updating VAERS data
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{"batchcode": "AU3921B", "histogram": {"Cerebrovascular accident": 1, "Dizziness": 1, "Headache": 1, "Tinnitus": 1}, "Adverse Reaction Reports": 4, "Deaths": 0, "Company": "MODERNA", "Life Threatening Illnesses": 0, "Disabilities": 0}
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{"batchcode": "AU3921B", "histogram": {"Dizziness": 3, "Headache": 2, "Lip swelling": 2, "Asthenia": 1, "Cerebrovascular accident": 1, "Dysgeusia": 1, "Dysphagia": 1, "Expired product administered": 1, "Extra dose administered": 1, "Feeling abnormal": 1, "Fungal infection": 1, "Gait disturbance": 1, "Injection site bruising": 1, "Injection site haemorrhage": 1, "Injection site hypoaesthesia": 1, "Injection site mass": 1, "Injection site pain": 1, "Injection site reaction": 1, "Paraesthesia": 1, "Rash": 1, "Swelling face": 1, "Tinnitus": 1, "Tremor": 1, "Unevaluable event": 1, "Wrong product administered": 1}, "Disabilities": 0, "Life Threatening Illnesses": 0, "Deaths": 0, "Company": "MODERNA", "Adverse Reaction Reports": 14}
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