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{"Adverse Reaction Reports": 6, "Company": "PFIZER\\BIONTECH", "Deaths": 0, "Disabilities": 1, "Hospitalizations": 1, "Life-Threatening Illnesses": 0, "batchcode": "31045BD", "histogram": {"Abdominal pain": 1, "Anaemia": 1, "Antiphospholipid antibodies": 1, "Antiphospholipid antibodies positive": 1, "Blindness": 1, "Breast pain": 1, "Deep vein thrombosis": 1, "Diarrhoea": 1, "Haematochezia": 1, "Immunisation": 1, "Inappropriate schedule of product administration": 3, "Interchange of vaccine products": 1, "Investigation": 1, "Joint range of motion decreased": 1, "Laboratory test": 1, "Loss of personal independence in daily activities": 1, "Lymph node pain": 1, "Lymphadenopathy": 1, "Mouth ulceration": 1, "Off label use": 2, "Optic nerve injury": 1, "Optic neuritis": 1, "Pain in extremity": 2, "Papilloedema": 1, "Peripheral swelling": 1, "Pleural effusion": 1, "Postmenopausal haemorrhage": 1, "Pruritus": 1, "Systemic lupus erythematosus": 1, "Ultrasound Doppler": 1, "Urticaria": 1, "Vaccination site pain": 1, "Von Willebrand's disease": 1}}