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3.1 KiB
JSON
1 line
3.1 KiB
JSON
{"Adverse Reaction Reports": 135, "Company": "PFIZER\\BIONTECH", "Deaths": 2, "Disabilities": 0, "Hospitalizations": 1, "Life-Threatening Illnesses": 1, "batchcode": "HF9300", "histogram": {"Abdominal pain": 1, "Agitation": 1, "Amnesia": 1, "Arthralgia": 2, "Atrial fibrillation": 1, "Blister": 2, "Blood cholesterol": 1, "Blood cholesterol increased": 1, "Blood creatinine increased": 1, "Blood fibrinogen increased": 1, "Blood lactate dehydrogenase increased": 1, "Blood lactic acid": 1, "Blood pressure increased": 1, "Blood test": 1, "Blood triglycerides": 1, "Blood triglycerides increased": 1, "Burning sensation": 1, "C-reactive protein": 1, "C-reactive protein increased": 1, "COVID-19": 11, "Carbon dioxide decreased": 1, "Cardioversion": 1, "Cellulitis": 1, "Chest X-ray": 1, "Chest pain": 1, "Chills": 2, "Colitis": 1, "Computerised tomogram head": 1, "Condition aggravated": 1, "Confusional state": 2, "Death": 1, "Delirium": 1, "Dizziness": 4, "Drug ineffective": 2, "Dyspnoea": 1, "Dysstasia": 1, "Erythema": 1, "Expired product administered": 68, "Extra dose administered": 3, "Face injury": 1, "Facial pain": 1, "Fall": 3, "Fatigue": 1, "Feeling abnormal": 1, "Feeling cold": 2, "Feeling hot": 1, "Fibrin D dimer": 1, "General physical health deterioration": 1, "Haemolysis": 1, "Haemolytic uraemic syndrome": 1, "Haemorrhage": 1, "Headache": 2, "Heart rate increased": 1, "Hyperaesthesia": 1, "Hyperhidrosis": 1, "Hyporesponsive to stimuli": 1, "Hypotension": 1, "Immediate post-injection reaction": 2, "Incorrect dose administered": 1, "Infection": 1, "Injection site erythema": 4, "Injection site induration": 2, "Injection site nodule": 1, "Injection site pain": 4, "Injection site rash": 1, "Injection site swelling": 1, "Injection site warmth": 2, "Insomnia": 1, "Laboratory test": 1, "Laboratory test abnormal": 1, "Lacrimation increased": 1, "Lip injury": 1, "Loss of consciousness": 2, "Lymphadenopathy": 3, "Magnetic resonance imaging": 1, "Malaise": 2, "Metabolic function test": 1, "Muscle tightness": 1, "Muscular weakness": 1, "Musculoskeletal disorder": 1, "Musculoskeletal stiffness": 2, "Myalgia": 2, "Nausea": 1, "Neck pain": 1, "Nervous system disorder": 1, "Neuralgic amyotrophy": 1, "No adverse event": 62, "Ocular discomfort": 1, "Ocular hyperaemia": 1, "Oxygen saturation decreased": 1, "Pain": 4, "Pain in extremity": 6, "Pain in jaw": 1, "Pallor": 1, "Papule": 1, "Peripheral coldness": 1, "Peripheral swelling": 1, "Poor quality product administered": 3, "Presyncope": 2, "Product administered to patient of inappropriate age": 5, "Product administration error": 3, "Product label confusion": 1, "Pruritus": 1, "Psoriasis": 2, "Pyrexia": 2, "Rash": 2, "Rash erythematous": 1, "Rash pruritic": 1, "Rectal haemorrhage": 1, "Renal failure": 1, "Respiratory tract congestion": 1, "Rhinorrhoea": 1, "SARS-CoV-2 test": 4, "Sensation of foreign body": 1, "Sepsis": 1, "Shock": 1, "Skin discolouration": 1, "Skin laceration": 1, "Syncope": 2, "Thrombotic thrombocytopenic purpura": 1, "Tinnitus": 1, "Unevaluable event": 1, "Vaccination failure": 9, "Vaccination site erythema": 1, "Vaccination site macule": 1, "Vaccination site pain": 1, "White blood cell count increased": 1}} |