Or. Admin. R. 411-086-0260 - Pharmaceutical Services
(1) Consulting
Pharmacist. Each facility shall have a consulting pharmacist who shall ensure
compliance with ORS Chapter 689, facility policy (OAR 411-085-0210) and this
rule.
(2) Pharmaceutical Services
Review. The Quality Assessment and Assurance Committee shall:
(a) Develop written policies and procedures
for safe and effective drug therapy, distribution and use;
(b) Oversee pharmaceutical services in the
facility, monitor the service to ensure accuracy and adequacy and make
recommendations for improvement; and
(c) Meet at least quarterly and document its
activities, findings and recommendations.
(3) Drug Supply, Storage and Labeling:
(a) Drug Room. Facilities without a pharmacy
shall have a drug room as defined in ORS Chapter 689, supervised by the
consulting pharmacist. Drug rooms shall contain only prescribed (legend and
non-legend) drugs, non-prescription (non-legend) stock drug supply and the
emergency medication kit authorized pursuant to this rule. Locked carts or
locked cupboards shall be used to prevent pilferage;
(b) Labels:
(A) All medications purchased or designated
for specific residents shall be labeled as prescribed for such
resident;
(B) If facility policy
allows medications accompanying the resident on admission to be used, the
medication must be identified as to the resident and medication and shall be
authorized for use only on the written order of the attending
physician.
(c) Storage.
Except as provided in subsection (4)(b) of this rule, all medications shall be
stored in the facility pharmacy, a drug room, or in a locked medication
cart;
(d) Stock Supply:
(A) Except as provided in section (6) of this
rule, a stock supply of prescription (legend) drugs may be maintained only
within a licensed pharmacy;
(B) A
stock supply of non-prescription drugs may be maintained in a drug room or
locked medication cart, but there must be a doctor's order for administering
such drugs. A stock supply of non-prescription drugs means those non-legend
medications supplied in the manufacturer's original package or repackaged by a
registered pharmacist and labeled in accordance with ORS Chapter 689.
(e) Resident Discharge. Medication
to accompany the resident upon discharge must be on the written order of the
physician;
(f) References.
References regarding use, dosage, contraindications, drug interactions, and
adverse reactions shall be available on drug products used in the
facility.
(4) Drug
Administration:
(a) Medications prescribed to
one resident shall not be administered to another;
(b) Self-administration. Facilities shall
have written policies and procedures allowing self-administration of
medication:
(A) All bedside medications,
except nitro-glycerine, shall be stored in closed, locked cupboards or
drawers;
(B) The consulting
pharmacist shall specify maximum quantities of medications to be stored at
bedside to ensure prevention of poisoning by confused or suicidal
residents.
(c) Stop
Order Policy. An automatic stop order policy shall be adopted and enforced.
This policy shall provide guidance when medications ordered are not
specifically limited as to time or number of doses. The policy shall be
developed by the Quality Assessment and Assurance Committee.
(5) Medication Review. Medications
shall be reviewed monthly by the consulting pharmacist and reordered by the
physician as necessary, but no less often than quarterly. The pharmacist shall
alert the DNS when drugs designated "less-than effective" ("DESI" drugs) by the
Federal Food and Drug Administration have been ordered and what alternative
medications may be available. The DNS shall notify the physician.
(6) Emergency Medication Kit:
(a) An emergency medication kit shall be
prepared and authorized by a registered pharmacist for use in the facility in
accordance with written facility policy. The contents shall be selected by the
Quality Assessment and Assurance Committee;
(b) The kit shall be sealed and stored in a
manner to prevent loss of drugs, but available to authorized personnel. The
vendor pharmacist shall be notified when the seal is broken. A record shall be
made that identifies each use of an emergency drug. The contents shall be
plainly indicated on the outside of the container;
(c) Any drug removed from the kit shall be
covered by a prescription and signed by the physician within 72
hours.
(7) Charges for
Drugs; Choice of Supplier. See OAR 411-085-0340.
(8) Documentation. The nursing staff shall
clearly and accurately document administration of pharmaceuticals and the
response thereto.
Notes
Stat. Auth.: ORS 410.070, 410.090 & 441.055
Stats. Implemented: ORS 441.055 & 441.615
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