Webb6 okt. 2024 · Displacement of statins from plasma proteins is unlikely to mediate clinically significant drug interactions. Statins have terminal elimination half-lives that range from less than 5 hours for fluvastatin, lovastatin, pravastatin and simvastatin, to 13 hours for pitavastatin, and between 15 and 30 hours for atorvastatin and rosuvastatin. WebbPitavastatin was used because it has fewer drug interactions than other statins. The study started in 2015 and included more than 100 sites in the US, Canada, Thailand, South Africa, Brazil, Peru, Haiti, Zimbabwe, Botswana, Uganda and India.
Pitavastatin RxWiki
Webb1 apr. 2024 · Call your doctor right away if you have stomach pain, bloating, nausea, vomiting, dark urine, light-colored stools, or yellow eyes or skin. These could be symptoms of liver damage. Make sure any doctor or dentist who … WebbConsidered clinically significant [see Dosage and Administration (2.4),Drug Interactions (7)] Cyclosporine: Pitavastatin 2 mg QD for 6 days + cyclosporine 2 mg/kg on Day 6: ↑ 4.6 fold † ↑ 6.6 fold † Erythromycin: Pitavastatin 4 mg single dose on Day 4 + erythromycin 500 mg 4 times daily for 6 days: ↑ 2.8 fold † ↑ 3.6 fold † Rifampin tool sets with case
Clinically relevant drug interactions between statins and ...
Webb18 feb. 2010 · The purpose of this study was to gain a better understanding of the transport mechanism of pitavastatin, a novel synthetic HMG-CoA reductase inhibitor ... The drug-drug interactions of pitavastatin (NK-104), a novel … Webb19 okt. 2024 · Pitavastatin: if clarithromycin is necessary, consider withholding or dose-reducing pitavastatin for the duration of antibiotic treatment and for two weeks after clarithromycin is discontinued. Use of an alternative antibiotic, for example azithromycin, may be considered. Most statins are metabolised in part by one or more hepatic cytochrome P450 enzymes, leading to an increased potential for drug interactions and problems with certain foods (such as grapefruit juice). The primary metabolism pathway of pitavastatin is glucuronidation. It is minimally metabolized by the CYP450 enzymes CYP2C9 and CYP2C8, but not by CYP3A4 (which is a common source of interactions in other statins). As a result, it is less likely to interact with drugs that are … tool sets on budget