{"batchcode": "015B22A", "histogram": {"Expired product administered": 101, "No adverse event": 85, "Inappropriate schedule of product administration": 16, "Product storage error": 16, "Incorrect product formulation administered": 15, "Headache": 4, "Nausea": 4, "Syncope": 4, "Wrong product administered": 4, "Asthenia": 3, "Chest pain": 3, "Dizziness": 3, "Chest discomfort": 2, "Cold sweat": 2, "Dyspnoea": 2, "Immunisation reaction": 2, "Incorrect dose administered": 2, "Loss of consciousness": 2, "Neck pain": 2, "Pain": 2, "Photophobia": 2, "Product administration error": 2, "Vomiting": 2, "Anion gap": 1, "Axillary mass": 1, "Axillary pain": 1, "Basophil count normal": 1, "Basophil percentage": 1, "Blood chloride normal": 1, "Blood creatinine normal": 1, "Blood glucose normal": 1, "Blood potassium normal": 1, "Blood pressure decreased": 1, "Blood sodium normal": 1, "Blood urea normal": 1, "Burning sensation": 1, "Capillary nail refill test": 1, "Carbon dioxide normal": 1, "Cough": 1, "Crying": 1, "Death": 1, "Dehydration": 1, "Diarrhoea": 1, "Differential white blood cell count": 1, "Electrocardiogram": 1, "Electrocardiogram QT prolonged": 1, "Electrocardiogram abnormal": 1, "Electrocardiogram normal": 1, "Emotional distress": 1, "Eosinophil count increased": 1, "Eosinophil percentage": 1, "Extra dose administered": 1, "Eye movement disorder": 1, "Fatigue": 1, "Feeling hot": 1, "Full blood count": 1, "Glomerular filtration rate normal": 1, "Granulocyte percentage": 1, "Haematocrit normal": 1, "Haemoglobin normal": 1, "Heart rate increased": 1, "Heart rate irregular": 1, "Hypertension": 1, "Immature granulocyte count": 1, "Injection site rash": 1, "Intermenstrual bleeding": 1, "Laboratory test": 1, "Lymph node pain": 1, "Lymphocyte count": 1, "Lymphocyte percentage decreased": 1, "Malaise": 1, "Mean cell haemoglobin concentration normal": 1, "Mean cell haemoglobin normal": 1, "Mean cell volume normal": 1, "Mean platelet volume normal": 1, "Monocyte count increased": 1, "Monocyte percentage": 1, "Nasopharyngitis": 1, "Neutrophil count increased": 1, "Neutrophil percentage increased": 1, "Pain in extremity": 1, "Platelet count normal": 1, "Poor quality product administered": 1, "Presyncope": 1, "Product administration interrupted": 1, "Product availability issue": 1, "Product temperature excursion issue": 1, "Pyrexia": 1, "Rash": 1, "Rash erythematous": 1, "Red blood cell count normal": 1, "Red cell distribution width normal": 1, "Rhinorrhoea": 1, "SARS-CoV-2 test": 1, "Skin warm": 1, "Sleep disorder": 1, "Suspected product contamination": 1, "Suspected product quality issue": 1, "Swelling face": 1, "Tachycardia": 1, "Tonsillitis": 1, "Tremor": 1, "Troponin normal": 1, "Unevaluable event": 1, "Vaccination error": 1, "Ventricular extrasystoles": 1, "White blood cell count increased": 1}, "Company": "MODERNA", "Adverse Reaction Reports": 165, "Disabilities": 0, "Life Threatening Illnesses": 0, "Deaths": 1}