Yes the drug is heavily metabolized by the liver’s P450 system, specicially CYP3A4.
cat.inist.fr/?aModele=afficheN&cpsidt=3688902
The drug has a near flat-dose response rate according to Merck’s materials as submitted to the FDA for the Propecia trials. Thus 0.25mg is almost the same effect as 5mg on DHT inhibition.
physics.upenn.edu/facultyinf … peciafda2/
If you are a psychiatrist, can you tell us what the consequences of inhibiting Allopregnanolone and THDOC synthesis, and interfering with GABA-A receptor function, would be?
So you are still on the drug? If so your symptoms will not likely clear up unless you quit. If you are a medical professional I would advise you to research this medication so you are aware of it’s many mechanisms of action beyond just “reducing DHT”… curious if you did in fact do this prior to taking it, or simply trusted Merck’s literature? 
Many people have their bloodwork on this forum after taking the drug and finding their Testosterone, LH, FSH crashed and have been left with symptoms of secondary hypogonadism and other hormonal imbalances. Drug is known to alter androgen/estrogen ratio in favor of Estrogens (gynecomastia), changes a man’s hormonal profile to match that of a 5AR2-deficient pseudohermaphrodite, and involutes the prostate – for starters.
I would advise you to get bloodwork if you plan on continuing the medication, also suggest you read the FAQ at top of this site. Unfortunately if you are having side effects, they will likely not go away unless you quit, no matter how much you reduce the dose (due to near flat-dose response).