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Introduction to Biopharmaceutics

Total questions: 15

Worksheet time: 11mins

Name
Class
Date
1.

In pharmacokinetics what does the acronym ADME stand for?

a)

adsorption, distribution, metabolism and excretion

b)

absolute, distribution, metastasis and excretion

c)

absorption, distribution, metabolism and excretion

d)

absorption, distillation, metabolism and excretion

2.

Applications of pharmacoki-

netics studies include:

a)

bioavailability measurements

b)

all of these

c)

correlation of pharmacological responses with

administered doses

d)

effects of physiological and pathological con-

ditions on drug disposition and absorption

· dosage adjustment of drugs in disease states, if

3.

What is the range of Tobramycin (Nebcin, Tobrex)?

a)

4–8 mg /L

b)

4-12 mg/L

c)

5-12 mg/L

d)

None of these

4.

What are the steps involved in developing a new drug ?

a)

Preclinical research

& Investigational New Drug (IND) Application

b)

Phase 1 trials

& Phase II trials

c)

Phase III trials ,

New Drug Application (NDA)

& Approval

d)

All of these

5.

Which of the following is the correct definition of bioavailability?

a)

Bioavailability describes the proportion of the drug administered that is metabolised very quickly and thus is not available to induce a physiological effect.

b)

Bioavailability describes the ability of the administered drug metabolites to cause undesirable physiological effects.

c)

Bioavailability is used to describe the fraction of the dose of drug administered that is present within the body and facilitates the desired physiological effects.

d)

Bioavailability is the length of time an administered drug is present in the body and thus is available to cause a physiological effect.

6.

Elimination is

a)

Absorption and metabolism

b)

Distribution and metabolism

c)

Metabolism and excretion

d)

Distribution and excretion

7.

The time the drug concentration is above the MEC.

a)

Elimination

b)

Absorption

c)

Duration of action

d)

Dosposition

8.

The transfer of a drug out of a dosage form and into the blood is called

a)

Absorption

b)

Metabolism

c)

Elimination

d)

Dissolution

9.

The time MEC is reachedc and the response occurs.

a)

site of action

b)

Therapeutic window

c)

Onset of action

d)

None of above

10.

The rate and extent of drug distribu-

tion is determined by:

a)

how well the tissues and/or organs are perfused

with blood

b)

the binding of drug to plasma proteins and

tissue components

c)

the permeability of tissue membranes to the

drug molecule.

11.

For the calculation of the volume of distribution (vd) one must take :

a)

Concentration of a substance in plasma

b)

A daily dose of drug

c)

Concentration of substance in urine

d)

Therapeutical width of drug action

12.

What is the unit of volume of distribution?

a)

mg

b)

mg/L

c)

L

d)

Cm

13.

What is Vd for total body water?

a)

40

b)

3

c)

17

d)

77

14.

77 is volume of distribution for ____________

a)

Atenolol

b)

Digoxin

c)

Felodipine

d)

Diazepam

15.

Reasons for the variation in concentration of drug distribution are:

a)

Tissue differences in rates of uptake of drugs: Blood flow and capillary permeability

b)

Differences in tissue/blood ratios at equilibrium: Dissolution of lipid-soluble drugs in adipose tissue, binding of drugs to intracellular sites, and plasma protein binding

c)

Apparent volume of distribution (Vd)