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1.4 KiB
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1 line
1.4 KiB
JSON
{"Adverse Reaction Reports": 131, "Company": "PFIZER\\BIONTECH", "Deaths": 1, "Disabilities": 1, "Hospitalizations": 2, "Life-Threatening Illnesses": 2, "batchcode": "FW1331", "histogram": {"Abdominal discomfort": 1, "Abdominal pain upper": 1, "Anxiety": 2, "Blood glucose decreased": 1, "Body temperature": 1, "COVID-19": 2, "Chest pain": 2, "Circumstance or information capable of leading to medication error": 1, "Cough": 1, "Death": 1, "Discontinued product administered": 28, "Dizziness": 3, "Drug ineffective": 2, "Dyspnoea": 1, "Expired product administered": 6, "Extra dose administered": 3, "Hyperhidrosis": 1, "Hypersensitivity": 1, "Hypotonia": 1, "Incorrect dose administered": 2, "Incorrect product formulation administered": 72, "Inflammatory bowel disease": 1, "Intensive care": 1, "Interchange of vaccine products": 1, "Laboratory test": 1, "Laboratory test normal": 1, "Loss of consciousness": 2, "Mobility decreased": 1, "No adverse event": 22, "Pain in extremity": 1, "Pallor": 1, "Posturing": 1, "Presyncope": 1, "Product administered to patient of inappropriate age": 3, "Product administration error": 10, "Product storage error": 1, "Rash": 1, "Rash erythematous": 1, "Rash papular": 1, "SARS-CoV-2 test": 2, "Skin warm": 1, "Subdural abscess": 1, "Subdural haematoma": 1, "Syncope": 1, "Throat tightness": 1, "Unevaluable event": 2, "Unresponsive to stimuli": 1, "Vomiting": 1, "Wrong product administered": 6}} |