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Sistemas de Notificação de Reações Adversas a Medicamentos ×
- Clinical Trial (2)
- Adverse event (2)
- Public Facilities (1)
- Hepatitis B Vaccines (1)
- Clinical Trial, Phase III (1)
- Drug-Related Side Effects and Adverse Reactions (1)
- On-Study Form (1)
- Common Data Elements (CDE) (1)
- Released Standard (1)
- Drug Therapy (1)
- Hepatitis B (1)
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Groupes Item: General information, Details Adverse Event
Groupes Item: Basic Data, Observed adverse drug reaction, Involved Drugs, Suspected Drug, Diseases, Anamnestic Specifics, Clinical Laboratory Tests, Therapy of adverse drug reaction, Outcome of the adverse drug reaction, Causality, Informed entities, Signatory Data, Manufacturer, Signature
Groupes Item: Administrative data, Solicited Adverse Events, Fever, Irritability/Fussiness, Drowsiness, Loss of Appetite, Vomiting, Diarrhea, In case of "Severe" Intensity of Crying: