Florida Senate - 2022                                    SB 1636
       
       
        
       By Senator Cruz
       
       
       
       
       
       18-01326-22                                           20221636__
    1                        A bill to be entitled                      
    2         An act relating to antiretroviral drugs; creating s.
    3         465.1861, F.S.; defining terms; authorizing
    4         pharmacists to order and dispense HIV preexposure and
    5         postexposure prophylaxis drugs without a prescription
    6         under certain circumstances; requiring pharmacists to
    7         complete specified training before ordering or
    8         dispensing such drugs without a prescription;
    9         authorizing pharmacists to order and dispense a
   10         specified supply of preexposure prophylaxis or a full
   11         course of postexposure prophylaxis, as applicable, to
   12         patients without prescriptions if certain conditions
   13         are met; authorizing the Board of Pharmacy, in
   14         consultation with the Board of Medicine, the
   15         Department of Health, and other relevant stakeholders,
   16         to adopt rules; creating s. 627.4291, F.S.; defining
   17         terms; prohibiting certain health insurers from
   18         requiring prior authorization or step-therapy
   19         protocols for certain antiretroviral drugs; providing
   20         an exception; prohibiting health insurers from
   21         refusing to cover, or allowing pharmacy benefit
   22         managers to refuse to cover, preexposure or
   23         postexposure prophylaxis drugs under certain
   24         circumstances; providing an effective date.
   25          
   26  Be It Enacted by the Legislature of the State of Florida:
   27  
   28         Section 1. Section 465.1861, Florida Statutes, is created
   29  to read:
   30         465.1861Antiretroviral drugs.—
   31         (1)As used in this section, the term:
   32         (a)“HIV” means the human immunodeficiency virus.
   33         (b)“Postexposure prophylaxis” means any of the following:
   34         1.A fixed-dose combination of 300 milligrams of tenofovir
   35  disoproxil fumarate with 200 milligrams of emtricitabine, taken
   36  once daily, in combination with either 400 milligrams of
   37  raltegravir, taken twice daily, or 50 milligrams of
   38  dolutegravir, taken once daily.
   39         2.A fixed-dose combination of 300 milligrams of tenofovir
   40  disoproxil fumarate with 200 milligrams emtricitabine, taken
   41  once daily, in combination with a fixed-dose combination of 800
   42  milligrams of darunavir and 100 milligrams of ritonavir, taken
   43  once daily.
   44         3.Any other drug or drug combination deemed by the board
   45  to meet the same clinical eligibility recommendations of the
   46  United States Centers for Disease Control and Prevention
   47  guidelines for antiretroviral postexposure prophylaxis after
   48  sexual, injection drug use, or other nonoccupational exposure to
   49  HIV.
   50         (c)“Preexposure prophylaxis” means a fixed-dose
   51  combination of 300 milligrams of tenofovir disoproxil fumarate
   52  with 200 milligrams of emtricitabine, or another drug or
   53  combination of drugs which the board deems to meet the clinical
   54  eligibility recommendations of the United States Centers for
   55  Disease Control and Prevention guidelines for preexposure
   56  prophylaxis for the prevention of HIV infection.
   57         (2)Notwithstanding any other law, a pharmacist may order
   58  or dispense an HIV preexposure or postexposure prophylaxis
   59  without a prescription in accordance with this section. Before
   60  ordering or dispensing such medicinal drug, a pharmacist must
   61  first complete a training program approved by the board which
   62  includes all of the following:
   63         (a)Training in the use of preexposure and postexposure
   64  prophylaxis.
   65         (b)Information about any financial assistance programs for
   66  preexposure and postexposure prophylaxis.
   67         (c)Any other topic the board deems appropriate. The board
   68  shall consult with the Board of Medicine, the department, and
   69  other relevant stakeholders when making such determinations.
   70         (3)A pharmacist may order or dispense up to two 30-day
   71  supplies of preexposure prophylaxis to a patient without a
   72  prescription if all of the following conditions are met:
   73         (a)The patient is HIV negative, as documented by a
   74  negative HIV test result obtained within the preceding 7 days
   75  from an HIV antigen or antibody test, an antibody-only test, or
   76  a rapid, point-of-care fingerstick blood test approved by the
   77  United States Food and Drug Administration. If the patient does
   78  not provide evidence of a negative HIV test in accordance with
   79  this paragraph, the pharmacist must order an HIV test. If the
   80  test results are not transmitted directly to the pharmacist, the
   81  pharmacist must verify the test results to his or her
   82  satisfaction. If the patient tests positive for HIV infection,
   83  the pharmacist or person administering the test must direct the
   84  patient to a primary care provider and provide to the patient a
   85  list of available providers and clinics in the region.
   86         (b)The patient does not report any signs or symptoms of
   87  acute HIV infection, as indicated on a self-reported checklist
   88  of acute HIV infection signs and symptoms provided by the
   89  pharmacist.
   90         (c)The patient does not report taking any contraindicated
   91  medications.
   92         (d)The pharmacist has not ordered two 30-day supplies of
   93  preexposure prophylaxis for the patient without a prescription
   94  in the preceding 2-year period.
   95         (e)The pharmacist provides counseling to the patient on
   96  the ongoing use of preexposure prophylaxis, to include, at a
   97  minimum, education about side effects, safety during pregnancy
   98  and breastfeeding, adherence to recommended dosing, and the
   99  importance of timely testing and treatment, as applicable, for
  100  HIV, renal function, hepatitis B, hepatitis C, sexually
  101  transmitted diseases, and pregnancy for individuals of child
  102  bearing capacity. A pharmacist may not allow a patient to waive
  103  this counseling.
  104         (f)The pharmacist informs the patient that he or she must
  105  be seen by a primary care provider to receive subsequent
  106  prescriptions for preexposure prophylaxis and that a pharmacist
  107  may order only up to two 30-day supplies without a prescription
  108  in one 2-year period for each patient.
  109         (g)The pharmacist documents and maintains in the pharmacy
  110  records system a record of each 30-day supply of preexposure
  111  prophylaxis ordered or dispensed to the patient without a
  112  prescription. The pharmacist or pharmacy must maintain such
  113  records for at least 4 years.
  114         (h)The pharmacist notifies the patient’s primary care
  115  provider that the pharmacist ordered or dispensed preexposure
  116  prophylaxis to the patient in accordance with this section. If
  117  the patient does not have a primary care provider or refuses
  118  consent to notify the patient’s primary care provider, the
  119  pharmacist must provide the patient a list of physicians,
  120  surgeons, clinics, or other health care service providers to
  121  contact regarding ongoing care for preexposure prophylaxis.
  122         (4)A pharmacist may order or dispense a full course of
  123  postexposure prophylaxis to a patient without a prescription if
  124  all of the following conditions are met:
  125         (a)The pharmacist screens the patient and determines that
  126  the exposure occurred within the previous 72 hours and the
  127  patient otherwise meets the clinical criteria for postexposure
  128  prophylaxis consistent with the applicable guidelines issued by
  129  the United States Centers for Disease Control and Prevention.
  130         (b)The pharmacist provides to the patient HIV testing that
  131  is deemed a waived test under the federal Clinical Laboratory
  132  Improvement Amendments of 1988 or the patient is willing to
  133  undergo HIV testing in accordance with s. 381.004. If the
  134  patient refuses to undergo HIV testing but is otherwise eligible
  135  for postexposure prophylaxis under this section, the pharmacist
  136  may order or dispense postexposure prophylaxis to the patient.
  137         (c)The pharmacist provides counseling to the patient on
  138  the use of postexposure prophylaxis, consistent with guidelines
  139  issued by the United States Centers for Disease Control and
  140  Prevention, to include, at a minimum, education about side
  141  effects, safety during pregnancy and breastfeeding, adherence to
  142  recommended dosing, and the importance of timely testing and
  143  treatment, as applicable, for HIV and sexually transmitted
  144  diseases. The pharmacist must also inform the patient of the
  145  availability of preexposure prophylaxis for persons who are at
  146  substantial risk of acquiring HIV. A pharmacist may not allow a
  147  patient to waive this counseling.
  148         (d)The pharmacist notifies the patient’s primary care
  149  provider that the pharmacist ordered or dispensed the
  150  postexposure prophylaxis in accordance with this section. If the
  151  patient does not have a primary care provider or refuses consent
  152  to notify the patient’s primary care provider, the pharmacist
  153  must provide the patient a list of physicians, surgeons,
  154  clinics, or other health care service providers to contact
  155  regarding follow-up care for postexposure prophylaxis.
  156         (5)The board, in consultation with the Board of Medicine,
  157  the department, and other relevant stakeholders, may adopt rules
  158  to implement this section.
  159         Section 2. Section 627.4291, Florida Statutes, is created
  160  to read:
  161         627.4291 Coverage of antiretroviral drugs.—
  162         (1)As used in this section, the term:
  163         (a)“AIDS” means acquired immune deficiency syndrome.
  164         (b)“Health insurer” means an authorized insurer offering
  165  health insurance as defined in s. 624.603, a managed care plan
  166  as defined in s. 409.962, or a health maintenance organization
  167  as defined in s. 641.19(12).
  168         (c)“HIV” means the human immunodeficiency virus.
  169         (d)“Insured” means a person who is covered under a policy
  170  delivered or issued for delivery in this state by a health
  171  insurer.
  172         (e)“Prior authorization” means a process by which an
  173  insured does not receive coverage for a particular prescription
  174  drug until the insured’s health care provider submits to the
  175  insured’s health insurer a request for approval and the health
  176  insurer determines that the prescription drug is covered by the
  177  insured’s policy.
  178         (f)“Step-therapy protocol” means a protocol or program
  179  that establishes the specific sequence in which prescription
  180  drugs determined as medically appropriate for an insured for a
  181  specified medical condition are covered by a policy.
  182         (2)Notwithstanding any other law, a health insurer
  183  providing major medical or similar comprehensive coverage or
  184  benefits to residents in this state on or after July 1, 2022,
  185  may not require prior authorization or a step-therapy protocol
  186  under the policy for a covered antiretroviral drug that is
  187  medically necessary for the prevention of HIV or AIDS,
  188  including, but not limited to, preexposure and postexposure
  189  prophylaxis, except as provided in subsection (3).
  190         (3)If the United States Food and Drug Administration has
  191  approved one or more therapeutic equivalents of a drug, device,
  192  or product for the prevention of HIV or AIDS, a health insurer
  193  is not required to cover all of the therapeutically equivalent
  194  versions without prior authorization or step-therapy protocols
  195  if at least one therapeutically equivalent version is covered
  196  without prior authorization or a step-therapy protocol.
  197         (4)A health insurer may not refuse to cover, or allow a
  198  pharmacy benefit manager to refuse to cover, preexposure or
  199  postexposure prophylaxis solely on the basis that it was ordered
  200  or dispensed by a licensed pharmacist in accordance with s.
  201  465.1861.
  202         Section 3. This act shall take effect July 1, 2022.