Ga. Comp. R. & Regs. R. 480-24-.08 - Crisis Stabilization Unit (CSU) Emergency Drug Kits
Emergency drug kits may be placed in licensed Crisis Stabilization Units (CSU) by the pharmacy of the consultant or vendor pharmacist provided the following conditions are met:
(1) A record of the drugs to be kept in an
emergency drug kit must be kept in the CSU and the provider pharmacy;
(2) Drugs shall not be accessed for use from
the emergency drug kit in an emergency situation without a prescription drug
order from a licensed practitioner. A valid, signed prescription drug order for
any such drug must be issued to the vendor pharmacy, supplying the emergency
drug kit, within 72 hours of the drug being taken from the kit;
(a) Whenever an emergency drug kit is
accessed and a drug is removed, personnel shall immediately reseal the kit with
a tamper-proof, serial-numbered seal, with the seal serial number to be
recorded in a log along with the name of the person removing the drug and
resealing the kit and date the kit was opened;
(3) Emergency drug kits shall be stored in
limited access areas and sealed to prevent unauthorized access and to insure a
proper environment for preservation of the drugs therein. The provider pharmacy
shall develop a method to readily determine if an emergency drug kit has been
accessed without authorization;
(4)
An emergency drug kit must be inventoried once a month by a pharmacist from the
provider pharmacy and sign a card attached to the kit indicating the date it
was inspected. The provider pharmacy must maintain an adequate record of such
inspections;
(5) Special Agents of
the GDNA shall have the authority to check emergency drug kits as well as the
records in the provider pharmacy to determine that drugs and records are
accurate and the emergency drug kit is being properly used;
(6) The provider pharmacy must apply on an
individual basis to the Board, in care of the GDNA Director, for approval to
place an emergency drug kit in each individual CSU and a copy of this approval
will be kept on file in both the CSU and the provider pharmacy. Upon
recommendation by the GDNA Director, the Board may revoke the approval for an
emergency drug kit in any CSU where abuse or misuse of drugs from the emergency
drug kit is noted;
(7) The Board
shall have the authority to approve on an individual basis the drugs and the
amounts of each individual drug allowed to be kept in an emergency drug kit.
Any change in the drugs and amounts kept in a kit must be submitted in writing
to the GDNA Director who shall make recommendations to the Board. After Board
approval, a copy of this approval will be maintained in the GDNA provider
pharmacy file and by the CSU. Any emergency drug kit approval becomes null and
void once the approved pharmacy ceases to provide that kit;
(8) Each solid oral dosage form placed in an
emergency drug kit must be individually labeled with the name and strength of
the drug, lot number, expiration date, and other appropriate cautionary
information; and
(9) The exterior
of an emergency drug kit shall be labeled so as to clearly and unmistakably
indicate that it is an emergency drug kit and is for "EMERGENCY USE ONLY", and
the label shall be physically signed and dated by the pharmacist who sealed the
kit. In addition, a listing of the drugs contained therein, including the name,
address, and telephone number(s) of the provider pharmacy shall be attached to
both the exterior and the interior of an emergency drug kit.
Notes
State regulations are updated quarterly; we currently have two versions available. Below is a comparison between our most recent version and the prior quarterly release. More comparison features will be added as we have more versions to compare.
No prior version found.