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The content of this website has been produced in line with the ABRYSVO®▼(Respiratory Syncytial Virus Vaccine [bivalent, recombinant]) Summary of Product Characteristics for Great Britain and is intended for Healthcare Professionals based in Great Britain only. ABRYSVO▼ Prescribing Information for Great Britain click here. ABRYSVO▼ Prescribing Information for Northern Ireland click here.

Dosing, administration and storage of ABRYSVO for pregnant women

Please refer to the Summary of Product Characteristics before administering this vaccine.
 

Reconstitute

  • ABRYSVO must be reconstituted prior to the administration by adding the entire contents of the pre-filled syringe of solvent to the vial containing the powder using the vial adapter.1
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One injection

  • Administered via a single 0.5mL dose intramuscular injection between 28 and 36 weeks of gestation.
  • Use in accordance with official recommendations.1

Store at 2°C-8°C

  • Do not freeze.1
  • ABRYSVO should be administered immediately after reconstitution.1
This content is for Great Britain only. If you reside in Northern Ireland, please refer to the Summary of Product Characteristics (SmPC) for more information.
Preparation of ABRYSVO


Watch a video on how to prepare ABRYSVO for administration.

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Safety Profile - Pregnant Women


Learn more about the safety information of ABRYSVO in pregnant women.

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Useful Resources


Explore the ABRYSVO resources section for useful videos and materials.

 VideosLoading Materials ABRYSVO (Respiratory Syncytial Virus Vaccine [bivalent, recombinant]) Summary of Product Characteristics for Great Britain. Available at: https://www.medicines.org.uk/emc/product/15309.
PP-A1G-GBR-0010. February 2024

Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search 

for MHRA Yellow Card in Google Play or Apple App Store

 

Adverse events should also be reported to Pfizer Medical Information on 01304 616161

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