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{"Adverse Reaction Reports": 17, "Company": "MODERNA", "Deaths": 0, "Disabilities": 0, "Hospitalizations": 1, "Life-Threatening Illnesses": 0, "batchcode": "023D21A", "histogram": {"Acoustic stimulation tests abnormal": 1, "Asthenia": 1, "Chills": 1, "Computerised tomogram thorax abnormal": 1, "Confusional state": 1, "Deafness neurosensory": 1, "Deafness unilateral": 1, "Deep vein thrombosis": 1, "Dizziness": 1, "Dyskinesia": 1, "Dyspnoea": 1, "Ear discomfort": 1, "Expired product administered": 2, "Extra dose administered": 1, "Eye movement disorder": 1, "Fall": 1, "Full blood count normal": 1, "Hypoaesthesia oral": 1, "Hypotonia": 1, "Immediate post-injection reaction": 1, "Inappropriate schedule of product administration": 1, "Influenza like illness": 1, "Injection site bruising": 1, "Injection site discolouration": 1, "Injection site erythema": 1, "Injection site nodule": 1, "Injection site pain": 2, "Injection site pruritus": 1, "Injection site swelling": 1, "Laboratory test normal": 1, "Nausea": 1, "Night sweats": 1, "Paraesthesia": 1, "Paraesthesia oral": 1, "Poor quality product administered": 1, "Product storage error": 1, "Pulmonary embolism": 1, "Rash": 1, "Rash erythematous": 1, "Syncope": 2, "Throat tightness": 1, "Tinnitus": 1, "Ultrasound Doppler abnormal": 1, "Unresponsive to stimuli": 1, "Urine odour abnormal": 1, "Vomiting": 1}}