059-2 Wyo. Code R. §§ 2-6 - Requirements for issuing valid prescriptions
(a) In order for a prescription drug to be
valid it must be issued for a legitimate medical purpose by a practitioner
acting in the usual course of his or her professional practice. The
responsibility for the proper prescribing of the prescription drug is upon the
prescribing practitioner, but a corresponding responsibility rests with the
pharmacist who dispenses the prescription.
(b) All non-controlled substance
prescriptions and refill authorizations shall contain the following:
(i) The patient's full name and date of
birth;
(ii) Name and strength of
the drug;
(iii) Quantity to be
dispensed, including refills, if applicable;
(iv) Directions for use;
(v) Date issued by the
practitioner;
(vi) The
practitioner's full name, address, telephone number; and
(vii) If a written or faxed prescription, the
recognizable signature of the issuing practitioner; or
(viii) If an electronically transmitted
prescription, the prescribing practitioner's electronic or digital signature;
or
(ix) If a verbal order, the name
of the authorized agent providing information, if other than
prescriber.
(c)
Prescriptions received from out-of-state practitioners are valid only to the
extent a practitioner licensed in Wyoming may prescribe that medication in
Wyoming.
(d) A prescription may not
be dispensed to a practitioner based on an order that is not issued for one
specific patient. A prescription order for "office use" is not a valid
order.
(e) Upon learning that a
practitioner/patient relationship has been terminated for reasons other than
discharge of the patient by the practitioner, a pharmacist utilizing his or her
professional judgment may honor a patient's request for remaining medication
refills, for a period not exceeding twelve (12) months.
(f) The pharmacist shall determine the
accuracy and authenticity of all prescriptions received. Pharmacists shall
request and document verification when necessary. If verification is refused,
the prescription shall not be filled.
(g) All prescription medication shall be
dispensed in child-resistant packaging, in accordance with the Poison
Prevention Packaging Act.
(i) The patient may
request a one-time or a blanket waiver from this requirement.
(ii) The practitioner, at the patient's
request, may request a one-time waiver only.
(iii) The pharmacist shall document a
one-time request on the prescription or in the patient profile
record.
(h) A written or
electronic record of a prescription shall be maintained and available for
inspection by agents of the Board for a period of two (2) years from the date
it is filed, as follows:
(i) The pharmacy
system shall be able to reproduce the original prescription information and
maintain it in a readily retrievable format;
(ii) A pharmacy shall be authorized to
maintain an exact digitized image of the prescription in an electronic
record-keeping system;
(iii) A
pharmacy may maintain any hard copy prescriptions in numerical or date order;
and
(iv) Disposal of the hard copy
must ensure privacy and confidentiality of the contents.
Notes
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