1 line
1.3 KiB
JSON
1 line
1.3 KiB
JSON
{"batchcode": "AR6965B", "histograms": [{"histogram": {"Incorrect product formulation administered": 1, "No adverse event": 1, "Product administration error": 1}, "batchcodes": ["018C22A", "AR6965B"]}, {"histogram": {"Incorrect product formulation administered": 209, "No adverse event": 191, "Wrong product administered": 88, "Incorrect dose administered": 30, "Product administered to patient of inappropriate age": 28, "Underdose": 21, "Expired product administered": 12, "Pain in extremity": 8, "Extra dose administered": 5, "Product label confusion": 5, "Product storage error": 4, "Chills": 2, "Fatigue": 2, "Injection site pain": 2, "Interchange of vaccine products": 2, "Poor quality product administered": 2, "Unevaluable event": 2, "Abdominal discomfort": 1, "Asthenia": 1, "Axillary pain": 1, "Decreased appetite": 1, "Feeding disorder": 1, "Feeling abnormal": 1, "Feeling hot": 1, "Headache": 1, "Inappropriate schedule of product administration": 1, "Laparotomy": 1, "Lymph node pain": 1, "Nausea": 1, "Pain": 1, "Product appearance confusion": 1, "Product lot number issue": 1, "Product packaging confusion": 1, "Tinnitus": 1, "Vaccination site pain": 1, "Vomiting": 1}, "batchcodes": ["AR6965B"]}], "Deaths": 0, "Lethality": 0.0, "Company": "MODERNA", "Adverse Reaction Reports": 363, "Disabilities": 0, "Life Threatening Illnesses": 0, "Severe reports": 0.0} |