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Pharmacotherapeutics for Advanced Practice Nurse Prescribers: Questions & Answers, Exams of Health sciences

A comprehensive q&a guide for advanced practice nurse prescribers, covering a wide range of topics related to pharmacotherapy. It includes questions and answers on various drugs, their side effects, contraindications, and appropriate uses. The guide also provides information on immunization, bariatric surgeries, and drug interactions. It is a valuable resource for nurse prescribers seeking to expand their knowledge and improve patient care.

Typology: Exams

2023/2024

Available from 04/18/2024

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DO NOT COPY
PHARMACOTHERAPEUTICS FOR ADVANCED PRACTICE NURSE
PRESCRIBERS,QUESTIONS & ANSWERS FULLY ANALYSED EDITION EXAM 100%
CORRECTLY/VERIFIED ANSWERS WITH SATISFACTION GUARANTEED SUCCESS
LATEST UPDATE ,5TH EDITION WOO ROBINSON TEST BANK, [GRADED A+.]
Chapter 1.
An Introduction to Pharmacogenetics
Multiple Choice
Identify the choice that best completes the statement or answers the question.
1. Genetic polymorphisms account for differences in metabolism, including:
1. Poor metabolizers, who lack a working enzyme
2. Intermediate metabolizers, who have one working, wild-type allele and one mutant
3. Extensive metabolizers, with two normally functioning alleles
4. All of the above
2. Up to 21% of Asians are ultra-rapid 2D6 metabolizers, leading to:
1. A need to monitor drugs metabolized by 2D6 for toxicity
2. Increased dosages needed of drugs metabolized by 2D6, such as the
selective seroto reuptake inhibitors
3. Decreased conversion of codeine to morphine by CYP 2D6
4. The need for lowered dosages of drugs, such as beta blockers
3. Rifampin is a nonspecific CYP450 inducer that may:
1. Lead to toxic levels of rifampin and must be monitored closely
2. Cause toxic levels of drugs, such as oral contraceptives, when coadministered
3. Induce the metabolism of drugs, such as oral contraceptives, leading to therapeutic
4. Cause nonspecific changes in drug metabolism
4. Inhibition of P-glycoprotein by a drug such as quinidine may lead to:
1. Decreased therapeutic levels of quinidine
2. Increased therapeutic levels of quinidine
3. Decreased levels of a coadministered drug, such as digoxin, that
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DO NO TCOP Y PHARMACOTHERAPEUTICS (^) FOR ADVANCED PRACTICE NURSE PRESCRIBERS,QUESTIONS & ANSWERS FULLY ANALYSED EDITION EXAM 100% CORRECTLY/VERIFIED ANSWERS WITH SATISFACTION GUARANTEED SUCCESS LATEST UPDATE ,5TH EDITION WOO ROBINSON TEST BANK, [GRADED A+.] Chapter 1. An Introduction to Pharmacogenetics Multiple Choice Identify the choice that best completes the statement or answers the question.

  1. Genetic polymorphisms account for differences in metabolism, including:
    1. (^) Poor metabolizers, who lack a working enzyme
    2. (^) Intermediate metabolizers, who have one working, wild-type allele and one mutant
    3. (^) Extensive metabolizers, with two normally functioning alleles
    4. (^) All of the above
  2. Up to 21% of Asians are ultra-rapid 2D6 metabolizers, leading to:
    1. (^) A need to monitor drugs metabolized by 2D6 for toxicity
    2. (^) Increased dosages needed of drugs metabolized by 2D6, such as the selective seroto reuptake inhibitors
    3. (^) Decreased conversion of codeine to morphine by CYP 2D
    4. (^) The need for lowered dosages of drugs, such as beta blockers
  3. Rifampin is a nonspecific CYP450 inducer that may:
    1. (^) Lead to toxic levels of rifampin and must be monitored closely
    2. (^) Cause toxic levels of drugs, such as oral contraceptives, when coadministered
    3. (^) Induce the metabolism of drugs, such as oral contraceptives, leading to therapeutic
    4. (^) Cause nonspecific changes in drug metabolism
  4. Inhibition of P-glycoprotein by a drug such as quinidine may lead to:
    1. (^) Decreased therapeutic levels of quinidine
    2. (^) Increased therapeutic levels of quinidine
    3. (^) Decreased levels of a coadministered drug, such as digoxin, that

DO NO TCOP Y PHARMACOTHERAPEUTICS (^) FOR ADVANCED PRACTICE NURSE PRESCRIBERS,QUESTIONS & ANSWERS FULLY ANALYSED EDITION EXAM 100% CORRECTLY/VERIFIED ANSWERS WITH SATISFACTION GUARANTEED SUCCESS LATEST UPDATE ,5TH EDITION WOO ROBINSON TEST BANK, [GRADED A+.] requires P-glycopr absorption and elimination

  1. (^) Increased levels of a coadministered drug, such as digoxin, that requires P-glycopro absorption and elimination
  2. Warfarin resistance may be seen in patients with VCORC1 mutation, leading to:
  3. (^) Toxic levels of warfarin building up
  4. (^) Decreased response to warfarin
  5. (^) Increased risk for significant drug interactions with warfarin
  6. (^) Less risk of drug interactions with warfarin
  7. Genetic testing for VCORC1 mutation to assess potential warfarin resistance is required prior to prescribing warfarin.
  8. (^) True
  9. (^) False
  10. Pharmacogenetic testing is required by the U.S. Food and Drug Administration prior to prescribing:
  11. (^) Erythromycin
  12. (^) Digoxin
  13. (^) Cetuximab

DO NO TCOP Y PHARMACOTHERAPEUTICS (^) FOR ADVANCED PRACTICE NURSE PRESCRIBERS,QUESTIONS & ANSWERS FULLY ANALYSED EDITION EXAM 100% CORRECTLY/VERIFIED ANSWERS WITH SATISFACTION GUARANTEED SUCCESS LATEST UPDATE ,5TH EDITION WOO ROBINSON TEST BANK, [GRADED A+.]

  1. (^) Increased elimination of active, nonmetabolized drug
  2. (^) Slowed metabolism of a prodrug into an active drug, leading to an accumulation of
  3. A provider may consider testing for CYP2D6 variants prior to starting tamoxifen for breast cancer to:
  4. (^) Ensure the patient will not have increased adverse drug reactions to the tamoxifen
  5. (^) Identify potential drug-drug interactions that may occur with tamoxifen
  6. (^) Reduce the likelihood of therapeutic failure with tamoxifen treatment
  7. (^) Identify poor metabolizers of tamoxifen

DO NO TCOP Y PHARMACOTHERAPEUTICS (^) FOR ADVANCED PRACTICE NURSE PRESCRIBERS,QUESTIONS & ANSWERS FULLY ANALYSED EDITION EXAM 100% CORRECTLY/VERIFIED ANSWERS WITH SATISFACTION GUARANTEED SUCCESS LATEST UPDATE ,5TH EDITION WOO ROBINSON TEST BANK, [GRADED A+.] Chapter 1. An Introduction to Pharmacogenetics Answer Section MULTIPLE CHOICE

  1. ANS: 4 PTS: 1
  2. ANS: 2 PTS: 1
  3. ANS: 3 PTS: 1
  4. ANS: 4 PTS: 1
  5. ANS: 2 PTS: 1
  6. ANS: 2 PTS: 1
  7. ANS: 3 PTS: 1
  8. ANS: 3 PTS: 1
  9. ANS: 2 PTS: 1

ANS:

1 PTS: 1

ANS:

2 PTS: 1

ANS:

3 PTS: 1

Chapter 2. Review of the Basic Principles of Pharmacology Multiple Choice Identify the choice that best completes the statement or answers the question.

  1. A patient’s nutritional intake and laboratory results reflect hypoalbuminemia. This is critical to prescribing because:
    1. Distribution of drugs to target tissue may be affected.
    2. The solubility of the drug will not match the site of absorption.
    3. There will be less free drug available to generate an effect.
    4. Drugs bound to albumin are readily excreted by the kidneys.
  2. Drugs that have a significant first-pass effect:
    1. Must be given by the enteral (oral) route only
    2. Bypass the hepatic circulation
    3. Are rapidly metabolized by the liver and may have little if any desired action
    4. Are converted by the liver to more active and fat-soluble forms
  3. The route of excretion of a volatile drug will likely be the:
    Kidneys
    1. Lungs
    2. Bile and feces
    3. Skin
  4. Medroxyprogesterone (Depo Provera) is prescribed intramuscularly (IM) to create a storage reservoir of the drug. Storage reservoirs:
  1. Assure that the drug will reach its intended target tissue
  2. Are the reason for giving loading doses
  3. Increase the length of time a drug is available and active
  4. Are most common in collagen tissues
  5. The NP chooses to give cephalexin every 8 hours based on knowledge of the drug’s:
  6. (^) Propensity to go to the target receptor 2.^ Biological half-life
  7. Pharmacodynamics
  8. Safety and side effects
  9. Azithromycin dosing requires that the first day’s dosage be twice those of the other 4 days of the prescription. This is considered a loading dose. A loading dose:
  10. Rapidly achieves drug levels in the therapeutic range
  11. Requires four- to five-half-lives to attain
  12. Is influenced by renal function
  13. Is directly related to the drug circulating to the target tissues
  14. The point in time on the drug concentration curve that indicates the first sign of a therapeutic effect is the:
  15. Minimum adverse effect level
  16. Peak of action
  1. An exaggerated response to competitive drug agonists
  2. Factors that affect gastric drug absorption include:
  3. Liver enzyme activity
  4. Protein-binding properties of the drug molecule 3.^ Lipid solubility of the drug
  5. (^) Ability to chew and swallow
  6. Drugs administered via IV:
  7. (^) Need to be lipid soluble in order to be easily absorbed 2.^ Begin distribution into the body immediately
  8. Are easily absorbed if they are nonionized
  9. May use pinocytosis to be absorbed
  10. When a medication is added to a regimen for a synergistic effect, the combined effect of the drugs is:
  11. The sum of the effects of each drug individually
  12. Greater than the sum of the effects of each drug individually
  13. Less than the effect of each drug individually
  14. Not predictable, as it varies with each individual
  15. Which of the following statements about bioavailability is true?
  16. Bioavailability issues are especially important for drugs with narrow therapeutic ranges or sustained- release mechanisms.
  17. All brands of a drug have the same bioavailability.
  18. Drugs that are administered more than once a day have greater bioavailability than

drugs given once daily.

  1. Combining an active drug with an inert substance does not affect bioavailability.
  2. Which of the following statements about the major distribution barriers (blood- brain or fetal-placental) is true?
  3. Water soluble and ionized drugs cross these barriers rapidly.
  4. The blood-brain barrier slows the entry of many drugs into and from brain cells.
  5. The fetal-placental barrier protects the fetus from drugs taken by the mother.
  6. Lipid-soluble drugs do not pass these barriers and are safe for pregnant women.
  7. Drugs are metabolized mainly by the liver via phase I or phase II reactions. The purpose of both of these types of reactions is to:
  8. Inactivate prodrugs before they can be activated by target tissues
  9. Change the drugs so they can cross plasma membranes
  10. Change drug molecules to a form that an excretory organ can excrete
  11. Make these drugs more ionized and polar to facilitate excretion
  12. Once they have been metabolized by the liver, the metabolites may be:
  13. More active than the parent drug
  14. Less active than the parent drug
  15. Totally “deactivated” so they are excreted without any effect 4. All of the above
  16. All drugs continue to act in the body until they are changed or excreted. The ability of the body to excrete drugs via the renal system would be increased by:
  17. Reduced circulation and perfusion of the kidney
  18. Chronic renal disease

Which of the following would reduce or inhibit this process?

  1. Protein malnutrition
  2. Iron-deficiency anemia
  3. Both 1 and 2 2
  4. The time required for the amount of drug in the body to decrease by 50% is called:
  5. (^) Steady state 2. Half-life
  6. Phase II metabolism
  7. Reduced bioavailability time
  8. An agonist activates a receptor and stimulates a response. When given frequently over time, the body may:
  9. Upregulate the total number of receptors
  10. Block the receptor with a partial agonist
  11. Alter the drug’s metabolism
  12. Downregulate the numbers of that specific receptor
  13. Drug antagonism is best defined as an effect of a drug that:
  14. (^) Leads to major physiological and psychological dependence 2.^ Is modified by the concurrent administration of another drug
  15. Cannot be metabolized before another dose is administered
  16. Leads to a decreased physiological response when combined with another drug
  17. Instructions to a client regarding self-administration of oral enteric- coated tablets should include which of the following statements?
  18. Neither 1 nor
  1. “Avoid any other oral medicines while taking this drug.”
  2. “If swallowing this tablet is difficult, dissolve it in 3 ounces of orange juice.”
  3. “The tablet may be crushed if you have any difficulty taking it.”
  4. “To achieve best effect, take the tablet with at least 8 ounces of fluid.”
  5. The major reason for not crushing a sustained-release capsule is that, if crushed, the coated beads of the drugs could possibly result in:
  6. Disintegration
  7. Toxicity
  8. Malabsorption
  9. Deterioration
  10. Which of the following substances is the most likely to be absorbed in the intestines rather than in the stomach?
  11. Sodium bicarbonate
  12. Ascorbic acid
  13. Salicylic acid
  14. Glucose
  15. Which of the following variables is a factor in drug absorption?
  16. (^) The smaller the surface area for absorption, the more rapidly the drug is absorbed. 2.^ A rich blood supply to the area of absorption leads to better absorption.
  17. The less soluble the drug, the more easily it is absorbed.
  18. Ionized drugs are easily absorbed across the cell membrane.

Chapter 2. Review of the Basic Principles of Pharmacology Answer Section MULTIPLE CHOICE

ANS

1 PTS: 1

ANS

3 PTS: 1

ANS

2 PTS: 1

ANS

3 PTS: 1

ANS

2 PTS: 1

ANS

1 PTS: 1

ANS

3 PTS: 1

ANS

4 PTS: 1

ANS

2 PTS: 1

AN

S

3 PTS: 1

AN

S

2 PTS: 1

12 AN 3 PTS: 1

. S

AN

S

2 PTS: 1

AN

S

2 PTS: 1

AN

S

1 PTS: 1

AN

S

2 PTS: 1

AN

S

3 PTS: 1

AN

S

4 PTS: 1

AN

S

4 PTS: 1

AN

S

2 PTS: 1

AN

S

4 PTS: 1

AN

S

3 PTS: 1

AN

S

4 PTS: 1

AN

S

2 PTS: 1

AN

S

4 PTS: 1

Chapter 3. Rational Drug Selection Multiple Choice Identify the choice that best completes the statement or answers the question.

  1. An NP would prescribe the liquid form of ibuprofen for a 6-year-old child because:
    1. Drugs given in liquid form are less irritating to the stomach. 2. A 6-year-old child may have problems swallowing a pill.
    2. Liquid forms of medication eliminate the concern for first-pass effect.
    3. Liquid ibuprofen does not have to be dosed as often as the tablet form.
  2. In deciding which of multiple drugs used to use to treat a condition, the NP chooses Drug A because it:
    1. Has serious side effects and it is not being used for a life-threatening condition
    2. Will be taken twice daily and will be taken at home
    3. Is expensive, but covered by health insurance
    4. None of these are important in choosing a drug
  3. A client asks the NP about the differences in drug effects between men and women. What is known about the differences between the pharmacokinetics of men and women?
    1. Body temperature varies between men and women.
    2. Muscle mass is greater in women.
    3. Percentage of fat differs between genders.
    4. Proven subjective factors exist between the genders.
  4. The first step in the prescribing process according to the World Health Organization is:
  1. Choosing the treatment
  2. Educating the patient about the medication 3. Diagnosing the patient’s problem
  3. (^) Starting the treatment
  4. Treatment goals in prescribing should:
  5. Always be curative 2. Be patient-centered
  6. Be convenient for the provider
  7. Focus on the cost of therapy
  8. The therapeutic goals when prescribing include(s):
  9. Curative
  10. Palliative
  11. Preventive
  12. All of the above
  13. When determining drug treatment, the NP prescriber should:
  14. Always use evidence-based guidelines
  15. Individualize the drug choice for the specific patient
  16. Rely on his or her experience when prescribing for complex patients
  17. Use the newest drug on the market for the condition being treated