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HowBadIsMyBatch/docs/data/histograms/Global/055F22B.json
2023-06-14 21:55:55 +02:00

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{"batchcode": "055F22B", "histogram": {"COVID-19": 11, "Fatigue": 6, "SARS-CoV-2 test": 6, "SARS-CoV-2 test positive": 6, "Blood pressure measurement": 3, "Cough": 3, "Malaise": 3, "Oropharyngeal pain": 3, "Arthritis": 2, "Dizziness": 2, "Dyspnoea": 2, "Headache": 2, "No adverse event": 2, "Pain in extremity": 2, "Pyrexia": 2, "Retching": 2, "Rhinorrhoea": 2, "Vaccination site pruritus": 2, "Vaccination site swelling": 2, "Vaccine breakthrough infection": 2, "Accidental underdose": 1, "Angiogram": 1, "Anosmia": 1, "Anticoagulant therapy": 1, "Arthralgia": 1, "Asthenia": 1, "Back pain": 1, "Blood pressure increased": 1, "COVID-19 immunisation": 1, "Cardiac imaging procedure normal": 1, "Catheterisation cardiac normal": 1, "Chest X-ray": 1, "Condition aggravated": 1, "Coronavirus test": 1, "Decreased appetite": 1, "Dry mouth": 1, "Dysgeusia": 1, "Ear infection": 1, "Echocardiogram": 1, "Electrocardiogram": 1, "Electrocardiogram normal": 1, "Exposure to SARS-CoV-2": 1, "Gastrooesophageal reflux disease": 1, "HIV test": 1, "Heart rate": 1, "Herpes zoster": 1, "Hypertension": 1, "Incorrect dose administered": 1, "Influenza like illness": 1, "Injection site pain": 1, "Insomnia": 1, "Intercepted product administration error": 1, "Interchange of vaccine products": 1, "Limb discomfort": 1, "Magnetic resonance imaging": 1, "Musculoskeletal pain": 1, "Myalgia": 1, "Myocardial infarction": 1, "Myocardial necrosis marker increased": 1, "Myocarditis": 1, "Nausea": 1, "Needle issue": 1, "Oedema peripheral": 1, "Pain": 1, "Paraesthesia": 1, "Pericarditis": 1, "Rash": 1, "Respiratory tract congestion": 1, "SARS-CoV-2 test negative": 1, "Salivary hypersecretion": 1, "Sluggishness": 1, "Spinal operation": 1, "Spinal pain": 1, "Syncope": 1, "Taste disorder": 1, "Throat irritation": 1, "Tremor": 1, "Troponin": 1, "Vaccination site erythema": 1, "Vaccination site haemorrhage": 1, "Ventricular extrasystoles": 1, "Visual impairment": 1, "Vomiting": 1, "Weight": 1, "Wrong product administered": 1, "X-ray normal": 1}, "Company": "MODERNA", "Adverse Reaction Reports": 28, "Disabilities": 0, "Life Threatening Illnesses": 0, "Deaths": 0}