Regulatory approval of Pfizer/BioNTech vaccine for COVID-19
Information for healthcare professionals and the public about the Pfizer/BioNTech vaccine.
Documents
Details
Information about the COVID-19 vaccine, approved by MHRA on 2 December 2020.
The Information for healthcare professionals document is a description of a medicinal product’s properties and the conditions attached to its use. It explains how to use and prescribe a medicine. It is used by healthcare professionals, such as doctors, nurses and pharmacists.
The Information for UK recipients document provides information for patients on using the medicine safely. This is based on the Information for healthcare professionals of the product.
The public assessment report is a scientific report, written by the MHRA. It explains how this product was assessed and its authorisation recommended, as well as its conditions of use. It is not intended to provide practical advice on how to use this product.
Find out more about the approval from our press release.
For further information on prioritising the first COVID-19 vaccine dose see the statement from the Joint Committee on Vaccination and Immunisation (JCVI).
Ingredients
The Medicines and Healthcare products Agency can confirm that the Pfizer/BioNTech COVID-19 vaccine does not contain any components of animal origin.
A full list of ingredients for the qualitative and quantitative composition of the vaccine can be found at point 2 in the Information for Healthcare Professionals on Pfizer/BioNtech Vaccine.
A full list of ingredients for the excipient composition of the vaccine can be found at point 6 in the Information for Healthcare Professionals on Pfizer/BioNtech Vaccine.
A full list of ingredients for the qualitative and quantitative composition of the vaccine and a full list of the excipient composition of the vaccine can be found at point 6 in the Information for Recipients of the Pfizer/BioNtech Vaccine.
Last updated
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Added information on fevers to Section 4 of Information for UK Recipients and section 4.8 of Information for Healthcare Professionals.
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Published new versions of the Conditions of Authorisation documents, with an additional clause relating to off-label prescribing
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We have updated the Product Information to state that the vaccine is manufactured with enough volume for six doses, if our latest guidance for Healthcare Professionals is followed.
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Updated HTML and PDF attachments for 'Conditions of authorisation for Pfizer BioNTech'
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Updated the Information for UK recipients and the Information for healthcare professionals documents, to reflect changes to the dosage interval, advice for women who are pregnant or breastfeeding and to those with allergies.
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Updated guidance for Healthcare Professionals on obtaining a sixth dose from a vial.
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Added an accessible HTML document: Summary of the Public Assessment Report
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Added the Public Assessment Report for the Pfizer/BioNTech COVID-19 vaccine
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Changes to section 4.2 and 6 of the Information for UK Healthcare Professionals to provide clarification following further feedback and update to section 4.4 to strengthen information on special warnings and precautions for use. Changes to warnings and precautions and clarification in section 6 of the Information for UK Recipients.
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Accessible HTML versions of both the 'Information for Healthcare Professionals on Pfizer/BioNTech COVID-19 vaccine' and the 'Information for UK recipients on Pfizer/BioNTech COVID-19 vaccine' are now available.
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A note regarding the ingredients has been added as well as an accessible HTML version of 'Conditions of Authorisation for Pfizer/BioNTech COVID-19 vaccine'. A reference to the Medicines Act 1968 has been corrected.
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Added new document: Conditions of Authorisation for Pfizer BioNTech COVID-19 vaccine.
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First published.
Update history
2024-08-08 11:23
Removed ‘Summary of Product Characteristics Comirnaty 30 micrograms/dose concentrate for age 12+ (purple cap)’ and ‘Patient Information Leaflet for Comirnaty 30 micrograms/dose concentrate for age 12+ (purple cap)’ Following the recent withdrawal of the licences for this Comirnaty (COVID-19 vaccines) vaccine.
2024-03-21 12:21
The product information of Comirnaty products has been updated following recent approval on PI updates (Sections 1, 2, and 4.8, and labelling) and shelf-life extension.
2023-12-22 09:51
Update to section 4.8 of the SmPC to update the safety information available in 12-15 year olds.
2023-09-05 14:35
Summary of Product Characteristics (SmPC) and Patient Information Leaflets (PIL) of the Comirnaty Omicron XBB.1.5 vaccines have been published.
2023-09-01 12:56
Summary of Product Characteristics (SmPC) and Patient Information Leaflets (PIL) updated to reflect:A variation to update the SmPC and PIL to reflect new posology for primary immunisation. The updates affect all the Comirnaty Original Products and Comirnaty Original/Omicron BA.4-5 products i.e., 5 products in total.A variation to update the SmPC and PIL to extend the shelf-life. The updates affect the Comirnaty Original 10 microgram/dose and 3 microgram/dose products and both Original/Omicron BA.4-5 products i.e., 4 products in total.Updates applicable from 24 August 2023
2023-06-05 15:35
Safety and immunogenicity information in the SmPC has been updated, based on six months post-booster dose follow-up data in recipients aged 16 year and older from studies C4591001 and C4591031.
2023-05-25 12:26
Updated Links and hyperlinks in ARCHIVE: Information for UK recipients on Pfizer/BioNTech COVID-19 vaccine (Regulation 174) attachment
2023-03-17 13:08
Updated SPCs and PILs for all Comirnaty products, to include: the uncommon side effect ‘dizziness’& longer-term clinical trial follow-up data in 5-11 year olds.
2023-01-06 16:09
Updated the purple cap SmPC
2022-12-09 16:48
Updated the Comirnaty purple, orange and maroon cap SmPCs and PILs.
2022-12-06 10:58
Product information has been added for a new presentation of the vaccine for use in those aged 6 months to 4 years.
2022-11-09 12:47
Comirnaty 10 micrograms concentrate for dispersion for injection (one of the licensed Comirnaty vaccines produced by Pfizer/BioNTech) has been approved for use as a booster for 5- to 11-year-olds. There has also been an update to the product information for the Comirnaty vaccines on myocarditis and pericarditis after a third dose and in the age group 5-11 years. This update reflects the most up to date information about these known side effects.
2022-08-16 10:51
Updates to the SmPC and PIL to include information about receiving a heterologous booster dose in individuals aged 18 years and over.Updated SmPC and PIL for the purple cap product (Comirnaty 30 micrograms/dose concentrate for dispersion for injection) – shelf life and transportation storage time information updated
2022-07-07 14:26
Conditions of Authorisation for COVID-19 Vaccine Pfizer/BioNTech (Comirnaty) updated. 2 quality specific obligations have now been fulfilled.
2022-05-24 16:40
Updated SpC and PIL for orange cap product (Comirnaty 10 micrograms/dose Concentrate for Dispersion for Injection – Shelf-life information updated.
2022-05-05 17:52
The website decision page for the mRNA COVID-19 vaccines has been updated to reflect the fact that the 15-minute observation period following vaccination has been removed for individuals aged 12 years and over who have no history of a severe allergic reaction.
2022-04-27 01:09
Updated information to Summary of Product Characteristics and Patient Information Leaflets (Purple Cap and Orange Cap)
2022-04-13 14:12
Updated shelf life from 9-months to 12-months for Comirnaty 30 microgram COVID-19 mRNA Vaccine (purple cap).Updated SmPC and PIL.
2022-03-25 11:36
Updated 30mg and 10mg PIL and SPC.
2022-03-14 15:16
PIL and SMPC Comirnaty 10 mg/dose concentrate: updated title to include reference to orange cap. Updated the shelf life life from 6 months to 9 months. SMPC and PIL Comirnaty 30mg/dose concentrate: Updated title to include reference to purple cap. Includes new reference to the fact there is now paediatric formulation available for children 5 to 11 years of age. Myo/pericarditis changed from a potential side effect of unknown frequency to “very rare”. Erythema multiforme added as a potential side effect with unknown frequency. Wording around shelf life updated.
2021-12-24 01:06
Information for Healthcare Professionals and UK recipients on COVID-19 Vaccine Pfizer/BioNTech (Regulation 174) was updated
2021-12-22 23:24
Added HTML document for Summary of product characteristics for Comirnaty 10 micrograms/dose concentrate for dispersion for injection
2021-12-22 14:43
Added Patient Information Leaflet and Summary of Product Characteristics for COVID-19 Vaccine Pfizer/BioNTech 10 micrograms
2021-12-14 16:28
Banner added to main page: The 15 minute observation period following a vaccination with Pfizer/BioNTech or Moderna will be temporarily suspended as part of measures to increase the booster rollout. Regulatory documents remain unchanged.
2021-12-03 11:33
The Pfizer/BioNTech vaccine (Comirnaty) Conditional Marketing Authorisation has been renewed: changes to the SmPC – section 9 and section 10.
2021-11-15 22:45
Updated sections of the Summary of Product Characteristics and Patient Information Leaflet for COVID-19 Vaccine Pfizer/BioNTech (Conditional Marketing Authorisation documents) to include information about receiving a 3rd/booster dose. Also to include two new reagents, Sodium Hydroxide and Hydrochloric Acid, which are used in small quantities during the preparation of one of the solutions used in the manufacturing process. The official International non-proprietary name ‘tozinameran’ has also been added.
2021-10-28 14:41
Updated figures in HCP information Table 5: Vaccine efficacy – First COVID-19 occurrence from 7 days after Dose 2 – participants without evidence of infection and with or without evidence of infection prior to 7 days after Dose 2 – adolescents 12 to 15 years of age evaluable efficacy (7 days) population
2021-10-27 17:50
Update to the summary of product characteristics and patient information leaflet for the Pfizer/BioNTech vaccine condition marketing authorisation documents
2021-10-27 17:50
Update to the summary of product characteristics and patient information leaflet for the Pfizer/BioNTech vaccine condition marketing authorisation documents
2021-10-27 11:56
Updated for both HCPs and public
2021-09-27 17:02
Extended vaccine shelf life from 6 months to now 9 months.
2021-06-04 11:03
Updated Conditions of Authorisation, Information for Healthcare Professionals and Information for UK Recipients documents in line with an extension to the current UK approval of the Pfizer/BioNTech COVID-19 vaccine that allows its use in 12- to 15-year-olds.
2021-05-20 16:29
Updated the Information for Healthcare Professionals, Information for UK recipients and Conditions of Authorisation documents. This is to reflect a change that once removed from the freezer, the undiluted vaccine has a maximum shelf life of up to 1 month (31 days). This was previously 5 days.
2021-03-31 17:14
Published new versions of the Conditions of Authorisation documents, with an additional clause in the Deployment section relating to transfers of frozen vials stored at ultra-low temperature and handling of temperature excursions
2021-03-09 16:11
Added information on fevers to Section 4 of Information for UK Recipients and section 4.8 of Information for Healthcare Professionals.
2021-01-28 11:45
Published new versions of the Conditions of Authorisation documents, with an additional clause relating to off-label prescribing
2021-01-26 17:18
We have updated the Product Information to state that the vaccine is manufactured with enough volume for six doses, if our latest guidance for Healthcare Professionals is followed.