Bill Text: MI HB5598 | 2015-2016 | 98th Legislature | Introduced
Bill Title: Insurance; health insurers; abuse-deterrent opioid analgesic drug; require coverage. Amends 1956 PA 218 (MCL 500.100 - 500.8302) by adding sec. 3406u.
Spectrum: Partisan Bill (Republican 5-0)
Status: (Introduced - Dead) 2016-04-27 - Bill Electronically Reproduced 04/26/2016 [HB5598 Detail]
Download: Michigan-2015-HB5598-Introduced.html
HOUSE BILL No. 5598
April 26, 2016, Introduced by Reps. Kesto, Crawford, Forlini, Lucido and Hughes and referred to the Committee on Insurance.
A bill to amend 1956 PA 218, entitled
"The insurance code of 1956,"
(MCL 500.100 to 500.8302) by adding section 3406u.
THE PEOPLE OF THE STATE OF MICHIGAN ENACT:
Sec. 3406u. (1) An expense-incurred hospital, medical, or
surgical policy or certificate delivered, issued for delivery, or
renewed in this state that provides pharmaceutical coverage and a
health maintenance organization contract that provides
pharmaceutical coverage shall provide coverage for at least 1
abuse-deterrent opioid analgesic drug product per opioid analgesic
ingredient.
(2) Cost sharing for brand-name abuse-deterrent opioid
analgesic drug products covered under this section must not exceed
the lowest cost-sharing level applied to brand-name prescription
drugs covered under the policy or contract.
(3) Cost sharing for generic abuse-deterrent opioid analgesic
drug products covered under this section must not exceed the lowest
cost-sharing level applied to generic prescription drugs covered
under the policy or contract.
(4) An insurer or health maintenance organization cannot
achieve compliance with this section by increasing patient cost
sharing or by issuing disincentives for prescribers.
(5) An insurer or health maintenance organization shall not
require an insured or enrollee to first use a non-abuse-deterrent
opioid analgesic drug product before providing coverage for an
abuse-deterrent opioid analgesic drug product.
(6) This section does not prohibit an insurer or health
maintenance organization from applying utilization review
requirements, including prior authorization, to abuse-deterrent
opioid analgesic drug products if the utilization review
requirements are applied to all opioid analgesic drug products with
the same type of drug release, immediate or extended.
(7) As used in this section:
(a) "Abuse-deterrent opioid analgesic drug product" means a
brand-name or generic opioid analgesic drug product approved by the
United States Food and Drug Administration with abuse-deterrence
labeling claims indicating its abuse-deterrent properties are
expected to deter or reduce its abuse.
(b) "Cost sharing" means any coverage limit, copayment,
coinsurance, deductible, or other out-of-pocket expense
requirements.
(c) "Opioid analgesic drug product" means a drug product that
contains an opioid agonist and that is indicated by the United
States Food and Drug Administration for the treatment of pain,
whether in an immediate release or extended release formulation and
whether or not the drug product contains other drug substances.
(d) "Prescriber" means that term as defined in section 17708
of the public health code, 1978 PA 368, MCL 333.17708.
Enacting section 1. This amendatory act takes effect 90 days
after the date it is enacted into law.