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Mosby's CT Exam Review Practice Test 1/Mosby's CT Simulated Exam 1 With Updated Answers

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Mosby's CT Exam Review Practice Test 1/Mosby's CT Simulated Exam 1 With Updated AnswersMULTIPLE CHOICE 1. Certain practitioners may prescribe medications. Which of the following practitioners would least likely have the right to write a prescription? a. Doctors of Pharmacy (PharmDs) b. Medical Doctors (MDs) c. Physician Assistants (PAs) d. Nurse Practitioners (NPs) ANS: A Generally, MDs, PAs, and NPs write prescriptions. Under certain conditions, a PharmDmaybe able to author prescriptions, but this is the exception, not the rule. DIF: Cognitive Level 1: Knowledge REF: p.98 2. Of the following laws and amendments regarding drugs in the United States, which was most recently passed? a. Pure Food and Drug Act b. Food Drug and Cosmetic Act c. Durham-Humphrey Act d. Kefauver-Harris Amendment ANS: D The Kefauver-Harris Amendment was passed in 1962; all the other listed laws and amendments were passed before then. DIF: Cognitive Level 1: Knowledge REF: p.99 3. Which of the following describes adulteration? a. “Prepared, packed, or held under unsanitary conditions” b. Labeling that is “false or misleading in any particular way” c. Failure to label “adequate directions for use” d. Failure to carry a label indicating “Warning—May be habit forming” if the product ONLYSTUDENTS STORE 2025 ALL THE BESTONLYSTUDENTS STORE 2 DO NOT COPY is habit forming ANS: A “Prepared, packed, or held under unsanitary conditions” describes adulteration. The other three choices describe misbranding. DIF: Cognitive Level 1: Knowledge REF: p.98 4. Which of the following describes misbranding? a. “Prepared, packed, or held under unsanitary conditions” b. Prepared in containers “composed, in whole or in part, of any poisonous or deleterious substance” c. Failure to label “adequate directions for use” d. Containing unsafe color additives DOWNLOAD THE Test Bank for Mosby's Pharmacy Technician Exam Review 4th Edition Mizner ANS: C Failure to label “adequate directions for use” describes misbranding. The other choices would best describe adulteration. DIF: Cognitive Level 1: Knowledge REF: p.98 5. You would expect to find all of the following except the ____ on a manufacturer’s drug label. a. physician’s name b. name and place of business of the manufacturer, packer, or distributor c. National Drug Code number d. statement of ingredients ANS: A On a manufacturer’s drug label you would expect to find the name and place of business of the manufacturer, packer, or distributor; National Drug Code number; and a statement of ingredients. The doctor’s name would be on a prescription label. DIF: Cognitive Level 3: Application ONLYSTUDENTS STORE 2025 ALL THE BESTONLYSTUDENTS STORE 3 DO NOT COPY REF: p.98 6. You would expect to find all the following except the ____ on an over-the-counter packagelabel. a. patient’s name b. active ingredients c. inactive ingredients d. National Drug Code number ANS: A A patient’s name might be typed on a prescription label that is affixed to an over-the- counter package, but it would not be found on the over-the-counter package label. One would findthe active and inactive ingredients as well as the National Drug Code number on the package label of an over-the-counter product. DIF: Cognitive Level 3: Application REF: p.98-99 7. The Durham-Humphrey Act did not include a provision that ________. a. separated drugs into legend and non-legend b. regulated the use of patient information c. required the supervision of a physician for prescribed medications d. refills could be phoned in from the physician’s office ANS: B The Durham-Humphrey Act of 1951 did not regulate the use of patient information; HIPAAdid that. The act did separate drugs into two categories, legend and non-legend, and didrequire the supervision of a physician for prescribed medications. The act also allowedrefills to be called in from a physician’s office. DIF: Cognitive Level 1: Knowledge REF: p.99 8. The Kefauver-Harris Amendment of 1962 did not include a provision that ________. a. requires all medications in the United States to be pure, safe, and effective b. controlled substances are placed in one of five schedules c. established procedures for both drug applications and investigational drugs ONLYSTUDENTS STORE 2025 ALL THE BESTONLYSTUDENTS STORE 4 DO NOT COPY DOWNLOAD THE Test Bank for Mosby's Pharmacy Technician Exam Review 4th Edition Mizner d. drug manufacturers are required to be responsible for good manufacturing processes ANS: B The Comprehensive Drug Abuse and Control Act of 1970 put controlled substances in fivecategories. The other three choices are part of the Kefauver-Harris Amendment of 1962. DIF: Cognitive Level 1: Knowledge REF: p.99 9. Which of the following drugs would be classified as Schedule I under the DEA’s guidelines?a. Oxycodone b. Hydrocodone c. Peyote d. Codeine ANS: C Peyote is a hallucinogenic and is classified as Schedule I. The other drugs would fall between Schedules II and V depending on their dosage form. DIF: Cognitive Level 1: Knowledge REF: p.105 10. Last night a local pharmacy had its safe broken into, and Schedule II drugs were stolen. Which form would need to be completed? a. DEA Form 106 b. DEA Form 41 c. DEA Form 222 d. DEA Form 22 ANS: A In the case of theft, a DEA Form 106 would need to be filled out after the police and local DEA diversion office were notified. DIF: Cognitive Level 1: Knowledge REF: p.110 11. Which DEA form must be completed to verify the destruction of Schedule II narcotics? ONLYSTUDENTS STORE 2025 ALL THE BESTONLYSTUDENTS STORE 5 DO NOT COPY a. DEA Form 106 b. DEA Form 41 c. DEA Form 222 d. DEA Form 22 ANS: B In the case of destruction of Schedule II narcotics, a DEA Form 41 would need to be filledout. DIF: Cognitive Level 1: Knowledge REF: p.113 12. The proper form to use when ordering Schedule II controlled substances for the pharmacy is DEA Form ________. a. 106 b. 41 c. 222 d. 22 DOWNLOAD THE Test Bank for Mosby's Pharmacy Technician Exam Review 4th Edition Mizner ANS: C For regular ordering of Schedule II medications, DEA Form 222 is used. DIF: Cognitive Level 1: Knowledge REF: p.107 13. The first letter of a prescriber’s DEA number would definitely not be ________. a. A b. B c. Q d. M ANS: C A, B, F, and M would be legitimate starting letters for a physician’s DEA number. DIF: Cognitive Level 1: Knowledge REF: p.107 14. How many refills are available on a Schedule II medication?

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ONLYSTUDENTS STORE 2025 ALL THE BEST


Chapter 02: Federal Requirements
Mizner: Mosby’s Pharmacy Technician Exam Review, 4th Edition

MULTIPLE CHOICE



1. Certain practitioners may prescribe medications. Which of the following practitioners
would
least likely have the right to write a prescription?
a. Doctors of Pharmacy (PharmDs)
b. Medical Doctors (MDs)
c. Physician Assistants (PAs)
d. Nurse Practitioners (NPs)

ANS: A
Generally, MDs, PAs, and NPs write prescriptions. Under certain conditions, a PharmD may
be able to author prescriptions, but this is the exception, not the rule.

DIF: Cognitive Level 1: Knowledge
REF: p.98



2. Of the following laws and amendments regarding drugs in the United States, which was
most
recently passed?
a. Pure Food and Drug Act
b. Food Drug and Cosmetic Act
c. Durham-Humphrey Act
d. Kefauver-Harris Amendment

ANS: D
The Kefauver-Harris Amendment was passed in 1962; all the other listed laws and
amendments were passed before then.

DIF: Cognitive Level 1: Knowledge
REF: p.99



3. Which of the following describes adulteration?
a. “Prepared, packed, or held under unsanitary conditions”
b. Labeling that is “false or misleading in any particular way”
c. Failure to label “adequate directions for use”
d. Failure to carry a label indicating “Warning—May be habit forming” if the product


ONLYSTUDENTS STORE 1 DO NOT COPY

,ONLYSTUDENTS STORE 2025 ALL THE BEST


is habit forming

ANS: A
“Prepared, packed, or held under unsanitary conditions” describes adulteration. The other
three choices describe misbranding.

DIF: Cognitive Level 1: Knowledge
REF: p.98



4. Which of the following describes misbranding?
a. “Prepared, packed, or held under unsanitary conditions”
b. Prepared in containers “composed, in whole or in part, of any poisonous or
deleterious substance”
c. Failure to label “adequate directions for use”
d. Containing unsafe color additives



DOWNLOAD THE Test Bank for Mosby's Pharmacy Technician Exam Review 4th
Edition Mizner
mynursytest.store
ANS: C
Failure to label “adequate directions for use” describes misbranding. The other choices
would
best describe adulteration.

DIF: Cognitive Level 1: Knowledge
REF: p.98



5. You would expect to find all of the following except the ____ on a manufacturer’s drug
label.
a. physician’s name
b. name and place of business of the manufacturer, packer, or distributor
c. National Drug Code number
d. statement of ingredients

ANS: A
On a manufacturer’s drug label you would expect to find the name and place of business of
the manufacturer, packer, or distributor; National Drug Code number; and a statement of
ingredients. The doctor’s name would be on a prescription label.

DIF: Cognitive Level 3: Application


ONLYSTUDENTS STORE 2 DO NOT COPY

, ONLYSTUDENTS STORE 2025 ALL THE BEST


REF: p.98



6. You would expect to find all the following except the ____ on an over-the-counter package
label.
a. patient’s name
b. active ingredients
c. inactive ingredients
d. National Drug Code number

ANS: A
A patient’s name might be typed on a prescription label that is affixed to an over-the-
counter
package, but it would not be found on the over-the-counter package label. One would find
the
active and inactive ingredients as well as the National Drug Code number on the package
label of an over-the-counter product.

DIF: Cognitive Level 3: Application
REF: p.98-99



7. The Durham-Humphrey Act did not include a provision that ________.
a. separated drugs into legend and non-legend
b. regulated the use of patient information
c. required the supervision of a physician for prescribed medications
d. refills could be phoned in from the physician’s office

ANS: B
The Durham-Humphrey Act of 1951 did not regulate the use of patient information; HIPAA
did that. The act did separate drugs into two categories, legend and non-legend, and did
require the supervision of a physician for prescribed medications. The act also allowed
refills
to be called in from a physician’s office.

DIF: Cognitive Level 1: Knowledge
REF: p.99



8. The Kefauver-Harris Amendment of 1962 did not include a provision that ________.
a. requires all medications in the United States to be pure, safe, and effective
b. controlled substances are placed in one of five schedules
c. established procedures for both drug applications and investigational drugs


ONLYSTUDENTS STORE 3 DO NOT COPY

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