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{"Adverse Reaction Reports": 56, "Company": "PFIZER\\BIONTECH", "Deaths": 1, "Disabilities": 0, "Hospitalizations": 2, "Life-Threatening Illnesses": 1, "batchcode": "HG9498", "histogram": {"Antineutrophil cytoplasmic antibody": 1, "Antinuclear antibody": 1, "Aortic aneurysm rupture": 1, "Asthenia": 3, "Axillary pain": 1, "Basophil count normal": 1, "Basophil percentage increased": 1, "Biopsy skin abnormal": 1, "Blood chloride increased": 1, "Blood culture": 1, "Blood glucose": 2, "Blood potassium normal": 1, "Blood sodium normal": 1, "Blood test": 1, "Blood urea": 1, "COVID-19": 5, "Carbon dioxide": 1, "Chest X-ray normal": 1, "Chest pain": 2, "Chills": 3, "Chronic obstructive pulmonary disease": 1, "Chronic pigmented purpura": 1, "Cold sweat": 1, "Computerised tomogram head normal": 1, "Condition aggravated": 1, "Confusional state": 1, "Contusion": 1, "Costochondritis": 1, "Decreased appetite": 2, "Device breakage": 2, "Device issue": 2, "Diplopia": 1, "Dizziness": 1, "Dyspnoea": 3, "Electrocardiogram normal": 1, "Eosinophil count normal": 1, "Eosinophil percentage": 1, "Erythema": 3, "Expired product administered": 15, "Extra dose administered": 1, "Eye pruritus": 1, "Eye swelling": 1, "Fatigue": 3, "Feeling abnormal": 1, "Feeling hot": 1, "Glycosylated haemoglobin": 1, "Gout": 1, "Headache": 2, "Hiccups": 1, "Hyperhidrosis": 2, "Hypersomnia": 1, "Hypotension": 1, "Hypoxia": 1, "Illness": 1, "Imaging procedure abnormal": 1, "Immature granulocyte count": 1, "Immediate post-injection reaction": 1, "Immune system disorder": 1, "Incorrect dose administered": 3, "Influenza like illness": 2, "Injected limb mobility decreased": 1, "Injection site bruising": 1, "Injection site erythema": 2, "Injection site haemorrhage": 1, "Injection site induration": 2, "Injection site inflammation": 1, "Injection site pain": 4, "Injection site reaction": 2, "Injection site swelling": 2, "Injection site warmth": 2, "Intensive care": 1, "Laboratory test": 1, "Lethargy": 2, "Lymphadenopathy": 2, "Lymphocyte count": 1, "Lymphocyte percentage increased": 1, "Malaise": 4, "Mass": 2, "Mean cell haemoglobin normal": 1, "Mean platelet volume normal": 1, "Mechanical ventilation": 1, "Metabolic function test": 1, "Monocyte count": 1, "Monocyte percentage increased": 1, "Muscular weakness": 1, "Musculoskeletal disorder": 1, "Musculoskeletal stiffness": 1, "Nasal congestion": 1, "Nausea": 2, "Neck pain": 2, "Nerve injury": 1, "Neuritis": 1, "Neutrophil count decreased": 1, "Neutrophil percentage decreased": 1, "No adverse event": 14, "Ocular hyperaemia": 1, "Oropharyngeal pain": 1, "Pain": 4, "Pain in extremity": 4, "Paraesthesia": 1, "Product administered at inappropriate site": 1, "Product administered to patient of inappropriate age": 4, "Productive cough": 1, "Pruritus": 3, "Pyrexia": 3, "Rash": 2, "Red blood cell count normal": 1, "Red blood cell nucleated morphology": 1, "Red blood cell sedimentation rate increased": 1, "Red cell distribution width normal": 1, "Road traffic accident": 1, "SARS-CoV-2 test": 2, "SARS-CoV-2 test positive": 1, "Sluggishness": 1, "Somnolence": 1, "Syncope": 3, "Throat irritation": 1, "Thrombocytopenia": 1, "Tremor": 1, "Urticaria": 1, "Vaccination failure": 3, "Vaccination site inflammation": 1, "Vaccination site pain": 1, "Vision blurred": 1, "Wheezing": 1}}