in breast milk; do not breastfeed while taking. CHILDREN: Safety and efficacy in children younger than 18 yr not established. Liver dysfunction: Use with caution in patients who consume substantial quantities of alcohol or who have a history of liver disease. LFTs: Perform LFTs before initiating therapy, q 4 to 6 wk during the first 3 mo of therapy, q 6 to 12 wk during the next 12 mo (or after a dose increase), and periodically (eg, q 6 mo) thereafter. Skeletal muscle effects: Rhabdomyolysis with renal dysfunction secondary to myoglobinuria has been reported with other drugs in this class. Temporarily withhold therapy in any patient experiencing an acute or serious condition predisposing to the development of renal failure secondary to rhabdomyolysis (eg, sepsis, hypotension). The risk of myopathy with other drugs in this class was found to be increased if therapy with either cyclosporine, gemfibrozil, erythromycin, or niacin is administered concurrently. Consider myopathy in any patient with diffuse myalgias, muscle tenderness or weakness, or marked elevations of CPK. Endocrine effects: Use caution when administering HMG-CoA reductase inhibitors with drugs that affect steroid levels or activity.


PATIENT CARE CONSIDERATIONS


 Administration/Storage

 Assessment/Interventions

 Patient/Family Education

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Copyright
© 2003 Facts and Comparisons
David S. Tatro
A to Z Drug Facts