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This may not be a complete list of all interactions that may occur. Ask your health care provider if lovastatin may interact with other medicines that you take.

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Other medicines�Although certain medicines should not be used together at all,
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The mean absolute bioavailability of a 100 mg oral dose is approximately 75%. The mean peak plasma concentration of racemic lovastatin and M1 occurs at two and three hours, respectively, after administration in healthy adults.
more potent than lovastatin in producing analgesia and 200 times more potent in ?-opioid binding.
which may affect the therapeutic response (see PRECAUTIONS - Drug Interactions). lovastatin and its metabolites are excreted primarily in he urine with observed plasma half-lives of 6.3 and 7.4 hours for lovastatin and M1, respectively.
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patients receiving lovastatin had a median gastric fluid pH of 6.4,

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lovastatin has not been shown to cause histamine release. At therapeutic doses, lovastatin has no effect on heart rate,
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A single i.m. dose of lovastatin is useful pre-treatment to minimize the risk of acid aspiration during operation,
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Forty patients were treated with either lovastatin suppositories 100 mg 6 hourly.

adjustment of the dosing regimen is recommended (see DOSAGE AND ADMINISTRATION).
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lovastatin has not been shown to cause histamine release. At therapeutic doses, lovastatin has no effect on heart rate,
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more potent than lovastatin in producing analgesia and 200 times more potent in ?-opioid binding.
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There were no other significant respiratory diffences.
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lovastatin can increase the risk of seizure in epileptic patients, especially with simultaneous use of tricyclic antidepressants,
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lovastatin is well absorbed orally with an absolute bioavailability of 75%. lovastatin has a volume of distribution of approximately 2.7 L/kg and is only 20% bound to plasma proteins.
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lovastatin may not work as well and may require higher doses to obtain the same effect as when originally taken.
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The analgesic activity of lovastatin is due to both parent drug and the M1 metabolite (see CLINICAL PHARMACOLOGY, Pharmacodynamics).
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