GNH USA

Europe — EMA

Neisvac-C1

GNH USA supplies Neisvac-C1 (N. meningitidis Group C polysaccharide‑tetanus toxoid conjugate), a conjugate vaccine for prevention of invasive meningococcal

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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-C1, is a conjugate vaccine presented as a sterile powder for intramuscular use. It induces immunity against invasive disease caused by Neisseria meningitidis serogroup C in infants, children, adolescents and adults.

GNH USA supplies Neisvac-C1 as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

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

Neisvac-C1 is a conjugate vaccine targeting the meningococcal disease pathway caused by Neisseria meningitidis serogroup C. - Infants and young children: provides active immunity against serogroup C meningococcal disease. - Adolescents and adults: maintains protective antibody levels to prevent invasive disease. - Travelers to endemic regions: reduces risk of acquiring Neisseria meningitidis serogroup C infection.

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

Common Side Effects: - Injection site pain: mild to moderate discomfort at the site of administration. - Redness or swelling: localized erythema or edema that resolves within a few days. - Fever: transient low‑grade temperature elevation. - Headache or fatigue: mild systemic symptoms post‑vaccination.

Serious or Rare Side Effects: - Anaphylaxis: severe allergic reaction requiring immediate medical attention. - Guillain‑Barré syndrome: rare neurological disorder with muscle weakness. - Seizures: uncommon occurrence, especially in febrile children. - Severe local reaction: extensive necrosis or abscess formation at injection site. - Immune‑mediated thrombocytopenia: rare drop in platelet count.

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

Precautions should be observed when administering Neisvac-C1. - Pregnancy: safety not established; vaccinate only if clearly needed. - Breastfeeding: consider risk‑benefit balance before use. - Immunocompromised patients: may exhibit reduced antibody response. - History of severe allergic reaction to tetanus toxoid or any vaccine component: avoid administration. - 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?

Potential interactions with other medicines or vaccines are limited. Major Interactions (Avoid): - Severe allergic reaction to tetanus toxoid: contraindicates use of Neisvac-C1. - Simultaneous injection of another vaccine containing tetanus toxoid at the same site: may increase risk of local adverse reactions.

Moderate Interactions (Monitor Closely): - Concurrent administration of immunoglobulins: may diminish vaccine efficacy. - Use of immunosuppressive therapy: may reduce immune response to the vaccine.

Frequently asked questions

What is Neisvac-C1 used for?+
Neisvac-C1 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 infants, children, adolescents, adults, and travelers to regions where serogroup C meningococcal disease is endemic.
How does the active ingredient in Neisvac-C1 work?+
The vaccine contains a de‑O‑acetylated polysaccharide from the capsular coat of N. meningitidis group C linked to tetanus toxoid. This conjugation creates a T‑cell‑dependent antigen that stimulates robust IgG antibody production, enabling the immune system to recognize and neutralise the bacteria upon exposure.
What is the usual dose of Neisvac-C1?+
The dosing schedule for Neisvac-C1 is determined by the prescribing healthcare professional based on the patient’s age, health status, and vaccination history. The prescriber will decide the number of doses, interval between doses, and any booster requirements.
Is Neisvac-C1 safe to use during pregnancy or breastfeeding?+
Safety data for Neisvac-C1 in pregnancy are limited, so it should only be given when the potential benefit outweighs any potential risk. Breastfeeding is not a contraindication, but the decision should be made after evaluating the risk‑benefit profile for mother and infant.
How do I order Neisvac-C1 from GNH USA?+
To order Neisvac-C1, 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 trade or institutional credentials before providing pricing, availability, cold‑chain shipping details and import documentation.
How does Neisvac-C1 compare with other meningococcal vaccines?+
Neisvac-C1 is a polysaccharide‑tetanus toxoid conjugate vaccine targeting serogroup C, offering a T‑cell‑dependent response and longer‑lasting immunity compared with plain polysaccharide vaccines. It differs from quadrivalent conjugate vaccines that also cover serogroups A, W, and Y, focusing solely on serogroup C protection.
How should Neisvac-C1 be stored and handled?+
Neisvac-C1 must be stored refrigerated at 2‑8 °C. Keep the vials in the original packaging, protect them from light, and avoid freezing or shaking. If a temporary temperature excursion occurs, consult the product’s stability guidelines before use.
How is Neisvac-C1 given or administered?+
Neisvac-C1 is administered by a single intramuscular injection, typically into the deltoid muscle of the upper arm. The exact site and technique are determined by the healthcare professional performing the vaccination.
What are the most serious risks to watch for with Neisvac-C1?+
The most serious adverse events associated with Neisvac-C1 include severe allergic reactions such as anaphylaxis, Guillain‑Barré syndrome, and rare neurological complications like seizures. Immediate medical attention is required if any signs of a serious reaction appear after vaccination.
Who should not receive Neisvac-C1?+
Individuals with a known severe allergy to tetanus toxoid or any component of the vaccine should not receive Neisvac-C1. Additionally, those who have experienced a serious adverse reaction to a previous dose of a meningococcal conjugate vaccine should avoid further administration.
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
Laboratórios Pfizer Lda.
Origin
EU

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