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{"Adverse Reaction Reports": 17, "Company": "MODERNA", "Deaths": 0, "Disabilities": 0, "Hospitalizations": 1, "Life-Threatening Illnesses": 0, "batchcode": "AS7166B", "histogram": {"Abdominal discomfort": 1, "Accidental overdose": 1, "Acute myocardial infarction": 1, "Blood test": 1, "Bundle branch block right": 1, "COVID-19": 1, "Chest pain": 1, "Chills": 2, "Confusional state": 1, "Cough": 1, "Dyspnoea": 1, "Electrocardiogram ST segment depression": 1, "Expired product administered": 5, "Exposure to SARS-CoV-2": 1, "Fatigue": 2, "Hangover": 1, "Headache": 3, "Hypertension": 1, "Incorrect product formulation administered": 1, "Injection site pain": 1, "Loss of personal independence in daily activities": 1, "Malaise": 1, "Memory impairment": 1, "Monoplegia": 1, "Nasal congestion": 1, "Nasopharyngitis": 1, "Nausea": 1, "No adverse event": 6, "Product storage error": 1, "Pyrexia": 2, "Rhinorrhoea": 1, "SARS-CoV-2 test positive": 1, "Somnolence": 1, "Troponin increased": 1, "Vaccination site pain": 1, "Wrong product administered": 1}} |