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Information about adverse event reporting can be found towards the bottom of the page

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AboutmRNA TechnologyMechanism of ActionDosing & AdministrationComirnaty Omicron XBB.1.5Dosing & Administration StorageComirnaty Omicron XBB.1.5 30mcg 12 years + (Grey cap)How to OrderComirnaty Omicron XBB.1.5 Supply for Great BritainResourcesMaterialsVideosEN - EnglishSelect a languageLanguagesEN - EnglishFR - Françias

Information on how to access prescribing information and adverse event reporting can be found at the bottom of the page.

How to order 
The information on this website relates to private provision of COMIRNATY Omicron XBB.1.5

There are several formulations of COMIRNATY Omicron XBB.1.5 used as part of the current NHS vaccination programme, information for which can be found here

For general enquiries related to Pfizer medicines, including COVID-19 vaccines, call 01304 616161. 

For queries regarding private supply of Pfizer COVID-19 vaccines, email [email protected]

COMIRNATY Omicron XBB.1.5 30mcg Single Dose Vial
  • Now available as COMIRNATY Omicron XBB.1.5 30mcg Single Dose Vial in Great Britain, for use in the private market, for those individuals 12 years of age and older who are not eligible for vaccination as part of the National Immunisation Programme1.
  • Single dose vials are available in packs of 10 vials (10 doses) at fridge temperature (2-8°C)1.
     
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Product Information

Learn more about the storage and administration

References

COMIRNATY Omicron XBB.1.5 Single Dose Vial Summary of Product Characteristics
PP-CMR-GBR-0557. April 2024

Adverse Event Reporting

Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. 

Healthcare professionals are asked to report any suspected adverse reactions via a Yellow card. Reporting forms and information can be found at https://coronavirus-yellowcard.mhra.gov.uk/ or search for MHRA Yellow Card in the Google Play or Apple App Store and include the batch/Lot number if available.

Alternatively, adverse events of concern in association with COMIRNATY can be reported to Pfizer Medical Information on 01304 616161 or via www.pfizersafetyreporting.com.

Please do not report the same adverse event(s) to both systems as all reports will be shared between Pfizer and MHRA (in an anonymised form) and dual reporting will create unnecessary duplicates.

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Marketing Authorisation
Holder: BioNTech
Manufacturing GmbH

COMIRNATY, COMIRNATY Omicron XBB.1.5, are based on BioNTech proprietary mRNA technology, developed by both BioNTech and Pfizer.


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.

 

Copyright © 2024 Pfizer Limited. All rights reserved.

 

VAT registration number GB201048427

PP-CMR-GBR-0512. January 2024
 

For UK Healthcare Professionals*

These pages are not intended for patients or for members of the general public. The healthcare professional web pages contain promotional content.

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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 for healthcare professional is members of the medical, dental, pharmacy and nursing professionals and any other persons who in the course of their professional activities may administer, prescribe, purchase, recommend or supply a medicine.

PP-UNP-GBR-7812. January 2024

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