{"Adverse Reaction Reports": 12, "Company": "PFIZER\\BIONTECH", "Deaths": 0, "Disabilities": 0, "Hospitalizations": 2, "Life-Threatening Illnesses": 2, "batchcode": "1K079A", "histogram": {"Ageusia": 1, "Arthralgia": 1, "Asthenia": 1, "Blood pressure decreased": 2, "Blood pressure measurement": 2, "Chest pain": 2, "Depressed level of consciousness": 1, "Dizziness": 1, "Dyspnoea": 1, "Guttate psoriasis": 1, "Heart rate increased": 1, "Hyperhidrosis": 1, "Hypertension": 1, "Immunisation": 2, "Insomnia": 1, "Interchange of vaccine products": 1, "Ischaemic cerebral infarction": 1, "Magnetic resonance imaging": 1, "Migraine": 1, "Myocardial infarction": 1, "Nausea": 1, "Off label use": 3, "Pain in extremity": 2, "Palpitations": 1, "Paraesthesia": 1, "Postmenopausal haemorrhage": 1, "Pruritus": 1, "Rash": 1, "SARS-CoV-2 test": 2, "Somnolence": 1, "Specialist consultation": 1, "Suspected COVID-19": 1, "Syncope": 1, "Tremor": 2, "Vision blurred": 1, "Visual field defect": 1, "Visual impairment": 1, "Vomiting": 1, "Wrong product administered": 2}}