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Pharmacology- Ch. 1-3 Review

Quiz by Kathryn Barnett

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40 questions
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  • Q1

    Drug standards

    Approval agency established by the 1938 Federal Food, Drug and Cosmetic Act.

    Require a prescription but not a DEA number

    Require a prescription and DEA number

    These were established by the 1906 Pure Food and Drug Act.

    30s
  • Q2

    Controlled (schedule) drug

    Approval agency established by the 1938 Federal Food, Drug, an Cosmetic Act

    Requires a prescription but not a DEA number.

    Requires a prescription and DEA number

    Enforcement agency established by the 1970 Controlled Substances Act.

    30s
  • Q3

    Legend Drug

    Approval agency established by the 138 Federal Food, Drug, and Cosmetic Act

    Requires a prescription and a DEA number. 

    Enforcement Agency

    Requires a prescription but not a DEA number.

    30s
  • Q4

    Orphan Drug

    Directory listing drugs by manufacturer and packaging type (s).

    Uniform strength, purity, and quality. 

    Drugs that treat a disease affecting a very small number of people. 

    These drugs require no prescription.

    30s
  • Q5

    NDC

    Directory listing of officially approved drugs (was originally two references). 

    Directory listing drugs by manufacturer and packaging type(s). 

    Uniform strength, purity, and quality

    These drugs require no prescription

    30s
  • Q6

    OTC

    Drugs that treat a disease affecting a very small number of people.

    These drugs require no prescription. 

    Uniform, strength, purity, and quality

    Directory listing of officially approved drugs (was originally two references).

    30s
  • Q7

    The pharmaceutical manufacturer has the authority to add additional active ingredients to a previously approved pharmaceutical product.

    False

    True

    30s
  • Q8

    The 1906 Pure Food and Drug Act established consumer protections to prevent the inclusion of "dangerous ingredients" without the knowledge of the consumer.

    True

    False

    30s
  • Q9

    Controlled Substance records are to be kept for 10 years.

    True

    False

    30s
  • Q10

    The NDC contains the manufacturer, product, and package information for all commercially available products. 

    False

    True

    30s
  • Q11

    The Controlled Substance Act sets tighter controls on ________________________. 

    Depressants, stimulants, psychedelics, narcotics, and anabolic steroids. 

    Antibiotics, diuretics, antihypertensives, and diabetic medications

    common cold/allergy medications

    common analgesics such as Tylenol or aspirin

    30s
  • Q12

    Prescriptions of the controlled substances listed in which of these schedules MAY be called into the pharmacy by healthcare workers other than the prescriber ________________. 

    Schedules 1 and 3

    Schedules 2 through 4

    Schedules 1 and 2 only

    Schedules 4 and 5 only

    30s
  • Q13

    Ototoxicity

    Increased reaction to sunlight, with the danger of intense sunburn.

    Damage to the kidneys resulting in impaired kidney function, decreased output, and renal failure.

    Method capitalizing part of a drug name to help avoid confusing look-alike-sound-alike drugs.

    Damage to the eight cranial nerve

    30s
  • Q14

    Nephrotoxicity

    Drug name using a number to help differentiate it from an almost identical product. 

    Method  capitalizing part of a drug name to help avoid confusing look-alike sound-alike drugs.

    Increased reaction to sunlight, with the danger of intense sunburn.

    Damage to the kidneys resulting in impaired kidney function, decreased output, and renal failure.

    30s
  • Q15

    Which name is the common or general name assigned to a drug and never capitalized? 

    Chemical name

    Official name

    Trade name

    Generic name

    30s

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