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{"Adverse Reaction Reports": 15, "Company": "PFIZER\\BIONTECH", "Deaths": 0, "Disabilities": 2, "Hospitalizations": 6, "Life-Threatening Illnesses": 3, "batchcode": "FD 9234", "histogram": {"Acute kidney injury": 1, "Anaphylactic reaction": 1, "Anti-thyroid antibody": 1, "Blood pressure increased": 1, "Blood thyroid stimulating hormone": 1, "Cerebellar haemorrhage": 1, "Cerebral ischaemia": 1, "Cerebrovascular accident": 1, "Diarrhoea": 1, "Dizziness": 2, "Dyspnoea": 1, "Ear haemorrhage": 1, "Epistaxis": 1, "Erectile dysfunction": 1, "Feeling hot": 1, "Haemorrhage": 1, "Headache": 2, "Hypertension": 1, "Hyperthyroidism": 1, "Inappropriate schedule of product administration": 1, "Interchange of vaccine products": 2, "Investigation": 1, "Leukaemia": 1, "Loss of libido": 1, "Magnetic resonance imaging": 3, "Maternal exposure during pregnancy": 1, "Myalgia": 2, "Off label use": 2, "Restlessness": 1, "Sudden hearing loss": 1, "Syncope": 1, "Taste disorder": 1, "Thrombophlebitis": 1, "Tinnitus": 1, "Tremor": 1, "Visual field defect": 1, "Visual impairment": 1, "White blood cell count": 1}}