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{"Adverse Reaction Reports": 27, "Company": "MODERNA", "Deaths": 0, "Disabilities": 1, "Hospitalizations": 3, "Life-Threatening Illnesses": 0, "batchcode": "024H22A", "histogram": {"Abdominal pain lower": 1, "Acute kidney injury": 1, "Acute respiratory failure": 1, "Aortic arteriosclerosis": 1, "Atrial fibrillation": 1, "Blood test": 2, "COVID-19": 2, "COVID-19 immunisation": 1, "Chest pain": 1, "Chills": 1, "Chronic respiratory failure": 1, "Computerised tomogram": 1, "Computerised tomogram thorax abnormal": 1, "Condition aggravated": 1, "Cough": 1, "Drug ineffective": 1, "Dysgeusia": 1, "Expired product administered": 9, "Headache": 1, "Hyperhidrosis": 1, "Hypertension": 1, "Inappropriate schedule of product administration": 1, "Interchange of vaccine products": 1, "Liver function test increased": 1, "Lung opacity": 1, "Muscle spasms": 1, "Nausea": 1, "No adverse event": 16, "Pain": 1, "Pruritus": 1, "Pulmonary fibrosis": 1, "Pyrexia": 1, "Respiratory failure": 1, "Rhinorrhoea": 1, "Skin mass": 1, "Syncope": 1, "Thrombocytopenia": 1, "Urticaria": 1, "Vaccination site erythema": 1, "Vaccination site inflammation": 1, "Vaccination site mass": 1, "Vaccination site pain": 1, "Vaccination site pruritus": 2, "Wrong product administered": 7}}