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Prevention

The current World Federation of Hemophilia guidelines for the management of haemophilia were developed using a formal evidence and consensus-based methodology that involved multidisciplinary healthcare professionals and well-informed people living with haemophilia.1

​​​​​​​In addition to the WFH guidelines, the British Society for Haematology have produced evidence-based guidelines to summarise best practice for the assessment and management of people living with haemophilia.2,3 

Nimenrix®

(meningococcal groups A, C, W-135 and Y conjugate vaccine) 

Nimenrix is indicated for active immunisation of individuals from the age of 6 weeks against invasive meningococcal disease caused by Neisseria meningitidis serogroups A, C, W-135, and Y.1

View Nimenrix Summary of Product Characteristics
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Trumenba®

(meningococcal group B vaccine (recombinant, adsorbed))

Trumenba is indicated for active immunisation of individuals 10 years and older to prevent invasive meningococcal disease caused by Neisseria meningitidis serogroup B.2

View Trumenba Summary of Product Characteristics
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References:Nimenrix®. Summary of Product Characteristics.Trumenba®. Summary of Product Characteristics.European Centre for Disease Prevention and Control (ECDC). Factsheet about meningococcal disease. Available at: https://www.ecdc.europa.eu/en/meningococcal-disease/factsheet Last Accessed August 2022.Mbaeyi, S., Duffy, J., McNamara, L.A. Meningococcal Disease. In: Hall, E., Wodi, A.P., Hamborsky J, et al., eds. Epidemiology and Prevention of Vaccine-Preventable Diseases. 14th ed. Centers for Disease Control and Prevention (CDC). Washington DC: Public Health Foundation; 2021.
TreatmentRead the WFH guidelines (3rd edition) Read the guidelines What is Meningococcal Disease?

Meningococcal disease refers to any illness caused by the bacterium Neisseria meningitidis.There are six common serogroups of bacteria that cause most meningococcal disease worldwide - A, B, C, W, X and Y.4

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Further information is available upon request

PP-NIM-IRL-0028 Date of Preparation: September 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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