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1 line
1.7 KiB
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{"Adverse Reaction Reports": 122, "Company": "MODERNA", "Deaths": 0, "Disabilities": 2, "Hospitalizations": 1, "Life-Threatening Illnesses": 1, "batchcode": "083B22A", "histogram": {"Abdominal pain": 1, "Abdominal pain upper": 1, "Amnesia": 1, "Anaemia": 1, "Arthralgia": 1, "Back pain": 1, "Bell's palsy": 1, "Blood test": 1, "Chills": 1, "Colon cancer": 1, "Computerised tomogram normal": 1, "Diarrhoea": 1, "Discontinued product administered": 1, "Dizziness": 2, "Dysphagia": 2, "Dyspnoea": 2, "Expired product administered": 42, "Extra dose administered": 3, "Facial paralysis": 1, "Fatigue": 3, "Flushing": 2, "Haematemesis": 1, "Headache": 2, "Hyperhidrosis": 2, "Hypertension": 2, "Hypoaesthesia": 1, "Hysteroscopy": 1, "Inappropriate schedule of product administration": 2, "Incorrect dose administered": 2, "Incorrect product formulation administered": 36, "Incorrect route of product administration": 1, "Injection site erythema": 1, "Injection site pain": 1, "Injection site pruritus": 1, "Interchange of vaccine products": 1, "Lacrimation increased": 1, "Liquid product physical issue": 1, "Musculoskeletal stiffness": 1, "Myalgia": 1, "Nausea": 3, "No adverse event": 54, "Pain": 2, "Pain in extremity": 3, "Paraesthesia": 2, "Peripheral swelling": 1, "Poor quality product administered": 2, "Product administered to patient of inappropriate age": 1, "Product availability issue": 2, "Product storage error": 19, "Product temperature excursion issue": 17, "Pruritus": 2, "Pyrexia": 2, "Rash": 3, "Skin reaction": 1, "Tenderness": 1, "Throat tightness": 1, "Ultrasound scan": 1, "Underdose": 2, "Unevaluable event": 6, "Vaginal haemorrhage": 1, "Weight increased": 1, "Wrong product administered": 13}} |