Nimenrix

RSS

meningococcal group A, C, W 135 and Y conjugate vaccine

Authorised
This medicine is authorised for use in the European Union.

Overview

This is a summary of the European public assessment report (EPAR) for Nimenrix. It explains how the Agency assessed the medicine to recommend its authorisation in the EU and its conditions of use. It is not intended to provide practical advice on how to use Nimenrix.
For practical information about using Nimenrix, patients should read the package leaflet or contact their doctor or pharmacist.

This EPAR was last updated on 03/04/2019

Authorisation details

Product details
Name
Nimenrix
Agency product number
EMEA/H/C/002226
Active substance
  • Neisseria meningitidis serogroup A polysaccharide conjugated to tetanus toxoid
  • Neisseria meningitidis serogroup C polysaccharide conjugated to tetanus toxoid / Neisseria meningitidis serogroup W-135 polysaccharide conjugated to tetanus toxoid
  • Neisseria meningitidis serogroup Y polysaccharide conjugated to tetanus toxoid
International non-proprietary name (INN) or common name
meningococcal group A, C, W 135 and Y conjugate vaccine
Therapeutic area (MeSH)
Meningitis, Meningococcal
Anatomical therapeutic chemical (ATC) code
J07AH08
Publication details
Marketing-authorisation holder
Pfizer Europe MA EEIG
Revision
26
Date of issue of marketing authorisation valid throughout the European Union
20/04/2012
Contact address

Boulevard de la Plaine 17
1050 Bruxelles
Belgium

Product information

28/02/2019 Nimenrix - EMEA/H/C/002226 - II/0084

Contents

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You are therefore advised to be selective about which sections or pages you wish to print.

Pharmacotherapeutic group

Vaccines

Therapeutic indication

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

Assessment history

Changes since initial authorisation of medicine

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