The Generic and Biosimilar Medicines Association (GBMA), the representative body of generic and biosimilar medicine suppliers in Australia, has recently published information resources for consumers and carers on biosimilars.
GBMA publishes information resources on biosimilars for consumers and carers
Biosimilars/General | Posted 13/11/2020 0 Post your comment
The GBMA has published a fact sheet providing information about the biosimilars of trastuzumab on the Pharmaceutical Benefits Scheme (PBS). The document outlines the trastuzumab biosimilars currently listed on the PBS (Trazimera®, Ogivri®, Herzuma®, Kanjinti® and Ontruzant®) and explains the process behind brand choice and brand substitution. It also explains the important role that biosimilar medicines play in the Australian healthcare system and provides links to further information.
GBMA Education, the educational arm of GBMA, has published several resources for consumers and carers about biosimilars. Brochures and fact sheets provide consumers and carers with the essentials on biosimilar medicines including an explanation of what they are, their regulation in Australia, and their beneficial role in the Australian healthcare system. The website now also features answers to the most frequently asked questions on biosimilar medicines, as well as links to recommended websites for further information including the PBS, the Therapeutic Goods Administration, and the Australian Government Department of Health.
Related articles
Biosimilar Awareness Week in Australia
GBMA publishes quarterly review of biosimilar literature
New Information on biosimilars from Australia and the US
Permission granted to reproduce for personal and non-commercial use only. All other reproduction, copy or reprinting of all or part of any ‘Content’ found on this website is strictly prohibited without the prior consent of the publisher. Contact the publisher to obtain permission before redistributing.
Copyright – Unless otherwise stated all contents of this website are © 2020 Pro Pharma Communications International. All Rights Reserved.
Research
Long-term real-world safety experience of biosimilars confirms concept of biosimilarity
Budget impact analysis of Rixathon introduction in Chile for non-Hodgkin lymphoma
News
FDA approves fifth ustekinumab biosimilar Imuldosa
EC approval for three ustekinumab biosimilar: Eksunbi, Fymskina, Otulfi
Comments (0)
Post your comment