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{"Adverse Reaction Reports": 16, "Company": "PFIZER\\BIONTECH", "Deaths": 3, "Disabilities": 3, "Hospitalizations": 2, "Life-Threatening Illnesses": 1, "batchcode": "162B2", "histogram": {"Bell's palsy": 2, "Blood glucose decreased": 1, "Blood glucose increased": 1, "Blood pressure measurement": 2, "Blood test": 1, "Body temperature": 1, "COVID-19": 1, "CSF test": 1, "Cardiac arrest": 1, "Cerebral infarction": 1, "Chest X-ray": 2, "Chest pain": 1, "Chills": 2, "Computerised tomogram head": 1, "Computerised tomogram thorax": 2, "Cough": 1, "Dizziness": 1, "Dry eye": 1, "Dry mouth": 1, "Dysphonia": 1, "Dyspnoea": 4, "Electrocardiogram": 2, "Erythema": 1, "Eyelid disorder": 1, "Fall": 1, "Glycosylated haemoglobin": 1, "Headache": 3, "Heart injury": 1, "Herpes zoster": 1, "Hyperhidrosis": 1, "Hypotension": 1, "Immunisation": 1, "Inappropriate schedule of product administration": 1, "Influenza like illness": 1, "Injected limb mobility decreased": 1, "Interchange of vaccine products": 1, "Lethargy": 1, "Magnetic resonance imaging": 1, "Malaise": 3, "Myalgia": 1, "Nausea": 2, "Off label use": 2, "Pain in extremity": 1, "Paraesthesia": 1, "Paraesthesia oral": 1, "Pneumonia": 1, "Product use issue": 1, "Pulmonary embolism": 1, "Pyrexia": 1, "Right ventricular dilatation": 1, "Right ventricular dysfunction": 1, "SARS-CoV-2 test": 6, "Sinus tachycardia": 1, "Skin laceration": 1, "Syncope": 1, "Ultrasound scan": 1, "Vomiting": 1, "Weight": 1}}