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Great BritainCOMIRNATY Omicron XBB.1.5 30mcgCOMIRNATY Omicron XBB.1.5 10mcgCOMIRNATY Omicron XBB.1.5 3mcgNorthern IrelandCOMIRNATY Omicron XBB.1.5 30mcgCOMIRNATY Omicron XBB.1.5 10mcgCOMIRNATY Omicron XBB.1.5 3mcg

COMIRNATY Omicron XBB.1.5 30 micrograms/dose dispersion (ready for use)

Full name: COMIRNATY Omicron XBB.1.5 30 micrograms/dose dispersion for injection COVID-19 mRNA Vaccine1

Indication: indicated for  active immunisation to prevent COVID-19 caused by SARS-CoV-2, in individuals 12 years of age and older.

The use of this vaccine should be in accordance with official recommendations.1

How does the Pfizer/BioNTech Vaccine COMIRNATY Omicron XBB.1.5 differ from Pfizer/BioNTech’s pre-existing COMIRNATY Vaccines?

COMIRNATY Omicron XBB.1.5 30 micrograms/dose dispersion (ready for use) is a monovalent vaccine adapted to target the Omicron XBB.1.5 COVID-19 variant.
 

Posology:
The dose of COMIRNATY Omicron XBB.1.5 is 0.3mL given intramuscularly.

There should be an interval of at least 3 months between administration of COMIRNATY Omicron XBB.1.5 and the last prior dose of a COVID-19 vaccine.

Please refer to 4.2 of the Summary of Product Characteristics for more information.

Administration: administered intramuscularly. The preferred site is the deltoid muscle of the upper arm. Do not dilute prior to use. Do not inject intravenously, subcutaneously or intradermally.

Pack size: 10 multidose vials1

Dilution status:  Ready for use. Do not dilute before use1

Refrigerated storage (2°C to 8°C) once thawed: 10 weeks storage and transportation within the 18-month shelf life. Once thawed the vaccine should not be re-frozen.1

Vial: 6 dose multidose vial1

Dose:  30 micrograms (0.3mL)1

Room temperature stability before use: the unopened vials can be stored for up to 12 hours at temperatures between 8oC and 30oC.1

Stability of opened vials: Chemical and physical in-use stability has been demonstrated for 12 hours at 2oC to 30oC, which includes up to 6 hours transportation time. From a microbiological point of view, unless the method of opening precludes the risks of microbial contamination, the product should be used immediately. If not used immediately, in use storage times and conditions are the responsibility of the user. Discard any unused vaccine 12 hours after first puncture.1

Click here for Summary of Product Characteristics

Verification, handling & preparation of COMIRNATY Omicron XBB.1.5 30 micrograms/dose dispersion (ready for use)

Undesirable Effects:

The safety of COMIRNATY Omicron XBB.1.5 is inferred from safety data of the prior COMIRNATY vaccine, given as first, second or subsequent doses.

The most common adverse reactions from COMIRNATY clinical trials and post-authorisation experience in individuals 12 years of age and older were:
 

Diarrhoea
Headache
Arthralgia/Myalgia
Injection site pain/swelling
Pyrexia*
Chills
Fatigue

* a higher frequency of pyrexia was observed after a second dose compared to a first dose

Before administering the vaccine, refer to the Summary of Product Characteristics for further details.

It is expected that the majority of vaccinating sites will receive this vaccine thawed and stored at 2 °C to 8 °C, ready for use.

References: 

  1. Comirnaty Omicron XBB.1.5 30 micrograms/dose dispersion for injection 12+ years COVID-19 mRNA Vaccine Summary of Product Characteristics, Northern Ireland. Available at https://www.emcmedicines.com/en-gb/northernireland/medicine?id=fb7b0598-d163-43b6-973b-284adbebbee6  (accessed: December 2023)
PP-CMR-GBR-0471. December 2023

Marketing Authorisation
Holder: BioNTech
Manufacturing GmbH

COMIRNATY, COMIRNATY Omicron XBB.1.5, COMIRNATY Original/Omicron BA.4-5 and COMIRNATY Original/Omicron BA.1 COVID-19 mRNA Vaccines, which are based on BioNTech proprietary mRNA technology, were developed by both BioNTech and Pfizer.


©2024 Pfizer Inc. All rights reserved. PP-CMR-GBR-0522  February 2024

*Healthcare Professionals ** Other Relevant Decision Makers

The product information provided in this site is intended only for Healthcare Professionals and Other Relevant Decision Makers resident in the United Kingdom. 

This website is brought to you by Pfizer Limited, a company registered in England and Wales under No. 526209 with its registered office at Ramsgate Road, Sandwich, Kent CT13 9NJ, VAT registration number GB201048427.

The products discussed may have different product labelling in other countries.​​​​​​​
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For Healthcare Professionals* and Other Relevant Decision Makers** only

This website is not intended for patients or for members of the general public. The website contains promotional content.

I confirm that I am a Healthcare Professional* or Other Relevant Decision Maker** resident in the United Kingdom.

If you select Yes – Great Britain: you will be directed to the Great Britain*** homepage. Information on this page is aligned to the Summary of Product Characteristics (SmPC) for Great Britain.

If you select Yes – Northern Ireland: you will be directed to the Northern Ireland homepage. Information on this page is aligned to the SmPC for Northern Ireland.


If you select 'No', you will be redirected to Pfizer.co.uk where you will be able to access reference information on Pfizer's prescription medicines.

*The ABPI Code definition of Healthcare Professional is members of the medical, dental, pharmacy and nursing professions and any other persons who in the course of their professional activities may administer, prescribe, purchase, recommend or supply a medicine.

**The ABPI Code definition of ‘Other Relevant Decision Makers’ particularly includes those with an NHS role who could influence in any way the administration, consumption, prescription, purchase, recommendation, sale, supply or use of any medicine but who are not health professionals.

*** Great Britain includes England, Scotland and Wales.

PP-CMR-GBR-0400 June 2023