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{"Adverse Reaction Reports": 13, "Company": "PFIZER\\BIONTECH", "Deaths": 0, "Disabilities": 0, "Hospitalizations": 0, "Life-Threatening Illnesses": 0, "batchcode": "GK0923", "histogram": {"Blood culture": 1, "Blood glucose": 1, "Blood glucose normal": 1, "Blood pressure fluctuation": 2, "Blood pressure increased": 1, "Blood pressure measurement": 2, "COVID-19": 4, "Chest X-ray": 1, "Chest pain": 1, "Discontinued product administered": 1, "Dizziness": 1, "Drug ineffective": 2, "Echocardiogram": 1, "Emotional distress": 1, "Fatigue": 1, "Head discomfort": 2, "Hypertension": 2, "Illness": 1, "Inappropriate schedule of product administration": 1, "Injected limb mobility decreased": 2, "Injection site infection": 1, "Injection site pain": 1, "Injection site reaction": 1, "Interchange of vaccine products": 1, "Magnetic resonance imaging": 1, "Nausea": 1, "No adverse event": 1, "Pain": 2, "Pain in extremity": 1, "Pneumonia": 1, "SARS-CoV-2 test": 2, "Vaccination failure": 2, "Vomiting": 1, "Wrong product administered": 1, "X-ray limb": 1}} |