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Frank Knoll
2024-04-07 22:59:07 +02:00
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docs/data/histograms/Global/HG4589.json
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{"batchcode": "HG4589", "histogram": {"Expired product administered": 5, "No adverse event": 5, "Pain in extremity": 5, "COVID-19": 3, "Fatigue": 3, "Malaise": 3, "Pain": 3, "Pruritus": 3, "SARS-CoV-2 test": 3, "Vaccination failure": 3, "Chest pain": 2, "Dizziness": 2, "Extra dose administered": 2, "Guillain-Barre syndrome": 2, "Heart rate increased": 2, "Inflammation": 2, "Injection site swelling": 2, "Loss of consciousness": 2, "Pallor": 2, "Rash": 2, "Swelling": 2, "Syncope": 2, "Tenderness": 2, "Abdominal discomfort": 1, "Acute myocardial infarction": 1, "Apnoea": 1, "Asthenia": 1, "Back pain": 1, "Balance disorder": 1, "Biopsy skin": 1, "Burning sensation": 1, "CSF protein increased": 1, "Chills": 1, "Consciousness fluctuating": 1, "Cough": 1, "Death": 1, "Disorientation": 1, "Electrocardiogram": 1, "Erythema": 1, "Eye pain": 1, "Failure to thrive": 1, "Fall": 1, "Feeling hot": 1, "Gait disturbance": 1, "Gait inability": 1, "Headache": 1, "Hyperhidrosis": 1, "Hypersensitivity": 1, "Hypersomnia": 1, "Hypoaesthesia": 1, "Hypotonia": 1, "Hypoxia": 1, "Imaging procedure": 1, "Immediate post-injection reaction": 1, "Immunoglobulin therapy": 1, "Inappropriate schedule of product administration": 1, "Injection site erythema": 1, "Injection site haemorrhage": 1, "Injection site rash": 1, "Injection site reaction": 1, "Injection site warmth": 1, "Interchange of vaccine products": 1, "Ischaemic cardiomyopathy": 1, "Joint swelling": 1, "Limb discomfort": 1, "Local reaction": 1, "Lymphadenopathy": 1, "Mechanical ventilation": 1, "Middle insomnia": 1, "Myocardial infarction": 1, "Nausea": 1, "Ocular discomfort": 1, "Oxygen saturation decreased": 1, "Peripheral swelling": 1, "Pharyngeal swelling": 1, "Photophobia": 1, "Poor quality product administered": 1, "Product temperature excursion issue": 1, "Pulse absent": 1, "Pyrexia": 1, "Respiratory arrest": 1, "Respiratory rate increased": 1, "Rhinorrhoea": 1, "Sedation": 1, "Sleep disorder": 1, "Swelling face": 1, "Swollen tongue": 1, "Unevaluable event": 1, "Unresponsive to stimuli": 1, "Upper-airway cough syndrome": 1, "Urticaria": 1, "Vomiting": 1, "Wheezing": 1}, "Company": "PFIZER\\BIONTECH", "Deaths": 2, "Life Threatening Illnesses": 2, "Disabilities": 1, "Adverse Reaction Reports": 41}
{"batchcode": "HG4589", "histogram": {"Expired product administered": 5, "No adverse event": 5, "Pain in extremity": 5, "COVID-19": 3, "Fatigue": 3, "Malaise": 3, "Pain": 3, "Pruritus": 3, "SARS-CoV-2 test": 3, "Vaccination failure": 3, "Chest pain": 2, "Dizziness": 2, "Extra dose administered": 2, "Guillain-Barre syndrome": 2, "Heart rate increased": 2, "Inflammation": 2, "Injection site swelling": 2, "Loss of consciousness": 2, "Pallor": 2, "Rash": 2, "Swelling": 2, "Syncope": 2, "Tenderness": 2, "Abdominal discomfort": 1, "Acute myocardial infarction": 1, "Apnoea": 1, "Asthenia": 1, "Back pain": 1, "Balance disorder": 1, "Biopsy skin": 1, "Burning sensation": 1, "CSF protein increased": 1, "Chills": 1, "Consciousness fluctuating": 1, "Cough": 1, "Death": 1, "Disorientation": 1, "Electrocardiogram": 1, "Erythema": 1, "Eye pain": 1, "Failure to thrive": 1, "Fall": 1, "Feeling hot": 1, "Gait disturbance": 1, "Gait inability": 1, "Headache": 1, "Hyperhidrosis": 1, "Hypersensitivity": 1, "Hypersomnia": 1, "Hypoaesthesia": 1, "Hypotonia": 1, "Hypoxia": 1, "Imaging procedure": 1, "Immediate post-injection reaction": 1, "Immunoglobulin therapy": 1, "Inappropriate schedule of product administration": 1, "Injection site erythema": 1, "Injection site haemorrhage": 1, "Injection site rash": 1, "Injection site reaction": 1, "Injection site warmth": 1, "Interchange of vaccine products": 1, "Ischaemic cardiomyopathy": 1, "Joint swelling": 1, "Limb discomfort": 1, "Local reaction": 1, "Lymphadenopathy": 1, "Mechanical ventilation": 1, "Middle insomnia": 1, "Myocardial infarction": 1, "Nausea": 1, "Ocular discomfort": 1, "Oxygen saturation decreased": 1, "Peripheral swelling": 1, "Pharyngeal swelling": 1, "Photophobia": 1, "Poor quality product administered": 1, "Product temperature excursion issue": 1, "Pulse absent": 1, "Pyrexia": 1, "Respiratory arrest": 1, "Respiratory rate increased": 1, "Rhinorrhoea": 1, "Sedation": 1, "Sleep disorder": 1, "Swelling face": 1, "Swollen tongue": 1, "Unevaluable event": 1, "Unresponsive to stimuli": 1, "Upper-airway cough syndrome": 1, "Urticaria": 1, "Vomiting": 1, "Wheezing": 1}, "Company": "PFIZER\\BIONTECH", "Adverse Reaction Reports": 41, "Deaths": 2, "Disabilities": 1, "Life Threatening Illnesses": 2}