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1.8 KiB
JSON
1 line
1.8 KiB
JSON
{"Adverse Reaction Reports": 145, "Company": "PFIZER\\BIONTECH", "Deaths": 0, "Disabilities": 1, "Hospitalizations": 3, "Life-Threatening Illnesses": 0, "batchcode": "GK1657", "histogram": {"Acute respiratory failure": 1, "Asthenia": 1, "Asthma": 1, "Back pain": 1, "Blood glucose normal": 1, "Body height": 1, "COVID-19": 3, "Chest pain": 1, "Chills": 1, "Condition aggravated": 1, "Cough": 1, "Dehydration": 1, "Dermatitis atopic": 1, "Diarrhoea": 1, "Discontinued product administered": 1, "Drug ineffective": 2, "Expired product administered": 31, "Extra dose administered": 1, "Eye swelling": 1, "Fatigue": 1, "Feeling hot": 1, "Gait disturbance": 1, "Headache": 3, "Hypersensitivity": 1, "Hypophagia": 1, "Inappropriate schedule of product administration": 2, "Incorrect dose administered": 9, "Incorrect product formulation administered": 29, "Injection site pain": 1, "Investigation": 1, "Loss of personal independence in daily activities": 1, "Maternal exposure during pregnancy": 1, "No adverse event": 18, "Obstructive sleep apnoea syndrome": 1, "Off label use": 1, "Oropharyngeal pain": 1, "Overdose": 3, "Pain": 2, "Pain in extremity": 3, "Peripheral swelling": 1, "Polymerase chain reaction": 1, "Poor quality product administered": 1, "Product administered to patient of inappropriate age": 8, "Product administration error": 2, "Product preparation error": 9, "Product preparation issue": 10, "Product storage error": 30, "Product use issue": 1, "Pruritus": 1, "Pyrexia": 2, "Rash erythematous": 1, "Rash pruritic": 1, "Rhinorrhoea": 1, "SARS-CoV-2 test": 1, "SARS-CoV-2 test positive": 1, "Swelling face": 1, "Transient ischaemic attack": 1, "Underdose": 5, "Unevaluable event": 2, "Urticaria": 1, "Vaccination site discomfort": 1, "Vaccination site erythema": 1, "Vomiting": 1, "Weight": 1, "Wrong product administered": 12}} |