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MARYVILLE NURS 615 PHARM EXAM 1 QUESTIONS AND ANSWERS $12.49   Add to cart

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MARYVILLE NURS 615 PHARM EXAM 1 QUESTIONS AND ANSWERS

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MARYVILLE NURS 615 PHARM EXAM 1 QUESTIONS AND ANSWERS

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  • October 11, 2024
  • 13
  • 2024/2025
  • Exam (elaborations)
  • Questions & answers
  • NURS 615 PHARM
  • NURS 615 PHARM
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MARYVILLE NURS 615 PHARM EXAM 1 QUESTIONS
AND ANSWERS

How does hypoalbuminemia affect the process of prescribing? - 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: - Answers-is considered a contraindication to administer
that drug.

What is the drugs half-life? - 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: - Answers-the time between drug administration and maximum
concentration of drug in the blood stream. Best therapeutic effect.

Duration of action: - 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? - Answers-The
first step is to define the patient's problem

The second step is to - Answers-specify the therapeutic objective

The third step is to - Answers-choose which drug or treatment is needed.

Step 4 of the WHO approach: - Answers-Start the treatment

Step 5 of the WHO approach: - Answers-Educate the patient

Step 6 of the WHO approach: - Answers-Monitor the treatment

Phase 1 of drug development: - Answers-The drug is tested on healthy volunteers

Phase 2 of drug development: - Answers-trials with people who have the disease for
which the drug is thought to be effective

Phase 3 of drug development: - 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: - 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 - 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: - Answers-The fastest route of absorption is
inhalation, and not as mistakenly considered the IV administration.

Why does absorption occur at a slower rate for oral, IM, SQ routes? - 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: - 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? - 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 - 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. - 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? - 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 - 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)

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