90-113.74C. Practitioner use of controlled substances reporting system; mandatory reporting of violations.
(a) Prior to initially prescribing a targeted controlled substance to a patient, a practitioner shall review the information in the controlled substances reporting system pertaining to the patient for the 12-month period preceding the initial prescription. For every subsequent three-month period that the targeted controlled substance remains a part of the patient's medical care, the practitioner shall review the information in the controlled substances reporting system pertaining to the patient for the 12-month period preceding the determination that the targeted controlled substance should remain a part of the patient's medical care. Each instance in which the practitioner reviews the information in the controlled substances reporting system pertaining to the patient shall be documented in the patient's medical record. In the event the practitioner is unable to review the information in the controlled substances reporting system pertaining to the patient because the system is not operational or there is some other temporary electrical or technological failure, this inability shall be documented in the patient's medical record. Once the electrical or technological failure has been resolved, the practitioner shall review the information in the controlled substances reporting system pertaining to the patient and the review shall be documented in the patient's medical record.
(b) A practitioner may, but is not required to, review the information in the controlled substances reporting system pertaining to a patient prior to prescribing a targeted controlled substance to the patient in any of the following circumstances:
(1) The controlled substance is to be administered to a patient in a health care setting, hospital, nursing home, outpatient dialysis facility, or residential care facility, as defined in G.S. 14-32.2.
(2) The controlled substance is prescribed for the treatment of cancer or another condition associated with cancer.
(3) The controlled substance is prescribed to a patient in hospice care or palliative care.
(c) The Department shall conduct periodic audits of the review of the controlled substances reporting system by prescribers. The Department shall determine a system for selecting a subset of prescriptions to examine during each auditing period. The Department shall report to the appropriate licensing board any prescriber found to be in violation of this section. A violation of this section may constitute cause for the licensing board to suspend or revoke a prescriber's license.
(d) For purposes of this section, a "practitioner" does not include a person licensed to practice veterinary medicine pursuant to Article 11 of Chapter 90 of the General Statutes. (2017-74, s. 12; 2018-76, s. 4.)
Structure North Carolina General Statutes
North Carolina General Statutes
Chapter 90 - Medicine and Allied Occupations
Article 5E - North Carolina Controlled Substances Reporting System Act.
§ 90-113.71 - Legislative findings and purpose.
§ 90-113.73A - Expand monitoring capacity; report.
§ 90-113.74 - Confidentiality.
§ 90-113.74D - Dispenser use of controlled substances reporting system.
§ 90-113.74E - Certification of diversion investigators and diversion supervisors.
§ 90-113.75 - Civil penalties; other remedies; immunity from liability.
§ 90-113.75A - Creation of Controlled Substances Reporting System Fund.
§ 90-113.75B - Annual report to General Assembly and licensing boards.