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{"Adverse Reaction Reports": 20, "Company": "MODERNA", "Deaths": 0, "Disabilities": 0, "Hospitalizations": 3, "Life-Threatening Illnesses": 0, "batchcode": "AS7167B", "histogram": {"Acute respiratory failure": 1, "Arthralgia": 3, "COVID-19": 2, "COVID-19 immunisation": 1, "Cardiac failure acute": 1, "Chills": 2, "Diarrhoea": 1, "Dysphonia": 1, "Expired product administered": 4, "Extra dose administered": 3, "Fatigue": 3, "Headache": 1, "Hypoaesthesia": 1, "Injection site pain": 1, "Injection site reaction": 1, "Interchange of vaccine products": 1, "Joint noise": 1, "Left ventricular failure": 1, "Lip swelling": 1, "Malaise": 1, "Musculoskeletal disorder": 1, "Myalgia": 2, "Nausea": 1, "No adverse event": 9, "Oropharyngeal pain": 1, "Pain": 2, "Pain in extremity": 1, "Paraesthesia": 1, "Periarthritis": 1, "Poor quality product administered": 1, "Product storage error": 2, "Product temperature excursion issue": 1, "Pyrexia": 3, "SARS-CoV-2 test": 1, "SARS-CoV-2 test positive": 1, "Sinus congestion": 1, "Swollen tongue": 1, "Wrong product administered": 2}}