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{"Adverse Reaction Reports": 136, "Company": "MODERNA", "Deaths": 0, "Disabilities": 0, "Hospitalizations": 1, "Life-Threatening Illnesses": 0, "batchcode": "AU5551B", "histogram": {"Abdominal pain": 1, "Accidental exposure to product": 1, "Arthralgia": 1, "Blood culture": 1, "Blood glucose normal": 1, "Bronchiolitis": 1, "C-reactive protein": 1, "C-reactive protein increased": 1, "Cellulitis": 1, "Chest X-ray": 1, "Chest pain": 1, "Condition aggravated": 1, "Cyanosis": 1, "Dizziness": 1, "Dyspnoea": 2, "Electrocardiogram": 1, "Epilepsy": 1, "Erythema": 1, "Expired product administered": 1, "Extra dose administered": 2, "Eye abrasion": 1, "Eye movement disorder": 1, "Eyelid irritation": 1, "Fatigue": 1, "Feeling abnormal": 1, "Full blood count": 1, "Headache": 2, "Immunisation reaction": 3, "Incorrect dose administered": 71, "Incorrect product formulation administered": 3, "Induration": 1, "Injection site discolouration": 1, "Injection site dryness": 1, "Injection site erythema": 1, "Injection site pain": 1, "Injection site rash": 1, "Lethargy": 1, "Loss of consciousness": 1, "Mass": 1, "Metabolic function test normal": 1, "Nausea": 1, "No adverse event": 53, "Ocular discomfort": 1, "Oedema peripheral": 1, "Pain": 1, "Peripheral swelling": 2, "Platelet count increased": 1, "Post-tussive vomiting": 1, "Product administered to patient of inappropriate age": 12, "Product dispensing error": 10, "Product label confusion": 5, "Product label issue": 4, "Product storage error": 5, "Prohormone brain natriuretic peptide": 1, "Pyrexia": 10, "Rash": 2, "Red blood cell sedimentation rate increased": 1, "Respiratory symptom": 1, "Rhinorrhoea": 1, "Seizure": 1, "Swelling of eyelid": 1, "Syncope": 1, "Trismus": 1, "Troponin": 1, "Underdose": 10, "Unevaluable event": 8, "Urine analysis": 1, "Urticaria": 3, "Vaccine positive rechallenge": 1, "Viral infection": 1, "Viral test negative": 1, "Vomiting": 1, "White blood cell count increased": 2, "Wrong product administered": 3}}