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{"Adverse Reaction Reports": 70, "Company": "PFIZER\\BIONTECH", "Deaths": 1, "Disabilities": 1, "Hospitalizations": 1, "Life-Threatening Illnesses": 1, "batchcode": "FL007", "histogram": {"Abdominal pain upper": 1, "Activated partial thromboplastin time prolonged": 1, "Anaphylactic reaction": 1, "Anxiety": 1, "Arthralgia": 1, "Arthritis": 1, "Autopsy": 1, "Blood immunoglobulin A increased": 1, "Blood pressure increased": 1, "Blood test": 2, "Breast pain": 1, "C-reactive protein increased": 1, "COVID-19": 2, "Cardio-respiratory arrest": 1, "Chest X-ray": 1, "Chest discomfort": 1, "Chest pain": 2, "Coagulation test abnormal": 1, "Coagulopathy": 1, "Complement factor C3 increased": 1, "Complement factor C4 increased": 1, "Condition aggravated": 3, "Conjunctivitis": 1, "Cough": 3, "Cyanosis": 2, "Death": 1, "Decreased activity": 1, "Diarrhoea": 1, "Dizziness": 4, "Dyspnoea": 2, "Echocardiogram": 1, "Electrocardiogram": 1, "Epistaxis": 1, "Expired product administered": 13, "Exposure to SARS-CoV-2": 1, "Extra dose administered": 1, "Eye movement disorder": 1, "Fall": 4, "Fatigue": 1, "Feeling abnormal": 2, "Feeling hot": 1, "Fibrin D dimer": 2, "Gastrointestinal disorder": 1, "Gastrointestinal haemorrhage": 1, "General physical health deterioration": 1, "Haematochezia": 1, "Head injury": 4, "Headache": 5, "Heart rate increased": 2, "Hypergammaglobulinaemia": 1, "Hyperglycaemia": 1, "Hypersensitivity": 1, "Illness": 1, "Immediate post-injection reaction": 1, "Inappropriate schedule of product administration": 2, "Incorrect dose administered": 6, "Incorrect product formulation administered": 3, "Incorrect route of product administration": 1, "Injection site pain": 2, "Intensive care": 2, "Interleukin level increased": 1, "Interleukin-2 receptor increased": 1, "International normalised ratio increased": 1, "Investigation": 1, "Joint swelling": 1, "Juvenile idiopathic arthritis": 1, "Laboratory test": 1, "Laboratory test abnormal": 1, "Lethargy": 1, "Lip swelling": 1, "Loss of consciousness": 2, "Magnetic resonance imaging abnormal": 1, "Malaise": 1, "Multisystem inflammatory syndrome in children": 1, "Muscular weakness": 1, "Musculoskeletal disorder": 1, "Musculoskeletal stiffness": 1, "Nausea": 3, "Nervousness": 1, "No adverse event": 9, "Oropharyngeal pain": 4, "Packed red blood cell transfusion": 1, "Pain in extremity": 1, "Painful respiration": 1, "Pharyngeal swelling": 1, "Platelet count increased": 1, "Product preparation error": 2, "Product preparation issue": 8, "Product storage error": 3, "Prothrombin time prolonged": 1, "Pruritus": 1, "Pulse absent": 1, "Pyrexia": 1, "Rash": 3, "Rash pruritic": 2, "Red blood cell sedimentation rate increased": 1, "Respiratory tract congestion": 3, "Rhinorrhoea": 1, "SARS-CoV-2 test": 1, "SARS-CoV-2 test negative": 2, "SARS-CoV-2 test positive": 1, "Shock haemorrhagic": 1, "Skin warm": 1, "Spinal cord infarction": 1, "Streptococcus test negative": 1, "Syncope": 3, "Throat tightness": 1, "Type 1 diabetes mellitus": 1, "Underdose": 7, "Unevaluable event": 2, "Unresponsive to stimuli": 3, "Urticaria": 1, "Vomiting": 2}}