[Congressional Bills 116th Congress]
[From the U.S. Government Publishing Office]
[H.R. 3408 Introduced in House (IH)]
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116th CONGRESS
1st Session
H. R. 3408
To amend title XVIII of the Social Security Act to require prescription
drug plan sponsors to include real-time benefit information as part of
such sponsor's electronic prescription program under the Medicare
program.
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IN THE HOUSE OF REPRESENTATIVES
June 21, 2019
Mr. Arrington (for himself and Mr. Olson) introduced the following
bill; which was referred to the Committee on Energy and Commerce, and
in addition to the Committee on Ways and Means, for a period to be
subsequently determined by the Speaker, in each case for consideration
of such provisions as fall within the jurisdiction of the committee
concerned
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A BILL
To amend title XVIII of the Social Security Act to require prescription
drug plan sponsors to include real-time benefit information as part of
such sponsor's electronic prescription program under the Medicare
program.
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 ``Shop Rx Act of 2019''.
SEC. 2. REQUIRING PRESCRIPTION DRUG PLAN SPONSORS TO INCLUDE REAL-TIME
BENEFIT INFORMATION AS PART OF SUCH SPONSOR'S ELECTRONIC
PRESCRIPTION PROGRAM UNDER THE MEDICARE PROGRAM.
Section 1860D-4(e)(2) of the Social Security Act (42 U.S.C. 1395w-
104(e)(2)) is amended--
(1) in subparagraph (D), by striking ``To the extent'' and
inserting ``Except as provided in subparagraph (F), to the
extent''; and
(2) by adding at the end the following new subparagraph:
``(F) Real-time benefit information.--
``(i) In general.--Not later than January
1, 2021, the program shall provide for the
real-time electronic transmission to
prescribing health care professionals, using
technology capable of integrating with such
professionals' electronic prescribing and
electronic health record systems, of
individual-specific formulary and benefit
information under a prescription drug plan with
respect to an individual enrolled in such plan.
Such information shall include, with respect to
the prescribing of a covered part D drug to
such individual, the following:
``(I) A description of any
clinically appropriate alternatives to
such drug included in the formulary of
such plan.
``(II) Information relating to
applicable cost-sharing requirements
for such drug and such alternatives,
including a description of any variance
in such requirements based on the
pharmacy dispensing such drug or such
alternatives.
``(III) Information relating to any
prior authorization or other
utilization management requirements
applicable to such drug and such
alternatives within the formulary of
such plan.
``(ii) Special rule for 2021.--The program
shall be deemed to be in compliance with clause
(i) for 2021 if the program complies with the
provisions of section 423.160(b)(7) of title
42, Code of Federal Regulations (or a successor
regulation), for such year.''.
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