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{"Adverse Reaction Reports": 106, "Company": "MODERNA", "Deaths": 1, "Disabilities": 1, "Hospitalizations": 1, "Life-Threatening Illnesses": 0, "batchcode": "063B22A", "histogram": {"Accidental underdose": 1, "Acute respiratory failure": 1, "COVID-19": 1, "Death": 1, "Expired product administered": 24, "Extra dose administered": 3, "General physical health deterioration": 1, "Head injury": 1, "Headache": 1, "Hypoaesthesia": 1, "Inappropriate schedule of product administration": 2, "Incorrect dose administered": 2, "Incorrect product formulation administered": 51, "Incorrect route of product administration": 1, "Lip swelling": 1, "Medication error": 1, "Myalgia": 1, "No adverse event": 29, "Paraesthesia": 1, "Pneumothorax": 1, "Poor quality product administered": 1, "Product administered to patient of inappropriate age": 1, "Product administration error": 1, "Product storage error": 6, "Product temperature excursion issue": 4, "Respiratory failure": 1, "SARS-CoV-2 test positive": 1, "Sepsis": 1, "Syncope": 1, "Underdose": 1, "Unevaluable event": 3, "Vaccination site erythema": 1, "Vaccination site pain": 1, "Vaccination site pruritus": 1, "Vaccination site rash": 1, "Vaccination site swelling": 1, "Wrong product administered": 9}}