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| | 102ND GENERAL ASSEMBLY
State of Illinois
2021 and 2022 HB3578 Introduced 2/22/2021, by Rep. Deb Conroy SYNOPSIS AS INTRODUCED: |
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Amends the Illinois Controlled Substances Act. Provides that a prescriber shall prescribe naloxone hydrochloride or another drug approved by the United States Food and Drug Administration for the complete or partial reversal of opioid depression to a patient if the patient presents with an increased risk for overdose, including a patient with a history of overdose, a patient with a history of substance use disorder, or a patient at risk for returning to a high dose of opioid medication to which the patient is no longer tolerant. Provides other requirements and exemptions. Makes other changes. Effective January 1, 2022.
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| | A BILL FOR |
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| | HB3578 | | LRB102 12604 KMF 17942 b |
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1 | | AN ACT concerning criminal law.
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2 | | Be it enacted by the People of the State of Illinois,
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3 | | represented in the General Assembly:
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4 | | Section 5. The Illinois Controlled Substances Act is |
5 | | amended by adding Section 315.7 as follows: |
6 | | (720 ILCS 570/315.7 new) |
7 | | Sec. 315.7. Prescriber requirements. |
8 | | (a) Notwithstanding any provision of law to the contrary, |
9 | | a prescriber shall: |
10 | | (1) Prescribe naloxone hydrochloride or another drug |
11 | | approved by the United States Food and Drug Administration |
12 | | for the complete or partial reversal of opioid depression |
13 | | to a patient when the patient presents with an increased |
14 | | risk for overdose, including a patient with a history of |
15 | | overdose, a patient with a history of substance use |
16 | | disorder, or a patient at risk for returning to a high dose |
17 | | of opioid medication to which the patient is no longer |
18 | | tolerant. |
19 | | (2) Consistent with the existing standard of care, |
20 | | provide education to patients receiving a prescription |
21 | | under paragraph (1) of this subsection (a) on overdose |
22 | | prevention and the use of naloxone hydrochloride or |
23 | | another drug approved by the United States Food and Drug |