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Vakzine, Hepatitis-B- ×
- Clinical Trial (173)
- Hepatitis B (108)
- Clinical Trial, Phase III (83)
- Vaccination (70)
- Adverse event (59)
- Vaccines (54)
- Hepatitis A Vaccines (52)
- Haemophilus influenzae type b (43)
- Gastroenterology (31)
- On-Study Form (29)
- Concomitant Medication (28)
- Signs and Symptoms (27)
- Meningococcal Vaccines (26)
- Tetanus (25)
- Bordetella pertussis (25)
- Diphtheria (25)
- Follow-Up Studies (24)
- Laboratories (24)
- Safety (22)
- Diphtheria-Tetanus-Pertussis Vaccine (16)
- Diphtheria-Tetanus-acellular Pertussis Vaccines (15)
- Drug-Related Side Effects and Adverse Reactions (15)
- Drug trial (15)
- Eligibility Determination (12)
- Physical Examination (11)
- Child (11)
- End of Study (11)
- Demography (10)
- Hepatitis A (9)
- Meningitis, Haemophilus (9)
- Drug Administration Routes (7)
- Informed Consent (7)
- Medical History Taking (7)
- Lost to Follow-Up (6)
- Infant (6)
- Office Visits (6)
- Patient Participation (6)
- Blood (5)
- Comparative Study (5)
- Fever (5)
- Immunogenetics (5)
- Immunologic Techniques (5)
- Appetite (4)
- Research Personnel (4)
- Drug Administration Schedule (4)
- Immunologic Memory (4)
- Pain (4)
- Vomiting (3)
- Body Temperature (3)
- Body Weight (3)
- Consent Forms (3)
- Symptom Assessment (3)
- Crying (3)
- Body Height (2)
- Pre-Study Form (2)
- Poliovirus Vaccine, Oral (1)
- Pregnancy (1)
- Random Allocation (1)
- Rotavirus (1)
- Smoking (1)
- BCG Vaccine (1)
- HIV Infections (1)
- Adverse Drug Reaction Reporting Systems (1)
- Clinical Trial, Phase II (1)
- Clinical Trial, Phase IV (1)
- Malaria Vaccines (1)
- Patient Selection (1)
- Observation (1)
- Pneumococcal Vaccines (1)
- Renal Insufficiency, Chronic (1)
- Infectious Disease Medicine (1)
- Pragmatic Clinical Trial (1)
- Common Data Elements (CDE) (1)
- General report (1)
- Trial screening (1)
- Document Tracking (1)
- Diarrhea (1)
- Abscess (1)
- Alcohol Drinking (1)
- Pharmaceutical Preparations (1)
- Hepatitis B e Antigens (1)
- Hepatitis B Surface Antigens (1)
- HIV (1)
- Influenza, Human (1)
- Malaria (1)
- Medical Records (1)
- Mothers (1)
- Pain Measurement (1)
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211 Resultados de la búsqueda.
Itemgroups: Conclusion, Clinical Research, Investigator Signature
Itemgroups: Administrative data, Occurrence of Serious Adverse Event, Elimination Criteria, Withdrawal from Study, Investigator's signature
Itemgroups: Follow-up studies, Study conclusion, Administrative documentation
Itemgroups: Follow-up Studies, Study conclusion
Itemgroups: Header, Study Conclusion, Administrative Data
Itemgroup: STUDY CONCLUSION FOR MENCEVAX™ ACWY 1/5th OF A DOSE STAGE
Itemgroups: Administration, Follow-up studies, Study conclusion, Investigator signature, Tracking Document Safety Follow-Up, Tracking Document Safety Follow-Up , Serious adverse event safety follow-up - Administrative, Serious adverse event safety follow-up, Serious adverse event safety follow-up - Study vaccine information, Serious adverse event safety follow-up - Concomitant medication/ Vaccination that could have contributed to this SAE, Serious adverse event safety follow-up - Relevant intercurrent illness & medical history that could have contributed to this SAE , Serious adverse event safety follow-up - Drug(s) used to treat this SAE , Serious adverse event safety follow-up - Surgical treatment for this SAE , Serious adverse event safety follow-up - Description , Serious adverse event safety follow-up - Comments , Serious adverse event safety follow-up - Investigator signature
Itemgroups: Patient Administration, Informed Consent, Demographics, Laboratory tests, Vaccination
Itemgroups: Tracking Document Safety Follow-Up, Administrative documentation
Itemgroups: Follow-up studies, Administrative documentation
Itemgroups: Tracking Document Safety Follow-Up, Administrative documentation
Itemgroups: Serious adverse events, Study vaccine information, Concomitant medication / vaccination, Intercurrent illness & medical history, Drug(s) used to treat SAE, SAE administative information