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

A

USDA

17
Q

who is responsible for agriculture and industrial chemicals, water

A

EPA

18
Q

who recalls unsafe consumer products

A

Consumer Products Safety Commision

19
Q

who is responsible for workplace chemical exposure

A

OSHA

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

A

caution

25
Q

the unintended effects

A

side effects

26
Q

the side effects that are negative

A

adverse effects

27
Q

the adverse effect of a drug resulting in drug poisoning

A

toxic effect/toxicity

28
Q

things that may alter the effects of a drug and should not be given at the same time

A

interaction

29
Q

the location within the body where the drug exerts its therapeutic effect

A

site of action

30
Q

the term for HOW a drug works

A

mechanism of action

31
Q

the area where the drug attaches itself to chemical structure on cells

A

receptor site