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Most interactions were pharmacokinetic, with most actually or theoretically affecting the metabolism of the affected product by way of the cytochrome P450 enzymes.

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A decrease in drug dosage by virtue of an interaction could make the drug ineffective; an increase in drug dosage could make it reach levels that produce side effects.

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Methadone is broken down by an unknown CP450 system enzyme, and there is concern about increased levels when taken with ritonavir.

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Responses to “Drug interactions”

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