GNH USA

Europe — EMA

Neisvac-C

GNH USA supplies Neisvac-C (Neisseria meningitidis Group C), a vaccine for prevention of invasive meningococcal disease caused by serogroup C.

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What is N. Meningitidis Group C (Strain C11) Polysaccharide (De-O-Acetylated) Conjugated To Tetanus Toxoid A?

Neisseria meningitidis Group C (Strain C11) polysaccharide (de-O-acetylated) conjugated to tetanus toxoid A, the active ingredient in Neisvac-C, is a vaccine presented as an injectable solution for intramuscular use. It induces active immunity to prevent invasive disease caused by Neisseria meningitidis serogroup C in at‑risk populations.

GNH USA supplies Neisvac-C as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

What is N. Meningitidis Group C (Strain C11) Polysaccharide (De-O-Acetylated) Conjugated To Tetanus Toxoid A used for?

Neisvac-C is a conjugate vaccine that targets meningococcal serogroup C infection. It is indicated for: - Invasive meningococcal disease caused by Neisseria meningitidis serogroup C: provides active immunity to prevent infection. - Outbreak control of serogroup C meningococcal disease: helps reduce transmission during epidemic situations. - Travel to regions with high serogroup C prevalence: offers protection for travelers at risk of exposure.

What are the side effects of N. Meningitidis Group C (Strain C11) Polysaccharide (De-O-Acetylated) Conjugated To Tetanus Toxoid A?

Neisvac-C may cause a range of post‑vaccination reactions. Monitoring and reporting are essential.

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 headache within 24 hours.

Serious or Rare Side Effects: - Anaphylaxis: severe allergic reaction requiring immediate medical attention. - Guillain‑Barré syndrome: rare demyelinating neuropathy. - Seizures: uncommon neurologic event. - Severe hypotension: marked drop in blood pressure after injection. - Acute allergic reaction: urticaria, angioedema, or bronchospasm.

What precautions apply to N. Meningitidis Group C (Strain C11) Polysaccharide (De-O-Acetylated) Conjugated To Tetanus Toxoid A?

Before administering Neisvac-C, consider the following safety measures. - Pregnancy: safety not established; use only if benefit outweighs risk. - Breastfeeding: limited data; consult healthcare professional. - Immunocompromised patients: vaccine may elicit a reduced immune response. - Prior allergic reaction to tetanus toxoid or any component: avoid vaccination. - Acute febrile illness: defer vaccination until recovery. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does N. Meningitidis Group C (Strain C11) Polysaccharide (De-O-Acetylated) Conjugated To Tetanus Toxoid A interact with?

Neisvac-C has limited known drug interactions, but caution is advised.

Major Interactions (Avoid): - Immunoglobulin therapy: may diminish vaccine‑induced antibody response. - Live bacterial vaccines administered concurrently: could interfere with immune response.

Moderate Interactions (Monitor Closely): - Antipyretics (e.g., acetaminophen, ibuprofen): may mask fever post‑vaccination. - Other injectable vaccines given on the same day: consider separate anatomical sites. - Corticosteroids or immunosuppressants: may reduce immunogenicity of the vaccine.

Frequently asked questions

What is Neisvac-C used for?+
Neisvac-C is a conjugate vaccine indicated to prevent invasive disease caused by Neisseria meningitidis serogroup C. It is used in individuals at risk of meningococcal infection, including travelers to endemic areas and during outbreak control.
How does the active ingredient in Neisvac-C work?+
The vaccine contains a de‑O‑acetylated polysaccharide from serogroup C linked to tetanus toxoid. This conjugate stimulates T‑cell help, leading to robust B‑cell production of anti‑polysaccharide antibodies that provide long‑lasting protection against the bacteria.
What is the usual dose of Neisvac-C?+
The dosing regimen for Neisvac-C is determined by the prescribing healthcare professional based on the patient’s age, health status, and local immunization guidelines. The prescriber will specify the number of doses and interval.
Is Neisvac-C safe during pregnancy or breastfeeding?+
Safety data for Neisvac-C in pregnancy and lactation are limited. It should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and after consultation with a qualified healthcare provider.
How do I order Neisvac-C from GNH USA?+
To order Neisvac-C, submit an enquiry on the product page at gnh-usa.com with the required quantity. GNH USA 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.
How does Neisvac-C compare with other meningococcal vaccines?+
Neisvac-C is a conjugate vaccine targeting serogroup C, whereas some alternatives are polysaccharide‑only or cover multiple serogroups (A, C, W, Y, B). Conjugate vaccines like Neisvac-C generally induce stronger, longer‑lasting immunity and are effective in younger children.
What are the storage and handling requirements for Neisvac-C?+
Neisvac-C must be stored refrigerated at 2‑8 °C. Keep the vial in its original packaging, protect it from light, and avoid freezing or shaking. Do not use the product if it has been exposed to temperatures outside this range.
How is Neisvac-C administered?+
Neisvac-C is given as a single intramuscular injection, typically into the deltoid muscle of the upper arm. The injection is performed by a qualified healthcare professional using aseptic technique.
What are the most serious risks associated with Neisvac-C?+
Serious adverse events, although rare, include anaphylaxis, Guillain‑Barré syndrome, severe allergic reactions, seizures, and profound hypotension. Any signs of a severe reaction require immediate medical attention.
Who should not receive Neisvac-C?+
Individuals with a known severe allergy to tetanus toxoid or any component of the vaccine should not receive Neisvac-C. It is also contraindicated in persons who have experienced a severe immediate hypersensitivity reaction after a previous dose.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
N. Meningitidis Group C (Strain C11) Polysaccharide (De-O-Acetylated) Conjugated To Tetanus Toxoid A
Route
Intramuscular Use
Manufacturer
Pfizer S.A.
Origin
EU

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