{"batchcode": "AR5186C", "histogram": {"Incorrect product formulation administered": 238, "No adverse event": 221, "Wrong product administered": 172, "Product temperature excursion issue": 106, "Poor quality product administered": 103, "Underdose": 70, "Incorrect dose administered": 53, "Product administered to patient of inappropriate age": 35, "Product administration error": 13, "Expired product administered": 11, "Extra dose administered": 6, "Product storage error": 5, "Inappropriate schedule of product administration": 3, "Medication error": 3, "Dizziness": 2, "Headache": 2, "Interchange of vaccine products": 2, "Pyrexia": 2, "Abdominal pain": 1, "Asthenia": 1, "Blood glucose normal": 1, "Blood test normal": 1, "COVID-19": 1, "Circumstance or information capable of leading to medication error": 1, "Cough": 1, "Exposure during pregnancy": 1, "Fatigue": 1, "Hyperhidrosis": 1, "Injection site pain": 1, "Loss of consciousness": 1, "Oropharyngeal pain": 1, "Pain in extremity": 1, "Presyncope": 1, "Product availability issue": 1, "Product label confusion": 1, "Product use issue": 1, "SARS-CoV-2 test positive": 1, "Unevaluable event": 1, "Vaccination error": 1}, "Company": "MODERNA", "Adverse Reaction Reports": 462, "Disabilities": 0, "Life Threatening Illnesses": 0, "Deaths": 0}