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Haemophilus influenzae tyyppi b ×
- Clinical Trial (150)
- Clinical Trial, Phase III (80)
- Hepatitis B (79)
- Neisseria meningitidis (71)
- Vaccines (70)
- Vaccination (57)
- Diphtheria-Tetanus-acellular Pertussis Vaccines (51)
- Adverse event (46)
- Hepatitis B Vaccines (43)
- Diphtheria-Tetanus-Pertussis Vaccine (29)
- Eligibility Determination (27)
- Concomitant Medication (26)
- Communicable Diseases (26)
- Tetanus (23)
- Bordetella pertussis (23)
- Meningococcal Vaccines (23)
- Diphtheria (23)
- Drug-Related Side Effects and Adverse Reactions (22)
- On-Study Form (22)
- Signs and Symptoms (21)
- Physical Examination (17)
- Laboratories (17)
- Immunologic Memory (13)
- Meningitis, Haemophilus (12)
- Demography (11)
- End of Study (10)
- Drug Administration Routes (10)
- Office Visits (10)
- Blood (9)
- Immunization, Secondary (8)
- Fever (7)
- Follow-Up Studies (7)
- Body Temperature (6)
- Informed Consent (6)
- Patient Reported Outcome (PRO) (5)
- Drug Administration Schedule (5)
- Patient Participation (5)
- Research Personnel (4)
- Medical History Taking (4)
- Pain (4)
- Appetite (3)
- Clinical Trial, Phase IV (3)
- Consent Forms (3)
- Pre-Study Form (3)
- Patient information (3)
- Comparative Study (3)
- Exanthema (3)
- Parotid Gland (3)
- Clinical Trial, Phase II (2)
- Medication Adherence (2)
- Seizures, Febrile (2)
- Abscess (2)
- Meningitis (2)
- Pain Measurement (2)
- Pharyngitis (1)
- Race Relations (1)
- Random Allocation (1)
- Salivary Glands (1)
- Therapeutics (1)
- Outcome Assessment (Health Care) (1)
- Clinical Trial, Phase I (1)
- Haemophilus Vaccines (1)
- Patient Selection (1)
- Dose Fractionation (1)
- Case Reports (1)
- Immune Reconstitution Inflammatory Syndrome (1)
- Lost to Follow-Up (1)
- General report (1)
- Compliance (1)
- Crying (1)
- Diagnosis (1)
- Pharmaceutical Preparations (1)
- Hematologic Tests (1)
- Hematology (1)
- Immune System (1)
- Infant (1)
- Infection (1)
- Meningism (1)
- Patient Compliance (1)
Table des matières
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169 Résultats de recherche.
Groupes Item: Administrative data, Check for Study Continuation, Elimination Criteria During The Study, Laboratory Tests - Blood
Groupes Item: Administrative data, Elimination Criteria During The Study, Contraindications To Subsequent Vaccination, Absolute Contraindications for InfanrixTM-IPV and Aventis PediacelTM Combination Vaccines, Precautions for Vaccination, Informed Consent, Demographics, Eligibility Check, Inclusion Criteria, Exclusion Criteria, Randomisation / Treatment Allocation, Physical Examination, Vaccine History, Laboratory Tests - Blood, Vaccine Administration, Vaccine, Vaccine 2, Non-administration, Unsolicited Adverse Events, Solicited Adverse Events - Local Symptoms, Solicited Adverse Events - Local Symptoms - Vaccine 2, Solicited Adverse Events, General Symptoms
- Hematologic Tests
- Drug-Related Side Effects and Adverse Reactions
- Blood
- Clinical Trial
- Immunization, Secondary
- Clinical Trial, Phase III
- Haemophilus influenzae type b
- Neisseria meningitidis
- Signs and Symptoms
- Vaccination
- Physical Examination
- On-Study Form
- Eligibility Determination
- Adverse event
- Laboratories
Groupes Item: Administrative data, Reason for non participation, Investigator's Signature, Study Conclusion, Status of treatment blind, Subject Withdrawal, Decision-making, Last Contact, Investigator's Signature
Groupes Item: Administrative data, Temperature, Temperature Log, Rash / Exanthem, Rash Event Log, Parotid / Salivary Gland Swelling, Parotid/Salivary Gland Swelling Events, Febrile Convulsions - Suspected Signs of Meningism, Febrile Convulsions Log, Reminder
Groupes Item: Administrative data, Booster Dose - Local Symptoms - Vaccine 1, Redness (Local Symptoms), Swelling (Local Symptoms), Pain (Local Symptoms), Booster Dose - Local Symptoms - Vaccine 2, Redness (Local Symptoms), Swelling (Local Symptoms), Pain (Local Symptoms), Booster Dose - Other Local Symptoms, Booster Dose - General Symptoms, Temperature (General Symptoms), Irritability / Fussiness (General Symptoms), Drowsiness (General Symptoms), Loss of Appetite (General Symptoms), Booster Dose - Other General Symptoms, Booster Dose - Medication, Reminder
Groupes Item: Administrative data, Dose 3 - Local Symptoms - Vaccine 1, Redness (Local Symptoms), Swelling (Local Symptoms), Pain (Local Symptoms), Dose 3 - Local Symptoms - Vaccine 2, Redness (Local Symptoms), Swelling (Local Symptoms), Pain (Local Symptoms), Dose 3 - Other Local Symptoms, Dose 3 - General Symptoms, Temperature (General Symptoms), Irritability / Fussiness (General Symptoms), Drowsiness (General Symptoms), Loss of Appetite (General Symptoms), Dose 3 - Other General Symptoms, Dose 3 - Medication, Reminder
Groupes Item: Administrative data, Dose 1 - Local Symptoms - Vaccine 1, Redness (Local Symptoms), Swelling (Local Symptoms), Pain (Local Symptoms), Dose 1 - Local Symptoms - Vaccine 2, Redness (Local Symptoms), Swelling (Local Symptoms), Pain (Local Symptoms), Dose 1 - Other Local Symptoms, Dose 1 - General Symptoms, Temperature (General Symptoms), Irritability / Fussiness (General Symptoms), Drowsiness (General Symptoms), Loss of Appetite (General Symptoms), Dose 1 - Other General Symptoms, Dose 1 - Medication, Reminder
Groupes Item: Administrative data, Dose 2 - Local Symptoms - Vaccine 1, Redness (Local Symptoms), Swelling (Local Symptoms), Pain (Local Symptoms), Dose 2 - Local Symptoms - Vaccine 2, Redness (Local Symptoms), Swelling (Local Symptoms), Pain (Local Symptoms), Dose 2 - Other Local Symptoms, Dose 2 - General Symptoms, Temperature (General Symptoms), Irritability / Fussiness (General Symptoms), Drowsiness (General Symptoms), Loss of Appetite (General Symptoms), Dose 2 - Other General Symptoms, Dose 2 - Medication, Reminder
Groupes Item: Administrative data, Concomitant Vaccination, Vaccination details, Concomitant Medication, Concomitant Medication Details, Non-Serious Adverse Events, Description of Event, Study Conclusion
Groupes Item: Administrative data, Check for Study Continuation, Elimination Criteria During The Study, Laboratory Tests - Blood
Groupes Item: Administrative data, Check for Study Continuation, Elimination Criteria During The Study, Vaccine Administration - Vaccine 1, Vaccine Administration - Vaccine 2, Non-administration, Unsolicited Adverse Events, Solicited Adverse Events - Local Symptoms, Solicited Adverse Events - Local Symptoms - Vaccine 2, Solicited Adverse Events, General Symptoms
Groupes Item: Administrative data, Check for Study Continuation, Vaccine Administration - Vaccine 1, Vaccine Administration - Vaccine 2, Non-administration, Unsolicited Adverse Events, Solicited Adverse Events - Local Symptoms, Solicited Adverse Events - Local Symptoms - Vaccine 2, Solicited Adverse Events, General Symptoms