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{"Adverse Reaction Reports": 8, "Company": "JANSSEN", "Deaths": 0, "Disabilities": 0, "Hospitalizations": 0, "Life-Threatening Illnesses": 0, "batchcode": "216D21A", "histogram": {"Asthenia": 1, "Balance disorder": 1, "Brain fog": 1, "Choking sensation": 1, "Computerised tomogram normal": 1, "Contusion": 1, "Dizziness": 2, "Electrocardiogram normal": 1, "Fall": 3, "Feeling hot": 1, "Fibrin D dimer normal": 1, "Head injury": 1, "Headache": 1, "Hyperhidrosis": 1, "Loss of consciousness": 1, "Malaise": 1, "No adverse event": 1, "Pain": 1, "Poor quality product administered": 2, "Product administered to patient of inappropriate age": 1, "Product storage error": 2, "Skin haemorrhage": 1, "Skin laceration": 1, "Syncope": 2, "Wound": 1}}