SB333 HJUD AM 4-3 NEW
The Committee on Judiciary moves to amend the bill on page 1, by striking out everything after the enacting clause and inserting in lieu thereof the following:
That §60A-9-4, §60A-9-5, and §60A-9-5a of the Code of West Virginia, 1931, as amended, be amended and reenacted; and that said code be amended by adding thereto a new section, designated §60A-9-9 all to read as follows:
ARTICLE 9. CONTROLLED SUBSTANCES MONITORING.
§60A-9-4. Required information.
(a) Whenever a medical services provider dispenses a controlled
substance listed in Schedule II, III or IV as established under the provisions
of article two of this chapter or an opioid antagonist, or whenever a
prescription for the controlled substance or opioid antagonist is filled by:
(i) A pharmacist or pharmacy in this state; (ii) a hospital, or other health
care facility, for outpatient use; or (iii) a pharmacy or pharmacist licensed
by the Board of Pharmacy, but situated outside this state for delivery to a
person residing in this state, the medical services provider, health care
facility, pharmacist or pharmacy shall, in a manner prescribed by rules
promulgated by the board under Board of Pharmacy pursuant to this
article, report the following information, as applicable:
(1) The name, address, pharmacy prescription number and Drug Enforcement Administration controlled substance registration number of the dispensing pharmacy or the dispensing physician or dentist;
(2) The full legal name, address and birth date of the person for whom the prescription is written;
(3) The name, address and Drug Enforcement Administration controlled substances registration number of the practitioner writing the prescription;
(4) The name and national drug code number of the Schedule II, III and IV controlled substance or opioid antagonist dispensed;
(5) The quantity and dosage of the Schedule II, III and IV controlled substance or opioid antagonist dispensed;
(6) The date the prescription was written and the date filled;
(7) The number of refills, if any, authorized by the prescription;
(8) If the prescription being dispensed is being picked up by
someone other than the patient on behalf of the patient, the first name, last
name and middle initial, address and birth date of the person picking up the
prescription as set forth on the person’s government-issued photo identification
card shall be retained in either print or electronic form until such time as
otherwise directed by rule promulgated by the board Board of
Pharmacy; and
(9) The source of payment for the controlled substance dispensed.
(b) Whenever a medical services provider treats a patient for an overdose that has occurred as a result of illicit or prescribed medication, the medical service provider shall report the full legal name, address and birth date of the person who is being treated, including any known ancillary evidence of the overdose. The Board of Pharmacy shall coordinate with the Division of Justice and Community Services and the Office of Drug Control Policy regarding the collection of overdose data.
(b) (c) The board Board of Pharmacy may
prescribe by rule promulgated under this pursuant to this article
the form to be used in prescribing a Schedule II, III, and IV substance or
opioid antagonist if, in the determination of the board Board of
Pharmacy, the administration of the requirements of this section would be
facilitated.
(c) (d) Products regulated by the provisions of article ten of
this chapter shall be subject to reporting pursuant to the provisions of this
article to the extent set forth in said article.
(d) (e) Reporting required by this section is not required for
a drug administered directly to a patient by a practitioner. Reporting is,
however, required by this section for a drug dispensed to a patient by a
practitioner. Provided, That the The quantity
dispensed by a prescribing practitioner to his or her own patient may not
exceed an amount adequate to treat the patient for a maximum of seventy-two hours with no greater
than two 72-hour
cycles dispensed in any fifteen-day period of time.
(e) (f) The Board of Pharmacy shall notify a physician
prescribing buprenorphine or buprenorphine/naloxone within sixty days of the
availability of the an abuse deterrent form of buprenorphine or
buprenorphine/naloxone is if approved by the Food and Drug
Administration as provided in FDA Guidance to Industry. Upon receipt of the
notice, a physician may switch their patients using buprenorphine or
buprenorphine/naloxone to the abuse deterrent form of the drug.
§60A-9-5. Confidentiality; limited access to records; period of retention; no civil liability for required reporting.
(a)(1) The information required by this article to be kept by the board
Board of Pharmacy is confidential and not subject to the provisions of
chapter twenty-nine-b of this code or obtainable
as discovery in civil matters absent a court order and is open to inspection
only by inspectors and agents of the board Board of Pharmacy,
members of the West Virginia State Police expressly authorized by the
Superintendent of the West Virginia State Police to have access to the
information, authorized agents of local law-enforcement agencies as members of a federally
affiliated drug task force, authorized agents of the federal Drug Enforcement
Administration, duly authorized agents of the Bureau for Medical Services, duly
authorized agents of the Office of the Chief Medical Examiner for use in post-mortem examinations, duly
authorized agents of the Office of Health Facility Licensure and Certification for
use in certification, licensure and regulation of health facilities, duly
authorized agents of licensing boards of practitioners in this state and other
states authorized to prescribe Schedules II, III and IV controlled substances,
prescribing practitioners and pharmacists, a dean of any medical school or
his or her designee located in this state to access prescriber level data to
monitor prescribing practices of faculty members, prescribers and residents
enrolled in a degree program at the school where he or she serves as dean, a
physician reviewer designated by an employer of medical providers to monitor
prescriber level information of prescribing practices of physicians, advance
practice registered nurses or physician assistant in their employ, and a chief
medical officer of a hospital or a physician designated by the chief executive
officer of a hospital who does not have a chief medical officer, for
prescribers who have admitting privileges to the hospital or prescriber level
information, and persons with an enforceable court order or regulatory
agency administrative subpoena. Provided, That all All
law-enforcement
personnel who have access to the Controlled Substances Monitoring Program
database shall be granted access in accordance with applicable state laws and
the board’s legislative Board of Pharmacy’s rules, shall be
certified as a West Virginia law-enforcement officer and shall have successfully completed training
approved by the board Board of Pharmacy. All information released
by the board Board of Pharmacy must be related to a specific
patient or a specific individual or entity under investigation by any of the
above parties except that practitioners who prescribe or dispense controlled
substances may request specific data related to their Drug Enforcement
Administration controlled substance registration number or for the purpose of
providing treatment to a patient: Provided, That the West Virginia
Controlled Substances Monitoring Program Database Review Committee established
in subsection (b) of this section is authorized to query the database to comply
with said subsection.
(2) Subject to the provisions of subdivision (1) of this
subsection, the board Board of Pharmacy shall also review the
West Virginia Controlled Substance Monitoring Program database and issue
reports that identify abnormal or unusual practices of patients who exceed
parameters as determined by the advisory committee established in this section.
The board Board of Pharmacy shall communicate with practitioners
and dispensers to more effectively manage the medications of their patients in
the manner recommended by the advisory committee. All other reports produced by
the board Board of Pharmacy shall be kept confidential. The board
Board of Pharmacy shall maintain the information required by this
article for a period of not less than five years. Notwithstanding any other
provisions of this code to the contrary, data obtained under the provisions of
this article may be used for compilation of educational, scholarly or
statistical purposes, and may be shared with the West Virginia Department of
Health and Human Resources for those purposes, as long as the identities of
persons or entities and any personally identifiable information, including
protected health information, contained therein shall be redacted, scrubbed or
otherwise irreversibly destroyed in a manner that will preserve the
confidential nature of the information. No individual or entity required to
report under section four of this article may be subject to a claim for civil
damages or other civil relief for the reporting of information to the board Board
of Pharmacy as required under and in accordance with the provisions of this
article.
(3) The board Board of Pharmacy shall establish an
advisory committee to develop, implement and recommend parameters to be used in
identifying abnormal or unusual usage patterns of patients in this state. This
advisory committee shall:
(A) Consist of the following members: A physician licensed by the
West Virginia Board of Medicine, a dentist licensed by the West Virginia Board
of Dental Examiners, a physician licensed by the West Virginia Board of
Osteopathic Medicine, a licensed physician certified by the American Board of
Pain Medicine, a licensed physician board certified in medical oncology
recommended by the West Virginia State Medical Association, a licensed
physician board certified in palliative care recommended by the West Virginia
Center on End of Life Care, a pharmacist licensed by the West Virginia Board of
Pharmacy, a licensed physician member of the West Virginia Academy of Family
Physicians, an expert in drug diversion and such other members as determined by
the board Board of Pharmacy.
(B) Recommend parameters to identify abnormal or unusual usage patterns of controlled substances for patients in order to prepare reports as requested in accordance with subdivision (2), subsection (a) of this section.
(C) Make recommendations for training, research and other areas that are determined by the committee to have the potential to reduce inappropriate use of prescription drugs in this state, including, but not limited to, studying issues related to diversion of controlled substances used for the management of opioid addiction.
(D) Monitor the ability of medical services providers, health care facilities, pharmacists and pharmacies to meet the 24-hour reporting requirement for the Controlled Substances Monitoring Program set forth in section three of this article, and report on the feasibility of requiring real-time reporting.
(E) Establish outreach programs with local law enforcement to provide education to local law enforcement on the requirements and use of the Controlled Substances Monitoring Program database established in this article.
(b) The board Board of Pharmacy shall create a West
Virginia Controlled Substances Monitoring Program Database Review Committee of
individuals consisting of two prosecuting attorneys from West Virginia
counties, two physicians with specialties which require extensive use of
controlled substances and a pharmacist who is trained in the use and abuse of
controlled substances. The review committee may determine that an additional
physician who is an expert in the field under investigation be added to the
team when the facts of a case indicate that the additional expertise is
required. The review committee, working independently, may query the database
based on parameters established by the advisory committee. The review committee
may make determinations on a case-by-case
basis on specific unusual prescribing or dispensing patterns indicated by
outliers in the system or abnormal or unusual usage patterns of controlled
substances by patients which the review committee has reasonable cause to
believe necessitates further action by law enforcement or the licensing board
having jurisdiction over the practitioners or dispensers under consideration. The
licensing board having jurisdiction over the practitioner or dispenser under
consideration shall report back to the Board of Pharmacy regarding any
findings, investigation or discipline resulting from the findings of the review
committee within thirty days of resolution of any action taken by the licensing
board resulting from the information provided by the Board of Pharmacy. The
review committee shall also review notices provided by the chief medical
examiner pursuant to subsection (h), section ten, article twelve, chapter sixty-one of this code and
determine on a case-by-case
basis whether a practitioner who prescribed or dispensed a controlled substance
resulting in or contributing to the drug overdose may have breached
professional or occupational standards or committed a criminal act when
prescribing the controlled substance at issue to the decedent. Only in those
cases in which there is reasonable cause to believe a breach of professional or
occupational standards or a criminal act may have occurred, the review
committee shall notify the appropriate professional licensing agency having
jurisdiction over the applicable practitioner or dispenser and appropriate law-enforcement agencies and
provide pertinent information from the database for their consideration. The
number of cases identified shall be determined by the review committee based on
a number that can be adequately reviewed by the review committee. The
information obtained and developed may not be shared except as provided in this
article and is not subject to the provisions of chapter twenty-nine-b of this code or obtainable
as discovering in civil matters absent a court order.
(c) The board Board of Pharmacy is responsible for
establishing and providing administrative support for the advisory committee
and the West Virginia Controlled Substances Monitoring Program Database Review
Committee. The advisory committee and the review committee shall elect a chair
by majority vote. Members of the advisory committee and the review committee
may not be compensated in their capacity as members but shall be reimbursed for
reasonable expenses incurred in the performance of their duties.
(d) The board Board of Pharmacy shall promulgate
rules with advice and consent of the advisory committee, in accordance with the
provisions of article three, chapter twenty-nine-a of this code. The legislative rules must include, but shall not
be limited to, the following matters:
(1) Identifying parameters used in identifying abnormal or unusual prescribing or dispensing patterns;
(2) Processing parameters and developing reports of abnormal or unusual prescribing or dispensing patterns for patients, practitioners and dispensers;
(3) Establishing the information to be contained in reports and the process by which the reports will be generated and disseminated; and
(4) Setting up processes and procedures to ensure that the privacy, confidentiality, and security of information collected, recorded, transmitted and maintained by the review committee is not disclosed except as provided in this section.
(e) Persons or entities with access to the West Virginia
Controlled Substances Monitoring Program database pursuant to this section may,
pursuant to rules promulgated by the board Board of Pharmacy,
delegate appropriate personnel to have access to said database.
(f) Good faith reliance by a practitioner on information contained in the West Virginia Controlled Substances Monitoring Program database in prescribing or dispensing or refusing or declining to prescribe or dispense a Schedule II, III, or IV controlled substance shall constitute an absolute defense in any civil or criminal action brought due to prescribing or dispensing or refusing or declining to prescribe or dispense.
(g) A prescribing or dispensing practitioner may notify law enforcement of a patient who, in the prescribing or dispensing practitioner’s judgment, may be in violation of section four hundred ten, article four of this chapter, based on information obtained and reviewed from the controlled substances monitoring database. A prescribing or dispensing practitioner who makes a notification pursuant to this subsection is immune from any civil, administrative or criminal liability that otherwise might be incurred or imposed because of the notification if the notification is made in good faith.
(h) Nothing in the article may be construed to require a practitioner to access the West Virginia Controlled Substances Monitoring Program database except as provided in section five-a of this article.
(i) The board Board of Pharmacy shall provide an
annual report on the West Virginia Controlled Substance Monitoring Program to
the Legislative Oversight Commission on Health and Human Resources
Accountability with recommendations for needed legislation no later than
January 1 of each year.
§60A-9-5a. Practitioner requirements to access database and conduct annual search of the database; required rulemaking.
(a)
All practitioners, as that term is defined in section one hundred one, article
two of this chapter who prescribe or dispense Schedule II, III or IV controlled
substances shall register with the West Virginia Controlled Substances
Monitoring Program and obtain and maintain online or other electronic access to
the program database: Provided, That compliance with the provisions of
this subsection must be accomplished within thirty days of the practitioner
obtaining a new license: Provided, however, That no licensing board
the Board of Pharmacy may renew a practitioner’s license without proof
that the practitioner meet the requirements of this subsection.
(b)
Upon initially prescribing or dispensing any pain-relieving controlled substance for a patient
for whom they are providing pain-relieving controlled substances as part of a course of
treatment for chronic, nonmalignant pain but who are not suffering from a
terminal illness and at
least annually thereafter should the practitioner or dispenser continue to
treat the patient with controlled substances, all persons with prescriptive or
dispensing authority and in possession of a valid Drug Enforcement
Administration registration identification number and, who are licensed by the
Board of Medicine as set forth in article three, chapter thirty of this code,
the Board of Registered Professional Nurses as set forth in article seven of
said chapter, the Board of Dental Examiners as set forth in article four of
said chapter and the Board of Osteopathic Medicine as set forth in article
fourteen of said chapter shall access the West Virginia Controlled Substances
Monitoring Program database for information regarding specific patients for
whom they are providing pain-relieving
controlled substances as part of a course of treatment for chronic,
nonmalignant pain but who are not suffering from a terminal illness. The information obtained from
accessing the West Virginia Controlled Substances Monitoring Program database
for the patient shall be documented in the patient’s medical record maintained
by a private prescriber or any inpatient facility licensed pursuant to the
provisions of chapter sixteen of this code. A pain-relieving controlled substance shall be
defined as set forth in section one, article three-a, chapter thirty of this code.
(c) The various boards mentioned in subsection (b) of this section shall promulgate both emergency and legislative rules pursuant to the provisions of article three, chapter twenty-nine-a of this code to effectuate the provisions of this section.
§60A-9-9. Drugs of concern designation.
(a) The Board of Pharmacy may designate certain drugs as drugs of concern which must be reported to the database established pursuant to this article. The designation of a drug of concern shall be reserved for drugs which have a high potential for abuse. Whenever a medical services provider dispenses a drug of concern or whenever a prescription for a drug of concern is filled by: (i) A pharmacist or pharmacy in this state; (ii) a hospital, or other health care facility, for outpatient use; or (iii) a pharmacy or pharmacist licensed by the Board of Pharmacy, but situated outside this state for delivery to a person residing in this state, the medical services provider, health care facility, pharmacist or pharmacy shall, in a manner prescribed by rules promulgated by the Board of Pharmacy under this article, report the following information, as applicable:
(1) The name, address, pharmacy prescription number and Drug Enforcement Administration controlled substance registration number of the dispensing pharmacy or the dispensing physician or dentist;
(2) The full legal name, address and birth date of the person for whom the prescription is written;
(3) The name, address and Drug Enforcement Administration controlled substances registration number of the practitioner writing the prescription;
(4) The name and national drug number of the drug of concern dispensed;
(5) The quantity and dosage of the drug of concern dispensed;
(6) The date the prescription was written and the date filled;
(7) The number of refills, if any, authorized by the prescription;
(8) If the prescription being dispensed is being picked up by someone other than the patient on behalf of the patient, the first name, last name and middle initial, address and birth date of the person picking up the prescription as set forth on the person’s government-issued photo identification card shall be retained in either print or electronic form until such time as otherwise directed by rule promulgated by the Board of Pharmacy; and
(9) The source of payment for the drug of concern dispensed.
(b) The penalties set forth in section seven of this article shall not apply to drugs listed as drugs of concern. Failure to report may be considered a violation of the practice act of the prescriber and may result in discipline by the appropriate licensing board.
(c) The Board of Pharmacy may promulgate emergency rules pursuant to the provisions of section fifteen, article three, chapter twenty-nine-a of this code to effectuate the provisions of this section.