A semilog graph paper is a graph paper in which the x-axis is a normal linear scale, but the y-axis is a logarithmic scale. Semilog graph paper allows plotting the data at logarithmic intervals without the need for logarithmic transformation.

The y-axis is divided into cycles, each represents 10-fold increase in values (a single log₁₀ unit).

The steady state is the condition when the rate of drug administration is equal to the rate of drug elimination.

When the drug is administered as a constant rate IV infusion, there will be one steady state concentration as long as the rate of administration and the rate of elimination do not change.

When drug administration involves repeated doses, the drug concentration-time profile during each of the dosing intervals ( τ ) will be identical at steady state. This means that the maximum, the minimum, and the average concentrations during each dosing interval will be similar at steady state.

The half life is the time required for the amount of the drug or the plasma concentration of the drug to decrease by 50% . The half life has units of time.

The half life of a drug is constant within a patient (dose and concentration independent) when the drug elimination process follows first-order kinetics.

However, the half life is concentration dependent when the elimination process is saturable (zero-order). The half life is usually longer at higher concentration.

The half life is a very important parameter, because it indicates how fast the drug is eliminated from the body.

The total body clearance is the volume of the plasma or blood that is completely cleared from the drug per unit time. It has units of vloume/time.

The CL_T is the sum of all organ clearances (i.e. renal clearance, metabolic clearance, and other clearances).

The CL_T for a drug is constant within a patient (dose and concentration independent) when the elimination process follows first-order kinetics.

When the drug elimination process follows zero-order kinetics the CL_T is concentration dependent. The CL_T is lower at higher drug concentration.

The volume of distribution is the apparent volume in which the drug can be distributed in. It is the factor that relates the amount of drug in the body to the concentration of the drug in the sampling site. It is not an actual volume, however it is a hypothetical volume determined by the drug distribution behavior.

The volume of distribution ranges from 3-5 liters to more than 25L/kg. Drugs with higher affinity for tissues, have higher volume of distribution.