EXAM #1: INTRODUCTION I & II Flashcards

1
Q

What is the definition of pharmacology?

A

Science concerned with the interaction of chemical substances with a biological target

**Specifically, what are the mechanisms that counteract disease?

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2
Q

What is the definition of pharmacy?

A

Science and profession concerned with:

  • Preparation
  • Dispensing
  • Proper utilization

of drug products.

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3
Q

What is toxicology?

A

Science of poisons and toxicity that focuses on the harmful effects of drugs/ their mechanisms

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4
Q

What is a prescription drug?

A

Agents whose sale is restricted and only available with an Rx from a LICENSED provider

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5
Q

What organization regulated prescription drugs at the federal level? What about the state level? What is the difference?

A
Federal= FDA 
State= controls licensure of providers that Rx
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6
Q

Outline the fives schedules of drugs.

A

I= high abuse potential, no medical use*

II= high abuse potential, WITH medical use

III= less abuse potential than I or II, low potential for dependence

IV= less abuse potential and dependence than III

V= less abuse and limited dependence

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7
Q

What is a nonprescription of OTC drug?

A

Drugs that can be sold with directions for safe use by the public

*****Note that there is wide variation in the marketing of these drugs for substances that are v. similar

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8
Q

Are nonprescription drugs regulated?

A

Yes, these drugs are also monitored by the FDA

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9
Q

What are the clinical considerations regarding OTC drugs that you should keep in mind as a provider?

A

1) May be a CHEAPER/ useful option for a patient
2) May EXACERBATE a medical condition
3) Drug INTERACTIONS
4) May be used INAPPROPRIATELY

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10
Q

What are the three basic steps of drug development?

A

1) Drug identification
2) In vitro experimentation and animal testing
3) Clinical testing

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11
Q

What happens once a drug is identified?

A

Animal testing occurs

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12
Q

What are the purposes of animal testing?

A
  • Drug characterization

- Determination of a lethal dose

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13
Q

What is the difference between phase I, II, III, and IV clinical testing?

A
I= Is the dose safe?
- Small # of patients 
II= Does it work?
- Small # of patients 
III= Is it better? RCT* 
IV= Should it stay?
- "Post-marketing studies"
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14
Q

What are the three names that are given to a drug?

A
  • Chemical name
  • Generic name
  • Trade name
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15
Q

What is the chemical name of a drug?

A

Standard chemical nomenclature denoting the chemical structure

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16
Q

What is the generic name of a drug?

A

Non-proprietary name of a drug derived from the chemical name*

This is the only name of a drug that will be given on boards

17
Q

What is the trade name of a drug?

A

Registered brand name or trademark given to a specific drug

18
Q

How are the five general methods for classifying drugs?

A
  • Drug action
  • Molecular target
  • Drug source
  • Chemical nature
  • Generic name
19
Q

What type of drug classification is “antiviral agent?”

A

Drug action

20
Q

What type of drug classification is “Beta-Blocker?”

A

Molecular target

21
Q

What type of drug classification is “atropine?”

A

Drug source

Atropine is a naturally occuring compound from the ATROPA genus of plants

22
Q

What type of drug classifications are the titles, “steroids, barbiturates, benzodiazepines?”

A

Chemical nature

23
Q

What type of drug classification is “atorvastatin?”

A

Generic name

24
Q

What is pharmacokinetics?

A

“What the body does to a drug.”

25
Q

What is pharmacodynamics?

A

“What the drug does to the body.”