Oklahoma 2024 Regular Session

Oklahoma House Bill HB3965 Compare Versions

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3128 STATE OF OKLAHOMA
3229
3330 2nd Session of the 59th Legislature (2024)
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3532 COMMITTEE SUBSTITUTE
3633 FOR
37-HOUSE BILL NO. 3965 By: McEntire and Echols of the
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42- Stanley of the Senate
34+HOUSE BILL NO. 3965 By: McEntire
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4740 COMMITTEE SUBSTITUTE
4841
4942 An Act relating to physician assistants ; amending 59
5043 O.S. 2021, Section 353.1a, which relates to the
5144 Oklahoma Pharmacy Act; clarifying which prescriptions
5245 for controlled dangerous substances pharmacists may
5346 dispense; amending 59 O.S. 2021, Sections 519.2,
5447 519.3, 519.6, 519.11, as amended by Section 1,
5548 Chapter 164, O.S.L. 2022 , and 521.2 (59 O.S. Supp.
5649 2023, Section 519.11) , which relate to the Physician
5750 Assistant Act; modifying definitions; increasing the
5851 number of Physician Assistant Committee members;
5952 clarifying certain requirements for the chair;
6053 increasing member requirements for a quorum; adding
6154 provisions regarding postgraduate clinical practice ;
6255 clarifying filing requirements for practice
6356 agreements; clarifying language regarding practicing
6457 medicine, prescribing drugs, and using medical
6558 supplies under a practice agreement ; modifying
6659 billing and payment authority; amending 63 O.S. 2021,
6760 Section 1-317, as amended by Section 1, Chapter 184,
6861 O.S.L. 2022 (63 O.S. Supp. 2023, Section 1 -317),
6962 which relates to the Oklahoma Public Health Code ;
7063 clarifying the authority of physician assistant s to
7164 carry out certain functions; amending 63 O.S. 2021,
7265 Sections 2-101, as last amended by Section 1, Chapter
7366 375, O.S.L. 2023, and 2-312, as amended by S ection 2,
7467 Chapter 184, O.S.L. 2 022 (63 O.S. Supp. 2023,
7568 Sections 2-101 and 2-312), which relate to the
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10369 Uniform Controlled Dangerous Substances Act ;
10470 modifying definitions related to physician
10571 assistants; clarifying which physician assistants may
10672 prescribe and administer certain controlled
10773 substances; repealing 59 O.S. 2021, Section 521. 4,
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108100 which relates to physician supervision and practice
109101 agreements; and declaring an emergency.
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115106 BE IT ENACTED BY THE PEOPLE OF THE STATE OF OKLAHOMA:
116107 SECTION 1. AMENDATORY 59 O.S. 2021, Section 353.1a, is
117108 amended to read as follows:
118109 Section 353.1a A. Prescribing authority shall be allowed,
119110 under the medical direction of a supervising physician, for an
120111 advanced practice nurse recognized by t he Oklahoma Board of Nursing
121112 in one of the following categories: advanced registered nurse
122113 practitioners, clinical nurse specialists, or certified nurse -
123114 midwives. The advanced practice nurse may write or sign, or
124115 transmit by word of mouth, telephone or o ther means of communication
125116 an order for drugs or medical supplies that is intended to be
126117 filled, compounded, or dispensed by a pharmacist. The supervising
127118 physician and the advanced practice nurse shall be identified at the
128119 time of origination of the pre scription and the name of the advanced
129120 practice nurse shall be printed on the prescription label.
130121 B. Pharmacists may dispense prescriptions for non -controlled
131122 prescription drugs authorized by an advanced practice nurse or
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159123 physician assistant, not located in Oklahoma, provided that they are
160124 licensed in the state in which they are actively prescr ibing.
161125 C. Pharmacists may only dispense prescriptions for controlled
162126 dangerous substances prescribed by an:
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163153 1. An advanced practice nurse or physician assistant licensed
164154 in the State of Oklahoma and supervi sed by an Oklahoma-licensed
165155 practitioner; or
166156 2. Physician assistant licensed in the State of Oklahoma and
167157 supervised by an Oklahoma-licensed practitioner .
168158 SECTION 2. AMENDATORY 59 O.S. 2 021, Section 519.2, is
169159 amended to read as follows:
170160 Section 519.2 As used in the Physicia n Assistant Act:
171161 1. "Board" means the State Board of Medical Li censure and
172162 Supervision;
173163 2. "Committee" means the Physician Assistant Committee;
174164 3. "Practice of medicine" means services which require train ing
175165 in the diagnosis, treatment and prevention of disease, including the
176166 use and administration of drugs, and whi ch are performed by
177167 physician assistants so long as such services are within the
178168 physician assistants ' skill,. For a physician assistant required to
179169 practice under supervision of a delegating physician, services form
180170 a component of the physician's scope of practice, and are provided
181171 with physician supervision, including authenticating by signature
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209172 any form that may be authenticated by the delegating physician 's
210173 signature with prior delegation by the physic ian;
211174 4. "Patient care setting" means and includes, but is not
212175 limited to, a physic ian's office, clinic, hospital, nursing home,
213176 extended care facility, p atient's home, ambulatory surgical center,
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214203 hospice facility or any other setting authorized by the del egating
215204 physician;
216205 5. "Physician assistant" means a health care professional,
217206 qualified by academic and clinical education and licensed by the
218207 State Board of Medical Licensure and Supervision, to practice
219208 medicine with physician supervision as a physician assistant;
220209 6. 5. "Delegating physician" means an individual holding a
221210 license in good standing as a physician from the State Board of
222211 Medical Licensure and Supervision or the State Board of Osteopathic
223212 Examiners, who supervises one or more physician assistants and
224213 delegates decision making pursuant to the practice agreement;
225214 7. 6. "Supervision" means overseeing or delegating the
226215 activities of the medical services rendered by a physician assistant
227216 through a practice agreement between a medical doctor or osteopathic
228217 delegating physician performing procedures or directly or indirectly
229218 involved with the treatment of a patient , and the physician
230219 assistant working jointly toward a common goal of providing
231220 services. Delegation shall be defined by the pra ctice agreement.
232221 The physical presence of the delegating physician is not required as
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260222 long as the delegating physician and physician assistant are or can
261223 be easily in contact with each other by telecommunication. At all
262224 times a physician assistant required to practice under supervision
263225 shall be considered an agent of the delegating phys ician;
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264252 8. 7. "Telecommunication" means the use of electroni c
265253 technologies to transmit words, sounds or images for interpersonal
266254 communication, clinical care (telemedicine) and review of electronic
267255 health records; and
268256 9. 8. "Practice agreement" means a written agreement between a
269257 physician assistant and the a delegating physician concerning the
270258 scope of practice of the physician assistant to only be determined
271259 by the delegating physician and the physician assistant based on the
272260 education, training, skills and experience of the physician
273261 assistant. The agreement shall i nvolve the joint formulation,
274262 discussion and agreement on the methods of supervision and
275263 collaboration for diagnosis, consultation and treatment of medical
276264 conditions and shall include the scope of and any limitations on
277265 prescribing. A practice agreement is require d for a physician
278266 assistant described in subsection C of Section 4 of this act.
279267 SECTION 3. AMENDATORY 59 O.S. 2021, Section 519.3, is
280268 amended to read as follows:
281269 Section 519.3 A. There is hereby created the Physician
282270 Assistant Committee, which shall be composed of seven (7) nine (9)
283271 members. Three Five members of the Commi ttee shall be physician
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311272 assistants appointed by the State Board of Medical Licensure and
312273 Supervision from a list of qualified individuals submitted by the
313274 Oklahoma Academy of Physician Assistant s. One member shall be a
314275 physician appointed by the Board fro m its membership. One member
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315302 shall be a physician appointed by the Board from a list of qualified
316303 individuals submitted by the Oklahoma State Medical Associatio n and
317304 who is not a member of the Board. One member shall be a physician
318305 appointed by the State Board of Osteopathic Examiners from its
319306 membership. One member shall be a physician appointed by the State
320307 Board of Osteopathic Examiners from a list of qualif ied individuals
321308 submitted by the Oklahoma Osteopathic Association and who is not a
322309 member of said board.
323310 B. The term of office for each member of the Committee shall be
324311 five (5) years.
325312 C. The Committee shall meet at least quarterly. At the initial
326313 meeting of each calendar year, the Committee members shall elect a
327314 chair from the physician assist ant members. The chair or his or her
328315 designee shall represent the Committee at all meeting s of the Board.
329316 Four Five members shall constitute a quorum for the pur pose of
330317 conducting official b usiness of the Committee.
331318 D. The State Board of Medical Licensu re and Supervision is
332319 hereby granted the power and authority to promulgate rules, which
333320 are in accordance with the provisions of Section 519.1 et seq. of
334321 this title, governing the requirements for licensure as a physician
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362322 assistant, as well as to establish standards for training, approve
363323 institutions for training, and regulate the standards of practi ce of
364324 a physician assistant after licensure, including the power of
365325 revocation of a license.
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366352 E. The State Board of Medical Licensure and Supervision is
367353 hereby granted the power and authority to investigate all
368354 complaints, hold hearings, subpoena witnesses and initiate
369355 prosecution concerning violations of Section 519.1 et seq. of this
370356 title. When such complaints involve physicians licensed by the
371357 State Board of Osteopathic Examiners, the State Board of Osteopathic
372358 Examiners shall be officially notified of such complaints.
373359 F. 1. The Committee shall advise the Board on al l matters
374360 pertaining to the practice of physician assistants.
375361 2. The Committee shall review and make recommendations to the
376362 Board on all applications for licensure as a physician assistant and
377363 all applications to practice which shall be approved by the Bo ard.
378364 When considering applic ants for licensure, to establish standards of
379365 training or approve institutions for training, the Committee shall
380366 include the Director, or designee, of all Physi cian Assistant
381367 educational programs conducted by institutions of hi gher education
382368 in the state as members.
383369 3. The Committee shall assist and advise the Board i n all
384370 hearings involving physician assistants who are deemed to be in
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412371 violation of Section 519.1 et seq. of this title or the rules of the
413372 Board.
414373 SECTION 4. AMENDATORY 59 O.S. 2021, Section 519.6, is
415374 amended to read as follows:
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416401 Section 519.6 A. No health care services may be performed by a
417402 physician assistant unless a current license is on file with and
418403 approved by the State Board of Medical Licensure and Supervision.
419404 B. A physician assistant with six thousand two hundred forty
420405 (6,240) or more hours of postgraduate clinical practice experience
421406 who has reported those hours to the Board shall not be requi red to
422407 practice under the supervision of a delegating physician.
423408 1. A physician assistant may report the completion of
424409 postgraduate clinical practice experience to the Board at any time
425410 after completion of at least six thousand two hundred forty (6,240)
426411 such hours.
427412 2. Hours earned prior to the enactment of this subsection shall
428413 be counted towards the six thousand two hundred forty (6,240) hours.
429414 3. The Board shall maintain, make available, and keep updated,
430415 on the Internet website of the Board , a list of physician assistants
431416 who have reported completion of six thousand two hundre d forty
432417 (6,240) or more postgraduate clinical pract ice experience hours.
433418 4. The Board shall, within ninety (90) days of enactment,
434419 prescribe a form for reporting post graduate clinical practice
435420 experience by a physician assistant. The Board shall make available
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463421 and keep updated on the Internet website of the Board the prescribed
464422 form. This reporting form may be filed electronically. The Board
465423 shall not charge a fee for reporting hours or filing of the
466424 prescribed form.
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467451 5. Nothing in this subsection shall prohibit a physician
468452 assistant from maintaining a practice agreement; however, such an
469453 agreement is not required for a physician assistant w ith the
470454 reported six thousand two hundred forty (6,240) hours of
471455 postgraduate clinical practice experience. Provided any practice
472456 agreements are subject to the req uirements of paragraphs 1, 2, 3,
473457 and 4 of subsection C of this section.
474458 6. Nothing in this subsection shall restrict the ability of the
475459 Board to require supervision as a part of disciplinary action
476460 against the license of a physician assistant .
477461 C. A physician assistant with less than six thousand two
478462 hundred forty (6,240) hours of postgraduate clinical practice
479463 experience or who has completed six thousand two hundred forty
480464 (6,240) hours but has not reported those hours t o the Board shall
481465 practice under the supervision of a delegating physician with the
482466 following requirements:
483467 1. All practice agreements and any amendments shall be filed
484468 with the State Board of Medical Licensure and Supervision within ten
485469 (10) business days of being executed. Practice agre ements may be
486470 filed electronically. The State Board of Medical Licensure and
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514471 Supervision shall not charge a fee for filing practice agreements or
515472 amendments of practice agreements.;
516473 B. 2. A physician assistant may have p ractice agreements with
517474 multiple allopathic or osteopathic physicians. Each physician shall
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518501 be in good standing with the State Board of Medical Licensure and
519502 Supervision or the State Boar d of Osteopathic Examiners.;
520503 C. 3. The delegating physician need not be physically present
521504 nor be specifically consulted before each delegated patient care
522505 service is performed by a physician assistant, so long as the
523506 delegating physician and physician assi stant are or can be easily in
524507 contact with one another by means of t elecommunication. In all
525508 patient care settings, the The delegating physician shall provide
526509 appropriate methods of participating in health care services
527510 provided by the physician assistant including:
528511 a. being responsible for the formulation or approval of
529512 all orders and protocols, whethe r standing orders,
530513 direct orders or any other orders or protocols, which
531514 direct the delivery of health care services provided
532515 by a physician assistant, and periodically reviewing
533516 such orders and protocols,
534517 b. regularly reviewing the health care services pr ovided
535518 by the physician assistant and any problems or
536519 complications encountered,
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564520 c. being available physically or through telemedicine or
565521 direct telecommunications for consultation, assistance
566522 with medical emergencies or pat ient referral,
567523 d. reviewing a sample of outpatient medical records.
568524 Such reviews shall take place at a site agreed upon
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569551 between the delegating physician and physician
570552 assistant in the pra ctice agreement which may also
571553 occur using electronic or virtual con ferencing, and
572554 e. that it remains clear that the physician assistant is
573555 an agent of the delegating physician; but, in no event
574556 shall the delegating physician be an employee of the
575557 physician assistant.;
576558 D. 4. In patients with newly diagnosed complex illnesses , the
577559 physician assistant shal l contact the delegating physician within
578560 forty-eight (48) hours of the physician assistant's initial
579561 examination or treatment and schedule the patient for ap propriate
580562 evaluation by the delegating physician as directed by the physician.
581563 The delegating physician shall determine which conditions qualify as
582564 complex illnesses based on the clinical setting and the skill and
583565 experience of the physician assistant .
584566 E. 1. D. A physician assistant under the direction of a
585567 delegating physician not practicing under a practice agreement may
586568 prescribe written and oral prescriptions and orders. The p hysician
587569 assistant not practicing under a practice agreement may prescribe
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615570 medical supplies, services, and drugs, including controlled
616571 medications in Schedules II III through V pursuant to Section 2-312
617572 of Title 63 of the Oklahoma Statutes, and medical supplies and
618573 services as delegated by the delegat ing physician and as approved by
619574 the State Board of Medical Licensure and Supervision after
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620601 consultation with the Sta te Board of Pharmacy on the Physician
621602 Assistant Drug Formulary . Physician assistants not practicing under
622603 a practice agreement may not dispense drugs, but may request,
623604 receive, and sign for professional samples and may distribute
624605 professional samples to patients .
625606 2. A physician assistant may write an order for a Schedule II
626607 drug for immediate or ongo ing administration on site. Prescriptions
627608 and orders for Schedule II drugs written by a physician assistant
628609 must be included on a written protocol determined by the delegating
629610 physician and approved by the medical staff committee of the
630611 facility or by direct verbal order of the delegating physician .
631612 Physician assistants may not dispense drugs, but may request,
632613 receive, and sign for professi onal samples and may distribute
633614 professional samples to patients.
634615 F. E. A physician assistant may perform health care s ervices in
635616 patient care settings as authorized by the delega ting physician
636617 practicing under a practice agreement m ay prescribe written and oral
637618 prescriptions and orders. The physician assistant practicing under
638619 a practice agreement may prescribe medical supplies, services, and
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666620 drugs, including controlled medications in Schedule s II through V
667621 pursuant to Section 2 -312 of Title 63 of the Oklahoma Statutes,
668622 written and oral prescriptions and orders only as delegated by the
669623 delegating physician and prescriptions and orders for Schedule II
670624 drugs written by such physician assistant sh all be included on a
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671651 written protocol det ermined by the delegating physician. Physician
672652 assistants practicing under a practice agreement may not dispense
673653 drugs, but may request, receive, and sign for professional samples
674654 and may distribute professional sa mples to patients. Provided that
675655 a physician assistant practicing under a practice agree ment may not
676656 prescribe any controlled medications in a Schedule that the
677657 delegating physician is not registered to prescribe .
678658 G. F. Each physician assistant licensed under the Physician
679659 Assistant Act shall keep his or her lice nse available for inspection
680660 at the primary place of business and shall, when enga ged in
681661 professional activitie s, identify himself or herself as a physician
682662 assistant.
683663 H. G. A physician assistant shall be bound by the provisions
684664 contained in Sections 725.1 through 725.5 of Title 59 of the
685665 Oklahoma Statutes this title.
686666 SECTION 5. AMENDATORY 59 O.S. 2 021, Section 519.11, as
687667 amended by Section 1, Chapter 164, O.S.L. 2022 (59 O.S. Supp. 2023,
688668 Section 519.11), is amended to read as follows:
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716669 Section 519.11 A. Nothing in the Physician Assistant Act shall
717670 be construed to prevent or restrict the practice, services or
718671 activities of any person s of other licensed professions or personnel
719672 supervised by licensed professions in th is state from perform ing
720673 work incidental to the practi ce of their profession or occupation,
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721700 if that person does not represent himself or herself as a physician
722701 assistant.
723702 B. Nothing stated in the Physician Assistant Act shall prevent
724703 any hospital from requiring the physician assistant o r the
725704 delegating physician to meet and maintain certain staff appointment
726705 and credentialing qualificatio ns for the privilege of practicing as,
727706 or utilizing, a physician assistant in the hospital.
728707 C. Nothing in the Physician Assistant Act shall be construe d to
729708 permit a physician assistant to practice medicine or prescribe drugs
730709 and medical supplies in this s tate except when suc h actions are
731710 performed under the supervision and at the direction of a physician
732711 or physicians approved by the State Board of Medic al Licensure and
733712 Supervision.
734713 D. Nothing herein shall be construed to require licensure under
735714 the Physician Assistant Act o f a physician assistant student
736715 enrolled in a physician assistant educational program accredited by
737716 the Accreditation Review Commiss ion on Education for t he Physician
738717 Assistant.
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766718 E. D. Notwithstanding any other provision of law, no one who is
767719 not a physician licensed to practice medicine in this state may
768720 perform acts restricted to such physicians pursuant to the
769721 provisions of Section 1-731 of Title 63 of t he Oklahoma Statutes.
770722 This paragraph is inseverable.
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771749 F. E. Nothing in the Physic ian Assistant Act sh all limit the
772750 activities of a physician assistant in the performance of their
773751 duties if the physician assistant is employed by or under contract
774752 with the United States Department of Veterans Affairs or if the
775753 physician assistant is employed by, under contract with, or
776754 commissioned by one of the uniformed services; provided, the
777755 physician assistant must be currently licensed in this state or any
778756 other state or currently credentialed as a physician assistant by
779757 the United States Department of Veterans Affairs or the applicable
780758 uniformed service. Any physician assistant who is employed by or
781759 under contract with the United States Department of Veterans Affairs
782760 or is employed by, under contract with, or commissioned by one of
783761 the uniformed services and practices outside of such employment,
784762 contract, or commission shall be subject to the Physician Assistant
785763 Act while practicing outside of such employment, contract, or
786764 commission. As used in this subsection, "uniformed services" shall
787765 have the same meaning as prov ided by Title 10 of the U.S . Code.
788766 SECTION 6. AMENDATORY 59 O.S. 2021, Section 521.2, is
789767 amended to read as follows:
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817768 Section 521.2 A. Payment for services within the physician
818769 assistant's scope of practice by a health insurance plan shall be
819770 made when ordered or performed by the ph ysician assistant, if the
820771 same service would have been covered if orde red or performed by a
821772 physician. An in-network A physician assistant shall be authorized
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822799 to bill for and receive direct payment for the medically necessary
823800 services the physician assist ant delivers.
824801 B. To ensure accountability and transparency for patients ,
825802 payers and the health care system, an in-network a physician
826803 assistant shall be identified a s the rendering professional in the
827804 billing and claims process when the physician assistan t delivers
828805 medical or surgical services to patients.
829806 C. No insurance comp any or third-party payer shall impose a
830807 practice, education, or collaboration requirement th at is
831808 inconsistent with or more rest rictive than existing phys ician
832809 assistant state laws o r regulations.
833810 SECTION 7. AMENDATORY 63 O.S. 2021, Section 1 -317, as
834811 amended by Section 1, Chapter 184, O.S.L. 2022 (63 O.S. Supp. 2023,
835812 Section 1-317), is amended to read as follows:
836813 Section 1-317. A. A death certificate for each death which
837814 occurs in this state sha ll be filed with the State Department of
838815 Health, within three (3) days after such death.
839816 B. The funeral director shall personally si gn the death
840817 certificate and shall be responsible for filing the death
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868818 certificate. If the funeral director is not availab le, the person
869819 acting as such who first assumes custody of a dead body in
870820 accordance with Section 1158 of Title 21 of the Oklahoma St atutes
871821 shall personally sign a nd file the death certificate. The personal
872822 data shall be obtained from the next of kin or t he best qualified
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873849 person or source available. The certificat e shall be completed as
874850 to personal data and delivered to the attending physician or the
875851 medical examiner responsible for completing the medical
876852 certification portion of the certificate of death within twenty-four
877853 (24) hours after the death. No later than July 1, 2012, the
878854 personal data, and no later than July 1, 2017, the me dical
879855 certificate portion, sha ll be entered into the prescribed electronic
880856 system provided by the State Registrar of Vital Statistics and the
881857 information submitted to the State Registr ar of Vital Statistics.
882858 The resultant certificate produced by the elect ronic system shall be
883859 provided to the physician or medical examiner for medical
884860 certification within twenty-four (24) hours after the death.
885861 C. The medical certification shall be comp leted and signed
886862 within forty-eight (48) hours after death by the physic ian,
887863 physician assistant, or advanced practice registered nurse in charge
888864 of the patient's care for the illness or conditio n which resulted in
889865 death, except when inquiry as to the ca use of death is required by
890866 Section 938 of this title. No later than July 1, 2017, the medical
891867 certification portion of certificate data shall be entered into the
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919868 prescribed electronic system prov ided by the State Reg istrar of
920869 Vital Statistics and the infor mation submitted to the State
921870 Registrar of Vital Statistics.
922871 D. In the event that the physician, physician assistant, or
923872 advanced practice registered nurse in charge of the patient's care
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924899 for the illness or conditio n which resulted in death is not in
925900 attendance at the time of death, the medical certification shall be
926901 completed and signed within forty-eight (48) hours after death by
927902 the physician, physician assistant, or advanced practice register ed
928903 nurse in attendance at the time of death, except:
929904 1. When the patient is under hospice care at the time of death,
930905 the medical certification may be signed by the hospice's medical
931906 director; and
932907 2. When inquiry as to the cause of death is required by Se ction
933908 938 of this title.
934909 Provided, that such certification, i f signed by other than the
935910 attending physician, physician assistant, or advanced practice
936911 registered nurse, shall note on the face the name of the attending
937912 physician, physician assistant, or advanced practice registered
938913 nurse and that the information show n is only as reported.
939914 E. A certifier completing cause of death on a ce rtificate of
940915 death who knows that a lethal drug, overdose or other means of
941916 assisting suicide within the meaning of Section s 3141.2 through
942917 3141.4 of this title caused or contributed t o the death shall list
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970918 that means among the chain of events under cause of death or list it
971919 in the box that describes how the injury occurred. If such means is
972920 in the chain of events under cause of death or in the b ox that
973921 describes how the injury occurre d, the certifier shall indicate
974922 "suicide" as the manner of death.
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975949 F. The authority of a physician assistant subject to subsection
976950 C of Section 4 of this act to carry out the functions described in
977951 this section shall be governed by the practice agreement as provided
978952 by Section 519.6 of Title 59 of the Oklahoma Statutes.
979953 SECTION 8. AMENDATORY 63 O.S. 2021, Sect ion 2-101, as
980954 last amended by Section 1, Chapter 375, O.S .L. 2023 (63 O.S. Supp.
981955 2023, Section 2-101), is amended to read as follows:
982956 Section 2-101. As used in the Uniform Controlled Dangerous
983957 Substances Act:
984958 1. "Administer" means the direct application of a controlled
985959 dangerous substance, whether by injection, inhalation, ingestion or
986960 any other means, to the body of a patient, animal or research
987961 subject by:
988962 a. a practitioner (or, in the presence of the
989963 practitioner, by the authorized agent of the
990964 practitioner), or
991965 b. the patient or research subject at the direction and
992966 in the presence of the practitioner;
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1020967 2. "Agent" means a peace officer appointed by and who acts on
1021968 behalf of the Director of the Oklahoma State Bureau of Narcotics and
1022969 Dangerous Drugs Control or an authorized person who acts on behalf
1023970 of or at the direction of a person who manufactures, distributes,
1024971 dispenses, prescribes, administers or uses for scientific purposes
1025972 controlled dangerous substances but does not include a common or
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1026999 contract carrier, public warehouser or employee thereof, or a person
10271000 required to register under the Uniform Controlled Dangerous
10281001 Substances Act;
10291002 3. "Board" means the Advisory Board to the Director of the
10301003 Oklahoma State Bureau of Narcotics and Dangerous Drugs Control;
10311004 4. "Bureau" means the Oklahoma State Bureau of Narcotics and
10321005 Dangerous Drugs Control;
10331006 5. "Coca leaves" includes cocaine and any compound,
10341007 manufacture, salt, derivative, mixture or preparation of coca
10351008 leaves, except derivatives of coca leaves which do not contain
10361009 cocaine or ecgonine;
10371010 6. "Commissioner" or "Director" means the Director of the
10381011 Oklahoma State Bureau of Narcotics and Dangerous Drugs Control;
10391012 7. "Control" means to add, remove or change the placement of a
10401013 drug, substance or immediate precursor under the Uniform Controlled
10411014 Dangerous Substances Act;
10421015 8. "Controlled dangerous substance" means a drug, substance or
10431016 immediate precursor in Schedules I through V of the Uniform
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10711017 Controlled Dangerous Substances Act or any drug, substance or
10721018 immediate precursor listed either temporarily or permanently as a
10731019 federally controlled substance. Any conflict between state and
10741020 federal law with regard to the particular schedule in which a
10751021 substance is listed shall be resolved in favor of state law;
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10761048 9. "Counterfeit substance" means a controlled substance which,
10771049 or the container or labeling of which without authorization, bears
10781050 the trademark, trade name or other identifying marks, imprint,
10791051 number or device or any likeness thereof of a manufacturer,
10801052 distributor or dispenser other than the person who in fact
10811053 manufactured, distributed or dispensed the substance;
10821054 10. "Deliver" or "delivery" means the actual, constructive or
10831055 attempted transfer from one person to another of a controlled
10841056 dangerous substance or drug paraphernalia, whether or not there is
10851057 an agency relationship;
10861058 11. "Dispense" means to deliver a controlled dangerous
10871059 substance to an ultimate user or human research subject by or
10881060 pursuant to the lawful order of a practitioner, including the
10891061 prescribing, administering, packaging, labeling or compounding
10901062 necessary to prepare the substance for such distribution.
10911063 "Dispenser" is a practitioner who delivers a controlled dangerous
10921064 substance to an ultimate user or human research subject;
10931065 12. "Distribute" means to deliver other than by administering
10941066 or dispensing a controlled dangerous substance;
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11221067 13. "Distributor" means a commercial entity engaged in the
11231068 distribution or reverse distribution of narcotics and dangerous
11241069 drugs and who complies with all regulations promulgated by the
11251070 federal Drug Enforcement Administration and the Oklahoma State
11261071 Bureau of Narcotics and Dangerous Drugs Control;
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11271098 14. "Drug" means articles:
11281099 a. recognized in the official United States Pharmacopeia,
11291100 official Homeopathic Pharmacopoeia of the United
11301101 States, or official National Formulary, or any
11311102 supplement to any of them,
11321103 b. intended for use in the diagnosis, cure, mitigation,
11331104 treatment or prevention of disease in man or other
11341105 animals,
11351106 c. other than food, intended to affect the structure or
11361107 any function of the body of man or other animals, and
11371108 d. intended for use as a component of any article
11381109 specified in this paragraph;
11391110 provided, however, the term drug does not include devices or their
11401111 components, parts or accessories;
11411112 15. "Drug-dependent person" means a person who is using a
11421113 controlled dangerous substance and who is in a state of psychic or
11431114 physical dependence, or both, arising from administration of that
11441115 controlled dangerous substance on a continuous basis. Drug
11451116 dependence is characterized by behavioral and other responses which
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11731117 include a strong compulsion to take the substance on a continuous
11741118 basis in order to experience its psychic effects, or to avoid the
11751119 discomfort of its absence;
11761120 16. "Home care agency" means any sole proprietorship,
11771121 partnership, association, corporation, or other organization which
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11781148 administers, offers, or provides home care services, for a fee or
11791149 pursuant to a contract for such services, to clients in their place
11801150 of residence;
11811151 17. "Home care services" means skilled or personal care
11821152 services provided to clients in their place of residence for a fee;
11831153 18. "Hospice" means a centrally administered, nonprofit or for-
11841154 profit, medically directed, nurse-coordinated program which provides
11851155 a continuum of home and inpatient care for the terminally ill
11861156 patient and the patient's family. Such term shall also include a
11871157 centrally administered, nonprofit or for-profit, medically directed,
11881158 nurse-coordinated program if such program is licensed pursuant to
11891159 the provisions of the Uniform Controlled Dangerous Substances Act.
11901160 A hospice program offers palliative and supportive care to meet the
11911161 special needs arising out of the physical, emotional and spiritual
11921162 stresses which are experienced during the final stages of illness
11931163 and during dying and bereavement. This care is available twenty-
11941164 four (24) hours a day, seven (7) days a week, and is provided on the
11951165 basis of need, regardless of ability to pay. "Class A" Hospice
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12231166 refers to Medicare-certified hospices. "Class B" refers to all
12241167 other providers of hospice services;
12251168 19. "Imitation controlled substance" means a substance that is
12261169 not a controlled dangerous substance, which by dosage unit
12271170 appearance, color, shape, size, markings or by representations made,
12281171 would lead a reasonable person to believe that the substance is a
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12291198 controlled dangerous substance. In the event the appearance of the
12301199 dosage unit is not reasonably sufficient to establish that the
12311200 substance is an imitation controlled substance, the court or
12321201 authority concerned should consider, in addition to all other
12331202 factors, the following factors as related to "representations made"
12341203 in determining whether the substance is an imitation controlled
12351204 substance:
12361205 a. statements made by an owner or by any other person in
12371206 control of the substance concerning the nature of the
12381207 substance, or its use or effect,
12391208 b. statements made to the recipient that the substance
12401209 may be resold for inordinate profit,
12411210 c. whether the substance is packaged in a manner normally
12421211 used for illicit controlled substances,
12431212 d. evasive tactics or actions utilized by the owner or
12441213 person in control of the substance to avoid detection
12451214 by law enforcement authorities,
1246-
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12731215 e. prior convictions, if any, of an owner, or any other
12741216 person in control of the object, under state or
12751217 federal law related to controlled substances or fraud,
12761218 and
12771219 f. the proximity of the substances to controlled
12781220 dangerous substances;
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12791247 20. "Immediate precursor" means a substance which the Director
12801248 has found to be and by regulation designates as being the principal
12811249 compound commonly used or produced primarily for use, and which is
12821250 an immediate chemical intermediary used, or likely to be used, in
12831251 the manufacture of a controlled dangerous substance, the control of
12841252 which is necessary to prevent, curtail or limit such manufacture;
12851253 21. "Laboratory" means a laboratory approved by the Director as
12861254 proper to be entrusted with the custody of controlled dangerous
12871255 substances and the use of controlled dangerous substances for
12881256 scientific and medical purposes and for purposes of instruction;
12891257 22. "Manufacture" means the production, preparation,
12901258 propagation, compounding or processing of a controlled dangerous
12911259 substance, either directly or indirectly by extraction from
12921260 substances of natural or synthetic origin, or independently by means
12931261 of chemical synthesis or by a combination of extraction and chemical
12941262 synthesis. "Manufacturer" includes any person who packages,
12951263 repackages or labels any container of any controlled dangerous
1296-
1297-HB3965 HFLR Page 26
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1322-
13231264 substance, except practitioners who dispense or compound
13241265 prescription orders for delivery to the ultimate consumer;
13251266 23. "Marijuana" means all parts of the plant Cannabis sativa
13261267 L., whether growing or not; the seeds thereof; the resin extracted
13271268 from any part of such plant; and every compound, manufacture, salt,
13281269 derivative, mixture or preparation of such plant, its seeds or
13291270 resin, but shall not include:
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13301297 a. the mature stalks of such plant or fiber produced from
13311298 such stalks,
13321299 b. oil or cake made from the seeds of such plant,
13331300 including cannabidiol derived from the seeds of the
13341301 marijuana plant,
13351302 c. any other compound, manufacture, salt, derivative,
13361303 mixture or preparation of such mature stalks (except
13371304 the resin extracted therefrom), including cannabidiol
13381305 derived from mature stalks, fiber, oil or cake,
13391306 d. the sterilized seed of such plant which is incapable
13401307 of germination,
13411308 e. for any person participating in a clinical trial to
13421309 administer cannabidiol for the treatment of severe
13431310 forms of epilepsy pursuant to Section 2-802 of this
13441311 title, a drug or substance approved by the federal
13451312 Food and Drug Administration for use by those
13461313 participants,
1347-
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13741314 f. for any person or the parents, legal guardians or
13751315 caretakers of the person who have received a written
13761316 certification from a physician licensed in this state
13771317 that the person has been diagnosed by a physician as
13781318 having Lennox-Gastaut syndrome, Dravet syndrome, also
13791319 known as severe myoclonic epilepsy of infancy, or any
13801320 other severe form of epilepsy that is not adequately
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13811347 treated by traditional medical therapies, spasticity
13821348 due to multiple sclerosis or due to paraplegia,
13831349 intractable nausea and vomiting, appetite stimulation
13841350 with chronic wasting diseases, the substance
13851351 cannabidiol, a nonpsychoactive cannabinoid, found in
13861352 the plant Cannabis sativa L. or any other preparation
13871353 thereof, that has a tetrahydrocannabinol concentration
13881354 not more than three-tenths of one percent (0.3%) and
13891355 that is delivered to the patient in the form of a
13901356 liquid,
13911357 g. any federal Food-and-Drug-Administration-approved drug
13921358 or substance, or
13931359 h. industrial hemp, from the plant Cannabis sativa L. and
13941360 any part of such plant, whether growing or not, with a
13951361 delta-9 tetrahydrocannabinol concentration not more
13961362 than three-tenths of one percent (0.3%) on a dry-
13971363 weight basis which shall only be grown pursuant to the
1398-
1399-HB3965 HFLR Page 28
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1424-
14251364 Oklahoma Industrial Hemp Program and may be shipped
14261365 intrastate and interstate;
14271366 24. "Medical purpose" means an intention to utilize a
14281367 controlled dangerous substance for physical or mental treatment, for
14291368 diagnosis, or for the prevention of a disease condition not in
14301369 violation of any state or federal law and not for the purpose of
14311370 satisfying physiological or psychological dependence or other abuse;
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14321397 25. "Mid-level practitioner" means an Advanced Practice
14331398 Registered Nurse as defined and within parameters specified in
14341399 Section 567.3a of Title 59 of the Oklahoma Statutes, or a certified
14351400 animal euthanasia technician as defined in Section 698.2 of Title 59
14361401 of the Oklahoma Statutes, or an animal control officer registered by
14371402 the Oklahoma State Bureau of Narcotics and Dangerous Drugs Control
14381403 under subsection B of Section 2-301 of this title within the
14391404 parameters of such officer's duties under Sections 501 through 508
14401405 of Title 4 of the Oklahoma Statutes;
14411406 26. "Narcotic drug" means any of the following, whether
14421407 produced directly or indirectly by extraction from substances of
14431408 vegetable origin, or independently by means of chemical synthesis,
14441409 or by a combination of extraction and chemical synthesis:
14451410 a. opium, coca leaves and opiates,
14461411 b. a compound, manufacture, salt, derivative or
14471412 preparation of opium, coca leaves or opiates,
1448-
1449-HB3965 HFLR Page 29
1450-BOLD FACE denotes Committee Amendments. 1
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14751413 c. cocaine, its salts, optical and geometric isomers, and
14761414 salts of isomers,
14771415 d. ecgonine, its derivatives, their salts, isomers and
14781416 salts of isomers, and
14791417 e. a substance, and any compound, manufacture, salt,
14801418 derivative or preparation thereof, which is chemically
14811419 identical with any of the substances referred to in
14821420 subparagraphs a through d of this paragraph, except
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14831447 that the words narcotic drug as used in Section 2-101
14841448 et seq. of this title shall not include decocainized
14851449 coca leaves or extracts of coca leaves, which extracts
14861450 do not contain cocaine or ecgonine;
14871451 27. "Opiate" or "opioid" means any Schedule II, III, IV or V
14881452 substance having an addiction-forming or addiction-sustaining
14891453 liability similar to morphine or being capable of conversion into a
14901454 drug having such addiction-forming or addiction-sustaining
14911455 liability. The terms do not include, unless specifically designated
14921456 as controlled under the Uniform Controlled Dangerous Substances Act,
14931457 the dextrorotatory isomer of 3-methoxy-n-methyl-morphinan and its
14941458 salts (dextromethorphan). The terms do include the racemic and
14951459 levorotatory forms;
14961460 28. "Opium poppy" means the plant of the species Papaver
14971461 somniferum L., except the seeds thereof;
1498-
1499-HB3965 HFLR Page 30
1500-BOLD FACE denotes Committee Amendments. 1
1501-2
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15251462 29. "Peace officer" means a police officer, sheriff, deputy
15261463 sheriff, district attorney's investigator, investigator from the
15271464 Office of the Attorney General, or any other person elected or
15281465 appointed by law to enforce any of the criminal laws of this state
15291466 or of the United States;
15301467 30. "Person" means an individual, corporation, government or
15311468 governmental subdivision or agency, business trust, estate, trust,
15321469 partnership or association, or any other legal entity;
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15331496 31. "Poppy straw" means all parts, except the seeds, of the
15341497 opium poppy, after mowing;
15351498 32. "Practitioner" means:
15361499 a. (1) a medical doctor or osteopathic physician,
15371500 (2) a dentist,
15381501 (3) a podiatrist,
15391502 (4) an optometrist,
15401503 (5) a veterinarian,
15411504 (6) a physician assistant or an Advanced Practice
15421505 Registered Nurse under the supervision of a
15431506 licensed medical doctor or osteopathic physician;
15441507 or a physician assistant,
15451508 (7) a scientific investigator, or
15461509 (8) any other person,
15471510 licensed, registered or otherwise permitted to
15481511 prescribe, distribute, dispense, conduct research with
1549-
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15761512 respect to, use for scientific purposes or administer
15771513 a controlled dangerous substance in the course of
15781514 professional practice or research in this state, or
15791515 b. a pharmacy, hospital, laboratory or other institution
15801516 licensed, registered or otherwise permitted to
15811517 distribute, dispense, conduct research with respect
15821518 to, use for scientific purposes or administer a
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15831545 controlled dangerous substance in the course of
15841546 professional practice or research in this state;
15851547 33. "Production" includes the manufacture, planting,
15861548 cultivation, growing or harvesting of a controlled dangerous
15871549 substance;
15881550 34. "State" means the State of Oklahoma or any other state of
15891551 the United States;
15901552 35. "Ultimate user" means a person who lawfully possesses a
15911553 controlled dangerous substance for the person's own use or for the
15921554 use of a member of the person's household or for administration to
15931555 an animal owned by the person or by a member of the person's
15941556 household;
15951557 36. "Drug paraphernalia" means all equipment, products and
15961558 materials of any kind which are used, intended for use, or fashioned
15971559 specifically for use in planting, propagating, cultivating, growing,
15981560 harvesting, manufacturing, comp ounding, converting, producing,
15991561 processing, preparing, testing, analyzing, packaging, repackaging,
1600-
1601-HB3965 HFLR Page 32
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1626-
16271562 storing, containing, concealing, injecting, ingesting, inhaling or
16281563 otherwise introducing into the human body, a controlled dangerous
16291564 substance in violation o f the Uniform Controlled Dangerous
16301565 Substances Act including, but not limited to:
16311566 a. kits used, intended for use, or fashioned specifically
16321567 for use in planting, propagating, cultivating, growing
16331568 or harvesting of any species of plant which is a
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16341595 controlled dangerous substance or from which a
16351596 controlled dangerous substance can be derived,
16361597 b. kits used, intended for use, or fashioned specifically
16371598 for use in manufacturing, compounding, converting,
16381599 producing, processing or preparing controlled
16391600 dangerous substances ,
16401601 c. isomerization devices used, intended for use, or
16411602 fashioned specifically for use in increasing the
16421603 potency of any species of plant which is a controlled
16431604 dangerous substance,
16441605 d. testing equipment used, intended for use, or fashioned
16451606 specifically for use in identifying, or in analyzing
16461607 the strength, effectiveness or purity of controlled
16471608 dangerous substances,
16481609 e. scales and balances used, intended for use, or
16491610 fashioned specifically for use in weighing or
16501611 measuring controlled dangerous substances,
1651-
1652-HB3965 HFLR Page 33
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16781612 f. diluents and adulterants, such as quinine
16791613 hydrochloride, mannitol, mannite, dextrose and
16801614 lactose, used, intended for use, or fashioned
16811615 specifically for use in cutting controlled dangerous
16821616 substances,
16831617 g. separation gins and sifters used, intended for use, or
16841618 fashioned specifically for use in removing twigs and
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16851645 seeds from, or in otherwise cleaning or refining,
16861646 marijuana,
16871647 h. blenders, bowls, containers, spoons and mixing devices
16881648 used, intended for use, or fashioned specifically for
16891649 use in compounding controlled dange rous substances,
16901650 i. capsules, balloons, envelopes and other containers
16911651 used, intended for use, or fashioned specifically for
16921652 use in packaging small quantities of controlled
16931653 dangerous substances,
16941654 j. containers and other objects used, intended for use,
16951655 or fashioned specifically for use in parenterally
16961656 injecting controlled dangerous substances into the
16971657 human body,
16981658 k. hypodermic syringes, needles and other objects used,
16991659 intended for use, or fashioned specifically for use in
17001660 parenterally injecting controlled dan gerous substances
17011661 into the human body,
1702-
1703-HB3965 HFLR Page 34
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17291662 l. objects used, intended for use, or fashioned
17301663 specifically for use in ingesting, inhaling or
17311664 otherwise introducing marijuana, cocaine, hashish or
17321665 hashish oil into the human body, such as:
17331666 (1) metal, wooden, acrylic, glass, stone, plastic or
17341667 ceramic pipes with or without screens, permanent
17351668 screens, hashish heads or punctured metal bowls,
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17361695 (2) water pipes,
17371696 (3) carburetion tubes and devices,
17381697 (4) smoking and carburetion masks,
17391698 (5) roach clips, meaning objects used to hold burning
17401699 material, such as a marijuana cigarette, that has
17411700 become too small or too short to be held in the
17421701 hand,
17431702 (6) miniature cocaine spoons and cocaine vials,
17441703 (7) chamber pipes,
17451704 (8) carburetor pipes,
17461705 (9) electric pipes,
17471706 (10) air-driven pipes,
17481707 (11) chillums,
17491708 (12) bongs, or
17501709 (13) ice pipes or chillers,
17511710 m. all hidden or novelty pipes, and
1752-
1753-HB3965 HFLR Page 35
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17791711 n. any pipe that has a tobacco bowl or chamber of less
17801712 than one-half (1/2) inch in diameter in which there is
17811713 any detectable residue of any controlled dangerous
17821714 substance as defined in this section or any other
17831715 substances not legal for possession or use;
17841716 provided, however, the term drug paraphernalia shall not include
17851717 separation gins intended for use in preparing tea or spice, clamps
17861718 used for constructing electrical equ ipment, water pipes designed for
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17871745 ornamentation in which no detectable amount of an illegal substance
17881746 is found or pipes designed and used solely for smoking tobacco,
17891747 traditional pipes of an American Indian tribal religious ceremony,
17901748 antique pipes that ar e thirty (30) years of age or older, or drug
17911749 testing strips possessed by a person for purposes of determining the
17921750 presence of fentanyl or a fentanyl-related compound;
17931751 37. a. "Synthetic controlled substance" means a substance:
17941752 (1) the chemical structure of which is substantially
17951753 similar to the chemical structure of a controlled
17961754 dangerous substance in Schedule I or II,
17971755 (2) which has a stimulant, depressant, or
17981756 hallucinogenic effect on the central nervous
17991757 system that is substantially similar to or
18001758 greater than the stimulant, depressant or
18011759 hallucinogenic effect on the central nervous
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18291760 system of a controlled dangerous substance in
18301761 Schedule I or II, or
18311762 (3) with respect to a particular person, which such
18321763 person represents or intends to have a stimulant,
18331764 depressant, or hallucinogenic effect on the
18341765 central nervous system that is substantially
18351766 similar to or greater than the stimulant,
18361767 depressant, or hallucinogenic effect on the
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18371794 central nervous system of a controlled dangerous
18381795 substance in Schedule I or II.
18391796 b. The designation of gamma butyrolactone or any other
18401797 chemical as a precursor, pursuant to Section 2-322 of
18411798 this title, does not preclude a finding pursuant to
18421799 subparagraph a of this paragraph that the chemical is
18431800 a synthetic controlled substance.
18441801 c. "Synthetic controlled substance" does not include:
18451802 (1) a controlled dangerous substance,
18461803 (2) any substance for which there is an approved new
18471804 drug application,
18481805 (3) with respect to a particular person any
18491806 substance, if an exemption is in effect for
18501807 investigational use, for that person under the
18511808 provisions of Section 505 of the Federal Food,
18521809 Drug and Cosmetic Act, Title 21 of the United
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18801810 States Code, Section 355, to the extent conduct
18811811 with respect to such substance is pursuant to
18821812 such exemption, or
18831813 (4) any substance to the extent not intended for
18841814 human consumption before such an exemption takes
18851815 effect with respect to that substance.
18861816 d. Prima facie evidence that a substance containing
18871817 salvia divinorum has been enhanced, concentrated or
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18881844 chemically or physically altered shall give rise to a
18891845 rebuttable presumption that the substance is a
18901846 synthetic controlled substance;
18911847 38. "Tetrahydrocannabinols" means all substances that have been
18921848 chemically synthesized to emulate the tetrahydrocannabinols of
18931849 marijuana, specifically including any tetrahydrocannabinols derived
18941850 from industrial hemp;
18951851 39. "Isomer" means the optical isomer, except as used in
18961852 subsections C and F of Section 2-204 of this title and paragraph 4
18971853 of subsection A of Section 2-206 of this title. As used in
18981854 subsections C and F of Section 2-204 of this title, isomer means the
18991855 optical, positional or geometric isomer. As used in paragraph 4 of
19001856 subsection A of Section 2-206 of this title, the term isomer means
19011857 the optical or geometric isomer;
19021858 40. "Hazardous materials" means materials, whether solid,
19031859 liquid or gas, which are toxic to human, animal, aquatic or plant
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19311860 life, and the disposal of which materials is controlled by state or
19321861 federal guidelines;
19331862 41. "Anhydrous ammonia" means any substance that exhibits
19341863 cryogenic evaporative behavior and tests positive for ammonia;
19351864 42. "Acute pain" means pain, whether resulting from disease,
19361865 accidental or intentional trauma or other cause, that the
19371866 practitioner reasonably expects to last only a short period of time.
19381867 Acute pain does not include chronic pain, pain being treated as part
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19391894 of cancer care, hospice or other end-of-life care, or pain being
19401895 treated as part of palliative care;
19411896 43. "Chronic pain" means pain that persists beyond the usual
19421897 course of an acute disease or healing of an injury. Chronic pain
19431898 may or may not be associated with an acute or chronic pathologic
19441899 process that causes continuous or intermittent pain over months or
19451900 years;
19461901 44. "Initial prescription" means a prescription issued to a
19471902 patient who:
19481903 a. has never previously been issued a prescription for
19491904 the drug or its pharmaceutical equivalent in the past
19501905 year, or
19511906 b. requires a prescription for the drug or its
19521907 pharmaceutical equivalent due to a surgical procedure
19531908 or new acute event and has previously had a
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19811909 prescription for the drug or its pharmaceutical
19821910 equivalent within the past year.
19831911 When determining whether a patient was previously issued a
19841912 prescription for a drug or its pharmaceutical equivalent, the
19851913 practitioner shall consult with the patient and review the medical
19861914 record and prescription monitoring information of the patient;
19871915 45. "Patient-provider agreement" means a written contract or
19881916 agreement that is executed between a practitioner and a patient,
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19891943 prior to the commencement of treatment for chronic pain using an
19901944 opioid drug as a means to:
19911945 a. explain the possible risk of development of physical
19921946 or psychological dependence in the patient and prevent
19931947 the possible development of addiction,
19941948 b. document the understanding of both the practitioner
19951949 and the patient regarding the patient-provider
19961950 agreement of the patient,
19971951 c. establish the rights of the patient in association
19981952 with treatment and the obligations of the patient in
19991953 relation to the responsible use, discontinuation of
20001954 use, and storage of opioid drugs, including any
20011955 restrictions on the refill of prescriptions or the
20021956 acceptance of opioid prescriptions from practitioners,
20031957 d. identify the specific medications and other modes of
20041958 treatment, including physical therapy or exercise,
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20321959 relaxation or psychological counseling, that are
20331960 included as a part of the patient-provider agreement,
20341961 e. specify the measures the practitioner may employ to
20351962 monitor the compliance of the patient including, but
20361963 not limited to, random specimen screens and pill
20371964 counts, and
20381965 f. delineate the process for terminating the agreement,
20391966 including the consequences if the practitioner has
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20401993 reason to believe that the patient is not complying
20411994 with the terms of the agreement. Compliance with the
20421995 "consent items" shall constitute a valid, informed
20431996 consent for opioid therapy. The practitioner shall be
20441997 held harmless from civil litigation for failure to
20451998 treat pain if the event occurs because of nonadherence
20461999 by the patient with any of the provisions of the
20472000 patient-provider agreement;
20482001 46. "Serious illness" means a medical illness or physical
20492002 injury or condition that substantially affects quality of life for
20502003 more than a short period of time. Serious illness includes, but is
20512004 not limited to, Alzheimer's disease or related dementias, lung
20522005 disease, cancer, heart failure, renal failure, liver failure or
20532006 chronic, unremitting or intractable pain such as neuropathic pain;
20542007 and
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20822008 47. "Surgical procedure" means a procedure that is performed
20832009 for the purpose of structurally altering the human body by incision
20842010 or destruction of tissues as part of the practice of medicine. This
20852011 term includes the diagnostic or therapeutic treatment of conditions
20862012 or disease processes by use of instruments such as lasers,
20872013 ultrasound, ionizing, radiation, scalpels, probes or needles that
20882014 cause localized alteration or transportation of live human tissue by
20892015 cutting, burning, vaporizing, freezing, suturing, probing or
20902016 manipulating by closed reduction for major dislocations or
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20912043 fractures, or otherwise altering by any mechanical, thermal, light-
20922044 based, electromagnetic or chemical means.
20932045 SECTION 9. AMENDATORY 63 O.S. 2021, Section 2-312, as
20942046 amended by Section 2, Chapter 184, O.S.L. 2022 (63 O. S. Supp. 2023,
20952047 Section 2-312), is amended to read as follows:
20962048 Section 2-312. A. A physician, podiatrist, optometrist or a
20972049 dentist who has complied with the registration req uirements of the
20982050 Uniform Controlled Dangerous Substances Act, in good faith and in
20992051 the course of such person's professional practice only, may
21002052 prescribe and administer controlled dangerous substances, or may
21012053 cause the same to be administered by medical or paramedical
21022054 personnel acting under the direction and supervision of the
21032055 physician, podiatrist, optometrist or dentist, and only may dispense
21042056 controlled dangerous substances pursuant to the provisions of
21052057 Sections 355.1 and 355.2 of Title 59 of the Oklahoma Statutes.
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21332058 B. A veterinarian who has complied with the registration
21342059 requirements of the Uniform Controlled Dangerous Substances Act, in
21352060 good faith and in the course of the professional practice of the
21362061 veterinarian only, and not for use by a human being, ma y prescribe,
21372062 administer, and dispense controlled dangerous substances and m ay
21382063 cause them to be administered by an assistant or orderly under the
21392064 direction and supervision of the veterinarian.
21402065 C. An advanced practice nurse who is recognized to prescribe by
21412066 the Oklahoma Board of Nursing as an advanced registered nurse
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21422093 practitioner, clinical nurse specialist or certified nurse-midwife,
21432094 who is subject to medical direction by a supervising physician,
21442095 pursuant to Section 567.3a of Title 59 of the Oklahoma Statut es, and
21452096 who has complied with the registration requirements of the Uniform
21462097 Controlled Dangerous Substances Act, in good faith and in the course
21472098 of professional practice only, may prescribe and administer Schedule
21482099 III, IV and V controlled dangerous substanc es.
21492100 D. An advanced practice nurse who is recognized to order,
21502101 select, obtain and administer drugs by the Oklahoma Board of Nursing
21512102 as a certified registered nurse anesthetist pursuant to Section
21522103 353.1b of Title 59 of the Oklahoma Statutes and who has comp lied
21532104 with the registration requirements of the Uniform Controlled
21542105 Dangerous Substances Act, in good faith and in the course of such
21552106 practitioner's professional practice only, may order, select, obtain
21562107 and administer Schedules II through V controlled danger ous
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21842108 substances in a preanesthetic preparation or evaluation; anesthesia
21852109 induction, maintenance or emergence; or postanesthesia care setting
21862110 only. A certified registered nurse anesthetist may order, select,
21872111 obtain and administer such drugs only during the perioperative or
21882112 periobstetrical period.
21892113 E. A physician assistant who is r ecognized to prescribe by the
21902114 State Board of Medical Licensure and Supervision under the medical
21912115 direction of a supervising physician, pursuant to Section 519.6 of
21922116 Title 59 of the Oklahoma Statutes, and who has complied with the
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21932143 registration requirements o f the Uniform Controlled Da ngerous
21942144 Substances Act, in good faith and in the course of professional
21952145 practice only, may prescribe and administer Schedule II through V
21962146 controlled dangerous substances subject to the restrictions in
21972147 Section 519.6 of Title 59 of the Oklahoma Statu tes.
21982148 SECTION 10. REPEALER 59 O.S. 2021, Section 521.4, is
21992149 hereby repealed.
22002150 SECTION 11. It being immediately necessary for t he preservation
22012151 of the public peace, health or safety, an emergency is hereby
22022152 declared to exist, by reason whereof this act shall take effect and
22032153 be in full force from and after its passage an d approval.
22042154
2205-COMMITTEE REPORT BY: COMMITTEE ON RULES, dated 02/28/2024 - DO PASS,
2206-As Amended and Coauthored.
2155+59-2-10555 LRB 02/27/24
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