pharmacodynamics and pharmacokinetics Flashcards

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1
Q

Two major divisions of pharmacology are:

A)

Biotransformation and elimination.

B)

Pharmacokinetics and pharmacodynamics.

C)

Active transport and diffusion.

D)

Pharmacognosy and biotransformation.

A

pharmacokinetics and pharmacodynamics

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2
Q

Which of the following factors is NOT a component of pharmacokinetics?

A)

Biotransformation

B)

Binding

C)

Distribution

D)

Absorption

A

Binding

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3
Q

Drug A requires the use of adenosine triphosphate (ATP) in order to move into the cellular membrane. This type of diffusion is known as:

A)

Osmosis.

B)

Facilitated.

C)

Elimination.

D)

Active transport.

A

active transport

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4
Q

Glucose in the bloodstream is a large molecule that cannot readily enter a cell unless it binds with insulin. This BEST describes:

A)

Osmosis.

B)

Diffusion.

C)

Carrier-mediated diffusion.

D)

Absorption.

A

carrier mediated diffusion

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5
Q

The term ________ describes the movement of molecules across a membrane down a pressure gradient from an area of higher pressure to and area of lower pressure normally resulting from hydrostatic forces.

A)

Active transport

B)

Carrier-mediated diffusion

C)

Osmosis

D)

Filtration

A

filtration

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6
Q

________ describes the movement of a medication from the site of application into the body and into the extracellular compartment.

A)

Osmosis

B)

Diffusion

C)

Elimination

D)

Absorption

A

absorption

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7
Q

Which of the following is NOT a factor in the absorption of a medication?

A)

pH of the medication

B)

Medication potency

C)

Concentration of the medication

D)

Surface area

A

pH of the medication

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8
Q

Which of the following forms of absorption is generally the slowest due to the decreased vascular supply?

A)

Intramuscular

B)

Sublingual

C)

Subcutaneous

D)

Intravenous

A

subcutaneous

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9
Q

________ BEST describes the process in which a medication is transported from the site of absorption to the site of action.

A)

Distribution

B)

Diffusion

C)

Active transport

D)

Elimination

A

distribution

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10
Q

You are treating a patient who suffers from renal disease and decreased perfusion of the kidneys. What effect will this have on the distribution of a drug that normally acts on kidneys, such as the diuretic medication Lasix?

A)

The drug will be present in increased concentrations at the kidneys resulting in toxicity.

B)

As the kidneys are a primary organ of elimination, the effects of the drug will be unchanged.

C)

The drug will most likely be metabolized by the liver resulting in the same effects systemically.

D)

The drug will be poorly delivered to the kidneys due to a decreased perfusion and will not produce the desired results.

A

the drug will be poorly delivered to the kidneys due to a decreased perfusion and will not produce the desired results

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11
Q

While researching the drug amiodarone, you read that the drug is considered to be highly protein bound upon entering the body. Knowing this, you can deduce that:

A)

The drug is largely ineffective when administered by intravenous route.

B)

The drug remains bound to proteins but will slowly release the active component when necessary resulting in a long half-life.

C)

Much of the drug remains active in the bloodstream and only a small percentage is bound in tissues.

D)

The drugs half-life will be relatively short due to the rapid elimination of the free, or unbound, percentage.

A

the drug remains bound to proteins but will slowly release the active component when necessary resulting in a long half lif

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12
Q

The blood-brain barrier is a preventive barrier that prevents MOST ________ medications from reaching the brain.

A)

Barbiturate

B)

Water-soluble

C)

Lipid-soluble

D)

Non-ionized, unbound

A

water-soluble

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13
Q

The process by which a medication passing through the liver may partially or completely inactivate many medications is known as:

A)

First-pass effect.

B)

Protein reservoir binding.

C)

Plasma binding effect.

D)

Prodrug effect.

A

first pass effect

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14
Q

A medication’s half-life refers to the:

A)

Removal of a medication from the body.

B)

Dose required to be therapeutic.

C)

Time required for the total dose of a medication to be decreased by one-half.

D)

Concentration of a drug.

A

time required for the total dose of a medication to be decreased by one half

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15
Q

________ is the length of time that a medication concentration is sufficient in the blood to produce a therapeutic response.

A)

Efficacy

B)

Affinity

C)

Half-life

D)

Duration of action

A

duration of action

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16
Q

Which of the following is the MOST common way that medications exert their actions?

A)

Changing the physical properties of a cell.

B)

Receptor site binding.

C)

Altering the normal metabolic pathway.

D)

Chemically combining with another chemical.

A

receptor site binding

17
Q

A medication such as nalbuphine binds with a specific receptor site causing an expected effect, but blocks another medication from triggering the receptor. This is known as a/an:

A)

Antagonist.

B)

Agonist-antagonist.

C)

Agonist.

D)

Beta blocker.

A

agonist- antagonist

18
Q

________ is the relative amount of a medication required to produce a desired response.

A)

Antagonism

B)

Therapeutic threshold

C)

Efficacy

D)

Potency

A

potency

19
Q

If a drug exceeds its therapeutic index, the drug will:

A)

Be present in the minimal level and may not cause the desired response.

B)

Be toxic to the patient.

C)

Not have any effect on the patient.

D)

Cause the desired response.

A

be toxic to the patient

20
Q

Which of the following statements is TRUE regarding medication administration to the children and elderly?

A)

Doses need to be significantly higher in both populations to produce the desired effect due to decreased liver functions.

B)

Pediatric patients have well developed livers, while elderly patients suffer from decreased liver function.

C)

Both populations should be treated the same as all patients as the therapeutic index does not change.

D)

Liver and kidney functions in both populations are altered leaving both susceptible to altered medication responses.

A

liver and kidney functions in both populations are altered leaving both susceptible to altered medication responses