Current through Reg. 50, No. 187; September 24, 2024
(1) It is the
responsibility of the licensee to ensure that individual unlicensed medication
assistants (UMA or UMAs) who will be administering medication to clients meet
all requirements of this rule.
(2)
Unlicensed medication assistants may administer only prescribed, prepackaged,
premeasured oral, topical nasal, and ophthalmic medications.
(3) UMAs may administer over the counter
(OTC) medications as currently prescribed by the client's health care
professional.
(4) UMAs may not:
(a) Administer medications by injection
including intra-muscular, intravenous or subcutaneous;
(b) Administer medication vaginally or
rectally; or
(c) Conduct glucose
monitoring.
(5) UMAs may
administer medications to a client only after the following requirements are
met for that client:
(a) A current informed
consent has been signed by the client or client's representative. The consent
must acknowledge and permit UMAs to administer specifically listed medications
prescribed by a licensed health care professional to the client. The informed
consent must be updated and signed annually;
(b) A written report for the client that
indicates the client's behavior and any past medication reactions must be
documented on the Medication Administration Record (MAR). The written report
and MAR must be updated if the client's behavior or medication reactions
change. Information included in the written report can be provided by the
client or client's representative, or another UMA or direct care staff person
who is familiar with the client. The person administering medications must be
familiar with the information included in the written report and MAR prior to
administering medications to clients; and,
(c) A determination is made that the client
to whom medication will be administered has not been deemed capable of
self-administration of his or her medications. The determination is to be made
by the facility through assessment and IDT review.
(6) Administration of medication by UMAs must
be under the supervision of a registered nurse or APRN.
(a) Supervision includes weekly monitoring of
medication and 24-hour availability of a registered nurse or APRN via telephone
or paging device;
(b) Prior to
assigning tasks to an UMA, the supervisory nurse must verify the training and
validation of the unlicensed medication assistant as required by this rule
chapter;
(c) The supervisory nurse
must communicate the assignment to the UMA and verify that the UMA understands
the assignment;
(d) Monitoring and
supervision of the completion of the assignment must be documented by the
supervising nurse;
(e) The
supervising nurse must participate in performance evaluations of the UMA
relative to performance of medication administration.
(7) Requirements governing acquiring,
receiving, dispensing, administering, disposing, labeling, and storage of
medication by UMAs include:
(a) Outdated
medication must be properly destroyed by the supervising nurse. The disposal
must be witnessed by one other staff of the facility and a record of the
medication disposal must be maintained by the facility and signed by the
supervising nurse and witness;
(b)
Torn, damaged, illegible or mislabeled prescription labels must be reported
immediately to the dispensing pharmacy or pharmacist;
(c) Clients must not miss the administration
of medications due to delays in refilling a prescription. It shall be the
responsibility of the supervising nurse to ensure that refills are ordered and
obtained in a timely manner;
(d) No
client shall be administered a prescription or OTC medication or treatment,
except upon the written order of the client's prescribing health care
professional.
(8) When
administering medications to clients, the UMA must:
(a) Wash his or her hands with soap and water
prior to administration of medication, or supervising the self-administration
of medication to clients. They must also wash their hands between the
administration of medication to each client and when there is a change in route
of administration;
(b) Prepare
medications for one individual client at a time in a quiet location that is
free from distraction;
(c)
Administer medications to one client at a time. To complete a client's
medication process, the medication of one client must be returned to the
portable or permanent medication storage unit and documentation made in the MAR
before administering medications to, or supervising the self-administration of,
medication for another client;
(d)
Administer medications to each client, at the time, with the dosage, and by the
route prescribed by the client's health care professional. Each time medication
is administered:
1. Conduct a triple-check of
the dosage and time of administration against the original medication container
label and the MAR before administering or supervising the self-administration
of the medication;
2. Confirm the
client to whom the medication is to be administered is the same client for whom
the medication has been prescribed or ordered;
3. Administer as prescribed and via the route
instructed by the client's prescribing health care professional;
4. Do not crush, dilute or mix medications
without written directions or instructions from the client's prescribing health
care professional;
5. Check the
expiration date before administering each medication. Medications with an
expiration date preceding the current date must not be administered;
6. Facilitate the correct positioning and use
any adaptive equipment or techniques required for that client for the proper
administration of medications.
(e) Ensure the oral medication administered
or supervised during self-administration has been completely ingested before
leaving the client. Directly observe the client for a period of at least twenty
minutes following the administration of a new medication ordered by the
client's prescribing health care professional. This observation period is to
immediately detect and react to possible side effects of the medication or to
document the effectiveness of the medication. UMAs must review the MAR for
special instructions regarding required observation of medications and the UMA
must monitor for side effects and effectiveness of all administered
drugs.
(f) Immediately record the
administration of the medication in the MAR.
Rulemaking Authority 400.9685, 400.967 FS. Law Implemented
400.9685, 400.967 FS.
New 12-21-15.