Ohio Admin. Code 4729:5-9-02.11 - Dispensing customized patient medication packages by an institutional pharmacy
In lieu of dispensing two or more dangerous drugs in separate containers, a pharmacist practicing at an institutional pharmacy may dispense a customized patient medication package. A customized patient medication package is a package for a specific patient comprising a series of containers and containing two or more prescribed solid oral dosage forms that complies with the following requirements:
(A)
The package is
designed, or each container is labeled, to indicate the day and time or period
of time when the contents within each container are to be taken by the
patient.
(B)
The number of drugs placed in each container cannot
exceed the capability of the container to prevent damage to the dosage
forms.
(C)
The quantity of the package dispensed may not be more
than a thirty-one-day supply.
(D)
The labels must
be of sufficient size to properly and clearly label a thirty-one-day or less
supply with all information required in accordance with this chapter of the
Administrative Code, including the use of accessory labels. When a customized
medication packaging is utilized, including dispensing of single unit packages,
the drugs shall be dispensed in a container or package with an affixed label
containing the following information:
(1)
Identification of
the dispensing pharmacy;
(2)
The patient's full name;
(3)
The date of
dispensing;
(4)
The non-proprietary and/or proprietary name of the
drug;
(5)
National drug code, universal product code, or
formulary code, if applicable, which may be embedded in a barcode or quick
response (QR) code on the label;
(6)
The strength of
the drug;
(7)
The pharmacy's expiration date or beyond-use date,
which shall not exceed the expiration date on the manufacturer's container or
six months from the date the drug was originally packaged, whichever date is
earlier. If multiple manufacturer containers are used, the expiration date
shall not exceed the expiration date on the manufacturer's container that will
expire first or six months from the date the drug was originally repackaged,
whichever date is earlier.
(E)
All drugs
dispensed to inpatients for self-administration or dispensed for outpatient use
shall also be labeled in accordance with rule
4729:5-5-06 of the
Administrative Code.
(F)
Dangerous drugs which have been dispensed in a
customized patient medication package may only be returned to stock or
re-dispensed in accordance with all the following:
(1)
The drugs have
not been in the possession of the ultimate user; and
(2)
The drugs have
not been placed in the same container with another dangerous drug (i.e. did not
come into direct contact with a different drug within the same
container).
(G)
The containers of a package are sealed or secured in
such a way that access to the drugs stored within is not possible without
leaving visible proof that such access has been attempted or
made.
(H)
Any pharmacy dispensing customized patient medication
packages in accordance with this rule must implement policies and procedures
that will exclude drugs having any of the following characteristics from such
packaging:
(1)
The U.S.P. monograph or official labeling requires
dispensing in the original container, unless there is documentation from the
manufacturer stating otherwise;
(2)
The drugs or
dosage forms are incompatible with packaging components or each
other;
(3)
The drugs are therapeutically incompatible when
administered simultaneously;
(4)
The drugs require
special packaging.
Replaces: 4729-17-10
Notes
Promulgated Under: 119.03
Statutory Authority: 3715.69, 3719.28, 4729.26
Rule Amplifies: 3715.64, 3719.08
Prior Effective Dates: 09/01/1985, 07/01/1991, 01/10/1996, 03/01/1999, 01/01/2009, 01/01/2010
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