Pharmacology Chap. 1-11 Flashcards

1
Q

Example: N-acetyl-para-aminophenol

A

Chemical Name

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2
Q

Example: (non-proprietary) acetaminophen

A

Generic Name

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3
Q

Example: (proprietary/brand) Tylenol

A

Trade Name

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4
Q

drug available in the body

A

Bioavailability

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5
Q

plants

A

Active Compounds

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6
Q

salts, Glycosides, oils, gums, and resins

A

Alkaloids

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7
Q

Fillers, vehicle, flavorings, and dye

A

Inactive Compounds

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8
Q

USPDI

A

United States Pharmacopeia-Drug Information

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9
Q

PDR

A

physicians desk reference

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10
Q

(1820) Recognized standard for drug purity

A

USP - United States Pharmacopeia

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11
Q

(1888) Standards for drug formulation

A

NF - National formulary

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12
Q

(1906) Protect public from mislabeled drugs

A

Pure food and Drug act

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13
Q

(1938) drugs must be properly tested

A

Food, Drug, and Cosmetic Act

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14
Q

Food and Drug Administration to monitor and regulate

A

FDA

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15
Q

content, name of drug, substances, warning, manufacture direction, statement must not be false or misleading

A

Label

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16
Q

(1952) Prescription vs. non prescription drugs dispensing of certain drugs by pharmacist limited to prescription by licensed health provider

A

Durham- Humphrey Amendment

17
Q

Hypnotic, narcotics, habit forming drugs

A

Legend Drug

18
Q

(1962) FDA empowered to supervise drug production, official name by FDA

A

Kefauver Harris

19
Q

(1970) 1. Drug-dependent, addiction 2. Funds for education, treatment 3. Drug control: Treasure - Justice Dept. 4. Control drug classified

A

Controlled Substance Act

20
Q

High abuse potential, May lead to severe dependence. No ACCEPTED MEDICAL USE.

A

Controlled Substances (C1)

21
Q

High abuse potential, may lead to severe dependence.

A

Controlled Substances (C2)

22
Q

Abuse potential less than schedules 1 & 2. May lead to moderate dependence.

A

Controlled Substances (C3)

23
Q

Moderate abuse potential. May lead to limited dependence.

A

Controlled Substances (C4)

24
Q

Small abuse potential. May lead to limited dependence.

A

Controlled Substances (C5)

25
Q

(1982) Made it where medicine bottles must have tamper resistant packaging

A

Tamper- Resistant packing regulation Act

26
Q

Alcohol and drug

A

State Control

27
Q

Antibiotics, Narcotics

A

Institution

28
Q

studies failed to demonstrate risk first trimester

A

FDA Pregnancy Categories (A)

29
Q

animals studies = failed to demonstrate risk, but no studies in pregnant women

A

FDA Pregnancy Categories (B)

30
Q

animal studies = adverse effect, no human studies; benefits may outweigh risks

A

FDA Pregnancy Categories (C)

31
Q

positive evidence of fetal risks, but benefits may outweigh risks

A

FDA Pregnancy Categories (D)

32
Q

Studies demonstrated fetal abnormalities, risks outweigh potential benefits.

A

FDA Pregnancy Categories (X)

33
Q

Properties of an Ideal Drug

A

effectiveness, safety, selectivity, reversible action, predictability, ease of administration, low cost, and chemical stability

34
Q

Purity, potency, bioavailability, efficacy, and safety/toxicity

A

Drug standards

35
Q

Developing interventions, outcome or patient goals

A

Planning

36
Q

Client education, medication administration, monitoring compliance

A

Implementation