Help:

This exercise is designed to simulate how the change in each of the pharmacokinetic and physiological parameters affects the plasma concentration-time profile after single iv and oral administration.

You are asked to select a value for each of the pharmacokinetic parameters (Dose, ka and Vd) and physiological parameters (Q and CLint )then click plot to simulate the drug concentration-time profile after iv or oral drug administration. The corresponding values for E, F and CLH will be displayed.

Adjust the values for the X and Y axes to see the entire plot by clicking the adjust x scale or adjust y scale buttons.