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{"Adverse Reaction Reports": 19, "Company": "MODERNA", "Deaths": 1, "Disabilities": 0, "Hospitalizations": 1, "Life-Threatening Illnesses": 1, "batchcode": "04C21A", "histogram": {"Axillary pain": 1, "Blood test": 1, "COVID-19": 2, "Condition aggravated": 1, "Death": 1, "Diarrhoea": 1, "Dizziness": 1, "Drug ineffective": 1, "Expired product administered": 4, "Extra dose administered": 1, "Fatigue": 1, "Flushing": 1, "Hyperhidrosis": 1, "Hypertension": 1, "Inappropriate schedule of product administration": 2, "Injected limb mobility decreased": 1, "Injection site erythema": 3, "Injection site induration": 1, "Injection site pain": 1, "Injection site pruritus": 2, "Injection site swelling": 2, "Injection site warmth": 1, "Interchange of vaccine products": 1, "Lethargy": 1, "Lymphadenopathy": 1, "Nausea": 1, "No adverse event": 1, "Oedema peripheral": 1, "Pain in extremity": 1, "Product storage error": 1, "Pruritus": 1, "SARS-CoV-2 test": 1, "Stool analysis": 1, "Swelling face": 1, "Syncope": 1, "Unresponsive to stimuli": 1}} |