NURS 5334 PHARM FINAL EXAM LATEST
ACTUAL EXAM 100 QUESTIONS AND CORRECT
DETAILED ANSWERS (VERIFIED ANSWERS )
|ALREADY GRADED A+
- What are the BON rules and regulations for prescriptive authority for the advance
- Texas is very restricted
- Describe the pharmacokinetic processes of absorption, distribution, metabolism and
- Absorption
- Drug’s movement from the site of administration into the blood.
- Distribution
- Metabolism
- Elimination
- Combination of metabolism and excretion
- Compare and contrast pharmacokinetics and pharmacodynamics of special
- Pediatrics—they have organ immaturity, elderly—they have organ degeneration,
- Analyze a drug interaction to determine an appropriate course of action.
- Basic mechanism of drug-drug interactions through pharmacokinetic interactions
- Identify medications with a narrow therapeutic index requiring drug level
- Discuss the effect of ionization and pH on absorption.
- Drugs that are weak acids are best absorbed in acidic environments. Acidic drugs
- Discuss factors affecting drug distribution.
- Competition for protein binding and alteration of extracellular pH
- Discuss barriers affecting drug distribution—such as placental membrane, blood
practice nurse?
elimination and how differences in these areas affect drug action.
1.Drug’s movement from the blood into the interstitial space of tissues and from there into cells.
1.Biotransformation is the enzymatically mediated alteration of drug structure.
populations—pediatrics, older adults and those that are pregnant.
loss of nephrons, excretion of drug is decreased and you have to give this population a lower dose of medication. Medication can pass through milk of lactating females.
are altered absorption, altered distribution, altered metabolism, and altered renal excretion.
monitoring.
1.
accumulate on the alkaline side, basic drugs accumulate on the acidic side known as ion trapping. Ionization of the drugs is pH dependent, when the pH and the fluid on one side of the membrane differs from the pH on the other side, drug molecules tend to accumulate on the side where the pH most favors ionization.
brain barrier and volume of distribution.
1. Placental membrane: drugs are easily passed through the placental membrance
- Blood brain barrier: the PGP pumps drugs back into the blood and thereby limits
their access to the brain.
3. Volume of distribution: 1 / 4
- Discuss the “first-pass effect”—what effect can this have on distribution of a drug?
- Rapid hepatic inactivation of certain oral drugs. When drugs are absorbed by the
GI tract, they are carried directly to the liver through the hepatic portal vein 2 / 4
before entering the systemic circulation. If the capacity of the liver to metabolize the drug is extremely high, this drug can be completely inactivated on its first pass through the liver.
- Discuss the significance of the Cytochrome P450 system on metabolism of drugs.
- It is a group of 12 closely related enzyme families. CYP1, CYP2, CYP3
- Discuss the major hepatotoxic drugs and possible effects on drug metabolism.
- List various routes of drug elimination—review normal renal function including
- Discuss terms used to describe drug actions-agonist, partial agonist, antagonist.
metabolize drugs. The other 9 families metabolize endogenous compounds (ex.Fatty acids, steroids).
1.
glomerular filtration, passive tubular reabsorption and active tubular secretion; describe the implications on drug clearance and how elimination affects prescribing.
1.
1. Agonist: molecules that activate receptors
- Partial agonist: Only has moderate intrinsic activity. Maximal effect that a partial
- Antagonist: Produce their effects by preventing receptor activation by endogenous
- Discuss the impact of food on drug absorption, drug metabolism and on drug toxicity
agonist can produce is lower than that of a full agonist.
regulatory molecules and drugs.
and action—as well as the timing of drug administration.
LIFESPAN
- Hepatic metabolism and GFR increase during pregnancy, dosages of some drugs
- Rate of albumin to water decreases
may need to be increased.
1.Third trimester: Renal blood flow is doubled and renal excretion is
accelerated (drugs excreted rapidly)
- Tone and mobility of bowel decrease
- Prolongation of drug effects Total (½ life increases)
- Understand stages of development in pregnancy
1. Conception: through week 2
2. Embryonic period: week 3-week 8
a) Gross malformations can be produced by teratogens
3. Fetal period: week 9-delivery
- Understand pregnancy labeling
- 3 categories now
a) Pregnancy, lactation, male & female reproductive potential
- How do you decrease risk in the infant during breastfeeding?
- How do pediatric patients differ in their response to medications?
- Absorption
1.Take meds immediately after breastfeeding, avoid drugs that have long half-lives, choose drugs that tend to be excluded from milk, avoid drugs that are known to be hazardous.
a) Oral? 3 / 4
1. Neonates: drug remain in the stomach longer which
increases the levels, low acidity can affect the absorption of acid labile drugs
b) Parenteral?
- Reponses are slow and erratic.
2. Infancy: absorption is more rapid than in neonates & adults
- Best avoided in infants
c) Transdermal?
- Greater skin permeability which increases topical drug
- Distribution
absorption and increases the risk for toxicity
a) Protein binding
1. Neonates: less protein-binding—increased availability of
highly protein bound drugs such as phenytoin, diazepam, and phenobarbital. Reduced dosages needed in these highly bound drugs.
b) Blood Brain Barrier
- Not fully developed at birth, drugs have easy access to the
- Metabolism
CNS, doses should be reduced.
a) Hepatic function?
- Liver hasn’t reached full maturation—sensitive to drugs
eliminated by the CYP450. Liver’s ability to metabolize drugs increases about one month after birth.
b) T half life
- Decreased by as much as 48-72 hours
- Excretion
a) Renal?
- GFR is significantly reduced at birth, drugs eliminated by
- What education needs to be given to parents?
- What to do if child spits out medication or throws it up
the kidneys must be given in a reduced dosage and longer dosing intervals.
2.Effective education: dosage size and timing, route, technique of
administration, duration of treatment, how to store the drug, nature and time course of the desired response, nature and time course of adverse reactions.
- How do you convert pounds to KG?
- Divide weight by 2.2
- What is definition of polypharmacy? Is polypharmacy always inappropriate?
What is Beer’s List?
1.Polypharmacy: 3 or more prescription drugs in conjunction-+ with 3 or
more dietary supplements.
- No
- / 4
3.List that identifies drugs with a high likelihood of causing adverse effects in the elderly