Rosuvastatin cyp

Rosuvastatin and pravastatin are mostly excreted unchanged with minor metabolism through CYP3A4 and CYP3A5, with their plasma levels not significantly. Rosuvastatin (Crestor), an HMG-CoA reductase inhibitor (statin), has a favorable pharmacologic profile, including its selective uptake by hepatic cells, hydrophilic nature

2024-03-29
    Effexor xr and energy
  1. 11622/smedj
  2. and, to a lesser extent, by CYP 2C19 and CYP 3A4 isoenzymes
  3. g
  4. In addition, the PK properties of statins also vary (Schachter, 2005)