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Updated: Aug 1, 2026

Trans-vivo Delayed Type Hypersensitivity Assay for Antigen Specific Regulation
Published on: May 2, 2013
Inadvertent administration of DTP and DT after age six as recorded in the Vaccine Adverse Event Reporting System
R K Zimmerman1, T R Pellitieri
1Department of Family Medicine and Clinical Epidemiology, University of Pittsburgh School of Medicine, PA 15261.
Insights
Individuals aged 7 and older are sometimes mistakenly given pediatric diphtheria-tetanus-pertussis (DTP) or diphtheria-tetanus (DT) vaccines instead of adult tetanus-diphtheria (Td) vaccines, potentially causing unnecessary adverse reactions.
Area of Science:
- Immunization practices
- Vaccine safety surveillance
- Pediatric vs. adult vaccination
Background:
- Pediatric diphtheria and tetanus toxoids and whole-cell pertussis vaccine (DTP) and pediatric diphtheria and tetanus toxoids (DT) are not recommended for individuals aged 7 years or older.
- This is due to a higher risk of adverse reactions and the low fatality rate of pertussis in this age group.
Observation:
- Analysis of Vaccine Adverse Event Reporting System (VAERS) data from July 1990 to March 1992 was conducted.
- Vaccine manufacturers were contacted to verify vaccine lot numbers and types.
Findings:
- Among individuals aged 7 and older in the VAERS database, 26 received DTP and 77 received DT.
- Verification revealed that out of 77 DT doses, only 8 were confirmed DT; 56 were actually adult tetanus-diphtheria (Td) vaccines, indicating significant reporting inaccuracies.
Implications:
- Individuals aged 7 years and older may be inadvertently receiving inappropriate vaccine formulations (DTP or DT), leading to unnecessary adverse events.
- The VAERS database, while useful for hypothesis generation, requires careful interpretation due to reporting errors and duplicate entries.
Objective:
Diphtheria and tetanus toxoids and whole-cell pertussis vaccine (DTP) and pediatric diphtheria and tetanus toxoids (DT) are not recommended for individuals > or = 7 years of age due to increased adverse reactions and the low pertussis case-fatality rate. Our objective was to determine if reactions to DTP and DT in individuals > or = 7 years of age were due to administration of pediatric DTP or DT instead of adult tetanus and diphtheria toxoids (Td), after adjusting for database inaccuracies.
Methods:
We analyzed data from the Vaccine Adverse Event Reporting System (VAERS) reported from July 1, 1990 through March 31, 1992. Vaccine manufacturers were contacted to verify whether lot numbers indicated DTP or DT.
Results:
According to VAERS's data, among individuals 7 years of age or older, 26 received DTP and 77 received DT. When lot numbers were compared with manufacturers' records, 8 of the 77 DT doses were confirmed; 11 had incorrect or missing lot numbers; one was a duplicate; 56 were Td; and one was neither DT nor Td. Alleged adverse reactions included fever, headache, and convulsions.
Conclusion:
Individuals > or = 7 years of age are inadvertently receiving DTP or DT and may be unnecessarily experiencing adverse reactions. The 1992 VAERS database offers opportunities to investigate hypotheses but should be interpreted with caution due to inaccuracies in reporting and duplicate entries.
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