Drug Interactions between Lipitor and mibefradil
This report displays the potential drug interactions for the following 2 drugs:
- Lipitor (atorvastatin)
- mibefradil
Interactions between your drugs
atorvastatin mibefradil
Applies to: Lipitor (atorvastatin) and mibefradil
CONTRAINDICATED: Rhabdomyolysis has been reported in patients receiving mibefradil and simvastatin. In vitro studies predict that mibefradil inhibits the metabolism of drugs that are substrates of the CYP450 microsomal pathway. HMG-CoA reductase inhibitors are metabolized to varying degrees by this pathway.
MANAGEMENT: The use of mibefradil with simvastatin and lovastatin is considered contraindicated, while the use of mibefradil with cerivastatin or atorvastatin is strongly discouraged by the manufacturers. Fluvastatin and pravastatin may be the preferred alternatives if an HMG-CoA reductase inhibitor must be used with mibefradil, since they are not significantly metabolized by the CYP450 pathway. Consideration should also be given to alternative antihypertensive therapy. However, if these agents must be used together, close observation for evidence of altered clinical effect is recommended. Additionally, the use of any HMG-CoA reductase inhibitor is not recommended in combination with mibefradil and either cyclosporine or tacrolimus, since additive inhibition of the metabolism of the HMG-CoA reductase inhibitor would be expected.
References (4)
- (2001) "Product Information. Posicor (mibefradil)." Roche Laboratories
- Muck W (2000) "Metabolic interactions between mibefradil and HMG-CoA reductase inhibitors: linking in vitro with in vivo information." Br J Clin Pharmacol, 49, p. 87-90
- Schmassmann-Suhijar D, Bullingham R, Gasser R, Schmutz J, Haefeli WE (1998) "Rhabdomyolysis due to interaction of simvastatin with mibefradil." Lancet, 351, p. 1929-30
- Holtzman CW, Wiggins BS, Spinler SA (2006) "Role of P-glycoprotein in statin drug interactions." Pharmacotherapy, 26, p. 1601-7
Drug and food interactions
atorvastatin food
Applies to: Lipitor (atorvastatin)
GENERALLY AVOID: Coadministration with grapefruit juice may increase the plasma concentrations of atorvastatin. The proposed mechanism is inhibition of CYP450 3A4-mediated first-pass metabolism in the gut wall by certain compounds present in grapefruit. When a single 40 mg dose of atorvastatin was coadministered with 240 mL of grapefruit juice, atorvastatin peak plasma concentration (Cmax) and systemic exposure (AUC) increased by 16% and 37%, respectively. Greater increases in Cmax (up to 71%) and/or AUC (up to 2.5 fold) have been reported with excessive consumption of grapefruit juice (>=750 mL to 1.2 liters per day). Clinically, high levels of HMG-CoA reductase inhibitory activity in plasma is associated with an increased risk of musculoskeletal toxicity. Myopathy manifested as muscle pain and/or weakness associated with grossly elevated creatine kinase exceeding ten times the upper limit of normal has been reported occasionally. Rhabdomyolysis has also occurred rarely, which may be accompanied by acute renal failure secondary to myoglobinuria and may result in death.
ADJUST DOSING INTERVAL: Fibres such as oat bran and pectin may diminish the pharmacologic effects of HMG-CoA reductase inhibitors by interfering with their absorption from the gastrointestinal tract.
MANAGEMENT: Patients receiving therapy with atorvastatin should limit their consumption of grapefruit juice to no more than 1 liter per day. Patients should be advised to promptly report any unexplained muscle pain, tenderness or weakness, particularly if accompanied by fever, malaise and/or dark colored urine. Therapy should be discontinued if creatine kinase is markedly elevated in the absence of strenuous exercise or if myopathy is otherwise suspected or diagnosed. In addition, patients should either refrain from the use of oat bran and pectin or, if concurrent use cannot be avoided, to separate the administration times by at least 2 to 4 hours.
References (7)
- Richter WO, Jacob BG, Schwandt P (1991) "Interaction between fibre and lovastatin." Lancet, 338, p. 706
- McMillan K (1996) "Considerations in the formulary selection of hydroxymethylglutaryl coenzyme a reductase inhibitors." Am J Health Syst Pharm, 53, p. 2206-14
- (2001) "Product Information. Lipitor (atorvastatin)." Parke-Davis
- Boberg M, Angerbauer R, Fey P, Kanhai WK, Karl W, Kern A, Ploschke J, Radtke M (1997) "Metabolism of cerivastatin by human liver microsomes in vitro. Characterization of primary metabolic pathways and of cytochrome P45 isozymes involved." Drug Metab Dispos, 25, p. 321-31
- Bailey DG, Malcolm J, Arnold O, Spence JD (1998) "Grapefruit juice-drug interactions." Br J Clin Pharmacol, 46, p. 101-10
- Lilja JJ, Kivisto KT, Neuvonen PJ (1999) "Grapefruit juice increases serum concentrations of atorvastatin and has no effect on pravastatin." Clin Pharmacol Ther, 66, p. 118-27
- Neuvonen PJ, Backman JT, Niemi M (2008) "Pharmacokinetic comparison of the potential over-the-counter statins simvastatin, lovastatin, fluvastatin and pravastatin." Clin Pharmacokinet, 47, p. 463-74
Therapeutic duplication warnings
No warnings were found for your selected drugs.
Therapeutic duplication warnings are only returned when drugs within the same group exceed the recommended therapeutic duplication maximum.
See also
Drug Interaction Classification
Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit. | |
Moderately clinically significant. Usually avoid combinations; use it only under special circumstances. | |
Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan. | |
No interaction information available. |
Further information
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