GNH USA

Europe — EMA

Neisvac-C

GNH USA supplies Neisvac-C (N. 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?

N. 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 is used to prevent invasive disease caused by Neisseria meningitidis serogroup C in individuals at risk.

GNH USA supplies Neisvac-C as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, clinics and vaccination centres 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 the meningococcal group C pathway to prevent serious bacterial infection.

- Invasive meningococcal disease (serogroup C): provides active immunity to prevent meningitis and septicemia caused by N. meningitidis group C. - Adolescents and young adults: reduces risk of serogroup C infection in this high‑risk age group. - Outbreak control and travel: used in vaccination campaigns to curb serogroup C outbreaks and protect travelers to endemic areas.

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, most of which are mild and self‑limiting.

Common Side Effects: - Injection site pain: soreness or tenderness at the injection site. - Redness or swelling: localized erythema or edema. - Fever: low‑grade temperature rise within 24‑48 hours. - Headache: mild to moderate headache after vaccination. - Fatigue: transient tiredness or malaise. - Myalgia: muscle aches in the days following injection.

Serious or Rare Side Effects: - Anaphylaxis: severe allergic reaction requiring immediate medical attention. - Guillain‑Barré syndrome: rare neurologic disorder with muscle weakness. - Seizures: occasional convulsive episodes, especially in infants. - Hypotension: sudden drop in blood pressure post‑injection. - Immune‑mediated thrombocytopenia: low platelet count with bleeding risk. - Severe local reaction: extensive necrosis or abscess at the injection site.

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.

- Allergy assessment: verify no known hypersensitivity to any vaccine component. - Acute illness: postpone vaccination in persons with moderate or severe febrile illness. - Observation: monitor for at least 15 minutes after injection for immediate hypersensitivity. - Concurrent vaccines: separate administration from live vaccines by at least 4 weeks. - Pregnancy and lactation: use only if benefits outweigh potential risks, as data are limited. - 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 may interact with other agents that affect immune response or vaccine efficacy.

Major Interactions (Avoid): - Other meningococcal conjugate vaccines: avoid simultaneous use to prevent antigenic interference. - Live bacterial vaccines (e.g., oral typhoid): avoid co‑administration within 4 weeks.

Moderate Interactions (Monitor Closely): - Immunosuppressive agents (corticosteroids, chemotherapy): may diminish antibody response. - Intravenous immunoglobulin or blood products: may interfere with vaccine efficacy if given within 4 weeks. - Antipyretics: may reduce fever but do not affect immunogenicity.

Frequently asked questions

What is Neisvac-C used for?+
Neisvac-C is a conjugate vaccine indicated for the prevention of invasive disease caused by Neisseria meningitidis serogroup C. It is administered to individuals at risk, including adolescents, travelers to endemic regions, and during outbreak control programs, to protect against meningitis and septicemia.
How does the active ingredient in Neisvac-C work?+
The active ingredient is a de‑O‑acetylated polysaccharide from N. meningitidis group C linked to tetanus toxoid. This conjugation creates a T‑cell‑dependent antigen that stimulates helper T‑cells and B‑cells, leading to the production of high‑affinity antibodies that specifically target the bacterial capsule, thereby preventing infection.
What is the usual dose of Neisvac-C?+
The dosing regimen for Neisvac-C is determined by the prescribing healthcare professional based on age, risk factors, and local immunization guidelines. The prescriber will decide the number of doses, interval between doses, and any booster requirements.
Is Neisvac-C safe to use during pregnancy or breastfeeding?+
Safety data for Neisvac-C in pregnancy and lactation are limited. It should only be administered when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision should be made by 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, specifying the required quantity. GNH USA supplies hospitals, pharmacies and procurement teams worldwide, and will request verification of trade or institutional credentials before providing pricing, availability, cold‑chain shipping details and import documentation.
How does Neisvac-C compare with other meningococcal vaccines?+
Neisvac-C is a group C conjugate vaccine, which offers a T‑cell‑dependent immune response and longer lasting protection compared with plain polysaccharide vaccines. Compared with broader multivalent conjugate vaccines, it targets only serogroup C, making it suitable for regions where that serogroup predominates or for specific outbreak control.
What are the storage and handling requirements for Neisvac-C?+
Neisvac-C must be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. The vaccine should be kept in its original packaging until use to maintain potency and stability.
How is Neisvac-C administered?+
Neisvac-C is given as an 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?+
The most serious risks include severe allergic reactions such as anaphylaxis, rare neurologic events like Guillain‑Barré syndrome, and immune‑mediated thrombocytopenia. Immediate medical attention is required if any signs of a serious reaction occur after vaccination.
Who should not receive Neisvac-C?+
Neisvac-C should not be given to individuals with a known severe allergy to any component of the vaccine, including the tetanus toxoid carrier. It is also contraindicated in persons who have experienced a previous severe reaction to a meningococcal conjugate vaccine.
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 Kft.
Origin
EU

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