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frankknoll
2024-09-08 18:21:35 +02:00
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commit dcd11b362c
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docs/SymptomsCausedByDrugs/data/ProportionalReportingRatios/vaccines/249.json
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{"Abdominal distension": 4.352179191775153, "Anaphylactic shock": 14.998257129528922, "Blood calcium decreased": 75.65609615152682, "Blood pressure decreased": 4.679325223171978, "Bronchial hyperreactivity": 729.1664017992144, "Drug hypersensitivity": 4.252496186615889, "Erythema": 2.270678167859293, "Gastritis erosive": 146.00098610311133, "Gastrointestinal haemorrhage": 4.852642484573176, "Hepatic enzyme increased": 6.024051232638052, "Hepatic function abnormal": 12.85936133982243, "Muscle contractions involuntary": 59.08739854093133, "Pulmonary alveolar haemorrhage": 50.65044261465893}
{"abortion spontaneous": 4.3, "angioedema": 7.18, "complication associated with device": 36.17, "device related infection": 15.25, "exposure during pregcy": 10.17, "hereditary angioedema": 710.44, "hospitalisation": 10.74, "inappropriate schedule of product administration": 25.26, "incorrect drug administration rate": 47.9, "infusion related reaction": 16.28, "laryngeal oedema": 12.42, "off label use": 2.66, "poor venous access": 125.68, "prescribed overdose": 31.39, "product dose omission issue": 9.42, "product use in unapproved indication": 5.47, "sepsis": 2.09, "sinusitis": 3.2, "staphylococcal infection": 8.21, "stress": 7.32, "therapeutic product effect decreased": 4.47, "therapy change": 701.76, "thrombosis": 2.45, "unevaluable event": 6.79, "vascular device infection": 150.93}