• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/42

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

42 Cards in this Set

  • Front
  • Back
Dr Harvey Wiley becomes chief chemist in the Division of Chem of Agriculture dept. Responsible to prevent adulteration of agriculture products
1883
Wily put together "poison squad", young men who volunteered to eat foods treated w/measured amts of chemical preservatives to measure safety
1902
1906
Pure Food and Drug Act (Wiley Act)
Pure Food And Drug Act
bureau of chemistry, prohibited misbranded or adulterated foods, drinks, or drugs and no false claims on labels. Required registration an listing of addicting substances
1911
Supreme Court ruled 1906 act did not prevent false therapeutic claims on labels
1912
Sherley amendment prohibited fraudulent therapeutic claims on labels
Elixir of Sulfanilamide
diethylene glycol, 107 deaths, helped FDC pass act of 1938
1938 act
Federal Food, Drug, and Cosmetic Act
Federal Food, Drug, and Cosmetic Act
required safety testing, accurate and complete labels, removed requirement of sherley amendment to prove intent to defraud, allowed factor inspections
1951
Durham Humphrey Amendment
1951 Required what?
Required statement, "caution: federal law prohibits dispensing without prescription" on all labels
"caution: federal law prohibits dispensing without prescription" on all labels on what drugs?
injection, hypnotics, narcotics, habit forming, toxic, investigational
1951 created what?
OTC
1962
Kefauver Harris Amendment
Kefauver Harris Amendment
testing for safety and effectiveness for new drugs and testing for those approved b/w 38 and 62
1994
dietary supplement health and education act
dietary supplement health and education act does
regulate labeling and therapeutic claims on dietary supplements
dietary supplement health and education act does not
require safety and effectiveness testing
1998
pediatric rule
pediatric rule
FDA requires manufacturers of new and existent biological products to assess safety and efficacy in children
Where do drugs come from?
natural, semi-synthetic, synthetic
M1 Ach
Gq
NE alpha 1 adrenergic
Gq
5-HT2
Gq
NE Beta-1
Gs
NE Alpha 2
Gi
DA D1
Gs
DA D2
Gi
AMPA
Cation channel
GABA B
Gi, Go
5HT-1
Gi
5-HT3
cation channel
decrease adenylate cyclase
Gi
increase adenylate cyclase
Gs
Increase phospholipase C
Gq
Increase phospholipase A
Gi
increase Ca release from intracellular stores
Gq
Activate K channels in PM
Gi
Increase cAMP stimulated protein Kinase A
Gs
Increase DAG stimulated Protein kinase C
Gq
Nicotinic receptors
cation channel
kappa opoid receptor
Gi, Go