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{"Adverse Reaction Reports": 42, "Company": "MODERNA", "Deaths": 0, "Disabilities": 1, "Hospitalizations": 2, "Life-Threatening Illnesses": 0, "batchcode": "021H22A", "histogram": {"Accidental underdose": 3, "Anticoagulant therapy": 1, "Aphasia": 1, "Atrial fibrillation": 1, "Blood test normal": 1, "COVID-19": 3, "COVID-19 immunisation": 1, "Cardiac disorder": 1, "Circumstance or information capable of leading to medication error": 1, "Drug ineffective": 1, "Dysarthria": 1, "Dysphonia": 1, "Echocardiogram": 1, "Electrocardiogram": 1, "Erythema": 1, "Expired product administered": 17, "Extra dose administered": 1, "Eye pain": 1, "Headache": 1, "Hemiplegia": 1, "Hypoxia": 1, "Inappropriate schedule of product administration": 1, "Incorrect dose administered": 2, "Incorrect product formulation administered": 1, "Intensive care": 1, "Interchange of vaccine products": 1, "Lymphadenopathy": 1, "Mental status changes": 1, "Migraine": 1, "Muscle spasms": 1, "Muscular weakness": 1, "Neurologic neglect syndrome": 1, "No adverse event": 28, "Pain": 1, "Product storage error": 10, "SARS-CoV-2 test": 1, "SARS-CoV-2 test positive": 1, "Skin warm": 1, "Urticaria": 1, "Vaccination site anaesthesia": 1, "Vaccination site discolouration": 1, "Vaccination site pain": 2, "Vaccination site paraesthesia": 1, "Vitrectomy": 1, "Wrong product administered": 5}}