Nur 641 E Final Exam Study Guide
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Terms in this set (181)
absorption, Pharmacokinetics involves
distribution,
metabolism,
excretion
,absorption from Pharmacokinetic absorption
the
administration
site either
directly or
indirectly in the
blood plasma
reversibly or Parmacokinetic distribution
irreversibly
move from the
bloodstream
into the
interstitial and
intracellular fluid
biotransformed Pharmacokinetics metabolism
via hepatic
metabolism or
by other tissue
,1. highest Intravenous medications
bioavailability
2. places entire
does into venin
thus bypassing
absorption
3. avoids hepatic
first pass
metabolism in
the liver
usually reached steady state medication
within 4-5 half
lives of the drug
, 1.the time drug half life
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
pharmacokinetic
s of a drug
drug is zero order (nonlinear)
metabolized at a
constant rate
per unit
Grand Canyon University
2025|Actual Exam Set Questions
And Verified Answers (Correct
solutions) | Get It 100% Accurate!!
Save
Terms in this set (181)
absorption, Pharmacokinetics involves
distribution,
metabolism,
excretion
,absorption from Pharmacokinetic absorption
the
administration
site either
directly or
indirectly in the
blood plasma
reversibly or Parmacokinetic distribution
irreversibly
move from the
bloodstream
into the
interstitial and
intracellular fluid
biotransformed Pharmacokinetics metabolism
via hepatic
metabolism or
by other tissue
,1. highest Intravenous medications
bioavailability
2. places entire
does into venin
thus bypassing
absorption
3. avoids hepatic
first pass
metabolism in
the liver
usually reached steady state medication
within 4-5 half
lives of the drug
, 1.the time drug half life
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
pharmacokinetic
s of a drug
drug is zero order (nonlinear)
metabolized at a
constant rate
per unit
