Pharmacology & Pharmacokinetics (Pearson MyLab & Mastering A&P) Flashcards

1
Q

[Pharmacology]

Which of the following schedules involves a pharmacist giving the customer the drug that does not require a prescription?

  • S7
  • S3
  • S1
  • S5
A

S3

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2
Q

[Pharmacokinetics]

Which one of the following is TRUE?

  • Protein binding reduces drug activity.
  • A drug that is bound to albumin can easily pass through biologic membrances.
  • Liver disease decreases plasma concentration of free drug.
  • A drug with low affinity for albumin will displace a drug with high affinity.
A

Protein binding reduces drug activity.

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3
Q

[Pharmacokinetics]

Which of the following involves the action of cytochrome enzymes in inactivating drugs?

  • Metabolism
  • Distribution
  • Excretion
  • Absorption
A

Metabolism

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4
Q

[Pharmacology]

Which of the following terms refers to the need to increase the dose of a drug in order to achieve the same therapeutic effect?

  • tolerance
  • toxicity
  • tachyphylaxis
  • desensitization
A

tolerance

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5
Q

[Pharmacology]

A drug binds completely with its receptor, but this binding results in reduced efficacy. What type of drug is this?

  • full agonist
  • non-competitive antagonist
  • competitive antagonist
  • partial agonist
A

non-competitive agonist

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6
Q

[Pharmacokinetics]

Which one of the following demonstrates that half-life is dependent on the starting concentration of a drug?

  • first-order kinetics
  • single-compartment model
  • zero-order elimination
  • two-compartment model
A

zero-order elimination

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7
Q

[Pharmacokinetics]

Which of the following routes of administration refers to crossing the skin barrier?

  • Sublingual
  • Rectal
  • Transdermal
  • Intramuscular
A

Transdermal

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8
Q

[Pharmacokinetics]

A patient received a drug at a dose of 100 mg. Its plasma concentration is 8 mg/L. What is the volume of distribution of the drug?

  • 8 L
  • 12.5 L
  • 125 L
  • 80 L
A

12.5 L

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9
Q

[Pharmacokinetics]

In a given population, the TD50 is 2 mg, and the LD50 is 40 mg. What is the therapeutic index of the drug?

  • 100
  • 20
  • 200
  • 50
A

20

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10
Q

[Pharmacology]

In a dose-response curve, what drug characteristic can be derived from the plateau (top right end)?

  • variability
  • maximal efficacy
  • therapeutic index
  • potency
A

maximal efficacy

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11
Q

[Pharmacology]

Which of the following items refers to a hepatic phenomenon that can reduce the concentration of the drug available in the blood after oral administration?

  • Ibuprofen
  • Panadol
  • Acetaminophen
  • Aspirin
A

Aspirin

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12
Q

[Pharmacokinetics]

The plasma concentration of the drug is found to be 2 mg/litre. The drug is known to have a volume of distribution of 50 litres for a person of his weight (70 kg). How much drug would you estimate is in his body (total body burden)?

  • 1 mg
  • 12.5 mg
  • 25 mg
  • 100 mg
A

25 mg

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13
Q

[Pharmacokinetics]

If drug A has a maximum safe concentration, 200 mg/L, then above this level a patient would commonly experience which of the following outcomes?

  • Desirable therapeutic effects
  • Suboptimal therapeutic effects
  • No side effects
  • Adverse side effects
A

Suboptimal therapeutic effects

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14
Q

[Pharmacokinetics]

Which one of the following is TRUE regarding first order kinetics?

  • Half-life is directly proportional to drug clearance.
  • Half-life is variable over time.
  • Half-life is independent of plasma concentration.
  • Half-life is inversely proportional to volume of distribution.
A

Half-life is variable over time.

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15
Q

[Pharmacokinetics]

Which one of the following is TRUE regarding half-life?

  • Half-life is unaffected by changes in clearance.
  • If clearance is doubled, half-life is doubled.
  • If the volume of distribution doubles, half-life is halved.
  • Half-life changes in relation to volume of distribution.
A

Half-life changes in relation to volume of distribution.

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16
Q

[Pharmacokinectics]

Which one of the following is TRUE regarding drug excretion?

  • If lipophilic drugs are slowly converted to hydrophilic metabolites, none is reabsorbed back to the blood.
  • Hydrophilic drugs are easily reaborbed by the kidneys.
  • Hydrophilic drugs are excreted by the kidneys.
  • If lipophilic drugs are rapidly converted to hydrophilic metabolites , renal reabsorption predominates.
A

Hydrophilic drugs are excreted by the kidneys.

17
Q

[Pharmacology]

If the ED50 is 10 mg and the LD50 is 200 mg, what is the therapeutic index?

  • 20
  • 100
  • 0.05
  • 2
A

20

18
Q

[Pharmacology]

Which of the following items refers to a hepatic phenomenon that can reduce the concentration of the drug available in the blood after oral administration?

  • distribution
  • absorption
  • desensitization
  • first pass metabolism
A

first pass metabolism

19
Q

[Pharmacokinetics]

Which one of the following facilitates deconjugation of a drug in the gut thus allowing enteral absorption?

  • glucuronidase
  • hydroxylase
  • cytochrome P450
  • oxidase
A

cytochrome P450

20
Q

[Pharmacokinectics]

Which of the following routes of administration will allow a drug to appear immediately in the bloodstream?

  • Subcutaneous
  • Intravenous
  • Topical
  • Oral
A

Intravenous