S.B. 41 Enrolled

1

DRUG UTILIZATION REVIEW BOARD
2 AMENDMENTS
3 2010 GENERAL SESSION
4 STATE OF UTAH
5 Chief Sponsor: Peter C. Knudson
6 House Sponsor: Ronda Rudd Menlove
7
8 LONG TITLE
9 General Description:
10 This bill amends the drug prior approval program within the state's Medicaid program.
11 Highlighted Provisions:
12 This bill:
13 . permits the Drug Utilization Review Board to consider costs, as well as other
14 factors, when determining whether a drug should be placed on the prior approval
15 program;
16 . amends notice requirements;
17 . amends number of days before implementation of a decision of the board;
18 . provides more discretion to the Drug Utilization Review Board to restrict the use of
19 a drug for off label indications; and
20 . makes technical changes.
21 Monies Appropriated in this Bill:
22 None
23 Other Special Clauses:
24 None
25 Utah Code Sections Affected:
26 AMENDS:
27 26-18-105, as last amended by Laws of Utah 2006, Chapter 14
28
29 Be it enacted by the Legislature of the state of Utah:

30 Section 1. Section 26-18-105 is amended to read:
31 26-18-105. Drug prior approval program.
32 [Any] (1) A drug prior approval program approved or implemented by the board shall
33 meet the following conditions:
34 [(1) no drug may] (a) except as provided in Subsection (2), a drug may not be placed
35 on prior approval for other than medical reasons;
36 [(2)] (b) the board shall hold a public hearing at least [90] 30 days prior to placing a
37 drug on prior approval;
38 [(3)] (c) notwithstanding the provisions of Section 52-4-202 , the board shall provide
39 not less than [30 days] 14 days' notice to the public before holding a public hearing under
40 Subsection [(2)] (1)(b);
41 [(4)] (d) the board shall consider written and oral comments submitted by interested
42 parties prior to or during the hearing held in accordance with Subsection [(2)] (1)(b);
43 [(5)] (e) the board shall provide evidence that placing a drug class on prior approval:
44 (i) will not impede quality of recipient care; and
45 (ii) that the drug class is subject to clinical abuse or misuse;
46 (f) the board shall reconsider its decision to place a drug on prior approval:
47 [(6)] (i) no later than nine months after any drug class is placed on prior approval[, it
48 shall be reconsidered in]; and
49 (ii) at a public hearing with notice as provided in Subsection [(3)] (1)(b);
50 [(7)] (g) the program shall provide [either telephone or fax] an approval or denial of a
51 request for prior approval:
52 (i) by either:
53 (A) fax;
54 (B) telephone; or
55 (C) electronic transmission;
56 (ii) at least Monday through Friday, except for state holidays; and
57 (iii) within 24 hours after receipt of the prior approval request;

58 [(8)] (h) the program shall provide for the dispensing of at least a 72-hour supply of
59 the drug on the prior approval program:
60 (i) in an emergency situation; or
61 (ii) on weekends or state holidays;
62 [(9)] (i) the program may [not] be applied to [prevent] allow acceptable medical use of
63 a drug on prior approval for appropriate off-label indications; and
64 [(10) any drug class placed on prior approval shall receive a majority vote by the
65 board for that placement, after meeting the requirements described in Subsections (1) through
66 (10).] (j) before placing a drug class on the prior approval program, the board shall:
67 (i) determine that the requirements of Subsections (1)(a) through (i) have been met;
68 and
69 (ii) by majority vote, place the drug class on prior approval.
70 (2) The board may, only after complying with Subsections (1)(b) through (j), consider
71 the cost:
72 (a) of a drug when placing a drug on the prior approval program; and
73 (b) associated with including, or excluding a drug from the prior approval process,
74 including:
75 (i) potential side effects associated with a drug; or
76 (ii) potential hospitalizations or other complications that may occur as a result of a
77 drug's inclusion on the prior approval process.