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{"Adverse Reaction Reports": 8, "Company": "PFIZER\\BIONTECH", "Deaths": 0, "Disabilities": 2, "Hospitalizations": 1, "Life-Threatening Illnesses": 0, "batchcode": "FE 8235", "histogram": {"Asthenia": 1, "Audiogram": 1, "COVID-19": 2, "Chest discomfort": 1, "Cough": 1, "Diarrhoea": 1, "Drug ineffective": 1, "Dyspnoea": 1, "Electronystagmogram": 1, "Epistaxis": 1, "Fatigue": 2, "Headache": 1, "Heart rate irregular": 1, "Hypoaesthesia": 1, "Increased upper airway secretion": 1, "Investigation": 1, "Limb discomfort": 1, "Lung disorder": 1, "Lymphadenopathy": 1, "Meniere's disease": 1, "Muscle spasms": 1, "Muscle strain": 1, "Myalgia": 2, "Nausea": 1, "Pain in extremity": 2, "Palpitations": 1, "Paraesthesia": 1, "Product administered at inappropriate site": 1, "Pyrexia": 1, "SARS-CoV-2 test": 1, "Sensory loss": 1, "Sinusitis": 1, "Specialist consultation": 1, "Stridor": 1, "Tachypnoea": 1, "Vaccination failure": 1}}