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{"Adverse Reaction Reports": 13, "Company": "PFIZER\\BIONTECH", "Deaths": 0, "Disabilities": 0, "Hospitalizations": 1, "Life-Threatening Illnesses": 0, "batchcode": "FK5168", "histogram": {"Abdominal pain upper": 1, "Adverse event": 1, "Anxiety": 1, "Biopsy": 1, "COVID-19": 3, "Condition aggravated": 1, "Cough": 1, "Dental cyst": 1, "Dental operation": 1, "Dizziness": 2, "Emotional disorder": 1, "Expired product administered": 1, "Fatigue": 3, "Inappropriate schedule of product administration": 1, "Injection site pain": 1, "Loss of personal independence in daily activities": 1, "Nausea": 3, "No adverse event": 1, "Paediatric autoimmune neuropsychiatric disorders associated with streptococcal infection": 1, "Product storage error": 1, "Pyrexia": 2, "Respiratory tract congestion": 1, "SARS-CoV-2 test": 2, "SARS-CoV-2 test positive": 1, "Tooth development disorder": 1, "Toothache": 1, "Underdose": 2, "Vaccination failure": 2, "Vomiting": 2, "X-ray dental abnormal": 1}}