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3 | because the prescription drug has been withdrawn from the | ||||||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