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Signes et symptômes ×
- Clinical Trial (90)
- Adverse event (40)
- Clinical Trial, Phase III (38)
- Vaccines (26)
- On-Study Form (25)
- Hepatitis B (25)
- Drug-Related Side Effects and Adverse Reactions (22)
- Hepatitis B Vaccines (21)
- Vaccination (19)
- Laboratories (16)
- Haemophilus influenzae type b (15)
- Physical Examination (12)
- Clinical Trial, Phase I (11)
- Safety (10)
- Gastroenterology (10)
- Restless Legs Syndrome (8)
- Measles-Mumps-Rubella Vaccine (8)
- Neisseria meningitidis (8)
- Neurology (8)
- Child (7)
- Influenza Vaccines (7)
- Diphtheria-Tetanus-acellular Pertussis Vaccines (6)
- Comparative Study (6)
- Fever (6)
- Hepatitis A (6)
- Medical History Taking (6)
- Pharmacokinetics (5)
- Streptococcal Infections (5)
- Streptococcal Vaccines (5)
- Concomitant Medication (5)
- Diabetes Mellitus, Type 2 (5)
- Pain (5)
- Diphtheria-Tetanus-Pertussis Vaccine (4)
- Hepatitis A Vaccines (4)
- Patient Reported Outcome (PRO) (4)
- Contraceptives, Oral, Combined (4)
- Eligibility Determination (4)
- Allergy and Immunology (4)
- Hepatitis (4)
- Influenza, Human (4)
- Patient Participation (4)
- Appetite (3)
- Vomiting (3)
- Biochemistry (3)
- Body Temperature (3)
- Crying (3)
- Headache (3)
- Meningitis, Haemophilus (3)
- Pain Measurement (3)
- Urinalysis (2)
- Biopsy (2)
- Clinical Trial, Phase II (2)
- Dopamine Agonists (2)
- Treatment Form (2)
- Patient information (2)
- Drug trial (2)
- Electrocardiogram (ECG) (2)
- Seizures, Febrile (2)
- Demography (2)
- Exanthema (2)
- Fatigue (2)
- Hematology (2)
- Immunization, Secondary (2)
- Informed Consent (2)
- Liver (2)
- Parotid Gland (2)
- Pharmacogenetics (1)
- Placebos (1)
- Pneumonia (1)
- Pregnancy (1)
- Rubella (1)
- Asthma (1)
- Temperature (1)
- Women (1)
- Pulmonary Medicine (1)
- Comorbidity (1)
- Chemotherapy, Adjuvant (1)
- Blood (1)
- Haemophilus Vaccines (1)
- Cross-Over Studies (1)
- Observation (1)
- Chickenpox Vaccine (1)
- Stroke (1)
- Multiple Sclerosis, Relapsing-Remitting (1)
- Pneumococcal Vaccines (1)
- Fish Proteins (1)
- Consent Forms (1)
- Chest Pain (1)
- Symptom Assessment (1)
- Myalgia (1)
- Baseline (1)
- Pre-Study Form (1)
- General report (1)
- Trial screening (1)
- End of Study (1)
- Chest X- ray (1)
- Coronary Disease (1)
- Depression (1)
- Depressive Disorder (1)
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90 Resultados de la búsqueda.
Itemgroups: Administrative, Pharmacogenetic Research, Prior Medication, Prior Medication , Baseline Signs and Symptoms, Baseline Signs and Symptoms - Investigator's Signature
Itemgroups: Previous chemotherapy, Comorbidities, Symptoms, Physical Examination, Complete Blood Count, Biochemistry, Serum Proteins, Electrocardiogram, Echocardiogram, Biopsie, Preservation of cellular samples, Cytogenetics, FISH (from bone marrow blood), Molecular Biology (peripheral blood), FISH (peripheral blood)
Itemgroups: Enrollment, Symptoms, Physical Examination, Complete Blood Count
Itemgroups: administrative data, signs and symptoms, events
Itemgroups: Introduction Information, General Information, Demographics, Laboratory tests, Study Conclusion, Serious Adverse Event, Investigator´s signature, Tracking Document
Itemgroups: Introductional information, General Information, Demographics, Laboratory tests, Study Conclusion, Serious Adverse Event, Investigator´s signature, Tracking Document
Itemgroups: Information, General Information, Demographics, Laboratory tests, Study Conclusion, Serious Adverse Event, Investigator´s signature, Tracking Document
Itemgroups: Administrative, Baseline Signs and Symptoms, Dosing Details (Day 1), Dosing Details (PK Visit), Dosing Details (Day 3 - 43; Extra Clinic Visit 1 - 3)
Itemgroups: Administrative Data, Events Common To Stroke Patients
Itemgroups: Administrative Data, Non-serious Adverse Event
Itemgroups: Administration, Check for Study Continuation , General Medical History / Physical Examination, Medical Condition, HCG Urine Pregnancy Test, Vaccine Administration, Vaccine Administration, Solicited Adverse Events - Local Symptoms, Solicited Adverse Events - General Symptoms, Unsolicited Adverse Events
Itemgroups: Administrative data, No event, Adverse Event