Title : Augmentative effects of fluvoxamine on duloxetine plasma levels in depressed patients.

Pub. Date : 2011 Nov

PMID : 21979923






3 Functional Relationships(s)
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1 Enzymes involved in duloxetine metabolism are cytochrome P450 isoenzymes (CYP) CYP1A2 and to a lesser extent CYP2D6 whereas the selective serotonin reuptake inhibitor Fluvoxamine is known to be a potent inhibitor of CYP1A2. Duloxetine Hydrochloride cytochrome P450 family 1 subfamily A member 2 Homo sapiens
2 Enzymes involved in duloxetine metabolism are cytochrome P450 isoenzymes (CYP) CYP1A2 and to a lesser extent CYP2D6 whereas the selective serotonin reuptake inhibitor Fluvoxamine is known to be a potent inhibitor of CYP1A2. Duloxetine Hydrochloride cytochrome P450 family 1 subfamily A member 2 Homo sapiens
3 Our findings indicate that duloxetine plasma levels can be enhanced by a potent CYP1A2 inhibition by FLX and that DLX, even in higher plasma levels, seems to be well tolerated. Duloxetine Hydrochloride cytochrome P450 family 1 subfamily A member 2 Homo sapiens