PC 707 Module 1 EXAM TEST QUESTIONS &
ANSWERS (A+ GRADED 100% VERIFIED) 2025
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Terms in this set (140)
Is the PDR considered No (only uses drug package inserts)
the best source of
evidence-based up to
date information for
prescribing?
What resource can help The Sanford Guide to Antimicrobial Therapy
guide usage with updates
on microbial resistant to
antibiotics?
What was passed to limit The Sunshine Act
the contributions of
pharmaceutical
companies can make to
influence provider
options?
What type of resource is Secondary resource
the textbook?
What is how the drug Pharmockinetics
moves through the
body?
What are the 4 different (1) absorption (2) excretion (3) distribution (4)
parts of pharmokinetics? metabolism
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What is the most Oral
common and safest route
to receive medication?
What is the route of (1) intestinal tract (2) portal vein (3) liver (4) hepatic
medication when taken artery (5) systemic circulation (6) hepatic vein
orally?
Where does absorption GI tract and small intestine
primarily take place?
What is the Absorption
pharmokinetic process of
how much drug ends up
in the body?
Because not all of the Bioavailability
administered dosage may
be dissolved or
absorbed or survive liver
passage, only a fraction
of an administered
dosage makes it to the
bloodstream. This is
called _______.
What is the maximum Peak Blood Level
blood level that is
achieved following drug
administration?
What is the process of Distribution
moving drugs throughout
the body?
What protein do most Albumin
drugs bind to?
If a drug is all bound in Less available
protein, is it more or less
available?
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, 5/27/25, 10:02 AM PC 707 Module 1 EXAM TEST QUESTIONS & ANSWERS (A+ GRADED 100% VERIFIED) 2025 LATEST!! Flashcards | Qui…
If a patient has more increase
protein binding, do you
need to increase or
decrease dosing of the
drug?
Drugs that are ________ are Protein bound
not able to activate
receptors unless they are
free
Stopping or starting a Protein bound drugs
drug that binds to plasma
protein changes the free
drug levels of other
__________.
What is a hypothetical Volume distribution
value that reflects the
volume in which a drug
would need to dissolved
to explain the
relationship between
dosage and blood
levels?
What is a drug that binds Agonist
to a receptor and
activates the receptor to
produce a biological
response?
What is a drug that binds Antagonist
to a receptor and does
not allow a drug to bind
thus making the drug
inactive?
Where are most drugs Kidneys
excreted?
Where do drugs break Liver (via enzymatic processes)
down in the body?
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