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{"Adverse Reaction Reports": 18, "Company": "MODERNA", "Deaths": 0, "Disabilities": 0, "Hospitalizations": 2, "Life-Threatening Illnesses": 0, "batchcode": "016H22A", "histogram": {"Adult failure to thrive": 1, "Arthritis": 1, "Atrial fibrillation": 1, "Body temperature": 1, "COVID-19": 2, "Chills": 1, "Computerised tomogram": 1, "Ear pain": 1, "Expired product administered": 1, "Gait disturbance": 2, "Haematuria": 1, "Headache": 1, "Hypertension": 1, "Incorrect product formulation administered": 1, "Influenza virus test negative": 1, "Limb injury": 1, "Mucosal discolouration": 1, "Musculoskeletal discomfort": 1, "Myalgia": 1, "No adverse event": 4, "Oropharyngeal pain": 1, "Pain": 1, "Pain in extremity": 1, "Paranasal sinus discomfort": 1, "Positron emission tomogram": 1, "Productive cough": 1, "Pyrexia": 1, "Renal pain": 1, "SARS-CoV-2 test": 1, "SARS-CoV-2 test negative": 1, "SARS-CoV-2 test positive": 2, "Tinnitus": 1, "Upper-airway cough syndrome": 2, "Urinary tract infection": 1, "Wrong product administered": 3, "X-ray abnormal": 1}} |