Spring 2023 - Exam 1

Spring 2023 - Exam 1

Professional Development

75 Qs

quiz-placeholder

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Spring 2023 - Exam 1

Spring 2023 - Exam 1

Assessment

Quiz

Professional Development

Professional Development

Practice Problem

Medium

Created by

nathan schirmacher

Used 2+ times

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75 questions

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1.

MULTIPLE CHOICE QUESTION

2 mins • 1 pt

A patient experiences a seizure as an adverse effect after taking a medication that was just released to the market a year ago. What organization should the patient report this side effect to?

FDA
DEA
MedWatch
Board of Pharmacy

2.

MULTIPLE CHOICE QUESTION

2 mins • 1 pt

Which organization is responsible for overseeing the distribution, sale, regulation, and destruction of controlled substances?

FDA
DEA
MedWatch
Board of Pharmacy

3.

MULTIPLE CHOICE QUESTION

2 mins • 1 pt

Fentanyl is classified as a C-II drug and Lyrica is classified as a C-V drug. A patient has stopped using Fentanyl and was prescribed Lyrica. Which of the following statements is correct regarding the categories and trends of controlled substances?

C-II drugs have higher potential for abuse than a C-V
C-V drugs have higher potential for abuse than a C-II
C-II drugs have lower potential for abuse than a C-IV
C-III drugs have lower potential for abuse than a C-IV

4.

MULTIPLE CHOICE QUESTION

2 mins • 1 pt

What is the minimum number of pharmacists that must be working with 3 pharmacy technicians in the hospital pharmacy?

3
2
6
5

5.

MULTIPLE CHOICE QUESTION

2 mins • 1 pt

Toradol is a medication that must be dispensed with a medication guide. What is true regarding medication guides?

Medication guides only need to be dispensed on the first fill of the prescription
Medication guides provide information to patients about adverse events and promote patient safety
Medication guides help keep track of controlled substace sales
Medication guides provide information to patients about therapeutic equivalence

6.

MULTIPLE CHOICE QUESTION

2 mins • 1 pt

What is the purpose of a new drug application?

It requires manufacturers to provide evidence of a drug's safety and efficacy before approval
It provides information about the comparison of two different drugs in terms of safety and efficacy
It allows manufacturers to compre information about drugs that are therapeutically equivalent
It mandates that all over the counter medications and supplements must be FDA approved before sale

7.

MULTIPLE CHOICE QUESTION

2 mins • 1 pt

A patient is enrolled in a clinical trail and is receiving a drug that is being tested for FDA apporval. What group is this patient in?

Control group
Intervention group
Therapeutic group
Prophylaxis group

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