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HowBadIsMyBatch/docs/data/histograms/Global/FE 6975.json
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{"batchcode": "FE 6975", "histogram": {"COVID-19": 4, "Inappropriate schedule of product administration": 4, "SARS-CoV-2 test": 4, "Arrhythmia": 2, "Drug ineffective": 2, "Headache": 2, "Lymphadenopathy": 2, "Paraesthesia": 2, "Pyrexia": 2, "Rash": 2, "Vaccination failure": 2, "Acute generalised exanthematous pustulosis": 1, "Ageusia": 1, "Anosmia": 1, "Apathy": 1, "Blood test": 1, "Body temperature": 1, "Breast discomfort": 1, "Chest discomfort": 1, "Chest pain": 1, "Circulatory collapse": 1, "Cough": 1, "Death": 1, "Dementia": 1, "Dermatitis": 1, "Dizziness": 1, "Dyspnoea": 1, "Eosinophilic granulomatosis with polyangiitis": 1, "Exercise tolerance decreased": 1, "Facial paralysis": 1, "Fatigue": 1, "Heavy menstrual bleeding": 1, "Herpes zoster": 1, "Hypersensitivity": 1, "Influenza": 1, "Interchange of vaccine products": 1, "Listless": 1, "Malaise": 1, "Monoplegia": 1, "Myalgia": 1, "Myocarditis": 1, "Nasopharyngitis": 1, "Off label use": 1, "Pain": 1, "Pain in extremity": 1, "Pericardial effusion": 1, "Pneumonia": 1, "Radial nerve palsy": 1, "Seizure": 1, "Venous thrombosis limb": 1, "Vitreous haemorrhage": 1, "Vomiting": 1}, "Company": "PFIZER\\BIONTECH", "Adverse Reaction Reports": 22, "Disabilities": 0, "Life Threatening Illnesses": 1, "Deaths": 1}