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This phase IV clinical study evaluates the safety of enterovirus 71 vaccine in children aged 6-35 months old by the method of both passive and active surveillance.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| two doses enterovirus 71 vaccine | Experimental | Two doses of enterovirus 71 vaccine will be given in aged 6-35 months old, 28 days interval. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| two doses enterovirus 71 vaccine | Biological | Two doses of enterovirus 71 vaccine will be given in children aged 6-35 months old, 28 days interval. |
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| Measure | Description | Time Frame |
|---|---|---|
| The rate of adverse reactions of enterovirus 71 Vaccine | Adverse reactions associated with vaccine will be observed in subjects after each vaccination. Solicited local adverse events include Pain, Redness, Swelling, Induration, Rash, Pruritus at injection site. solicited general adverse events include Fever, Nausea, Vomiting, Diarrhea, Decreased appetite, Be agitated (irritability, abnormal crying), fatigue, allergy | 28 days |
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Inclusion Criteria:
Exclusion Criteria:
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