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Nurs 615 Pharm Exam 1 – Maryville Questions And Correct
Verified Answers Latest Update 2024/2025 Best Exam Top
Ranked To Score A+ For Success
How does hypoalbuminemia affect the process of prescribing? - CORRECT ANSWERS
Low albumin = more free drug (bc the drug can't bind to albumin aka protein) =
increased adverse effects
What is a Black Box Warning: - CORRECT ANSWERS is considered a contraindication to
administer that drug.
What is the drugs half-life? - CORRECT ANSWERS Half-life specifically means the
amount of time it takes for an administered drug to be halfway cleared from the system.
Peak of action: - CORRECT ANSWERS the time between drug administration and
maximum concentration of drug in the blood stream. Best therapeutic effect.
Duration of action: - CORRECT ANSWERS the time between onset of action and
metabolism of drug below the minimum needed for an effect. The length of time you
have the drug in your system.
According to the WHO what is the first step in the prescribing process? - CORRECT
ANSWERS The first step is to define the patient's problem
The second step is to - CORRECT ANSWERS specify the therapeutic objective
The third step is to - CORRECT ANSWERS choose which drug or treatment is needed.
Step 4 of the WHO approach: - CORRECT ANSWERS Start the treatment
Step 5 of the WHO approach: - CORRECT ANSWERS Educate the patient
Step 6 of the WHO approach: - CORRECT ANSWERS Monitor the treatment
Phase 1 of drug development: - CORRECT ANSWERS The drug is tested on healthy
volunteers
,Nurs 615 Pharm Exam 1 – Maryville Questions And Correct
Verified Answers Latest Update 2024/2025 Best Exam Top
Ranked To Score A+ For Success
Phase 2 of drug development: - CORRECT ANSWERS trials with people who have the
disease for which the drug is thought to be effective
Phase 3 of drug development: - CORRECT ANSWERS Large numbers of patients in
medical research centers receive the drug in phase 3. This larger sampling provides
information about infrequent or rare adverse effects. The FFA will approve a new drug
application if phase 3 studies are satisfactory.
Phase 4 of drug development: - CORRECT ANSWERS This phase is voluntary and
involves postmarket surveillance of the drug's therapeutic effects at the completion of
phase 3. The pharmaceutical company receives reports from doctors and other health
care professionals about the therapeutic results and adverse effects of the drug. Some
medications, for example, have been found to be toxic and have been removed from the
market after their initial release.
Explain first pass metabolism - CORRECT ANSWERS much of the drug is lost in the
absorption process. The liver metabolizes many drugs, thus reduces the bioavailabilty of
the drug.
What is the fasted route of absorption: - CORRECT ANSWERS The fastest route of
absorption is inhalation, and not as mistakenly considered the IV administration.
Why does the GI tract take longer to absorb? - CORRECT ANSWERS The GI tract is lined
with epithelial cells; drugs must permeate through these cells in order to be absorbed
into the circulatory system.
What is One particular cellular barrier that may prevent absorption of a given drug? -
CORRECT ANSWERS the cell membrane. Cell membranes are essentially lipid bilayers
which form a semipermeable membrane. Pure lipid bilayers are generally permeable
only to small and uncharged solutes, hence whether or not a molecule is ionized will
affect its absorption, since ionic molecules are charged.
What is solubility? - CORRECT ANSWERS Solubility favors charged species,
permeability favors neutral species. Some molecules have special exchange proteins and
channels to facilitate movement from the lumen into the circulation.
, Nurs 615 Pharm Exam 1 – Maryville Questions And Correct
Verified Answers Latest Update 2024/2025 Best Exam Top
Ranked To Score A+ For Success
Why does absorption occur at a slower rate for oral, IM, SQ routes? - CORRECT
ANSWERS Absorption occurs at a slower rate because the complex membrane systems
of GI mucosal layers, muscle, and skin delay drug passage.
The ability of a drug to cross a cell membrane depends on: - CORRECT ANSWERS
whether the drug is water or lipid (fat) soluble. Lipid-soluble drugs easily cross through
cell membranes; water-soluble drugs can't. Lipid-soluble drugs can also cross the blood-
brain barrier and enter the brain.
As a drug travels through the body, it comes in contact with? - CORRECT ANSWERS
proteins such as the plasma protein albumin. The drug can remain free or bind to the
protein. The portion of a drug that's bound to a protein is inactive and can't exert a
therapeutic effect. Only the free, or unbound, portion remains active. A drug is said to be
highly protein-bound if more than 80% of the drug is bound to protein.
Identify drug metabolism and the role of isoenzymes in the p450 system - CORRECT
ANSWERS CYPs are the are the major enzymes involved in drug metabolism accounting
for about 75% of the total metabolism.
Naturally occurring compounds may induce or inhibit CYP activity. - CORRECT
ANSWERS For example, bioactive compounds found in grapefruit juice and some other
fruit juices including dihydroxy forgotten and parasitin A have been found to inhibit
CYP3a4 mediated metabolism of certain medications leading to increased bioavailability
and the strong possibility of overdosing.
What does grapefruit have to do with CYP? - CORRECT ANSWERS Grapefruit is an
inhibitor and will decrease the metabolism of drugs by the cyp enzymes
When 2 drugs are both metabolized by the p450 system the drug should be - CORRECT
ANSWERS administered at separate times to prevent the metabolism of one drug
resulting in toxic effects of the other drug. (because it would have less protein to bind
too, thus more free floating drug)
What is the efficacy of a drug? - CORRECT ANSWERS Efficacy is the maximum response
achievable from a drug. Effectiveness refers to the ability of the drug to produce a
beneficial effect.
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