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NURS 682 Pharmacology Opener Review Exam 2025

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what the body does to the drug (absorption, distribution, metabolism, excretion) - Correct Ans-Pharmacokinetics what the drug does to the body; mechanism of action Pharmacodynamic study= determining the effect of a specific medication dose in treating a disease - Correct Ans-Pharmacodynamics -Percent of dose enter systemic circulation after PO administration *Fraction of the administered drug that reaches systemic circulation* - Correct Ans-Bioavailability LESS drug there is in circulation and in the tissue, higher first pass effect ex. Simvastatin - Correct Ans-Lower bioavailability the more of the drug that reaches systemic circulation, Lower first pass effect ex. Atorvastatin - Correct Ans-Higher bioavailability Time to maximum drug level observed - Correct Ans-Tmax maximum or peak concentration of drug observed after administration - Correct Ans-Cmax Vd = (amount of drug in the body) / (plasma drug concentration) -distribution of a medication between plasma and the rest of the body; the volume in which the amount of drug would need to be uniformly distributed to produce the observed blood concentration ex. Vancomycin in serum testing for trough levels - Correct Ans-Volume of distribution -Healthy adults 20-30 vs. 60-80 -Older adults get more dehydrated -Medications that are lipophilic will stay longer in the older adult and older adults get -Liver shrinks with age and albumin is synthesized in the liver. There is freer drug available in highly protein bound drugs—-Decrease in serum albumin -Most drugs are biotransformed in the liver, with older adults there is slower transformation and longer half lives - Correct Ans-Volume of distribution: age related changes Aging -less free water, more body fat -lower average serum albumin Hydration Status Compartment and volume - Correct Ans-Factors that influence volume of distribution Biostranformation and/or excretion of oral drug by hepatic mechanisms -occurs prior to entering GI tract Drugs absorbed from the GI tract Extensive hepatic citon Ex. IV vs oral dosages - Correct Ans-First Pass Effect (pre-systemic elimination) Works primarily by stimulating the activity of a receptor site binds to a receptor, causes an effect similar to endogenous compound - Correct Ans-Agonists Clinical action= occupying a receptor site and inhibiting its endogenous activity - Correct Ans-Antagonist small differences in drug dose or blood concentration can be fatal Any pharmaceutical which has 2-fold difference between the minimum toxic concentration and minimum effective concentration in blood - Correct Ans-Narrow therapeutic Index Greater distance between effective dose and toxic dose Ex. Fluoxetine does NOT need drug monitoring - Correct Ans-Wide therapeutic index Drug absorption, distribution, metabolism, excretion Influence dose requirements and/or adverse effects - Correct Ans-Pharmacogenetics: PK genetic influences Drug targets: Receptors, transporters, intracellular signaling pathways, enzymes and metabolic pathways Influence drug efficacy - Correct Ans-Pharmacogenetics: PD genetic influences

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NURS



NURS 682 Pharmacology Opener Review
Exam 2025
what the body does to the drug (absorption, distribution, metabolism, excretion) -
Correct Ans-Pharmacokinetics

what the drug does to the body; mechanism of action

Pharmacodynamic study= determining the effect of a specific medication dose in
treating a disease - Correct Ans-Pharmacodynamics

-Percent of dose enter systemic circulation after PO administration
*Fraction of the administered drug that reaches systemic circulation* - Correct Ans-
Bioavailability

LESS drug there is in circulation and in the tissue, higher first pass effect

ex. Simvastatin - Correct Ans-Lower bioavailability

the more of the drug that reaches systemic circulation, Lower first pass effect

ex. Atorvastatin - Correct Ans-Higher bioavailability

Time to maximum drug level observed - Correct Ans-Tmax

maximum or peak concentration of drug observed after administration - Correct Ans-
Cmax

Vd = (amount of drug in the body) / (plasma drug concentration)

-distribution of a medication between plasma and the rest of the body; the volume in
which the amount of drug would need to be uniformly distributed to produce the
observed blood concentration

ex. Vancomycin in serum testing for trough levels - Correct Ans-Volume of distribution

-Healthy adults 20-30 vs. 60-80
-Older adults get more dehydrated
-Medications that are lipophilic will stay longer in the older adult and older adults get
-Liver shrinks with age and albumin is synthesized in the liver. There is freer drug
available in highly protein bound drugs—->Decrease in serum albumin
-Most drugs are biotransformed in the liver, with older adults there is slower
transformation and longer half lives - Correct Ans-Volume of distribution: age related
changes

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Aging
-less free water, more body fat
-lower average serum albumin

Hydration Status

Compartment and volume - Correct Ans-Factors that influence volume of distribution

Biostranformation and/or excretion of oral drug by hepatic mechanisms
-occurs prior to entering GI tract

Drugs absorbed from the GI tract

Extensive hepatic metabolism.extraciton

Ex. IV vs oral dosages - Correct Ans-First Pass Effect (pre-systemic elimination)

Works primarily by stimulating the activity of a receptor site

binds to a receptor, causes an effect similar to endogenous compound - Correct Ans-
Agonists

Clinical action= occupying a receptor site and inhibiting its endogenous activity - Correct
Ans-Antagonist

small differences in drug dose or blood concentration can be fatal

Any pharmaceutical which has <2-fold difference between the minimum toxic
concentration and minimum effective concentration in blood - Correct Ans-Narrow
therapeutic Index

Greater distance between effective dose and toxic dose

Ex. Fluoxetine does NOT need drug monitoring - Correct Ans-Wide therapeutic index

Drug absorption, distribution, metabolism, excretion

Influence dose requirements and/or adverse effects - Correct Ans-Pharmacogenetics:
PK genetic influences

Drug targets: Receptors, transporters, intracellular signaling pathways, enzymes and
metabolic pathways

Influence drug efficacy - Correct Ans-Pharmacogenetics: PD genetic influences



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Ventricular repolarization prolongation

Ectopic beats with long pause follow by baseline rhythm beat with marked prolonged
QT interval

Underlying risk factors + Adding medications with QT prolonging effects

Known: Amiodarone, Haldol - Correct Ans-Drugs with QT prolongation

OLDER AGE - Correct Ans-Known risk of QT prolongaiton

Older adults have....
-less % body weight as water
-less lean muscle mass
-higher % weight as fat
-LOWER SERIUM ALBUMIN**
-lower relative kidney weight
-less relative hepatic blood flow - Correct Ans-Summary of Age-Related Changes

Unconditionally inappropriate meds & Generally best avoided regardless of
circumstances
Usually alternative available

Conditioned upon disease state & dose
Likely only to be inappropriate in specific context - Correct Ans-Beer's Criteria

Beer's Criteria

**Avoid medications with systemic anticholinergic ridged effect due to risk of confusion,
urinary retention, constipation, visual disturbance and hypotension

DO NOT continue unwise practices that are seen in daily clinical settings

Have multiple choices in a drug class, choose a product with a shorter half life

While PD (pharmakodynamics) doesn't change with gaining some age-related changes
will result in less drug effect

**In the elder: loss of B-2 receptor sites
Less bronchodilator effect with -terol meds - Correct Ans-Age-related changes that
impact drug effect / general pharm rules for the elder

blood urea nitrogen

Evaluation of the amount of nitrogen in the blood in urea form



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Urea= metabolism by-product of proteins by liver, removed from the blood by kidneys -
Correct Ans-BUN

Breakdown product of muscle creatinine phosphate and is usually produced at fairly
constant rate by the body (depending on muscles mass)

**Creatinine is greater with higher muscle mass and lower with low muscle mass** -
Correct Ans-Creatinine

Usually less than 20:1 in presence of appropriate hydration
-Reduced in order hydration

Often elevated in renal disease
-In absence of renal disease, can be transiently elevated in dehydration, ingestion of
extreme amounts of protein, upper/lower GI bleed - Correct Ans-BUN: Creatinine
(BUN:Cr)

Used to calculate GFR to take into account differences b/t male and female

USE IBW

Cr Cl in men
(140-age) x wt in kg/(72 x sCr)

Cr Cl in women
(140-age) x wt in kg/(72 x sCr) x 0.85 - Correct Ans-Cockcroft-Gault equation

Category B= best

Animal studies have not demonstrated fetal risk but no controlled study in humans OR
Animal studies have shown adverse effect but not demonstrated in human study

Beta-lactation abx
-Penicillins
-Cephalosporins

Macrolides
-Azithromycin, erythromycin but NOT clarithromycin - Correct Ans-Antibiotic use in
pregnancy: Category B

No controlled study in humans available
Studies in animals have revealed. Adverse effects on the fetus
-Embryocidal
-Teratogenic
-Other



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