Product image of Nimenrix (Tetanus Toxoid, N. Meningitidis Group C Polysaccharide, N. Meningitidis Group Y Polysaccharide, Neis) supplied by GNH India

Nimenrix

Active Ingredient:
Tetanus Toxoid, N. Meningitidis Group C Polysaccharide, N. Meningitidis Group Y Polysaccharide, Neis
Origin:
EU

Nimenrix (Tetanus Toxoid, N. Meningitidis Group C Polysaccharide, N. Meningitidis Group Y Polysaccharide, Neis)

Meningococcal (A, C, W-135, Y) conjugate vaccine, the active ingredient in Nimenrix, is a vaccine presented as a 0.5 mL injectable solution for intramuscular use. It is indicated for the prevention of invasive meningococcal disease caused by Neisseria meningitidis serogroups A, C, W-135 and Y in individuals from 2 months up to 55 years of age.

GNH India supplies Nimenrix as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring quality and regulatory compliance across global markets.

Manufacturer / TM Owner

Pfizer Europe Ma Eeig

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Indications & Clinical Uses

Nimenrix is a conjugate vaccine that targets meningococcal polysaccharides to prevent invasive disease. It is used in the following clinical situations:

  • Invasive meningococcal disease (A, C, W-135, Y): Provides active immunity to prevent infection by these serogroups.
  • Primary vaccination (children ≥2 months): Establishes protective antibody levels in the pediatric population.
  • Booster immunization (adolescents and adults): Restores waning immunity and maintains long‑term protection.

How It Works

  • The vaccine contains capsular polysaccharides from Neisseria meningitidis serogroups A, C, W‑135 and Y covalently linked to tetanus toxoid. Conjugation converts the polysaccharide antigens into T‑cell‑dependent forms, prompting helper‑T‑cell activation, robust B‑cell antibody production, and the generation of opsonophagocytic antibodies that facilitate bacterial clearance.

Side Effects

Nimenrix is generally well tolerated, but injection‑related and systemic reactions can occur.

Common Side Effects

  • Injection site pain: mild to moderate discomfort at the injection site.
  • Redness or swelling: localized erythema or edema.
  • Fever: transient low‑grade temperature rise.
  • Headache: mild to moderate headache within 24 hours.
  • Fatigue: temporary tiredness post‑vaccination.
  • Myalgia: mild muscle aches.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Guillain‑Barré syndrome: rare neurological disorder.
  • Seizures: infrequent convulsive episodes.
  • Severe hypotension: marked drop in blood pressure.
  • Acute allergic reaction: angioedema or urticaria.
  • Vaccine‑associated meningococcal disease: extremely rare occurrence.

Precautions & Warnings

Before administering Nimenrix, consider the following precautions:

  • Pregnancy: safety not established; evaluate risk‑benefit with a healthcare professional.
  • Breastfeeding: unknown safety profile; weigh potential benefits against risks.
  • Age limitation: not recommended for individuals older than 55 years.
  • Known allergy: avoid if hypersensitivity to any vaccine component is documented.
  • Immunocompromised patients: may exhibit reduced antibody response.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Vaccines can interact with other therapies; monitor accordingly.

Major Interactions (Avoid)

  • Severe allergic reaction to any vaccine component: contraindicates use.
  • Prior anaphylaxis to a meningococcal conjugate vaccine: contraindicates administration.

Moderate Interactions (Monitor Closely)

  • Concurrent administration of blood products containing immunoglobulins: may diminish vaccine efficacy.
  • Live bacterial vaccines given within 4 weeks: could interfere with immune response.
  • High‑dose corticosteroids started within 2 weeks: may impair antibody generation.
  • Use of antipyretics before vaccination: may blunt antibody response.
  • Simultaneous receipt of other vaccines: generally safe but may increase local reactogenicity.

Frequently Asked Questions

Nimenrix is a conjugate vaccine indicated to prevent invasive meningococcal disease caused by Neisseria meningitidis serogroups A, C, W‑135 and Y. It is used for primary vaccination in children from two months of age and for booster doses in adolescents and adults up to 55 years to maintain protective immunity.

The vaccine contains polysaccharide antigens from four meningococcal serogroups that are chemically linked to tetanus toxoid. This conjugation creates a T‑cell‑dependent antigen, stimulating helper‑T‑cells and B‑cells to produce high‑affinity antibodies that opsonize the bacteria, leading to their clearance by the immune system.

The prescribed dose of Nimenrix is determined by the treating clinician. Typically, a single 0.5 mL intramuscular injection is administered according to national immunisation schedules, with booster doses given at recommended intervals for continued protection.

Safety data for Nimenrix in pregnancy and lactation are limited. Health professionals should assess the potential benefits against any unknown risks before vaccinating pregnant or breastfeeding individuals. Consultation with a physician is essential to make an informed decision.

To order Nimenrix, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, cold‑chain shipping details and any necessary import documentation.

Nimenrix is a quadrivalent conjugate vaccine covering serogroups A, C, W‑135 and Y, similar to other conjugates such as Menactra® and Menveo®. Compared with polysaccharide‑only vaccines, conjugates like Nimenrix generate a stronger, longer‑lasting T‑cell‑dependent immune response and are suitable for younger children.

Nimenrix must be stored refrigerated at 2 °C to 8 °C. Keep the vials in their original packaging, protect them from light, and avoid freezing or shaking. If the cold chain is broken, the product should not be used.

Nimenrix is given as a single 0.5 mL intramuscular injection. The preferred injection sites are the deltoid muscle of the upper arm for adults and the anterolateral thigh for infants and young children, following aseptic technique.

Serious adverse events, although rare, include anaphylaxis, severe allergic reactions, Guillain‑Barré syndrome, seizures, and profound hypotension. Immediate medical attention is required if any of these symptoms develop after vaccination.

Nimenrix is contraindicated in individuals with a known severe allergy to any vaccine component or who have experienced anaphylaxis after a previous meningococcal conjugate vaccine. It is also not recommended for persons older than 55 years or for those with uncontrolled severe immunodeficiency without medical guidance.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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