Meningococcal group A Diphtheria Conjugate Vaccine

Meningococcal group A Diphtheria Conjugate Vaccine Uses, Dosage, Side Effects, Food Interaction and all others data.

Presence of bacteriocidal anti-capsular meningococcal antibodies associated with protection from invasive meningococcal disease.

Meningococcal serogroup A, C, Y and W-l 35 capsular polysaccharide antigens individually conjugated to diphtheria toxoid protein carrier.

Induces production of bactericidal antibodies directed against the capsular polysaccharides of serogroups A, C, Y and W-l 35.

Trade Name Meningococcal group A Diphtheria Conjugate Vaccine
Generic Meningococcal group A Diphtheria Conjugate Vaccine
Type
Therapeutic Class Vaccines, Anti-sera & Immunoglobulin
Manufacturer
Available Country
Last Updated: September 19, 2023 at 7:00 am
Meningococcal group A Diphtheria Conjugate Vaccine
Meningococcal group A Diphtheria Conjugate Vaccine

Uses

Meningococcal infection

Dosage

Meningococcal group A Diphtheria Conjugate Vaccine dosage

The dosing schedule for individuals initiating vaccination is as follows:

Infants: 2 Months of Age: administered as a four-dose series at 2,4, 6, and 12 months of age.

Children: 7 Months through 23 Months of Age: administered as a two-dose series with the second dose administered in the second year of life and at least three months after the first dose.

Children: 2 Years through 10 Years of Age: administered as a single dose. For children 2 years through 5 years of age at continued high risk of meningococcal disease, a second dose may be administered 2 months after the first dose.

Adolescents and Adults: 11 Years through 55 Years of Age: administered as a single dose.

Side Effects

Common solicited adverse reactions (>10%) among children initiating vaccination at 2 months of age and receiving the four-dose series were tenderness (24-41%) and erythema at injection site (11-15%), irritability (42-57%), sleepiness (29-50%), persistent crying (21-41 %), change in eating habits (17-23%), vomiting (5-11%) and diarrhea (8-16%).

Common solicited adverse reactions (>10%) among children initiating vaccination at 7 months through 23 months of age and receiving the two-dose series were tenderness (10-16%) and erythema at injection site (12-15%), irritability (27-40%), sleepiness (17-29%), persistent crying (12-21%), change in eating habits (12-20%) and diarrhea (10-16%).

Common solicited adverse reactions (>10%) among children 2 years through 10 years of age who received injection site pain (31%), erythema (23%), irritability (18%), induration (16%), sleepiness (14%), malaise (12%), and headache (11%). Common solicited adverse reactions (>10%) among adolescents and adults who received were pain at the injection site (41%), headache (30%), myalgia (18%), malaise (16%) and nausea (10%).

Precaution

Guillain-Barre syndrome. Preventing & managing allergic vaccine reactions. Thrombocytopenia or bleeding disorders. Immunocompromised person. Pregnancy & lactation.

Interaction

Live vaccines. Reduced immunological response with immunosuppresants.

Pregnancy & Breastfeeding use

Pregnancy Category-C. Animal reproduction studies have shown an adverse effect on the fetus and there are no adequate and well-controlled studies in humans, but potential benefits may warrant use of the drug in pregnant women despite potential risks

Contraindication

Severe allergic reaction (e.g., anaphylaxis) after a previous dose , any component of this vaccine, or any other CRM197, diphtheria toxoid or meningococcal-containing vaccine is a contraindication to administration

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