Prescription Drug Monitoring Program (216-RICR-20-20-3)

A.These regulations are promulgated pursuant to the authority set forth in R.I. Gen. Laws §§ 21-28-3.18(d)(2) and 21-28-3.32(n)(3), and are established for the purpose of defining minimum standards for the transfer of electronic data between the Department of Health and pharmacies for schedule II, III, IV, and V controlled substances, and opioid antagonists.

A.Pharmacies that do not have a Rhode Island Controlled Substance Registration (CSR) pursuant to R.I. Gen. Laws § 21-28-3.02(a) are not required to report the dispensing of schedule II, III, IV, and V controlled substances and opioid antagonists to the prescription drug monitoring program (PDMP).

A.Wherever used in this Part, the following terms shall be construed as follows:

1."Controlled substance" means as defined in R.I. Gen. Laws § 21-28-1.02(8).

2.“Department" means the Rhode Island Department of Health.

3.“Nonresident pharmacy" means a pharmacy located outside Rhode Island in any state in the United States or any province or territory of Canada that ships, mails, or delivers prescription drugs and/or devices to a patient or person in Rhode Island.

4.“Parent or legal guardian” means the custodial parent for a person under eighteen (18) years of age or the legal guardian with responsibility for healthcare decisions for a person of any age.

5.“Pharmacy” means that portion or part of a premise where prescriptions are compounded and dispensed, including that portion utilized for the storage of prescription or legend drugs.

6.“Practitioner” means a physician, physician assistant, dentist, veterinarian, nurse or other person duly authorized by law in the state in which they practice to prescribe drugs.

A.A pharmacy licensed as a retail pharmacy that dispenses schedule II, III, IV, or V controlled substances or opioid antagonists shall transmit prescription dispensing data for these substances to the Department in accordance with §§ 3.5(A) and (B) of this Part.

1.A pharmacy licensed as an institutional pharmacy that dispenses schedule II, III, IV, or V controlled substances or opioid antagonists shall transmit prescription dispensing data for these substances to the Department when dispensed to outpatients only and shall not be required to submit zero fill reports.

a.A pharmacy that possesses a Rhode Island Controlled Substance Registration (CSR) pursuant to R.I. Gen. Laws § 21-28-3.02(a) which does not dispense any controlled substances shall report “zero fills,” every twenty-four (24) hours.

b.Any pharmacy that does not possess a Rhode Island Controlled Substance Registration (CSR) is not required to submit “zero fills” reports.

2.A pharmacy licensed as a non-resident pharmacy shall be considered a pharmacy for the purpose of compliance with the reporting requirements of this Part.

A.A pharmacy that dispenses schedule II, III, IV, or V controlled substances or opioid antagonists to a person, who is not an inpatient of a hospital, shall transmit electronically to the Department the information stated in R.I. Gen. Laws § 21-28-3.32(b).

B.A pharmacy licensed as a retail pharmacy or a nonresident pharmacy shall transmit the required prescription information by means of a secure web-based data system, or other approved electronic methods, designated by the Department.

1.Pursuant to R.I. Gen. Laws § 21-28-3.18(n), A pharmacy shall transmit the information required pursuant to this Part one (1) business day following the date of dispensing.

2.A pharmacy shall transmit the information required pursuant to this Part to the Department in such a manner as to ensure the confidentiality of the information in compliance with all applicable federal and state statutes and regulations, including the federal Health Insurance Portability and Accountability Act of 1996 (HIPAA).

3.Notification to the prescribing physician by the pharmacist for refusal to fill a prescription is pursuant to R.I. Gen. Laws § 21-28-3.32(k).

A.The Department shall only disclose information obtained pursuant to this Part in accordance with R.I. Gen. Laws § 21-28-3.32(a).

B.A patient may request from the dispensing pharmacy correction of any inaccurate information contained within the PDMP in accordance with the procedure specified by R.I. Gen. Laws § 5-37.3-5(c).

C.Maintenance of records of information disclosed is pursuant to R.I. Gen. Laws § 21-28-3.32(e).

D.Removal of prescription information contained within the PDMP is pursuant to R.I. Gen. Laws § 21-28-3.32(f).

E.Notification of improper disclosure is pursuant to R.I. Gen. Laws § 21-28-3.32(g).

F.Notification to patients of the PDMP is pursuant to R.I. Gen. Laws § 21-28-3.32(h).

G.Department disclosure of information to patients is pursuant to R.I. Gen. Laws § 21-28-3.32(c).

A.The Department shall ensure the privacy of patients and confidentiality of patient information transmitted or obtained is maintained in accordance with applicable state and federal laws, rules, and regulations.

1.No person shall access information in the PDMP except to the extent and for the purposes authorized by § 3.6(A) of this Part.

A.The Department may evaluate the prescription information received from pharmacies for the purposes of preventing controlled substance diversion, public health initiatives, and statistical reporting.

A.Notwithstanding the provisions of § 3.6(A) of this Part, a pharmacist or prescriber is allowed to share access to the PDMP with an authorized designee of the practitioner and/or pharmacist, to consult the PDMP on the practitioner's and/or pharmacist's behalf, or with a medical director of the practitioner's practice for quality improvement activities within the practice, provided that the requirements of R.I. Gen. Laws § 21-28-3.32(a)(3) are satisfied.