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1.2 KiB
JSON
1 line
1.2 KiB
JSON
{"Adverse Reaction Reports": 37, "Company": "PFIZER\\BIONTECH", "Deaths": 0, "Disabilities": 0, "Hospitalizations": 0, "Life-Threatening Illnesses": 0, "batchcode": "FW1333", "histogram": {"Acupuncture": 1, "Ageusia": 1, "Arthralgia": 2, "Asthenia": 2, "Balance disorder": 1, "COVID-19": 2, "Cough": 1, "Decreased appetite": 1, "Discomfort": 1, "Discontinued product administered": 1, "Dizziness": 2, "Drug ineffective": 1, "Expired product administered": 1, "Extra dose administered": 2, "Eye irritation": 1, "Fatigue": 4, "Headache": 1, "Hyperhidrosis": 1, "Hypertension": 1, "Incorrect dose administered": 2, "Incorrect product formulation administered": 10, "Interchange of vaccine products": 1, "Lymphadenopathy": 1, "Malaise": 1, "Medication error": 1, "Mobility decreased": 1, "Myalgia": 1, "Nausea": 2, "Neck pain": 1, "No adverse event": 8, "Oropharyngeal pain": 1, "Pain": 3, "Pain in extremity": 4, "Paranasal sinus discomfort": 1, "Product administered to patient of inappropriate age": 1, "Pyrexia": 1, "Respiratory tract congestion": 1, "SARS-CoV-2 test": 1, "SARS-CoV-2 test positive": 1, "Sneezing": 1, "Underdose": 1, "Unevaluable event": 11, "Wrong product administered": 1}} |