ID | 1017 |
Name of the vaccine | Decavac |
Microbe | Bacteria |
Disease name | Diphtheria |
Name of bacteria | Corynebacterium diphtheriae |
Type of vaccine | Combination |
Nucleic acid content | DNA |
Age | 7 years and older |
Description of the vaccine | Tetanus and diphtheria toxoids adsorbed (Td vaccine). |
Name of the manufacturer | Sanofi Pasteur Inc. |
Name of the manufacturing country | United States |
Year of manufacture | 1955 |
Clinical Phase status | Approved |
Bacterial strain | Gram-positive bacillus. |
Efficacy | NA |
Vaccine formulation | Sterile suspension |
Dosage | Primary Immunization - three 0.5 mL doses.
Routine booster - in children 11-12 years of age and every 10 years. |
Mechanism of action | Serum diphtheria antitoxin level-
0.01 IU/mL - lowest protection level.
0.1 IU/mL - Protective
Greater than or equal to 1.0 IU/mL - Long term protection |
Route of administration | Intramuscular |
Indications | Active immunization for the prevention of tetanus and diphtheria. |
Export | NA |
Approval | US FDA |
Adjuvant | Alum |
Repurposing | For tetanus also. |
Side effects of vaccine | Pain, headache, injection site swelling and erythema, muscle weakness, tiredness, diarrhoea, chills, nausea, sore and swollen joints. |
Post vaccination | NA |
Dose type | Combination doses |
Interspecies transfer | NA |
PubMed identifier | NA |
Clinical trial number | NA |
Reference | https://www.rxlist.com/decavac-drug.htm#description |
Other name | NA |
Additional Links | NA
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