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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 ta26 KB (3,487 words) - 14:06, 2 February 2023
- [[Mass screening|Screening]] for [[Cytochrome P-450]] 2C9 polymorphisms may improve [[warfarin]] dosing cmopared to the Ageno a5 KB (713 words) - 17:34, 10 February 2024
- ** Hepatically metabolized by [[cytochrome P-450]] [http://www.ncbi.nlm.nih.gov/sites/entrez/?db=gene&cmd=Retrieve&dopt=summ ===Cytochrome P-450===35 KB (4,629 words) - 08:41, 6 May 2024
- ...holesterolemia]] and elevated [[liver]] [[Cytochrome_P-450#Drug_Metabolism|cytochrome p-450 measurements]]. Reproductive studies in rats resulted in no observable effe10 KB (1,538 words) - 15:31, 8 March 2023
- ...y contribute<ref name="pmid18541823"/>, in some cases due to an abnormal [[cytochrome P-450]] 3A5 allele that may reduce metabolism of [[cortisol]] and [[corticosteron9 KB (1,159 words) - 14:09, 2 February 2023
- ...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, S14 KB (1,963 words) - 10:30, 28 August 2013
- ...The most important role is in the [[heme]] protein of [[hemoglobin]] and [[cytochrome P-450]], and secondarily for [[myoglobin]], which transports oxygen into muscle c8 KB (1,113 words) - 19:55, 28 September 2010
- ...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/Safe11 KB (1,448 words) - 14:12, 2 February 2023
- **Non-thienopyridine [[ticagrelor]] does not undergo metabolism by [[cytochrome P-450]] and is a reversible binder12 KB (1,658 words) - 08:52, 28 June 2011
- ...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=sum16 KB (2,243 words) - 11:52, 2 February 2023
- 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/ |t39 KB (5,361 words) - 17:35, 10 February 2024
- 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-nu42 KB (5,794 words) - 14:08, 2 February 2023
- ''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]].52 KB (7,136 words) - 22:53, 6 April 2014
- ...l |issn=}}</ref> that are not metabolized by the CYP3A4 [[isoenzyme]] of [[cytochrome P-450]] ([[naproxen]] is not metabolized by CYP3A4). Combining [[glucocorticoid]]23 KB (3,133 words) - 17:51, 17 June 2024
- ...y contribute<ref name="pmid18541823"/>, in some cases due to an abnormal [[cytochrome P-450]] 3A5 allele that may reduce metabolism of [[cortisol]] and [[corticosteron53 KB (7,057 words) - 13:53, 5 June 2024
- * [[Cytochrome P-450]]25 KB (3,396 words) - 13:29, 2 April 2024