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1.8 KiB
JSON
1 line
1.8 KiB
JSON
{"Adverse Reaction Reports": 50, "Company": "MODERNA", "Deaths": 0, "Disabilities": 0, "Hospitalizations": 3, "Life-Threatening Illnesses": 0, "batchcode": "061F22A", "histogram": {"Accidental underdose": 11, "Acute kidney injury": 1, "Acute respiratory failure": 1, "Ageusia": 1, "Anaemia of chronic disease": 1, "Anosmia": 1, "Arthralgia": 1, "Arthritis": 1, "Asthenia": 1, "Atrial fibrillation": 1, "Back disorder": 1, "Blister": 1, "Blood test": 1, "Blood test abnormal": 1, "COVID-19": 7, "Chills": 1, "Computerised tomogram": 1, "Condition aggravated": 1, "Coronary artery bypass": 1, "Cough": 4, "Diarrhoea": 1, "Drug hypersensitivity": 1, "Dry mouth": 1, "Dyspnoea": 1, "Dyspnoea at rest": 1, "Electrocardiogram abnormal": 1, "Erythema": 1, "Expired product administered": 10, "Exposure to SARS-CoV-2": 1, "Fatigue": 3, "Headache": 1, "Hyperkalaemia": 1, "Hypersensitivity": 1, "Hypoaesthesia": 1, "Inappropriate schedule of product administration": 1, "Incorrect dose administered": 2, "Influenza like illness": 1, "Insomnia": 1, "Lethargy": 1, "Magnetic resonance imaging head": 1, "Malaise": 1, "Myalgia": 1, "Nasal congestion": 1, "Nasopharyngitis": 1, "No adverse event": 32, "Nodule": 1, "Oropharyngeal pain": 3, "Pain": 2, "Paraesthesia": 1, "Peripheral swelling": 1, "Pneumonia": 1, "Product administered to patient of inappropriate age": 1, "Product storage error": 9, "Pruritus": 1, "Pulmonary embolism": 1, "Pyrexia": 4, "Rash": 2, "Respiratory tract congestion": 3, "Rhinorrhoea": 1, "SARS-CoV-2 test": 1, "SARS-CoV-2 test negative": 1, "SARS-CoV-2 test positive": 4, "Sneezing": 1, "Splint application": 1, "Syringe issue": 1, "Tenderness": 1, "Tendonitis": 1, "Tinnitus": 1, "Transient ischaemic attack": 1, "Underdose": 5, "Vaccine breakthrough infection": 2, "Wrong product administered": 5, "X-ray limb abnormal": 1}} |