updating data for batch codes

docs/SymptomsCausedByDrugs/data/ProportionalReportingRatios/vaccines/72.json

@@ -1 +1 @@
-{"anti-insulin antibody positive": 72.08, "blindness": 2.26, "blindness unilateral": 3.22, "blood glucose abnormal": 36.23, "blood glucose decreased": 25.77, "blood glucose fluctuation": 43.34, "blood glucose increased": 28.84, "cataract": 4.52, "circumstance or information capable of leading to medication error": 5.26, "cold sweat": 4.1, "device breakage": 4.18, "device defective": 14.28, "device delivery system issue": 11.09, "device issue": 36.78, "device leakage": 10.84, "device malfunction": 4.2, "device operational issue": 230.69, "device use issue": 10.84, "diabetes mellitus inadequate control": 47.07, "diabetic coma": 14.3, "diabetic ketoacidosis": 12.06, "diabetic metabolic decompensation": 34.63, "diabetic retinopathy": 15.43, "disability": 4.25, "drug ineffective": 3.15, "expired product administered": 13.74, "exposure during pregcy": 3.74, "exposure via breast milk": 3.85, "extra dose administered": 8.06, "eye haemorrhage": 2.0, "foot fracture": 2.76, "glycosylated haemoglobin increased": 18.35, "hospitalisation": 2.58, "hunger": 6.52, "hyperglycaemia": 55.92, "hyperinsulinaemic hypoglycaemia": 75.19, "hypoglycaemia": 47.31, "hypoglycaemic coma": 26.25, "hypoglycaemic seizure": 30.54, "hypoglycaemic unconsciousness": 33.68, "incorrect dose administered": 4.58, "incorrect dose administered by device": 24.84, "injection site bruising": 7.28, "injection site discolouration": 7.63, "injection site haemorrhage": 8.31, "injection site hypersensitivity": 7.49, "intentional product misuse": 2.93, "ketoacidosis": 16.66, "lipodystrophy acquired": 23.73, "liquid product physical issue": 9.34, "localised infection": 2.89, "loss of consciousness": 3.26, "medication error": 5.95, "multiple use of single-use product": 96.79, "nervousness": 3.49, "premature baby": 2.38, "product administration error": 4.8, "product complaint": 7.23, "product quality issue": 8.88, "product storage error": 26.23, "product use issue": 4.02, "renal disorder": 2.47, "sopor": 14.27, "therapeutic product effect delayed": 9.85, "therapeutic response decreased": 3.27, "thirst": 2.84, "visual impairment": 4.04, "weight increased": 2.66, "wrong product administered": 58.14, "wrong technique in device usage process": 7.48, "wrong technique in product usage process": 2.36}
+{"abdominal discomfort": 2.91, "adjustment disorder with depressed mood": 228.06, "adverse drug reaction": 19.27, "alopecia": 3.9, "amnesia": 8.86, "anti-cyclic citrullinated peptide antibody positive": 115.8, "arthropathy": 17.94, "blepharospasm": 45.58, "blood cholesterol increased": 26.19, "c-reactive protein abnormal": 43.74, "c-reactive protein increased": 12.54, "condition aggravated": 2.38, "contraindicated product administered": 26.75, "delirium": 13.73, "discomfort": 7.71, "dislocation of vertebra": 535.0, "drug hypersensitivity": 17.35, "drug ineffective": 3.21, "drug intolerance": 8.71, "duodenal ulcer perforation": 65.3, "epilepsy": 6.87, "gait disturbance": 3.16, "general physical health deterioration": 4.23, "grip strength decreased": 75.08, "hand deformity": 35.92, "hepatic enzyme increased": 6.64, "hypersensitivity": 3.18, "inflammation": 5.49, "infusion related reaction": 14.66, "injury": 12.44, "joint swelling": 5.04, "mobility decreased": 8.13, "musculoskeletal stiffness": 7.86, "product use in unapproved indication": 2.36, "psoriasis": 4.73, "psoriatic arthropathy": 32.43, "rheumatic fever": 381.19, "rheumatoid arthritis": 8.01, "rheumatoid factor positive": 119.43, "sleep disorder": 3.08, "therapeutic product effect decreased": 14.28, "treatment failure": 6.19}