[Congressional Bills 118th Congress]
[From the U.S. Government Publishing Office]
[S. 5271 Introduced in Senate (IS)]
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118th CONGRESS
2d Session
S. 5271
To require the Administrator of the Drug Enforcement Administration to
temporarily exempt buprenorphine from the Suspicious Orders Report
System for the remainder of the opioid public health emergency.
_______________________________________________________________________
IN THE SENATE OF THE UNITED STATES
September 25, 2024
Mr. Heinrich introduced the following bill; which was read twice and
referred to the Committee on the Judiciary
_______________________________________________________________________
A BILL
To require the Administrator of the Drug Enforcement Administration to
temporarily exempt buprenorphine from the Suspicious Orders Report
System for the remainder of the opioid public health emergency.
Be it enacted by the Senate and House of Representatives of the
United States of America in Congress assembled,
SECTION 1. SHORT TITLE.
This Act may be cited as the ``Broadening Utilization of Proven and
Effective Treatment for Recovery Act'' or the ``BUPE for Recovery
Act''.
SEC. 2. REMOVAL OF BUPRENORPHINE PRODUCTS FROM SORS DURING OPIOID
PUBLIC HEALTH EMERGENCY.
(a) Temporary Exemption.--The Administrator of the Drug Enforcement
Administration shall temporarily exempt any buprenorphine product
approved for the treatment of opioid use disorder from the Suspicious
Orders Report System established under 312 of the Controlled Substances
Act (21 U.S.C. 832), including subsection (a)(3) of that section, until
that date that is 270 days after the date on which the public health
emergency with respect to opioids declared by the Secretary of Health
and Human Services pursuant to section 319 of the Public Health Service
Act (42 U.S.C. 247d) on October 26, 2017, expires.
(b) Report.--Not later than 90 days after the date of the
expiration of the public health emergency described in subsection (a),
the Department of Justice and the Department of Health and Human
Services shall--
(1) conduct a comprehensive report that indicates if the
temporary exemption under subsection (a) resulted in increased
access to buprenorphine treatment for patients experiencing
opioid use disorder; and
(2) make a recommendation to the White House and Congress
about whether buprenorphine should remain in the Suspicious
Orders Report System and be subject to related reporting
requirements after the expiration of the public health
emergency described in subsection (a).
(c) Sense of Congress.--It is the sense of Congress that Congress
is concerned by reports of patients not being able to fill
buprenorphine prescriptions for the treatment of opioid use disorder at
pharmacies. Reports indicate that pharmacies are unable or unwilling to
stock sufficient buprenorphine products, in part because of the
Suspicious Orders Report System and related reporting requirements. A
temporary exemption of buprenorphine products approved for the
treatment of opioid use disorder from Suspicious Order Report System
requirements would allow the Federal Government to collect relevant
data and assess whether a permanent exemption should be established.
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