ID | 1097 |
Name of the vaccine | Td Adsorbed |
Microbe | Bacteria |
Disease name | Tetanus (Lock Jaw) |
Name of bacteria | Clostridium tetani |
Type of vaccine | Toxoid |
Nucleic acid content | DNA |
Age | 7 years and older |
Description of the vaccine | Tetanus and diphtheria toxoids adsorbed. |
Name of the manufacturer | Sanofi Pasteur Ltd |
Name of the manufacturing country | Canada |
Year of manufacture | 2012 |
Clinical Phase status | Approved |
Bacterial strain | An obligate anaerobic bacillus, which is gram positive. |
Efficacy | NA |
Vaccine formulation | Suspension for injection |
Dosage | Primary immunisation - Three doses.
Booster- Single dose at 10 year interval. |
Mechanism of action | Serum tetanus antitoxin level:
at least 0.01 IU/mL: Minimum protective level
at least 0.1 IU/mL : Protective
1.0 IU/mL: Long term protection
|
Route of administration | Intramuscular |
Indications | Immunization against tetanus and diphtheria. |
Export | NA |
Approval | NA |
Adjuvant | Aluminium phosphate |
Repurposing | For diphtheria also. |
Side effects of vaccine | Pain, swelling, redness, fever, chills and sore joints. |
Post vaccination | NA |
Dose type | Combination (4 doses) |
Interspecies transfer | NA |
PubMed identifier | NA |
Clinical trial number | NA |
Reference | http://www.violinet.org/vaxquery/vaccine_detail.php?c_vaccine_id=771&keywords= |
Other name | NA |
Additional Links | https://pdf.hres.ca/dpd_pm/00020609.PDF
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