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1.1 KiB
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1 line
1.1 KiB
JSON
{"Adverse Reaction Reports": 361, "Company": "MODERNA", "Deaths": 0, "Disabilities": 0, "Hospitalizations": 0, "Life-Threatening Illnesses": 0, "batchcode": "AR6965B", "histogram": {"Abdominal discomfort": 1, "Asthenia": 1, "Axillary pain": 1, "Chills": 2, "Decreased appetite": 1, "Expired product administered": 12, "Extra dose administered": 5, "Fatigue": 2, "Feeding disorder": 1, "Feeling abnormal": 1, "Feeling hot": 1, "Headache": 1, "Inappropriate schedule of product administration": 1, "Incorrect dose administered": 30, "Incorrect product formulation administered": 208, "Injection site pain": 2, "Interchange of vaccine products": 2, "Laparotomy": 1, "Lymph node pain": 1, "Nausea": 1, "No adverse event": 190, "Pain": 1, "Pain in extremity": 8, "Poor quality product administered": 2, "Product administered to patient of inappropriate age": 27, "Product appearance confusion": 1, "Product label confusion": 5, "Product lot number issue": 1, "Product packaging confusion": 1, "Product storage error": 4, "Tinnitus": 1, "Underdose": 21, "Unevaluable event": 2, "Vaccination site pain": 1, "Vomiting": 1, "Wrong product administered": 88}} |