updating VAERS data
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{"batchcode": "GJ6743", "histogram": {"Acute respiratory failure": 5, "Hypoxia": 5, "COVID-19": 3, "Pyrexia": 3, "Wrong product administered": 3, "Body temperature": 2, "Cardiac failure congestive": 2, "Cerebrovascular accident": 2, "Drug ineffective": 2, "Fatigue": 2, "Hypotension": 2, "Incorrect product formulation administered": 2, "SARS-CoV-2 test": 2, "Sepsis": 2, "Symptom recurrence": 2, "Syncope": 2, "Acute myocardial infarction": 1, "Angioedema": 1, "Aortic aneurysm": 1, "Aortic arteriosclerosis": 1, "Asthenia": 1, "Blood glucose normal": 1, "Blood thyroid stimulating hormone": 1, "COVID-19 pneumonia": 1, "Chills": 1, "Chronic respiratory failure": 1, "Coagulopathy": 1, "Confusional state": 1, "Dark circles under eyes": 1, "Deep vein thrombosis": 1, "Discomfort": 1, "Expired product administered": 1, "Extra dose administered": 1, "Facial pain": 1, "Full blood count": 1, "Glycosylated haemoglobin": 1, "Headache": 1, "Hepatic enzyme": 1, "Hepatic enzyme increased": 1, "Hot flush": 1, "Hypersensitivity": 1, "Incorrect dose administered": 1, "Interchange of vaccine products": 1, "Investigation": 1, "Lipids": 1, "Loss of consciousness": 1, "Metabolic function test": 1, "Nausea": 1, "No adverse event": 1, "Obstructive sleep apnoea syndrome": 1, "Pain": 1, "Pneumonia": 1, "Poor quality product administered": 1, "Product administered to patient of inappropriate age": 1, "Product administration error": 1, "Product storage error": 1, "Respiratory failure": 1, "Seasonal allergy": 1, "Swelling face": 1, "Tinnitus": 1, "Transient ischaemic attack": 1, "Vaccination failure": 1, "Vaccination site haemorrhage": 1, "Vaccination site pain": 1, "Vertigo": 1, "Vertigo positional": 1, "Vitamin D": 1}, "Life Threatening Illnesses": 0, "Deaths": 0, "Company": "PFIZER\\BIONTECH", "Adverse Reaction Reports": 35, "Disabilities": 0}
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{"batchcode": "GJ6743", "histogram": {"Acute respiratory failure": 8, "Hypoxia": 6, "COVID-19": 4, "Hypotension": 3, "Pyrexia": 3, "Wrong product administered": 3, "Acute myocardial infarction": 2, "Body temperature": 2, "Cardiac failure congestive": 2, "Cerebrovascular accident": 2, "Coronary artery disease": 2, "Drug ineffective": 2, "Fatigue": 2, "Incorrect product formulation administered": 2, "SARS-CoV-2 test": 2, "Sepsis": 2, "Symptom recurrence": 2, "Syncope": 2, "Angina pectoris": 1, "Angioedema": 1, "Aortic aneurysm": 1, "Aortic arteriosclerosis": 1, "Asthenia": 1, "Asthma": 1, "Attention deficit hyperactivity disorder": 1, "Blood glucose normal": 1, "Blood thyroid stimulating hormone": 1, "COVID-19 pneumonia": 1, "Carotid artery stenosis": 1, "Chills": 1, "Chronic respiratory failure": 1, "Coagulopathy": 1, "Confusional state": 1, "Dark circles under eyes": 1, "Deep vein thrombosis": 1, "Discomfort": 1, "Expired product administered": 1, "Extra dose administered": 1, "Facial pain": 1, "Full blood count": 1, "Gangrene": 1, "Glycosylated haemoglobin": 1, "Headache": 1, "Hepatic enzyme": 1, "Hepatic enzyme increased": 1, "Hot flush": 1, "Hypersensitivity": 1, "Hypervolaemia": 1, "Hypoaesthesia": 1, "Inappropriate schedule of product administration": 1, "Incorrect dose administered": 1, "Interchange of vaccine products": 1, "Investigation": 1, "Lipids": 1, "Loss of consciousness": 1, "Metabolic encephalopathy": 1, "Metabolic function test": 1, "Nausea": 1, "Night sweats": 1, "No adverse event": 1, "Obstructive sleep apnoea syndrome": 1, "Overdose": 1, "Pain": 1, "Paraesthesia": 1, "Pneumonia": 1, "Poor quality product administered": 1, "Product administered to patient of inappropriate age": 1, "Product administration error": 1, "Product storage error": 1, "Respiratory failure": 1, "Seasonal allergy": 1, "Subarachnoid haemorrhage": 1, "Swelling face": 1, "Tinnitus": 1, "Transient ischaemic attack": 1, "Vaccination failure": 1, "Vaccination site haemorrhage": 1, "Vaccination site pain": 1, "Vertigo": 1, "Vertigo positional": 1, "Vitamin D": 1}, "Disabilities": 0, "Company": "PFIZER\\BIONTECH", "Deaths": 0, "Adverse Reaction Reports": 43, "Life Threatening Illnesses": 0}
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