AB1011: Bill Text

AB1011,1 Section 1 . 20.435 (1) (ck) of the statutes is created to read:

AB1011,2,4 20.435 (1) (ck) Epinephrine for ambulances. A sum sufficient for the department of health services to purchase and provide epinephrine for ambulances under s. 256.158.

AB1011,2 Section 2 . 102.425 (1) (c) of the statutes is amended to read:

AB1011,2,7 102.425 (1) (c) “Drug product equivalent" has the meaning given in s. 450.13 (1e) (a).

AB1011,3 Section 3. 256.158 of the statutes is created to read:

AB1011,2,9 256.158 Epinephrine for ambulances. (1) In this section:

AB1011,2,11 (a) “Ambulance service provider” means an ambulance service provider that is a public agency, volunteer fire department, or nonprofit corporation.

AB1011,2,13 (b) “Draw-up epinephrine” means epinephrine that is administered intramuscularly using a needle and syringe and drawn up from a vial or ampule.

AB1011,2,15 (c) “Draw-up epinephrine kit” means a single-use vial or ampule of draw-up epinephrine and a syringe for administration to a patient.

AB1011,3,8 (2) From the appropriation under s. 20.435 (1) (ck), the department shall purchase and provide to ambulance service providers without charge a set of 2 epinephrine auto-injectors or a set of 2 draw-up epinephrine kits for each ambulance operating in the state. On an ongoing basis, the department shall, upon request from an ambulance service provider, provide to the ambulance service provider a replacement set of 2 epinephrine auto-injectors or a set of 2 draw-up epinephrine kits. The department shall allow the ambulance service provider to choose between epinephrine auto-injectors and draw-up epinephrine kits.

AB1011,4 Section 4 . 450.11 (4g) (a) 2. of the statutes is amended to read:

AB1011,3,11 450.11 (4g) (a) 2. “Drug product equivalent" has the meaning given in s. 450.13 (1e) (a).

AB1011,5 Section 5. 450.13 (title) of the statutes is amended to read:

AB1011,3,15 450.13 (title) Using drug product equivalent in dispensing prescriptions; therapeutic exchange for drug products prescribed to counteract anaphylaxis.

AB1011,6 Section 6. 450.13 (1e) of the statutes is renumbered 450.13 (1e) (intro.) and amended to read:

AB1011,3,18 450.13 (1e) Definition Definitions. (intro.) In this section, “drug:

AB1011,3,23 (a) “Drug product equivalent" means a drug product that is designated the therapeutic equivalent of another drug product by the federal food and drug administration as set forth in the latest edition of or supplement to the federal food and drug administration's Approved Drug Products with Therapeutic Equivalence Evaluations.

AB1011,7 Section 7. 450.13 (1e) (b) of the statutes is created to read:

AB1011,4,2 450.13 (1e) (b) “Therapeutic class” means a group of similar drug products that are used to treat a specific condition.

AB1011,8 Section 8. 450.13 (5m) of the statutes is created to read:

AB1011,4,9 450.13 (5m) Therapeutic interchange for drugs counteracting anaphylaxis. (a) Notwithstanding subs. (1s) to (4), for a drug product prescribed to counteract anaphylaxis, a pharmacist may substitute a drug product with another drug product in the same therapeutic class that would, in the opinion of the pharmacist, have a substantially equivalent therapeutic effect even though the substitute drug product is not a drug product equivalent, provided all of the following conditions are met:

AB1011,4,14 1. A prescribing practitioner has not indicated, by writing on the face of the prescription order or, with respect to a prescription order transmitted electronically, by designating in electronic format that a substitution of the drug product prescribed may not be made under this subsection. If such indication is made, the pharmacist shall dispense the prescription with the specific drug product prescribed.

AB1011,4,17 2. The drug product substitution is intended to ensure formulary compliance with the consumer's health insurance plan or, in the case of a consumer without insurance, to lower the cost to the patient while maintaining safety.

AB1011,4,20 3. The consumer opts in to the drug product substitution, and the pharmacist clearly informs the consumer of the differences in the drug products and specifies that the consumer may refuse the substitution.

AB1011,4,24 (b) If a pharmacist substitutes a drug product prescribed to counteract anaphylaxis under this subsection, the pharmacist must ensure that the prescriber's directions and quantity are modified to allow for equivalent dispensing to what was originally prescribed.

AB1011,5,3 (c) Within 5 business days after the dispensing of a drug product substitute under this subsection, the dispensing pharmacist or the pharmacist's designee shall do one of the following:

AB1011,5,9 1. Make an entry of the specific drug product provided to the patient, including the name of the product and the manufacturer. Entry into an electronic records system as described in this paragraph is presumed to provide notice to the prescribing practitioner. The communication shall be conveyed by making an entry that is electronically accessible to the prescribing practitioner through one of the following:

AB1011,5,10 a. An interoperable electronic medical records system.

AB1011,5,11 b. An electronic prescribing technology.

AB1011,5,12 c. A pharmacist benefit management system.

AB1011,5,13 d. A pharmacy record.

AB1011,5,19 2. If a pharmacist is unable to make an entry as provided in subd. 1., communicate the drug product substitute dispensed to the prescribing practitioner using facsimile, telephone, electronic transmission, or another prevailing means, except that communication under this paragraph is not required if a refill of the drug product is not changed from the product dispensed on the prior filling of the prescription.

AB1011,6,4 (d) Notwithstanding pars. (a) to (c), a pharmacist who dispenses a drug product prescribed for a patient in a hospital may, for a drug product prescribed to counteract anaphylaxis, substitute a drug product with another drug product in the same therapeutic class that would in the opinion of the pharmacist, have a substantially equivalent therapeutic effect even though the substitute drug product is not a drug product equivalent, if the pharmacist dispenses the drug product substitute in accordance with written guidelines or procedures previously established by a pharmacy and therapeutics committee of the hospital and approved by the hospital's medical staff and use of the drug product substitute has been approved for a patient during the period of the patient's stay within the hospital by any of the following:

AB1011,6,5 1. The patient's individual physician.

AB1011,6,8 2. The patient's advanced practice nurse prescriber, if the advanced practice nurse prescriber has entered into a written agreement to collaborate with a physician.

AB1011,6,9 3. The patient's physician assistant.

AB1011,6,10 (End)