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1 line
1.2 KiB
JSON
{"Adverse Reaction Reports": 12, "Company": "PFIZER\\BIONTECH", "Deaths": 0, "Disabilities": 1, "Hospitalizations": 2, "Life-Threatening Illnesses": 2, "batchcode": "FA 1027", "histogram": {"Allergy to vaccine": 1, "Amnesia": 1, "Asthenia": 1, "Blood fibrinogen": 1, "Blood test": 1, "Body temperature": 1, "Cerebral venous sinus thrombosis": 1, "Cerebrovascular accident": 2, "Chest X-ray": 1, "Chest discomfort": 1, "Chest pain": 1, "Chills": 1, "Decreased appetite": 1, "Depression": 1, "Diarrhoea": 1, "Disturbance in attention": 1, "Drug ineffective": 1, "Dyspnoea": 2, "Electric shock sensation": 1, "Fatigue": 1, "Feeling abnormal": 1, "Fibrin D dimer": 1, "Formication": 1, "Headache": 5, "Hypoaesthesia": 2, "Liver function test": 1, "Lymphadenopathy": 1, "Magnetic resonance imaging head": 1, "Malaise": 1, "Maternal exposure during pregnancy": 1, "Memory impairment": 2, "Myalgia": 1, "Nausea": 3, "Nerve injury": 1, "Pain": 1, "Palpitations": 1, "Paraesthesia": 2, "Photosensitivity reaction": 1, "Platelet count": 1, "Product administration error": 1, "Pyrexia": 2, "SARS-CoV-2 test": 2, "Sinus headache": 1, "Somnolence": 1, "Suspected COVID-19": 1, "Syncope": 3, "Tremor": 1, "Wrong technique in product usage process": 1}} |