OAR 855-019-0265
Administration of Drugs
(1)
In accordance with ORS 689.655 (Power to administer drugs and devices), a pharmacist may administer a drug or device as specified in this rule.(2)
A pharmacist who administers a drug or device must:(a)
Observe, monitor, report, and otherwise take appropriate action regarding desired effect, side effect, interaction, and contraindication associated with administering the drug or device; and(b)
Ensure a record is kept for three years of such activities. This record shall include but is not limited to:(A)
Patient identifier;(B)
Drug or device and strength;(C)
Route and site of administration;(D)
Date and time of administration;(E)
Pharmacist identifier.(3)
The pharmacist must be acting:(a)
Under the direction of or pursuant to a lawful prescription or order issued by a licensed practitioner acting within the scope of the practitioner’s practice or;(b)
In accordance with a written protocol or collaborative drug therapy agreement with a licensed practitioner.(4)
The pharmacist must be able to document that they have received training on the drug or device to be administered and the route of administration. Such training may include a program approved by the ACPE, curriculum based programs from an ACPE-accredited college, state or local health department programs, training by an appropriately qualified practitioner, or programs approved by the Board.(5)
The pharmacist may administer a drug or device in conjunction with training the patient or the patient’s caregiver how to administer or self-administer the drug or device.
Source:
Rule 855-019-0265 — Administration of Drugs, https://secure.sos.state.or.us/oard/view.action?ruleNumber=855-019-0265
.