1 | 1 | | H.B. No. 3286 |
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2 | 2 | | |
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3 | 3 | | |
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4 | 4 | | AN ACT |
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5 | 5 | | relating to prescription drug benefits under Medicaid and the child |
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6 | 6 | | health plan program. |
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7 | 7 | | BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF TEXAS: |
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8 | 8 | | SECTION 1. Subchapter B, Chapter 531, Government Code, is |
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9 | 9 | | amended by adding Section 531.0691 to read as follows: |
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10 | 10 | | Sec. 531.0691. VENDOR DRUG PROGRAM INCLUSION. (a) The |
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11 | 11 | | commission shall ensure that the vendor drug program includes all |
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12 | 12 | | drugs and national drug codes made available under the federal |
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13 | 13 | | Medicaid Drug Rebate Program if a certificate of information form |
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14 | 14 | | to request the drug's inclusion in the vendor drug program has been |
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15 | 15 | | submitted to the commission and: |
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16 | 16 | | (1) approved by the commission; or |
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17 | 17 | | (2) subject to Subsection (b), is pending review by |
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18 | 18 | | the commission. |
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19 | 19 | | (b) On receipt of a certificate of information form to |
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20 | 20 | | request the addition to the Texas Drug Code Index of a drug that is |
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21 | 21 | | available under the federal Medicaid Drug Rebate Program, the |
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22 | 22 | | commission shall, if the commission determines that the drug is |
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23 | 23 | | appropriate for dispensing through an outpatient pharmacy, |
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24 | 24 | | provisionally make the drug available under the vendor drug program |
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25 | 25 | | for a period that expires on the earlier of: |
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26 | 26 | | (1) the 90th day after the date the form was submitted; |
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27 | 27 | | or |
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28 | 28 | | (2) the date the commission makes a determination |
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29 | 29 | | regarding whether to approve or deny the drug's inclusion on the |
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30 | 30 | | vendor drug program formulary. |
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31 | 31 | | (c) The commission shall: |
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32 | 32 | | (1) denote the provisional availability of a drug |
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33 | 33 | | under this section; and |
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34 | 34 | | (2) remove a drug made provisionally available under |
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35 | 35 | | the vendor drug program: |
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36 | 36 | | (A) on the expiration of the 90-day period |
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37 | 37 | | prescribed by Subsection (b)(1); or |
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38 | 38 | | (B) if applicable, on the date the commission |
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39 | 39 | | denies the drug's inclusion on the vendor drug program formulary. |
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40 | 40 | | SECTION 2. Chapter 533, Government Code, is amended by |
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41 | 41 | | adding Subchapter C to read as follows: |
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42 | 42 | | SUBCHAPTER C. PRESCRIPTION DRUG BENEFITS UNDER CERTAIN OUTPATIENT |
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43 | 43 | | PHARMACY BENEFIT PLANS |
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44 | 44 | | Sec. 533.071. PREFERRED DRUG LIST EXCEPTIONS. (a) The |
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45 | 45 | | commission shall adopt rules allowing exceptions to the preferred |
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46 | 46 | | drug list if: |
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47 | 47 | | (1) the drug required under the preferred drug list: |
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48 | 48 | | (A) is contraindicated; |
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49 | 49 | | (B) will likely cause an adverse reaction in or |
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50 | 50 | | physical or mental harm to the recipient; or |
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51 | 51 | | (C) is expected to be ineffective based on the |
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52 | 52 | | known clinical characteristics of the recipient and the known |
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53 | 53 | | characteristics of the prescription drug regimen; |
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54 | 54 | | (2) the recipient previously discontinued taking the |
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55 | 55 | | preferred drug at any point in the recipient's clinical history and |
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56 | 56 | | for any length of time because the drug: |
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57 | 57 | | (A) was not effective; |
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58 | 58 | | (B) had a diminished effect; or |
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59 | 59 | | (C) resulted in an adverse event; |
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60 | 60 | | (3) the recipient was prescribed and is taking a |
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61 | 61 | | nonpreferred drug in the antidepressant or antipsychotic drug class |
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62 | 62 | | and the recipient: |
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63 | 63 | | (A) was prescribed the nonpreferred drug before |
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64 | 64 | | being discharged from an inpatient facility; |
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65 | 65 | | (B) is stable on the nonpreferred drug; and |
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66 | 66 | | (C) is at risk of experiencing complications from |
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67 | 67 | | switching from the nonpreferred drug to another drug; or |
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68 | 68 | | (4) the preferred drug is not available for reasons |
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69 | 69 | | outside of the Medicaid managed care organization's control, |
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70 | 70 | | including because: |
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71 | 71 | | (A) the drug is in short supply according to the |
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72 | 72 | | Food and Drug Administration Drug Shortages Database; or |
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73 | 73 | | (B) the drug's manufacturer has placed the drug |
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74 | 74 | | on backorder or allocation. |
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75 | 75 | | (b) An exception provided under this section does not |
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76 | 76 | | subject the Medicaid managed care plan to liquidated damages for |
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77 | 77 | | failing to comply with the preferred drug list. |
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78 | 78 | | SECTION 3. Section 531.072, Government Code, is amended by |
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79 | 79 | | adding Subsections (b-3), (g), and (h) to read as follows: |
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80 | 80 | | (b-3) Notwithstanding Subsection (b), the preferred drug |
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81 | 81 | | lists must contain all therapeutic equivalents for a generic drug |
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82 | 82 | | on the preferred drug list. |
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83 | 83 | | (g) The commission shall develop an expedited review |
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84 | 84 | | process to consider requests from managed care organizations and |
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85 | 85 | | providers to add drugs to the preferred drug list. |
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86 | 86 | | (h) The commission shall grant temporary non-preferred |
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87 | 87 | | status to new drugs that are available but have not yet been |
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88 | 88 | | reviewed by the drug utilization review board and establish |
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89 | 89 | | criteria for authorizing drugs with temporary non-preferred |
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90 | 90 | | status. |
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91 | 91 | | SECTION 4. Section 531.073(b), Government Code, is amended |
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92 | 92 | | to read as follows: |
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93 | 93 | | (b) The commission shall establish procedures for the prior |
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94 | 94 | | authorization requirement under the Medicaid vendor drug program to |
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95 | 95 | | ensure that the requirements of 42 U.S.C. Section 1396r-8(d)(5) and |
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96 | 96 | | its subsequent amendments are met. Specifically, the procedures |
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97 | 97 | | must ensure that: |
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98 | 98 | | (1) [a prior authorization requirement is not imposed |
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99 | 99 | | for a drug before the drug has been considered at a meeting of the |
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100 | 100 | | Drug Utilization Review Board under Section 531.0736; |
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101 | 101 | | [(2)] there will be a response to a request for prior |
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102 | 102 | | authorization by telephone or other telecommunications device |
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103 | 103 | | within 24 hours after receipt of a request for prior authorization; |
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104 | 104 | | and |
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105 | 105 | | (2) [(3)] a 72-hour supply of the drug prescribed will |
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106 | 106 | | be provided in an emergency or if the commission does not provide a |
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107 | 107 | | response within the time required by Subdivision (1) [(2)]. |
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108 | 108 | | SECTION 5. Sections 531.0736(c) and (d), Government Code, |
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109 | 109 | | are amended to read as follows: |
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110 | 110 | | (c) The executive commissioner shall determine the |
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111 | 111 | | composition of the board, which must: |
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112 | 112 | | (1) comply with applicable federal law, including 42 |
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113 | 113 | | C.F.R. Section 456.716; |
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114 | 114 | | (2) include three [two] representatives of managed |
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115 | 115 | | care organizations [as nonvoting members], all [one] of whom must |
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116 | 116 | | be physicians or pharmacists [a physician and one of whom must be a |
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117 | 117 | | pharmacist]; |
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118 | 118 | | (3) include at least 17 physicians and pharmacists |
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119 | 119 | | who: |
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120 | 120 | | (A) provide services across the entire |
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121 | 121 | | population of Medicaid recipients and represent different |
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122 | 122 | | specialties, including at least one of each of the following types |
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123 | 123 | | of physicians: |
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124 | 124 | | (i) a pediatrician; |
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125 | 125 | | (ii) a primary care physician; |
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126 | 126 | | (iii) an obstetrician and gynecologist; |
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127 | 127 | | (iv) a child and adolescent psychiatrist; |
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128 | 128 | | and |
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129 | 129 | | (v) an adult psychiatrist; and |
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130 | 130 | | (B) have experience in either developing or |
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131 | 131 | | practicing under a preferred drug list; and |
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132 | 132 | | (4) include a consumer advocate who represents |
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133 | 133 | | Medicaid recipients. |
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134 | 134 | | (d) Notwithstanding any other law, members [Members] |
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135 | 135 | | appointed under Subsection (c)(2) may attend quarterly and other |
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136 | 136 | | regularly scheduled meetings, but may not: |
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137 | 137 | | (1) attend portions of the executive sessions in which |
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138 | 138 | | confidential drug pricing information is shared; or |
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139 | 139 | | (2) access confidential drug pricing information. |
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140 | 140 | | SECTION 6. If before implementing any provision of this Act |
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141 | 141 | | a state agency determines that a waiver or authorization from a |
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142 | 142 | | federal agency is necessary for implementation of that provision, |
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143 | 143 | | the agency affected by the provision shall request the waiver or |
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144 | 144 | | authorization and may delay implementing that provision until the |
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145 | 145 | | waiver or authorization is granted. |
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146 | 146 | | SECTION 7. This Act takes effect September 1, 2023. |
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147 | 147 | | ______________________________ ______________________________ |
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148 | 148 | | President of the Senate Speaker of the House |
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149 | 149 | | I certify that H.B. No. 3286 was passed by the House on May 5, |
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150 | 150 | | 2023, by the following vote: Yeas 142, Nays 0, 1 present, not |
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151 | 151 | | voting; and that the House concurred in Senate amendments to H.B. |
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152 | 152 | | No. 3286 on May 25, 2023, by the following vote: Yeas 139, Nays 0, |
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153 | 153 | | 1 present, not voting. |
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154 | 154 | | ______________________________ |
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155 | 155 | | Chief Clerk of the House |
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156 | 156 | | I certify that H.B. No. 3286 was passed by the Senate, with |
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157 | 157 | | amendments, on May 21, 2023, by the following vote: Yeas 31, Nays |
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158 | 158 | | 0. |
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159 | 159 | | ______________________________ |
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160 | 160 | | Secretary of the Senate |
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161 | 161 | | APPROVED: __________________ |
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162 | 162 | | Date |
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163 | 163 | | __________________ |
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164 | 164 | | Governor |
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