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updating VAERS data

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frankknoll
2023-06-30 18:37:49 +02:00
parent cc22841df8
commit b36f0bc5c8
9120 changed files with 9120 additions and 9120 deletions
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docs/data/histograms/Global/FP7136.json
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{"batchcode": "FP7136", "histogram": {"Incorrect product formulation administered": 165, "No adverse event": 61, "Discontinued product administered": 47, "Unevaluable event": 18, "Wrong product administered": 11, "Incorrect dose administered": 8, "Expired product administered": 7, "Product storage error": 7, "Pruritus": 5, "Dizziness": 4, "Extra dose administered": 4, "Headache": 4, "Loss of consciousness": 4, "Nausea": 4, "Pyrexia": 4, "Syncope": 4, "Circumstance or information capable of leading to medication error": 3, "Computerised tomogram": 3, "Dyspnoea": 3, "Electrocardiogram": 3, "Hyperhidrosis": 3, "Inappropriate schedule of product administration": 3, "Injection site pain": 3, "Palpitations": 3, "Product administration error": 3, "Rash": 3, "Vaccination error": 3, "Body temperature": 2, "Dysphagia": 2, "Fatigue": 2, "Interchange of vaccine products": 2, "Laboratory test": 2, "Migraine": 2, "Muscle spasms": 2, "Pain in extremity": 2, "Pallor": 2, "Pharyngeal swelling": 2, "Product administered to patient of inappropriate age": 2, "Product label issue": 2, "SARS-CoV-2 test": 2, "Seizure": 2, "Urticaria": 2, "Vomiting": 2, "Alopecia": 1, "Axillary pain": 1, "Blood glucose normal": 1, "Blood lactic acid": 1, "Blood pressure abnormal": 1, "Blood pressure decreased": 1, "Blood test": 1, "Bradycardia": 1, "COVID-19 immunisation": 1, "Chest X-ray": 1, "Chest discomfort": 1, "Chills": 1, "Computerised tomogram abdomen": 1, "Computerised tomogram thorax": 1, "Culture": 1, "Death": 1, "Dehydration": 1, "Diarrhoea": 1, "Drug screen": 1, "Electrocardiogram abnormal": 1, "Epistaxis": 1, "Fall": 1, "Feeling abnormal": 1, "Feeling hot": 1, "Fibrin D dimer": 1, "Full blood count": 1, "Gait disturbance": 1, "Heart rate increased": 1, "Human chorionic gonadotropin": 1, "Hypotonic-hyporesponsive episode": 1, "Immediate post-injection reaction": 1, "Inflammation": 1, "Influenza A virus test": 1, "Influenza B virus test": 1, "Injection site pruritus": 1, "Injection site swelling": 1, "Injection site warmth": 1, "Lethargy": 1, "Lipase": 1, "Lymphadenopathy": 1, "Malaise": 1, "Metabolic function test": 1, "Myalgia": 1, "Orthostatic hypotension": 1, "Pain": 1, "Pharyngeal hypoaesthesia": 1, "Product preparation error": 1, "Product use issue": 1, "Respiration abnormal": 1, "Respiratory syncytial virus test": 1, "Scan with contrast": 1, "Seizure like phenomena": 1, "Tachycardia": 1, "Tremor": 1, "Trendelenburg position": 1, "Troponin I": 1, "Unresponsive to stimuli": 1, "Urine analysis": 1, "Vaccination site pain": 1, "Vaccination site swelling": 1}, "Disabilities": 0, "Adverse Reaction Reports": 297, "Deaths": 1, "Life Threatening Illnesses": 0, "Company": "PFIZER\\BIONTECH"}
{"batchcode": "FP7136", "histogram": {"Incorrect product formulation administered": 165, "No adverse event": 61, "Discontinued product administered": 47, "Unevaluable event": 18, "Wrong product administered": 11, "Incorrect dose administered": 8, "Expired product administered": 7, "Product storage error": 7, "Pruritus": 5, "Dizziness": 4, "Extra dose administered": 4, "Headache": 4, "Loss of consciousness": 4, "Nausea": 4, "Pyrexia": 4, "Syncope": 4, "Circumstance or information capable of leading to medication error": 3, "Computerised tomogram": 3, "Dyspnoea": 3, "Electrocardiogram": 3, "Hyperhidrosis": 3, "Inappropriate schedule of product administration": 3, "Injection site pain": 3, "Palpitations": 3, "Product administration error": 3, "Rash": 3, "Vaccination error": 3, "Body temperature": 2, "Dysphagia": 2, "Fatigue": 2, "Interchange of vaccine products": 2, "Laboratory test": 2, "Migraine": 2, "Muscle spasms": 2, "Pain in extremity": 2, "Pallor": 2, "Pharyngeal swelling": 2, "Product administered to patient of inappropriate age": 2, "Product label issue": 2, "SARS-CoV-2 test": 2, "Seizure": 2, "Urticaria": 2, "Vomiting": 2, "Alopecia": 1, "Axillary pain": 1, "Blood glucose normal": 1, "Blood lactic acid": 1, "Blood pressure abnormal": 1, "Blood pressure decreased": 1, "Blood test": 1, "Bradycardia": 1, "COVID-19 immunisation": 1, "Chest X-ray": 1, "Chest discomfort": 1, "Chills": 1, "Computerised tomogram abdomen": 1, "Computerised tomogram thorax": 1, "Culture": 1, "Death": 1, "Dehydration": 1, "Diarrhoea": 1, "Drug screen": 1, "Electrocardiogram abnormal": 1, "Epistaxis": 1, "Fall": 1, "Feeling abnormal": 1, "Feeling hot": 1, "Fibrin D dimer": 1, "Full blood count": 1, "Gait disturbance": 1, "Heart rate increased": 1, "Human chorionic gonadotropin": 1, "Hypotonic-hyporesponsive episode": 1, "Immediate post-injection reaction": 1, "Inflammation": 1, "Influenza A virus test": 1, "Influenza B virus test": 1, "Injection site pruritus": 1, "Injection site swelling": 1, "Injection site warmth": 1, "Lethargy": 1, "Lipase": 1, "Lymphadenopathy": 1, "Malaise": 1, "Metabolic function test": 1, "Myalgia": 1, "Orthostatic hypotension": 1, "Pain": 1, "Pharyngeal hypoaesthesia": 1, "Product preparation error": 1, "Product use issue": 1, "Respiration abnormal": 1, "Respiratory syncytial virus test": 1, "Scan with contrast": 1, "Seizure like phenomena": 1, "Tachycardia": 1, "Tremor": 1, "Trendelenburg position": 1, "Troponin I": 1, "Unresponsive to stimuli": 1, "Urine analysis": 1, "Vaccination site pain": 1, "Vaccination site swelling": 1}, "Life Threatening Illnesses": 0, "Company": "PFIZER\\BIONTECH", "Adverse Reaction Reports": 297, "Disabilities": 0, "Deaths": 1}