Kansas Statutes
Article 16 - Regulation Of Pharmacists
65-1685 Same; database information privileged and confidential; persons authorized to receive data; advisory committee review of information.

65-1685. Same; database information privileged and confidential; persons authorized to receive data; advisory committee review of information. (a) The prescription monitoring program database, all information contained therein and any records maintained by the board, or by any entity contracting with the board, submitted to, maintained or stored as a part of the database, shall be privileged and confidential, shall not be subject to subpoena or discovery in civil proceedings and may only be used for investigatory or evidentiary purposes related to violations of state or federal law and regulatory activities of entities charged with administrative oversight of those persons engaged in the prescribing or dispensing of scheduled substances and drugs of concern, shall not be a public record and shall not be subject to the Kansas open records act, K.S.A. 45-215 et seq., and amendments thereto, except as provided in subsections (c) and (d).
(b) The board shall maintain procedures to ensure that the privacy and confidentiality of patients and patient information collected, recorded, transmitted and maintained is not disclosed to persons except as provided in subsections (c) and (d).
(c) The board is hereby authorized to provide data in the prescription monitoring program to the following persons:
(1) Persons authorized to prescribe or dispense scheduled substances and drugs of concern, for the purpose of providing medical or pharmaceutical care for their patients;
(2) an individual who requests the individual's own prescription monitoring information in accordance with procedures established by the board;
(3) designated representatives from the professional licensing, certification or regulatory agencies charged with administrative oversight of those persons engaged in the prescribing or dispensing of scheduled substances and drugs of concern;
(4) local, state and federal law enforcement or prosecutorial officials engaged in the administration, investigation or enforcement of the laws governing scheduled substances and drugs of concern subject to the requirements in K.S.A. 22-2502, and amendments thereto;
(5) designated representatives from the department of health and environment regarding authorized medicaid program recipients;
(6) persons authorized by a grand jury subpoena, inquisition subpoena or court order in a criminal action;
(7) personnel of the prescription monitoring program advisory committee for the purpose of operation of the program;
(8) personnel of the board for purposes of administration and enforcement of this act or the uniform controlled substances act, K.S.A. 65-4101 et seq., and amendments thereto;
(9) persons authorized to prescribe or dispense scheduled substances and drugs of concern, when an individual is obtaining prescriptions in a manner that appears to be misuse, abuse or diversion of scheduled substances or drugs of concern; and
(10) medical examiners, coroners or other persons authorized under law to investigate or determine causes of death.
(d) The prescription monitoring program advisory committee established pursuant to K.S.A. 65-1689, and amendments thereto, is authorized to review and analyze the data for purposes of identifying patterns and activity of concern.
(1) If a review of information appears to indicate a person may be obtaining prescriptions in a manner that may represent misuse or abuse of controlled substances and drugs of concern, the advisory committee is authorized to notify the prescribers and dispensers who prescribed or dispensed the prescriptions. If the review identifies patterns or other evidence sufficient to create a reasonable suspicion of criminal activity, the advisory committee is authorized to notify the appropriate law enforcement agency.
(2) If a review of information appears to indicate that a violation of state or federal law relating to prescribing controlled substances and drugs of concern may have occurred, or that a prescriber or dispenser has knowingly prescribed, dispensed or obtained controlled substances and drugs of concern in a manner that is inconsistent with recognized standards of care for the profession, the advisory committee shall determine whether a report to the professional licensing, certification or regulatory agencies charged with administrative oversight of those persons engaged in prescribing or dispensing of controlled substances and drugs of concern or to the appropriate law enforcement agency is warranted.
(A) For purposes of such determination the advisory committee may, in consultation with the appropriate regulatory agencies and professional organizations, establish criteria regarding appropriate standards and utilize volunteer peer review committees of professionals with expertise in the particular practice to create such standards and review individual cases.
(B) The peer review committee or committees appointed herein shall have authority to request and receive information in the prescription monitoring program database from the director of the prescription monitoring program.
(C) If the determination is made that a referral to a regulatory or law enforcement agency is not warranted but educational or professional advising might be appropriate, the advisory committee may refer the prescribers or dispensers to other such resources.
(e) The board is hereby authorized to provide data in the prescription monitoring program to public or private entities for statistical, research or educational purposes after removing information that could be used to identify individual practitioners, dispensers, patients or persons who received prescriptions from dispensers.
History: L. 2008, ch. 104, § 5; L. 2012, ch. 107, § 5; May 17.

Structure Kansas Statutes

Kansas Statutes

Chapter 65 - Public Health

Article 16 - Regulation Of Pharmacists

65-1625 Title of act.

65-1626 Pharmacy act; definitions.

65-1626a Practice of pharmacy defined; persons engaged as pharmacists.

65-1627 Grounds for revocation, suspension, placement in probationary status, denial, temporary suspension or temporary limitation of license for pharmacist, permit for retail dealer or registration for pharmacy, manufacturer, distributor or logistic...

65-1627a Same; jurisdiction of board; petition, who may file; stipulation, order based thereon.

65-1627b Same; direction by board to file petition or to prosecute.

65-1627c Same; form of petition, rules.

65-1627f Same; powers of board; term of suspension, probation or revocation; hearing; orders.

65-1627h Costs of proceedings.

65-1627j Subpoenas.

65-1627k Certain records of board of pharmacy confidential; exceptions.

65-1627l Conditions of probation or disciplinary action; compliance inspections and audits; payment of costs.

65-1628 Order; judicial review.

65-1628a Review bond.

65-1629 Inspection of drugs by board; samples; analyses; publication of results.

65-1630 Rules and regulations.

65-1631 Licensure required of pharmacists; qualification of applicants; application for licensure by examination; reciprocal licensure; fees; applicants from schools outside the United States.

65-1632 Renewal of license; fee; denial; conditions; continuing education; inactive status license; reinstatement after nonrenewal; penalty fee.

65-1633 Change of mailing address or email address of pharmacist.

65-1634 Responsibility for quality of drugs sold; adulteration or mislabeling unlawful.

65-1635 Dispensing and administering of drugs by duly licensed practitioners, nurses and other persons; in-person encounter not required.

65-1635a Administration of vaccine; education and reporting requirements; exceptions; delegation of authority prohibited; "pharmacist" defined.

65-1636 Sale of drugs limited to pharmacies; violations; exceptions.

65-1637 Prescription orders; requirements; compounding, filling and refilling of prescriptions; refusal to fill; brand exchange; interchangeable biological products.

65-1637a Institutional drug rooms; supervision and record-keeping; rules and regulations.

65-1637c Pharmacist required to be in charge of pharmacy; filling of certain prescriptions; refusal to fill; brand exchange. [See Revisor's Note]

65-1637d Automated prescription drug dispensing systems; pharmacist required to supervise; rules and regulations.

65-1637e Compounding of drugs and distribution of compounded drugs; rules and regulations.

65-1638 Sale of drugs and poisons by registered pharmacist.

65-1640 Act not applicable to manufacture or to certain sales of poisons.

65-1641 Display of pharmacist license; when unlawful.

65-1642 Equipment of pharmacy; records of prescription orders; medication profile record system; electronic transmission of prescription drug orders; application of federal drug supply chain security act.

65-1643 Registration or permit required; pharmacies, manufacturers, wholesale distributors, third-party logistics providers, automated dispensing systems, auctions, sales, distribution or dispensing of samples, retailers, institutional drug rooms, ve...

65-1643d Registration as manufacturer or virtual manufacturer; information required in application; criteria for grant or denial; state board of pharmacy rules and regulations; inspections; registration of manufacturer or virtual manufacturer license...

65-1644 Duplicate licenses, registrations and permits; fees.

65-1645 Applications for registrations and permits; renewals; forms; establishment of fees; establishment of retail dealer classes; display of registrations and permits; expiration dates; penalty fee for renewal after lapse; proration of fees.

65-1646 Violations of act or rules and regulations; penalty; revocation or suspension of registration or permit; notice and hearing.

65-1647 Repeated violations of act or rules and regulations may be enjoined.

65-1648 Distribution and control of prescription medications by a medical care facility pharmacy, health department, indigent health care clinic, federally qualified health center or family planning clinic; maintenance and use of emergency medication...

65-1649 Invalidity of part.

65-1650 Regulation of advertising of prescription-only drugs; exceptions and exclusions.

65-1651 Sections part of and supplemental to pharmacy act.

65-1652 Immunity from liability in civil actions for reporting, communicating and investigating certain information concerning alleged malpractice incidents and other information; conditions.

65-1653 References to registered pharmacists deemed to apply to licensed pharmacists.

65-1654 Privileged communications.

65-1655 Information required of applicant for registration as a wholesale distributor; factors in reviewing qualifications of applicants; denial of application if not in public interest; qualifications of personnel; inspection by the board; rules and...

65-1655a Information required of applicant for registration as third-party logistics provider; factors for reviewing qualifications of applicants; denial of application if not in public interest; inspection by the board; rules and regulations.

65-1655b Information required of applicant for registration as outsourcing facility; factors for reviewing qualifications of applicants; denial of application if not in public interest; inspection by the board; rules and regulations.

65-1656 Filling transferred prescriptions; exceptions and conditions; common electronic prescription files authorized; rules and regulations.

65-1657 Nonresident pharmacy registration; information required; civil fine; regulatory requirements; drug product selection rules; interstate delivery guidelines; disciplinary action; pharmacies prohibited from advertising unless registered; penalti...

65-1658 Civil fines for violations.

65-1659 Pharmacies authorized to place certain drugs with home health agencies and hospices; protocols for drug handling and storage; review and inspection; definitions.

65-1660 Dialysates, devices or drugs designated by board for treatment of persons with chronic kidney failure; inapplicability of pharmacy act; rules and regulations.

65-1662 Veterinary medical teaching hospital pharmacy; distribution and control of prescription-only drugs; pharmacist in charge.

65-1663 Registration of pharmacy technicians; applications; registration fee; qualifications for registration; restrictions on tasks performed; expiration and renewal of registration; grounds for denial of application or registration; revocation, sus...

65-1668 Utilization of unused medications act; not applicable to certain medications.

65-1669 Same; definitions.

65-1670 Same; duties of the board of pharmacy; duties of qualifying center or clinic.

65-1671 Same; criteria for accepting unused medications; dispensing.

65-1672 Same; participation; adult care homes; powers and duties of a qualifying center or clinic.

65-1673 Same; criminal and civil liability under the act.

65-1674 Same; rules and regulations; duties of the board of pharmacy.

65-1675 Same; duties of the secretary of health and environment; records.

65-1676 Registration of pharmacist interns; applications; registration fee; qualifications for registration; expiration and renewal; revocation, suspension or limitation; change of name, address or email address; responsibilities of pharmacist and ph...

65-1677 Collaborative drug therapy management advisory committee; purpose and membership.

65-1680 Epinephrine kits in schools; rules and regulations.

65-1681 Prescription monitoring program act.

65-1682 Same; definitions.

65-1683 Same; required information to be submitted by dispenser; rules and regulations; waiver; acceptance of gifts and grants.

65-1684 Same; charges and fees prohibited.

65-1685 Same; database information privileged and confidential; persons authorized to receive data; advisory committee review of information.

65-1686 Same; another agency as contractor.

65-1687 Same; maintenance of records.

65-1688 Same; act does not create civil liability or duty.

65-1689 Same; advisory committee created; members; terms.

65-1690 Same; advisory committee in cooperation with other entities.

65-1691 Same; board consultation with advisory committee; annual report.

65-1692 Same; rules and regulations.

65-1693 Same; penalties.

65-1694 Same; veterinary prescription monitoring program task force; study; members; report.

65-1694a Same; prescription monitoring program fund created.

65-1695 Continuous quality improvement program; purpose; confidential peer review documents; rules and regulations.

65-1696 State board of pharmacy; fingerprinting and criminal history.

65-16,101 Statewide electronic logging system for sale of methamphetamine precursor act; definitions.

65-16,102 Same; maintenance of program by the board of pharmacy; rules and regulations; waiver and liability.

65-16,103 Same; no cost charged to pharmacies; funding of program.

65-16,104 Same; confidential information; authorized access to data in the log.

65-16,105 Same; another agency or private vendor as contractor; maintenance and destruction of records; educational program for pharmacies; annual report.

65-16,106 Same; rules and regulations.

65-16,107 Same; penalties.

65-16,108 Same; short title.

65-16,121 Pharmacy audit integrity act.

65-16,122 Same; definitions.

65-16,123 Same; procedural requirements.

65-16,124 Same; audit reports; recoupment and repayment of funds; access to audit information.

65-16,125 Same; final report; availability.

65-16,126 Same; application of the act.

65-16,127 Emergency opioid antagonists; dispensing, storing and administering; duties of the state board of pharmacy and first responder agencies; rules and regulations.

65-16,128 Electronic transmission of prescription orders required, when; exceptions.

65-16,129 Pharmacists authorized to administer drugs, when; exceptions.

65-16,130 Telepharmacy; definitions; requirements for operation; state board of pharmacy rules and regulations.