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HowBadIsMyBatch/docs/SymptomsCausedByVaccines/data/ProportionalReportingRatios/vaccines/PNC15.json
2023-11-25 10:28:44 +01:00

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{"Accident at work": 661.2263347100867, "Accidental exposure to product": 5.693055130091035, "Angiogram pulmonary": 16.48210969493693, "Anosmia": 2.271664661341588, "Blood glucose fluctuation": 14.672975864855088, "Brain scan abnormal": 33.424457737841784, "CSF culture": 16.042554594452735, "CSF glucose normal": 9.207803387985738, "CSF lymphocyte count increased": 30.85303023868458, "CSF protein increased": 3.487301671670216, "CSF test abnormal": 3.228401186017347, "CSF white blood cell count increased": 10.616127367560066, "Cerebral arteriovenous malformation haemorrhagic": 715.7511713593096, "Circumstance or information capable of leading to medication error": 4.005956301561028, "Crying": 9.403824524064468, "Device leakage": 34.379570608286905, "Endotracheal intubation": 5.080897558356923, "Eosinophil count abnormal": 240.64499930680296, "Eye inflammation": 6.015671181369658, "Gram stain negative": 28.878204778133824, "Herpes simplex test negative": 10.678947888314044, "Imaging procedure artifact": 190.01683797735367, "Injection site rash": 2.0256657290106643, "Injection site warmth": 2.3197758185030226, "Injury associated with device": 116.55005226127972, "Intracranial aneurysm": 16.407185413657903, "Laboratory test normal": 2.361554749296276, "Life support": 18.230356378872404, "Limb injury": 2.7117529017763053, "Localised infection": 9.278817901145391, "Magnetic resonance imaging spinal abnormal": 7.663337355624213, "Meningitis aseptic": 10.647444967788903, "Middle ear effusion": 12.071933875804836, "Muscle strength abnormal": 27.555388694227524, "Needle issue": 95.2050973919912, "No adverse event": 6.114872173197689, "Occupational exposure to product": 20.165595989269487, "Poor quality device used": 3304.6168582710998, "Product administration error": 6.074279740399545, "Product label confusion": 30.85303023868458, "Product quality issue": 5.013034408802501, "Product storage error": 5.589620962336209, "Product use complaint": 257.811460026471, "Recalled product administered": 15.831453060627496, "Red blood cell sedimentation rate normal": 2.105794648055095, "Reversed hot-cold sensation": 171.92624067305954, "Scratch": 5.544384478023565, "Skin laceration": 34.185213725598764, "Spinal disorder": 19.83316687896092, "Spondylolisthesis": 82.05383843379558, "Syringe issue": 262.4003935975557, "Thecal sac compression": 888.0865757061689, "Vaccination site erythema": 2.1271675970195365, "Vaccination site urticaria": 6.586519819035233, "Vertebral foraminal stenosis": 54.69867133197926, "Wound": 36.92936034300444, "Wrong product administered": 7.13157826450229, "Wrong technique in product usage process": 2.538213742910817, "X-ray of pelvis and hip": 14.915521093486092}