1 line
3.2 KiB
JSON
1 line
3.2 KiB
JSON
{"Adverse Reaction Reports": 313, "Company": "PFIZER\\BIONTECH", "Deaths": 1, "Disabilities": 0, "Hospitalizations": 3, "Life-Threatening Illnesses": 0, "batchcode": "FP7136", "histogram": {"Acute polyneuropathy": 1, "Acute respiratory failure": 2, "Agitation": 1, "Alopecia": 1, "Angiogram pulmonary abnormal": 1, "Anxiety": 1, "Axillary pain": 1, "Blood glucose normal": 1, "Blood lactic acid": 1, "Blood pressure abnormal": 1, "Blood pressure decreased": 1, "Blood test": 1, "Body temperature": 2, "Bradycardia": 1, "Bronchoalveolar lavage normal": 1, "Bronchoscopy": 1, "COVID-19 immunisation": 1, "COVID-19 pneumonia": 1, "Chest X-ray": 1, "Chest discomfort": 1, "Chills": 1, "Circumstance or information capable of leading to medication error": 3, "Computerised tomogram": 3, "Computerised tomogram abdomen": 1, "Computerised tomogram thorax": 1, "Condition aggravated": 1, "Culture": 1, "Death": 1, "Dehydration": 1, "Demyelinating polyneuropathy": 1, "Depression": 1, "Diarrhoea": 1, "Discontinued product administered": 50, "Dizziness": 4, "Drug screen": 1, "Dysphagia": 2, "Dyspnoea": 4, "Electrocardiogram": 3, "Electrocardiogram abnormal": 1, "Epistaxis": 1, "Expired product administered": 14, "Exposure during pregnancy": 1, "Extra dose administered": 5, "Fall": 1, "Fatigue": 2, "Feeling abnormal": 1, "Feeling hot": 1, "Fibrin D dimer": 1, "Full blood count": 1, "Gait disturbance": 1, "Headache": 4, "Heart rate increased": 1, "Human chorionic gonadotropin": 1, "Hyperhidrosis": 3, "Hypotonic-hyporesponsive episode": 1, "Hypoxia": 1, "Immediate post-injection reaction": 1, "Inappropriate schedule of product administration": 3, "Incorrect dose administered": 8, "Incorrect product formulation administered": 165, "Inflammation": 1, "Influenza A virus test": 1, "Influenza B virus test": 1, "Injection site pain": 3, "Injection site pruritus": 1, "Injection site swelling": 1, "Injection site warmth": 1, "Interchange of vaccine products": 2, "Laboratory test": 2, "Lethargy": 1, "Leukocytosis": 1, "Lipase": 1, "Loss of consciousness": 4, "Lung infiltration": 1, "Lung opacity": 1, "Lymphadenopathy": 1, "Malaise": 1, "Metabolic function test": 1, "Migraine": 2, "Muscle spasms": 2, "Myalgia": 1, "Mycobacterium test negative": 1, "Nausea": 4, "Neurogenic bladder": 1, "No adverse event": 69, "Orthostatic hypotension": 1, "Pain": 1, "Pain in extremity": 2, "Pallor": 2, "Palpitations": 3, "Pharyngeal hypoaesthesia": 1, "Pharyngeal swelling": 2, "Product administered to patient of inappropriate age": 2, "Product administration error": 3, "Product label issue": 2, "Product preparation error": 1, "Product storage error": 7, "Product use issue": 1, "Productive cough": 1, "Pruritus": 6, "Pyrexia": 4, "Rash": 4, "Respiration abnormal": 1, "Respiratory syncytial virus test": 1, "SARS-CoV-2 test": 2, "SARS-CoV-2 test positive": 1, "Scan with contrast": 1, "Seizure": 2, "Seizure like phenomena": 1, "Sputum culture": 1, "Syncope": 4, "Tachycardia": 1, "Tremor": 1, "Trendelenburg position": 1, "Troponin I": 1, "Unevaluable event": 18, "Unresponsive to stimuli": 1, "Urine analysis": 1, "Urticaria": 2, "Vaccination error": 4, "Vaccination site pain": 1, "Vaccination site swelling": 1, "Vomiting": 2, "White blood cell count increased": 1, "Wrong product administered": 13}} |