| Drug | Interaction | Comments |
|---|---|---|
| Amlodipine | Modest increase in atorvastatin exposure | Not clinically relevant |
| Antacids | Decreased plasma atorvastatin concentrations | |
| Anticoagulants, oral (e.g., warfarin) | Pharmacologic interaction (e.g., increased PT) unlikely | |
| Azole antifungals |
Itraconazole: 2.5 to threefold increase in atorvastatin AUC Increased risk of myopathy |
Consider using lower initial and maintenance dosages of atorvastatin |
| Bile acid sequestrants | Decreased plasma atorvastatin concentrations | Administer statins ≥1 hour before or at least 2–4 hours after the resin |
| Cyclosporine | 8.7-fold increase in atorvastatin AUC; increased risk of myopathy and/or rhabdomyolysis |
Carefully monitor patients for manifestations of unexplained muscle pain, tenderness, or weakness, particularly following initiation of atorvastatin therapy or an increase in dosage Atorvastatin dosage should not exceed 10 mg daily |
| Digoxin | Increased plasma digoxin concentrations | Monitor appropriately |
| Diltiazem | Increased plasma atorvastatin concentrations | |
| Efavirenz | Possible variable reductions in plasma atorvastatin concentrations | |
| Fibric acid derivatives |
Increased risk of myopathy Fenofibrate: Decreased or increased AUC of atorvastatin reported |
Concomitant use generally should be avoided; if used concomitantly, initiate atorvastatin at low or moderate dosages and consider using lower maintenance dosages of atorvastatin |
| Grapefruit juice (particularly >1.2 L daily) | Increased bioavailability of atorvastatin | |
| HIV protease inhibitors (combination of ritonavir plus saquinavir, combination of lopinavir plus ritonavir) |
Combination of ritonavir plus saquinavir: Threefold increase in atorvastatin AUC and increased risk of myopathy Combination of lopinavir plus ritonavir: 5.9-fold increase in atorvastatin AUC and increased risk of myopathy |
Carefully monitor patients for manifestations of unexplained muscle pain, tenderness, or weakness, particularly following initiation of atorvastatin therapy or an increase in dosage of either drug Consider using lower initial and maintenance dosages of atorvastatin In patients receiving the combination of ritonavir and saquinavir, or the combination of lopinavir and ritonavir, use of atorvastatin dosages >20 mg daily requires appropriate clinical assessment to ensure that the lowest effective dosage is employed |
| Macrolide antibiotics (i.e., clarithromycin, erythromycin) |
Clarithromycin: 4.4-fold increase in atorvastatin AUC and increased risk of myopathy Erythromycin: Increased plasma atorvastatin concentrations and increased risk of myopathy |
Carefully monitor patients for manifestations of unexplained muscle pain, tenderness, or weakness, particularly following initiation of atorvastatin therapy and an increase in dosage of either drug Consider using lower initial and maintenance dosages of atorvastatin In patients receiving clarithromycin, use of atorvastatin dosages >20 mg daily requires appropriate clinical assessment to ensure that the lowest effective dosage is employed |
| Niacin (antilipemic dosages) | Increased risk of myopathy |
Use low dosages of niacin and carefully monitor patients for manifestations of unexplained muscle pain, tenderness, or weakness, particularly following initiation of atorvastatin therapy or an increase in dosage of either drug Consider using lower initial and maintenance dosages of atorvastatin |
| Oral contraceptives | Increased bioavailability of norethindrone and ethinyl estradiol | Caution when selecting an oral contraceptive |
| Rifampin | Possible variable reductions in plasma atorvastatin concentrations | Administer simultaneously, because delayed administration of atorvastatin following administration of rifampin associated with substantial reductions in plasma atorvastatin concentrations |








