CH 1 INTRO TO DRUGS

Question 1

A nurse working in radiology administers iodine to a patient who is having a computed tomography (CT) scan. The nurse working on the oncology unit administers chemotherapy to patients who have cancer. At the Public Health Department, a nurse administers a measles-mumps-rubella (MMR) vaccine to a 14-month-old child as a routine immunization. Which branch of pharmacology best describes the actions of all three nurses?

A) Pharmacoeconomics
B) Pharmacotherapeutics
C) Pharmacodynamics
D) Pharmacokinetics

Answer 1

Ans: B

Feedback:
Pharmacology is the study of the biologic effects of chemicals. Nurses are involved with clinical pharmacology or pharmacotherapeutics, which is a branch of pharmacology that deals with the uses of drugs to treat, prevent, and diagnose disease. The radiology nurse is administering a drug to help diagnose a disease. The oncology nurse is administering a drug to help treat a disease. Pharmacoeconomics includes any costs involved in drug therapy. Pharmacodynamics involves how a drug affects the body and pharmacokinetics is how the body acts on the body.

Question 2

2. A physician has ordered intramuscular (IM) injections of morphine, a narcotic, every 4 hours as needed for pain in a motor vehicle accident victim. The nurse is aware this drug has a high abuse potential. Under what category would morphine be classified?

A) Schedule I
B) Schedule II
C) Schedule III
D) Schedule IV

Answer 2

Ans: B
Feedback:
Narcotics with a high abuse potential are classified as Schedule II drugs because of severe dependence liability. Schedule I drugs have high abuse potential and no accepted medical use. Schedule III drugs have a lesser abuse potential than II and an accepted medical use. Schedule IV drugs have low abuse potential and limited dependence liability.

Question 3

3. When involved in phase III drug evaluation studies, what responsibilities would the nurse have?

A) Working with animals who are given experimental drugs
B) Choosing appropriate patients to be involved in the drug study
C) Monitoring and observing patients closely for adverse effects
D) Conducting research to determine effectiveness of the drug

Answer 3

Ans: C
Feedback:
Phase III studies involve use of a drug in a vast clinical population in which patients are asked to record any symptoms they experience while taking the drugs. Nurses may be responsible for helping collect and analyze the information to be shared with the Food and Drug Administration (FDA) but would not conduct research independently because nurses do not prescribe medications. Use of animals in drug testing is done in the preclinical trials. Select patients who are involved in phase II studies to participate in studies where the participants have the disease the drug is intended to treat. These patients are monitored closely for drug action and adverse effects. Phase I studies involve healthy human volunteers who are usually paid for their participation. Nurses may observe for adverse effects and toxicity.

Question 4

4. What concept is considered when generic drugs are substituted for brand name drugs?

A) Bioavailability
B) Critical concentration
C) Distribution
D) Half-life

Answer 4

Ans: A
Feedback:
Bioavailability is the portion of a dose of a drug that reaches the systemic circulation and is available to act on body cells. Binders used in a generic drug may not be the same as those used in the brand name drug. Therefore, the way the body breaks down and uses the drug may differ, which may eliminate a generic drug substitution. Critical concentration is the amount of a drug that is needed to cause a therapeutic effect and should not differ between generic and brand name medications. Distribution is the phase of pharmacokinetics, which involves the movement of a drug to the body’s tissues and is the same in generic and brand name drugs. A drug’s half-life is the time it takes for the amount of drug to decrease to half the peak level, which should not change when substituting a generic medication.

Question 5

5. A nurse is assessing the patient’s home medication use. After listening to the patient list current medications, the nurse asks what priority question?

A) “Do you take any generic medications?”
B) “Are any of these medications orphan drugs?”
C) “Are these medications safe to take during pregnancy?” D) “Do you take any over-the-counter medications?”

Answer 5

Ans: D
Feedback:
It is important for the nurse to specifically question use of over-the-counter medications because patients may not consider them important. The patient is unlikely to know the meaning of “orphan drugs” unless they too are health care providers. Safety during pregnancy, use of a generic medication, or classification of orphan drugs are things the patient would be unable to answer but could be found in reference books if the nurse wishes to research them.

Question 6

6. After completing a course on pharmacology for nurses, what will the nurse know?

A) Everything necessary for safe and effective medication administration
B) Current pharmacologic therapy; the nurse will not require ongoing education for 5
years.
C) General drug information; the nurse can consult a drug guide for specific drug
information.
D) The drug actions that are associated with each classification of medication

Answer 6

Ans: C
Feedback:
After completing a pharmacology course nurses will have general drug information needed for safe and effective medication administration but will need to consult a drug guide for specific drug information before administering any medication. Pharmacology is constantly changing, with new drugs entering the market and new uses for existing drugs identified. Continuing education in pharmacology is essential to safe practice. Nurses tend to become familiar with the medications they administer most often, but there will always be a need to research new drugs and also those the nurse is not familiar with because no nurse knows all medications.

Question 7

7. A nurse is instructing a pregnant patient concerning the potential risk to her fetus from a Pregnancy Category B drug. What would the nurse inform the patient?

A) “Adequate studies in pregnant women have demonstrated there is no risk to the
fetus.”
B) “Animal studies have not demonstrated a risk to the fetus, but there have been no
adequate studies in pregnant women.”
C) “Animal studies have shown an adverse effect on the fetus, but there are no
adequate studies in pregnant women.”
D) “There is evidence of human fetal risk, but the potential benefits from use of the
drug may be acceptable despite potential risks.”

Answer 7

Ans: B
Feedback:
Category B indicates that animal studies have not demonstrated a risk to the fetus. However, there have not been adequate studies in pregnant women to demonstrate risk to a fetus during the first trimester of pregnancy and no evidence of risk in later trimesters. Category A indicates that adequate studies in pregnant women have not demonstrated a risk to the fetus in the first trimester or in later trimesters. Category C indicates that animal studies have shown an adverse effect on the fetus, but no adequate studies in humans. Category D reveals evidence of human fetal risk, but the potential benefits from the use of the drugs in pregnant women may outweigh potential risks.

Question 8

8. Discharge planning for patients leaving the hospital should include instructions on the use of over-the-counter (OTC) drugs. Which comment by the patient would demonstrate a good understanding of OTC drugs?

A) “OTC drugs are safe and do not cause adverse effects if taken properly.”
B) “OTC drugs have been around for years and have not been tested by the Food and
Drug Administration (FDA).”
C) “OTC drugs are different from any drugs available by prescription and cost less.”
D) “OTC drugs could cause serious harm if not taken according to directions.”

Answer 8

Ans: D
Feedback:
It is important to follow package directions because OTCs are medications that can cause serious harm if not taken properly. OTCs are drugs that have been determined to be safe when taken as directed; however, all drugs can produce adverse effects even when taken properly. They may have originally been prescription drugs that were tested by the FDA or they may have been grandfathered in when the FDA laws changed. OTC education should always be included as a part of the hospital discharge instructions.

Question 9

9. What would be the best source of drug information for a nurse?

A) Drug Facts and Comparisons
B) A nurse’s drug guide
C) A drug package insert
D) The Physicians’ Drug Reference (PDR)

Answer 9

Ans: B
Feedback:
A nurse’s drug guide provides nursing implications and patient teaching points that are most useful to nurses in addition to need-to-know drug information in a very user friendly organizational style. Lippincott’s Nursing Drug Guide (LNDG) has drug monographs organized alphabetically and includes nursing implications and patient teaching points. Numerous other drug handbooks are also on the market and readily available for nurses to use. Although other drug reference books such as Drug Facts and Comparisons, PDR, and drug package inserts can all provide essential drug information, they will not contain nursing implications and teaching points and can be more difficult to use than nurse’s drug guides.

Question 10

10. The nurse is preparing to administer a medication from a multidose bottle. The label is torn and soiled but the name of the medication is still readable. What is the nurse’s priority action?

A) Discard the entire bottle and contents and obtain a new bottle.
B) Find the drug information and create a new label for the bottle.
C) Ask another nurse to verify the contents of the bottle.
D) Administer the medication if the name of the drug can be clearly read.

Answer 10

Ans: A
Feedback:
When the drug label is soiled obscuring some information the safest action by the nurse is to discard the bottle and contents because drug labels contain a great deal of important information, far more than just the name of the drug. Concentration of the drug, expiration date, administration directions, and precautions may be missing from the label and so put the patient at risk. Looking up drug information in a drug handbook or consulting with another nurse will not supply the expiration date or concentration of medication. Be safe and discard the bottle and its contents.

Question 11

11. What aspect of pharmacology does a nurse study? (Select all that apply.)

A) Chemical pharmacology
B) Molecular pharmacology
C) Impact of drugs on the body
D) The body's response to a drug
E) Adverse and anticipated drug effects

Answer 11

Ans: C, D, E
Feedback:
Nurses study pharmacology from a pharmacotherapeutic level, which includes the effect of drugs on the body, the body’s response to drugs, and both expected and unexpected drug effects. Chemical and molecular pharmacology (Options A and B) are not included in nursing pharmacology courses.

Question 12

12. The nurse, providing patient teaching about home medication use to an older adult, explains that even when drugs are taken properly they can produce negative or unexpected effects. What are these negative or unexpected effects called?

A) Teratogenic effects
B) Toxic effects
C) Adverse effects
D) Therapeutic effects

Answer 12

Ans: C
Feedback:
Negative or unexpected effects are known as adverse or side effects. Teratogenic effects are adverse effects on the fetus and not a likely concern for an older adult. Toxic effects occur when medication is taken in larger than recommended dosages caused by an increase in serum drug levels. Therapeutic effects are the desired actions for which the medication is prescribed.

Question 13

13. After administering a medication, for what would the nurse assess the patient?

A) Drug effects
B) Allergies
C) Pregnancy
D) Preexisting conditions

Answer 13

Ans: A
Feedback:
After the medication is administered, the nurse assesses the patient for drug affects, both therapeutic and adverse. The nurse would assess the patient for allergies, preexisting conditions, and pregnancy before administering a medication.

Question 14

14. The nurse receives an order to administer an unfamiliar medication and obtains a nurse’s drug guide published four years earlier. What is the nurse’s most prudent action?

A) Find a more recent reference source.
B) Use the guide if the drug is listed.
C) Ask another nurse for drug information.
D) Verify the information in the guide with the pharmacist.

Answer 14

Ans: A
Feedback:
The nurse is responsible for all medications administered and must find a recent reference source to ensure the information learned about the medication is correct and current. Using an older drug guide could be dangerous because it would not contain the most up-to-date information. Asking another nurse or the pharmacist does not guarantee accurate information will be obtained and could harm the patient if the information is wrong.

Question 15

15. What would the nurse provide when preparing a patient for discharge and home medication self-administration?

A) Personal contact information to use if the patient has questions
B) Thorough medication teaching about drugs and the drug regimen
C) Over-the-counter medications to use to treat potential adverse effects
D) A sample size package of medication to take home until prescription is filled

Answer 15

Ans: B
Feedback:
The nurse is responsible for providing thorough medication teaching about drugs and the drug regimen to ensure the patient knows how to take the medication and when to notify the provider. The nurse never provides personal contact information to a patient. If adverse effects arise, the patient is taught to call the health care provider and should not self-medicate with over-the-counter drugs, which could mask serious symptoms. The nurse never dispenses medication because it must be properly labeled for home use; this is done by the pharmacy.

Question 16

16. In response to the patient’s question about how to know whether drugs are safe, the nurse explains that all medications undergo rigorous scientific testing controlled by what organization?

A) Food and Drug Administration (FDA)
B) Drug Enforcement Agency (DEA)
C) Centers for Disease Control and Prevention (CDC)
D) Joint Commission on Accreditation of Healthcare Organizations (JCAHO)

Answer 16

Ans: A
Feedback:
The FDA is responsible for controlling and regulating the development and sale of drugs in the United States, allowing new drugs to enter the market only after being subjected to rigorous scientific testing. The DEA regulates and controls the use of controlled substances. The CDC monitors and responds to infectious diseases. The JCAHO is an accrediting body that inspects acute care facilities to ensure minimum standards are met.

Question 17

17. The nurse, assisting with Phase I drug studies, is talking with a woman who asks, “Why can’t I participate in this study?” What would be the nurse’s best response?

A) Drugs pose a greater risk to women of reproductive age.
B) Drugs are only tested on men because they are stronger.
C) Women are more prone to adverse effects from medications.
D) Drugs affect women differently than they affect women.

Answer 17

Ans: A
Feedback:
Phase I drug trials usually involve healthy male volunteers because chemicals may exert an unknown and harmful effect on ova in women which could result in fetal damage when the woman becomes pregnant. Drugs are tested on both men and women, but women must be fully informed of risks and sign a consent stating they understand the potential for birth defects. Women are not more prone to adverse effects of medications. Although some drugs may affect women differently than men, this is a rationale for why drugs need to be tested on women, not an explanation of why women are not included in a phase I study.

Question 18

18. The patient tells the nurse about a new drug being tested to treat the disease she was diagnosed with and asks the nurse whether the doctor can prescribe a medication still in the preclinical phase of testing. What is the nurse’s best response?

A) “The doctor would have to complete a great deal of paperwork to get approval to
prescribe that drug.”
B) “Sometimes pharmaceutical companies are looking for volunteers to test a new
drug and the doctor could give them your name.”
C) “Drugs in the preclinical phase of testing are only tested on animals and so would
not be available to you.”
D) “Drugs in the preclinical phase of testing are given only to healthy young men and
so would not be available to you.”

Answer 18

Ans: C
Feedback:
During the preclinical phase of testing drugs are tested on animals and are not available to patients. In phase I, the drug is tested on volunteers who are usually healthy young men. It is only in phase III studies that the drug is made available to prescribers who agree to closely monitor patients getting the medication.

Question 19

19. The nurse is caring for a patient who had a severe, acute, previously unseen adverse effect of a drug in Phase III testing. The patient asks, “After all the testing done on this drug, didn’t they know this adverse effect could occur?” What is the nurse’s best response? (Select all that apply.)
    A) “Pharmaceutical companies sometimes underreport problems to make more money.”
    B) “Your response to this medication will be reported to the drug company and the Food and Drug Administration (FDA).”
    C) “When a drug begins to be used by a large clinical market, new adverse effects may be found.”
    D) “The pharmaceutical company weighs the benefits of the drug with the severity of adverse effects.”
    E) After a drug reaches phase III testing it is considered an accepted drug and will not be recalled.”

Answer 19

Ans: B,C
Feedback:
When a new and unexpected adverse effect occurs, especially one of a serious nature, it is reported to the drug company who reports it to the FDA immediately. When a large number of people begin using the drug in phase III studies, it is not unusual to identify adverse effects not previously noted. It would be both unprofessional and inaccurate to imply that pharmaceutical companies put profit ahead of patient concern because lawsuits would remove any potential profit if a drug proves harmful. The FDA is responsible for weighing risk versus benefit in deciding whether to allow the drug to move to the next phase of testing. Drugs found to have serious adverse effects can be removed from the market at any time.

Question 20

20. The telephone triage nurse receives a call from a patient asking for a prescription for a narcotic to manage his surgical pain. The nurse explains that narcotic prescriptions must be written and cannot be called in to the pharmacy. The patient says, “Why are narcotics so difficult to get a prescription for?” What is the nurse’s best response?

A) “The Drug Enforcement Agency (DEA) determines the risk for addiction and the Food and Drug Administration (FDA) enforces their control.”
B) “The increase in the number of drug addicts has made the rules stronger.”
C) “The Centers for Disease Control and Prevention (CDC) regulates use of
controlled substances to reduce the risk of injury.”
D) “Controlled substances like narcotics are controlled by the FDA and the DEA.”

Answer 20

Ans: D
Feedback:
Controlled substances are controlled by the FDA and the DEA: the DEA enforces control while the FDA determines abuse potential. Regulations related to controlled substances have remained strict and specific and have not been significantly impacted by substance abusers. The CDC is not involved in control of narcotics and other controlled substances.

Question 21

21. The nurse explains the Drug Enforcement Agency’s (DEA’s) schedule of controlled substances to the nursing assistant who asks, “Do you ever get a prescription for Schedule I medications?” What is the nurse’s best response?

A) “Schedule I medications have no medical use so they are not prescribed.”
B) “Schedule I medications have the lowest risk for abuse and do not require a prescription.”
C) “Schedule I medications are only prescribed in monitored units for patient safety.”
D) “Schedule I medications are found in antitussives and antidiarrheals sold over the
counter.”

Answer 21

Ans: A
Feedback:
Schedule I medications have no medical use and are never prescribed. Schedule V medications have the lowest risk for abuse and are found mostly in antitussives and antidiarrheals but they are not sold over the counter.

Question 22

22. The nurse, working on the maternity unit, receives a call from a pregnant woman asking how she can know whether a medication is safe to take while pregnant. What is the nurse’s best response?

A) “You can take any drug indicated as a Category A.”
B) “No medications should be taken during pregnancy.”
C) “Never take medication until you receive approval from your health care
provider.”
D) “Most medications are safe but you need to weigh benefit against risk.”

Answer 22

Ans: C
Feedback:
The best response to a pregnant woman asking about medication usage is to talk with her obstetric practitioner because the best advice will come from someone who knows their health and pregnancy history. While Category A drugs have no known risk, they may be contraindicated by the woman’s health condition or pregnancy issues and many pregnant women would not know what it means to be a Category A drug. Medications can be helpful during pregnancy if taken safely and appropriately. Although risk benefit needs to be weighed, it should occur with advice from the obstetric practitioner.

Question 23

23. A patient asks the nurse, “What is a Drug Enforcement Agency (DEA) number?” What is the nurse’s best response?

A) “DEA Numbers are given to physicians and pharmacists when they register with
the DEA to prescribe and dispense controlled substances.”
B) “Physicians must have a DEA number in order to prescribe any type of
medication for patients.”
C) “DEA numbers are case numbers given when someone breaks the law involving a
controlled substance.”
D) “DEA numbers are contact numbers to talk with someone at the DEA when
questions arise about controlled substances.”

Answer 23

Ans: A
Feedback:
All pharmacists and physicians must register with the DEA. They are given numbers that are required before they can dispense or prescribe controlled substances. DEA numbers are only needed when prescribing controlled substances. A DEA number is neither a case number nor a phone number.

Question 24

24. When moving to another state, what is the nurse responsible for becoming familiar with?

A) Local policies and procedures for controlled substance administration
B) Local provider’s Drug Enforcement Agency (DEA) number for prescribing
controlled substances
C) The agency monitoring controlled substances in the new state
D) Board of Nursing regulations of controlled substances in the new state

Answer 24

Ans: A
Feedback:
The nurse needs to learn local policies and procedures for controlled substance administration because they can vary with some local governments more rigorous than others. Nurses do not memorize a provider’s DEA numbers. The DEA is a federal agency that monitors controlled substances in all states. State boards of nursing do not regulate controlled substances but may regulate how controlled substances are administered by nurses.

Question 25

25. The patient looks at the prescription provided by the doctor and asks the nurse whether he can request a generic substitution. The nurse answers “No” when noting what on the prescription?

A) No refills
B) DAW
C) Brand name used on prescription
D) Patient older than 65 years of age

Answer 25

Ans: B
Feedback:
DAW stands for “dispense as written” and means that the doctor does not want a generic substituted for the prescribed medication. Requesting no refills does not preclude the substitution of a generic medication. Even when the brand name is ordered, the pharmacist can substitute a generic equivalent so long as the prescriber does not write DAW. Generic substitutions are not impacted by the patient’s age.

Question 26

26. The patient asks the nurse why generic drugs would be used and voices concerns that only the brand name product will be safe. What is the nurse’s best response?

A) “Generic drugs are often less expensive.”
B) “Some quality control problems have been found with generic drugs.”
C) “Most generic drugs are very safe and can be cost effective as well.”
D) “Although initial cost is higher for a brand name it may cost less in the long run.”

Answer 26

Ans: C
Feedback:
Most generic medications are completely safe and may be identical to the brand name drug except generic medications are often less expensive, but this does not address the patient’s concern about safety. Although some quality control issues have occurred in the past, this does not address the patient’s concerns regarding safety or explain why generic drugs are prescribed and used. Although some doctors believe initial cost is higher but will cost less over time, this response also does not address the patient’s concerns.

Question 27

27. While studying for the test, the nursing student encounters the following drug: papaverine (Pavabid). What does the nursing student identify the name Pavabid as?

A) The generic name
B) The chemical name
C) The brand name
D) The chemical and generic name

Answer 27

Ans: C
Feedback:
Several clues indicate the brand name including capitalization of the first letter in the name and in parentheses. Generic names are not capitalized; chemical names are descriptions of the chemistry of the medication resulting in complicated names.

Question 28

28. The patient is prescribed a medication that was just placed in Phase IV study. The patient tells the nurse, “This medication is too expensive. Could the doctor order a generic form of this medication?” What is the nurse’s most accurate response?

A) “Medications are not produced in generic form until the patent expires, which
normally takes several years.”
B) “You can request the generic form but the binder used may make the drug less
effective for this medication.”
C) “The generic form of the medication would not be any less expensive because this
is a relatively new medication.”
D) “Generic medications are lower quality drugs and that would mean you would not
be getting the best treatment available.”

Answer 28

Ans: A
Feedback:
When a new drug enters the market, it is given a time-limited patent; generic forms of the medication cannot be produced until the patent expires. Because no generic version of this drug will exist because it is so new, it is impossible to predict what binder will be used or what the cost would be.

Question 29

29. The nurse learns that a drug needed by the patient is classified as an orphan drug and recognizes what as a reason for this classification? (Select all that apply.)

A) The drug is rarely prescribed.
B) The drug has dangerous adverse effects.
C) The drug treats a rare disease.
D) The patent on the medication is still effective.
E) Production by a company that only manufactures drugs.

Answer 29

Ans: A, B, C
Feedback:
Drugs are classified as orphan drugs when they are not financially viable for a drug company to produce either because of risk for lawsuits about adverse effects or because the drug is not prescribed, which is often seen in rare diagnoses. Generic drugs are not produced until the patent expires, but this has no impact on classifying a particular drug as an orphan drug. Generic drugs are often produced by companies that only manufacture drugs without conducting research, but this has no bearing on the classification of orphan drugs.

Question 30

30. While collecting a medication history, the patient admits to doubling the recommended dosage of an over-the-counter (OTC) medication, saying “It’s harmless or they would require a prescription.” What is the nurse’s best response?

A) “OTC drugs are serious medications and carry serious risks if not taken as
directed.”
B) “Taking medications like that is careless and you could kill yourself doing it.”
C) “Sometimes you need to take more than the package directs to treat the
symptoms.”
D) “Did you notify your doctor of the increased dosage you were taking?”

Answer 30

Ans: A
Feedback:
OTC drugs are no less a medication than prescription drugs and carry the same types of risks for overdosage and toxicity if directions are not followed. Although increasing the dosage is careless and dangerous, it is important to use the information as a teaching opportunity rather than scolding the patient. Agreeing with the patient or asking her if she talked to the doctor misses the teaching opportunity, which could be harmful for the patient.

Question 31

31. The patient asks the nurse, “Is it safe to take over-the-counter (OTC) medications with prescription medications?” What is the nurse’s best response? (Select all that apply.)

A) “OTC medications can interact with prescription medications.”
B) “It is important to tell your doctor all medications you take, including OTC.”
C) “OTC medications could mask or hide signs and symptoms of a disease.”
D) “You should avoid taking any OTC medication when taking prescription drugs.”
E) “Taking OTC medications can make your prescription medication more
effective.”

Answer 31

Ans: A, B, C
Feedback:
OTC medications can interact with prescription medications or other OTC so it is always important to consult your pharmacist and provider for advice. To provide the most accurate instruction, the health care provider must know all medications taken including dietary supplements, OTC, and prescription. OTC medications could mask or hide symptoms of a disease so it is always important to consult a physician if symptoms persist. OTC medications are not prohibited when taking prescription drugs as long as no drug interaction occurs. How an OTC will impact a prescription medication varies depending on the medications involved, so it is incorrect to say it will make the prescription drug more effective.

Question 32

32. Before administering a prescription medication, what information does the nurse find on the drug label? (Select all that apply.)

A) Brand name
B) Generic name
C) Drug concentration 
D) Expiration date
E) Adverse effects

Answer 32

Ans: A, B, C, D Feedback:
Prescription drug labels will contain the brand name, generic name, drug concentration, and expiration date. Adverse effects will not be listed on drug labels.

Question 33

33. The nurse is preparing a medication that is new to the market and cannot be found in the nurse’s drug guide. Where can the nurse get the most reliable information about this medication?

A) Package insert
B) Another nurse
C) Drug manufacturer
D) Physician

Answer 33

Ans: A
Feedback:
The most reliable information about the drug can be found on the package insert supplied by the manufacturer because it was prepared according to strict Food and Drug Administration (FDA) regulations. Asking another nurse or the physician is not reliable and cannot be verified as accurate. It would not be realistic to call the drug manufacturer for information.

Question 34

34. The nurse explains that what drug resource book is compiled from package inserts?

A) Nurses Drug Guide
B) Physicias’s Desk Reference (PDR)
C) Drug Facts and Comparisons
D) AMA Drug Evaluations

Answer 34

Ans: B
Feedback:
The PDR is a compilation of information found on package inserts. The Nurses Drug Guide uses more easily understood language and incorporates nursing considerations and patient teaching points. Drug Facts and Comparisons includes cost comparison, often not found in other drug resource guides. The AMA Drug Evaluations is far less biased than the PDR and includes drugs still in the research stage of development.