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Clinical Information Clinical Information Burden of meningococcal disease Serogroup distribution Nimenrix® immunogenicity Nimenrix® persistence Nimenrix® dose and administration Real-world impact Summary Important Safety Information Abbreviated Prescribing Information Support and Services Support and Services VideosWebinarsSelf-detail Presentations

Nimenrix® dose & administration

Dosing schedule

Nimenrix® is approved as a single dose from 12 months of age.2

Nimenrix® is a licensed meningococcal conjugate vaccine for serogroups A, C, W-135, and Y that can be administered at age 6 weeks with no upper age limit and with broad age indication2

Adapted from Nimenrix (Meningococcal group A, C, W-135 and Y conjugate vaccine). [Local product document]. May 2022.

Safety profile

Preparation & Storage

Nimenrix® can be administered in a few steps.2

Route of administration2
Immunisation should carried out by intramuscular injection only. In infants, the recommended injection site is the anterolateral aspect of the thigh. In individuals aged ≥1 year, the recommended injection site is the anterolateral aspect of the thigh or the deltoid muscle.

Nimenrix® allows concomitant administration with the standard vaccine calendar.2


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*In some situations, consideration may be given to administering an additional primary dose or a booster dose of Nimenrix®
Nimenrix® should be used in accordance with official recommendations2
A second dose of Nimenrix® may be considered appropriate for some individuals.

DTaP, Diphtheria, tetanus, acellular pertussis; HiB, Haemophilus influenzae type B; IPV, Inactivated polio vaccine; HepB, Hepatitis B.

  1. Stein-Zamir C, Shoob H, Sokolov I, Kunbar A, Abramson N, Zimmerman D. The clinical features and long-term sequelae of invasive meningococcal disease in children. Pediatr Infect Dis J. 2014;33(7):777-779.
  2. Nimenrix (Meningococcal group A, C, W-135 and Y conjugate vaccine). Egyptian Drug Authority leaflet approval date: 19/10/2022 Revision date: May 2022.
Click here for Nimenrix® Prescribing Information Loading

Approval Code: BF0098OA686/052023
Invalidation date: 10/05/2025


Adverse events should be reported. Adverse events can be reported to [email protected]

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