Transcript L2_Pharmacy Law & Et..

Pharmacy Law &
Ethics
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1.
The Basis of Pharmacy Law

The law is both a body of information and a system within which that information is used to
resolve conflicts and preserve order within society. To understand the law, one must both
know the information that forms the basis of the law, and also appreciate how that
information supports particular social interests such as public health or individual freedom.
Pharmacy law is a body of information about drags, drug distribution, and drug therapy.
The information is used by legislatures, administrative agencies, and courts of law, to
assure that all parties to whom responsibilities have been assigned by society meet those
responsibilities.

When tilings have not gone well in drug therapy, legal authorities are likely to ask who was
in a position of responsibility prior to the problem having developed, and then to ask that
the responsible person (or persons) account for actions taken. A requirement that this
explanation of actions be provided is known as accountability. If the responsible person or
persons providing the accounting fail to furnish an acceptable explanation for the
conduct, then liability will be imposed. Liability is legal recognition that an acceptable
accounting was not provided by a party who was in a position of responsibility when a
problem occurred.

The law defines a set of responsibilities for pharmacists and for others who are formally
involved with medication use. The law also provides a mechanism through which adverse
outcomes are reviewed by affording responsible persons an opportunity to account for
their actions and avoid liability through a satisfactory accounting.
The Purpose of Pharmacy L aw
 Pharmacy law protects patients from harm that might occur if medications were
used in ways that unreasonably increase the risk of their causing harm. Some
pharmacy laws relate to all drugs and the hazard s of using them for therapeutic
reasons. Other laws relate to a subset of drugs that have the potential for abuse,
and these laws seek to restrict inappropriate use while not interfering with
legitimate use.
 In studying pharmacy law. the primary goal is to address the question: "How far
should government go to protect people who use medications from the
consequences of their own choices in drug therapy?" This is both an empirical
question and a normative question, because it asks both what the rules are and
what the rules ought to be. To fully appreciate pharmacy laws, it is important to
understand what is required and why. as well as understand that pharmacy law
is dynamic and can be changed to protect the public in ways that extend
beyond the status quo.
 Most laws exist for a reason, and pharmacy laws are no exception to this general
rule. Restrictions on the use of chemicals as drags and restrictions on individual
practice of pharmacy exist because the open market would fail to protect the
public if any old chemical could be used as a drug and if anyone could practice
pharmacy. The public would be unnecessarily exposed to risks of harm from
dangerous chemicals and dangerous dispensers of them. This prospect of harm
is a reason to regulate, and it justifies legal restrictions on drag distribution.
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The Structure of Pharmacy Law
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Pharmacy is regulated at the federal and state levels. Federal rules primarily relate to the
drug product, while state rules primarily relate to the people who practice pharmacy and
the practice sites withing which they perform their professional duties, As a general rule,
pharmacists are required to comply with the most restrictive law. if both state and federal
law address a specific issue and if they conflict on that issue. For example, if under federal
law a particular drug is not restricted to prescription-only sale, but under state law there is
such a restriction, pharmacists may not sell the thug without a prescription, because state
law would be more strict. It is important, however, to assure that apparently conflicting
laws really do relate to the same issue.
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At both the federal and state levels there are administrative agencies, legislatures, and
courts that decide whether and how pharmacists must comply with particular rules.
Administrative agencies such as the board of pharmacy, at the state level, and the Food
and Drug Administration (FDA) or the Drug Enforcement Administration (DBA), at the
federal level, make rules for pharmacists and they enforce their own rules as well as rules
made by the state and federal legislatures. State legislatures and the United States
Congress establish a general framework of rules and enforcement processes, by enacting
laws such as the state pharmacy act and the federal Food Drug & Cosmetic Act (FDCA).
It is important to remember that the answer to a question of pharmacy law may be found
in either the administrative rules or the relevant legislation, and that a legal question has
not been thoroughly researched until both sources have been consulted.
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The History of Pharmacy Law

Pharmacy is an old profession that traces its history back at least 4,000 years ago, when people
who prepared medications were different from those who decided what medications people
needed to use. Even in the early years of the pharmacy profession, the distinction between
medication prescribers and medications preparers was noted in the law, due to the need to
avoid conflicts of interest. As American pharmacy began to formally develop in the early 19th
Century, the need to regulate the profession became evident, and by the end of that century
most states had enacted pharmacy practice acts with boards of pharmacy empowered to
make and enforce rules for the profession. The self-regulation approach, through a board of
pharmacy, persists today, even though there have been frequent calls for more public oversight
in the regulation of pharmacy and of the other health care professions.
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Federal regulation of drugs began only in 1906 with passage of the Pure Food and Drag Act. This
legislation was a classic example of "indirect regulation," because it. merely provided that
labeling on medications be truthful and not adulterated, allowing consumers to make decisions
for themselves. It did not prevent the marketing of dangerous chemicals as drugs. In 1938, the
Food, Drag & Cosmetic Act (FDCA) was passed. This act, as amended, forms the basis of drag
regulation today. The 1938 law required that new drags be shown to be safe prior to their
marketing. Thus, this was a first step toward "direct regulation," because it made decisions for
consumers. Several subsequent amendments have added requirements to the FDCA. in 1952,
the prescription-only requirement became effective, creating two classes of drugs: those
available without a prescription and those available only with a prescription. In 1961, an
amendment required proof of efficacy, in addition to safety, prior to marketing of a new drag.
The 1984 amendment made is easier to market generic equivalents of drags, but granted
patent term extension to the innovators of new drugs, under certain conditions. The FDA
Modernization Act of 1997 is the most recent amendment to clarify pharmacist responsibilities in
drug distribution.
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The Federal Food, Drag & Cosmetic Act
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Passed by the United States Congress in 1938, and amended many times since
then, the FDCA serves as the basis for drug regulation in the United States. The
FDCA is both simple and complex at the same time. The simplicity is that it
specifies only three basic illegal acts; adulteration, misbranding, and the placing
into interstate commerce of an unapproved new drag. The complexity is that
many activities are included under the umbrella of these three basis illegal acts.
If you are ever challenged to explain why something you know to be illegal is
illegal under the FDCA, a safe explanation would be to assert that the activity is
either adulteration, misbranding, or the placing into interstate commerce of an
unapproved new drug.
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I.
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Important to a thorough understanding of the FDCA is a knowledge of how the
FDCA defines the terms to which it frequently refers. Whether an activity falls
outside or inside a definition under the act may well determine
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whether the activity is lawful or unlawful. Some of the most important definitions
follow. The language is quoted directly from the FDCA. Numerations refer to
subsections of Section 321, Title 21, of the United States Code.
Definitions
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(g) (I) The term "drug" means (A) articles recognized hi the official United States
Pharmacopoeia, official Homoeopathic Pharmacopoeia of the United States, or official
National Formulary, or any supplement to any of them; and (B) articles intended for use in
the diagnosis, cure., mitigation, treatment, or prevention of disease in man or other
animals; and (C) articles (other than food) intended to affect the structure or any function
of the body of man or other animals; and (D) articles intended for use as a component of
any article specified in clause (A), (B), or (C). A food or dietary supplement for which a
claim.... is made in accordance with the requirements of section 403(f) [21 USCS § 343(r)J is
not a drug solely because the label or the labeling contains such a claim, A food, dietary
ingredient, or dietary supplement for which a truthful and not misleading statement is
made in accordance with section 403(f)(6) [21 USCS § 343(f)(6)] is not a drug under clause
(C) solely because the label or the labeling contains such a statement,
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Note that the definition of "drug" is in dependent on the intended use of the article, not on
the actual use of it. And the relevant intent is that of the provider of the article, not the
user of the article. A single article may be a drug in one context, and not be a drag in
another context, because the intent of the provider clmnges between the two contexts.
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Note also that subsections (B) and (C) differ significantly, because in (B) an article can be
a drug due to its intended use in therapeutics, while in (C) and article can be a drug
merely due to its intended use in affecting the structure or function of the body.
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fh) The term "device",.. means an instrument, apparatus, implement, machine,
contrivance, implant, in vitro reagent, or other similar or related article, including any
component, part, or accessary, which is~-
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recognized in the official National Formulary, or the United States Pharmacopeia, or any
supplement to them,
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intended for use in the diagnosis of disease or other conditions, or in the cure, mitigation,
treatment, or prevention of disease, in man or other animals, or
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intended to affect the structure or any function of the body of man or other animals, and
which does not achieve its primary intended purposes through chemical action within or
on the body of man or other animals and which is not dependent upon being
metabolized for the achievement of its primary intended purposes,

Note that the principle distinction between drugs and devices is that drugs achieve their
intended purpose through chemical action while devices do not. Sometimes the
distinction between drugs and devices is blurry, and it is important to ask in what way the
article achieves its intended purpose. The terms "drug" and "device" are mutually exclusive.
A single article cannot be both.
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(i) The term "cosmetic" means (1) articles intended to be rubbed, poured, sprinkled, or
sprayed on, introduced into, or otherwise applied to the human body or any part thereof
for cleansing, beautifying, promoting attractiveness, or altering the appearance, and (2)
articles intended for use as a component of any such articles; except that such term shall
not include soap.
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The FDCA definition of "cosmetic" is relatively consistent with the lay usage of that term.
The terms "cosmetic" and "drug" are not mutually exclusive. A single article can be both.
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(j) The term "official compendium" means the official United States
Pharmacopoeia, official Homoeopathic Pharmacopoeia of the United States,
official National Formulary, or any supplement to any of them.
Official Compendia set standards with which those who are responsible for drug
formulation and distribution must comply. Many of the requirements for drugs are
not explicitly stated within the FDCA because the act defers to an official
compendium and merely requires compliance with compendial standards. This
does not mean that there are no legally mandated standards; only that the
standards are contained within a compendium mat is adopted by reference
within the act.
(k) The term "label" means a display of written, printed, or graphic matter upon
the immediate container of any article.
(m) The term "labeling " means all labels and other written, printed, or graphic
matters (I) upon any article or any of its containers or wrappers, or (2)
accompanying such article.
Note that "labeling" includes the "label" It is to the labeling that attention usually
turns when decisions are made about the intend of a provider of an article. It is
the labeling that will frequently make the difference between an act being legal
or illegal. Because the FDCA is oriented toward the product, rather than the
prescribers and dispensers of the product, the labeling is considered part of the
product.

(p) The term "new drug" means—

(I) Any drug (except a new animal drug or an animal feed bearing or containing a new
animal drug) the composition of which is such that such drug is not generally recognized,
among experts qualified by scientific training and experience to evaluate the safety and
effectiveness of drugs, as safe and effective for use under the condition prescribed,
recommended, or suggested in the labeling thereof except that such a drug not so
recognized shall not be deemed to be a "new drug" if at any time prior to the enactment
of tins Act [enacted June 25, 1938] it was subject to the Food and Drugs Act of June 30,
1906, as amended, and if at such time its labeling contained the same representations
concerning the conditions of its use; or (2) Any drug (except a new animal drug or an
animal feed bearing or containing a new animal drug) the composition of which is such
that such drug, as a result of investigations to determine its safety and effectiveness for use
under such conditions, has become so recognized, but which has not, otherwise than in
such investigations, been media a material extent or for a material time under such
conditions.

Note that whether a drug is "new" or "not new" (most people who are familiar with
pharmacy law use the phrase "not new" drug rather than "old" drug), depends on its
general recognition as safe and effective under the conditions suggested in the labeling.
As the labeling changes, perceptions of newness may change. Only new drugs must be
shown to be safe and effective prior to their being place into interstate commerce, "Not
new" drags must meet all other relevant requirements for drugs (i.e., adulteration and
misbranding provisions), but not those applicable to new drugs, because they are not
new.
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2.
Adulteration
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A drug may be adulterated either because it is actually adulterated or because it is deemed to be
adulterated due to some requirement for proper storage or handling not having been met. The FDCA adopts
a take-no-chances approach. It also recognizes the practical difficulties of proving that an article actually is
adulterated. Thus, the act creates circumstances under which the assumption is made that an article must be
adulterated. These assumptions are virtually impossible to rebut. The language of the act follows. Numerations
refer to subsections of Section 351, Title 21, of tire United States Code.
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A drug or device shall be deemed to be adulterated-
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(a)(1) If it consists in whole or in part of any filthy, putrid, or decomposed substance; or (2)(A) if it has been
prepared, packed, or held under insanitary conditions whereby it may have been contaminated with filth, or
whereby it may have been rendered injurious to health; or (B) if it is a drug and the methods used in, or the
facilities or controls used for, its manufacture, processing, packing, or holding do not conform to or are not
operated or administered in conformity with current good manufacturing practice to assure that such drug
meets the requirements of this Act as to safety and has the identity and strength, and meets the quality and
purity characteristics, which it purparts or is represented to possess;,..
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If it purports to be or is represented as a drug the name of which is recognized in an official compendium, and
its strength differs from, or its quality or purity falls below, the standard set forth in such compendium.. . .
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If it is not subject to the provisions of paragraph (b) of this section and its strength differs from, or its purity or
quality falls below, that which it purports or is represented to possess.
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Note that a drug may be adulterated either because it is actually adulterated in some way (contamination
by a foreign substance, for example), or because it has been deemed to be adulterated due to the possibility
of its being adulterated (by being held under unsanitary conditions, for example).
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C.
Misbranding
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The FDCA requires that any information a manufacturer places on the label of a drug be
truthful and not misleading. In addition, the act imposes certain mandatory disclosure
requrements. So a provider of drugs cannot get cute and omit information that is
mandated, else the provider will violate the disclosure requirement. And the provider
cannot disclose in a misleading way or the provider will violate the basic requirement of
truth. This is essentially a "Catch 22" situation, in which the only way out is fall and truthful
(not misleading) disclosure. The language of the act follows. Numerations refer to
subsections of Section 352, Title 21, of the United States Code.
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A drug or device shall be deemed to be misbranded-
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(a) If its labeling is false or misleading in any particular. Health care economic information
provided to a formulary committee, or other similar entity, in the course of the committee
or the entity earning out its responsibilities for the selection of drugs for managed care or
other similar organizations, shall not be considered to be false or misleading under this
paragraph if the health care economic information directly relates to an indication
approved under section SOS [21 USCS § 355] or under section 351 (a) of the Public Health
Service Act [42 USCS § 262(a)] for such drug and is based on competent and reliable
scientific evidence.... In this paragraph, the term "health care economic information"
means any analysis that identifies, measures, or compares the economic consequences,
including the costs of the represented health outcomes, of the use of a drug to the use of
another drug, to another health care intervention, or to no intervention.
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If in package form unless it bears a label containing (I) the name and place of business of the
manufacturer, packer, or distributor; and (2) an accurate statement of the quantity of the
contents in terms of weight, measure, or numerical count: Provided, That under clause (2) of this
paragraph reasonable variations shall be permitted, and exemptions as to small packages shall
be established, by regulations prescribed by the Secretary.
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If any word, statement, or other information required by or under authority of this Act to appear
on the label or labeling is not prominently placed thereon with such conspicuousness (as
compared with other words, statements, designs, or devices, in the labeling) and in such terms
as to render it likely to be read and understood by the ordinary individual under customary
conditions of purchase and use.
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Unless its labeling bears (I) adequate directions for use; and (2) such adequate warnings against
use in those pathological conditions or by children where its use may be dangerous to health, or
against unsafe dosage or methods or duration of administration or application, in such manner
and form, as are necessary for the protection of users, except that where any requirement of
clause (I) of this paragraph, as applied to any drug or device, is not necessary for the protection
of the public health, the Secretary shall promulgate regulations exempting such drug or device
from such requirement.
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If it purports to be a drug the name of which is recognized in an official compendium, unless it is
packaged and labeled as prescribed therein.. . .
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(ft) If it has been found by the Secretary to be a drug liable to deterioration, unless it is
packaged in such form and manner, and its label bears a statement of such precautions, as the
Secretary shall by regulations require as necessary for the protection of the public health....
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(i) If it is a drug and its container is so made, formed, or filled as to be misleading, or (2) if it is an imitation of
another drug; or (3) if it is offered for sale under the name of another drug.
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(j) If it is dangerous to health when used in the dosage, or manner or with the frequency or duration
prescribed, recommended, or suggested in the labeling thereof.
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(n) In the case of any prescription drug distributed or offered for sale in any State, unless the manufacturer,
packer, or distributor thereof includes in all advertisements and other descriptive printed matter issued or
caused to be issued by the manufacturer, packer, or distributor with respect to that dug a true statement of
(J) the established name as defined in section 502(e) [subsec. (e) of this section], printed prominently and in
type at least half as large as that used for any- trade or brand name thereof (2) the formula showing
quantitatively each ingredient of such drug to the extent required for labels under section 502(e) [subsec. (e)
of this section], and (3) such other information in brief summary relating to side effects, contraindications, and
effectiveness as shall be required in regulations which shall be issued by the Secretary.
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Note that the general purpose of the misbranding provisions is to assure that accurate and complete
information accompanies every drag product. This requirement applies to advertisements as well as to other
product-related materials.
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4,
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One of the most controversial aspects of the FDCA is the restrictive provision regarding the approval of new
drugs. The Food and Drug Administration (FDA) is criticized by some because it is too lenient in its interpretation
of the FDCA and permits new drugs to be marketed without adequate studies for safety and efficacy, while
others criticize the agency for being too strict and preventing the use of perfectly safe and effective remedies
that are needed by people who are ill and near death. In response to these criticisms, the agency has
attempted to speed tip approval of those new drugs that represent a significant advance in therapy, while
continuing to maintain a healthy skepticism regarding new drugs that are not as likely to advance therapy
and have the potential to cause significant harm. The language of the act follows. Numerations refer to
subsections of Section 355, Title 21, of the United States Code.
New Drug Approval
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No person shall introduce or deliver for introduction into interstate commerce any new drug, unless an
approval of an application filed pursuant to subsection (b) or (j) is effective with respect to such drug.
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(I) Any per son may file with the Secretary an application with respect to any drug subject to the provisions of
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have been made to show whether or not such drug is safe for use and whether such drug is effective in use;
(B) a full list of the articles used as components of such drug; (C) a full statement of the composition of such
drug; (D) a full description of the methods used in, and the facilities and controls used for, the manufacture,
processing, and packing of such drug; (E) such samples of such drug and of the articles used as components
thereof as the Secretary may require; and (F) specimens of the labeling proposed to be used for such drug.

The information that must be included in an NDA is quite specific, and the brief list cited above is misleading in
its simplicity. In fact, an NDA includes massive amounts of information beyond what is described here,
because often FDA reviewers require additional information to maintain a "comfort zone" regarding product
safety and efficacy. In addition to safety and efficacy information, product sponsors must include information
about the patent status of the product they sponsor.
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5.
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Some medications are so potentially hazardous to health that the law recognizes they are not capable of
being labeled for safe and effective use without medical supervision, For these drugs, a prescription is required
before a pharmacist may dispense them to a patient. These drugs must bear the "federal legend" on the label
affixed to each stock bottle provided to pharmacists. When dispensed to patients, these drugs must be
labeled with specific .information required by the RDCA, but under such circumstances the drug is exempt
from most requirements of the misbranding provisions. Other drugs are of such a character that they can be
labeled for safe and effective use without medical supervision, thus they are available without a prescription.
'lire FDCA specifies the conditions and characteristics that will cause a drug to be classified as Rx or otc. The
language of the act follows. Numerations refer to subsections of Section 353, Title 21, of the United States
Code.
Prescription Exemption
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(b)(1) A drug intended for use by man which—
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because of its toxicity or other potentiality for harmful effect, or the method of its use, or the collateral measures
necessary to its use, is not safe for use except under the supervision of a practitioner licensed by law to administer such
drug; or
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is limited by an approved application under section 505 [21 USCS § 355] to me under the professional supervision of a
practitioner licensed by law to administer such drug,
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shall be dispensed only (i) upon a written prescription of a practitioner licensed by law to administer such drug, or (ii)
upon an oral prescription of such practitioner which is reduced promptly to writing and filed by the pharmacist, or (Hi)
by refilling any such written or oral prescription if such refilling is authorized by the prescribe)' either in the original
prescription or by oral order which is reduced promptly to writing and filed by the pharmacist. The act of dispensing a
drug contrary to the provisions of this paragraph shall be deemed to be an act which results in the drug being
misbranded while held for sale.
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Note the two ways for a product to be classified as prescription-only; (1) lack of safety if used without medical
supervision, and (2) the sponsor's request for prescription-only classification in the products NDA. Note also the three
ways in which a prescription may be authorized by a prescriber; (1) in writing. (2) verbal authorization, and (3) refilling a
written or verbal order. Finally, note that the dispensing of a prescription drag without a prescription is a misbranding
violation, because the law says so; regardless of the truthfulness and non-misleading nature of the drug labeling.
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(2) Any dug dispensed by filling or refilling a written or oral prescription of a practitioner licensed by law to administer
such drug shall be. exempt from the requirements of section 502 [21 USCS § 352], except paragraphs (a), (i)(2) and (3),
(k), and (I) [21 USCS § 352(a), (i)(2), (3), (k), (I)], and the packaging requirements of paragraphs (§)• (M atf d (p) [21
USCS § 352(g), (h), (p)], if the drug bears a label containing the name and address of the dispenser, the serial number
and date of the prescription or of its filling, the name of the prescriber, and, if stated in the prescription, the name of
the patient, and the directions for use and cautionary statements, if any, contained in such prescription. This
exemption shall not apply to any drug dispensed in the course of the conduct of a business of dispensing drugs
pursuant to diagnosis by mail, or to a drug dispensed in violation of paragraph (1) of this subsection.
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Note the information that is required to appear on the label of a drug prescribed for a patient, when the drug is
dispensed to the patient. Some pieces of information are mandatory for every prescription, other pieces of information
need be included on the label only when they are contained in the prescription. The very important effect of this
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section is to exempt from most important misbranding provisions those drugs that are dispensed pursuant to a
prescription and are properly labeled. This is the reason why requirements such as the "adequate directions for
use" requirement need not be met by pharmacists dispensing properly labeled drugs pursuant to a
prescription; the drug is exempt from that requirement,
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The Administrator may by regulation remove drugs subject to section 505 [21 USCS § 355] from the
requirements of paragraph (J) of this subsection when such requirements are not necessary for the protection
of the public health,
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(A) A drug that is subject to paragraph (1) shall be deemed to be misbranded if at any time prior to
dispensing the label of the drug fails to bear, at a minimum, the symbol "Rx only".
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(B) A drug to which paragraph (J) does not apply shall be deemed to be misbranded if at any time prior to
dispensing the label of the drug bears the symbol described in subparagraph (A).
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Note that drugs may be switched from prescription to non-prescription status. They must contain the federal
legend, which is now "Rx Only," but used to be "Caution: Federal law prohibits dispensing without a
prescription." If the label of a non-prescription drug contains this federal legend, then the drug is misbranded.
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6.
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It would be nice to think that all parties involved in drug development, marketing, and distribution could be
trusted to voluntarily comply with requirements of the FDCA, and that there would be no need to actually
enforce tire law through penalties. Actually, voluntary compliance with the act is quite prevalent, but
occasionally there are those who "test the waters" by going out on a limb and conducting themselves in ways
that the law simply cannot allow. Very rarely there are others who simply have no respect for the law or for the
public health, and they conduct themselves in ways that cannot be tolerated. In either event, the FDCA
contains within it provisions to penalize those who fail to voluntarily comply with the law. These penalties vary in
severity, and can be used as necessary to protect the public health. The language of the act follows.
Numerations refer to subsections of Section 331, Title 21, of the United States Code.
Prohibited Acts
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The following acts and the causing thereof are hereby prohibited:
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The introduction or delivery for introduction into interstate commerce of any food, drug, desice, or cosmetic
that is adulterated or misbranded.
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The adulteration or misbranding of any food, drug, device, or cosmetic, in interstate commerce.
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The receipt in interstate commerce of any food, drug, device, or cosmetic that is adulterated or misbranded,
and the delivery or proffered delivery thereof for pay or otherwise.
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The introduction or delivery for introduction into interstate commerce of any article in violation of section 404
or 505 [21 USCS § 344 or 355].
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• Note that the bad stuff that cannot be done relates primarily to adulteration, misbranding, and the placing
into interstate commerce of an unapproved new drug. When these violations occur, the FDA may initiate
injunction proceedings to prevent further distribution of a drug, it may seize the drug, and it may criminally
prosecute those responsible for the violation. The act also allows the FDA to issue a warning letter to alert
violators of possible problems and to permit voluntary compliance. The product recalls that are often
publicized are theoretically voluntary, because there is no statutory authority to require them. However, the
FDA can enforce the statute strongly against those who do not "voluntarily" withdraw their product when
asked to do so. FDA does classify voluntary recalls. A Class I recall applies when there is a reasonable
probability that the product will cause serious adverse health consequences or death. A Class II recall applies
when the product may cause temporary or medically reversible adverse health consequences, but the
probability of serious adverse consequences is remote. A Class III recall applies when a product is not likely to
cause adverse health consequences.
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Ill,
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A significant component of the federal Comprehensive Drug Abuse Prevention and Control Act of 1970, the
federal Controlled Substances Act (CSA) establishes rules that empower the Drag Enforcement Administration
(DEA) to assure that drags intended for medical use are not diverted to nonmedical uses. Pharmacists, as
custodians of the nation's medicinal drug supply find themselves significantly involved in police activities in
which they have little interest and no training. However.
The Federal Conn-oiled Substances Act
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there is no escaping the reality that the law requires pharmacists to do their best to assure that the drags pharmacists control do not end up
in the wrong hands. The basic structure of the CSA is to place all potentially abused drugs in one of five schedules. People and places that
are authorized to possess these drugs are then required to be registered with the DEA. Specific records must be kept so that the
whereabouts of any controlled substance can be followed from cradle to grave. Of particular interest to pharmacists are rules relating to
dispensing of controlled substances pursuant to a prescription. The failure to keep controlled substances within authorized medical channels
exposes to discipline the person or persons responsible for diversion outside authorized medical channels.
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A.

The CSA uses specific words and phrases in ways that might not be anticipated from their ordinary day-today meaning. To fully appreciate
the functioning of the CSA. one must understand how the act uses these words and phrases. Some of the most important definitions follow.
The language is quoted directly from the CSA. Numerations refer to subsections of Section 802, Title 21, of the United States Code.

As used in this title:

(1)
The term "addict" means any individual who habitually uses any narcotic drug so as to endanger the public
morals, health, safety, or welfare, or who is so far addicted to the use of narcotic drugs as to have lost the power of
self-control with reference to his addiction,

Note that a patient who is using controlled substances to treat a medical condition, and who becomes habituated to the controlled
substances, is not an "addict" under the CSA.

(2)
The term "administer" refers to the direct application of a controlled substance to the body of a patient or
research subject by--

a practitioner (or, in his presence, by his authorized agent), or

the patient or research subject at the direction and in the presence of the practitioner, whether such application be by injection, inhalation,
ingestion, or any other means.

(6) The term "controlled substance" means a drug or other substance, or immediate precursor, included in schedule!, II, III, IV, or V of part B of
this title [21 USCS§ 812]. The term does not include distilled spirits, wine, malt beverages, or tobacco, as those terms are defined or used in
subtitle E of the Internal Revenue Code of 1954 [26 WCS §§ 5001 et seq,].

(8) The terms "deliver" or "delivery" mean the actual, constructive, or attempted transfer of a controlled substance or a listed chemical,
whether or not there exists an agency relationship.
Definitions

(10) The term "dispense" means to deliver a controlled substance to an ultimate user or research subject by, or
pursuant to the lawful order of, a practitioner, including the prescribing and administering of a controlled
substance and the packaging, labeling, or compounding necessary to prepare the substance for such
delivery. The term "dispenser" means a practitioner who so delivers a controlled substance to an ultimate user
or research subject.

(12) The term "drug" has the meaning given that term by section 201(g)(1) of the Federal Food, Drug, and
Cosmetic Act [21 USCS § 321(g)(4)].

(21) The term "practitioner" means a physician, dentist, veterinarian, scientific investigator, pharmacy, hospital,
or other person licensed, registered, or otheivise permitted, by the United States or the jurisdiction in which he
practices or does research, to distribute, dispense, conduct research with respect to, administer, or use in
teaching or chemical analysis, a controlled substance in the course of professional practice or research.

2.

Under the CSA, the DEA is given responsibility to schedule controlled substances in five categories knows as
Schedules I through V. The restrictions on controlled substances vary according the schedule in which the
controlled substance has been placed. Controlled substances in Schedule I are the most restrictively
controlled, and controlled substances in Schedule V are the least restrictively controlled. Of course, there are
many medicinal agents that are not controlled at all because they have no abuse potential, and these drugs
are the least restricted because they fall into no schedule. The language below is quoted directly from the
CSA. Numerations refer to subsections of Section 812. Title 21, of the United States Code.

a) Establishment. There are established five schedules of controlled substances, to be known as schedules III,
III, IV, and V. Such schedules shall initially consist of the substances listed in this section. The schedules
established by this section shall be updated and republished on a semiannual basis during the two-year
period beginning one year after the date of enactment of this title [enacted Oct, 2 7, 1970] and shall be
updated and republished on an annual basis thereafter.
Controlled Substance Schedules

(b) Placement on schedules; findings required. Except where control is required by United States obligations under an international treaty,
convention, or protocol, in effect on the effective date of this part, and except in the case of an immediate precursor, a drug or other substance
may not be placed in any schedule unless the findings required for such schedule are made with respect to such drug or other substance. The
findings required for each of the schedules are as follows:

(1)

(A) The drug or other substance has a high potential for abuse.

(3) The drug or other substance has no currently accepted medical use in treatment in the United States.

(C) There is a lack of accepted safety for me of the drug or other substance under medical supervision.

(2)

The drug or other substance has a high potential for abuse.

The drug or other substance has a currently accepted medical use in treatment in the United States or a currently accepted medical use with
severe restrictions.

(C)
Abuse of the drug or other substances may lead to severe psychological or physical dependence.
(B) SCHEDULE III

The drug or other substance has a potential for abuse less than the drugs or other substances in schedules I and I J.

The drug or other substance has a currently accepted medical me in treatment in the United States.

Abuse of the drug or other substance may lead to moderate or low physical dependence or high psychological dependence.

(4)

The drug or other substance has a low potential for abuse relative to the drugs or other substances in schedule III.

The drug or other substance has a currently accepted medical use in treatment in the United States,

Abuse of the drug or other substance may lead to limited physical dependence or psychological dependence relative to the drugs or other
substances in schedule III.

(5)
SCHEDULE 1.
SCHEDULE II.
SCHEDULE W.
SCHEDULE V.

The drug or other substance has a low potential for abuse relative to the drugs or other substances in schedule III.

The drug or other substance has a currently accepted medical use in treatment in the United States,

Abuse of the drug or other substance may lead to limited physical dependence or psychological dependence relative to the drugs or other
substances in schedule III.

(5)

The drug or other substance has a low potential for abuse relative to the drugs or other substances in schedule IV.

The drug or other substance has a currently accepted medical me in treatment in the United States.

Abuse of the drug or other substance may lead to limited physical dependence or psychological dependence relative to the drugs or other
substances in schedule IV.

Note that the schedules of controlled substances are based on the potential for abuse, the recognition of a medical use, and the possibility of
physical or psychological dependence.

C.

Under the CSA, only certain parties are permitted to possess controlled substances legally. These parties must be registered with the DEA, or they
must be exempt from registration. For example, a pharmacist who meets the licensure requirements of the state where the pharmacist is practicing,
may possess controlled substances to patients as long as the pharmacist practices in a pharmacy that is registered with the DEA. The pharmacist
need not personally be registered with the DEA. The language below is quoted directly from the CSA. Numerations refer to subsections of Section
822, Title 21. of the United States Code.

(a)

Every person who manufactures or distributes any controlled substance or list I chemical, or who proposes to engage in the manufacture or
distribution of any controlled substance or list I chemical, shall obtain annually a registration issued by the Attorney General in accordance with the
rules and regulations promulgated by him.

Every person who dispenses, or who proposes to dispense, any controlled substance, shall obtain from the Attorney General a registration issued in
accordance with the rules and regulations promulgated try him. The Attorney General shall, by regulation, determine, the period of such
registrations. Innocent, however, shall such registrations be issued for less than one year nor for more than three years.
SCHEDULE V.
Registration
Annual registration.

(b)
Authorized activities. Persons registered by the Attorney General under this title to manufacture, distribute, or dispense
controlled substances or list I chemicals are authorized to possess, manufacture, distribute, or dispense such substances or chemicals
(including any such activity in the conduct of research) to the extent authorized by their registration and in conformity with the other
provisions of this title.

Waiver. The Attorney General may, by regulation, waive the requirement for registration of certain manufacturers, distributors, or
dispensers if he finds it consistent with the public health and safety.

Separate registration. A separate registration shall be required at each principal place of business or professional practice where the
applicant manufactures, distributes, or dispenses controlled substances or list I chemicals.

Inspection, The Attorney General is authorized to inspect the establishment of a registrant or applicant for registration in accordance
with the rules and regulations promulgated by him.

Note that the registration for dispensers is currently effective for a period of three years.

4,

Every transaction in which controlled substances change hands must be recorded. This means generally that the receipt of controlled
substances must be recorded as must the dispersal of controlled substances. In addition, there are requirements for the periodic
inventory of controlled substances. Based on records kept of controlled substances, it should be possible to discern, for any registrant,
what controlled substances are on hand, where they came from, and where controlled substances have gone to. The language
below is quoted directly from the CSA. Numerations refer to subsections of Section 827, Title 21, of the United States Code.

(b) Availability of records. Every inventory or other record required under this section (1) shall be in accordance with, and contain such
relevant information as may be required by, regulations of the Attorney General, (2) shall (A) be maintained separately from all other
records of the registrant, or (B) alternatively, in the case of nonnarcotic controlled substances, be in such form that information
required by the Attorney General is readily retrievable from the ordinary business records of the registrant, and (3) shall be kept and be
mailable, for at least two years, for inspection and copying by officers or employees of the United States authorized by the Attorney
General.
Records

E Prescriptions

The most frequent method through which controlled substances are dispersed by a pharmacy is through a prescription, issued by a
licensed prescriber and filled for a patient. Because this method of dispersion is so commonplace, specific rules have been developed
to guide appropriateness of it. These rules are intended to assure that all prescriptions filled by pharmacists for controlled substances
have been issued for a medical purpose, and will not result in diversion to nonmedical use. The DEA issues regulations that expand on
the CSA requirements, to assure that prescriptions are in such a form as to make it likely that they have been issued for a medical
purpose. The language below is quoted directly from the CSA. Numerations refer to subsections of Section 829, Title 21. of the United
States Code.

(a)
Schedule II substances. Except when dispensed directly by a practitioner, other than a pharmacist, to an ultimate
user, no controlled substance m schedule II, which is a prescription drug as determined under the Federal Food,
Drug, and Cosmetic Act [21 USCS §§ 301 et seq.J, may be dispensed without the written prescription of a
practitioner, except that in emergency situations, as prescribed by the Secretary by regulation after consultation
with the Attorney General, such drug may be dispensed upon oral prescription in accordance with section 503(b) of
that Act [21 USCS § 353(b)]. Prescriptions shall be retained in conformity with the requirements of section 307 of
this title [21 USCS § 82 7], No prescription for a controlled substance in schedule II may be refilled

Note that Schedule II prescriptions must be in writing, except in the case of particular narrowly circumscribed situations in which oral
prescriptions are permitted. Schedule II prescriptions may never be refilled. Never! End of story!!

(b)
Schedule 111 and IV substances. Except when dispensed directly by a practitioner, other than a pharmacist, to an
ultimate user, no controlled substance in schedule III or IV, which is a prescription drug as determined under the
Federal Food, Drug, and Cosmetic Act [21 USCS § 301 et seq.J, may be dispensed without a written or oral
prescription in conformity with section 503(b) of that Act [21 USCS § 353(b)]. Such prescriptions may not be filled
or refilled more than six months after the date thereof or be refilled more than five times after the date of the prescription unless
renewed by the practitioner,

This is the "five times in six months rule under which Schedule III and IV prescriptions may be refilled if authorized by the prescriber. during
the six months following the issuance of the prescription,

(c) Schedule V substances. No controlled substance in schedule V which is a drug may be distributed or dispensed other than for a
medical purpose.

Note that for prescriptions issued for Schedule V controlled substances there is no hard and fast time limit on refills, but there is the basic
requirement of a medical purpose.

IV.

Pharmacy ethics is a branch of medical ethics that provides a framework for pharmacists to use in resolving questions about what
ought to be done in pharmacy practice. To conduct an ethical exercise requires that one ask nonnative questions about what should
be done, rather than that: one ask only legal questions about what must be done, or empirical questions about why something is
done. To address a question from an ethical perspective requires that one reflect on the morality of a situation; that one ask what will
be the impact on others of one's own action and whether one can justify one's action to a higher authority.

A.

Modern medical ethics has its roots in two classical theories known as deontology and utilitarianism. It is a gross oversimplification to say
that the deontological view is idealistic, while the utilitarian view is consequentialist. but that is an effective way of beginning to think of
these two differing approaches to ethical theory. The deontologist is generally considered to be means and ends oriented, while the
utilitarian is usually considered to be ends oriented only. In other words, for the deontologist the process matters more than the result,
while for the utilitarian if is the result that matters most.
Introduction to Pharmacy Ethics
Ethical Theories

Consider the hypothetical situation of a clinical investigator who believes that a new drug to treat cancer will produce uncomfortable
but temporary side effects. To persuade subjects to volunteer for clinical trials, the researcher is tempted to not disclose information
about the side effects, reasoning that the overall good of proving the drag effective will benefit a large number of furture patients,
and will override the harm resulting from the side effects experienced by the small number of subjects in the clinical trial. This approach
will likely be deemed invalid and inappropriate by both those who adhere to the idealistic, deontological view, and those who are
adherents of the consequentialist, utilitarian view. But the criticisms these two theories offer of the plan will be different. Under the
deontological view, one would likely argue that it is morally wrong ever to lie or to use a subject merely as a means to an end. The
deontologist will be critical of the process that violates the principles of truth telling and respect for persons. On the other hand, the
utilitarian would likely assert that if the deception is ever disclosed, future research would be impaired because prospective subjects
would be distrustful of researchers and would not volunteer. The result of decreased participation in research would be unacceptable
to the utilitarian. The withholding of information would do more harm than good. So, while the two theories might lead to the same
conclusion about the unethical nature of the research, the theoretical basis of the conclusion would differ significantly.

B.

Principle-based ethics has at times been criticized as too methodic and not sufficiently sensitive to the individual differences of ethical
cases, but the study of pharmacy ethics would be incomplete without a description of the four basic ethical principles that apply in
pharmacy ethics. The purpose of ethical principles is to determine the right of patients under the principles, and to then permit a
decision about pharmacist duties that correlate with those rights. The primary objective of the principle-based approach is to enable a
pharmacist to justify to himself or herself, and to others, the action taken in a given situation.

The principle of autonomy (respect for persons) requires that individuals be permitted to make their own evaluations and choices when
their own interests are at stake. If individuals are viewed as moral agents with their own unique approach to life (their own values,
interests, attitudes and beliefs), then it would be disrespectful of individuals to reject their considered judgments or to deny them the
liberty to act on those judgments. Autonomous individuals are at liberty to perform whatever actions they wish, as long as another
autonomous individual's actions are not infringed, even if the actions appear to be foolish or unwise based upon conventional and
generally accepted wisdom. For example, under the principle of autonomy, a person who is a competent decision-maker is free to use
a medication in a way that is less than optimally sale and effective, if the generally recognized k*right way" to use the drug interferes
with the person's lifestyle.
Ethical Principles

The principle of nonmaleficence (doing no harm) requires that pharmacists refrain from acting in ways that will cause harm or injury to
others. A pharmacist who fails to counsel patients, for fear that the patients will discontinue using a drug if information about the drug is
disclosed, is adhering to the principle of nonmaleficence, because it is through acts of commission mat this principle is violated.
Nonmaleficence prohibits both deliberate harmful action (substituting one generic drug product for another without authorization and
without evidence of bioequivalence) and unintentional harm (inadvertently using the sig code for "take one tablet four times daily" for
the label of a digoxin prescription that has directed the patient to take only one tablet daily.

The principle of beneficence (doing good) requires positive action to (I) prevent what is bad, (2) remove bad or evil, and (3) do or
promote good. It is through acts of omission that this principle is violated. For example, the pharmacist described above who neglects
to counsel patients is violating the principle of beneficence, because information about medications generally helps patients use their
medications the correct way. Health care providers, including pharmacists, have at times used the principle of beneficence as
justification for doing for patients what, in the care provider's view, is best for the patient even if the patient prefers that it not be done.
Beneficence of this type is sometimes referred to as "paternalism.** A paternalistic act toward a patient is an act that is done
benevolently, either contrary to the patient's expressed wishes, or without considering the patient's wishes.

The principle of justice (fairness) requires that all benefits and burdens be distributed equally. It requires that people be given that to
which they are entitled. Distributive justice requires that resources be allocated in a fair way. Corrective justice requires that one who
has harmed another place the banned person back in a position the person would have been in had the harm not occurred (as well
as this can be done with resources available). Justice is a principle that is difficult to apply in a practice setting, but it greatly facilitates
the decisions made by policy makers,

C.
Ethical Problem-solving Ethical principles are useful to one who ponders the value of the pharmacy profession and the
relationship of pharmacists with their patients. Yet, without a framework for decision-making, ethical principles are of little use. Because
pharmacists, and other health care professionals, need a method for solving ethical problems, ethicists have suggested an approach
that seeks first to define the ethical dilemma and then to suggest the best potential resolution of the dilemma.

The first step in ethical problem-solving is to clarify facts. Sometimes disagreements can be traced to misunderstandings of
fact rather than to differences of opinion. Once the facts are clarified, tire dispute may evaporate, because the
disagreement does not exist. Alternatively, the parties to a disagreement may realize that they simply must agree to
disagree, because a difference in factual interpretation is unavoidable. In either event, there is no point in proceeding to
treat the problem as if it were conceptual instead of factual, it may be the case that one party to a disagreement is
mistaken about a fact. It is far easier to clarify a mistaken fact than it is to reach agreement on ethical principles, so the
potential to solve a problem through clarification offsets is tempting when faced with the possibility of an arduous discussion
of esoteric principles.

The second step is to clarify concepts. For example, there are concepts such as the "right to health care," or "unacceptable
risk." that may seem to be the basis of a disagreement, when clarification of these concepts will resolve the controversy.
Perhaps the disagreeing parties were really talking about the same thing but did not realize it.

Step three is to clarify principles. This is the time to apply the concepts of autonomy, beneficence, nonmaleficence and
justice to a specific fact situation. By asking what result each of the four major principles would produce to solve tire
problem, those who are involved with ethical analysis can determine the patient's rights and the correlative pharmacist
duties. Usually this exercise will require some sort of decision regarding the weight to afford a specific principle in balancing
that principle against another. The problem-solving that can result from this approach is not as scientifically objective as is
the clinical drug trial, but it is useful in helping gather information and consider alternatives.

D,

The American Pharmaceutical Association has adopted a Code of Ethics that is intended to present to the public the
principles on which the pharmacy profession bases its professional duties. This code is not as useful in practice as one might
wish it to be, Seldom will a practitioner of pharmacy find an unequivocal answer to a questions of rights and wrongs in
The APhA Code of Ethics
practice by simply "looking up the answer" in the APhA Code of Ethics. But the code serves the profession well as a
general statement of ideals.

Code of Ethics for Pharmacists

PREAMBLE

Pharmacists are health professionals who assist individuals in making the best use of medications. This Code, prepared and
supported by pharmacists, is intended to state publicly the principles that form the fundamental basis of the roles and
responsibilities of pharmacists. These principles, based on moral obligations and virtues, are established to guide pharmacists
in relationships with patients, health professionals, and society.

I. A pharmacist respects the covenantal relationship between the patient and pharmacist.

Considering the patient-pharmacist relationship as a covenant means that a pharmacist has moral obligations in response to
the gift of trust received from society. In return for this gift, a pharmacist promises to help individuals achieve optimum benefit
from their medications, to be committed to their welfare, and to maintain their trust.

II.
A
pharmacist
confidential manner.

A pharmacist places concern for the well-being of the patient at the center of professional practice. In doing so, a.
pharmacist considers needs stated by the patient as well as those defined by health science. A pharmacist is dedicated to
protecting the dignity of the patient. With a caring attitude and a compassionate spirit a pharmacist focuses on serving the
patient in a private and confidential manner.

III.
promotes
the
good
of
every
patient
A pharmacist respects the autonomy and dignity of each patient.
in
a
caring,
compassionate,
and

A pharmacist promotes the right of self-determination and recognizes individual self-worth by encouraging patients
to participate in decisions about their health. A pharmacist communicates with patients in terms that are
understandable, hi all cases, a pharmacist respects personal and cultural differences among patients.

IV.

A pharmacist has a duty to tell the truth and to act with conviction of conscience. A pharmacist avoids
discriminatory practices, behavior or work conditions that impair professional judgment, and actions that
compromise dedication to the best interests of patients.

V.

A pharmacist has a duty to maintain knowledge and abilities as new medications, devices, and technologies
become available and as health information advances.

VI.
A
pharmacist
professionals.

When appropriate, a pharmacist asks for the consultation of colleagues or other health professionals or refers the
patient. A pharmacist acknowledges that colleagues and other health professionals may differ in the beliefs and
values they apply to the care of the patient.

VII.
A pharmacist acts with honesty and integrity in professional relationships.
A pharmacist maintains professional competence.
respects
the
values
and
abilities
A pharmacist selves individual, community, and societal needs.

of
colleagues
and
other
health

The primary obligation of a pharmacist is to individual patients. However, the obligations of a pharmacist may at
times extend beyond the individual to the community and society. In these situations, the pharmacist recognizes the
responsibilities that accompany these obligations and acts accordingly.

VIII.

When health resources are allocated, a pharmacist is fair and equitable, balancing the needs of patients
A pharmacist seeks justice in the distribution of health resources.