№ lp_1_2_59497
File format: docx Character count: 75461 File size: 379 KB
Year: 2020
Region / city: Australia
Subject: Influenza Vaccination
Document Type: Resubmission for listing
Agency / institution: Pharmaceutical Benefits Advisory Committee (PBAC)
Author: Sanofi-Aventis Australia Pty Ltd
Target Audience: Healthcare providers, public health authorities
Period of validity: From 2020 onward
Approval Date: July 2019
Date of amendments: July 2019
Price: 8 / 10 USD
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Inactivated trivalent influenza vaccine (Split Virion) suspension for injection, 180mcg single dose in 0.5mL, Fluzone High-Dose, Australia, 2017–2018
Year: 2017
Country: Australia
Vaccine type: Inactivated trivalent influenza vaccine (TIV-HD)
Manufacturer: Sanofi-Aventis Australia Pty Ltd
Product form: Suspension for injection, 180mcg single dose in 0.5mL
Regulatory approval: TGA registration December 2017
Target population: Persons aged 65 years and older
Purpose: Listing on National Immunisation Program (NIP)
Comparative analysis: Cost-minimisation versus standard quadrivalent influenza vaccine (QIV)
Advisory review: PBAC and ATAGI evaluation
Implementation considerations: Cold chain capacity, provider communication, monitoring adverse events
Inactivated trivalent influenza vaccine (Split Virion) suspension for injection, 180mcg single dose in 0.5mL, Fluzone High-Dose, Australia, 2017–2018
Year: 2017
Country: Australia
Vaccine type: Inactivated trivalent influenza vaccine (TIV-HD)
Manufacturer: Sanofi-Aventis Australia Pty Ltd
Product form: Suspension for injection, 180mcg single dose in 0.5mL
Regulatory approval: TGA registration December 2017
Target population: Persons aged 65 years and older
Purpose: Listing on National Immunisation Program (NIP)
Comparative analysis: Cost-minimisation versus standard quadrivalent influenza vaccine (QIV)
Advisory review: PBAC and ATAGI evaluation
Implementation considerations: Cold chain capacity, provider communication, monitoring adverse events
Topics: Sanofi–Aventis VIRION Fluzone