Florida 2025 2025 Regular Session

Florida House Bill H0149 Introduced / Bill

Filed 01/14/2025

                       
 
HB 149   	2025 
 
 
 
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A bill to be entitled 1 
An act relating to claims for adverse reactions to 2 
vaccines and drugs under the Medicaid and medically 3 
needy programs; providing a short title; creating s. 4 
409.9043, F.S.; requiring the Agency for Health Care 5 
Administration to expedite the review and payment 6 
process for claims related to adverse reactions to 7 
vaccines, immunizing agents, and emergency 8 
countermeasure drugs under the Medicaid and Florida 9 
Medicaid medically needy programs; requiring the 10 
agency to publish certain information on its website; 11 
requiring the agency to seek federal approval for a 12 
specified purpose under certain circumstances and to 13 
adopt rules; providing an effective date. 14 
 15 
Be It Enacted by the Legislature of the State of Florida: 16 
 17 
 Section 1. This act may be cited as the "Cody's Law: 18 
Florida No Vaccine-Injured Patient Left Behind." 19 
 Section 2.  Section 409.9043, Florida Statutes, is created 20 
to read: 21 
 409.9043  Claims for advers e reactions to vaccines, 22 
immunizing agents, and emergency countermeasure drugs under the 23 
Medicaid and medically needy programs. — 24 
 (1)  The Agency for Health Care Administration shall, under 25     
 
HB 149   	2025 
 
 
 
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the Medicaid program and the Florida Medicaid medically needy 26 
program, expedite the review and payment process for a claim in 27 
which the physician has diagnosed a severe, debilitating, life -28 
threatening, or lifelong injury caused by the administration of 29 
a vaccine or other immunizing agent or an adverse reaction to an 30 
emergency countermeasure drug if the vaccine, immunizing agent, 31 
or emergency countermeasure drug is recommended by the United 32 
States Food and Drug Administration or the Department of Health 33 
of this state. 34 
 (2)(a)  The agency shall publish on its website: 35 
 1.  A list of medical conditions related to a vaccine, 36 
immunizing agent, or emergency countermeasure drug for the 37 
expedited claims described in subsection (1). 38 
 2.  A list of potential adverse reactions found in the 39 
manufacturer's product insert of a vaccine, immunizing agent, or 40 
drug which are deemed critical, severe, or temporarily or 41 
permanently disabling by the agency or the physicians who make 42 
the diagnoses in the claims described in subsection (1). 43 
 3.  Any new medical condition related to a vaccine, 44 
immunizing agent, or emergency countermeasure drug which arises. 45 
 4.  Any future vaccine, immunizing agent, or emergency 46 
countermeasure drug or treatment deemed appropriate by the 47 
agency or by the physicians who make the diagnoses in the claims 48 
described in subsection (1). 49 
 (b)  The agency shall also inform its website visitors of 50     
 
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the content of this section, including the requirements under 51 
subsection (1), so that physicians or other health care 52 
providers may best serve patients who have urgent medical needs 53 
as a result of an injury caused by the administration of a 54 
vaccine or other immunizing agent or an adverse reaction to an 55 
emergency countermeasure drug. 56 
 (3)  The agency shall seek federal approval, if necessary, 57 
to implement this section and shall adopt ru les to administer 58 
this section. 59 
 Section 3. This act shall take effect July 1, 2025. 60