| ID | 1071 |
| Name of the vaccine | Daptacel |
| Microbe | Bacteria |
| Disease name | Tetanus (Lock Jaw) |
| Name of bacteria | Clostridium tetani |
| Type of vaccine | Inactivated |
| Nucleic acid content | DNA |
| Age | 6 weeks to 6 years |
| Description of the vaccine | Diphtheria, Tetanus Toxoids and Acellular Pertussis Vaccine Adsorbed (DTaP vaccine). |
| Name of the manufacturer | Sanofi Pasteur Limited |
| Name of the manufacturing country | Canada |
| Year of manufacture | 2002 |
| Clinical Phase status | Approved |
| Bacterial strain | An obligate anaerobic bacillus, which is gram positive. |
| Efficacy | After the third dose, 100% achieved tetanus antitoxin levels of greater than or equal to 0.10 IU/mL. While 98.8% achieved levels of greater than or equal to 1.0 IU/mL after the fourth dose. |
| Vaccine formulation | Suspension for injection |
| Dosage | The five dose immunization series administered at 2, 4, 6 and 15-20 months of age, and at 4-6 years. |
| Mechanism of action | Serum tetanus antitoxin level of greater than or equal to 0.1 IU/mL is protective. |
| Route of administration | Intramuscular |
| Indications | Used to complete the immunization series in infants who have received 1 or more doses of whole-cell pertussis DTP. |
| Export | Distributed by- Sanofi Pasteur Inc., USA |
| Approval | US FDA |
| Adjuvant | Aluminium phosphate |
| Repurposing | Could be used for diphtheria and pertussis. |
| Side effects of vaccine | Fussiness, inconsolable crying, and decreased activity/lethargy, fever, tenderness, redness and increase in arm circumference. |
| Post vaccination | NA |
| Dose type | Combination doses |
| Interspecies transfer | NA |
| PubMed identifier | NA |
| Clinical trial number | NCT00258895 |
| Reference | https://www.fda.gov/media/74035/download |
| Other name | NA |
| Additional Links | NA
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