by M Deodhar 2024 Cited by 49The drug is extensively metabolized by several cytochrome P450 (CYP450) enzymes and subjected to a myriad of CYP450-mediated drug interactions.
In addition, discontinuation of concomitantly used CYP450 3A4 2B6, 2C19, or 2C9 inducers may also result in an increase in methadone plasma concentration. Follow patients closely for respiratory depression and sedation, and consider dose reduction with changes to drugs affecting CYP450 isoenzymes listed above.
The drug is extensively metabolized by several cytochrome P450 (CYP450) enzymes and subjected to a myriad of CYP450-mediated drug interactions. In a multidrug regimen, preemptive mitigation of drug drug interactions requires knowledge of fluoxetine actions on these CYP450 enzymes.
The cytochrome P450 (CYP450) enzymes are essential to produce numerous agents, including cholesterol and steroids. Learn about how they work, usages, side effects, and a list of drugs.
The cytochrome P450 (CYP450) enzymes are essential to produce numerous agents, including cholesterol and steroids. Learn about how they work, usages, side effects, and a list of drugs.
Drugs that induce CYP450 enzymes taking metronidazole with phenytoin, phenobarbital, or other drug that stimulate CYP450 enzymes can cause metronidazole to leave the body too quickly; Please note that this list may not be complete, and other interactions with drugs not listed here may occur. Metronidazole and Clindamycin
medication regimen and lifestyle factors is important when prescribing drugs metabolized by CYP450 enzymes. Make list private. Cancel
bupropion. Bupropion inhibits CYP450 2D6. Drug Interactions atomoxetine. Bupropion is metabolized by CYP450 2B6; the maximum dose of naltrexone-bupropion
The primary form of drug metabolism for most statins occurs through CYP450 enzymes. The most prevalent CYP450 enzyme subcategories for statin
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