Considerations for the US health-system pharmacist in a world of biosimilars
As numerous biosimilar products are forecast to enter the US market in the coming years, health-system pharmacists will be faced with novel challenges while incorporating them into clinical practice. The current regulatory approval framework and guidance from the US Food and Drug Administration do n...
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2020-02-01
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doaj-860f255fe4f44e449a6b67b5a822e63e2020-11-25T03:05:53ZengBioExcel Publishing LtdDrugs in Context1740-43982020-02-0191710.7573/dic.2019-12-1Considerations for the US health-system pharmacist in a world of biosimilarsAndrea ZlatkusTodd BixbyKavitha GoyalAs numerous biosimilar products are forecast to enter the US market in the coming years, health-system pharmacists will be faced with novel challenges while incorporating them into clinical practice. The current regulatory approval framework and guidance from the US Food and Drug Administration do not address many real-world scenarios that pharmacists will encounter. We provide an overview of the evolving healthcare landscape shaped by the entry of multiple biosimilars, including for a given reference product, and their impact on the healthsystem pharmacist with respect to formulary assessment, implementation, and education of various health-system stakeholders, including patients.https://www.drugsincontext.com/considerations-for-the-us-health-system-pharmacist-in-a-world-of-biosimilars/biologicsbiosimilarsclinical pharmacistsdrug substitutionpharmacoeconomicsrheumatology |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Andrea Zlatkus Todd Bixby Kavitha Goyal |
spellingShingle |
Andrea Zlatkus Todd Bixby Kavitha Goyal Considerations for the US health-system pharmacist in a world of biosimilars Drugs in Context biologics biosimilars clinical pharmacists drug substitution pharmacoeconomics rheumatology |
author_facet |
Andrea Zlatkus Todd Bixby Kavitha Goyal |
author_sort |
Andrea Zlatkus |
title |
Considerations for the US health-system pharmacist in a world of biosimilars |
title_short |
Considerations for the US health-system pharmacist in a world of biosimilars |
title_full |
Considerations for the US health-system pharmacist in a world of biosimilars |
title_fullStr |
Considerations for the US health-system pharmacist in a world of biosimilars |
title_full_unstemmed |
Considerations for the US health-system pharmacist in a world of biosimilars |
title_sort |
considerations for the us health-system pharmacist in a world of biosimilars |
publisher |
BioExcel Publishing Ltd |
series |
Drugs in Context |
issn |
1740-4398 |
publishDate |
2020-02-01 |
description |
As numerous biosimilar products are forecast to enter the US market in the coming years, health-system pharmacists will be faced with novel challenges while incorporating them into clinical practice. The current regulatory approval framework and guidance from the US Food and Drug Administration do not address many real-world scenarios that pharmacists will encounter. We provide an overview of the evolving healthcare landscape shaped by the entry of multiple biosimilars, including for a given reference product, and their impact on the healthsystem pharmacist with respect to formulary assessment, implementation, and education of various health-system stakeholders, including patients. |
topic |
biologics biosimilars clinical pharmacists drug substitution pharmacoeconomics rheumatology |
url |
https://www.drugsincontext.com/considerations-for-the-us-health-system-pharmacist-in-a-world-of-biosimilars/ |
work_keys_str_mv |
AT andreazlatkus considerationsfortheushealthsystempharmacistinaworldofbiosimilars AT toddbixby considerationsfortheushealthsystempharmacistinaworldofbiosimilars AT kavithagoyal considerationsfortheushealthsystempharmacistinaworldofbiosimilars |
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