Utah Code § 58-17b-627

Prescription of drugs or devices by a pharmacist
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(1) Beginning January 1, 2022, a pharmacist may prescribe a prescription drug or device if:
(a) prescribing the prescription drug or device is within the scope of the pharmacist's training and
experience;
(b) the prescription drug or device is designated by the division by rule under Subsection (3)(a);
and
(c) the prescription drug or device is not a controlled substance that is included in Schedules I, II,
III, or IV of:
(i) Section 58-37-108; or
(ii) the federal Controlled Substances Act, Title II, P.L. 91-513.
(2) Nothing in this section requires a pharmacist to issue a prescription for a prescription drug or
device.

(3) The division shall make rules in accordance with Title 63G, Chapter 3, Utah Administrative
Rulemaking Act, to:
(a) designate the prescription drugs or devices that may be prescribed by a pharmacist under this
section, beginning with prescription drugs or devices that address a public health concern that
is designated by the Department of Health and Human Services, including:
(i) post-exposure HIV prophylaxis;
(ii) pre-exposure HIV prophylaxis;
(iii) self-administered hormonal contraceptives;
(iv) smoking cessation;
(v) naloxone;
(vi) fluoride;
(vii) vaccines; and
(viii) epinephrine.
(b) create guidelines that a pharmacist must follow when prescribing a prescription drug or
device, including guidelines:
(i) for notifying the patient's primary care or other health care provider about the prescription;
and
(ii) to prevent the over-prescription of drugs or devices including but not limited to antibiotics;
(c) address when a pharmacist should refer the patient to an appropriate health care provider or
otherwise encourage the patient to seek further medical care; and
(d) implement the provisions of this section.
(4) The division shall make rules under Subsection (3) in collaboration with:
(a) individuals representing pharmacies and pharmacists;
(b) individuals representing physicians and advanced practice clinicians; and
(c)
(i) if the executive director of the Department of Health and Human Services is a physician, the
executive director of the Department of Health and Human Services;
(ii) if the executive director of the Department of Health and Human Services is not a physician,
a deputy director who is a physician in accordance with Subsection 26B-1-203(4); or
(iii) a designee of the individual described in Section 26B-1-203.
(5) Before November 1 of each year, the division, in consultation with the individuals described in
Subsection (4), shall:
(a) develop recommendations for statutory changes to improve patient access to prescribed
drugs in the state; and
(b) report the recommendations developed under Subsection (5)(a) to the Health and Human
Services Interim Committee.

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