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Arexvy▼ (Respiratory Syncytial Virus (RSV) vaccine (recombinant, adjuvanted)
AREXVY▼: Protection from RSV starts here1
AREXVY is indicated for active immunisation for the prevention of RSV-LRTD* in adults aged 60 years and older and adults aged 50- 59 years who are at increased risk for RSV disease.1
Date of preparation: September 2024 | PM-IE-RSA-WCNT-240001
*RSV-LRTD=respiratory syncytial virus-associated lower respiratory tract disease
References: 1. Arexvy SPC, www.medicines.ie (accessed September 2024).
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References
- Cahn P, Sierra Madero J, Arribas JR, et al. Durable efficacy of dolutegravir (DTG) plus lamivudine (3TC) in antiretroviral treatment-naïve adults with HIV-1 infection—3-year results from the GEMINI studies. Presented at: HIV Glasgow 2020; October 5-8, 2020; Virtual. Poster P018.
- Arexvy, Summary of Product Characteristics (SPC), available at: https://www.medicines.ie/medicines/arexvy-powder-and-suspension-for-suspension-for-injection-35441/spc. Last Accessed: September 2024
- Zejula, Summary of Product Characteristics (SPC), available at: https://www.medicines.ie/medicines/zejula-100-mg-hard-capsules-35060/spc Last Accessed: September 2024
- Shingrix, Summary of Product Characteristics (SPC), available at: https://www.medicines.ie/medicines/shingrix-powder-and-suspension-for-suspension-for-injection-herpes-zoster-vaccine-recombinant-adjuvanted--35192/spc Last Accessed: September 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.
▼ These medicinal products are subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reactions.
Trade marks are owned by or licensed to the GSK group of companies.
PM-IE-NA-WCNT-220010 Date of Preparation: September 2024
