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{"Adverse Reaction Reports": 103, "Company": "MODERNA", "Deaths": 0, "Disabilities": 0, "Hospitalizations": 1, "Life-Threatening Illnesses": 0, "batchcode": "060B22A", "histogram": {"Blood culture negative": 1, "COVID-19": 1, "COVID-19 pneumonia": 1, "Cardiomegaly": 1, "Chest X-ray abnormal": 1, "Computerised tomogram": 1, "Disturbance in attention": 1, "Dizziness": 1, "Dyspnoea": 1, "Electrocardiogram": 1, "Expired product administered": 91, "Fall": 1, "Full blood count": 1, "Headache": 1, "Hemiparesis": 1, "Hemiplegic migraine": 1, "Inappropriate schedule of product administration": 2, "Incorrect dose administered": 1, "Incorrect product formulation administered": 2, "Intercepted medication error": 1, "Interchange of vaccine products": 1, "Leukocytosis": 1, "Liver function test": 1, "Lung infiltration": 1, "Lung opacity": 1, "Migraine": 1, "No adverse event": 95, "Pain in extremity": 1, "Poor quality product administered": 1, "Positive airway pressure therapy": 1, "Product administration error": 1, "Product storage error": 84, "Product temperature excursion issue": 2, "Pulmonary oedema": 1, "Renal function test": 1, "Respiratory symptom": 1, "SARS-CoV-2 test positive": 1, "Urine analysis": 1, "Urticaria": 1, "Wrong product administered": 2}}