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final pharma 2nd exam

Total questions: 20

Worksheet time: 30mins

Name
Class
Date
1.

GABA receptors are an example of which of the following receptors type

a)

DNA- linked intracellular receptors

b)

Tyrosine kinase-linked receptors

c)

G-protein-linked receptors

d)

None of the above

2.

Absorption of vitamin B12/intrinsic factor complex by the ileum has occurred under

a)

Facilitated diffusion

b)

Simple diffusion

c)

Endocytosis

d)

Active transport

3.

Which of the following drug(s) is(are) considered a liver microsomal inducer(s):

a)

Phenobarbitone

b)

Testosterone

c)

Na-valporate

d)

Cimetidine

4.

Urinary excretion of amphetamine can be increased by

a)

Using activated charcoal

b)

Use of vitamin C

c)

Decrease urine pH

d)

b and c

5.

All of the following are physical mechanisms of drugs except:

a)

Demulcent

b)

Osmosis

c)

Neutralization

d)

Adsorption

6.

If two drugs have the same efficacy and safety, it is called:

a)

Bioequivalence

b)

Therapeutically equivalence

c)

Bioavailability

d)

a and b

7.

Hemodialysis is useful in treatment of acute toxicity by drugs have:

a)

Low Vd

b)

Low toxicity c

c)

Low bioavailability

d)

a andc

8.

Which of the following is the example for conversion of drug to toxic metabolite:

a)

Phenacetin to paracetamol

b)

Enalapril to Enalaprilater

c)

Methanol to formaldehyde

d)

Non of the bove

9.

The dose required to achieve therapeutic effect in an adult is called

a)

Loading dose

b)

Median effective dose

c)

Therapeutic dose

10.

10-Females usually require smaller doses than males of the same age because

a)

Female sex hormones

b)

Higher body fat

c)

Menstrual cycle

d)

A and B

11.

G-coupled receptor type-i (Gi) like M2-recptors is mediated by:

a)

Increase DAG

b)

Decrcased cyclic AMP

c)

Increase phospholipase-c

d)

A and C

12.

Drug first pass metabolism can be overcome by:

a)

Change the route of drug administration

b)

Use of long-acting formulation

c)

Use of unionized form of the drug

d)

None of the above

13.

Transfer of the drug from the site of administration to the systemic circulation.

a)

Absorption

b)

Distribution

c)

Metabolism

d)

Excretion

14.

Drugs that are extensively bound to plasma proteins and drugs that have a very

high molecular weight are distributed in:

a)

Plasma only

b)

Plasma and interstitial fluid

c)

Interstitial fluid only

d)

All compartments

15.

Drugs that are of low molecular weight, non-ionized, and lipophilic are distributed

in:

a)

Plasma only

b)

Plasma and interstitial fluid

c)

Interstitial fluid only

d)

All compartments

16.

Volume of distribution may be increased by:

a)

Renal failure

b)

Liver failure

c)

Dehydration

d)

A and B

17.

Concerning pharmacokinetics, pick the INCORRECT statement of the following:

a)

Passive diffusion occurs with concentration gradient.

b)

Ionized drugs cannot cross cell membranes.

c)

Active transport needs both energy and carrier.

d)

Conjugation with glucuronic acid is a phase I biotransformation reaction

18.

Prodrug is the drug that:

a)

Converted from active to inactive

b)

Converted from inactive to active

c)

Converted from active-to-active

d)

Converted from inactive to inactive

19.

Lipophilic drugs have the ability to be used in all the following steps EXCEPT:

a)

Difficulty excreted from kidney

b)

Pass Blood brain barrier

c)

Poorly absorbed from GIT

d)

Pass placental barrier

20.

Oral bioavailability of drug 70% means

a)

70% of the drug can reach blood

b)

30% of the drug is lost

c)

70% of the drug is lost

d)

A and B