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frankknoll
2023-04-19 09:53:36 +02:00
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docs/data/histograms/Global/061F22A.json
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{"batchcode": "061F22A", "histograms": [{"histogram": {"No adverse event": 32, "Accidental underdose": 11, "Expired product administered": 10, "Product storage error": 9, "COVID-19": 5, "Underdose": 5, "Wrong product administered": 5, "Oropharyngeal pain": 3, "Pyrexia": 3, "SARS-CoV-2 test positive": 3, "Cough": 2, "Incorrect dose administered": 2, "Respiratory tract congestion": 2, "Arthralgia": 1, "Arthritis": 1, "Back disorder": 1, "Blood test abnormal": 1, "Condition aggravated": 1, "Diarrhoea": 1, "Dry mouth": 1, "Dyspnoea": 1, "Erythema": 1, "Exposure to SARS-CoV-2": 1, "Fatigue": 1, "Headache": 1, "Inappropriate schedule of product administration": 1, "Influenza like illness": 1, "Myalgia": 1, "Nasal congestion": 1, "Nasopharyngitis": 1, "Pain": 1, "Peripheral swelling": 1, "Product administered to patient of inappropriate age": 1, "Pruritus": 1, "Rash": 1, "SARS-CoV-2 test": 1, "Splint application": 1, "Syringe issue": 1, "Tendonitis": 1, "Vaccine breakthrough infection": 1, "X-ray limb abnormal": 1}, "batchcodes": ["061F22A"]}], "Life Threatening Illnesses": 0, "Adverse Reaction Reports": 41, "Deaths": 0, "Company": "MODERNA", "Severe reports": null, "Lethality": null, "Disabilities": 0}
{"batchcode": "061F22A", "histogram": {"No adverse event": 32, "Accidental underdose": 11, "Expired product administered": 10, "Product storage error": 9, "COVID-19": 5, "Underdose": 5, "Wrong product administered": 5, "Oropharyngeal pain": 3, "Pyrexia": 3, "SARS-CoV-2 test positive": 3, "Cough": 2, "Incorrect dose administered": 2, "Respiratory tract congestion": 2, "Arthralgia": 1, "Arthritis": 1, "Back disorder": 1, "Blood test abnormal": 1, "Condition aggravated": 1, "Diarrhoea": 1, "Dry mouth": 1, "Dyspnoea": 1, "Erythema": 1, "Exposure to SARS-CoV-2": 1, "Fatigue": 1, "Headache": 1, "Inappropriate schedule of product administration": 1, "Influenza like illness": 1, "Myalgia": 1, "Nasal congestion": 1, "Nasopharyngitis": 1, "Pain": 1, "Peripheral swelling": 1, "Product administered to patient of inappropriate age": 1, "Pruritus": 1, "Rash": 1, "SARS-CoV-2 test": 1, "Splint application": 1, "Syringe issue": 1, "Tendonitis": 1, "Vaccine breakthrough infection": 1, "X-ray limb abnormal": 1}, "Adverse Reaction Reports": 41, "Disabilities": 0, "Deaths": 0, "Life Threatening Illnesses": 0, "Company": "MODERNA"}