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...84">{{cite journal |author=Mega JL, Close SL, Wiviott SD, ''et al'' |title=Cytochrome P-450 Polymorphisms and Response to Clopidogrel |journal=N. Engl. J. Med. |volume ...Mega JL, Close SL, Wiviott SD, Shen L, Hockett RD, Brandt JT et al.| title=Cytochrome p-450 polymorphisms and response to clopidogrel. | journal=N Engl J Med | year= 2

===Cytochrome P-450=== {{main|cytochrome P-450}}

Escitalopram is metabolised by [[cytochrome P-450]] CYP3A4 and [[Cytochrome P-450 CYP2C19|CYP2C19]].

...ome P-450]] (microsomal) enzyme system. ... minimal effects of the drug on cytochrome P-450 enzymes have been suggested, and additional experience with long-term thera

Propranolol is metabolized in the liver by several isoenzymes of [[cytochrome P-450]].

Methadone is metabolized by [[cytochrome P-450]].

...statin]], [[simvastatin]], or [[gemfibrozil]] that are metabolized by [[cytochrome P-450]] may increase bleeding when added to patients taking [[warfarin]].<ref n

...interactions. Tables are available to check for drug interactions due to [[cytochrome P-450]] interactions.<ref>{{cite web |url=http://medicine.iupui.edu/flockhart/ |t ** http://drug-interactions.com - [[Cytochrome P-450]]

...nazole increases cell permeability by interacting with 14-α demethylase, a cytochrome P-450 enzyme necessary in the conversion of [[lanosterol]] to [[ergosterol]], a n

...other [[azole]]-based antifungal agents, it inhibits 14-alpha-methylase, a cytochrome P-450 enzyme that converts [[lanosterol]] to [[ergosterol]], an essential compone

...84">{{cite journal |author=Mega JL, Close SL, Wiviott SD, ''et al'' |title=Cytochrome P-450 Polymorphisms and Response to Clopidogrel |journal=N. Engl. J. Med. |volume

It is not metabolized by [[cytochrome P-450]] [http://www.ncbi.nlm.nih.gov/sites/entrez/?db=gene&cmd=Retrieve&dopt=summ

'''Cytochrome P-450''' is a "superfamily of hundreds of closely related hemeproteins found thro Cytochrome P-450's role in drug metabolism is described by Wolf:<ref name="pmid10723863">{{c

...gn prostatic hypertrophy]]. Both of these medications are metaoblized by [[cytochrome P-450 CYP3A4]].Dutasteride may better prevent acute urinary retention rates than

...agents, itraconazole interacts with 14-<math>\alpha</math>-demethylase, a cytochrome P-450 enzyme necessary to convert [[lanosterol]] to [[ergosterol]], an essential

It is metabolized by [[cytochrome P-450]] [http://www.ncbi.nlm.nih.gov/sites/entrez/?db=gene&cmd=Retrieve&dopt=summ

...medications that induce [[cytochrome P-450]].<ref name="pmid18579817"/> [[Cytochrome P-450]] is a [[hemeprotein]] that consists of a [[heme]] group and [[heme]] is ir

Colchicine is metabolized by the CYP3A4 [[isoenzyme]] of [[cytochrome P-450]] and may interact with other durgs with similar metabolism.<ref name="pmid

Buprenorphine is metabolized by [[cytochrome P-450]], specifically the .<ref name="pmid15743975">{{cite journal| author=Picard

...ncluding [[antidepressant]]s. Coadministration of drugs that inhibit the [[cytochrome P-450]] CYP2D6 and CYP3A4 metabolism of [[antidepressant]]s may increase the risk