Frage 1
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The NP is reading the literature about a drug. The article reports that the drug is potent. The NP knows that this means that the drug:
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Produces its effect at low doses
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Produces strong effects at any dose
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Requires high doses to produce its effects
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Is very likely to cause adverse effects
Frage 2
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Except for gene therapy, which statements are true about drug-receptor interactions? SELECT ALL THAT APPLY
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Drugs can mimic the actions of endogenous molecules.
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Receptors for drugs do not respond to hormones and neurotransmitters produced by the body.
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The binding of a drug to its receptor is usually irreversible.
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Drugs can block the actions of endogenous molecules.
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Drugs can give the cell new functions.
Frage 3
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Which assessment findings suggest hypersensitivity of the receptors when a patient suddenly stops taking atenolol (Tenormin), a beta 2 receptor antagonist that slows the heart rate?
Frage 4
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A patient who has over dosed on methadone HCL (Metadol), an opiate, is brought to the emergency department unresponsive with severely depressed respirations. The patient receives intravenous naloxone HCL (Narcan), an opiod antagonist, with a dramatic improvement in the level of consciousness and respiratory rate and effort within minutes. Which is the priority action 45-60 minutes after the naloxone HCL is administered?
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Assess for the return of pain because the effect of the naloxone HCL should be peaking.
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Assess the need to administer another dose of naloxone HCL because the respiratory and CNS depression may return as the medication effect ends.
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Prepare to administer the drug intramuscularly if the drug has not taken effect.
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Prepare to counter act the effects of the opiod withdrawal.
Frage 5
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When the therapeutic index of a drug is narrow, what should the NP expect?
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Blood levels of the drug would be monitored throughout the therapy.
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The drug would produce the desired effect at low doses.
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The drug would produce many adverse effects at low doses.
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The drug would only be used in an emergency.
Frage 6
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Pharmacodynamics includes the study of how drugs work.
Frage 7
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Phase 2 of the dose response relationship starts at the point when the therapeutic effect does not increase with the increasing dose.
Frage 8
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Maximal efficacy is defined as the largest effect that a drug can produce.
Frage 9
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Potency is defined as the dose of drug needed to get the desired effect.
Frage 10
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Two drugs in the same therapeutic class with different recommended doses (2mg vs. 200mg) can have equal effects.
Frage 11
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A drug that stimulates a family of receptors that are transcription factors does not reach a therapeutic effect until taken regularly for 2wks.
Frage 12
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A drug that is selective for specific receptors will produce more unintended effects than a nonselective drug.
Frage 13
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If a drug is selective for specific receptors it is safe.
Frage 14
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Affinity is the strength of attraction between a drug and its receptor.
Frage 15
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Drugs with high intrinsic activity cause an intense response.
Frage 16
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An agonist blocks the stimulation of a receptor.
Frage 17
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If a receptor is constantly bombarded by a drug, the cell can down-regulate and decrease the response to the drug.
Frage 18
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If a patient suddenly stops taking an antagonist drug, he can have a hypersensitivity of the receptor and overstimulation.
Frage 19
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The ED 50 is usually the recommended dose for the drug.
Frage 20
Antworten
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Change in drug structure; makes drug more hydrophilic
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Change in drug structure/movement out of the body
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Movement of drug from blood into tissues/cells
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Movement of drug into and out of the body; what body does to drug
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Movement of drug into the blood
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Movement of drug out of the body
Frage 21
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Change in drug structure; makes drug more hydrophilic
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Change in drug structure/movement out of the body
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Movement of drug from blood into tissues/cells
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Movement of drug into and out of the body; what body does to drug
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Movement of drug into the blood
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Movement of drug out of the body
Frage 22
Antworten
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Change in drug structure; makes drug more hydrophilic
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Change in drug structure/movement out of the body
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Movement of drug from blood into tissues/cells
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Movement of drug into and out of the body; what body does to drug
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Movement of drug into the blood
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Movement of drug out of the body
Frage 23
Antworten
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Change in drug structure; makes drug more hydrophilic
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Change in drug structure/movement out of the body
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Movement of drug from blood into tissues/cells
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Movement of drug into and out of the body; what body does to drug
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Movement of drug into the blood
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Movement of drug out of the body
Frage 24
Antworten
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Change in drug structure; makes drug more hydrophilic
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Change in drug structure/movement out of the body
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Movement of drug from blood into tissues/cells
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Movement of drug into and out of the body; what body does to drug
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Movement of drug into the blood
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Movement of drug out of the body
Frage 25
Antworten
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Change in drug structure; makes drug more hydrophilic
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Change in drug structure/movement out of the body
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Movement of drug from blood into tissues/cells
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Movement of drug into and out of the body; what body does to drug
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Movement of drug into the blood
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Movement of drug out of the body
Frage 26
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Which of the following labs would suggest to the NP that a patient may be at risk for drug toxicity secondary to impaired excretion?
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AST 72 IU
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INR 4.2
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eGFR 30mL/min
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WBC 13,000 mm3
Frage 27
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What is the priority action to assist a patient in PACU to promote excretion of most anesthetics?
Frage 28
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Lanoxin (Digoxin) is a drug with a narrow therapeutic index. Which interventions would be critical for the NP to implement? SELECT ALL THAT APPLY.
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Administer the medication only on a PRN basis.
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Monitor the patient for therapeutic and toxic effects
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Be diligent about the timing of drug administration
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Monitor blood levels of the drug
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Teach the patient that the drug takes several weeks to reach its peak effect
Frage 29
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Grapefruit juice inhibits the CYP 450 system enzymes (CYP3A4 enzyme specifically) and inhibits p-glycoprotein in the intestines for days after ingestion. This especially affects calcium channel blockers, benzodiazepines, cyclosporine, and “statin” drugs. The NP would explain to the patient that ingesting grapefruit juice causes:
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Excessive first-pass effect
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Excess levels of drug in the blood
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Lack of therapeutic drug effect
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Rapid excretion of the drug
Frage 30
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A patient receiving Vancomycin for a serious infection, has been ordered to have a peak and trough level drawn. When would the NP order these blood levels to be obtained?
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Peak level 1.5-hours after infusion and trough level 30 minutes before the next dose.
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Peak level 1.5-hours before infusion is started and trough level immediately after infusion of the drug is completed.
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Peak level while the drug is infusing and trough level trough level immediately after infusion of the drug is completed.
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Peak level while the drug is infusing and trough level 30 minutes before the next dose.
Frage 31
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A patient has stopped taking levothyroxine (Synthroid) 3 days ago. The drug has a half-life of 7 days. The patient tells the NP that the drug must not have been necessary because he/the patient does not feel any different. Which of the following is the basis of the NP’s explanation for this phenomenon?
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The patient’s dose was probably too high, so the drug is still working.
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The patient could not have been taking the drug as prescribed.
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The drug probably was not needed if the pt. has not experienced symptoms.
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The drug’s previous doses have not been completely eliminated from the body.
Frage 32
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The NP prescribes the following medications for a patient: glyburide (Diabeta) 10mg by mouth daily for diabetes and quinapril HCL (Accupril) 20mg by mouth daily for hypertension. The NP should advise Quinipril (ACEI) potentiates the action of glyburide (sulfonylureas) so the patient should be cautioned to monitor for signs and symptoms of hypoglycemia. The dose of the glyburide may need adjustment. In addition, the meds (specially the glyburide) should be administered with breakfast.
Frage 33
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Which of the following is true for a drug that acts as a reversibly-binding partial agonist?
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The effect of the drug cannot be overcome by an increase in the endogenous agonist.
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The drug will have an effect on the Emax of the endogenous agonist.
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The drug will have an effect on EC50 of the endogenous agonist.
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The drug will effectively decrease the efficacy of the endogenous agonist.
Frage 34
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Which of the following is most dependent on a drug's EC50?
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Drug potency.
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Drug efficacy.
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Volume of Distribution.
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Therapeutic Index.
Frage 35
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In the following illustration, which drug is the most efficacious?
Frage 36
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In the following illustration, if B is an endogenous agonist, A is most likely?
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A competitive inhibitor.
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A noncompetitive inhibitor.
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An allosteric potentiator.
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It is impossible to tell based in the information in this graph.
Frage 37
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In the follow graph, which of the following parameters is a comparison of ED50 to LD50?
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Therapeutic Index
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Standard Safety Margin
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Therapeutic Window
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None of the above
Frage 38
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Which of the following is not a factor influencing drug membrane passage?
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Molecular size
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Lipid solubility
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Volume of distribution
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Degree of ionization
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Concentration gradient
Frage 39
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The fraction of drug reaching circulation following administration is known by which abbreviation?
Frage 40
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Which of the following routes of absorption are in the correct order in terms of rate of absorption?
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intravenous = subcutaneous > inhalational > intramuscular > oral
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intravenous = inhalational > subcutaneous > intramuscular > oral
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intravenous = inhalational > intramuscular > oral > subcutaneous
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intravenous = inhalational > intramuscular > subcutaneous > oral
Frage 41
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Which of the following is true regarding the graph below?
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Drug B has an availability equal to that of drug A.
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Drug C has a rate equal to that of drug A.
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The availability of B & C are dictated by their peak plasma concentration.
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The difference in AUC between A and C dictate their relative availabilities.
Frage 42
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Concerning drug receptor interactions, the constant Kd refers to:
SELECT ALL THAT APPLY
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maximal physiological effect
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maximal binding
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the drug concentration required to occupy 50% of receptors
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drug concentration that results in half-maximal physiological response
Frage 43
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Signal transduction involves G protein coupled receptor systems:
SELECT ALL THAT APPLY
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biogenic amines
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peptide hormones
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eicosanoids
Frage 44
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Example(s) of second messenger effect(s):
SELECT ALL THAT APPLY
Frage 45
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EC50 mainly reflects a drug's:
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maximal effect
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potency
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lethality
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ease of elimination
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safety
Frage 46
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Physiological processes mediated by the intracellular second messenger, cyclic AMP:
SELECT ALL THAT APPLY
Frage 47
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Drug effects are thought to be proportional to the number of occupied receptors
Frage 48
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Nitric oxide mediates this effect on vascular smooth muscle:
Frage 49
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Receptors are usually:
Frage 50
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Longer-lasting physiological response to drug:
Frage 51
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True statement(s) concerning competitive inhibition:
SELECT ALL THAT APPLY
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competitive in addition is based on reversible drug/antagonist binding at receptor sites
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with competitive inhibition, the dose-effects curve the shifted to the left
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with competitive inhibition, maximal drug effect cannot be obtained, even at high agonist concentrations
Frage 52
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Example(s) of endogenous ligands that interact with membrane-integrated ion channels and affect(s) ion conductance.
SELECT ALL THAT APPLY
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acetylcholine
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GABA
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glutamate
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aspartate
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glycine
Frage 53
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Example(s) of (a) receptor(s) which is/are enzyme(s):
SELECT ALL THAT APPLY
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dihydrofolate reductase
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acetylcholinesterase
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monoamine oxidase
Frage 54
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Primary mechanism by which cAMP effects are terminated:
Frage 55
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An example of a receptor which is a structural protein.
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Na/K ATPase
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acetylcholinesterase
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tubulin
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DNA
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phospholipase C
Frage 56
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An example of an agent that exerts much of its effects through intracellular receptors that in complex form binds to DNA response elements:
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acetylcholine
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dopamine
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corticosteroids
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diltiazem
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atropine
Frage 57
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Factors that may cause variation in drug responsiveness:
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changes in the number or function of receptors
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tachyphylaxis
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idiosyncratic drug responses
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hypersensitivity reactions
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all of the above
Frage 58
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Major roles of receptors:
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determine rate of drug elimination
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determine drug action selectivity
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provide a means of blocking drug action as well as mediating drug action
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act as drug storage sites
Frage 59
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Concerning oral administration -- disadvantages
SELECT ALL THAT APPLY
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least economical
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drug taken orally may cause emesis
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drug taken orally may be destroyed by gastric acidity
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drug taken orally may be metabolized by gastrointestinal flora
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drug taken orally may be inconsistently absorbed due to the presence of food
Frage 60
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Factors That Can Affect Pharmacokinetics
SELECT ALL THAT APPLY
Frage 61
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Factors That Affect Bioavailability:
SELECT ALL THAT APPLY
Frage 62
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Factors affecting absorption:
SELECT ALL THAT APPLY
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Formulation
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Mechanics of absorption
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pH
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Molecular size
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Lipophilicity
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2nd messengers
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Cellular environment
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Ionization
Frage 63
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Most drugs are strong acids (-) or bases (+)
Frage 64
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Uncharged drugs are more lipid soluble
Frage 65
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Ionized drug molecules more lipid soluble
Frage 66
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You can create a non-ionized form of an acidic drug by placing it in an acidic environment
Frage 67
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Drugs with low molecular weight pass through membrane pores more easily
Frage 68
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Active transport is drug movement from area of higher
concentration to lower concentration
Frage 69
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Biotransformation reactions occur first with Phase I followed by Phase II.
Frage 70
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CYP cytochromes are non-specific, so they could all act on the same drugs.
Frage 71
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Biotransformation occurs:
SELECT ALL THAT APPLY
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liver
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intestines
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skin
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lungs
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kidney
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brain
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muscles
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heart
Frage 72
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During Phase II biotransformation, drugs can conjugate with which of the following:
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glucoronic acid
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sulphuric acid
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acetic acid
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amino acid
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all of the above
Frage 73
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Conjugation occurs during Phase I of biotransformation
Frage 74
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Enzyme induction can cause potential toxicity
Frage 75
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Only certain drugs are hepatotoxic
Frage 76
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Alcoholism and fatty liver disease affect drug metabolism
Frage 77
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Factors that affect drug metabolism:
SELECT ALL THAT APPLY
Antworten
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Age
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Comorbidities
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Liver dysfunction
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Gender
Frage 78
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In an 18-month-old baby, these factors could affect biotransformation:
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P-450 enzymes not fully developed
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blood brain barrier not fully developed
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intestinal enzymes not fully developed
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renal system not fully developed
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none of the above
Frage 79
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A drug must be biotransformed to be excreted
Frage 80
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Clearance is the sum of elimination from liver, kidneys, and GI tract.
Frage 81
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All drugs are excreted by the kidneys.
Frage 82
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After age [blank_start]50[blank_end] people lose [blank_start]10[blank_end] percent of kidney nephrons
every decade.
Frage 83
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You see a pt with HTN. You've given him a prescription for an antihypertensive BID. He returns in 30 days and his blood pressure is 150/85. He admits to noncompliance with BID dosing. You educate him about the importance of taking the medication as prescribed, because once daily is not enough to maintain adequate blood levels. This is an example of:
Frage 84
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A patient is taking multiple doses of 100 mg of metoprolol. At what does of medication will the patient reach steady state?
[blank_start]_____[blank_end] mg
Frage 85
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A patient is given a single dose of morphine for pain relief before leaving the hospital. Since he can't drive while under the influence, he wants to know how long until he can drive. The half-life if morphine is 2 hours. What is your answer?
Antworten
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2 hours
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4 hours
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6 hours
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8 hours
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10 hours
Frage 86
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What substances are excreted via the lungs?
Antworten
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Alcohol
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Liquid
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Gas
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Volatile substance
Frage 87
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Your pregnant patient develops a DVT. You place her on heparin. She mentions she doesn't like shots. Should you place her on warfarin instead to increase medication compliance?
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Yes, drug compliance is very important. Because DVTs are so serious, increasing drug compliance is the primary concern.
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No, heparin is better for the baby.
Frage 88
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Until age 2, children have [blank_start]80[blank_end]% body water, in contrast to adults, who have [blank_start]60[blank_end]%.
Frage 89
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Despite differences in body makeup, infants and children have consistent rates of absorption.
Frage 90
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A laboratory is conducting a study to assess the safety, efficacy, and potency of a group of drugs before allowing the agents to proceed to clinical trials. The figure shows the dose-response curves for four different drugs from the same class of medications (Drugs A, B, C, & D). Which of the following is true regarding these medications?
Antworten
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Drug A has greater efficacy than Drug D
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Drug D has greater efficacy than Drug A
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Drug A has greater potency than Drug D
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Drug D has greater potency than Drug A
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All four drugs (A,B,C,D) have equal potencies
Frage 91
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An overweight patient comes to see you about heart palpitations and high blood pressure. You're trying to decide between a once-daily beta blocker and one given every 6 hours. You feel the once-daily is the best choice. Is this correct?
Antworten
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Yes, this is the best choice because once-daily will help with medication compliance.
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No, this is not the best choice because your patient is overweight.
Frage 92
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Characteristics of fat-soluble drugs:
cell membrane potential [blank_start]_____[blank_end]
pH [blank_start]_____[blank_end]
molecular size [blank_start]_____[blank_end]
Half-life [blank_start]_____[blank_end]
Vd [blank_start]_____[blank_end]
Ionization [blank_start]_____[blank_end]
Absorption [blank_start]_____[blank_end]
Route of administration [blank_start]_____[blank_end]
Metabolized by [blank_start]_____[blank_end]
Frage 93
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Characteristics of water-soluble drugs:
cell membrane potential [blank_start]_____[blank_end]
pH [blank_start]_____[blank_end]
molecular size [blank_start]_____[blank_end]
Half-life [blank_start]_____[blank_end]
Vd [blank_start]_____[blank_end]
Ionization [blank_start]_____[blank_end]
Absorption [blank_start]_____[blank_end]
Route of administration [blank_start]_____[blank_end]
Metabolized by [blank_start]_____[blank_end]
Antworten
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Cross on their own
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Use 2nd messengers
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Acidic
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Basic
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Large
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Small
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Long
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Short
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High
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Low
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Charged
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Uncharged
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Difficult to absorb
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Easily absorbed
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PO
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IV
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It doesn't really matter
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Kidneys
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Liver