Sen. Sara Feigenholtz

Filed: 5/5/2026

 

 


 

 


 
10400HB2584sam002LRB104 08321 BAB 37256 a

1
AMENDMENT TO HOUSE BILL 2584

2    AMENDMENT NO. ______. Amend House Bill 2584 by replacing
3everything after the enacting clause with the following:
 
4    "Section 5. The Illinois Insurance Code is amended by
5changing Section 356z.60 as follows:
 
6    (215 ILCS 5/356z.60)
7    Sec. 356z.60. Coverage for abortifacients, hormonal
8therapy, and human immunodeficiency virus pre-exposure
9prophylaxis and post-exposure prophylaxis.
10    (a) As used in this Section:
11    "Abortifacients" means any medication administered to
12terminate a pregnancy as prescribed or ordered by a health
13care professional.
14    "Health care professional" means a physician licensed to
15practice medicine in all of its branches, licensed advanced
16practice registered nurse, or physician assistant.

 

 

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1    "Hormonal therapy medication" means hormonal treatment
2administered to treat gender dysphoria.
3    "Therapeutic equivalent version" means drugs, devices, or
4products that can be expected to have the same clinical effect
5and safety profile when administered to patients under the
6conditions specified in the labeling and that satisfy the
7following general criteria:
8        (1) it is approved as safe and effective;
9        (2) it is a pharmaceutical equivalent in that it:
10            (A) contains identical amounts of the same active
11        drug ingredient in the same dosage form and route of
12        administration; and
13            (B) meets compendial or other applicable standards
14        of strength, quality, purity, and identity;
15        (3) it is bioequivalent in that:
16            (A) it does not present a known or potential
17        bioequivalence problem and it meets an acceptable in
18        vitro standard; or
19            (B) if it does present such a known or potential
20        problem, it is shown to meet an appropriate
21        bioequivalence standard;
22        (4) it is adequately labeled; and
23        (5) it is manufactured in compliance with Current Good
24    Manufacturing Practice regulations adopted by the United
25    States Food and Drug Administration.
26    (b) An individual or group policy of accident and health

 

 

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1insurance amended, delivered, issued, or renewed in this State
2on or after January 1, 2024 shall provide coverage for all
3abortifacients, hormonal therapy medication, human
4immunodeficiency virus pre-exposure prophylaxis, and
5post-exposure prophylaxis drugs approved by the United States
6Food and Drug Administration, and follow-up services related
7to that coverage, including, but not limited to, management of
8side effects, medication self-management or adherence
9counseling, risk reduction strategies, and mental health
10counseling. This coverage shall include drugs approved by the
11United States Food and Drug Administration that are prescribed
12or ordered for off-label use for the purposes described in
13this Section. On or after the effective date of this
14amendatory Act of the 104th General Assembly, this coverage
15shall include pre-PrEP HIV screening, sexually transmitted
16infection screening, kidney function analysis, routine
17laboratory testing, and routine provider visits.
18    (c) The coverage required under subsection (b) is subject
19to the following conditions:
20        (1) If the United States Food and Drug Administration
21    has approved one or more therapeutic equivalent versions
22    of an abortifacient drug, a policy is not required to
23    include all such therapeutic equivalent versions in its
24    formulary so long as at least one is included and covered
25    without cost sharing and in accordance with this Section.
26        (2) If an individual's attending provider recommends a

 

 

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1    particular drug approved by the United States Food and
2    Drug Administration based on a determination of medical
3    necessity with respect to that individual, the plan or
4    issuer must defer to the determination of the attending
5    provider and must cover that service or item without cost
6    sharing.
7        (3) If a drug is not covered, plans and issuers must
8    have an easily accessible, transparent, and sufficiently
9    expedient process that is not unduly burdensome on the
10    individual or a provider or other individual acting as a
11    patient's authorized representative to ensure coverage
12    without cost sharing.
13    The conditions listed under this subsection (c) also apply
14to drugs prescribed for off-label use as abortifacients.
15    (d) Except as otherwise provided in this Section, a policy
16subject to this Section shall not impose a deductible,
17coinsurance, copayment, or any other cost-sharing requirement
18on the coverage provided. The provisions of this subsection do
19not apply to coverage of procedures to the extent such
20coverage would disqualify a high-deductible health plan from
21eligibility for a health savings account pursuant to the
22federal Internal Revenue Code, 26 U.S.C. 223.
23    (e) Except as otherwise authorized under this Section, a
24policy shall not impose any restrictions or delays on the
25coverage required under this Section.
26    (f) The coverage requirements in this Section for

 

 

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1abortifacients do not, pursuant to 42 U.S.C. 18054(a)(6),
2apply to a multistate plan that does not provide coverage for
3abortion.
4    (g) If the Department concludes that enforcement of any
5coverage requirement of this Section for abortifacients may
6adversely affect the allocation of federal funds to this
7State, the Department may grant an exemption to that
8requirement, but only to the minimum extent necessary to
9ensure the continued receipt of federal funds.
10(Source: P.A. 102-1117, eff. 1-13-23; 103-462, eff. 8-4-23.)
 
11    Section 10. The Prior Authorization Reform Act is amended
12by adding Section 52 as follows:
 
13    (215 ILCS 200/52 new)
14    Sec. 52. Prior authorization for certain prescription
15drugs; prohibited. A health insurance issuer may not require
16prior authorization for the following prescription drug types
17and their therapeutic equivalents approved by the United
18States Food and Drug Administration: human immunodeficiency
19virus pre-exposure prophylaxis and post-exposure prophylaxis
20medication or human immunodeficiency virus treatment
21medication. This Section does not apply to a health care plan
22serving Medicaid populations that provides, arranges for, pays
23for, or reimburses the cost of any health care service for
24persons who are enrolled under the Illinois Public Aid Code;

 

 

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1however, nothing in this Section shall be construed to limit
2or otherwise diminish any coverage requirements, patient
3protections, or access standards applicable to the medical
4assistance program under the Illinois Public Aid Code,
5including, but not limited to, Section 5-5, Section 5-16.8, or
6any other provision of the Illinois Public Aid Code regarding
7coverage of human immunodeficiency virus pre-exposure
8prophylaxis and post-exposure prophylaxis medication or human
9immunodeficiency virus treatment medication. This Section does
10not apply to the State Employees Group Insurance Program or
11any health care plan established or maintained under the State
12Employees Group Insurance Act of 1971.
 
13    Section 99. Effective date. This Act takes effect January
141, 2028.".