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1.2 KiB
JSON
1 line
1.2 KiB
JSON
{"Adverse Reaction Reports": 235, "Company": "PFIZER\\BIONTECH", "Deaths": 0, "Disabilities": 0, "Hospitalizations": 0, "Life-Threatening Illnesses": 0, "batchcode": "HE2391", "histogram": {"Blood glucose normal": 1, "Circumstance or information capable of leading to medication error": 1, "Decreased appetite": 1, "Dizziness": 3, "Dysgeusia": 1, "Dyspnoea": 1, "Erythema": 1, "Expired product administered": 89, "Extra dose administered": 3, "Fall": 1, "Fatigue": 1, "Foaming at mouth": 1, "Head injury": 2, "Headache": 1, "Hyperhidrosis": 2, "Hypotonia": 1, "Incorrect dose administered": 17, "Lethargy": 1, "Loss of consciousness": 3, "Lymphadenopathy": 1, "Malaise": 1, "Muscle twitching": 1, "Nausea": 1, "No adverse event": 71, "Overdose": 1, "Pain": 1, "Pallor": 2, "Product administered to patient of inappropriate age": 45, "Product administration error": 2, "Product expiration date issue": 1, "Product storage error": 9, "Pruritus": 1, "Pyrexia": 1, "Refusal of vaccination": 1, "Seizure": 1, "Swelling": 2, "Syncope": 6, "Tearfulness": 1, "Tremor": 1, "Underdose": 52, "Unevaluable event": 3, "Urine analysis normal": 1, "Urticaria": 2, "Vomiting": 1, "Wrong patient received product": 1, "Wrong product administered": 15}} |