ID | 1137 |
Name of the vaccine | NEISVAC-C |
Microbe | Bacteria |
Disease name | Meningococcal disease |
Name of bacteria | Neisseria meningitidis |
Type of vaccine | Conjugate |
Nucleic acid content | DNA |
Age | From 8 weeks |
Description of the vaccine | Monovalent Meningococcal group C conjugate vaccine. |
Name of the manufacturer | Pfizer |
Name of the manufacturing country | New Zealand |
Year of manufacture | 2008 |
Clinical Phase status | Approved |
Bacterial strain | Gram-negative diplococcus. |
Efficacy | No protective efficacy studies conducted with NeisVac-C vaccine. |
Vaccine formulation | Semi-opaque white to off-white suspension |
Dosage | Infants 8 weeks to 11 months: Two doses 8 weeks apart. Booster at 12 months of age.
12 months and under 7 years: Single dose. Booster dose if still at risk 2-3 years later.
Greater than 7 years: Single dose. Booster dose if at risk 5 years later. |
Mechanism of action | T-cell dependent response. |
Route of administration | Intramuscular |
Indications | Prevention of invasive disease caused by Neisseria meningitidis serogroup C. |
Export | NA |
Approval | NA |
Adjuvant | Aluminium hydroxide hydrate |
Repurposing | NA |
Side effects of vaccine | In infants and children: Mild fever, decreased appetite, irritability, malaise.
In adults : Headache |
Post vaccination | NA |
Dose type | Both |
Interspecies transfer | NA |
PubMed identifier | NA |
Clinical trial number | NA |
Reference | https://www.immune.org.nz/vaccines/available-vaccines/neisvac-c |
Other name | NA |
Additional Links | NA
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