updating VAERS data
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{"batchcode": "FX5095", "histogram": {"Incorrect product formulation administered": 31, "No adverse event": 29, "Incorrect dose administered": 9, "Expired product administered": 8, "Product preparation issue": 8, "Discontinued product administered": 7, "Underdose": 7, "Pyrexia": 5, "Rash": 4, "Vomiting": 4, "Cough": 3, "Interchange of vaccine products": 3, "Product administration error": 3, "Unevaluable event": 3, "Wrong product administered": 3, "Chills": 2, "Decreased appetite": 2, "Dyspnoea": 2, "Inappropriate schedule of product administration": 2, "Influenza virus test negative": 2, "Insomnia": 2, "Irritability": 2, "Lethargy": 2, "Pain": 2, "Pharyngeal erythema": 2, "Product administered to patient of inappropriate age": 2, "Respiratory tract congestion": 2, "SARS-CoV-2 test negative": 2, "Streptococcus test negative": 2, "Abdominal pain": 1, "Alopecia": 1, "Anxiety": 1, "Blister": 1, "Blood glucose": 1, "Body temperature": 1, "Body temperature increased": 1, "COVID-19 screening": 1, "Chest X-ray normal": 1, "Circumstance or information capable of leading to medication error": 1, "Diarrhoea": 1, "Ear infection": 1, "Erythema": 1, "Extra dose administered": 1, "Feeling hot": 1, "Hypersensitivity": 1, "Hypoxia": 1, "Influenza A virus test": 1, "Influenza B virus test": 1, "Injection site haemorrhage": 1, "Injury associated with device": 1, "Nasopharyngitis": 1, "Obesity": 1, "Poor quality product administered": 1, "Product preparation error": 1, "Product storage error": 1, "Product use issue": 1, "Pruritus": 1, "Rash erythematous": 1, "Rash papular": 1, "Rash pruritic": 1, "Rhinorrhoea": 1, "Secretion discharge": 1, "Streptococcus test": 1, "Urticaria": 1, "Vaccination error": 1}, "Life Threatening Illnesses": 1, "Deaths": 0, "Company": "PFIZER\\BIONTECH", "Adverse Reaction Reports": 107, "Disabilities": 0}
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{"batchcode": "FX5095", "histogram": {"Incorrect product formulation administered": 31, "No adverse event": 29, "Incorrect dose administered": 9, "Expired product administered": 8, "Product preparation issue": 8, "Discontinued product administered": 7, "Underdose": 7, "Pyrexia": 5, "Rash": 4, "Vomiting": 4, "Cough": 3, "Interchange of vaccine products": 3, "Product administration error": 3, "Unevaluable event": 3, "Wrong product administered": 3, "Chills": 2, "Decreased appetite": 2, "Dyspnoea": 2, "Inappropriate schedule of product administration": 2, "Influenza virus test negative": 2, "Insomnia": 2, "Irritability": 2, "Lethargy": 2, "Pain": 2, "Pharyngeal erythema": 2, "Product administered to patient of inappropriate age": 2, "Respiratory tract congestion": 2, "SARS-CoV-2 test negative": 2, "Streptococcus test negative": 2, "Abdominal pain": 1, "Alopecia": 1, "Anxiety": 1, "Blister": 1, "Blood glucose": 1, "Body temperature": 1, "Body temperature increased": 1, "COVID-19 screening": 1, "Chest X-ray normal": 1, "Circumstance or information capable of leading to medication error": 1, "Diarrhoea": 1, "Ear infection": 1, "Erythema": 1, "Extra dose administered": 1, "Feeling hot": 1, "Hypersensitivity": 1, "Hypoxia": 1, "Influenza A virus test": 1, "Influenza B virus test": 1, "Injection site haemorrhage": 1, "Injury associated with device": 1, "Nasopharyngitis": 1, "Obesity": 1, "Poor quality product administered": 1, "Product preparation error": 1, "Product storage error": 1, "Product use issue": 1, "Pruritus": 1, "Rash erythematous": 1, "Rash papular": 1, "Rash pruritic": 1, "Rhinorrhoea": 1, "Secretion discharge": 1, "Streptococcus test": 1, "Urticaria": 1, "Vaccination error": 1}, "Disabilities": 0, "Company": "PFIZER\\BIONTECH", "Deaths": 0, "Adverse Reaction Reports": 107, "Life Threatening Illnesses": 1}
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