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NUR 641E Midterm Exam Study Guide| Questions And Well Elaborated Solutions Graded A| Latest updates $9.89   Add to cart

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NUR 641E Midterm Exam Study Guide| Questions And Well Elaborated Solutions Graded A| Latest updates

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NUR 641E Midterm Exam Study Guide| Questions And Well Elaborated Solutions Graded A| Latest updates Pharmacokinetics - answer -The process by which drugs are absorbed, distributed within the body, metabolized, and excreted. -what the body does to the drug First pass - answer -the fact that ...

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  • October 31, 2024
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  • NUR 641E
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NUR 641E Midterm Exam Study Guide|
Questions And Well Elaborated Solutions Graded
A| Latest updates
Pharmacokinetics - answer -The process by which drugs are absorbed, distributed
within the body, metabolized, and excreted.
-what the body does to the drug

First pass - answer -the fact that a medication in the GI tract passes through the
liver before entering other organs

does not - answer -bioequivalence does/does not affect bioavailability

Bioequivalence - answer -relative therapeutic effectiveness of chemically
equivalent drugs.

Bioavailability (is affected by) - answer --chemical instability
-solubility
-first pass metabolism

Cytochrome P450 - answer --enzymes that function to metabolize potentially toxic
compounds, including drugs and products of endogenous metabolism such as
bilirubin, principally in the liver.
-genetics influence presence of enzymes
-affects metabolism of warfarin, antidepressants, antiepileptics, and statins.
-the levels of these drugs are higher when taken with certain drugs that are
inhibitors (ex. warfarin with omeprazole) because there is competition for enzyme
metabolism.
-inducers lead to decreased plasma concentration of drug.

cytochrome p450 inducer - answer -An inducer increases the metabolism of a
substrate resulting in a decreased level or effect of the substrate

, cytochrome p450 inhibitor - answer -An inhibitor decreases the metabolism of a
substrate resulting in an increased level or effect of the substrate.

Clopidogrel - answer -prodrug that must be activated by hepatic CYP2C19
metabolism; individuals who are poor metabolizers may not form the active
metabolite and have reduced antiplatelet response

half-life (determines) - answer -how often a drug is administered

4-5 - answer -steady state is reached in _-_ times the half-life

Warfarin (MOA) - answer --Vitamin K antagonist
-Factors II, VII, IX, X
-takes several days to take effect
-monitor INR

Vitamin K - answer -warfarin antidote

Heparin (MOA) - answer --rapid anticoagulation by binding with antithrombin III
and inhibits factors IXa, Xa, XIIa, and XIII
-aPTT monitoring (low dose SQ does not require monitoring)

Apixaban (MOA) - answer -direct factor Xa inhibitor

parenteral administration - answer --directly into systemic circulation
-poor absorption or unstable in GI tract (ex. heparin, insulin), rapid absorption,
unable to take meds PO
-IV, IM, SQ, ID

IV - answer --into the vein
-can be given through bolus (rapid peak) or infusion (lower peak, longer duration)
-ex. rocuronium (neuromuscular blocker)

IM - answer --aqua solutions absorbed rapidly

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