NSG 100 Exam 3 Flashcards
(126 cards)
The patient is receiving two different drugs. At current dosages and dosage forms, both drugs have the same concentration of active ingredients. Which term is used to identify this principle?
a. Bioequivalent
b. Synergistic
c. Prodrugs
d. Steady-state
a. Bioequivalent
Rationale: Two drugs absorbed into the circulation in the same amount (in specific dosage forms) have the same bioavailability; thus, they are bioequivalent.
A drug’s steady state is the physiologic state in which the amount of drug removed via elimination is equal to the amount of drug absorbed from each dose.
The term synergistic refers to two drugs, given together, with a resulting effect that is greater than the sum of the effects of each drug given alone.
A prodrug is an inactive drug dosage form that is converted to an active metabolite by various biochemical reactions once it is inside the body.
When given an intravenous medication, the patient says to the nurse, “I usually take pills. Why does this medication have to be given in the arm?” What is the nurse’s best answer?
a. “The medication will cause fewer adverse effects when given intravenously.”
b. “The intravenous medication will have delayed absorption into the body’s tissues.”
c. “The action of the medication will begin sooner when given intravenously.”
d. “There is a lower chance of allergic reactions when drugs are given intravenously.”
c. “The action of the medication will begin sooner when given intravenously.”
Rationale: An intravenous (IV) injection provides the fastest route of absorption. The IV route does not affect the number of adverse effects, nor does it cause delayed tissue absorption (it results in faster absorption). The IV route does not affect the number of allergic reactions.
The nurse is administering parenteral drugs. Which statement is true regarding parenteral drugs?
a. Parenteral drugs bypass the first-pass effect.
b. Absorption of parenteral drugs is affected by reduced blood flow to the stomach.
c. Absorption of parenteral drugs is faster when the stomach is empty.
d. Parenteral drugs exert their effects while circulating in the bloodstream.
a. Parenteral drugs bypass the first-pass effect.
Rationale: Drugs given by the parenteral route bypass the first-pass effect.
Reduced blood flow to the stomach and the presence of food in the stomach apply to enteral drugs (taken orally), not to parenteral drugs.
Parenteral drugs must be absorbed into cells and tissues from the circulation before they can exert their effects; they do not exert their effects while circulating in the bloodstream.
When monitoring the patient receiving an intravenous infusion to reduce blood pressure, the nurse notes that the patient’s blood pressure is extremely low, and the patient is lethargic and difficult to awaken. This would be classified as which type of adverse
drug reaction?
a. Adverse effect
b. Allergic reaction
c. Idiosyncratic reaction
d. Pharmacologic reaction
d. Pharmacologic reaction
Rationale: A pharmacologic reaction is an extension of a drug’s normal effects in the body. In this case, the antihypertensive drug lowered the patient’s blood pressure levels too much.
The other options do not describe a pharmacologic reaction. An adverse effect is a predictable, well-known adverse drug reaction that results in minor or no changes in patient management.
An allergic reaction (also known as a hypersensitivity reaction) involves the patient’s immune system.
An idiosyncratic reaction is unexpected and is defined
as a genetically determined abnormal response to normal dosages of a drug.
The nurse is reviewing pharmacology terms for a group of newly graduated nurses. Which sentence defines a drug’s half-life?
a. The time it takes for the drug to cause half of its therapeutic response
b. The time it takes for one-half of the original amount of a drug to reach the target cells
c. The time it takes for one-half of the original amount of a drug to be removed from the body
d. The time it takes for one half of the original amount of a drug to be absorbed into the circulation
c. The time it takes for one-half of the original amount of a drug to be removed from the body
Rationale: A drug’s half-life is the time it takes for one-half of the original amount of a drug to be removed from the body. It is a measure of the rate at which drugs are removed from the body. The other options are incorrect definitions of half-life.
When administering drugs, the nurse remembers that the duration of action of a drug is defined as which of these?
a. The time it takes for a drug to elicit a therapeutic response
b. The amount of time needed to remove a drug from circulation
c. The time it takes for a drug to achieve its maximum therapeutic response
d. The time period at which a drug’s concentration is sufficient to cause a therapeutic response
d. The time period at which a drug’s concentration is sufficient to cause a therapeutic response
Rationale: Duration of action is the time during which drug’s concentration is sufficient to elicit a therapeutic response.
The other options do not define duration of action. A drug’s onset of action is the time it takes for the drug to elicit a therapeutic response.
A drug’s peak effect is the time it takes for the drug to reach its maximum therapeutic response.
Elimination is the length of time it takes to remove a drug from circulation.
When reviewing the mechanism of action of a specific drug, the nurse reads that the drug works by selective enzyme interaction. Which of these processes describes selective enzyme interaction?
a. The drug alters cell membrane permeability.
b. The drug’s effectiveness within the cell walls of the target tissue is enhanced.
c. The drug is attracted to a receptor on the cell wall, preventing an enzyme from binding to that receptor.
d. The drug binds to an enzyme molecule and inhibits or enhances the enzyme’s action with the normal target cell.
d. The drug binds to an enzyme molecule and inhibits or enhances the enzyme’s action with the normal target cell.
Rationale: With selective enzyme interaction, the drug attracts the enzymes to bind with the drug instead of allowing the enzymes to bind with their normal target cells.
As a result, the target cells are protected from the action of the enzymes. This results in a drug effect.
The actions described in the other options do not occur with selective enzyme interactions.
When administering a new medication to a patient, the nurse reads that it is highly protein-bound. Assuming that the patient’s albumin levels are normal, the nurse would expect which result, as compared to a medication, that is not highly protein-bound?
a. Renal excretion will be faster.
b. The drug will be metabolized quickly.
c. The duration of action of the medication will be shorter.
d. The duration of action of the medication will be longer.
d. The duration of action of the medication will be longer.
Rationale: Drugs that are bound to plasma proteins are characterized by a longer duration of action. Protein binding does not make renal excretion faster, does not speed up drug metabolism, and does not cause the duration of action to be shorter.
The patient is experiencing chest pain and needs to take a sublingual form of nitroglycerin. Where does the nurse instruct the patient to place the tablet?
a. Under the tongue
b. On top of the tongue
c. At the back of the throat
d. In the space between the cheek and the gum
a. Under the tongue
Rationale: Drugs administered via the sublingual route are placed under the tongue. Drugs administered via the buccal route are placed in the space between the cheek and the gum; oral drugs are swallowed. The other options are incorrect.
The nurse is administering medications to the patient who is in renal failure resulting from end-stage renal disease. The nurse is aware that patients with kidney failure would most likely have problems with which pharmacokinetic phase?
a. Absorption
b. Distribution
c. Metabolism
d. Excretion
d. Excretion
Rationale: The kidneys are the organs that are most responsible for drug excretion. The renal function does not affect the absorption and distribution of a drug. Renal function may affect the metabolism of drugs to a small extent.
A patient who has advanced cancer is receiving opioid medications around the clock to keep him comfortable as he nears the end of his life. Which term best describes this type of therapy?
a. Palliative therapy
b. Maintenance therapy
c. Empiric therapy
d. Supplemental therapy
a. Palliative therapy
Rationale: The goal of palliative therapy is to make the patient as comfortable as possible.
It is typically used in the end stages of illnesses when all attempts at curative therapy have failed.
Maintenance therapy is used for the treatment of chronic illnesses such as hypertension.
Empiric therapy is based on clinical probabilities and involves drug administration when a certain pathologic
condition has an uncertain but high likelihood of occurrence based on the patient’s initial presenting symptoms.
Supplemental therapy (or replacement therapy) supplies the body with a substance needed to maintain normal function.
The patient is stating that he has a headache and asks the nurse which over-the-counter medication form would work the fastest to help reduce the pain. Which medication form will the nurse suggest?
a. A capsule
b. A tablet
c. An enteric-coated tablet
d. A powder
d. A powder
Rationale: Of the types of oral medications listed, the powder form would be absorbed the fastest, thus having a faster onset. The tablet, the capsule, and, finally, the enteric-coated tablet would be absorbed next, in that order.
The nurse will be injecting a drug into the superficial skin layers immediately underneath the epidermal layer of skin. Which route does this describe?
a. Intradermal
b. Subcutaneous
c. Intramuscular
d. Transdermal
a. Intradermal
Rationale: Injections under the more superficial skin layers immediately underneath the epidermal layer of skin and into the dermal layer are known as intradermal injections.
Injections into the fatty subcutaneous tissue under the dermal layer of skin are referred to as subcutaneous injections.
Injections into the muscle beneath the subcutaneous fatty tissue are referred to as intramuscular injections.
Transdermal drugs are applied to the skin via an adhesive patch.
Which drugs would be affected by the first-pass effect when administered? (Select all that apply.)
a. Morphine given by IV push injection
b. Sublingual nitroglycerin tablets
c. Diphenhydramine (Benadryl) elixirs
d. Levothyroxine (Synthroid) tablets
e. Transdermal nicotine patches
f. Esomeprazole (Nexium) capsules
g. Penicillin given by IV piggyback infusion
c. Diphenhydramine (Benadryl) elixirs
d. Levothyroxine (Synthroid) tablets
e. Transdermal nicotine patches
Rationale: Orally administered drugs (elixirs, tablets, and capsules) undergo the first-pass effect, because they are metabolized in the liver after being absorbed into the portal circulation from the small intestine.
IV medications (IV push and IV piggyback) enter the
bloodstream directly and do not go directly to the liver. Sublingual tablets and transdermal patches also enter the bloodstream without going directly to the liver, thus avoiding the first-pass effect.
Drug transfer to the fetus is more likely during the last trimester of pregnancy for which reason?
a. Decreased fetal surface area
b. Increased placental surface area
c. Enhanced blood flow to the fetus
d. Increased amount of protein-bound drug in maternal circulation
c. Enhanced blood flow to the fetus
Rationale: Drug transfer to the fetus is more likely during the last trimester of pregnancy as a result of enhanced blood flow to the fetus.
The other options are incorrect. Increased fetal surface area, not decreased, is a factor that affects drug transfer to the fetus.
The placenta’s surface area does not increase during this time. Drug transfer is increased because of an increased amount of free drugs, not protein-bound drugs, in the mother’s circulation.
The nurse is monitoring a patient who is in the 26th week of pregnancy and has developed gestational diabetes and pneumonia. She is given medications that pose a possible fetal risk, but the potential benefits may warrant the use of the medications in her
situation. The nurse recognizes that these medications are in which U.S. Food and Drug Administration pregnancy safety category?
a. Category X
b. Category B
c. Category C
d. Category D
d. Category D
Rationale: Pregnancy category D fits the description given.
Category B indicates no risk to animal fetus; information for humans is not available.
Category C indicates adverse effects reported in animal fetus; information for humans is not available.
Category X
consists of drugs that should not be used in pregnant women because of reports of fetal abnormalities and positive evidence of fetal risk in humans.
When discussing dosage calculation for pediatric patients with a clinical pharmacist, the nurse notes which type of dosage calculation is used most commonly in pediatric calculations?
a. West nomogram
b. Clark rule
c. Height-to-weight ratio
d. Milligram per kilogram of body weight formula
d. Milligram per kilogram of body weight formula
Rationale: The milligram per kilogram formula, based on body weight, is the most common method of calculating doses for pediatric patients.
The other options are available methods but are not the most commonly used. The height-to-weight ratio is not used.
The nurse is assessing a newly admitted 83-year-old patient and determines that the patient is experiencing polypharmacy. Which statement most accurately illustrates polypharmacy?
a. The patient is experiencing multiple illnesses.
b. The patient uses one medication for an illness several times per day.
c. The patient uses over-the-counter drugs for an illness.
d. The patient uses multiple medications simultaneously.
d. The patient uses multiple medications simultaneously.
Rationale: Polypharmacy usually occurs when a patient has several illnesses and takes medications for each of them, possibly prescribed by different specialists who may be unaware of other treatments the patient is undergoing.
The other options are incorrect.
Polypharmacy addresses the medications taken, not just the illnesses.
Polypharmacy means the patient is taking several different medications, not just one, and can include prescription drugs, over-the-counter medications, and herbal products.
The nurse is aware that confusion, forgetfulness, and increased risk for falls are common responses in an elderly patient who is taking which type of drug?
a. Laxatives
b. Anticoagulants
c. Sedatives
d. Antidepressants
c. Sedatives
Rationale: Sedatives and hypnotics often cause confusion, daytime sedation, ataxia, lethargy, forgetfulness, and increased risk for falls in the
elderly.
Laxatives, anticoagulants, and antidepressants may cause adverse effects in the elderly, but not the ones specified in the question.
For accurate medication administration to pediatric patients, the nurse must take into account which criteria?
a. Organ maturity
b. Renal output
c. Body temperature
d. Height
a. Organ maturity
Rationale: To administer medications to pediatric patients accurately, one must take into account organ maturity, body surface area, age, and weight.
The other options are incorrect; renal output and body temperature are not considerations, and height alone is not sufficient.
The nurse recognizes that an elderly patient may experience a reduction in the stomach’s ability to produce hydrochloric acid. This change may result in which effect?
a. Delayed gastric emptying
b. Increased gastric acidity
c. Decreased intestinal absorption of medications
d. Altered absorption of some drugs
d. Altered absorption of some drugs
Rationale: Reduction in the stomach’s ability to produce hydrochloric acid is an aging-related change that results in a decrease in gastric acidity and may alter the absorption of some drugs.
The other options are not results of reduced hydrochloric acid production.
The nurse is administering drugs to neonates and will consider which factor may contribute the most to drug toxicity?
a. The lungs are immature.
b. The kidneys are small.
c. The liver is not fully developed.
d. Excretion of the drug occurs quickly.
c. The liver is not fully developed.
Rationale: A neonate’s liver is not fully developed and cannot detoxify many drugs. The other options are incorrect. The lungs and kidneys do not play major roles in drug metabolism.
Renal excretion is slow, not fast, because of organ immaturity, but this is not the factor that contributes the most to drug toxicity.
An 83-year-old woman has been given a thiazide diuretic to treat heart failure. She and her daughter should be told to watch for which problems?
a. Constipation and anorexia
b. Fatigue, leg cramps, and dehydration
c. Daytime sedation and lethargy
d. Edema, nausea, and blurred vision
b. Fatigue, leg cramps, and dehydration
Rationale: Electrolyte imbalance, leg cramps, fatigue, and dehydration are common complications when thiazide diuretics are given to elderly
patients.
The other options do not describe complications that occur when these drugs are given to the elderly.
An elderly patient with a new diagnosis of hypertension will be receiving a new prescription for an antihypertensive drug. The nurse expects which type of dosing to occur with this drug therapy?
a. Drug therapy will be based on the patient’s weight.
b. Drug therapy will be based on the patient’s age.
c. The patient will receive the maximum dose that is expected to reduce the blood pressure.
d. The patient will receive the lowest possible dose at first, and then the dose will be increased as needed.
d. The patient will receive the lowest possible dose at first, and then the dose will be increased as needed.
Rationale: As a general rule, dosing for elderly patients should follow the admonition, “Start low, and go slow,” which means to start with the lowest possible dose (often less than an average adult dose) and increase the dose slowly, if needed, based on patient response. The
other responses are incorrect.