Toxicology Exam 1 - Pt 1 Flashcards

1
Q

any substance that when administered produces a change in function

A

drug

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2
Q

study of adverse effects of chemical, physical or biological agents

A

toxicology

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3
Q

the study of the uses, effects and modes of action of drugs

A

pharmacology

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4
Q

the act that was the first attempt to protect consumers by having drugs meet a minimum standard of strength purity and quality in each batch and having them label dangerous ingredients

A

1906 pure food and drug act

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5
Q

the act which allowed the FDA to demand evidence of safety for new drugs and issue standards for food and conduct factory inspections

A

1938 federal food, drug and cosmetic act

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6
Q

the amendment in which states drugs can only be purchased if a patient has a prescription from a licensed practitioner

A

1951 FD&C Durham-Humphrey Amendment

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7
Q

the amendment in which states there must be approval of new food additives

A

1958 FD&C Food Additives Amendment

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8
Q

what are some exceptions to the 1958 FD&C Food Additives Amendment

A

substances that have generally been recognized as safe and substances which the FDA or USDA has approved for use in food prior to the passage of this amendment

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9
Q

the amendment in which states there must be approval for all color additives

A

1960 FD&C color additives amendment

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10
Q

the amendment in which there is a requirement for standard labeling to list adverse reactions to contraindications and prove drug safety and effectiveness

A

1962 FD&C Kefauver-Harris Amendment

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11
Q

the act which regulates the dispensing of drugs that have the potential for abuse

A

1970 Comprehensive Drug Abuse Prevent and Control Act (commonly referred to as the Controlled Substances Act)

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12
Q

the act in which the FDA is responsible for taking acton against unsafe dietary supplements

A

1994 Dietary Supplements Health and Education Act

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13
Q

the act which reinvestigated pesticide tolerance levels and developed stricter pesticide safety standards

A

1996 food quality protection act

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14
Q

Who is responsible for food labelling/nutrition, food ingredients/packaging, pharmaceuticals, supplements, vaccines, tobacco

A

FDA

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15
Q

Who is responsible for controlled substances only, schedules of abused drugs

A

DEA

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16
Q

who is responsible for food distribution and school lunch programs

17
Q

who is responsible for agriculture and industrial chemicals, water

18
Q

who recalls unsafe consumer products

A

Consumer Products Safety Commision

19
Q

who is responsible for workplace chemical exposure

20
Q

is “tylenol” a brand name or a generic name?

A

is Brand/Trade name

Acetaminophen would be the Generic Name

21
Q

The intended physiological effect of a drug

A

Therapeutic Effect

22
Q

the medical condition for which the drug is meant to be used

A

Indication

23
Q

the conditions for which the drug should not be used

A

contra indication

24
Q

the conditions or types of patients that warrant closer observation for specific side effects

25
the unintended effects
side effects
26
the side effects that are negative
adverse effects
27
the adverse effect of a drug resulting in drug poisoning
toxic effect/toxicity
28
things that may alter the effects of a drug and should not be given at the same time
interaction
29
the location within the body where the drug exerts its therapeutic effect
site of action
30
the term for HOW a drug works
mechanism of action
31
the area where the drug attaches itself to chemical structure on cells
receptor site