2014 Rules Revisions, Wyoming Controlled
Substances Act
By Allyson Dolence, PharmD Candidate, University of Wyoming
School of Pharmacy
Several housekeeping adjustments were made throughout the
act, including spelling, numbering, and formatting corrections, as
well as the deletion of outdated definitions and wording in Chapter
1. Chapter 2, Hearings, was updated to outline the procedures for
complaints and hearings. Changes to Chapter 3, Fees for Registration
and Re-registration, were minimal. Chapter 4 was not revised.
Chapter 5, formerly Rules of Practice and Procedure, has been
repealed because the process for contested case hearings is now
listed in Chapter 2.
Several important changes have been made to Chapter 6, Issuing,
Filing, and Filling of Prescriptions. The identification of patients
has been moved from Chapter 2 to Section 7. Section 10 clarifies
what a pharmacist can change on a Schedule II prescription. After
approval from the prescribing practitioner, the pharmacist is permitted
to change the drug strength, drug quantity, directions for use,
and dosage form. The pharmacist is permitted to add or change
the patient’s address with proper verification without consulting
the prescribing practitioner. The prescribing practitioner’s Drug
Enforcement Administration (DEA) registration number may be
added to a prescription drug order after consulting the prescribing
practitioner or verifying the number from another reliable source.
Required information may appear on the front or back of the prescription
drug order, and computer-generated data satisfies these
requirements. Any change made by the pharmacist shall be documented
and shall include the date, the name of person consulted,
and the initials of the pharmacist. A pharmacist is not permitted to
change the patient’s name, CS prescribed (except for generic substitution
permitted by state law), the date issued, or the prescriber’s
signature. Section 11 lists the process for multiple prescriptions
for a 90-day supply of Schedule II CS. An individual practitioner
may issue multiple prescriptions authorizing the patient to receive
a total of up to a 90-day supply of a Schedule II CS provided the
following conditions are met: each separate prescription is issued
for a legitimate medical purpose by a practitioner acting in the usual
course of professional practice; each individual prescription is dated
with the date it was prescribed and contains all other information
required by Chapter 6; the practitioner provides written instructions
on each prescription indicating the earliest date on which a
pharmacy may fill each prescription; and the practitioner concludes
that providing the patient with multiple prescriptions in this manner
does not create an undue risk of diversion or abuse.
Notable changes were also made to Chapter 8, Prescription Drug
Monitoring Program. These include updates to the process for
registering and using the online program (WORxPDMP.com). All
faxed (paper) requests must include the DEA registration number
for the pharmacy or practitioner. Pharmacists and practitioners
may request patient profiles electronically provided the following
conditions are met: the pharmacist or practitioner must first register
for access to the online system using the online registration; the
Board staff will activate the online access; and the Board staff shall
discontinue access to any pharmacist or practitioner whose license,
DEA registration, or Wyoming Controlled Substance Registration
has lapsed, been revoked, or suspended.
Chapter 4, Records and Inventories, was not revised, as it was
updated in 2011, and no further revisions are needed at this time.
Chapter 7, Administrative Inspections, was reviewed by the Board
and no revisions were made.quoted from here
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