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, and Neisseria meningitidis group C polysaccharide, the active ingredients in Neisvac-C, is a vaccine presented as a vaccine for intramuscular use. It prevents tetanus and provides immunity against Neisseria meningitidis group C infection in individuals at risk.
GNH India supplies Neisvac-C as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

Pfizer B.V.

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Indications & Clinical Uses

Neisvac-C is a combination vaccine that targets bacterial toxin and capsular polysaccharide disease pathways. It is indicated for:

  • Tetanus: induces protective antibodies that neutralize tetanus toxin.
  • Neisseria meningitidis group C infection: stimulates antibodies against the group C polysaccharide capsule to prevent invasive meningococcal disease.
  • Travel to endemic regions: provides protection against group C meningococcal disease for travelers and pilgrims.

How It Works

  • Neisvac-C contains purified tetanus toxoid, an algeldrate adjuvant, and a de‑O‑acetylated polysaccharide from Neisseria meningitidis group C. The toxoid elicits a T‑cell‑dependent response that generates anti‑tetanus toxin antibodies, while the polysaccharide induces a B‑cell‑mediated response against the bacterial capsule. Algeldrate enhances antigen presentation, resulting in robust, long‑lasting humoral immunity against both pathogens.

Side Effects

Neisvac-C is generally well tolerated, but injection‑related reactions and rare systemic events have been reported.

Common Side Effects

  • Injection site pain: mild to moderate discomfort at the injection site.
  • Redness or swelling: localized erythema and edema.
  • Fever: low‑grade temperature rise within 24‑48 hours.
  • Headache: transient mild headache.
  • Fatigue: temporary tiredness.
  • Myalgia: muscle aches near the injection area.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Guillain‑Barré syndrome: rare demyelinating neuropathy.
  • Seizures: infrequent neurologic events.
  • Severe hypotension: marked drop in blood pressure.
  • Persistent high fever: prolonged temperature elevation.
  • Severe local necrosis: extensive tissue damage at injection site.

Precautions & Warnings

Prior to administration, consider the following safety measures:

  • Pregnancy: safety not established; vaccinate only if benefit outweighs risk.
  • Breastfeeding: no known adverse effects, but consult a healthcare professional.
  • Immunocompromised patients: vaccine may elicit reduced immune response.
  • Known allergy: avoid if hypersensitivity to any vaccine component exists.
  • Acute illness: postpone vaccination during moderate or severe febrile illness.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Vaccination may be influenced by concurrent therapies or other immunizations.

Major Interactions (Avoid)

  • Live bacterial or viral vaccines: concurrent administration may interfere with immune response.
  • Immunoglobulin therapy: can neutralize vaccine antigens and diminish effectiveness.

Moderate Interactions (Monitor Closely)

  • Immunosuppressive drugs (e.g., corticosteroids, chemotherapy): may reduce antibody production.
  • Antipyretics taken prophylactically: could mask early fever signals.
  • Blood products administered within 48 hours: may lower vaccine efficacy.

Frequently Asked Questions

Neisvac-C is a combination vaccine indicated for the prevention of tetanus and for protection against infection caused by Neisseria meningitidis group C. It is administered to individuals who need immunity against these bacterial diseases, including travelers to endemic areas.

The vaccine contains tetanus toxoid, which stimulates the immune system to produce antibodies that neutralize tetanus toxin, and a de‑O‑acetylated polysaccharide from Neisseria meningitidis group C that induces antibodies against the bacterial capsule. An algeldrate adjuvant enhances the overall immune response.

The dosing schedule for Neisvac-C is determined by the prescribing healthcare professional based on age, health status, and vaccination history. The prescriber will specify the number of doses, interval between doses, and any booster requirements.

Safety data for Neisvac-C in pregnancy are limited, so vaccination should only be considered if the potential benefit outweighs any risk. Breastfeeding is not known to be contraindicated, but mothers should discuss vaccination with their healthcare provider.

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

Neisvac-C combines tetanus toxoid with a group C meningococcal polysaccharide in a single injection, offering protection against both diseases simultaneously. Some alternatives provide separate tetanus or broader meningococcal coverage (e.g., conjugate vaccines covering multiple serogroups), which may be preferred in different clinical contexts.

Neisvac-C must be stored refrigerated at 2‑8 °C. Keep the vials in the original packaging, protect them from light, and avoid freezing or shaking the product. Do not use if the cold chain has been broken.

Neisvac-C is given by intramuscular injection, typically into the deltoid muscle of the upper arm. The injection should be performed by a qualified healthcare professional using aseptic technique.

Serious adverse events, although rare, include anaphylaxis, Guillain‑Barré syndrome, severe hypotension, and high‑grade fever. Immediate medical attention is required if any signs of a severe allergic reaction or neurological symptoms develop after vaccination.

Individuals with a known hypersensitivity to tetanus toxoid, algeldrate, the meningococcal polysaccharide, or any other vaccine component should not receive Neisvac-C. Those with severe acute illness should defer vaccination until recovery.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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