Drug X S-warfarin Agents that DECREASE metabolism (inhibit or compete for cytochrome P450) are more important than those that increase metabolism

Drug X R-warfarin and S-warfarin Must also consider that both forms of warfarin can interact with other drugs

Both inhibitors and substrates of a particular CYP isozyme decrease the metabolism of substrates of that isozyme  increased efficacy Inducers increase the metabolism of substrates  decreased efficacy For example, for CYP 2C9, both amiodarone and carvedilol will increase the efficacy of celecoxib, but barbiturates will reduce it

In other words, drugs in the inhibitor and inducer columns can affect drugs in the substrate column, but substrates don’t affect inhibitors and inducers

Substrates can affect other substrates

Taking up the case of warfarin, the active enantiomer is S-warfarin which is metabolized by CYP 2C9.

That means we have to be most concerned by drugs that inhibit CYP 2C i.e., amiodarone, cimetidine, etc., and especially fluvoxamine.

Drug X S-warfarin Drug X R&S-warfarin We also have to worry about drug interactions where warfarin causes an adverse drug interaction with another drug.

Neither warfarin enantiomer is an inducer or an inhibitor of CYP enzymes. So the drugs that could interact are ones that are substrates for the CYP isozymes that EITHER R- or S-warfarin is a substrate of. So you could expect interactions with amitriptyline, carvedilol, amitriptyline and alfentanil (reading just the first drug in the substrate list for each affected isozyme)