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NUR 641 E FINAL EXAM STUDY GUIDE GRAND CANYON UNIVERSITY QUESTIONS WITH DETAILED VERIFIED ANSWERS

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absorption, distribution, metabolism, excretion Ans: Pharmacokinetics involves absorption from the administration site either directly or indirectly in the blood plasma Ans: Pharmacokinetic absorption reversibly or irreversibly move from the bloodstream into the interstitial and intracellular fluid Ans: Parmacokinetic distribution biotransformed via hepatic metabolism or by other tissue Ans: Pharmacokinetics metabolism 1. highest bioavailability 2. places entire does into venin thus bypassing absorption 3. avoids hepatic first pass metabolism in the liver Ans: Intravenous medications usually reached within 4-5 half lives of the drug Ans: steady state medication time required for the elimination process to reduce concentration of the drug to one half what it was at initial administration mines drug frequency 4. predicts length of toxic effects absorption, distribution, metabolism, excretion Ans: Pharmacokinetics involves absorption from the administration site either directly or indirectly in the blood plasma Ans: Pharmacokinetic absorption reversibly or irreversibly move from the bloodstream into the interstitial and intracellular fluid Ans: Parmacokinetic distribution biotransformed via hepatic metabolism or by other tissue Ans: Pharmacokinetics metabolism 1. highest bioavailability 2. places entire does into venin thus bypassing absorption 3. avoids hepatic first pass metabolism in the liver Ans: Intravenous medications usually reached within 4-5 half lives of the drug Ans: steady state medication time required for the elimination process to reduce concentration of the drug to one half what it was at initial administration mines drug frequency 4. predicts length of toxic effects

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NUR 641
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NUR 641

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December 8, 2025
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Written in
2025/2026
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NUR 641 E FINAL EXAM STUDY GUIDE
GRAND CANYON UNIVERSITY
QUESTIONS WITH DETAILED VERIFIED
ANSWERS
absorption, distribution, metabolism, excretion Ans: Pharmacokinetics
involves

absorption from the administration site either directly or indirectly in the
blood plasma Ans: Pharmacokinetic absorption

reversibly or irreversibly move from the bloodstream into the interstitial
and intracellular fluid Ans: Parmacokinetic distribution

biotransformed via hepatic metabolism or by other tissue Ans:
Pharmacokinetics metabolism

1. highest bioavailability

2. places entire does into venin thus bypassing absorption

3. avoids hepatic first pass metabolism in the liver Ans: Intravenous
medications

usually reached within 4-5 half lives of the drug Ans: steady state
medication

1.the time required for the elimination process to reduce 2.the
concentration of the drug to one half what it was at initial administration

3.determines drug frequency

4. predicts length of toxic effects

5. constant first order pharmacokinetics of a drug Ans: drug half life

, Page | 2

drug is metabolized at a constant rate per unit Ans: zero order
(nonlinear)

metabolizes 50% drugs

inhibit: grapefruit juice

- increase drug -> adverse effects

may have enhanced activity with any other CYP3A4 Ans: CYP3A4

1. discovery or laboratory for development

2. Phase 1 begins with animal testing

3. phase 2 human subjects

4. compare drug to placebo or other drug that is effective

5.FDA then reviews result and determines approval

6. Post market study to determine other side effects that were not seen
while lab testing Ans: Six steps in drug development process

1.Institute of Safe mediation Practice

2. Institute of Medicine

3. Joint commission

4.National Coordinating Council form mediation error reporting and
prevention

5. Food and Drug Administration (safe use initiative) Ans: organizations
for medication safety

1.Also known as a side effect, an undesirable reaction that accompanies
the principal response for which the drug was taken include allergic
reactions and adverse drug effects

, Page | 3

2. Either pharmacological or idiosyncratic

3. 85-90% of ADRs are pharmacological

4. Reporting is not mandated by FDA thus are not commonly reported

5. usually preventable occur in hospital and nursing homes due to med
errors

6. Polypharmacy, multiple doctors and multiple pharmacies increase risk
Ans: Adverse Drug Reaction (ADR)

1. end in pril: lisinopril, captopril, enalapril, ramipril, benazepril and
fosinopril

2. suppress release of angiotensin converting enzyme

3. side effects include cough and angioedema, with angioedema the
medication should be discontinued Ans: Angiotensin-converting enzyme
(ACE) inhibitors

1. -sartan: candesartan, eprosartan, ibesartan, Isosartan, telmisartan,
valsartan

2.block angiotensin 11 receptors Ans: Angiotensin II Receptor Blockers
(ARBs)

Essential HTN accounts for 90% of cases and is also called primary,
secondary may be caused by CKD Ans: Essential vs Secondary HTN

use: angina pectoris

action: dilate veins and arteries and thereby reducing ischemia and
relieving pain by decreasing myocardial O2 consumption

Side effects: throbbing HA, flushing, hypotension tachycardia

available: IV, SL, topical ointment and transdermal patch

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