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{"Adverse Reaction Reports": 17, "Company": "MODERNA", "Deaths": 0, "Disabilities": 0, "Hospitalizations": 2, "Life-Threatening Illnesses": 1, "batchcode": "3030701", "histogram": {"Angiogram": 1, "Arthralgia": 2, "Asthenia": 1, "Balance disorder": 1, "Blood glucose increased": 1, "Cardiac disorder": 1, "Cellulitis": 1, "Chest X-ray": 1, "Confusional state": 1, "Device failure": 1, "Device malfunction": 1, "Dizziness": 2, "Dyspnoea": 1, "Dyspnoea exertional": 1, "Echocardiogram": 1, "Electrocardiogram": 1, "Expired product administered": 2, "Extra dose administered": 2, "Fatigue": 1, "Full blood count": 1, "Full blood count normal": 1, "Headache": 1, "Hypoaesthesia": 1, "Incorrect dose administered": 1, "Influenza": 1, "Injection site dryness": 1, "Injection site erythema": 1, "Injection site pruritus": 1, "Injection site swelling": 2, "Insomnia": 1, "International normalised ratio": 1, "Malaise": 1, "Metabolic function test": 2, "Needle issue": 1, "No adverse event": 5, "Palpitations": 1, "Paraesthesia": 1, "Patient uncooperative": 1, "Product administered to patient of inappropriate age": 1, "Pulmonary embolism": 1, "Pyrexia": 1, "Tachycardia": 1}}