For a particular drug, in a patient with liver disease the FFP went up and the hepatic clearance went down as compared to healthy patients. What is the most likely cause of this observation?

Drug A, a calcium channel blocker, is 97% plasma protein bound (fup = 0.03); its hepatic plasma clearance is 475 mL/min. Predict the clearance (ml/min) in a patient with hypoalbumenia such that their fup is 0.055. (Use the full equations and do not simplify based on “E” status (i.e low, intermediate or high E).

Drug Q has a V of 2.0 L/kg. What loading dose (mg) (i.v. bolus) is required to rapidly attain a Cp of 15 mg/liter? 

The volume of hepatic blood/plasma flow from which drug is completely removed in a specified time is known as

Drug Q has a V of 2.0 L/kg. What loading dose (mg) (i.v. bolus) is required to rapidly attain a Cp of 15 mg/liter? 

The elimination rate constant (KE) can be calculated from

For a particular drug, in a patient with liver disease the FFP went up and the hepatic clearance went down as compared to healthy patients. What is the most likely cause of this observation?

Which of the following does not involve pharmacokinetics?

How would you like another five points?

Which molecule is most likely to get filtered through the glomerular basement membrane?