Bills · 2019-2020 Regular Session
Relating to: epinephrine for ambulances, therapeutic interchange for drug products prescribed to counteract anaphylaxis, and making an appropriation. (FE)
Drugs Health services department of — Health Medical service Pharmacy
- Introduced, stopped here
- Passes Assembly, not reached
- Passes Senate, not reached
- Governor signs, not reached
- Law, not reached
Unfamiliar terms? Glossary
What this bill does
Plain-language analysis by the nonpartisan Legislative Reference Bureau
This bill requires that the Department of Health Services purchase and provide
to ambulance service providers without charge a set of two epinephrine
auto-injectors or a set of two draw-up epinephrine kits for each ambulance
operating in the state. Under the bill, an ambulance service provider means an
ambulance service provider that is a public agency, volunteer fire department, or
nonprofit corporation. The bill also requires that, on an ongoing basis, DHS must,
upon request, provide replacement sets to ambulance service providers.
Also, for drug products prescribed to counteract anaphylaxis, this bill allows,
if certain conditions are met, a pharmacist to 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. The bill also provides that
a pharmacist who dispenses a drug product for a patient in a hospital may, for a drug
product prescribed to counteract anaphylaxis, under the same conditions applicable
for drug product equivalents under current law, 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. Current law defines a
“drug product equivalent” as 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
, commonly known as the Orange Book. As with substitution of drug
product equivalents under current law, the therapeutic class substitutions allowed
under the bill do not apply to biological products.
Sponsors
Full history
- Mar 20, 2020 · Assembly
Introduced by Representatives Vining, Spreitzer, Anderson, Brostoff, Cabrera, Fields, Hebl, Kolste, Neubauer, Ohnstad, Shankland, Sinicki, Stubbs, Subeck and Zamarripa; cosponsored by Senators Hansen, Jacque, Larson, Ringhand, Schachtner, Smith, L. Taylor and Wirch
- Mar 20, 2020 · Assembly
Read first time and referred to Committee on Health
- Apr 1, 2020 · Assembly
Failed to pass pursuant to Senate Joint Resolution 1