.
Fluvastatin is a member of the HMG-CoA reductase inhibitor family of drugs that blocks the body’s production of cholesterol. Fluvastatin is used to lower elevated cholesterol and to slow or prevent hardening of the arteries.
Interactions with Dietary Supplements
Coenzyme Q10
In a randomized, double-blind trial, blood levels of coenzyme Q10 (CoQ10) were measured in 45
people with high cholesterol treated with lovastatin or
pravastatin (drugs related to fluvastatin) for 18
weeks.1 A significant decline in blood levels of CoQ10 occurred with either drug.
One study found that supplementation with 100 mg of CoQ10 prevented declines in CoQ10 when
taken with simvastatin (another HMG-CoA reductase
inhibitor drug).2 Many doctors recommend that people taking HMG-CoA reductase
inhibitor drugs such as fluvastatin also supplement with approximately 100 mg CoQ10 per day,
although lower amounts, such as 10–30 mg per day, might conceivably be effective in
preventing the decline in CoQ10 levels.
Niacin
Niacin is the form of vitamin B3 used to lower cholesterol. Fluvastatin and niacin used
together have been shown to be more effective than either drug alone.3 High-dose
niacin taken with lovastatin (a drug closely related to fluvastatin) may cause muscle
disorders (myopathy) that can become serious (rhabdomyolysis).4 5 Such
problems appear to be uncommon.6 7 No interactions have yet been
reported with fluvastatin and niacin. Nonetheless, until more is known, people taking both
fluvastatin and niacin should be monitored for muscle disorders by the prescribing
physician.
Vitamin A
A study of 37 people with high cholesterol
treated with diet and HMG-CoA reductase inhibitors found blood vitamin A levels increased
during two years of therapy.8 Until more is known, people taking HMG-CoA reductase
inhibitors, including fluvastatin, should have blood levels of vitamin A monitored if they
intend to supplement vitamin A.
Interactions with Foods and Other Compounds
Food
Fluvastatin is equally effective taken with or without food in the evening.9
Alcohol
In a study of 31 people with primary
hypercholesterolemia treated with fluvastatin, six weeks of daily, moderate alcohol
consumption slowed the absorption and metabolism of fluvastatin but did not interfere with its
effectiveness.10
Summary of Interactions for Fluvastatin
| Depletion or interference | Coenzyme Q10 |
|---|---|
| Adverse interaction | Vitamin A* |
| Side effect reduction/prevention | None known |
| Supportive interaction | None known |
| Reduced drug absorption/bioavailability | None known |
| Other (see text) | Niacin |
For the convenience of the reader, the information in the summary is categorized as follows: “Depletion or interference” indicates the drug may deplete or interfere with the absorption or function of the supplement or herb. “Adverse interaction” indicates that the supplement or herb used together with the drug may result in undesirable effects. “Side effect reduction/prevention” indicates the supplement or herb may reduce the likelihood and/or severity of a potential side effect caused by the drug. “Supportive interaction” indicates the supplement or herb may support or aid the function of the drug. “Reduced drug absorption/bioavailability” indicates that the supplement or herb may decrease the absorption and/or activity of the drug in the body. An asterisk (*) next to an item in the summary indicates that the interaction is supported only by weak, fragmentary, and/or contradictory scientific evidence.
References:
1. Mortensen SA, Leth A, Agner E, Rohde M. Dose-related decrease of serum coenzyme Q10 during treatment with HMG-CoA reductase inhibitors. Mol Aspects Med 1997;18(suppl):S137–44.
2. Bargossi AM, Grossi G, Fiorella PL, et al. Exogenous CoQ10 supplementation prevents plasma ubiquinone reduction induced by HMG-CoA reductase inhibitors. Molec Aspects Med 1994;15(suppl):s187–93.
3. Jacobson TA, Chin MM, Fromell GJ, et al. Fluvastatin with and without niacin for hypercholesterolemia. Am J Cardiol 1994;74:149–54.
4. Garnett WR. Interactions with hydroxymethylglutaryl-coenzyme A reductase inhibitors. Am J Health Syst Pharm 1995;52:1639–45.
5. Yee HS, Fong NT. Atorvastatin in the treatment of primary hypercholesterolemia and mixed dyslipidemias. Ann Parmacother 1998;32:1030–43.
6. Jacobson TA, Amorosa LF. Combination therapy with fluvastatin and niacin in hypercholesterolemia: a preliminary report on safety. Am J Cardiol 1994;73:25D–9D.
7. Jokubaitis LA. Fluvastatin in combination with other lipid-lowering agents. Br J Pract Suppl 1996;77A:28–32.
8. Muggeo M, Zenti MG, Travia D, et al. Serum retinol levels throughout 2 years of cholesterol-lowering therapy. Metabolism 1995;44:398–403.
9. Dujovne CA, Davidson MH. Fluvastatin administration at bedtime versus with the evening meal: a multicenter comparison of bioavailability, safety, and efficacy. Am J Med 1994;96:37S–40S.
10. Smit JW, Wijnne HJ, Schobben F, et al. Effects of alcohol and fluvastatin on lipid metabolism and hepatic function. Ann Intern Med 1995;122:678–80.
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