New Jersey Administrative Code
Title 10 - HUMAN SERVICES
Chapter 44B - MANUAL OF STANDARDS FOR COMMUNITY CARE RESIDENCES
Subchapter 5 - HEALTH SERVICES
Section 10:44B-5.2 - Medication

Universal Citation: NJ Admin Code 10:44B-5.2

Current through Register Vol. 56, No. 18, September 16, 2024

(a) When an individual cannot administer his or her own medication due to intellectual or behavioral disabilities, as determined by the IDT and recorded in the service plan, the licensee or his or her alternate, who has successfully completed medication training, shall give it to the individual to take exactly as prescribed, and assure that the medication is taken.

1. The licensee, and when necessary, the trained alternate, shall maintain a medication administration record of all medications taken where assistance is required. The licensee, and when necessary, the alternate, shall complete the medication administration record as he or she was trained to do by the placing agency. The medication record shall include:
i. The signature of any persons administering medication followed by his or her initials;

ii. The brand name and, if applicable, generic name of the medication;

iii. The dosage;

iv. The date and time of administration;

v. A record of each dosage at the time it is administered, identified by the initials of the person administering the medication;

vi. Documentation of the proper code for instances when a medication is not administered; and

vii. A list of all known allergies.

2. Errors in medication documentation or administration shall be recorded on the medication record at the time of their occurrence.

3. Medications may be changed or discontinued only upon written documentation from the physician or nurse practitioner, which shall be maintained in the individual's file.

(b) Individuals who have the potential to be self-medicating shall be assessed by the IDT and the results of this assessment shall be recorded in the service plan and reviewed annually by the IDT.

1. Only those individuals who have been determined by the IDT to be self-medicating, and who have documentation of such in their service plan, which shall include a current Self-Medication Assessment, shall administer their own medications.

2. Upon determination by the IDT as documented in the service plan that an individual is capable of self-medication, no daily medication administration record is required; however, the licensee shall maintain in the individual's record all copies of prescriptions/physician's orders for currently prescribed medications, as well as all documentation from the physician for any changes and/or discontinuations of medications.

3. The licensee shall be familiar with all medications being taken by the individual who self-medicates, their side effects, and where they are stored.

4. Medications administered by injection may be self-administered if there is documentation of the individual's successful training by licensed medical personnel. This determination shall be approved by the IDT and included in the service plan.

5. Only a licensee who has documentation of successful completion of training from licensed medical personnel may administer medication by injection.

(c) Medications shall only be administered to or used by the person for whom they are prescribed.

(d) The licensee shall ensure that an adequate supply of medication is maintained for the individual at all times.

(e) The licensee shall dispose of expired and discontinued medications in such a manner so that they cannot be ingested or used by anyone in or out of the home.

(f) The licensee shall supervise the storage and accessibility of all medication, assuring access only by authorized persons.

1. Medication shall be stored separately from all food, household cleaners, insecticides, poisons, etc.

2. All medications shall be kept in their original containers and shall be properly identified.
i. Medications obtained from a pharmacist shall include a pharmacy label with the individual's name, medication name, frequency of dosing, and dosage amount, in accordance with the physician's prescription.

ii. Medications available over-the-counter shall include the manufacturer's label identifying the content and strength of the medication, exactly matching the physician's order.

3. Pill planners shall not be utilized.

4. The licensee may not repackage medications from one container to another container for administration by another person. Medications that are to be administered by another person shall be maintained in the original container that has been obtained directly from the pharmacy.

(g) The licensee shall be familiar with all medications being administered to the individual, their purpose, and side effects.

(h) Medication errors and drug reactions shall be reported at the time of the occurrence to the individual's physician or nurse practitioner and case manager and documented in the individual's file.

Disclaimer: These regulations may not be the most recent version. New Jersey may have more current or accurate information. We make no warranties or guarantees about the accuracy, completeness, or adequacy of the information contained on this site or the information linked to on the state site. Please check official sources.
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