What did the Federal Controlled Substances Act do? Why was it implemented? - ANSWER Legislators
very concerned in the 1960s about legal and illegal drugs being abused
They were given the opportunity to design an act/law
Created the DEA to promulgate and enforce the law
Created a closed system between: manufacturer, distributors, prescriber, dispenser, and patient.
What did the Pure Food and Drug Act of 1906 do? - ANSWER Prohibited the adulteration and
misbranding of foods and drugs in interstate commerce; DID NOT have to be proven safe or effective;
did not require the label to list ingredients, directions for use, or provide warnings
What did the Food, Drug, and Cosmetic Act do? (started in 1938) - ANSWER Provides for the
comprehensive regulation of all drugs introduced into interstate (and most intrastate) commerce
Under this act no new drug may be marketed and sold unless it has been proved SAFE ONLY for its
intended use and approved by the FDA
Labels must contain adequate directions for use and warnings about habit-forming properties of certain
drugs
Describe the FDCA - ANSWER The purpose of the FDCA is to protect consumers from adulterated or
misbranded foods, drugs, cosmetics, or devices; provided that no new drug could be marketed until
proven safe for use under the conditions described on the label and approved by the FDA; also started
the labeling requirements; applies to devices as well; all drugs before 1938 are exempt from the
requirement that new drugs be proven safe
,If you get in trouble with the board of pharmacy can you get in trouble with the government too? What
about the a lawsuit with a patient? - ANSWER Yes, you can have an administrative lawsuit, a civil lawsuit,
and a criminal lawsuit separately for the same offense
What did the Durham-Humphrey Amendment of 1951 do? - ANSWER Established 2 classes of drugs;
prescription and OTC
Allows refills on prescriptions and oral prescriptions
Per the Durham-Humphrey Amendment; what must be labeled on a prescription medication - ANSWER
Caution: federal law prohibits dispensing without a Rx; they do not need adequate directions for use like
OTC (talking about the MANUFACTURERS label here; there is no take this medication x amount of times
daily on the manufacturer labeling)
What did the Kefauver-Harris Amendment of 1962 do? - ANSWER Required all drugs to not only be
proven safe but also EFFECTIVE
Transferred the regulation of drug advertising from the FTC to the FDA
The efficacy requirement made by the Kefauver-Harris Amendment included all drugs marketed during
what time period - ANSWER 1938-1962; drugs produced before 1938 were just grandfathered in and did
not have to prove their efficacy
What did the Orphan Drug Act of 1983 do? - ANSWER Provided tax and exclusive licensing incentives for
manufacturers to develop agents for the treatment of rare disease or conditions (those conditions that
affect < 200,000 Americans)
What did the Drug Price Competition and Patent Term Restoration Act of 1984 do? - ANSWER Made
generic drugs more readily available to the public and at the same time provided incentives for
manufacturers to develop new drugs
,Eliminated the need for generic to prove safety and efficacy thus allowing new generics to get approved
more easily
What did the Prescription Drug Marketing Act of 1987 do? - ANSWER Established sales restrictions and
recordkeeping requirements for prescription drug samples
Prohibits hospitals and other healthcare entities from selling drugs to other businesses (because the
hospitals were getting the drugs for a discount then reselling them)
Requires state licensing of wholesalers
Prohibits ANY SAMPLES for any reason in a retail pharmacy
Bans importation of prescription drugs except by manufacturers and for emergency use
Mandates record keeping requirements for drug samples for 3 years
What is the Prescription Drug User Fee Act of 1992 - ANSWER Drug companies volunteered to pay tax
and the money was used to hire more FDA scientist in hopes to speed up NDA reviews; however the
price of drugs just went up to cover the fee being paid by the drug manufacturers
What did the Dietary Supplement Health and Education Act (DSHEA) of 1994 do? - ANSWER Provided
laws on the regulation of dietary supplements; forced the FDA to treat these products more as food
than drugs
Define dietary supplement per the law - ANSWER A product that is intended for *ORAL* ingestion,
intended to supplement the diet, and contains any one or more of the following: a vitamin, mineral,
herb or other botanical, an amino acid, dietary substance or use by humans to supplement the diet by
increasing the total dietary intake and a concentrate, metabolite, constituent, extract or combination of
the previous.
, All dietary supplements must be claimed as - ANSWER A dietary supplement; they CANNOT say they are
drugs or anything else on the labeling
Dietary supplement manufacturers may not make these claims - ANSWER Disease Claims
Dietary supplement manufacturers may only make these types of claims - ANSWER Structure / Function
The label can't say that it will cure or prevent but it can say "will support or maintain"
Dietary Supplements must have this on the labeling - ANSWER "This statement has not been evaluated
by the FDA. This product is not intended to diagnose, treat, cure or prevent any disease."
Who enforces drug advertising? - ANSWER FDA
Who enforces dietary supplement advertising - ANSWER FTC
Do dietary supplements have to be safe and/or effective? - ANSWER No
How does a dietary supplement get pulled off the market? - ANSWER The FDA cannot act until the
dietary supplement is proven to be dangerous; the products should not be adulterated or misbranded
(passed in 2007); however since little to no testing is conducted on these products it would be difficult
to tell if they are adulterated or misbranded
Can you put a bunch of publications regarding how awesome a dietary supplement is on the self with
the dietary supplement to get people to purchase the product? - ANSWER No; here are the rules:
Dietary supplement publications must be reprinted in their ENTIRETY
You cannot have any information that is FALSE or MISLEADING
very concerned in the 1960s about legal and illegal drugs being abused
They were given the opportunity to design an act/law
Created the DEA to promulgate and enforce the law
Created a closed system between: manufacturer, distributors, prescriber, dispenser, and patient.
What did the Pure Food and Drug Act of 1906 do? - ANSWER Prohibited the adulteration and
misbranding of foods and drugs in interstate commerce; DID NOT have to be proven safe or effective;
did not require the label to list ingredients, directions for use, or provide warnings
What did the Food, Drug, and Cosmetic Act do? (started in 1938) - ANSWER Provides for the
comprehensive regulation of all drugs introduced into interstate (and most intrastate) commerce
Under this act no new drug may be marketed and sold unless it has been proved SAFE ONLY for its
intended use and approved by the FDA
Labels must contain adequate directions for use and warnings about habit-forming properties of certain
drugs
Describe the FDCA - ANSWER The purpose of the FDCA is to protect consumers from adulterated or
misbranded foods, drugs, cosmetics, or devices; provided that no new drug could be marketed until
proven safe for use under the conditions described on the label and approved by the FDA; also started
the labeling requirements; applies to devices as well; all drugs before 1938 are exempt from the
requirement that new drugs be proven safe
,If you get in trouble with the board of pharmacy can you get in trouble with the government too? What
about the a lawsuit with a patient? - ANSWER Yes, you can have an administrative lawsuit, a civil lawsuit,
and a criminal lawsuit separately for the same offense
What did the Durham-Humphrey Amendment of 1951 do? - ANSWER Established 2 classes of drugs;
prescription and OTC
Allows refills on prescriptions and oral prescriptions
Per the Durham-Humphrey Amendment; what must be labeled on a prescription medication - ANSWER
Caution: federal law prohibits dispensing without a Rx; they do not need adequate directions for use like
OTC (talking about the MANUFACTURERS label here; there is no take this medication x amount of times
daily on the manufacturer labeling)
What did the Kefauver-Harris Amendment of 1962 do? - ANSWER Required all drugs to not only be
proven safe but also EFFECTIVE
Transferred the regulation of drug advertising from the FTC to the FDA
The efficacy requirement made by the Kefauver-Harris Amendment included all drugs marketed during
what time period - ANSWER 1938-1962; drugs produced before 1938 were just grandfathered in and did
not have to prove their efficacy
What did the Orphan Drug Act of 1983 do? - ANSWER Provided tax and exclusive licensing incentives for
manufacturers to develop agents for the treatment of rare disease or conditions (those conditions that
affect < 200,000 Americans)
What did the Drug Price Competition and Patent Term Restoration Act of 1984 do? - ANSWER Made
generic drugs more readily available to the public and at the same time provided incentives for
manufacturers to develop new drugs
,Eliminated the need for generic to prove safety and efficacy thus allowing new generics to get approved
more easily
What did the Prescription Drug Marketing Act of 1987 do? - ANSWER Established sales restrictions and
recordkeeping requirements for prescription drug samples
Prohibits hospitals and other healthcare entities from selling drugs to other businesses (because the
hospitals were getting the drugs for a discount then reselling them)
Requires state licensing of wholesalers
Prohibits ANY SAMPLES for any reason in a retail pharmacy
Bans importation of prescription drugs except by manufacturers and for emergency use
Mandates record keeping requirements for drug samples for 3 years
What is the Prescription Drug User Fee Act of 1992 - ANSWER Drug companies volunteered to pay tax
and the money was used to hire more FDA scientist in hopes to speed up NDA reviews; however the
price of drugs just went up to cover the fee being paid by the drug manufacturers
What did the Dietary Supplement Health and Education Act (DSHEA) of 1994 do? - ANSWER Provided
laws on the regulation of dietary supplements; forced the FDA to treat these products more as food
than drugs
Define dietary supplement per the law - ANSWER A product that is intended for *ORAL* ingestion,
intended to supplement the diet, and contains any one or more of the following: a vitamin, mineral,
herb or other botanical, an amino acid, dietary substance or use by humans to supplement the diet by
increasing the total dietary intake and a concentrate, metabolite, constituent, extract or combination of
the previous.
, All dietary supplements must be claimed as - ANSWER A dietary supplement; they CANNOT say they are
drugs or anything else on the labeling
Dietary supplement manufacturers may not make these claims - ANSWER Disease Claims
Dietary supplement manufacturers may only make these types of claims - ANSWER Structure / Function
The label can't say that it will cure or prevent but it can say "will support or maintain"
Dietary Supplements must have this on the labeling - ANSWER "This statement has not been evaluated
by the FDA. This product is not intended to diagnose, treat, cure or prevent any disease."
Who enforces drug advertising? - ANSWER FDA
Who enforces dietary supplement advertising - ANSWER FTC
Do dietary supplements have to be safe and/or effective? - ANSWER No
How does a dietary supplement get pulled off the market? - ANSWER The FDA cannot act until the
dietary supplement is proven to be dangerous; the products should not be adulterated or misbranded
(passed in 2007); however since little to no testing is conducted on these products it would be difficult
to tell if they are adulterated or misbranded
Can you put a bunch of publications regarding how awesome a dietary supplement is on the self with
the dietary supplement to get people to purchase the product? - ANSWER No; here are the rules:
Dietary supplement publications must be reprinted in their ENTIRETY
You cannot have any information that is FALSE or MISLEADING
