Pharm Mt 1 Part IV

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Pharm Mt 1 Part IV - Quiz

Principles of Pharm (pgs. 26-39; skipped 31-35)


Questions and Answers
  • 1. 

    What detemerines whether an agonist is strong or weak?

  • 2. 

    What is the conversion from lbs to kg?

  • 3. 

    Briefly describe the 4 categories involved int he FDA Pregnancy Risk Factor Categories.

  • 4. 

    Which of the drug monograph sections should an OD review o find info on the half life, onset of action, binding mechanism and elimination?

    • A.

      Indications

    • B.

      Mech of action

    • C.

      Pharmacokinetics/dynamics

    • D.

      Administration

    Correct Answer
    C. Pharmacokinetics/dynamics
    Explanation
    question from lecture

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  • 5. 

    The SCr is a _____ sensitive indicator of renal function than the BUN.

    Correct Answer
    more
    Explanation
    pg. 26

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  • 6. 

    What category for Pregnancy Risk Factors is a contra-indication in women who are or may become pregnant?

    • A.

      A

    • B.

      C

    • C.

      D

    • D.

      X

    • E.

      Both options C and D

    Correct Answer
    D. X
    Explanation
    pg. 37

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  • 7. 

    Which of the following is NOT involved in the hepatobiliary excretion process?

    • A.

      Liver

    • B.

      Bile

    • C.

      Gall bladder

    • D.

      None of the above (all are involved)

    Correct Answer
    D. None of the above (all are involved)
    Explanation
    liver --> gall bladder --> bile --> feces

    pg. 26

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  • 8. 

    Use of actual body weight in obese patients may significanly _______ CrCl.

    Correct Answer
    overestimate
    Explanation
    In obese patients, need to use adujusted body weight (ABW) instead when calculating CrCl and doses.

    pg. 26

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  • 9. 

    High doses of agonists can overcome non-competitive antagonism.

    • A.

      True

    • B.

      False

    Correct Answer
    B. False
    Explanation
    non-competitive antagonism: antagonist binds to sites OTHER THAN the agonist-binding domain

    pg. 29

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  • 10. 

    Renal dose adjustments are not usually needed unless the CrCl is less than ____mL/min.

    • A.

      10

    • B.

      25

    • C.

      50

    • D.

      65

    Correct Answer
    C. 50
    Explanation
    Some drugs do not need to be adjusted until the clearance is lower..

    pg. 27

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  • 11. 

    DNA transcription, steroid production, stimulation of red blood production are all examples of what type of event in response to drug binding to receptor sites?

    • A.

      Activation of cellular function

    • B.

      Inhibition of cellular function

    • C.

      Activation of biochemical processes

    • D.

      Opening or closing of ionic channels

    Correct Answer
    A. Activation of cellular function
    Explanation
    pg. 28

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  • 12. 

    The creatinine clearance of a female is what percent of a males?

    • A.

      55%

    • B.

      65%

    • C.

      75%

    • D.

      85%

    Correct Answer
    D. 85%
    Explanation
    pg.26

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  • 13. 

    How strongly a drug molecule binds to a binding site is referred to as:

    • A.

      Binding strength

    • B.

      Affiliation

    • C.

      Affinity

    • D.

      Affixation

    Correct Answer
    C. Affinity
    Explanation
    pg. 28

    The dissociation constant (K sub D) describes the degree of a drug's affinity for the receptor site. This is the concentration of drug in solution necessary for 50% of given receptors to be occupied (pg. 29)

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  • 14. 

    ________ is a concept often used when comparing the effects in the same class of drugs.

    • A.

      Irreversible antagonism

    • B.

      Drug efficiency

    • C.

      Drug efficacy

    • D.

      Drug potency

    Correct Answer
    D. Drug potency
    Explanation
    -vs-
    Drug efficacy: used when comparing the effects od drugs in DIFFERENT classes or which have different mechs of

    pg. 29

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  • 15. 

    Where do agonists bind?

    • A.

      Intracellular receptors

    • B.

      Plasma membranes

    • C.

      Nuclear membranes

    • D.

      All of the above

    • E.

      More than one of the above

    Correct Answer
    E. More than one of the above
    Explanation
    agonists are drugs which change or affect cellular physiology by binding to INTRACELLULAR RECEPTORS or PLASMA MEMBRANES

    (pg. 29)

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  • 16. 

    What drug info monograph section should an OD review in order to find info on how the drug actually works?

    • A.

      Indications

    • B.

      Mechanism of action

    • C.

      Pharmakodynamics

    • D.

      Dosage

    Correct Answer
    B. Mechanism of action
    Explanation
    question from lecture

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  • 17. 

    The margin between the therapeutic dose and the lethal dose of a drug is termed _____.

    • A.

      Therapeutic index

    • B.

      Lethal index

    • C.

      Margin of safety

    • D.

      Margin of death

    Correct Answer
    C. Margin of safety
    Explanation
    pg. 30

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  • 18. 

    High doses of agnosits can overcome competitive antagonism.

    • A.

      True

    • B.

      False

    Correct Answer
    A. True
    Explanation
    Competitive antagonism: antagonist competes with agonists for receptor site

    pg. 29

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  • 19. 

    The amount of drug required to produce 50% of the maximal response that the drug is capable of inducing is the definition for ___________.

    Correct Answer
    drug potency
  • 20. 

    What Pregnancy Risk Factor Category corresponds to a drug that has no animal or female studies available to determine risks.

    • A.

      A

    • B.

      B

    • C.

      C

    • D.

      D

    • E.

      X

    Correct Answer
    C. C
    Explanation
    pg. 37

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Our quizzes are rigorously reviewed, monitored and continuously updated by our expert board to maintain accuracy, relevance, and timeliness.

  • Current Version
  • Mar 20, 2022
    Quiz Edited by
    ProProfs Editorial Team
  • Dec 11, 2011
    Quiz Created by
    Tseemore
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