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DƯỢC LÍ Goodman & Gilman's The Pharmacological Basis of Therapeutics 12th, 2010

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APPENDIX I

PRINCIPLES OF PRESCRIPTION ORDER WRITING AND PATIENT COMPLIANCE

Table AI–1

Controlled Substance Schedules

Schedule I (examples: heroin, methylene dioxymethamphetamine,

lysergic acid diethylamide, mescaline, and all

salts and isomers thereof):

1. High potential for abuse.

2. No accepted medical use in the U.S. or lacks accepted

safety for use in treatment in the U.S. May be used for

research purposes by properly registered individuals.

Schedule II (examples: morphine, oxycodone, fentanyl,

meperidine, dextroamphetamine, cocaine, amobarbital):

1. High potential for abuse.

2. Has a currently accepted medical use in the U.S.

3. Abuse of substance may lead to severe psychological

or physical dependence.

Schedule III (examples: anabolic steroids, nalorphine,

ketamine, certain schedule II substances in suppositories,

mixtures, or limited amounts per dosage unit):

1 Abuse potential less than substances in schedule I or

schedule II.

2. Has a currently accepted medical use in the U.S.

3. Abuse of substance may lead to moderate to low physical

dependence or high psychological dependence.

Schedule IV (examples: alprazolam, phenobarbital,

meprobamate, modafinil):

1. Abuse potential less than substances in schedule III.

2. Has a currently accepted medical use in the U.S.

3. Abuse of substance may lead to limited physical or

psychological dependence relative to substances in

schedule III.

Schedule V (examples: buprenorphine, products containing

a low dose of an opioid plus a non-narcotic ingredient

such as cough syrup with codeine a and guaifenesin, antidiarrheal

tablets with diphenoxylate and atropine):

1. Low potential for abuse relative to schedule IV.

2. Has a currently accepted medical use in the U.S.

3. Some schedule V products may be sold in limited

amounts without a prescription at the discretion of the

pharmacist; however, if a physician wishes a patient to

receive one of these products, it is preferable to provide

a prescription.

a

Although codeine is a schedule II drug, its dosage in cough syrups is

regarded as sufficiently low to permit their classification as schedule

V substances.

A statement such as “refill prn” (refill as needed) is not

appropriate, as it could allow the patient to misuse the

medicine or neglect medical appointments. If no refills

are desired, “zero” (not “0”) should be written in the

refill space to prevent alteration of the prescriber’s

intent. Refills for controlled substances are discussed

later, in “Refills” under “Controlled Substances.”

Concern about the rising cost of healthcare has

favored the dispensing of so-called “generic” drugs. A

drug is called by its generic name (in the U.S., this is the

U.S. Adopted Name or USAN) or the manufacturer’s

proprietary name, called the trademark, trade name, or

brand name. In most states in the U.S., pharmacists

have the authority to dispense generic drugs rather than

brand-name medications. The physician can request

that the pharmacist not substitute a generic for a

branded medication by indicating this on the prescription

(“do not substitute”), although this generally is

unnecessary because the U.S. Food and Drug

Administration (FDA) requires that generic medications

meet the same bioequivalence standards as their

brand-name counterparts. In some jurisdictions, prescriptions

may not be filled with a generic substitution

unless specifically permitted on the prescription.

Occasions when substituting generic medications is discouraged

are limited to products with specialized

release systems and narrow therapeutic indices, or

when substantial patient confusion and potential noncompliance

may be associated with substitution.

Choice and Amount of Drug Product

Dispensed

Inappropriate choice of drugs by physicians is a problem

in prescribing. As learned recently with the

cyclooxygenase-2 (COX-2) inhibitors, a drug’s therapeutic

promise or popularity is not proof of its overall

clinical superiority or safety (Topol, 2004). Physicians

must rely on unbiased sources when seeking drug information

that will influence their prescribing habits; use

of the original medical literature will ensure instruction

of the prescriber’s best judgment.

The amount of a drug to be dispensed should be

clearly stated and should be only that needed by the

patient. Excessive amounts should never be dispensed,

because this not only is expensive for the patient but

may lead to accumulation of medicines, which can lead

to harm to the patient or members of the patient’s family

if used inappropriately. It is far better to have several

refills of a prescription than to have more than necessary

prescribed at one time.

The Prescription as a Commodity

Prescribers must be aware that patients may visit their

doctor to “get” a prescription. Indeed, in an era when

the time spent between physician and patient is ever

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