Kan. Admin. Regs. § 68-2-20 - Pharmacist's function in filling a prescription
(a) As used in this
regulation, each of the following terms shall have the meaning specified in
this subsection:
(1) "Prescriber" means a
"practitioner" as defined by
K.S.A. 65-1626 and amendments thereto, a "mid-level
practitioner" as defined by
K.S.A. 65-1626 and amendments thereto, or a person
authorized to issue a prescription by the laws of another state.
(2) "Legitimate medical purpose," when used
regarding the dispensing of a prescription drug, means that the prescription
for the drug was issued with a valid preexisting patient-prescriber
relationship rather than with a relationship established through an
internet-based questionnaire.
(b) Except as provided in subsection (c),
judgmental functions that constitute the filling or refilling of a prescription
shall be performed only by a pharmacist or by a pharmacist intern under the
direct supervision of a licensed pharmacist and shall consist of the following
steps:
(1) Read and interpret the
prescription of the prescriber;
(2)
limit any filling or refilling of a prescription to one year from the date of
origin, except as provided by
K.S.A. 65-1637 and
K.S.A. 65-4123, and amendments thereto;
(3) verify the compounding, counting, and
measuring of ingredients and document the accuracy of the
prescription;
(4) personally offer
to counsel each patient or the patient's agent with each new prescription
dispensed, once yearly on maintenance medications and, if the pharmacist deems
appropriate, with prescription refills in accordance with subsection
(e);
(5) ensure the proper
selection of the prescription medications, devices, or suppliers as authorized
by law; and
(6) interpret and
verify patient medication records and perform drug regimen reviews.
(c) The pharmacist-in-charge shall
prohibit all other pharmacy personnel from performing those judgmental
functions restricted to the pharmacist. The following judgmental functions
shall be performed only by a pharmacist and shall not be delegated:
(1) Final verification of the accuracy of a
completed compound or prescription;
(2) documentation of the pharmacist's final
verification in the pharmacy record; and
(3) direct supervision of a pharmacist intern
or pharmacy technician.
(d) Any pharmacist may delegate nonjudgmental
functions to a pharmacist intern or pharmacy technician. Each pharmacist shall
conduct in-process and final checks associated with the preparation of
medications, except as provided by
K.A.R.
68-7-11.
(e) In order to comply with subsection (b),
the pharmacist or the pharmacist intern under the pharmacist's direct
supervision shall perform the following:
(1)
Personally offer to counsel each patient or the patient's agent with each new
prescription dispensed, once yearly on maintenance medications and, if the
pharmacist deems appropriate, with prescription refills. Any pharmacist may
authorize an exception to the verbal counseling requirement on a case-by-case
basis for the continuation of therapy prescriptions issued more frequently than
once yearly;
(2) provide the verbal
counseling required by this regulation in person or by the utilization of a
telephone or other communication service available to the patient or patient's
agent if the prescription is not collected at the pharmacy;
(3) when appropriate, provide alternative
forms of patient information to supplement verbal patient counseling. These
supplemental forms of patient information may include written information,
leaflets, pictogram labels, video programs, and auxiliary labels on the
prescription vials. However, the supplemental forms of patient information
shall not be used as a substitute for the verbal counseling required by this
regulation;
(4) encourage proper
patient drug utilization and medication administration. The pharmacist shall
counsel the patient or patient's agent on those elements that, in the
pharmacist's professional judgment, are significant for the patient. These
elements may include the following:
(A) The
name and a description of the prescribed medication or device;
(B) the dosage form, dosage, route of
administration, and duration of therapy;
(C) special directions and precautions for
preparation, administration, and use by the patient;
(D) common side effects, adverse effects or
interactions, or therapeutic contraindications that could be encountered; the
action required if these effects, interactions, or contraindications occur; and
any activities or substances to be avoided while using the
medication;
(E) techniques for
self-monitoring drug therapy;
(F)
proper storage requirements and disposal instructions; and
(G) action to be taken in the event of a
missed dose; and
(5)
expressly notify the patient or the patient's agent if a brand exchange has
been exercised.
(f)
Except as required by
K.S.A. 65-16,127 and amendments thereto for the
dispensing of an emergency opioid antagonist, nothing in this regulation shall
be construed to require a pharmacist to provide the required patient counseling
if either of the following occurs:
(1) The
patient or the patient's agent refuses counseling.
(2) The pharmacist, based upon professional
judgment, determines that the counseling could be detrimental to the patient's
care.
(g) Each pharmacist
shall make a reasonable effort to ensure that any prescription, regardless of
the means of transmission, has been issued for a legitimate medical purpose by
a prescriber.
Notes
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