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1.2 KiB
JSON
1 line
1.2 KiB
JSON
{"Adverse Reaction Reports": 39, "Company": "PFIZER\\BIONTECH", "Deaths": 0, "Disabilities": 0, "Hospitalizations": 2, "Life-Threatening Illnesses": 0, "batchcode": "FY3680", "histogram": {"Brain natriuretic peptide increased": 1, "Cardiac valve disease": 1, "Circumstance or information capable of leading to medication error": 1, "Coronary artery dilatation": 1, "Discontinued product administered": 3, "Echocardiogram": 1, "Expired product administered": 2, "Extra dose administered": 2, "Full blood count abnormal": 1, "Immune thrombocytopenia": 1, "Immunoglobulin therapy": 1, "Inappropriate schedule of product administration": 1, "Incorrect dose administered": 2, "Incorrect product formulation administered": 9, "Incorrect route of product administration": 1, "Laboratory test abnormal": 1, "Malaise": 1, "Multisystem inflammatory syndrome in children": 1, "No adverse event": 11, "Petechiae": 1, "Platelet count decreased": 1, "Poor quality product administered": 1, "Product preparation issue": 2, "Product storage error": 1, "Pyrexia": 2, "SARS-CoV-2 antibody test positive": 1, "Thrombocytopenia": 1, "Underdose": 4, "Unevaluable event": 4, "Urticaria": 1, "Wrong product administered": 4}} |