Tetanus Clinical Trial
Official title:
Evaluation of Safety and Efficacy Through Post Market Surveillance for Infanrix™, the DTaP Mixed Vaccine
The purpose of this study was to investigate the following questions through post-marketing
surveillance:
- Unknown/Unexpected adverse events and the serious adverse events.
- The circumstances in which the adverse events occurred under the practical application.
- Factors considered to have influence on safety.
- Factors considered to have influence on efficacy.
- Miscellaneous - Facts about mechanism, efficacy and safety which were not clearly known
due to the inherent problems of the drugs.
n/a
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
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