Exam 1 Version 2 Flashcards
Package inserts are intended to be used by:
-Distributors
-Healthcare professionals
-Patients
-Wholesalers
-Healthcare professionals
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Please review the Package Inserts Part I activity in the Drug Information Resources course.
FDA may approve a Biologics License Application if the biologic proves to be:
-Researched and branded
-Researched and effective
-Safe and effective
-Safe and branded
: Safe and effective
Which schedule of controlled substances is Valium classified under?
Select one:
-II
-III
-IV
-V
The correct answer is: IV
Which is a principle of HIPAA?
-To counsel patients on new and refill prescription medications
-To dispense prescription medications with child-resistant packaging
-To dispense certain prescription medications with a Medication Guide
-To use and disclose the minimum necessary amount of protected information
-To use and disclose the minimum necessary amount of protected information
To use and disclose the minimum necessary amount of protected information
Mrs. Trent brings a prescription into your community pharmacy for clozapine. What is a requirement of the Clozapine REMS program?
-Eligibility check
-Predispense Authorization code
-Risk Management Authorization number
-Copy of the Patient-Prescriber Acknowledgement form
Answer: Predispense Authorization code
What are the five key components of the patient care process?
-Get, analyze, dispense, bill, evaluate
-Obtain, review, prepare, execute, counsel -Gather, examine, develop, action, educate
-Collect, assess, plan, implement, follow up
-Collect, assess, plan, implement, follow up
When is a DEA 222 form used?
-Sending expired Schedule Il drugs to the wholesaler x
-Destroying expired Schedule Il drugs at the pharmacy
-Sending expired Schedule Il drugs to the reverse distributor
-Destroying expired Schedule Il drugs with a witness present
Sending expired Schedule Il drugs to the reverse distributor
——Please review the Controlled Substances: Transfers, Disposal, and Diversion activity in the Controlled Substances course.
The Food, Drug, and Cosmetic Act of 1938:
-Set requirements for dispensing controlled substances
-Prohibits the sale of misbranded and adulterated products *
-Created two classes of medications, prescription and nonprescription
-Requires manufacturers to prove a drug’s purity, strength, and safety before it can be sold
is: Requires manufacturers to prove a drug’s purity, strength, and safety before it can be sold
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Please review the Laws Affecting Prescription Dispensing Part I activity in the Laws Affecting Prescription Dispensing course.
For an involuntary recall, who requires the recalled drug to be removed from pharmacy shelves?
-Board of Pharmacy
-Food and Drug Administration
-Center for Disease Control and Prevention
-Occupational Safety and Health Administration
Food and Drug Administration
Which DAW code means that no product selection is indicated and substitution is allowed?
-0
-2
-3
-7
-0
Which section of the package insert provides the signs and symptoms for when a patient takes too much of the medication?
-Clinical Pharmacology
-Drug Abuse and Dependence
-Nonclinical Toxicology
-Overdosage
-Overdosage
According to federal law, which controlled substances must be kept in a secure, locked location on a patient care unit?
-Only Schedule Il
-Only Schedule II and III
-Only Schedule II, Ill, and IV x
-Any controlled substance
-Any controlled substance
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Please review the Controlled Substances: Dispensing activity in the Controlled Substances course.
According to federal law, which medication can be called into the pharmacy under most circumstances?
-Actiq
-Avinza
-Forinal
-Focalin
-Fiorinal
Which section of the NDC identifies the name, strength, and dosage form of the medication:
-First
-Second
-Third
-Fourth
-Second
A drug that contains the same active ingredient, but is a different strength is considered a:
-Pharmacologic alternative
-Pharmacologic equivalent
-Therapeutic alternative
-Therapeutic equivalent
-Pharmacologic alternative
