Atorvastatin
[98 cents per tablet]
ADMINISTRATION ROUTES:
- PO
ALTERNATIVE NAMES:
- Lipitor
ICU INDICATIONS:
- secondary prevention in patients with coronary artery disease
- treatment of hypercholesterolaemia
PRESENTATION AND ADMINISTRATION:
- PO:
10mg, 20mg, 40mg and 80mg strengths (white). Tablets may be crushed and adminstered via NG tube.
DOSAGE:
- PO:
Commenced at 10-20mg daily at night; slowly increase to a maximum of 80mg if required.
DOSAGE IN RENAL FAILURE AND RENAL REPLACEMENT THERAPY:
- Dose as in normal renal function
DOSAGE IN PAEDIATRICS:
- PO:
Familial hypercholesterolaemia:
0.2mg/kg daily, increased every 4 weeks to a maximum of 1.6mg/kg daily.
CLINICAL PHARMACOLOGY:
- Atorvastatin is a selective, competitive inhibitor of HMG-CoA reductase. Atorvastatin is rapidly absorbed after oral administration; maximum plasma concentrations occur within 1-2 hours. It can be taken with or without food.
CONTRAINDICATIONS:
- Active liver disease or unexplained persistent elevations of serum transaminases.
- Hypersensitivity to any component of this medication.
WARNINGS
- Liver Dysfunction:
HMG-CoA reductase inhibitors, like some other lipid-lowering therapies, have been associated with biochemical abnormalities of liver function. - Skeletal Muscle:
Rare cases of rhabdomyolysis with acute renal failure secondary to myoglobinuria have been reported with atorvastatin and with other drugs in this class.
PRECAUTIONS
- General:
Patients should be advised to report promptly unexplained muscle pain, tenderness, or weakness, particularly if accompanied by malaise or fever. - Laboratory Tests:
CK should be measured if there is concern about development of myopathy due to statins. - Drug/Laboratory Test Interactions:
None known
IMPORTANT DRUG INTERACTIONS FOR THE ICU
- The risk of myopathy during treatment with other drugs of this class is increased with concurrent administration of cyclosporine, fibric acid derivatives, niacin (nicotinic acid), erythromycin, and azole antifungals
- When multiple doses of atorvastatin and digoxin were coadministered, steady-state plasma digoxin concentrations increased by approximately 20%. Patients taking digoxin should be monitored appropriately.
ADVERSE REACTIONS
- Body as a Whole:
Malaise - Digestive System:
Constipation, derangement of LFTs, flatulence, dyspepsia, and abdominal pain - Nervous System:
Insomnia, dizziness, paresthesia, somnolence - Skin:
Pruritus - Musculoskeletal:
Myalgia, myopathy































