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{"Adverse Reaction Reports": 8, "Company": "PFIZER\\BIONTECH", "Deaths": 0, "Disabilities": 0, "Hospitalizations": 1, "Life-Threatening Illnesses": 1, "batchcode": "EK-5730", "histogram": {"Alopecia": 1, "Catheter placement": 1, "Chest X-ray": 1, "Chest pain": 1, "Computerised tomogram thorax abnormal": 1, "Cough": 2, "Diarrhoea": 1, "Dizziness": 2, "Dyspnoea": 2, "Echocardiogram normal": 1, "Electrocardiogram": 1, "Electrocardiogram normal": 1, "Fatigue": 2, "Feeling abnormal": 1, "Headache": 1, "Hyperhidrosis": 1, "Injection site reaction": 1, "Intensive care": 1, "Loss of consciousness": 1, "Mobility decreased": 1, "Muscle tightness": 1, "Nausea": 1, "Neck pain": 1, "Off label use": 1, "Pain": 1, "Paraesthesia": 1, "Product use issue": 1, "Pulmonary embolism": 1, "Pyrexia": 1, "SARS-CoV-2 test": 1, "SARS-CoV-2 test negative": 2, "Throat irritation": 1, "Ultrasound Doppler": 1, "Vomiting": 1}}