98TH GENERAL ASSEMBLY
State of Illinois
2013 and 2014
SB3109

 

Introduced 2/7/2014, by Sen. Pat McGuire

 

SYNOPSIS AS INTRODUCED:
 
225 ILCS 80/15.1

    Amends the Illinois Optometric Practice Act of 1987. Permits a licensed optometrist to prescribe Dihydrocodeinone (Hydrocodone) with one or more active, non-narcotic ingredients only in a quantity sufficient to provide treatment for up to 72 hours, and only if such formulations are reclassified as Schedule II by the U.S. Food and Drug Administration.


LRB098 18318 ZMM 53453 b

 

 

A BILL FOR

 

SB3109LRB098 18318 ZMM 53453 b

1    AN ACT concerning regulation.
 
2    Be it enacted by the People of the State of Illinois,
3represented in the General Assembly:
 
4    Section 2. The Illinois Optometric Practice Act of 1987 is
5amended by changing Section 15.1 as follows:
 
6    (225 ILCS 80/15.1)
7    (Section scheduled to be repealed on January 1, 2017)
8    Sec. 15.1. Diagnostic and therapeutic authority.
9    (a) For purposes of the Act, "ocular pharmaceutical agents"
10means topical anesthetics, topical mydriatics, topical
11cycloplegics, topical miotics and mydriatic reversing agents,
12anti-infective agents, anti-allergy agents, anti-glaucoma
13agents (except oral carbonic anhydrase inhibitors, which may be
14prescribed only in a quantity sufficient to provide treatment
15for up to 72 hours), anti-inflammatory agents (except oral
16steroids), over-the-counter agents, analgesic agents, anti-dry
17eye agents, and agents for the treatment of hypotrichosis.
18    (a-3) In addition to ocular pharmaceutical agents that fall
19within the categories set forth in subsection (a) of this
20Section, the Board may add a pharmaceutical agent approved by
21the FDA or class of agents for the purpose of the diagnosis or
22treatment of conditions of the eye and adnexa after
23consideration of the agent's systemic effects, side effects,

 

 

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1and the use of the agent within the practice of optometry. The
2Board shall consider requests for additional agents and make
3recommendations within 90 days after the receipt of the
4request.
5    Within 45 days after the Board's recommendation to the
6Department of a pharmaceutical agent or class of agents, the
7Department shall promulgate rules necessary to allow for the
8prescribing or administering of the pharmaceutical agent or
9class of agents under this Act.
10    (a-5) Ocular pharmaceutical agents administered by
11injection may be used only for the treatment of anaphylaxis.
12    (a-10) Oral pharmaceutical agents may be prescribed for a
13child under 5 years of age only in consultation with a
14physician licensed to practice medicine in all its branches.
15    (a-15) The authority to prescribe a Schedule III, IV, or V
16controlled substance shall include only analgesic agents only
17in a quantity sufficient to provide treatment for up to 72
18hours. The prescription of a Schedule II controlled substance
19is prohibited, except for Dihydrocodeinone (Hydrocodone) with
20one or more active, non-narcotic ingredients only in a quantity
21sufficient to provide treatment for up to 72 hours, and only if
22such formulations of Dihydrocodeinone are reclassified as
23Schedule II by the U.S. Food and Drug Administration.
24    (b) A licensed optometrist may remove superficial foreign
25bodies from the human eye and adnexa and may give orders for
26patient care to a nurse licensed to practice under Illinois

 

 

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1law.
2    (c) An optometrist's license shall be revoked or suspended
3by the Department upon recommendation of the Board based upon
4either of the following causes:
5        (1) grave or repeated misuse of any ocular
6    pharmaceutical agent; and
7        (2) the use of any agent or procedure in the course of
8    optometric practice by an optometrist not properly
9    authorized under this Act.
10    (d) The Secretary of Financial and Professional Regulation
11shall notify the Director of Public Health as to the categories
12of ocular pharmaceutical agents permitted for use by an
13optometrist. The Director of Public Health shall in turn notify
14every licensed pharmacist in the State of the categories of
15ocular pharmaceutical agents that can be utilized and
16prescribed by an optometrist.
17(Source: P.A. 97-170, eff. 7-22-11.)