Missouri 2025 Regular Session

Missouri Senate Bill SB17 Latest Draft

Bill / Introduced Version Filed 12/04/2024

                             
FIRST REGULAR SESSION 
SENATE BILL NO. 17 
103RD GENERAL ASSEMBLY  
INTRODUCED BY SENATOR MAY. 
0105S.01I 	KRISTINA MARTIN, Secretary  
AN ACT 
To repeal section 195.080, RSMo, and to enact in lieu thereof one new section relating to opioid 
prescriptions. 
 
Be it enacted by the General Assembly of the State of Missouri, as follows: 
     Section A.  Section 195.080, RSMo, is repealed and one ne w 1 
section enacted in lieu thereof, to be known as section 195.080, 2 
to read as follows:3 
     195.080.  1.  Except as otherwise provided in this 1 
chapter and chapter 579, this chapter and chapter 579 shall 2 
not apply to the following cases:  prescribing,  3 
administering, dispensing or selling at retail of liniments, 4 
ointments, and other preparations that are susceptible of 5 
external use only and that contain controlled substances in 6 
such combinations of drugs as to prevent the drugs from 7 
being readily extracted from such liniments, ointments, or 8 
preparations, except that this chapter and chapter 579 shall 9 
apply to all liniments, ointments, and other preparations 10 
that contain coca leaves in any quantity or combination. 11 
     2.  Unless otherwise provided i n sections 334.037, 12 
334.104, and 334.747, a practitioner, other than a 13 
veterinarian, shall not issue an initial prescription for 14 
more than a seven-day supply of any opioid controlled 15 
substance upon the initial consultation and treatment of a 16 
patient for acute pain.  Upon any subsequent consultation 17 
for the same pain, the practitioner may issue any 18   SB 17 	2 
appropriate renewal, refill, or new prescription in 19 
compliance with the general provisions of this chapter and 20 
chapter 579.  Prior to issuing an initial prescription for  21 
an opioid controlled substance, a practitioner shall consult 22 
with the patient regarding the quantity of the opioid and 23 
the patient's option to fill the prescription in a lesser 24 
quantity and shall inform the patient of the risks 25 
associated with the opioid prescribed.  If, in the  26 
professional medical judgment of the practitioner, more than 27 
a seven-day supply is required to treat the patient's acute 28 
pain, the practitioner may issue a prescription for the 29 
quantity needed to treat the p atient; provided, that the 30 
practitioner shall document in the patient's medical record 31 
the condition triggering the necessity for more than a seven - 32 
day supply and that a nonopioid alternative was not 33 
appropriate to address the patient's condition.  The  34 
provisions of this subsection shall not apply to 35 
prescriptions for opioid controlled substances for a patient 36 
who is currently undergoing treatment for cancer or sickle 37 
cell disease, is receiving hospice care from a hospice 38 
certified under chapter 19 7 or palliative care, is a 39 
resident of a long-term care facility licensed under chapter 40 
198, or is receiving treatment for substance abuse or opioid 41 
dependence. 42 
     3.  A pharmacist or pharmacy shall not be subject to 43 
disciplinary action or other civi l or criminal liability for 44 
dispensing or refusing to dispense medication in good faith 45 
pursuant to an otherwise valid prescription that exceeds the 46 
prescribing limits established by subsection 2 of this 47 
section. 48 
     4.  Unless otherwise provided in t his section, the  49 
quantity of Schedule II controlled substances prescribed or 50   SB 17 	3 
dispensed at any one time shall be limited to a thirty -day  51 
supply.  The quantity of Schedule III, IV or V controlled 52 
substances prescribed or dispensed at any one time shall b e  53 
limited to a ninety-day supply and shall be prescribed and 54 
dispensed in compliance with the general provisions of this 55 
chapter and chapter 579.  The supply limitations provided in 56 
this subsection may be increased up to three months if the 57 
physician describes on the prescription form or indicates 58 
via telephone, fax, or electronic communication to the 59 
pharmacy to be entered on or attached to the prescription 60 
form the medical reason for requiring the larger supply.   61 
The supply limitations provided i n this subsection shall not 62 
apply if: 63 
     (1)  The prescription is issued by a practitioner 64 
located in another state according to and in compliance with 65 
the applicable laws of that state and the United States and 66 
dispensed to a patient located in anot her state; or 67 
     (2)  The prescription is dispensed directly to a member 68 
of the United States Armed Forces serving outside the United 69 
States. 70 
     5.  The partial filling of a prescription for a 71 
Schedule II substance is permissible as defined by 72 
regulation by the department of health and senior services. 73 
     6.  (1)  Prior to issuing an initial prescription for a 74 
Schedule II controlled substance or any other opioid pain 75 
reliever in a course of treatment for acute or chronic pain 76 
and prior to issuing a third prescription of the same in the 77 
same course of treatment, a practitioner shall discuss with 78 
the patient, or the patient's parent or guardian if the 79 
patient is under eighteen years of age and is not 80 
emancipated, the risks associated with the drugs being  81 
prescribed, including, but not limited to, the following: 82   SB 17 	4 
     (a)  The risks of addiction and overdose associated 83 
with opioid drugs and the dangers of taking opioid drugs 84 
with alcohol, benzodiazepines, and other central nervous 85 
system depressants; 86 
     (b)  The reasons why the prescription is necessary; 87 
     (c)  Alternative treatments that may be available; and 88 
     (d)  The risks associated with the use of the drugs 89 
prescribed, specifically that opioids are highly addictive, 90 
even when taken as prescribed; that there is a risk of 91 
developing a physical or psychological dependence on the 92 
controlled substance; and that the risks of taking more 93 
opioids than prescribed, or mixing sedatives, 94 
benzodiazepines, or alcohol with opioids, may res ult in  95 
fatal respiratory depression. 96 
     (2)  The practitioner shall include a note in the 97 
patient's medical record that the patient or the patient's 98 
parent or guardian has discussed with the practitioner the 99 
risks of developing a physical or psycholo gical dependence  100 
on the controlled substance and alternative treatments that 101 
may be available.  The consultation described in this 102 
subsection shall satisfy the consultation requirements of 103 
subsection 2 of this section for initial prescriptions for 104 
more than a seven-day supply of any opioid controlled 105 
substance. 106 
     (3)  The provisions of this subsection shall not apply 107 
to a prescription for a patient who is in active treatment 108 
for cancer, receiving hospice care from a hospice certified 109 
under chapter 197 or palliative care, is a resident of a 110 
long-term care facility licensed under chapter 198, or is 111 
receiving treatment for substance abuse or opioid dependence. 112 
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