updating VAERS data
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{"batchcode": "HG2282", "histogram": {"Dizziness": 4, "Pruritus": 4, "Blood pressure increased": 3, "Erythema": 3, "Headache": 3, "Injection site pain": 3, "Nausea": 3, "Syncope": 3, "Chills": 2, "Fatigue": 2, "Loss of consciousness": 2, "Pyrexia": 2, "Urticaria": 2, "Vaccination site pain": 2, "Abdominal discomfort": 1, "Administration site pruritus": 1, "Anxiety": 1, "Arthralgia": 1, "Body temperature": 1, "Cardiac flutter": 1, "Confusional state": 1, "Disorientation": 1, "Extra dose administered": 1, "Eye pain": 1, "Heart rate increased": 1, "Hypertension": 1, "Hypotension": 1, "Illness": 1, "Immunisation reaction": 1, "Inappropriate schedule of product administration": 1, "Injected limb mobility decreased": 1, "Injection site erythema": 1, "Injection site haemorrhage": 1, "Injection site warmth": 1, "Laboratory test": 1, "Lip pruritus": 1, "Malaise": 1, "Myalgia": 1, "No reaction on previous exposure to drug": 1, "Pain": 1, "Palpitations": 1, "Paraesthesia oral": 1, "Presyncope": 1, "Product preparation issue": 1, "Rash": 1, "Rash erythematous": 1, "Rash pruritic": 1, "Seizure": 1, "Skin discolouration": 1, "Skin warm": 1, "Swelling": 1, "Swelling face": 1, "Swelling of eyelid": 1, "Vision blurred": 1, "Wrong technique in device usage process": 1}, "Company": "PFIZER\\BIONTECH", "Adverse Reaction Reports": 27, "Disabilities": 0, "Life Threatening Illnesses": 0, "Deaths": 0}
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{"batchcode": "HG2282", "histogram": {"Dizziness": 4, "Pruritus": 4, "Blood pressure increased": 3, "Erythema": 3, "Headache": 3, "Injection site pain": 3, "Nausea": 3, "Syncope": 3, "Chills": 2, "Fatigue": 2, "Loss of consciousness": 2, "Pyrexia": 2, "Urticaria": 2, "Vaccination site pain": 2, "Abdominal discomfort": 1, "Administration site pruritus": 1, "Anxiety": 1, "Arthralgia": 1, "Body temperature": 1, "Cardiac flutter": 1, "Confusional state": 1, "Disorientation": 1, "Extra dose administered": 1, "Eye pain": 1, "Heart rate increased": 1, "Hypertension": 1, "Hypotension": 1, "Illness": 1, "Immunisation reaction": 1, "Inappropriate schedule of product administration": 1, "Injected limb mobility decreased": 1, "Injection site erythema": 1, "Injection site haemorrhage": 1, "Injection site warmth": 1, "Laboratory test": 1, "Lip pruritus": 1, "Malaise": 1, "Myalgia": 1, "No reaction on previous exposure to drug": 1, "Pain": 1, "Palpitations": 1, "Paraesthesia oral": 1, "Presyncope": 1, "Product preparation issue": 1, "Rash": 1, "Rash erythematous": 1, "Rash pruritic": 1, "Seizure": 1, "Skin discolouration": 1, "Skin warm": 1, "Swelling": 1, "Swelling face": 1, "Swelling of eyelid": 1, "Vision blurred": 1, "Wrong technique in device usage process": 1}, "Adverse Reaction Reports": 27, "Deaths": 0, "Company": "PFIZER\\BIONTECH", "Life Threatening Illnesses": 0, "Disabilities": 0}
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