2014 -- S 2523

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LC004341

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     STATE OF RHODE ISLAND

IN GENERAL ASSEMBLY

JANUARY SESSION, A.D. 2014

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A N   A C T

RELATING TO FOOD AND DRUGS - UNIFORM CONTROLLED SUBSTANCES ACT

     

     Introduced By: Senators Ottiano, Lombardi, Nesselbush, Satchell, and Felag

     Date Introduced: February 27, 2014

     Referred To: Senate Health & Human Services

     It is enacted by the General Assembly as follows:

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     SECTION 1. Section 21-28-3.32 of the General Laws in Chapter 21-28 entitled "Uniform

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Controlled Substances Act" is hereby amended to read as follows:

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     21-28-3.32. Electronic prescription database. -- (a) The information contained in any

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prescription drug monitoring database maintained by the department of health pursuant to section

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3.18 of this chapter shall be disclosed only:

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      (1) To a practitioner who certifies that the requested information is for the purpose of

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evaluating the need for or providing medical treatment for a current patient to whom the

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practitioner is prescribing or considering prescribing a controlled substance;

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      (2) To a pharmacist who certifies that the requested information is for a current client to

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whom the pharmacist is dispensing or considering dispensing a controlled substance;

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     (3) To an authorized designee of the practitioner and/or pharmacist who is qualified to

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access the information in accordance with rules promulgated by the department of health.

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      (3)(4) Pursuant to a valid search warrant based on probable cause to believe a violation

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of federal or state criminal law has occurred and that specified information contained in the

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database would assist in the investigation of the crime;

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      (4)(5) To a patient who requests his or her own prescription information, or the parent or

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legal guardian of a minor child who requests the minor child's prescription information;

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      (5)(6) To a health professional regulatory board that documents, in writing, that the

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requested information is necessary for an investigation related to licensure, renewal or

 

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disciplinary action involving the applicant, licensee or registrant to whom the requested

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information pertains;

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      (6)(7) To any vendor or contractor with whom the department has contracted to establish

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or maintain the electronic system of the prescription drug monitoring database; or

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      (7)(8) To public or private entities for statistical, research, or educational purposes, after

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removing the patient and prescriber information that could be used to identify individual patients.

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This shall not include entities receiving a waiver from the institutional review board.

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      (b) Information stored in the prescription drug monitoring database shall include only the

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following:

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      (1) Patient's first and last name, and/or patient identification number; provided, however,

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the patient's social security number shall not be recorded in whole or in part, patient sex, patient

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date of birth, and patient address;

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      (2) Prescribing practitioner's name and drug enforcement administration prescriber

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information number;

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      (3) Prescribing practitioner's office or hospital contact information;

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      (4) Prescription name, prescription number, prescription species code, national drug code

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number, prescription dosage, prescription quantity, days' supply, new-refill code, number of

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refills authorized, date the prescription was written, date the prescription was filled, payment

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type; provided, however, no credit card number shall be recorded in whole or in part; and

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      (5) The drug enforcement administration pharmacy number of the pharmacy filling the

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prescription.

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      (c) The department shall disclose any information relating to a patient maintained in the

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prescription drug monitoring database to that patient, at no cost to the patient, within thirty (30)

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business days after the department receives a written request from the patient for the information.

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This information shall include the records maintained by the department pursuant to subsection

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(e). Notwithstanding the above, the department may, at the request of the law enforcement

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agency, withhold for up to sixty (60) days following the conclusion of a law enforcement

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investigation, the disclosure to the patient that information has been obtained pursuant to

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subdivision (a)(3).

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      (d) A patient may request from the dispensing pharmacy correction of any inaccurate

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information contained within the prescription drug monitoring database in accordance with the

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procedure specified by subsection 5-37.3-5(c).

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      (e) The department shall, for the period of time that prescription information is

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maintained, maintain records of the information disclosed through the prescription drug

 

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monitoring database, including, but not limited to:

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      (1) The identity of each person who requests or receives information from the

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prescription drug monitoring database and the organization, if any, the person represents;

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      (2) The information released to each person or organization and the basis for its release

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under subsection (a); and

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      (3) The dates the information was requested and provided.

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      (f) Prescription information contained within the prescription drug monitoring database

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shall be removed no later than five (5) years from the date the information is entered into the

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database. Records in existence prior to the enactment of this section shall be removed no later

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than ten (10) years from the date the information is entered into the database.

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      (g) The department shall promptly notify any affected individual of an improper

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disclosure of information from the prescription drug monitoring database or a breach in the

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security of the prescription drug monitoring database that poses a significant risk of disclosure of

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patient information to an unauthorized individual.

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      (h) At the time of signing a prescription which is required by the department to be

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entered into the prescription drug monitoring database, the prescribing practitioner shall inform

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the patient in writing of the existence of the prescription drug monitoring database, the patient's

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right to access their own prescription information, and the name and contact information of the

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agency operating the program.

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      (i) No person shall access information in the prescription monitoring database except to

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the extent and for the purposes authorized by subsection (a).

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      (j) In any civil action allowing a violation of this chapter, the court may award damages,

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including punitive damages, and reasonable attorneys' fees and costs to a prevailing plaintiff, and

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injunctive and any other appropriate relief.

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      (k) Any pharmacist who, in his or her professional judgment, refuses to fill a prescription

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based on information contained within the prescription drug monitoring database shall inform the

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prescribing physician within twenty-four (24) hours.

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     (l) All practitioners shall, as a condition of the initial registration or renewal of the

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practitioner’s authority to prescribed controlled substances, register with the prescription drug

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monitoring database maintained by the department of health.

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     SECTION 2. This act shall take effect upon passage.

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EXPLANATION

BY THE LEGISLATIVE COUNCIL

OF

A N   A C T

RELATING TO FOOD AND DRUGS - UNIFORM CONTROLLED SUBSTANCES ACT

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     This act would permit an authorized designee of a practitioner and/or pharmacist, who is

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qualified, to access the information contained in any prescription drug monitoring database

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maintained by the department of health. It would further require practitioners to register with the

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prescription drug monitoring database, upon initial registration or renewal of the practitioner’s

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authority to prescribe controlled substances.

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     This act would take effect upon passage.

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