140
72.7k
Chapter:

Pharmacodynamics & Pharmacokinetics Solved MCQs

in Pharmacological Principles

These multiple-choice questions (MCQs) are designed to enhance your knowledge and understanding in the following areas: Biology .

Chapters

Chapter: Pharmacodynamics & Pharmacokinetics
1.

Which of the following drugs has an average half life of 50 hours?

A. Nortriptylline
B. Digoxin
C. Trimethoprim
D. Valproic acid
E. Lithium
Answer» B. Digoxin
2.

All of the following have 100% oral bioavailability EXCEPT

A. Valproic acid
B. Trimethoprim
C. Digoxin
D. Diazepam
E. Lithium
Answer» C. Digoxin
3.

All of the following drugs are >90% plasma protein bound EXCEPT

A. Diazepam
B. Frusemide
C. Fluoxetine
D. Gentamicin
E. Warfarin
Answer» D. Gentamicin
4.

Which of the following drugs has a volume of distribution >2000 ℓ/70kg?

A. Aspirin
B. Imipramine
C. Digoxin
D. Propranolol
E. Chloroquine
Answer» E. Chloroquine
5.

What is the half life of a drug with a volume of distribution of 100ℓ/70kg and a clearance of 7ℓ/hr/70kg

A. 5 hours
B. 10 hours
C. 12.5 hours
D. 15 hours
E. 20 hours
Answer» B. 10 hours
6.

All of the following drugs exhibit flow dependent elimination EXCEPT

A. Atenolol
B. Isoniazid
C. Propoxyphene
D. Amitriptylline
E. Lignocaine
Answer» A. Atenolol
7.

Which of the following undergoes a phase I hydrolysis reaction? (biotransformation)

A. Ethanol
B. Naloxone
C. Morphine
D. Lignocaine
E. Diazepam
Answer» D. Lignocaine
8.

Which of the following undergoes acetylation in the liver? (Phase 2 biotransformation)

A. Isoniazid
B. Acetaminophen
C. Salicylic acid
D. Epinephrine
E. Diazepam
Answer» A. Isoniazid
9.

A D Response B C Concentration Which of these drugs is the most efficacious?

A. Drugs A and B
B. Drug C
C. Drugs A and D
D. Drugs D and C
E. Drug A
Answer» C. Drugs A and D
10.

Referring to the graph in question 9 – which of the drugs is most potent?

A. A
B. B
C. C
D. D
E. A and B
Answer» A. A
11.

EC50 is

A. Measured with a radioactive receptor
B. Always equal to Kd
C. Drug concentration with 50% receptors bound
D. Representation of the receptors affinity for drug binding
E. Drug concentration with 50% of maximal drug effect
Answer» E. Drug concentration with 50% of maximal drug effect
12.

Which of the following will NOT alter the volume of distribution of a drug?

A. Cardiac failure
B. Clearance
C. Age
D. Burns
E. Pleural effusion
Answer» B. Clearance
13.

Volume of distribution equals

A. Dose given/plasma concentration
B. Total amount of drug in the body/plasma concentration
C. Urine drug concentration/plasma concentration
D. Dose given/urine concentration
E. Urine drug concentration/plasma concentration
Answer» B. Total amount of drug in the body/plasma concentration
14.

Which of the following drugs undergoes rate limited elimination?

A. Lignocaine
B. Morphine
C. Warfarin
D. Propanolol
E. Aspirin
Answer» E. Aspirin
15.

Ligand gated channel receptors include all of the following EXCEPT

A. GABA
B. Aspartate
C. Glycine
D. Glutamate
E. Ach-muscarinic
Answer» E. Ach-muscarinic
16.

Regarding receptor regulation

A. Receptor down regulation occurs over hours – days
B. Receptor responses to drugs often “desensitise” with time – this desensitisation is usually irreversible
C. The mechanism of agonist induced desensitisation of the nicotinic Ach receptor has been worked out in detail
D. All “internalised” receptors are degraded by lysosomes
E. None of the above are correct
Answer» A. Receptor down regulation occurs over hours – days
17.

Which of the following acts on intracellular receptors

A. Serotonin
B. Glucagon
C. Corticosteroids
D. GABA
E. Insulin
Answer» C. Corticosteroids
18.

Which of the following has ↑ bioavailability in the neonate when compared with older children/adults?

A. Penicillin
B. Digoxin
C. Acetaminophen
D. Diazepam
E. Phenobarbital
Answer» A. Penicillin
19.

First order kinetics

A. Means rate of reaction is proportional to concentration
B. Are more common than zero order kinetics
C. Apply to exponential processes
D. Generally apply to high plasma concentrations (>20mg/100ml) of ethanol
E. Result in steady state concentrations after multiple dosing
Answer» D. Generally apply to high plasma concentrations (>20mg/100ml) of ethanol
20.

A single compartment model means that

A. One exponential term describes the decreasing plasma concentration of the drug
B. A single exponential term describes the rise in plasma concentration following oral administration
C. The drug does not penetrate tissues
D. The drug is restricted to the ECF
E. The drug is highly ionised
Answer» A. One exponential term describes the decreasing plasma concentration of the drug

Done Studing? Take A Test.

Great job completing your study session! Now it's time to put your knowledge to the test. Challenge yourself, see how much you've learned, and identify areas for improvement. Don’t worry, this is all part of the journey to mastery. Ready for the next step? Take a quiz to solidify what you've just studied.