Pharmacology Chap. 1-11 Flashcards

(36 cards)

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

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
(1982) Made it where medicine bottles must have tamper resistant packaging
Tamper- Resistant packing regulation Act
26
Alcohol and drug
State Control
27
Antibiotics, Narcotics
Institution
28
studies failed to demonstrate risk first trimester
FDA Pregnancy Categories (A)
29
animals studies = failed to demonstrate risk, but no studies in pregnant women
FDA Pregnancy Categories (B)
30
animal studies = adverse effect, no human studies; benefits may outweigh risks
FDA Pregnancy Categories (C)
31
positive evidence of fetal risks, but benefits may outweigh risks
FDA Pregnancy Categories (D)
32
Studies demonstrated fetal abnormalities, risks outweigh potential benefits.
FDA Pregnancy Categories (X)
33
Properties of an Ideal Drug
effectiveness, safety, selectivity, reversible action, predictability, ease of administration, low cost, and chemical stability
34
Purity, potency, bioavailability, efficacy, and safety/toxicity
Drug standards
35
Developing interventions, outcome or patient goals
Planning
36
Client education, medication administration, monitoring compliance
Implementation