Bill Text For HB2801 - Engrossed

 1|ENGROSSED HOUSE                                                        |
  |BILL NO. 2801                        By: Marti of the House            |
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  |                                         Stanley of the Senate         |
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 7|       [ antipsychotic drugs - vendor drug program                     |
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 8|         disorders - prior authorization - effective date ]            |
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11|BE IT ENACTED BY THE PEOPLE OF THE STATE OF OKLAHOMA:                  |
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12|    SECTION 1.     AMENDATORY     56 O.S. 2021, Section 204, is        |
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13|amended to read as follows:                                            |
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14|    Section 204.  A.  Except as otherwise provided, the Oklahoma       |
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15|Health Care Authority shall be authorized and directed to establish    |
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16|a vendor drug program to provide any drugs that have been approved     |
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17|and designated as safe and effective by the federal Food and Drug      |
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18|Administration, and that are prescribed by a licensed medical,         |
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19|dental, podiatric, or osteopathic practitioner for eligible            |
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20|recipients of assistance payments suffering from painful or            |
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21|life-endangering diseases or other persons who are suffering from a    |
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22|catastrophic illness.                                                  |
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23|    B.  The Authority shall, in accordance with federal law, not be    |
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24|obligated to cover any outpatient drugs of a manufacturer which has    |
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arsid16532362 ENGR. H. B. NO. 2801                                 Page 1
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 1|not entered into or which does not have in effect a rebate agreement   |
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 2|with the Secretary of Health and Human Services on behalf of the       |
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 3|state.                                                                 |
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 4|    C.  Such program shall, to the fullest extent possible, be         |
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 5|established and maintained in conjunction with existing federal        |
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 6|programs of prescribed drugs so as to earn the maximum of federal      |
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 7|financial participation.  Exempt from the provisions of this section   |
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 8|are the following drugs or classes of drugs, or their medical uses:    |
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 9|    1.  Agents when used for anorexia or weight gain;                  |
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10|    2.  Agents when used to promote fertility;                         |
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11|    3.  Agents when used for cosmetic purposes or hair growth;         |
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12|    4.  Agents when used for the symptomatic relief of coughs and      |
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13|colds;                                                                 |
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14|    5.  Agents when used to promote smoking cessation;                 |
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15|    6.  Prescription vitamins and mineral products, except prenatal    |
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16|vitamins and fluoride preparations;                                    |
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17|    7.  Nonprescription drugs;                                         |
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18|    8.  Covered outpatient drugs when the manufacturer seeks to        |
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19|require as a condition of sale that associated tests or monitoring     |
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20|services be purchased exclusively from the manufacturer or its         |
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21|designee;                                                              |
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22|    9.  Drugs described in paragraph 3 of subsection c of Section      |
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23|107 of the Drug Amendments of 1962, 21 U.S.C., Section 107(c)(3),      |
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24|and identical, similar or related drugs, within the meaning of         |
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arsid16532362 ENGR. H. B. NO. 2801                                 Page 2
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 1|paragraph 1 of subsection b of Section 310.6 of Title 21 of the Code   |
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 2|of Federal Regulations;                                                |
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 3|    10.  Barbiturates; or                                              |
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 4|    11.  Benzodiazepines;                                              |
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 5|provided, however, the Authority shall be authorized to include        |
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 6|specific drugs within these categories for reimbursement based upon    |
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 7|specific medical need.                                                 |
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 8|    D.  The Authority shall be authorized to establish a prospective   |
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 9|drug utilization review program for the H2 Antagonists; provided       |
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10|that such limitations are in compliance with federal Food and Drug     |
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11|Administration Agency-approved product labeling.                       |
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12|    E.  The Authority shall approve a prior authorization request      |
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13|for any Food and Drug Administration approved atypical antipsychotic   |
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14|that is not on the preferred drug list for the treatment and           |
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15|prevention of mood disorders with psychotic symptoms including         |
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16|bipolar disorders, schizophrenia, and schizotypal or delusion          |
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17|disorders.  Medications included under this section shall be           |
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18|available at parity to other branded medications in the same class.    |
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19|Approval shall be based on patient's claims history or health care     |
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20|provider attestation of one of the following conditions for the        |
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21|Medicaid client:                                                       |
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22|    1.  A trial and failure of any preferred atypical antipsychotic    |
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23|in the preceding three hundred sixty-five (365) days; or               |
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arsid16532362 ENGR. H. B. NO. 2801                                 Page 3
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 1|    2.  The patient is stable on an atypical antipsychotic that is     |
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 2|not included on the preferred drug list.                               |
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 3|    SECTION 2.  This act shall become effective November 1, 2025.      |
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 4|    Passed the House of Representatives the 10th day of March, 2025.   |
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  |                                     Presiding Officer of the House    |
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  |    Passed the Senate the ___ day of __________, 2025.                 |
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11|                                    Presiding Officer of the Senate    |
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arsid16532362 ENGR. H. B. NO. 2801                                 Page 4
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