Rehash Flashcards
- The study of drugs and their interaction in general with living systems is known as:
a. Pharmacokinetics
b. Clinical pharmacology
c. Pharmacotherapeutics
d. Pharmacology
d. pharmacology
In teaching a continuing education class in pharmacology, the instructor tests the class regarding concepts learned about pharmacodynamics. Which statement made by a student best demonstrates the understanding regarding these concepts:
a. “Routes of administration are components of pharmacodynamics.”
b. “Receptor binding is the main component of pharmacodynamics.”
c. “Metabolism is a component of pharmacodynamics.”
d. “Age and gender are components of pharmacodynamics.”
b. “Receptor binding is the main component of pharmacodynamics.”
Among the characteristics for an “ideal drug”, what are the three important characteristics that are considered to be the most important for a drug?
a. Predictability, stability and effectiveness
b. Safety, reversibility and ease of administration
c. Safety, effectiveness and selectivity
d. Stability, safety and selectivity
c. Safety, effectiveness and selectivity
A nurse is teaching a continuing education class on pharmacology. The nurse is evaluating the participants’ knowledge and poses the question, “When a disease process triggers increased metabolism of the drug, the disease has altered the drug’s ___________.”
a. Pharmacodynamics
b. Pharmacotherapeutics
c. Pharmacokinetics
d. Selectivity
c. Pharmacokinetics
The intensity of any drug action is determined by
a. What dosage is administered
b. How the dosage is administered
c. How the drug is handled by the body
d. All of the above
d. All of the above
A patient while being administered the drug questions the nurse, “What do you mean that most drug actions are reversible?” The nurse’s best response is that most drug effects _____________________________________.
a. Diminish when given in low doses
b. Diminish as it wears out from the system
c. Reverse when given in high doses
d. Reverse when given in low doses
b. Diminish as it wears out from the system
A patient with type I diabetes mellitus arrives at the clinic with complaints of low blood sugar. The nurse questions the patient regarding compliance with medications. The patient states that she gives herself more insulin per dose so she doesn’t have to take it as often. Which of the following area does the nurse need to educate the patient on?
a. Pharmacokinetics
b. Pharmacodynamics
c. Administration
d. Chemical stability
c. Administration
Which aspect of the baseline assessment would be the most important before a drug that is known to cause hepatotoxicity is to be administered to a patient?
a. The patient’s blood pressure measurement
b. The patient’s liver function tests
c. The patient’s electrocardiogram (EKG)
d. The patient’s mental status
b. The patient’s liver function tests
The nurse is ready to administer an anti-hypertensive agent and on assessing finds out the blood pressure is 108/75 (normal 100/80). What action should the nurse take to determine if it is safe to administer the drug?
a. Note the current blood pressure levels and give the medication and monitor the patient
because he has hypertension
b. Hold the medication, as the patient’s blood pressure is too high to administer the drug.
c. Administer the medication because the medication is prescribed.
d. Assess the patients baseline blood pressure levels before and after the last dose of the medication, to determine if the medication should be administered.
d. Assess the patients baseline blood pressure levels before and after the last dose of the medication, to determine if the medication should be administered.
A patient has been taking a brand-name drug and his insurance plan change requires the use of generic drugs since they are available and approved by the FDA. The patient asks if he should pay out of his pocket for the brand-name drug. The nurse’s response should be based on the fact that:
a. Trade name drugs contain active ingredients than generic drugs and he should
pay out of his pocket
b. Generic drugs have therapeutic equivalency to their brand-name counterparts and its ok to start with the generic drugs
c. Generic drugs usually are not the same dosage as brand-name drugs and he should
pay out of his pocket
d. Continuing to use the brand-name drug will prevent confusion and therefore he should
pay out of his pocket
b. Generic drugs have therapeutic equivalency to their brand-name counterparts and its ok to start with the generic drugs
An adult patient is receiving antibiotics as drug therapy for an infection and has developed hearing loss. The nurse realizes that this is a side effect of the drug. This action has occurred during which step of the nursing process?
a. Baseline assessment
b. Evaluation
c. Planning
d. Implementation
b. Evaluation
When discussing the types of drug names such as Ibuprofen / 2,4,(isobutylphenyl) propionic acid / Advil, it is because we are discussing their ________________ name.
a. Chemical / Generic / Trade
b. Generic / Chemical / Trade
c. Trade / Generic / Chemical
d. Trade/ Chemical/ Generic
b. Generic / Chemical / Trade
The nurse is caring for several patients and prepares to administer morning medications. Which among the following is the most high-risk patient that the nurse should monitor after administering the drugs?
a. The pediatric patient admitted with a broken arm
b. The active elderly patient admitted with a right hip fracture
c. The young adult patient with a history of kidney disease
d. The 26-year-old female admitted with asthma
c. The young adult patient with a history of kidney disease
All drugs have a chemical, a generic and a trade name. Learning the generic name for a drug is important for nurses/practitioners. Why?
a. The generic name is the same as trade name
b. Generic names are easy to recall and pronounce
c. The generic name of the drug will be the same no matter what the trade name is
d. There are several generic names for a drug with one given trade name
c. The generic name of the drug will be the same no matter what the trade name is
Which legislation gives the power to the FDA, for the first time, to require drug companies to conduct pediatric clinical trials on new drugs that may be used in children?
a. Controlled Substance Act (1970)
b. Food and Drug Administration Modernization Act (FDAMA, 1997)
c. Pediatric Research Equity Act (PREA) of 2003
d. The Best Pharmaceutical for Children Act (BPCA) in 2002
c. Pediatric Research Equity Act (PREA) of 2003
The Harris-Kefauver amendment that was created after the thalidomide tragedy sought to strengthen all aspects of drug regulation. It required
a. Proof of effectiveness before a new drug could be marketed
b. That drugs be free of adulterants
c. All new drugs undergo testing for toxicity
d. Testing procedures be done for adverse effects before a new drug is released
a. Proof of effectiveness before a new drug could be marketed
The rationale for the 1992 changes in the Food and Drug Administration regulations to permit accelerated approval of drugs for the treatment of life-threatening or severely debilitating disease was to:
a. Allow for marketing before completion of Phase III in drug trials
b. Ensure that the unknown risks associated with early approval are balanced by the need for effective drugs
c. Change the rules because existing FDA regulations were too easy for potentially non-effective drugs
d. Accelerate approval of new drugs to give physicians the option of using them even before knowing their effectiveness
b. Ensure that the unknown risks associated with early approval are balanced by the need for effective drugs
A researcher working for a pharmaceutical company is providing orientation to a new nurse researcher. The researcher determines that further education is needed when the nurse states that
a. Preclinical testing takes place in animals b. Phase I involves normal volunteers
c. Phase III involves patients
d. The manufacturer applies for FDA approval after phase II
d. The manufacturer applies for FDA approval after phase II
When a new drug is subjected to clinical trial while there is an already existing drug in treatment for the condition, what would the control drug be in this clinical trial ?
a. A placebo sugar pill
b. A control sugar pill
c. The already existing drug
d. All of the above
c. The already existing drug
The terminology used to describe the clinical trial drug study where both health professional and the patient do not know what drug they are receiving in the trial is a(n) \_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_ study. a. Single blind b. Open label c. Cross over d. Double blind
d. Double blind
The most common way through which drugs cross the membrane is via direct penetration. From the following list, identify the one that can cross the membrane more readily:
a. Molecules that are hydrophilic/lipophobic
b. Molecules that are hydrophobic/lipophilic
c. Small molecules that are charged
d. Large molecules that are charged
b. Molecules that are hydrophobic/lipophilic
Select the accurate statement with regard to drugs and pH dependent ionization (ion trapping). Aspirin when taken with antacid will be ____________________________.
a. Absorbed more from the stomach at that pH because they are non-ionized
b. Trapped more in the stomach at that pH because they will ionize
c. Degraded more in the stomach at that pH
d. Absorbed normally as they don’t ionize
b. Trapped more in the stomach at that pH because they will ionize
Under most circumstances, intramuscular (IM) injections are to be avoided; however, there are some advantages to this route. Identify the advantage in using IM from the following list:
a. IM route is the least painful
b. IM route is the least expensive
c. The IM route is superior when administering poorly soluble drugs
d. IM injections are safer than the other drug administration routes
c. The IM route is superior when administering poorly soluble drugs
Some drugs under go first- pass effect where as others undergo enterohepatic recirculation. The first-pass effect primarily alters a drug’s _____________, whereas enterohepatic circulation alters a drugs’s ________________.
a. Absorption. metabolism
b. Distribution, metabolism
c. Metabolism, distribution
d. Metabolism, excretion.
c. Metabolism, distribution
The nurse is reading research about a drug. The literature states that the drug is potent. This means the drug
a. Produces its maximal effects at low doses
b. Produces strong effects at only high doses
c. Produces toxic effects at even low doses
d. All of the above
a. Produces its maximal effects at low doses
Grape fruit juice consumed along with certain drugs plays a major effect on the plasma levels of the drug. The “grape fruit juice effect” is most associated with:
a. Altered absorption in the stomach
b. Increased excretion in the urine
c. Decreased binding to plasma proteins
d. Effects on drug metabolism
d. Effects on drug metabolism
A patient with a history of cardiac problems is admitted to a telemetry unit. The patient needs administration of digoxin (Lanoxin) immediately. The drug has a longer half- life. As a prescriber what would be your best action?
a. Administer the same amount every day (for 4 half lives) until it reaches plateau
b. Administer double the dose every day until it reaches the plateau
c. Administer high and low doses alternatively every day
d. Administer a high dose to reach plateau, followed by a lower dose for maintenance
d. Administer a high dose to reach plateau, followed by a lower dose for maintenance
On Monday (Sep 1) a patient begins taking a daily dose of a drug with a half-life of 3 days. If the patient takes the same dose every day, on what day will the plasma drug levels reach a plateau?
a. Sep 4, Thursday
b. Sep 13, Saturday
c. Sep 7, Sunday
d. Sep 10, Wednesday
b. Sep 13, Saturday
. A patient has been taking medication for his asthma condition. His condition has improved and the doctor has ordered him to stop taking his medication. How much of the drug will still remain in the patient at the end of three half-lives?
a. 50%
b. 6.25%
c. 25%
d. 12.5%
d. 12.5%
When comparing a drug that has a strong attraction to albumin with one that has a weaker attraction, the nurse would anticipate that the distribution of the free drug with the strong attraction would be:
a. Higher than the distribution of the drug with the weaker attraction.
b. No different from the distribution of the drug with the weaker attraction
c. Lower than the distribution of the drug with the weaker attraction
d. Equal as far as free drug distribution goes
c. Lower than the distribution of the drug with the weaker attraction
Select the accurate statement regarding competitive antagonists
a. They bind at a site different than the site where endogenous compounds bind
b. They produce pharmacologic effects by causing receptor activation
c. They are stronger in the absence of an agonist compound
d. They have a higher affinity than an agonist compound
c. They are stronger in the absence of an agonist compound
Drug A has an ED50 of 10 mg & a LD50 of 20 mg. Drug B has an ED50 of 10 mg and a LD50 of 100 mg. Based on this information, which statement is TRUE about A & B?
a. A is more potent than B
b. A is more safer than B
c. B is more potent than A
d. B is more safer than A
d. B is more safer than A
A scientist tests a new drug for pain relief and finds that it provides pain relief at a range of dosages. The overall pain relief (magnitude of response) produced by this drug is almost double of that of available medications at the same tested dosage. What can be said about this new drug?
a. The drug is very potent than the existing drugs
b. The drug is more efficient (more efficacy) than the existing drugs
c. The drug is less efficient (less efficacy) than the existing drugs
d. The drug is less potent than the existing drugs
b. The drug is more efficient (more efficacy) than the existing drugs
Endogenous ligands such as acetylcholine and GABA act through receptors that are
a. Cell membrane embedded enzymes
b. G-Protein coupled receptors systems
c. Transcription factors
d. Ligand-gated ion channels
d. Ligand-gated ion channels
Dose–response relationships can be explained by drug-receptor interaction theories. According to the modified occupancy theory differences in potency between two drugs can be explained by the
a. Difference in affinities towards the receptor
b. Difference in avidities towards the receptor
c. Difference in their intrinsic activity towards the receptor
d. Difference in desensitization of the receptor
a. Difference in affinities towards the receptor
Education on pharmacology is taking place on the nursing unit. The discussion involves the receptor sensitivity of a medication. The presenter asks one nurse to provide an example situation for hyper-sensitization. The nurse’s response would be:
a. The degradation of more receptors
b. Continuous exposure to an agonist
c. Internalization and recycling of receptors
d. Continuous exposure to an antagonist
d. Continuous exposure to an antagonist
The nurse is providing nursing education regarding receptor-less drugs to a group of college students. Which example of a receptor-less drug given by a student would indicate a need for further teaching?
a. Antiseptics
b. Chelating agents
c. Saline laxatives
d. morphine
d. morphine
The following combination of drugs when taken together is a good example for reduced therapeutic (or adverse) effect that is detrimental
a. Morphine and Naloxone
b. Propanalol and albuterol
c. Sublactam and warfarin
d. all of the above
b. Propanalol and albuterol
When one drug alters the absorption of a second drug taken at the same time for example: tetracyclines taken along with antacids or calcium tablets, the interaction would be classified as:
a. A direct chemical reaction.
b. Pharmacodynamic.
c. Pharmacokinetic.
d. Combined toxicity
c. Pharmacokinetic
When one drug works to decrease acidity in the stomach by directly neutralizing the acid (antacid) and another drug decreases stomach acidity by preventing the production of acid in the stomach (Prilosec), how would the interaction be classified?
a. A direct chemical reaction
b. Pharmacodynamic
c. Pharmacokinetic
d. Combined toxicity
b. Pharmacodynamic
When taking monoamine oxidase inhibitors for treating depression, consumption of food items such as fermented cheese, chianti wine etc., rich in the following compound should be avoided to prevent any potential hypertensive crisis:
a. Monoamine
b. Tyrosine
c. Tryptamine
d. Tyramine
d. Tyramine
A patient who has taken antipsychotics for treatment develops “tardive dyskinesia” that resembles parkinson’s disease. This adverse drug reaction would be classified as:
a. An allergic reaction
b. An iatrogenic disease
c. An idiosyncratic effect
d. A teratogenic effect
b. An iatrogenic disease
A nurse is providing patient education regarding the development of drug tolerance. Which statement made by the nurse is correct with regard to the development of drug tolerance?
a. “Drug tolerance is only seen with the use of opioids.”
b. “The patient will require a greater dosage of drug for the same effect to be achieved if tolerance has developed.”
c. “The patient needs a lower dose of the medication until the drug is discontinued.”
d. “Addiction is likely to develop if the drug is decreased, leading to tolerance.”
b. “The patient will require a greater dosage of drug for the same effect to be achieved if tolerance has developed.”
Most people who receive succinylcholine as a muscle paralyzer have a brief response lasting only a few minutes. But a person who has a very prolonged effect from the drug at a standard dosage is experiencing:
a. An anaphylactic reaction.
b. An idiosyncratic effect.
c. An iatrogenic response.
d. A physical dependence.
b. An idiosyncratic effect.
A patient’s unique genetic makeup can lead to variability in drug response. Which of the following is a good example of varied response due to different genetic makeup?
a. Digitalis treatment and increased mortality in women
b. Severe skin reactions in Asians due to consumption of anti-seizure medication Carbamazapine
c. Barbiturates and increased metabolism of drugs
d. all of the above
b. Severe skin reactions in Asians due to consumption of anti-seizure medication
Carbamazapine
Repeated dosing within a short period of time with a drug may lead to a situation referred to as __________________, where the drug effect is lost. Nitroglycerin is a good example for this condition.
a. Idiosyncratic effect
b. Tachyphylaxis
c. Anaphylaxis
d. Iatrogenic effect
b. Tachyphylaxis`
Neuropharmacologic agents can cause which of the following effects?
a. Decreased neurotransmitter synthesis
b. Increased neurotransmitter degradation
c. Direct activation of receptor
d. All of the above
d. All of the above
A nurse is discussing the functions of the parasympathetic and the sympathetic nervous system with a group of nursing students. Which statement made by one of the student indicates a need for further teaching?
a. “The parasympathetic nervous system regulates the digestive functions of the body.”
b. “The sympathetic nervous system regulates the cardiovascular system.”
c. “The sympathetic nervous system implements the fight-or-flight response.”
d. “The parasympathetic nervous system regulates body temperature.”
d. “The parasympathetic nervous system regulates body temperature.”
The receptor subtype and the neurotransmitter involved in sweat glands in the body:
a. Acetylcholine and nicotinic (Nm) receptors
b. Norepinephrine and beta1 receptors
c. Epinephrine and muscarinic receptors (M)
d. Acetylcholine and muscarinic receptors (M)
d. Acetylcholine and muscarinic receptors (M)
Skeletal muscle contraction involves the following neurotransmitter and the receptor
subtype:
a. acetylcholine and nicotinic(Nn type)
b. acetyl choline and muscarinic (M) type
c. acetylcholine and nicotinic (Nm type)
d. norepinephrine and alpha 1 type
c. acetylcholine and nicotinic (Nm type)
A prescriber has ordered bethanechol (Urecholine) for a postoperative patient who has urinary retention. The nurse reviews the patient’s chart before giving the drug. Which part of the patient’s history would be a contraindication to using this drug?
a) Asthma as a child
b) Intestinal obstruction
c) Hypertension
d) Hypothyroidism
b) Intestinal obstruction
Acetylcholine (Miochol-E) has limited therapeutic indication due to its selectivity at cholinergic receptors. Miochol is indicated primarily for:
a) Reducing excessive secretions and mucus in a postoperative patients
b) Lowering intraocular pressure in patients with glaucoma
c) Inhibiting muscular activity in the bladder
d) Producing rapid miosis in cataract surgery
d) Producing rapid miosis in cataract surgery
A prescriber has ordered pilocarpine (Pilocar). A nurse understands that the drug stimulates muscarinic receptors and would expect the drug to have which action?
a) Reduce excessive secretions in a postoperative patient
b) Lower intraocular pressure in patients with glaucoma
c) Inhibit muscular activity in the bladder
d) Prevent hypertensive crisis
b) Lower intraocular pressure in patients with glaucoma
A patient has developed muscarinic antagonist toxicity from ingestion of an unknown chemical. The nurse should prepare to administer which medication?
a) Atropine (Sal-Tropine) IV
b) Physostigmine (Antilirium)
c) An acetylcholinesterase activator
d) Pseudoephedrine
b) Physostigmine (Antilirium)
A nurse plans to administer atropine (Sal-Tropine) to a patient on multiple concurrent medications. The nurse feels confident that which class of drugs would be safe to administer with atropine?
a) Antihistamines
b) Tricyclic antidepressants
c) Phenothiazine antipsychotics
d) Narcotic analgesics
d) Narcotic analgesics
Anticholinergic agents that are selective for M3 receptors are commonly used treat overactive bladders. Identify the anticholinergic agent below used for overactive bladder treatment and is highly M3 receptor selective :
a) Echothiopate (phospholine)
b) Darifinecin (Enablex)
c) Bethenachol (Urechol)
d) Atropine (Sal-tropine, Atropen)
b) Darifinecin (Enablex)
A nurse working in the emergency department is assigned to a child who is arriving by ambulance after being involved in a spill of organophosphate insecticides. What will the nurse expect to be the initial priority for treating this child?
a) Administering diphenhydramine to control secretions
b) Giving beta blockers to prevent tachycardia
c) Providing mechanical ventilation and oxygen
d) Reporting the spill to the Environmental Protection Agency
c) Providing mechanical ventilation and oxygen
A nurse has arrived at work late and missed report. While reviewing the patient’s medications, the nurse notes that the patient is on an irreversible cholinesterase inhibitor. The nurse understands that the only indication for an irreversible cholinesterase inhibitor would be:
a) Glaucoma.
b) Muscular dystrophy
c) Myasthenia gravis
d) Hypertension
a) Glaucoma.
Acetylcholinesterase inhibitors are not only given for treatment of Mysthenia Gravis but four specific acetylcholinesterase inhibitors have been indicated for treatment for Alzheimer’s as well. Identify the one acetylcholinesterase inhibitor used for Alzheimer’s treatment from the list below:
a) Neostigamine (Prostigmin)
b) Physostigamine (Antilirium)
c) Edrophonium (Tensilon/Reversol/Enlon)
d) Rivastigamine (Exelon)
d) Rivastigamine (Exelon)
A nurse is providing education to the other nurses on the unit on how to differentiate between a myasthenic crisis and a cholinergic crisis. To show that they understand the difference, the nurses could state that they should
a) ask the patient about occupation and family history
b) administer atrophine and monitor the patient
c) administer edrophonium (Tensilon/Reversol/enlon) and monitor the response
d) assess serum levels of succinyl choline
c) administer edrophonium (Tensilon/Reversol/enlon) and monitor the response