Product image of Neisvac-C (Tetanus Toxoid, Algeldrate, N. Meningitidis Group C (Strain C11) Polysaccharide (De-O-Acetylated)) supplied by GNH India

Neisvac-C

Active Ingredient:
Tetanus Toxoid, Algeldrate, N. Meningitidis Group C (Strain C11) Polysaccharide (De-O-Acetylated)
Origin:
EU

Neisvac-C (Tetanus Toxoid, Algeldrate, N. Meningitidis Group C (Strain C11) Polysaccharide (De-O-Acetylated))

Tetanus toxoid, algeldrate, Neisseria meningitidis group C (strain C11) polysaccharide (de‑O‑acetylated), the active ingredient in Neisvac‑C, is a vaccine presented as an injectable solution for intramuscular use. It is employed to induce protective immunity against tetanus and against meningococcal disease caused by Neisseria meningitidis group C in individuals requiring immunisation.

GNH India supplies Neisvac‑C as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to EU quality standards and provides cold‑chain logistics for biologic products.

Manufacturer / TM Owner

Pfizer Europe Ma Eeig

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Indications & Clinical Uses

Neisvac‑C is a tetanus and meningococcal conjugate vaccine used in immunisation programmes to prevent specific bacterial infections.

  • Tetanus: provides active immunity that protects against tetanus toxin in individuals of all ages.
  • Meningococcal group C disease: induces antibodies against the polysaccharide capsule of Neisseria meningitidis group C, reducing risk of invasive meningitis.
  • Routine immunisation schedules: can be incorporated into childhood or adult booster schedules to maintain protective antibody levels.

How It Works

  • Neisvac‑C contains purified tetanus toxoid and de‑O‑acetylated polysaccharide from Neisseria meningitidis group C conjugated to algeldrate. After intramuscular injection, the toxoid is processed by antigen‑presenting cells, stimulating B‑cell production of anti‑tetanus toxin antibodies. The polysaccharide component is presented as a T‑cell dependent antigen, prompting a robust IgG response against the meningococcal capsule, thereby establishing active, long‑lasting immunity.

Side Effects

Injection of Neisvac‑C may be associated with local and systemic reactions, most of which are mild and transient.

Common Side Effects

  • Injection site pain: mild soreness at the site of administration.
  • Redness or swelling: localized erythema or edema.
  • Low‑grade fever: temperature rise up to 38 °C within 24 hours.
  • Headache: mild to moderate headache following vaccination.
  • Fatigue: transient tiredness lasting a day or two.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Guillain‑Barré syndrome: rare neurological disorder potentially triggered post‑vaccination.
  • Seizures: uncommon occurrence, especially in individuals with pre‑existing neurologic conditions.
  • Severe local reaction: extensive swelling or necrosis at injection site.
  • Thrombotic events: very rare clotting disorders reported in isolated cases.

Precautions & Warnings

Before administering Neisvac‑C, healthcare professionals should observe several precautionary measures to ensure safety.

  • Allergy assessment: verify no known hypersensitivity to tetanus toxoid, algeldrate or meningococcal polysaccharide.
  • Acute illness: postpone vaccination in persons with moderate or severe febrile illness until recovery.
  • Prior reaction: avoid repeat dosing in individuals who experienced a severe allergic response to a previous dose.
  • Pregnancy considerations: use only if the benefit outweighs potential risk and after medical consultation.
  • Immunocompromised patients: anticipate possible reduced antibody response and monitor serology.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Vaccines can interact with other medicines or biologics, affecting efficacy or safety.

Major Interactions (Avoid)

  • Live vaccines: avoid simultaneous administration with live attenuated vaccines to prevent interference.
  • Immunoglobulin therapy: concurrent use may diminish the immune response to the vaccine.
  • Blood products: transfusion within 48 hours may reduce vaccine effectiveness.

Moderate Interactions (Monitor Closely)

  • Antipyretics: analgesics such as acetaminophen may mask fever, a sign of reaction.
  • Immunosuppressive drugs: may lower antibody production, requiring serological monitoring.
  • Corticosteroids: high‑dose steroids can attenuate the immune response, consider timing of vaccination.

Frequently Asked Questions

Neisvac‑C is a combination vaccine that protects against tetanus and meningococcal disease caused by Neisseria meningitidis group C. It is administered to individuals who need immunisation against these bacterial infections, typically as part of routine or catch‑up vaccination programmes.

The tetanus toxoid component stimulates the immune system to produce antibodies that neutralise tetanus toxin, while the de‑O‑acetylated polysaccharide from meningococcal group C, conjugated to algeldrate, is presented as a T‑cell dependent antigen, prompting a strong IgG response that targets the bacterial capsule.

The specific dose and schedule of Neisvac‑C are determined by the prescribing healthcare professional based on the patient’s age, health status and local immunisation guidelines. The product is supplied as a single‑dose injectable solution for intramuscular administration.

The safety of Neisvac‑C in pregnancy has not been fully established, so it should be used only if the potential benefit justifies any possible risk to the fetus. Breastfeeding is not a contraindication, but mothers should discuss vaccination with their healthcare provider.

To order Neisvac‑C, 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.

Neisvac‑C combines tetanus toxoid with a de‑O‑acetylated meningococcal group C polysaccharide, offering protection against both diseases in a single injection. Compared with monovalent tetanus vaccines, it adds meningococcal coverage, and versus separate meningococcal vaccines it reduces the number of injections required.

Neisvac‑C must be stored at 2‑8 °C (refrigerated). It should be kept in its original packaging, protected from light, and must not be frozen or shaken to maintain vaccine potency.

Neisvac‑C is given as a single intramuscular injection, usually into the deltoid muscle of adults or the anterolateral thigh in infants and young children, following the dosing schedule recommended by the prescriber.

Serious adverse events, although rare, can include anaphylactic reactions, Guillain‑Barré syndrome, severe local tissue reactions, seizures, and rare thrombotic events. Any signs of severe allergic reaction or neurological symptoms after vaccination should be evaluated promptly by a healthcare professional.

Neisvac‑C should be avoided in individuals with a known severe allergy to any of its components, those who have experienced a serious reaction to a previous dose, or in persons for whom a contraindication to tetanus or meningococcal vaccination has been documented. Clinical judgement is required for other special populations.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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