Module 1 Flashcards

1
Q

Modern medical uses of drugs

A
  1. Therapeutic uses
  2. Preventive uses
  3. diagnostic uses
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2
Q

Drugs derived from…

A

Plant, animal or mineral sources

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3
Q

Drugs derived from Plant sources

A
  1. digitalis (Lanoxin)
  2. scopolamine
  3. ephedrine
  4. galantamine
  5. aspirin
  6. morphine
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4
Q

Digitalis (Lanoxin)

A

is derived from foxglove plant (it is used in CHF to decrease contraction of the heart)

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5
Q

Scopolamine

A

derived from the belladonna plant and was used by Italian women as cosmetics to dilate the eyes

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6
Q

ephedrine

A

comes from the ephedra species and is used as a bronchodilator and decongestant

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7
Q

galantamine (Reminyl)

A

is a new drug, derived from daffodil bulbs, and used to treat Alzheimer disease

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8
Q

Aspirin (acetylsalicylic acid)

A

comes from the Bark of the willow tree. It is used to decrease inflammation, relieve pain, reduce a fever, and prevent platelets form “sticking together”

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9
Q

morphine

A

derived from opium poppies

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10
Q

Botox

A

is a much diluted form of the botulinum toxin (deadly form of food poisoning)
is used extensively for cosmetic treatment of facial wrinkle
it is also used by injection for muscle spasticity and to treat migraine H.A

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11
Q

Drugs derived from Animal sources

A
  1. Thyroid Hormone
  2. Premarin
  3. Insulin
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12
Q

Drugs derived from Mineral sources

A
  1. Potassium
  2. Lithium
  3. Iron
  4. Calcium
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13
Q

Thyroid Hormone

A

from various animals

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14
Q

Premarin (estrogen)

A

from pregnant Mares urine

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15
Q

Insulin

A

used to come from the pancreases of cows and pis

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16
Q

What is meant by patent medicine

A

were proprietary drug formulations commonly sold out of the backs of wagons and then cars, before the institution of strong federal and state drug laws.

  • The ingredients of a patent drug were usually not labelled, with the manufacturer claiming “trade secrets”
  • refers to medical compounds of questionable effectiveness sold under a variety of names and labels.
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17
Q

Wiley Act 1906

A

The Pure Food and Drug Act 1906 stipulated that food and drug manufacturers use “pure ingredients and accurate labeling”
***first federal drug legislation

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18
Q

FDA

A

Food and Drug Administration
***has the authority to “pull a drug” off the market for valid reasons, or force the manufacturers or correct misleading advertising about their drugs

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19
Q

The FDCA 1938

A

Food, Drug, and Cosmetic Act of 1938
Introduced many provisions previously lacking (not only requiring”purity” of ingredients, but also mandating “safety tests” on proposed new drugs

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20
Q

FDA Protections

A

Recalls certain drug and food lots because of various types of manufacturing defects:

  1. contamination
  2. the “shelf-life” is not as long as advertised
  3. ingredients have fallen “below the tolerance standard”
  4. new or worse than expected “side effects” are uncovered
21
Q

DSHEA

A

Dietary Supplements and Health Education Act

22
Q

FDA Modernization Act 1997

A

FDA reforms in the AIDS Era - 1997 pres Clinton signed into law a major update to the FDCA. “shortened approval time”

23
Q

The Three Names of Drugs

A
  1. Chemical
  2. Generic
  3. Trade or Brand
24
Q

SR

A

SLOW RELEASE

25
Q

DS

A

Double Strength

26
Q

Slow-K

A

slow release form of potassium

27
Q

b.i.d

A

twice a day

28
Q

IND

A

Investigational New Drug

29
Q

Clinical (human) trials

A

there are three classic phases of clinical trials

  1. phase 1 - involve a small number 10 - 100 - healthy
  2. phase 2 - larger group of volunteer 50 - 500 - have the disease. new drug fails to live up to its potential, it dropped during this phase.
  3. phase 3 - large patient groups (with the disease being tested)
30
Q

double–blind study group

A

the observer and the patient DO NOT know if the patient is on the study drug of placebo.

31
Q

OTC

A

Over-the -counter

32
Q

Sublingual

A

drug is NOT swallowed but placed under the tongue to be absorbed by the large blood vessels found there.

33
Q

Nasogastric

A

drug is given through an NG tube

34
Q

Gastrostomy Tube

A

is surgically placed directly into the stomach or small intestines (routes of drug administration)

35
Q

Rectal Suppositories

A

are a solid form of glycerin or cocoa butter and are especially useful in the very young or if the patient is vomiting

36
Q

Vaginal Creams and Suppositories

A

for treatment of infections and irritations of the vaginal tract

37
Q

Topicals

A

Creams and ointments, eye drops, Nasal Sprays

38
Q

Transdermally

A

Patches applied to the skin. Steady blood levels can be achieved in some medication.

39
Q

Inhalation

A

is a very effective way to give some aerosolized liquid medications (and very fine powders) to achieve a fast active response.

40
Q

Parenteral

A

Not oral. Anything given by injection

41
Q

Subcutaneous (insulin shots) and Intraderma (allergy shots)

A

given just under the skin but above the muscle layer

42
Q

IM

A

Intramuscular

means injection directly into muscles, which are well supplied with blood vessels so drugs are absorbed more quickly

43
Q

IV

A

Intravenous

is the fastest parenteral injection

44
Q

DSHEA 1994

A

Restricts FDA regulation of dietary supplements

45
Q

Orphan Drug Act 1983

A

Facilitated development of drugs for “unprofitable” disorders.

46
Q

Controlled Substances Act 1970

A

restricted drugs by addiction potential and abuse

47
Q

Prescription Drug Amendment

A

defined with medications is Rx and which one is OTC

48
Q

Harrison Nacrcotic Act 1914

A

regulate and restrict addictive supstances