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Proton pump inhibitors are metabolized by the CYP2C19 isoenzyme of [[cytochrome P-450]]. Lanzoprazole is the strongest inhibitor of CYP2C19,<ref name="pmid152581 ...are metabolized by the [[Cytochrome P-450 CYP2C19|CYP2C19]] isoenzyme of [[cytochrome P-450]], may or may not increase adverse cardiac events when given to patients ta

[[Mass screening|Screening]] for [[Cytochrome P-450]] 2C9 polymorphisms may improve [[warfarin]] dosing cmopared to the Ageno a

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

...holesterolemia]] and elevated [[liver]] [[Cytochrome_P-450#Drug_Metabolism|cytochrome p-450 measurements]]. Reproductive studies in rats resulted in no observable effe

...y contribute<ref name="pmid18541823"/>, in some cases due to an abnormal [[cytochrome P-450]] 3A5 allele that may reduce metabolism of [[cortisol]] and [[corticosteron

...en statins are given with patients who are also taking inhibitors of the [[cytochrome P-450]] isoenzyme 3A4.<ref name="pmid23778904">{{cite journal| author=Patel AM, S

...The most important role is in the [[heme]] protein of [[hemoglobin]] and [[cytochrome P-450]], and secondarily for [[myoglobin]], which transports oxygen into muscle c

...ion]] has issued a warning to not use higher doses because of use of the [[cytochrome P-450]] system and also arrhythmias.<ref>{{cite web |url= http://www.fda.gov/Safe

**Non-thienopyridine [[ticagrelor]] does not undergo metabolism by [[cytochrome P-450]] and is a reversible binder

...rular filtration rate]]. Atenolol is ''not'' metabolized in the liver by [[cytochrome P-450]] [http://www.ncbi.nlm.nih.gov/sites/entrez/?db=gene&cmd=Retrieve&dopt=sum

Some interactions are due to the system of [[cytochrome P-450]] enzymes used to clear drugs from the body. These interactions can be comp ...g metabolism. Tables are available to check for drug interactions due to [[cytochrome P-450]] interactions.<ref>{{cite web |url=http://medicine.iupui.edu/flockhart/ |t

Some opioids are metabolized by [[cytochrome P-450]] and [[cytochrome P-450 CYP2D6]].<ref name="pmid19059064">{{cite journal| author=Reynolds KK, Ramey ...ast to [[hydrocodone]], [[oxycodone]] and [[codeine]] and metabolized by [[cytochrome P-450 CYP2D6]] which may lead to variable [[pharmacokinetics]] due to [[single-nu

''CYP2C9'' is an [[isoenzyme]] of [[cytochrome P-450]]. [[Genetic polymorphism|Polymorphisms]] of CYP2C9 explain another 10% of * Interference with warfarin metabolism by [[cytochrome P-450]] CYP2C9 [[isoenzyme]].

...l |issn=}}</ref> that are not metabolized by the CYP3A4 [[isoenzyme]] of [[cytochrome P-450]] ([[naproxen]] is not metabolized by CYP3A4). Combining [[glucocorticoid]]

...y contribute<ref name="pmid18541823"/>, in some cases due to an abnormal [[cytochrome P-450]] 3A5 allele that may reduce metabolism of [[cortisol]] and [[corticosteron

* [[Cytochrome P-450]]