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updating VAERS data

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frankknoll
2023-07-21 21:22:26 +02:00
parent 3a3a1804d5
commit 3d5af723f8
9155 changed files with 16837 additions and 16823 deletions
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docs/data/histograms/Global/FW1331.json
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{"batchcode": "FW1331", "histogram": {"Incorrect product formulation administered": 68, "Discontinued product administered": 22, "No adverse event": 21, "Product administration error": 8, "Expired product administered": 4, "COVID-19": 3, "Dizziness": 3, "Drug ineffective": 3, "Extra dose administered": 3, "Product administered to patient of inappropriate age": 3, "SARS-CoV-2 test": 3, "Wrong product administered": 3, "Anxiety": 2, "Chest pain": 2, "Incorrect dose administered": 2, "Loss of consciousness": 2, "Unevaluable event": 2, "Abdominal discomfort": 1, "Abdominal pain upper": 1, "Blood glucose decreased": 1, "Body temperature": 1, "Circumstance or information capable of leading to medication error": 1, "Cough": 1, "Death": 1, "Dyspnoea": 1, "Hyperhidrosis": 1, "Hypersensitivity": 1, "Hypotonia": 1, "Inflammatory bowel disease": 1, "Intensive care": 1, "Interchange of vaccine products": 1, "Laboratory test": 1, "Laboratory test normal": 1, "Mobility decreased": 1, "Pain in extremity": 1, "Pallor": 1, "Posturing": 1, "Presyncope": 1, "Product storage error": 1, "Rash": 1, "Rash erythematous": 1, "Rash papular": 1, "Skin warm": 1, "Subdural abscess": 1, "Subdural haematoma": 1, "Syncope": 1, "Throat tightness": 1, "Unresponsive to stimuli": 1, "Vomiting": 1}, "Deaths": 1, "Adverse Reaction Reports": 122, "Disabilities": 1, "Company": "PFIZER\\BIONTECH", "Life Threatening Illnesses": 2}
{"batchcode": "FW1331", "histogram": {"Incorrect product formulation administered": 71, "Discontinued product administered": 28, "No adverse event": 21, "Product administration error": 10, "Expired product administered": 6, "Wrong product administered": 5, "COVID-19": 3, "Dizziness": 3, "Drug ineffective": 3, "Extra dose administered": 3, "Product administered to patient of inappropriate age": 3, "SARS-CoV-2 test": 3, "Anxiety": 2, "Chest pain": 2, "Incorrect dose administered": 2, "Loss of consciousness": 2, "Unevaluable event": 2, "Abdominal discomfort": 1, "Abdominal pain upper": 1, "Blood glucose decreased": 1, "Body temperature": 1, "Circumstance or information capable of leading to medication error": 1, "Cough": 1, "Death": 1, "Dyspnoea": 1, "Hyperhidrosis": 1, "Hypersensitivity": 1, "Hypotonia": 1, "Inflammatory bowel disease": 1, "Intensive care": 1, "Interchange of vaccine products": 1, "Laboratory test": 1, "Laboratory test normal": 1, "Mobility decreased": 1, "Pain in extremity": 1, "Pallor": 1, "Posturing": 1, "Presyncope": 1, "Product storage error": 1, "Rash": 1, "Rash erythematous": 1, "Rash papular": 1, "Skin warm": 1, "Subdural abscess": 1, "Subdural haematoma": 1, "Syncope": 1, "Throat tightness": 1, "Unresponsive to stimuli": 1, "Vomiting": 1}, "Life Threatening Illnesses": 2, "Deaths": 1, "Company": "PFIZER\\BIONTECH", "Adverse Reaction Reports": 131, "Disabilities": 1}