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1.1 KiB
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1 line
1.1 KiB
JSON
{"Adverse Reaction Reports": 10, "Company": "PFIZER\\BIONTECH", "Deaths": 0, "Disabilities": 0, "Hospitalizations": 1, "Life-Threatening Illnesses": 0, "batchcode": "FF82222", "histogram": {"Asthenopia": 1, "Back pain": 1, "Blood pressure measurement": 1, "Burning sensation": 1, "COVID-19": 1, "Cardiac monitoring": 1, "Chest discomfort": 1, "Deafness": 1, "Diarrhoea": 1, "Drug ineffective": 1, "Dyspnoea": 1, "Dyspnoea exertional": 1, "Electrocardiogram": 1, "Erythema": 1, "Extra dose administered": 1, "Fatigue": 2, "Gastrooesophageal reflux disease": 1, "Greater trochanteric pain syndrome": 1, "Headache": 1, "Hyperaesthesia": 1, "Immunisation": 2, "Inappropriate schedule of product administration": 1, "Interchange of vaccine products": 2, "Joint effusion": 1, "Magnetic resonance imaging": 2, "Malaise": 1, "Migraine": 1, "Muscle twitching": 1, "Nasal congestion": 1, "Off label use": 3, "Oropharyngeal pain": 1, "Pain": 1, "Paraesthesia": 1, "Peripheral swelling": 1, "Product use issue": 1, "SARS-CoV-2 test": 5, "Tendon disorder": 1, "Tremor": 1, "Ultrasound scan": 1, "Vaccination site pain": 1, "Vomiting": 1}} |