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Concomitant Medication ×
- Clinical Trial (132)
- Adverse event (52)
- Vaccination (28)
- Hematology (18)
- Hypereosinophilic Syndrome (17)
- Clinical Trial, Phase III (16)
- Hepatitis B (16)
- Asthma (15)
- Meningococcal Vaccines (15)
- Clinical Trial, Phase II (14)
- Pulmonary Medicine (12)
- Vital Signs (12)
- Laboratories (11)
- Hepatitis B Vaccines (10)
- Haemophilus influenzae type b (10)
- Pulmonary Disease, Chronic Obstructive (9)
- Multiple Myeloma (9)
- Clinical Trial, Phase I (8)
- Electrocardiogram (ECG) (8)
- Compliance (8)
- Gastroenterology (8)
- Pharmacokinetics (6)
- Signs and Symptoms (6)
- Tetanus (6)
- Bordetella pertussis (6)
- Drug trial (6)
- Diabetes Mellitus, Type 2 (6)
- Diphtheria (6)
- Hepatitis A (6)
- Medical Oncology (6)
- Meningitis, Meningococcal (6)
- Drugs, Investigational (5)
- Diphtheria-Tetanus-Pertussis Vaccine (5)
- Diabetes Mellitus (5)
- Medical Records (5)
- Therapeutics (4)
- Topotecan (4)
- AML (4)
- Chest X- ray (4)
- Non Small Cell Lung Cancer (4)
- Drug Therapy (4)
- Infection (4)
- Lung Neoplasms (4)
- Macular Edema (4)
- Ophthalmology (4)
- Pharmacogenetics (3)
- Physical Examination (3)
- Risk Factors (3)
- Purpura, Thrombocytopenic, Idiopathic (3)
- Chemotherapy, Adjuvant (3)
- Clinical Trial, Phase IV (3)
- Blood Transfusion (3)
- Pneumococcal Vaccines (3)
- Child (3)
- Healthy Volunteers (3)
- Treatment Form (3)
- Type 2 Diabetes (3)
- Allergy and Immunology (3)
- Glucocorticoids (3)
- HIV (3)
- Leukemia (3)
- Liver (3)
- Lymphoma, Non-Hodgkin (3)
- Pneumonia (2)
- Pregnancy Tests (2)
- Arthritis, Rheumatoid (2)
- Research Personnel (2)
- Rhinitis, Allergic, Perennial (2)
- Self-Assessment (2)
- Thrombocytopenia (2)
- Thrombosis (2)
- Bacterial Infections (2)
- HIV Infections (2)
- Urinalysis (2)
- Blood (2)
- Diphtheria-Tetanus-acellular Pertussis Vaccines (2)
- Small Cell Lung Carcinoma (2)
- Administration, Inhalation (2)
- Drug-Related Side Effects and Adverse Reactions (2)
- CML (2)
- Trial screening (2)
- End of Study (2)
- CTC code (2)
- Imatinib mesylate (2)
- Bone marrow biopsy (2)
- CTC grade (2)
- Routine documentation (2)
- Drug Administration Routes (2)
- Endocrinology (2)
- Hypersensitivity (2)
- Impetigo (2)
- Medical History Taking (2)
- Meningitis, Haemophilus (2)
- Methotrexate (2)
- Philadelphia Chromosome (1)
- Placebos (1)
- Arthritis (1)
- Questionnaires (1)
- Rectal Neoplasms (1)
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158 Sökresultat.
Item-grupper: Patient administration, Concomitant Medications
Item-grupp: Concomitant Agent
Item-grupper: Liver Events, Investigational Product (Liver)
Item-grupper: Date of Visit/ Assessment , Completion of Visit Assessments, Run- In Failure, Investigator Siganture , Date of Visit/ Assessment , Randomisation Criteria, Run- In Failure , Investigator Siganture , ICS/ LABA Concomitant Medications, Randomisation Number, Investigatinal Product, Vital Signs, Candidiasis Examination, Electronically transferred lab data, Device Use Assessment, Subject Withdrawal Status, Electronically transferred lab data , Liver Events Assessment
Item-grupp: Concomitant Medications
Item-grupper: Administrative documentation, Concomitant medication, Comments
Item-grupp: Concomitant Medication Details
Item-grupper: administrative data, COPD concomitant medication, COPD concomitant medication documentation, concomitant medication, concomitant medication
Item-grupper: Date of Visit/ Assessment, Adverse Event/ Concomitant Medication/ Repeat Assessment Check Questions, Non- serious Adverse Event, Serious Adverse Event, Relevant medical conditions/ risk factors, Relevant Concomitant/ Treatment Medications, Relevant Diagnostic Results, Investigational Product, General Narrative Comments, Concomitant Medication, Electronically transferred lab data, Vital signs , 12- Lead ECG, ECG Abnormalities, Pharmacodynamics - Cortisol , Pharmacodynamics Results - Glucose, Pharmacodynamics Results - Potassium, Pharmacokinetics Blood - FF/GW642444M , Defective Inhaler, X Ray Pneumonia Confirmation
Item-grupp: Log Status
Item-grupper: Administrative documentation, Concomitant Agent
Item-grupper: Randomisation, Serious Adverse Event Entry, Seriousness, Relevant Concomitant/Treatment Medication, Relevant Medical Conditions/Risk Factors, Relevant Diagnosis Results, Rechallenge, Investigational Product, General narrative comments, Non Clinical