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{"Adverse Reaction Reports": 7, "Company": "PFIZER\\BIONTECH", "Deaths": 0, "Disabilities": 1, "Hospitalizations": 1, "Life-Threatening Illnesses": 1, "batchcode": "FE 3064", "histogram": {"Abscess": 1, "Adnexa uteri pain": 1, "Anaphylactic reaction": 1, "Angioedema": 1, "Arthralgia": 1, "Back pain": 1, "Blood pressure measurement": 1, "Blood pressure systolic increased": 1, "Body temperature": 1, "Chest discomfort": 1, "Computerised tomogram thorax": 1, "Confusional state": 1, "Dizziness": 1, "Dyshidrotic eczema": 1, "Dysmenorrhoea": 1, "Dyspnoea": 1, "Electrocardiogram": 1, "Empyema": 1, "Exercise tolerance decreased": 1, "Fatigue": 3, "Feeling hot": 1, "Fibrin D dimer": 1, "Full blood count": 1, "Gait disturbance": 1, "Haematemesis": 1, "Headache": 1, "Heart rate": 1, "Heart rate increased": 1, "Heavy menstrual bleeding": 1, "Hyperhidrosis": 1, "Influenza": 1, "Insomnia": 1, "Menstruation delayed": 1, "Neck pain": 1, "Oxygen saturation": 1, "Oxygen saturation decreased": 1, "Pain": 1, "Paraesthesia": 1, "Platelet count": 1, "Product administered to patient of inappropriate age": 1, "Pruritus": 1, "Pulmonary embolism": 1, "Rash": 2, "Syncope": 1, "Tremor": 1, "Ultrasound Doppler": 1, "Urinary incontinence": 1, "Uterine pain": 1}}