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frankknoll
2024-04-07 22:15:42 +02:00
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docs/data/histograms/Global/HG4675.json
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{"batchcode": "HG4675", "histogram": {"COVID-19": 5, "No adverse event": 4, "Pain in extremity": 4, "Dizziness": 3, "Drug ineffective": 3, "Dyspnoea": 3, "Extra dose administered": 3, "Product administered to patient of inappropriate age": 3, "Chest discomfort": 2, "Inappropriate schedule of product administration": 2, "Incorrect dose administered": 2, "Injection site erythema": 2, "Injection site swelling": 2, "Loss of consciousness": 2, "Nausea": 2, "Pain": 2, "Palpitations": 2, "Product administration error": 2, "SARS-CoV-2 test": 2, "Vision blurred": 2, "Wrong product administered": 2, "Angiogram normal": 1, "Arthralgia": 1, "Asthenia": 1, "Back pain": 1, "Balance disorder": 1, "Blister": 1, "Blood creatine phosphokinase increased": 1, "Blood creatinine increased": 1, "Blood pressure increased": 1, "Blood test normal": 1, "Body height": 1, "Body height decreased": 1, "Brain fog": 1, "Brain natriuretic peptide increased": 1, "Cardiac monitoring normal": 1, "Catheterisation cardiac normal": 1, "Chest pain": 1, "Computerised tomogram head normal": 1, "Condition aggravated": 1, "Death": 1, "Dyspnoea exertional": 1, "Echocardiogram normal": 1, "Electrocardiogram T wave inversion": 1, "Electrocardiogram normal": 1, "Expired product administered": 1, "Fall": 1, "Fatigue": 1, "Fibrin D dimer increased": 1, "Flushing": 1, "Gait inability": 1, "Head injury": 1, "Heart rate increased": 1, "Immediate post-injection reaction": 1, "Incorrect route of product administration": 1, "Injection site bruising": 1, "Injection site pain": 1, "Injection site pruritus": 1, "Injection site warmth": 1, "Magnetic resonance imaging normal": 1, "Mobility decreased": 1, "Muscle spasms": 1, "Myocarditis": 1, "Myositis": 1, "Nerve conduction studies abnormal": 1, "Nerve injury": 1, "Neuralgic amyotrophy": 1, "Presyncope": 1, "Product administered at inappropriate site": 1, "Pyrexia": 1, "Rash": 1, "Seizure": 1, "Sleep disorder": 1, "Swelling": 1, "Syncope": 1, "Tinnitus": 1, "Transient ischaemic attack": 1, "Troponin increased": 1, "Unresponsive to stimuli": 1, "Vaccination failure": 1, "X-ray": 1}, "Deaths": 1, "Disabilities": 2, "Adverse Reaction Reports": 39, "Company": "PFIZER\\BIONTECH", "Life Threatening Illnesses": 0}
{"batchcode": "HG4675", "histogram": {"COVID-19": 7, "No adverse event": 4, "Pain in extremity": 4, "SARS-CoV-2 test": 4, "Dizziness": 3, "Drug ineffective": 3, "Dyspnoea": 3, "Extra dose administered": 3, "Product administered to patient of inappropriate age": 3, "Vaccination failure": 3, "Chest discomfort": 2, "Inappropriate schedule of product administration": 2, "Incorrect dose administered": 2, "Injection site erythema": 2, "Injection site swelling": 2, "Loss of consciousness": 2, "Nausea": 2, "Pain": 2, "Palpitations": 2, "Product administration error": 2, "Vision blurred": 2, "Wrong product administered": 2, "Angiogram normal": 1, "Arthralgia": 1, "Asthenia": 1, "Back pain": 1, "Balance disorder": 1, "Blister": 1, "Blood creatine phosphokinase increased": 1, "Blood creatinine increased": 1, "Blood pressure increased": 1, "Blood test normal": 1, "Body height": 1, "Body height decreased": 1, "Brain fog": 1, "Brain natriuretic peptide increased": 1, "Cardiac monitoring normal": 1, "Catheterisation cardiac normal": 1, "Chest pain": 1, "Computerised tomogram head normal": 1, "Condition aggravated": 1, "Death": 1, "Dyspnoea exertional": 1, "Echocardiogram normal": 1, "Electrocardiogram T wave inversion": 1, "Electrocardiogram normal": 1, "Expired product administered": 1, "Fall": 1, "Fatigue": 1, "Fibrin D dimer increased": 1, "Flushing": 1, "Gait inability": 1, "Head injury": 1, "Heart rate increased": 1, "Immediate post-injection reaction": 1, "Incorrect route of product administration": 1, "Injection site bruising": 1, "Injection site pain": 1, "Injection site pruritus": 1, "Injection site warmth": 1, "Magnetic resonance imaging normal": 1, "Mobility decreased": 1, "Muscle spasms": 1, "Myocarditis": 1, "Myositis": 1, "Nerve conduction studies abnormal": 1, "Nerve injury": 1, "Neuralgic amyotrophy": 1, "Presyncope": 1, "Product administered at inappropriate site": 1, "Pyrexia": 1, "Rash": 1, "Seizure": 1, "Sleep disorder": 1, "Swelling": 1, "Syncope": 1, "Thrombosis": 1, "Tinnitus": 1, "Transient ischaemic attack": 1, "Troponin increased": 1, "Unresponsive to stimuli": 1, "X-ray": 1}, "Adverse Reaction Reports": 41, "Company": "PFIZER\\BIONTECH", "Deaths": 1, "Life Threatening Illnesses": 0, "Disabilities": 2}