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{"Adverse Reaction Reports": 17, "Company": "PFIZER\\BIONTECH", "Deaths": 2, "Disabilities": 3, "Hospitalizations": 2, "Life-Threatening Illnesses": 1, "batchcode": "FE8163", "histogram": {"Ageusia": 1, "Anaphylactic reaction": 1, "Anosmia": 1, "Blood pressure increased": 3, "Blood pressure measurement": 2, "COVID-19": 3, "COVID-19 screening": 1, "Chest discomfort": 1, "Cough": 3, "Diarrhoea": 1, "Disturbance in attention": 1, "Dizziness": 2, "Drug ineffective": 3, "Dyspnoea": 3, "Echocardiogram": 1, "Eczema": 1, "Erythema": 1, "Fatigue": 2, "Feeling abnormal": 1, "Haemoglobin": 1, "Hypoaesthesia": 1, "Limb discomfort": 1, "Malaise": 1, "Menstrual disorder": 1, "Myalgia": 1, "Myelodysplastic syndrome": 1, "Nasopharyngitis": 1, "Nerve conduction studies": 1, "Palpitations": 1, "Panic attack": 1, "Paraesthesia": 1, "Pericarditis": 1, "Phlebitis": 1, "Platelet count": 1, "Pruritus": 1, "Pulmonary embolism": 1, "Pyrexia": 2, "SARS-CoV-2 test": 2, "Skin lesion": 1, "Syncope": 3, "Tachycardia": 1, "Ultrasound scan": 1, "Urticaria": 1, "VIth nerve paralysis": 1, "Visual impairment": 1, "White blood cell count": 1}}