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{"Adverse Reaction Reports": 169, "Company": "MODERNA", "Deaths": 0, "Disabilities": 0, "Hospitalizations": 0, "Life-Threatening Illnesses": 0, "batchcode": "AR4504B", "histogram": {"Accidental underdose": 1, "Asthenia": 1, "Atrial fibrillation": 1, "Back pain": 1, "Colonoscopy": 1, "Condition aggravated": 1, "Expired product administered": 23, "Extra dose administered": 3, "Fatigue": 1, "Feeling abnormal": 1, "Feeling of relaxation": 1, "Heart rate abnormal": 1, "Illness": 1, "Inappropriate schedule of product administration": 1, "Incorrect dose administered": 14, "Incorrect product formulation administered": 77, "Injection site pain": 1, "Interchange of vaccine products": 4, "Nasopharyngitis": 1, "Nervousness": 1, "No adverse event": 68, "Pain in extremity": 3, "Product administered to patient of inappropriate age": 15, "Product administration error": 1, "Product storage error": 13, "Pyrexia": 1, "SARS-CoV-2 test": 1, "Underdose": 4, "Unevaluable event": 3, "Wrong product administered": 41}}