Pharmacy Practice Ch 3 Exam

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32 Terms

1
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When a generic manufacturer files an abbreviated NDA with the FDA, it must prove 

 

Bioequivalence

2
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Deceptive advertising by manufacturers of dietary supplements is regulated by the 

 

FTC

3
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The FDA monitors the incidence and risk of adverse drug reactions to vaccines on the market with 

 

VAERS

4
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Select the TRUE statement regarding an active ingredient 

 

It exerts the desired therapeutic effect

5
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What is the function of a vaccine?

 

to produce Immunity to disease

6
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What defines a synthesized drug?

 

An imitation of naturally occurring substances

7
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What is the field of study that examines the relationship between an individual's genes and his or her body's response to a drug? 

 

Pharmacogenomics

8
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What is true about an inert ingredient

 

It has no pharmacological effect

9
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What is the purpose of a pharmacodynamic Agent

 

to alter body functioning

10
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The FDA's medical product safety reporting program for the health professions, and patients and consumers

Medwatch

11
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What Discovery let to the emphasis on sterility and cleanliness in the practice of medicine and manufacture of pharmaceuticals? 

 

Germ Theory

12
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Which of the following would be classified as drugs by the FDA?

 

homeopathic medications

13
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Probiotics are Microorganisms that

 

promote positive digestive health

14
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Which of these is not a Hormone therapy 

 

nitroglycerine

15
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Why is the generic drug application submitted to the FDA called abbreviated?

 

It only need to prove bioequivalence

16
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Why does the FDA require OTC product labeling to list active and inactive ingredients?

 

prevent allergic reactions

17
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To fill a prescription and bill insurance for Xanax, a pharmacy technician will need the prescriber's

 

NPI and DEA number

18
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Based on significant incidents of adverse drug reactions, who has the power to recall, or pull drugs off the market?

 

FDA

19
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If a drug have the possibility of an extreme ADR,  this information must be included in the 

 

Product package insert's black box and the patient's information printout

20
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The discovery of the existence of microbes and their role in causing illness is known as the 

 

germ theory

21
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The process by which patients are protected from harmful germs during surgery or medical procedures is called

 

aseptic technique

22
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The hormone insulin was discovered and isolated for the treatment of diabetes due to the difficulties in the functioning of the 

 

pancreas

23
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Antineoplastic drugs are classified as

 

destructive agent

24
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When receiving a prescription to fill and talking to a patient, you should get a complete _______________ to prevent the patient form having a bad reaction to the drug

 

allergy history

25
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If a liquid antibiotic had flavoring added to improve the taste what type ingredient would that be? 

 

inert

26
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What document signed by a research-study participant states the purpose and the risk o the research in easy to understand terms?

 

informed consent form

27
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If you are helping a patient find a good quality vitamin, what marking on the label identifies the supplement is good quality?

 

USP verified

28
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Which of the following statements about dietary supplements approval process is true?

 

Supplements are considered to be food, not drugs

29
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The FDA monitors the incidence and risk of adverse drug reactions to new drugs on the market with

AERS

30
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A medications that targets specific needs in the body is?

 

Therapeutic

31
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What classification of drugs are natural substances combined with laboratory substances?

 

Semisynthetic drugs

32
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Where do would you find the NDC number on a stock bottle

 

At the top of the bottle or in the bar code