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AboutAboutAbout APEXXNARMechanism of actionClinical programmeClinical programmeAPEXXNAR clinical study overviewAPEXXNAR adverse drug reactionsAdministration
An expanded level of protection in adults 18 years of age and older1,2APEXXNAR® helps to protect against the 20 Streptococcus pneumoniae serotypes in the vaccine1Serotype Coverage1

APEXXNAR adds 7 serotypes to Prevenar 13® (Pneumococcal polysaccharide conjugate vaccine [13-valent, adsorbed]). Help protect your patients from pneumococcal pneumonia and invasive pneumococcal disease in only one dose.1


 

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Conjugation matters1,3

Conjugate vaccines are designed to deliver long-lasting immunity.1,3
 

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Study Overview

APEXXNAR was evaluated for safety and immunogenicity across a diverse patient population1,4-6

 

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View Summary of Product Characteristics Apexxnar® Loading Prevenar 13® LoadingGuidelines

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▼ 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.

References:APEXXNAR® Summary of Product Characteristics.Prevenar 13® Summary of Product Characteristics.Froes F, Roche N, Blasi F. Pneumococcal vaccination and chronic respiratory diseases. Int J Chron Obstruct Pulmon Dis. 2017;12:3457-3468.ClinicalTrials.gov. Trial to evaluate the safety and immunogenicity of a 20-valent pneumococcal conjugate vaccine in pneumococcal vaccine-naïve adults. Available at: https://clinicaltrials.gov/ct2/show/NCT03760146 Last Accessed: August 2022.ClinicalTrials.gov. Trial to evaluate the safety and immunogenicity of 3 lots of 20-valent pneumococcal conjugate vaccine in pneumococcal vaccine-naïve adults. Available at: https://clinicaltrials.gov/ct2/show/NCT03828617 Last Accessed: August 2022.ClinicalTrials.gov. Trial to evaluate the safety and immunogenicity of a 20-valent pneumococcal vaccine in adults 65 years of age or older with prior pneumococcal vaccination. Available at: https://clinicaltrials.gov/ct2/show/NCT03835975 Last Accessed: August 2022.

Legal Category: S1A
Further information is available upon request

PP-PNR-IRL-0013 Date of Preparation: August 2022

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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