Biopharmaceutics MCQs | Part-4

The movement of drug from the dosage formulation to the blood:

The time for which the drug concentration is above the MEC:

The process of metabolism and excretion:

The transfer of drugs and their metabolites from the liver to the bile in the gall bladder, then into the intestine, and then back into circulation:

The decrease in hepatic enzyme activity that results in reduced metabolism of drugs:

The time a drug will stay in the stomach before it is emptied into the small intestine:

The blood filtering process of the nephron:

The relative amount of an administered dose that reaches the general circulation and the rate at which this occurs:

The comparison of bioavailability between two dosage forms:

Linear Pharmacokinetics is:

The characteristic of non-linear pharmacokinetics include:

The drug concentration between Minimum Effective Concentration and Maximum Safe
Concentration is called:

Which of the following is not a pharmacokinetic parameters that describe the plasma level
time curve?

The unit of k for zero order reaction is:

When rate is independent of the reactant concentration, then it is called:

The concentration of drug in plasma above which toxic effects are precipitated is known
as:

Which of the following methods are used to determine Area Under curve?

USP Apparatus 5 is:

______ is the ratio of the mean residence time to the absorption time.

Which route of drug administration shows 100% Bioavailability?

The Initial distribution of drug into the tissue is determined chiefly by:

The absorption of drugs like (quaternary ammonium compounds, sulphonic acid) are
explained by:

Which of the following process is also called "cell drinking"?

Which of the following is a not mechanism of drug absorption through GIT:

Fick's law is used for study of: