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Maternal ImmunisationMaternal ImmunisationMaternal Immunisation HomepageSafety ProfileDosingOlder AdultsOlder Adults HomepageOlder Adults HomepageSafety ProfileDosingPreparationUseful ResourcesUseful ResourcesOlder AdultsOlder Adults HomepageOlder Adults HomepageSafety ProfileDosingVideosMaterials

Disclaimer: This information is valid only for healthcare professionals in Bahrain, Oman, Qatar & UAE.

Abrysvo™ (Respiratory syncytial virus vaccine) is available, marketed and has a Health Registry only in Bahrain, Oman, Qatar & UAE. The advertising or promotion carried out for Abrysvo™ (Respiratory syncytial virus vaccine) is only directed to health professionals in Bahrain, Oman, Qatar & UAE.

Information on how to access Abrysvo™ (Respiratory syncytial virus vaccine) prescribing information and adverse event reporting can be found at the bottom of the page.

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

Most local and systemic reactions in maternal participants were mild to moderate in severity and resolved within 2-3 days of onset.1

In pregnant women at 24-36 weeks of gestation, the most frequently reported adverse reactions were vaccination site pain (41%), headache (31%), and myalgia (27%).1

Tabulated Adverse Events (AE) in pregnant women

Please refer to the SmPC for additional safety information.


No safety signals were detected in infants up to 24 months of age.1

The incidences of AEs reported within 1 month after birth in infants were similar in the ABRYSVO group (37%) and the placebo group (35%).1
The safety profile of ABRYSVO was evaluated in phase 3 clinical studies. Pregnant women (n=3,682) at 24-36 weeks of gestation were evaluated after receiving a single dose of vaccine.1

Contraindications1

Hypersensitivity to the active substances or to any of the excipients listed in section 6.1 of the SmPC.

Special warnings and precautions for use1
 

TraceabilityIn order to improve the traceability of biological medicinal products, the name and the batch number of the administered product should be clearly recorded.Hypersensitivity and anaphylaxisAppropriate medical treatment and supervision should always be readily available in case of an anaphylactic event following the administration of the vaccine.Anxiety-related reactionsAnxiety-related reactions, including vasovagal reactions (syncope), hyperventilation or stress-related reactions may occur in association with vaccination as a psychogenic response to the needle injection. It is important that procedures are in place to avoid injury from fainting.Concurrent illnessVaccination should be postponed in individuals suffering from an acute febrile illness. However, the presence of a minor infection, such as a cold, should not result in the deferral of vaccination.Thrombocytopenia and coagulation disordersABRYSVO should be given with caution to individuals with thrombocytopenia or any coagulation disorder since bleeding or bruising may occur following an intramuscular administration to these individualslmmunocompromised individualsThe efficacy and safety of the vaccine have not been assessed in immunocompromised individuals, including those receiving immunosuppressant therapy. The efficacy of ABRYSVO may be lower in immunosuppressed individuals.
ABRYSVO - Maternal Immunisation

Learn more about maternal immunisation 1vith ABRYSVO

 

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Preparation of ABRYSVO

Watch a video on how to prepare ABRYSVO for administration.

 

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Dosing - Pregnant Women

Find out more about the dosing information of ABRYSVO for maternal patients.

 

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1. Abrysvo™ (Respiratory syncytial virus vaccine) Local Product Document Revision Date: August 2023 for Oman, Qatar, UAE and October 2024 for Bahrain.

Prescribing Information:

Bahrain Prescribing Information
Oman Prescribing Information
Qatar Prescribing Information
UAE Prescribing Information

PP-A1G-BHR-0040

This information is valid only for healthcare professionals in Bahrain, Oman, Qatar & UAE.

Report Adverse Events 

If you'd like to report an adverse event related to a Pfizer Product from Gulf (UAE, Bahrain, Qatar, Oman and Kuwait), please send an email with the adverse event details to: [email protected]

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Copyright © 2024 Pfizer Gulf FZ LLC. All rights reserved.

 

i- The product information provided in this site is intended only for Healthcare Professionals of UAE, Kuwait, Qatar, Bahrain, Oman.

 

ii- The information contained on this website is offered for educational purposes only and does not represent medical advice, diagnosis, treatment or a professional recommendation. Pfizer will not be responsible for the use or interpretation of the information by the user of the website.

 

iii- The products discussed herein may have a different product labeling than authorized in your country and may not be available in some territories.
 

PP-UNP-BHR-0298
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