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updating VAERS data

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frankknoll
2024-02-03 16:45:53 +01:00
parent 4491bbbc80
commit ef570808b6
9502 changed files with 10006 additions and 63765 deletions
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docs/data/histograms/Global/FY3680.json
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{"batchcode": "FY3680", "histogram": {"No adverse event": 11, "Incorrect product formulation administered": 9, "Underdose": 4, "Unevaluable event": 4, "Wrong product administered": 4, "Discontinued product administered": 3, "Expired product administered": 2, "Extra dose administered": 2, "Incorrect dose administered": 2, "Product preparation issue": 2, "Pyrexia": 2, "Brain natriuretic peptide increased": 1, "Cardiac valve disease": 1, "Circumstance or information capable of leading to medication error": 1, "Coronary artery dilatation": 1, "Echocardiogram": 1, "Full blood count abnormal": 1, "Immune thrombocytopenia": 1, "Immunoglobulin therapy": 1, "Inappropriate schedule of product administration": 1, "Incorrect route of product administration": 1, "Laboratory test abnormal": 1, "Malaise": 1, "Multisystem inflammatory syndrome in children": 1, "Petechiae": 1, "Platelet count decreased": 1, "Poor quality product administered": 1, "Product storage error": 1, "SARS-CoV-2 antibody test positive": 1, "Thrombocytopenia": 1, "Urticaria": 1}, "Disabilities": 0, "Life Threatening Illnesses": 0, "Deaths": 0, "Company": "PFIZER\\BIONTECH", "Adverse Reaction Reports": 39}
{"batchcode": "FY3680", "histogram": {"No adverse event": 11, "Incorrect product formulation administered": 9, "Underdose": 4, "Unevaluable event": 4, "Wrong product administered": 4, "Discontinued product administered": 3, "Expired product administered": 2, "Extra dose administered": 2, "Incorrect dose administered": 2, "Product preparation issue": 2, "Pyrexia": 2, "Brain natriuretic peptide increased": 1, "Cardiac valve disease": 1, "Circumstance or information capable of leading to medication error": 1, "Coronary artery dilatation": 1, "Echocardiogram": 1, "Full blood count abnormal": 1, "Immune thrombocytopenia": 1, "Immunoglobulin therapy": 1, "Inappropriate schedule of product administration": 1, "Incorrect route of product administration": 1, "Laboratory test abnormal": 1, "Malaise": 1, "Multisystem inflammatory syndrome in children": 1, "Petechiae": 1, "Platelet count decreased": 1, "Poor quality product administered": 1, "Product storage error": 1, "SARS-CoV-2 antibody test positive": 1, "Thrombocytopenia": 1, "Urticaria": 1}, "Deaths": 0, "Disabilities": 0, "Adverse Reaction Reports": 39, "Company": "PFIZER\\BIONTECH", "Life Threatening Illnesses": 0}