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{"Adverse event": 4.02219839339429, "Atrial fibrillation": 2.5556926464388265, "Cardiac disorder": 4.501018091845299, "Cerebrovascular accident": 4.285635311507412, "Depressed mood": 2.050213171226122, "Depression": 2.416578072400478, "Dyspepsia": 2.408050438087031, "Flatulence": 3.17188018200651, "Gastrointestinal disorder": 2.948208807080858, "Glomerular filtration rate decreased": 21.12201785750508, "Hospitalisation": 3.4804074557423306, "Impaired work ability": 5.213511559014525, "Implantable defibrillator insertion": 95.1580602402994, "Inappropriate schedule of product administration": 4.172117018832758, "Nasal congestion": 2.8220767946630883, "Nephrolithiasis": 4.086116711126249, "Neuropathy peripheral": 4.080614936935806, "Poor quality sleep": 11.020034157197278, "Pre-existing condition improved": 171.6906000939662, "Product dose omission in error": 44.89261774555358, "Product dose omission issue": 13.547254056044514, "Product physical issue": 22.632470588815448, "Proteinuria": 10.428904441011738, "Renal disorder": 2.8780641748972275, "Renal impairment": 3.52735308160889, "Rhinorrhoea": 5.519666429598175, "Sinusitis": 2.801534104790178, "Surgery": 4.916651430912984, "Temperature intolerance": 21.084889731617096, "Transient ischaemic attack": 5.38140934991934, "Weight increased": 2.4688031127314165, "Wrong technique in product usage process": 2.434036577458104}