Immunisation resources


Page last updated 5 March 2026

Immunisations in your state or territory 

Access specific immunisation information relevant to your state or territory:

 

2026 Influenza vaccination advice now available

The Australian Technical Advisory Group on Immunisation (ATAGI) has released its 2026 influenza vaccination advice ahead of this year’s flu season.

See '2026 influenza vaccination' section below. 
 

Intranasal live-attenuated influenza vaccine 

The intranasal live-attenuated influenza vaccine (LAIV) FluMist® has been approved for use in Australia for children aged 2 years to under 18 years, and will be available in early 2026.

See '2026 influenza vaccination' section below. 


Counterfeit Rabies vaccine (Abhayrab®) reported in India

Counterfeit Abhayrab® rabies vaccines have been circulating in India since 2023. Travellers vaccinated there since November 2023 may be unprotected and should replace invalid doses with Australian‑registered vaccines. ATAGI has released guidance for immunisation providers. 

Read ATAGI guidance 


Australian Technical Advisory Group on Immunisation (ATAGI) has released its 2026 influenza vaccination advice ahead of this year’s flu season.

Annual influenza vaccination is recommended when it becomes available in April 2026, before the start of the influenza season.

You must report all influenza vaccinations, both National Immunisation Program (NIP) and privately purchased, to the Australian Immunisation Register (AIR).

Healthcare provider recommendation is the strongest predictor of a person's decision to vaccinate. Please familiarise yourself with the latest advice and resources as they become available and discuss these with your patients.
 

Key points and updates for 2026

  • For adults aged 65 years and over, both the NIP funded adjuvanted vaccine (Fluad®) and the private market high dose influenza vaccine (Fluzone High-Dose) are equally preferentially recommended over standard influenza vaccines.
  • Flucelvax®, a cell-based vaccine, is NIP funded for people aged 5 to 64 years with medical conditions that put them at increased risk of complications from influenza. There is no preferential recommendation between Flucelvax® and standard dose egg-based influenza vaccines.
  • In 2026, the intranasally administered live attenuated influenza vaccine (LAIV) will be available for the first time in Australia for children aged 2–17 years by private prescription, and through statebased immunisation programs in New South Wales, Queensland, South Australia and Western Australia (See 'Intranasal live-attenuated influenza vaccine' section below).
  • Influenza vaccines can be co-administered with other vaccines.

The factsheet also includes specific advice on:

  • special considerations for travelling patients
  • children aged six months to less than five years 
  • pregnant women
  • Aboriginal and Torres Strait Islander People
  • people aged 65 years and over
  • medically at-risk patients.
Read full ATAGI advice
 

Eligibility for influenza vaccines funded by the National Immunisation Program (NIP)

Annual influenza vaccination is funded under the NIP for:

  • all children aged 6 months to < 5 years;
  • ​all adults aged ≥65 years; 
  • ​pregnant women at any stage of pregnancy
  • First Nations people aged 6 months and over
  • People aged 6 months and over with certain medical conditions (see conditions outlined in ATAGI advice).

​Some states and territory governments also fund influenza vaccines for other groups. Please refer your state or territory health department website (links at the top of this page) for more information.


Intranasal live-attenuated influenza vaccine 

The intranasal live-attenuated influenza vaccine (LAIV) FluMist® has been approved for use in Australia for children aged 2 years to under 18 years, and will be available in early 2026.

Some states have announced funding for use of the intranasal vaccine for eligible children, including: 
NSW: children aged two years to under five years
SA: children aged two to five years
QLD: children aged two to five years (inclusive) from 1 March
WA: children aged two to under 12.
Please refer your state or territory health department website (links at the top of this page) for more information.

The LAIV is available for children aged 2–17 years by private prescription.

The National Centre for Immunisation Research and Surveillance has released influenza resources that addres the new intranasal LAIV, including:


Key resources:

 

Stay up-to-date

Further advice and resources will be available on the Department of Health, Disability and Ageing website as it becomes available.

You can also subscribe to receive the latest updates on National Immunisation Program (NIP).

 

The National Immunisation Program (NIP) Schedule is a series of immunisations given at specific times from birth through to adulthood.

The Department of Health and Aged Care’s National Immunisation Program (NIP) Schedule webpage contains information on:

  • the NIP Schedule
  • catch-up immunisations
  • State and territory immunisation schedules
  • International immunisation schedules

You can subscribe to the program’s mailing list to receive all the latest updates.

State and territory health departments also fund some additional vaccines. Access further information on state and territory schedules via the appropriate link at the top of this page.
 

Changes to childhood pneumococcal vaccine under the NIP 

Subsequent to advice from the Australian Technical Advisory Group on Immunisation (ATAGI), the government has made changes to the National Immunisation Program (NIP) in relation to the childhood pneumococcal vaccine schedule. 

Prevenar 20 was introduced into the NIP on 1 September 2025 to replace Prevenar 13 and Pneumovax 23 on the childhood schedule.

The introduction of Prevenar 20 simplifies the vaccine schedule, reduces the number of doses and covers more strains of the disease.

All First Nations children will receive 4 doses, making the program consistent across all states and territories.

Children under 5 years, who have:

  • not yet started their pneumococcal schedule should receive 3 doses of Prevenar 20.
  • previously received 1 or 2 doses of Prevenar 13 should receive Prevenar 20 for all subsequent doses to complete the recommended vaccination course (where  required).
  • already completed a Prevenar 13 vaccination course who are due for a Pneumovax 23 booster should receive 1 dose of Prevenar 20 instead. Do not delay vaccination, if required, Pneumovax 23 can still be used (while stock is available).

Further advice is available in the Australian Immunisation Handbook
 

COVID-19 vaccinations no longer recommended for healthy infants and children under the age of 18

Please note that the COVID-19 vaccine is not recommended for healthy infants, children or adolescents under the age of 18 who do not have medical conditions that increase their risk of severe illness. The risk of severe illness has been deemed as extremely low in this cohort over the course of the pandemic, and benefits of vaccination are not considered to outweigh the potential harms.

For further guidance and recommendations regarding COVID-19 vaccinations, visit the Department of Health, Disability and Ageing’s COVID-19 webpage.
 

Respiratory Syncytial Virus (RSV) vaccine now available for eligible pregnant women under the NIP

The Abrysvo® vaccine has now been listed on the NIP, meaning eligible women who are at 28 to 36 weeks pregnancy will be able to receive the maternal RSV vaccine for free through the NIP, to protect their infant against RSV from birth and in their first few months of life.

The Department of Health and Aged Care are encouraging all GPs/general practices to:
  • Order the RSV maternal vaccine, Abrysvo®, through the usual channels in your state or territory.
  • Promote the free vaccine to eligible pregnant women, emphasising your recommendation as a trusted health professional.
  • Consider opportunities to co-administer the RSV vaccine with the recommended whooping cough and influenza vaccines where appropriate.
  • Ensure vaccine safety by verifying you are correctly administering the Abrysvo® RSV vaccine to your patient.
  • Report all RSV and NIP vaccines you administer to the Australian Immunisation Register.
  • Stay informed by subscribing to the NIP mailing list for the latest NIP updates.
RSV vaccine resources:

At the Australian Technical Advisory Group on Immunisation (ATAGI) in November 2025, several key issues were discussed. A report has been developed for GPs to provide updates on:

  • the decline of immunisation coverage in Australia
  • the 2025 flu season
  • new influenza products in 2026
  • how you as a GP can assist. 
Read the report

 

All vaccines administered to a patient should be recorded by the vaccine provider to the AIR, irrespective of whether they were administered as part of the NIP or privately.

It is now mandatory to upload a record of administration of the following vaccines to the AIR:

  • COVID-19
  • seasonal influenza
  • vaccines given under the National Immunisation Program (NIP)
  • Japanese encephalitis virus (JEV)

Mandatory data elements when uploading a record include:

  • relevant vaccines: COVID-19, influenza, NIP and JEV vaccines
  • how to report: electronic, or if this is not reasonably practical then in written form
  • when to report: within 24 hours, and no more than 10 working days after the vaccination
  • personal information: Medicare number (if applicable), name, contact details, date of birth, gender
  • vaccine information: brand name, dose number and batch number, date given, for COVID19 vaccines – vial serial number (if known)
  • provider information: provider number, name and contact details.

The Department of Health, Disability and Ageing's Using the Australian Immunisation Register webpage contains information on:

  • mandatory reporting to the AIR
  • using the AIR to check a patient’s immunisation history
  • identifying patients who are due/overdue a vaccine
  • recording vaccine administration
  • record accuracy
  • vaccination information payments.
 

Antenatal reporting to be mandatory within the AIR from 1 March 2025

From 1 March 2025 it became mandatory for all vaccination providers to report to the AIR information about whether an individual was pregnant at the time of vaccine administration.
 

The collection of antenatal data is important to ensure the AIR contains a complete and reliable dataset to enable the monitoring of:

  • immunisation coverage and administration; and

  • the effectiveness and safety of maternal vaccines and vaccination programs. 

A new bespoke antenatal indictor has now been added to the AIR to support this reporting requirement.

Next steps:
You can report antenatal information to the AIR through clinical software or the AIR site, using either the:

  • antenatal indicator - the new indicator will be rolled out in clinical software throughout 2025. You can update to the latest version of your clinical software to make sure the latest functionality is available
  • vaccine type field - if the new Antenatal indicator is not yet available in your clinical software, you must report antenatal information to the AIR using the ‘Antenatal’ option under the ‘Vaccine type’ field.

Please contact your software provider if you are wanting to know when the new antenatal indicator will be available in your clinical software.

For further information on reporting information to the AIR, please visit the Services Australia website or contact immunisation.registers@health.gov.au
 

Update to COVID-19 vaccine names with the AIR

COVID-19 vaccine names will no longer display the manufacturer name within the AIR. For example, the ‘Pfizer Comirnaty XBB.1.5’ vaccine will display as ‘Comirnaty XBB.1.5’. 
This simplifies the display of COVID-19 vaccines and aligns with how other vaccines are recorded in the AIR. 

The AIR vaccine codes for COVID-19 vaccines remain the same. Further information about AIR vaccine codes and vaccine brand names is available on the Services Australia website.

 

The Australian Immunisation Handbook provides national clinical guidance on the safest and most effective use of vaccines.

The Handbook’s recommendations are developed by the Australian Technical Advisory Group on Immunisation (ATAGI) and approved by the National Health and Medical Research Council (NHMRC).

You can find the latest statements by ATAGI on immunisation on the Department of Health, Disability and Ageing webpage.

 

There will be scenarios where it is not appropriate to administer a vaccine due to a valid medical reason – be it temporarily or long-term. In such cases the person will require an Immunisation Medical Exemption.

Eligible GPs can provide an Immunisation Medical Exemption using the AIR site using HPOS (you’ll need an individual PRODA account) or via vaccination reporting software. If you don't have access to either of these, you can record a medical exemption using the Australian Immunisation Register (AIR) - immunisation medical exemption form (IM011).

Someone who is not able to receive a vaccine may require evidence, for example, to receive family assistance payments or be eligible to attend school or childcare. Having this recorded in AIR provides that evidence.


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