pharmacodynamics and pharmacokinetics Flashcards
Two major divisions of pharmacology are:
A)
Biotransformation and elimination.
B)
Pharmacokinetics and pharmacodynamics.
C)
Active transport and diffusion.
D)
Pharmacognosy and biotransformation.
pharmacokinetics and pharmacodynamics
Which of the following factors is NOT a component of pharmacokinetics?
A)
Biotransformation
B)
Binding
C)
Distribution
D)
Absorption
Binding
Drug A requires the use of adenosine triphosphate (ATP) in order to move into the cellular membrane. This type of diffusion is known as:
A)
Osmosis.
B)
Facilitated.
C)
Elimination.
D)
Active transport.
active transport
Glucose in the bloodstream is a large molecule that cannot readily enter a cell unless it binds with insulin. This BEST describes:
A)
Osmosis.
B)
Diffusion.
C)
Carrier-mediated diffusion.
D)
Absorption.
carrier mediated diffusion
The term ________ describes the movement of molecules across a membrane down a pressure gradient from an area of higher pressure to and area of lower pressure normally resulting from hydrostatic forces.
A)
Active transport
B)
Carrier-mediated diffusion
C)
Osmosis
D)
Filtration
filtration
________ describes the movement of a medication from the site of application into the body and into the extracellular compartment.
A)
Osmosis
B)
Diffusion
C)
Elimination
D)
Absorption
absorption
Which of the following is NOT a factor in the absorption of a medication?
A)
pH of the medication
B)
Medication potency
C)
Concentration of the medication
D)
Surface area
pH of the medication
Which of the following forms of absorption is generally the slowest due to the decreased vascular supply?
A)
Intramuscular
B)
Sublingual
C)
Subcutaneous
D)
Intravenous
subcutaneous
________ BEST describes the process in which a medication is transported from the site of absorption to the site of action.
A)
Distribution
B)
Diffusion
C)
Active transport
D)
Elimination
distribution
You are treating a patient who suffers from renal disease and decreased perfusion of the kidneys. What effect will this have on the distribution of a drug that normally acts on kidneys, such as the diuretic medication Lasix?
A)
The drug will be present in increased concentrations at the kidneys resulting in toxicity.
B)
As the kidneys are a primary organ of elimination, the effects of the drug will be unchanged.
C)
The drug will most likely be metabolized by the liver resulting in the same effects systemically.
D)
The drug will be poorly delivered to the kidneys due to a decreased perfusion and will not produce the desired results.
the drug will be poorly delivered to the kidneys due to a decreased perfusion and will not produce the desired results
While researching the drug amiodarone, you read that the drug is considered to be highly protein bound upon entering the body. Knowing this, you can deduce that:
A)
The drug is largely ineffective when administered by intravenous route.
B)
The drug remains bound to proteins but will slowly release the active component when necessary resulting in a long half-life.
C)
Much of the drug remains active in the bloodstream and only a small percentage is bound in tissues.
D)
The drugs half-life will be relatively short due to the rapid elimination of the free, or unbound, percentage.
the drug remains bound to proteins but will slowly release the active component when necessary resulting in a long half lif
The blood-brain barrier is a preventive barrier that prevents MOST ________ medications from reaching the brain.
A)
Barbiturate
B)
Water-soluble
C)
Lipid-soluble
D)
Non-ionized, unbound
water-soluble
The process by which a medication passing through the liver may partially or completely inactivate many medications is known as:
A)
First-pass effect.
B)
Protein reservoir binding.
C)
Plasma binding effect.
D)
Prodrug effect.
first pass effect
A medication’s half-life refers to the:
A)
Removal of a medication from the body.
B)
Dose required to be therapeutic.
C)
Time required for the total dose of a medication to be decreased by one-half.
D)
Concentration of a drug.
time required for the total dose of a medication to be decreased by one half
________ is the length of time that a medication concentration is sufficient in the blood to produce a therapeutic response.
A)
Efficacy
B)
Affinity
C)
Half-life
D)
Duration of action
duration of action