Test 1 Review Flashcards

0
Q

Drug not protected by a trademark but regulated by the FDA

A

Generic name

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1
Q

Brand name given to a drug by its manufacturer

A

Trade name

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2
Q

Drug that does not require a prescription, non legend drug:

A

Over the counter

OTC

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3
Q

Purity

A

Standard that specifies the type or concentration

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4
Q

Potency

A

Concentration of active ingredients in a medication

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5
Q

Quality

A

Condition of ensuring that each time a medication is taken as ordered or In compliance with the manufacturers directions, it meets the same drug standards

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6
Q

Efficacy

A

Ability of a drug to produce the desired chemical change in the body

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7
Q

Placebo

A

Medication with no pharmacologic or therapeutic effect that is used to satisfy a patients psychologic need for medication

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8
Q

Who controls prescriptions

A

DEA & FDA

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9
Q

Who regulates the development of drugs

A

FDA

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10
Q

Who oversees responsibility for purity, safety, identity and strength of meds:

A

FDA

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11
Q

What do the letters FDA represent

A

Food and drug administration

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12
Q

What department is the FDA a division of

A

Department of health and human services

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13
Q

What do the letters DEA represent

A

Drug enforcement agencies

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14
Q

What is the DEA’s function as related to pharmacology

A

Regulates and enforces the manufacturing of dangerous and potentially abusive drugs

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15
Q

What do the letters BNDD

A

Bureau of narcotics and dangerous drugs

16
Q

What is the BNDD’s function

A

Register all persons who manufacture, dispense, prescribe, & administer any controlled substances

17
Q

What do the letters USP represent

A

U.S. pharmacopoeia

18
Q

What is the purpose of the USP

A

Book that contains official standards to which a drug was manufactured

19
Q

Investigational new drug testing is completed on

A

Animals

20
Q

Preclinical testing is done/completed on

A

Animals

21
Q

What records must a physician keep when using drugs on the DEA scheduled list

A

(1) log of scheduled drugs on hand and dispensed
(2) copies of suppliers invoice as a receipt for the drug
(3) DEA / BNDD registration #

22
Q

Are drug standards the same everywhere in the world

A

No

23
Q

Are over the counter drugs regulated, if so by who

A

Yes, FDA

24
Q

Name of first act to address narcotics

A

Harrison narcotic act or federal narcotic act of 1914

25
Q

NF

A

National formulary

26
Q

What is the function of the NF

A

Branch that approves the national formulary

27
Q

What agency follows the potential for abusive drugs

A

DEA

28
Q

Describe how controlled substances should be handled in the office

A

Keep separate & securely locked, double locked for opiates.
Stocks should be minimal.
Inventory controlled substances every 2yrs.
Notify DEA if theft occurs.
Must surrender expired meds to DEA.

29
Q

What type of drugs must the physician have permission to dispose of

A

Scheduled & non-scheduled drugs

out dated controlled substances

30
Q

Responsibilities of physicians office related to drug samples

A

Can accept on Dr’s discretion, can’t be sold, Dr must sign, only Dr can sign, must be packaged, kept locked, document samples given to patients on their charts, dispose of unused samples properly, can’t give back to drug rep, can’t use outdated samples, can’t repackage, report abuse of coworker, don’t allow to leave any meds they want, must be approved

31
Q

Schedule 1

A

Highest potential for abuse-not prescribed

32
Q

Schedule 2

A

Highest potential for abuse. Rx only. No refills.

33
Q

Schedule 3

A

Moderate potential for abuse. Rx only. 5 refills within 6 months

34
Q

Schedule 4

A

Lower potential for abuse Rx only 5 refills within 6 months

35
Q

Schedule 5

A

Lowest, over the counter

36
Q

Will drugs always stay on same schedule

A

No

37
Q

211 drugs for potential abuse under what act

A

Comprehensive drug abuse and control act of 1970