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2.4 KiB
JSON
1 line
2.4 KiB
JSON
{"Adverse Reaction Reports": 97, "Company": "MODERNA", "Deaths": 0, "Disabilities": 1, "Hospitalizations": 4, "Life-Threatening Illnesses": 1, "batchcode": "044C22A", "histogram": {"Acute kidney injury": 1, "Anaemia": 1, "Angiogram pulmonary": 1, "Anhedonia": 1, "Aphasia": 1, "Arthralgia": 2, "Asthenia": 1, "Asthma": 1, "Biopsy kidney": 1, "Blood magnesium": 1, "Blood test normal": 1, "Blood thyroid stimulating hormone normal": 1, "Body temperature": 1, "Bradykinesia": 1, "Brain natriuretic peptide increased": 1, "COVID-19 immunisation": 1, "Cardiac failure congestive": 1, "Chest X-ray": 1, "Condition aggravated": 1, "Cough": 1, "Depression": 1, "Diarrhoea": 1, "Discomfort": 1, "Discontinued product administered": 1, "Dyspnoea": 3, "Electrocardiogram": 1, "Electrocardiogram abnormal": 1, "Erectile dysfunction": 1, "Expired product administered": 44, "Exposure during pregnancy": 2, "Extra dose administered": 8, "Fatigue": 1, "Fibrin D dimer": 1, "Full blood count": 1, "Full blood count normal": 1, "Gait disturbance": 1, "Headache": 1, "Hypersensitivity": 1, "Hypoaesthesia": 1, "Hypokalaemia": 1, "Hypoxia": 1, "Immediate post-injection reaction": 1, "Inappropriate schedule of product administration": 7, "Incorrect dose administered": 2, "Incorrect product formulation administered": 7, "Incorrect route of product administration": 1, "Infarction": 1, "Inflammation": 1, "Interchange of vaccine products": 1, "Joint range of motion decreased": 1, "Knee operation": 1, "Laboratory test": 2, "Libido decreased": 1, "Localised oedema": 1, "Magnetic resonance imaging": 2, "Maternal exposure during pregnancy": 1, "Metabolic function test": 1, "Metabolic function test normal": 1, "Mobility decreased": 1, "Myelopathy": 1, "Myocardial infarction": 1, "Nasal congestion": 1, "Neck pain": 2, "No adverse event": 52, "Oedema peripheral": 1, "Pain": 3, "Pain in extremity": 2, "Palpitations": 1, "Pneumonia": 1, "Product administered to patient of inappropriate age": 1, "Product administration error": 1, "Product administration interrupted": 1, "Product storage error": 8, "Productive cough": 1, "Pruritus": 1, "Pulmonary oedema": 1, "Pyrexia": 2, "Rash": 1, "SARS-CoV-2 test": 1, "Shoulder injury related to vaccine administration": 1, "Sleep disorder": 3, "Swelling face": 1, "Tinnitus": 1, "Ultrasound Doppler normal": 1, "Underdose": 1, "Unevaluable event": 3, "Urine analysis": 1, "Walking aid user": 1, "Wheezing": 1, "Wrong product administered": 2, "X-ray": 1, "X-ray normal": 1}} |