1 line
1.4 KiB
JSON
1 line
1.4 KiB
JSON
{"Adverse Reaction Reports": 113, "Company": "MODERNA", "Deaths": 0, "Disabilities": 0, "Hospitalizations": 0, "Life-Threatening Illnesses": 0, "batchcode": "AS1417B", "histogram": {"Accidental underdose": 2, "Anion gap abnormal": 1, "Blood urea nitrogen/creatinine ratio": 1, "C-reactive protein": 1, "COVID-19": 1, "Chills": 1, "Circumstance or information capable of leading to medication error": 2, "Discontinued product administered": 24, "Expired product administered": 26, "Extra dose administered": 3, "Febrile convulsion": 1, "Full blood count": 1, "Inappropriate schedule of product administration": 5, "Incorrect dose administered": 2, "Incorrect product formulation administered": 16, "Injection site erythema": 1, "Injection site induration": 1, "Injection site pain": 1, "Injection site rash": 1, "Injection site warmth": 1, "Interchange of vaccine products": 2, "Laboratory test": 1, "Metabolic function test": 1, "No adverse event": 68, "Poor quality product administered": 2, "Product expiration date issue": 1, "Product label confusion": 3, "Product label issue": 1, "Product preparation error": 2, "Product storage error": 14, "Product temperature excursion issue": 3, "Pyrexia": 3, "Rash": 1, "SARS-CoV-2 test": 1, "Sleep disorder": 1, "Tachycardia": 1, "Underdose": 6, "Unevaluable event": 3, "Vaccination error": 3, "Vomiting": 2, "Wrong product administered": 22}} |