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1 | AN ACT concerning regulation.
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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 Managed Care Reform and Patient Rights Act | |||||||||||||||||||||
5 | is amended by changing Sections 45.1 and 45.2 as follows: | |||||||||||||||||||||
6 | (215 ILCS 134/45.1) | |||||||||||||||||||||
7 | Sec. 45.1. Medical exceptions procedures required. | |||||||||||||||||||||
8 | (a) Every health carrier that offers a qualified health | |||||||||||||||||||||
9 | plan, as defined in the federal Patient Protection and | |||||||||||||||||||||
10 | Affordable Care Act of 2010 (Public Law 111-148), as amended by | |||||||||||||||||||||
11 | the federal Health Care and Education Reconciliation Act of | |||||||||||||||||||||
12 | 2010 (Public Law 111-152), and any amendments thereto, or | |||||||||||||||||||||
13 | regulations or guidance issued under those Acts (collectively, | |||||||||||||||||||||
14 | "the Federal Act"), directly to consumers in this State shall | |||||||||||||||||||||
15 | establish and maintain a medical exceptions process that allows | |||||||||||||||||||||
16 | covered persons or their authorized representatives to request | |||||||||||||||||||||
17 | any clinically appropriate prescription drug when (1) the drug | |||||||||||||||||||||
18 | is not covered based on the health benefit plan's formulary; | |||||||||||||||||||||
19 | (2) the health benefit plan is discontinuing coverage of the | |||||||||||||||||||||
20 | drug on the plan's formulary for reasons other than safety or | |||||||||||||||||||||
21 | other than because the prescription drug has been withdrawn | |||||||||||||||||||||
22 | from the market by the drug's manufacturer; (3) the | |||||||||||||||||||||
23 | prescription drug alternatives required to be used in |
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1 | accordance with a step therapy requirement (A) has been | ||||||
2 | ineffective in the treatment of the enrollee's disease or | ||||||
3 | medical condition or, based on both sound clinical evidence and | ||||||
4 | medical and scientific evidence, the known relevant physical or | ||||||
5 | mental characteristics of the enrollee, and the known | ||||||
6 | characteristics of the drug regimen, is likely to be | ||||||
7 | ineffective or adversely affect the drug's effectiveness or | ||||||
8 | patient compliance or (B) has caused or, based on sound medical | ||||||
9 | evidence, is likely to cause an adverse reaction or harm to the | ||||||
10 | enrollee; or (4) the number of doses available under a dose | ||||||
11 | restriction for the prescription drug (A) has been ineffective | ||||||
12 | in the treatment of the enrollee's disease or medical condition | ||||||
13 | or (B) based on both sound clinical evidence and medical and | ||||||
14 | scientific evidence, the known relevant physical and mental | ||||||
15 | characteristics of the enrollee, and known characteristics of | ||||||
16 | the drug regimen, is likely to be ineffective or adversely | ||||||
17 | affect the drug's effective or patient compliance. | ||||||
18 | (b) The health carrier's established medical exceptions | ||||||
19 | procedures must require, at a minimum, the following: | ||||||
20 | (1) Any request for approval of coverage made verbally | ||||||
21 | or in writing (regardless of whether made using a paper or | ||||||
22 | electronic form or some other writing) at any time shall be | ||||||
23 | reviewed by appropriate health care professionals. | ||||||
24 | (2) The health carrier must, within 72 hours after | ||||||
25 | receipt of a request made under subsection (a) of this | ||||||
26 | Section, either approve or deny the request. In the case of |
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1 | a denial, the health carrier shall provide the covered | ||||||
2 | person or the covered person's authorized representative | ||||||
3 | and the covered person's prescribing provider and | ||||||
4 | pharmacist with the reason for the denial, an alternative | ||||||
5 | covered medication, if applicable, and information | ||||||
6 | regarding the procedure for submitting an appeal to the | ||||||
7 | denial. | ||||||
8 | (3) In the case of an expedited coverage determination, | ||||||
9 | the health carrier must either approve or deny the request | ||||||
10 | within 24 hours after receipt of the request. In the case | ||||||
11 | of a denial, the health carrier shall provide the covered | ||||||
12 | person or the covered person's authorized representative | ||||||
13 | and the covered person's prescribing provider with the | ||||||
14 | reason for the denial, an alternative covered medication, | ||||||
15 | if applicable, and information regarding the procedure for | ||||||
16 | submitting an appeal to the denial. | ||||||
17 | (c) Notwithstanding any other provision of this Section, | ||||||
18 | nothing in this Section shall be interpreted or implemented in | ||||||
19 | a manner not consistent with the Federal Act.
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20 | (Source: P.A. 98-1035, eff. 8-25-14.) | ||||||
21 | (215 ILCS 134/45.2) | ||||||
22 | Sec. 45.2. Prior authorization form; prescription | ||||||
23 | benefits. | ||||||
24 | (a) Notwithstanding any other provision of law, on and | ||||||
25 | after January 1, 2015, a health insurer that provides |
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1 | prescription drug benefits must, within 72 hours after receipt | ||||||
2 | of a paper or electronic prior authorization form from a | ||||||
3 | prescribing provider or pharmacist, either approve or deny the | ||||||
4 | prior authorization. In the case of a denial, the insurer shall | ||||||
5 | provide the prescriber and pharmacist with the reason for the | ||||||
6 | denial, an alternative covered medication, if applicable, and | ||||||
7 | information regarding the denial. | ||||||
8 | In the case of an expedited coverage determination, the | ||||||
9 | health insurer must either approve or deny the prior | ||||||
10 | authorization within 24 hours after receipt of the paper or | ||||||
11 | electronic prior authorization form. In the case of a denial, | ||||||
12 | the health insurer shall provide the prescriber with the reason | ||||||
13 | for the denial, an alternative covered medication, if | ||||||
14 | applicable, and information regarding the procedure for | ||||||
15 | submitting an appeal to the denial. | ||||||
16 | (b) This Section does not apply to plans for beneficiaries | ||||||
17 | of Medicare or Medicaid. | ||||||
18 | (c) For the purposes of this Section: | ||||||
19 | "Pharmacist" has the same meaning as set forth in the | ||||||
20 | Pharmacy Practice Act. | ||||||
21 | "Prescribing provider" includes a provider authorized to | ||||||
22 | write a prescription, as described in subsection (e) of Section | ||||||
23 | 3 of the Pharmacy Practice Act, to treat a medical condition of | ||||||
24 | an insured.
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25 | (Source: P.A. 98-1035, eff. 8-25-14.)
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26 | Section 99. Effective date. This Act takes effect upon |
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1 | becoming law.
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