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{"Adverse Reaction Reports": 8, "Company": "PFIZER\\BIONTECH", "Deaths": 0, "Disabilities": 1, "Hospitalizations": 1, "Life-Threatening Illnesses": 0, "batchcode": "FF5107", "histogram": {"Acute motor-sensory axonal neuropathy": 1, "Angiogram": 1, "Blood test": 1, "Candida infection": 1, "Cardiac failure congestive": 1, "Cerebral venous sinus thrombosis": 1, "Cerebral venous thrombosis": 1, "Chest pain": 1, "Coronary artery insufficiency": 1, "Echocardiogram": 1, "Electroneuromyography": 1, "Eructation": 1, "Fluid retention": 1, "Furuncle": 1, "Heart rate increased": 1, "Hypoaesthesia": 1, "Hypokinesia": 1, "Impaired work ability": 1, "Inappropriate schedule of product administration": 3, "Interchange of vaccine products": 1, "Investigation": 1, "Lymphadenopathy": 2, "Magnetic resonance imaging": 1, "Magnetic resonance imaging head": 1, "Migraine": 1, "Off label use": 1, "Pain in extremity": 1, "Peripheral sensorimotor neuropathy": 1, "Sinus rhythm": 1, "Systolic dysfunction": 1, "Ultrasound Doppler": 1, "Ultrasound breast": 1, "Ultrasound scan": 1, "Visual impairment": 1, "Weight": 1, "Weight increased": 1}}