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APEXXNAR is indicated for active immunisation for the prevention of invasive disease and pneumonia caused by Streptococcus pneumoniae in individuals 18 years of age and older.1
Apexxnar may be administered concomitantly with seasonal influenza vaccine (QIV; surface antigen, inactivated, adjuvanted) and COVID-19 mRNA vaccine (nucleoside modified).1
Manifestations of pneumococcal disease include:3
▼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. Refer to section 4.8 for how to report adverse reactions.
APEXXNAR® was evaluated for safety and immunogenicity across a diverse patient population.1,4-6
Conjugate vaccines like APEXXNAR are designed to deliver long-lasting immunity.1,7
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Adverse events should be reported. Report an adverse event to your national reporting system (HPRA Pharmacovigilance)
Adverse events should also be reported to Pfizer Medical Information on 1800 633 363
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PP-UNP-IRL-0176. January 2023