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- Poliomyelitis (11)
- Tetanus (11)
- Clinical Trial (11)
- Diphtheria (11)
- Hepatitis B (11)
- Vaccination (10)
- Adverse event (7)
- Medical Records (3)
- Office Visits (3)
- Medication Adherence (1)
- Concomitant Medication (1)
- End of Study (1)
- Demography (1)
- Eligibility Determination (1)
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11 Resultados de la búsqueda.
Itemgroups: Administrative Documentation, Continuation status, Clinical Trials, Collection of blood specimen for laboratory procedure
Itemgroups: Administrative Documentation, Exclusion Criteria, During, Clinical Trials, Vaccination, Medical contraindications, Informed Consent, Demographics Domain, Eligibility Determination, Inclusion, Exclusion Criteria, Randomization, Medical History, Physical Examination, Collection of blood specimen for laboratory procedure, Vaccination, Administration of Vaccine, Adverse Event, Symptoms, Local, Adverse Event, General symptom, Adverse Event, Vaccination
Itemgroups: Administrative Documentation, Continuation status, Clinical Trials, Vaccination, Administration of Vaccine, Adverse Event, Symptoms, Local, Adverse Event, General symptom, Adverse Event, Vaccination
Itemgroups: Administrative Documentation, Continuation status, Clinical Trials, Vaccination, Administration of Vaccine, Adverse Event, Symptoms, Local, Adverse Event, General symptom, Adverse Event, Vaccination
Itemgroups: Administrative Documentation, Pharmaceutical Preparations
Itemgroups: Administrative documentation, Non-serious Adverse Event
Itemgroups: Administrative Documentation, Adverse Event, Symptoms, Local, Symptoms, Local, Other, Adverse Event, General symptom, General symptom, Other, Pharmaceutical Preparations
Itemgroups: Administrative Documentation, Adverse Event, Symptoms, Local, Symptoms, Local, Other, Adverse Event, General symptom, General symptom, Other, Pharmaceutical Preparations
Itemgroups: Administrative Documentation, Adverse Event, Symptoms, Local, Symptoms, Local, Other, Adverse Event, General symptom, General symptom, Other, Pharmaceutical Preparations
Itemgroups: Administrative Documentation, Concomitant Agent, Vaccination
Itemgroups: Administrative documentation, Follow-Up Studies, Serious Adverse Event, Treatment Status, Blinded Clinical Study, Exclusion Criteria, Withdraw, Investigator Signature