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updating VAERS data

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frankknoll
2023-06-30 18:37:49 +02:00
parent cc22841df8
commit b36f0bc5c8
9120 changed files with 9120 additions and 9120 deletions
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docs/data/histograms/Global/GL2042.json
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{"batchcode": "GL2042", "histogram": {"Headache": 3, "COVID-19": 2, "Expired product administered": 2, "Nausea": 2, "Oropharyngeal pain": 2, "Pain in extremity": 2, "Abdominal distension": 1, "Alanine aminotransferase": 1, "Arrhythmia": 1, "Aspartate aminotransferase": 1, "Back pain": 1, "Blood albumin": 1, "Blood alkaline phosphatase": 1, "Blood bilirubin": 1, "Blood calcium": 1, "Blood chloride": 1, "Blood creatinine": 1, "Blood creatinine increased": 1, "Blood glucose": 1, "Blood potassium": 1, "Blood sodium": 1, "Blood urea": 1, "Carbon dioxide": 1, "Carbon dioxide decreased": 1, "Chest discomfort": 1, "Chronic respiratory failure": 1, "Contusion": 1, "Deep vein thrombosis": 1, "Diarrhoea": 1, "Disorientation": 1, "Dizziness": 1, "Drug ineffective": 1, "Dry skin": 1, "Dyskinesia oesophageal": 1, "Ear pain": 1, "Epistaxis": 1, "Fall": 1, "Feeling cold": 1, "Globulin": 1, "Head injury": 1, "Hypersensitivity": 1, "Immediate post-injection reaction": 1, "Incorrect dose administered": 1, "Incorrect product formulation administered": 1, "Injection site erythema": 1, "Interchange of vaccine products": 1, "Loss of consciousness": 1, "Lumbar radiculopathy": 1, "Musculoskeletal stiffness": 1, "Myalgia": 1, "No adverse event": 1, "Oxygen saturation decreased": 1, "Pallor": 1, "Palpitations": 1, "Peripheral swelling": 1, "Poor quality product administered": 1, "Product administration error": 1, "Protein total": 1, "Pulmonary embolism": 1, "Respiratory failure": 1, "SARS-CoV-2 test": 1, "Symptom recurrence": 1, "Tenderness": 1, "Tinnitus": 1, "Vaccination failure": 1, "Vertigo": 1, "Vision blurred": 1, "Wrong product administered": 1}, "Disabilities": 0, "Adverse Reaction Reports": 16, "Deaths": 0, "Life Threatening Illnesses": 0, "Company": "PFIZER\\BIONTECH"}
{"batchcode": "GL2042", "histogram": {"Headache": 3, "COVID-19": 2, "Expired product administered": 2, "Nausea": 2, "Oropharyngeal pain": 2, "Pain in extremity": 2, "Abdominal distension": 1, "Alanine aminotransferase": 1, "Arrhythmia": 1, "Aspartate aminotransferase": 1, "Back pain": 1, "Blood albumin": 1, "Blood alkaline phosphatase": 1, "Blood bilirubin": 1, "Blood calcium": 1, "Blood chloride": 1, "Blood creatinine": 1, "Blood creatinine increased": 1, "Blood glucose": 1, "Blood potassium": 1, "Blood sodium": 1, "Blood urea": 1, "Carbon dioxide": 1, "Carbon dioxide decreased": 1, "Chest discomfort": 1, "Chronic respiratory failure": 1, "Contusion": 1, "Deep vein thrombosis": 1, "Diarrhoea": 1, "Disorientation": 1, "Dizziness": 1, "Drug ineffective": 1, "Dry skin": 1, "Dyskinesia oesophageal": 1, "Ear pain": 1, "Epistaxis": 1, "Fall": 1, "Feeling cold": 1, "Globulin": 1, "Head injury": 1, "Hypersensitivity": 1, "Immediate post-injection reaction": 1, "Incorrect dose administered": 1, "Incorrect product formulation administered": 1, "Injection site erythema": 1, "Interchange of vaccine products": 1, "Loss of consciousness": 1, "Lumbar radiculopathy": 1, "Musculoskeletal stiffness": 1, "Myalgia": 1, "No adverse event": 1, "Oxygen saturation decreased": 1, "Pallor": 1, "Palpitations": 1, "Peripheral swelling": 1, "Poor quality product administered": 1, "Product administration error": 1, "Protein total": 1, "Pulmonary embolism": 1, "Respiratory failure": 1, "SARS-CoV-2 test": 1, "Symptom recurrence": 1, "Tenderness": 1, "Tinnitus": 1, "Vaccination failure": 1, "Vertigo": 1, "Vision blurred": 1, "Wrong product administered": 1}, "Life Threatening Illnesses": 0, "Company": "PFIZER\\BIONTECH", "Adverse Reaction Reports": 16, "Disabilities": 0, "Deaths": 0}