Legislation Flashcards

(31 cards)

1
Q

What infection control is needed for airborne protection?

A

Eyewear, gloves, mask

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2
Q

What infection control is needed for contact protection?

A

Eyewear, gloves, gown, mask

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3
Q

What infection control is needed for droplet protection?

A

Eyewear, gloves, gown, mask

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4
Q

What is the orphan drug act?

A

An act to motivate development and provision of new, effective drugs for rare diseases

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5
Q

What is pharmacology?

A

Study of drugs and their interactions with the body

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6
Q

What is a drug?

A

Chemical used to diagnose, treat, or prevent disease

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7
Q

What is pharmacokinetics?

A

What the body does to drugs

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8
Q

What is pharmacodynamics?

A

What the drug does to the body

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9
Q

What is toxicology?

A

Study of poisonous substances

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10
Q

What are the five main sources of drugs?

A
Plants
Animals
Minerals and mineral products
Laboratory produced chemicals 
DNA produced drugs
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11
Q

What is the oldest source of drugs?

A

Plants

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12
Q

What is included in animal drug products?

A

Hormones (eg insulin)
Enzymes
Oils and fats

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13
Q

What is included in mineral drug products?

A

Inorganic material (eg. sodium bicarbonate)

Metallic/non-metallic are combined with other ingredients to form acids, bases, and salts

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14
Q

What is included in laboratory (synthetic) drugs?

A

Medications created in the lab (eg. Fentanyl, adenosine)

Reordering of genetic information to develop bacteria that produces medication (eg. Glucagon, Hep B vaccine)

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15
Q

What is the drug approval process?

A

Animal studies on at least two animal species. If successful…

Clinical trials

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16
Q

What is phase 1 of clinical trials?

A

Tested in healthy volunteers to compare with animal data. Uses safe doses

17
Q

What is phase 2 of clinical drug trials?

A

50-300 patients in a double-blind experiment

In double blind, neither the administrator (eg. Doctor) or the patients know what drug they are receiving

18
Q

What is phase 3 of clinical drug trials?

A

Large patient groups (1000’s) lasting several years to evaluate efficacy and side effects

19
Q

What is phase 4 of clinical drug trials?

A

A new drug submission to Health Products and Food Branch

20
Q

What are the six purposes of drug therapy?

A
  1. Diagnosis
  2. Treatment (EMS)
  3. Prevention - vaccines
  4. Health maintenance
  5. Cure - antibiotics
  6. Contraception
21
Q

What are the sources of drug information?

A
Internet (good and bad)
Drug manufacturers 
Package inserts
Pharmacists
Medical journals
22
Q

What is a chemical drug name?

A

The chemical composition and molecular structure

It is the most detailed

23
Q

What is a generic drug name?

A

The name given to a drug prior to becoming a trade name and is usually suggested by manufacturer

Not capitalized
Available for use by other drug companies
Often based on chemical composition

24
Q

What is a drug trade name?

A

The name given to a drug by a specific manufacturer

“Brand name” is always capitalized
Registered as a trademark
Often based on the drugs action, or what it is meant to treat

25
What is drug standardization?
Drugs must be uniform and consistent in strength (potency) when offered on the market Between 95-105% every time
26
What are the special considerations for meds in pregnant or lactating women?
Potential for drug to cross placental barrier and affect fetus Breastfeeding while taking meds
27
What are the special drug considerations for pediatrics?
May require smaller dose Or may require smaller amount because of high concentration Note: dosing often based on weight/surface area of child
28
What are special drug considerations for geriatrics?
May be taking multiple meds - poly pharmacy Body organs may be slower causing altered effects and accumulation Some meds have narrow therapeutic and toxic thresholds
29
What is the Controlled Drug and Substances Act?
Governs the production, registration, distribution, and possession of narcotics and controlled substances
30
What is the Food and Drug Act?
Protects the public from mislabeled, poisonous, or harmful food and medications
31
What is the Canadian Food and Drug Act?
Regulations for drug manufacture and sale (amended yearly)