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VACCINE DESIGN

Arexvy includes both an antigen component and an adjuvant system

Mechanism of Action

By combining the RSVPreF3 antigen with an adjuvant system (AS01_E), AREXVY induces antigen-specific cellular immune response and neutralising antibodies that help protect against RSV-associated LRTD.¹

EFFICACY

Review efficacy data against RSV-LRTD for your patients aged 60 years and older.¹

LEARN MORE

ADMINISTRATION

Review details on dosing and administration of AREXVY to learn about the reconstitution process.

LEARN MORE

SAFETY

AREXVY has a Clinically acceptable safety profile.¹

LEARN MORE

Abbreviations

LRTD=lower respiratory tract disease; RSV=respiratory syncytial virus; RSVPreF3=recombinant RSV glycoprotein F stabilised in the pre-fusion conformation.

References

Arexvy SPC, https://www.medicines.ie/medicines/arexvy-powder-and-suspension-for-suspension-for-injection-35441/spc. Accessed April 2024

Adverse events should be reported directly to the Health Products Regulatory Authority (HPRA) on their website: www.hpra.ie. Adverse events should also be reported to GlaxoSmithKline on 1800 244 255.

▼This medicinal product is subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reactions.

PM-IE-RSA-WCNT-230002 | May 2024

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Registered in Ireland: GlaxoSmithKline (Ireland) Limited, a private company limited by shares, and a member of the GlaxoSmithKline group of companies. Registered in Ireland with Company Number 15513.
Registered office: 12 Riverwalk, Citywest Business Campus, Dublin 24, Ireland.

PM-IE-NA-WCNT-230003

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