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H.B. 381

             1     

PRESCRIPTION DRUG AMENDMENTS

             2     
2011 GENERAL SESSION

             3     
STATE OF UTAH

             4     
Chief Sponsor: Paul Ray

             5     
Senate Sponsor: ____________

             6     
             7      LONG TITLE
             8      General Description:
             9          This bill amends provisions related to drug utilization requirements for the state
             10      Medicaid program.
             11      Highlighted Provisions:
             12          This bill:
             13          .    prohibits the state Medicaid program from requiring step therapy for a drug
             14      prescribed for the treatment of pain; and
             15          .    permits a requirement for the use of a generic equivalent for a drug prescribed for
             16      the treatment of pain.
             17      Money Appropriated in this Bill:
             18          None
             19      Other Special Clauses:
             20          None
             21      Utah Code Sections Affected:
             22      AMENDS:
             23          26-18-2.4, as last amended by Laws of Utah 2009, Chapter 324
             24     
             25      Be it enacted by the Legislature of the state of Utah:
             26          Section 1. Section 26-18-2.4 is amended to read:
             27           26-18-2.4. Medicaid drug program -- Preferred drug list.


             28          (1) A Medicaid drug program developed by the department under Subsection 26-18-2.3
             29      (2)(f):
             30          (a) shall, notwithstanding Subsection 26-18-2.3 (1)(b), be based on clinical and
             31      cost-related factors which include medical necessity as determined by a provider in accordance
             32      with administrative rules established by the Drug Utilization Review Board;
             33          (b) may include therapeutic categories of drugs that may be exempted from the drug
             34      program;
             35          (c) may include placing some drugs, except the drugs described in Subsection (2), on a
             36      preferred drug list to the extent determined appropriate by the department;
             37          (d) notwithstanding the requirements of Part 2, Drug Utilization Review Board, shall
             38      immediately implement the prior authorization requirements for a non-preferred drug that is in
             39      the same therapeutic class as a drug that is:
             40          (i) on the preferred drug list on the date that this act takes effect; or
             41          (ii) added to the preferred drug list after this act takes effect; and
             42          (e) except as prohibited by Subsections 58-17b-606 (4) and (5), the prior authorization
             43      requirements established under Subsections (1)(c) and (d) shall permit a health care provider or
             44      the health care provider's agent to obtain a prior authorization override of the preferred drug list
             45      through the department's pharmacy prior authorization review process, which shall:
             46          (i) provide either telephone or fax approval or denial of the request within 24 hours of
             47      the receipt of a request that is submitted during normal business hours of Monday through
             48      Friday from 8 a.m. to 5 p.m.;
             49          (ii) provide for the dispensing of a limited supply of a requested drug as determined
             50      appropriate by the department in an emergency situation, if the request for an override is
             51      received outside of the department's normal business hours; and
             52          (iii) require the health care provider to provide the department with documentation of
             53      the medical need for the preferred drug list override in accordance with criteria established by
             54      the department in consultation with the Pharmacy and Therapeutics Committee.
             55          (2) (a) For purposes of this Subsection (2), "immunosuppressive drug":
             56          (i) means a drug that is used in immunosuppressive therapy to inhibit or prevent
             57      activity of the immune system to aid the body in preventing the rejection of transplanted organs
             58      and tissue; and


             59          (ii) does not include drugs used for the treatment of autoimmune disease or diseases
             60      that are most likely of autoimmune origin.
             61          (b) A preferred drug list developed under the provisions of this section may not
             62      include:
             63          (i) a psychotropic or anti-psychotic drug; or
             64          (ii) an immunosuppressive drug.
             65          (c) The state Medicaid program shall reimburse for a prescription for an
             66      immunosuppressive drug as written by the health care provider for a patient who has undergone
             67      an organ transplant. For purposes of Subsection 58-17b-606 (4), and with respect to patients
             68      who have undergone an organ transplant, the prescription for a particular immunosuppressive
             69      drug as written by a health care provider meets the criteria of demonstrating to the Department
             70      of Health a medical necessity for dispensing the prescribed immunosuppressive drug.
             71          (d) (i) Notwithstanding the requirements of Part 2, Drug Utilization Review Board, the
             72      state Medicaid drug program may not require the use of step therapy for immunosuppressive
             73      drugs, or drugs prescribed for the treatment of pain, without the written or oral consent of the
             74      health care provider and the patient.
             75          (ii) The prohibition of the use of step therapy for drugs prescribed for the treatment of
             76      pain does not prohibit the program from requiring a patient to first use a generically equivalent
             77      drug.
             78          (3) The department shall report to the Health and Human Services Interim Committee
             79      and to the Health and Human Services Appropriations Subcommittee prior to November 1,
             80      [2010] 2011, regarding the savings to the Medicaid program resulting from the use of the
             81      preferred drug list permitted by Subsection (1).




Legislative Review Note
    as of 2-10-11 9:52 AM


Office of Legislative Research and General Counsel


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