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{"Adverse Reaction Reports": 5, "Company": "JANSSEN", "Deaths": 0, "Disabilities": 0, "Hospitalizations": 1, "Life-Threatening Illnesses": 0, "batchcode": "207H21A", "histogram": {"Abdominal pain upper": 1, "Asthenia": 1, "Biopsy": 1, "Blood pressure decreased": 1, "Blood pressure measurement": 1, "Body temperature": 2, "COVID-19 immunisation": 2, "Chills": 1, "Electrocardiogram": 1, "Feeling abnormal": 1, "Gait disturbance": 1, "Headache": 2, "Heart rate irregular": 1, "Herpes virus test": 1, "Inappropriate schedule of product administration": 1, "Magnetic resonance imaging": 1, "Malaise": 1, "Muscle spasms": 1, "Myocardial ischaemia": 1, "Nausea": 3, "Neoplasm": 1, "Off label use": 3, "Pain": 1, "Pain in extremity": 1, "Paralysis": 1, "Product administered to patient of inappropriate age": 1, "Pyrexia": 4, "Renal failure": 1, "Syncope": 2, "Treponema test": 1, "Vaccination site pain": 1, "Vertigo": 1, "Vomiting": 2, "Vulvovaginal injury": 1, "X-ray": 1}}