1 line
1.9 KiB
JSON
1 line
1.9 KiB
JSON
{"Adverse Reaction Reports": 180, "Company": "PFIZER\\BIONTECH", "Deaths": 0, "Disabilities": 0, "Hospitalizations": 1, "Life-Threatening Illnesses": 0, "batchcode": "GD1857", "histogram": {"Abnormal behaviour": 1, "Asthenia": 1, "Back pain": 1, "Blood alkaline phosphatase increased": 1, "Blood creatine phosphokinase": 1, "Blood test": 1, "C-reactive protein normal": 1, "Chills": 2, "Circumstance or information capable of leading to medication error": 1, "Continuous glucose monitoring": 1, "Differential white blood cell count normal": 1, "Discomfort": 1, "Discontinued product administered": 4, "Dizziness": 1, "Electroencephalogram": 1, "Encephalitis autoimmune": 1, "Erythema multiforme": 1, "Expired product administered": 28, "Extra dose administered": 2, "Fatigue": 1, "Full blood count normal": 2, "Gait disturbance": 1, "Gait inability": 1, "Hallucination, auditory": 1, "Hallucination, visual": 1, "Headache": 1, "Hyperaesthesia": 1, "Hypoglycaemia": 1, "Hyporesponsive to stimuli": 1, "Inappropriate schedule of product administration": 2, "Incorrect dose administered": 18, "Incorrect product formulation administered": 78, "Injection site induration": 1, "Injection site swelling": 1, "Laboratory test normal": 1, "Lethargy": 2, "Lumbar puncture": 1, "Magnetic resonance imaging head": 1, "Metabolic function test normal": 1, "Musculoskeletal pain": 1, "No adverse event": 41, "Pain": 2, "Pain in extremity": 2, "Pallor": 2, "Personality change": 1, "Product administered to patient of inappropriate age": 13, "Product administration error": 2, "Product preparation error": 3, "Product preparation issue": 13, "Product storage error": 6, "Pyrexia": 3, "Rash": 1, "Red blood cell sedimentation rate normal": 1, "Respiratory rate increased": 1, "Seizure": 1, "Tearfulness": 1, "Tenderness": 1, "Tremor": 1, "Ultrasound testes": 1, "Underdose": 8, "Unevaluable event": 2, "Urticaria": 1, "Vaccination error": 1, "Vomiting": 1, "Wrong product administered": 9}} |