regenerating tables
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{"batchcode": "007CZ1A", "histogram": {"Fatigue": 5, "Pain": 4, "Pain in extremity": 4, "Injection site pain": 3, "Nausea": 3, "Arthralgia": 2, "Chills": 2, "Dizziness": 2, "Headache": 2, "Injection site pruritus": 2, "Injection site swelling": 2, "Mobility decreased": 2, "Pyrexia": 2, "Urticaria": 2, "Abdominal discomfort": 1, "Abdominal distension": 1, "Breast pain": 1, "Breast swelling": 1, "Breast tenderness": 1, "Burning sensation": 1, "Colitis ulcerative": 1, "Cough": 1, "Demyelination": 1, "Diarrhoea": 1, "Dysmenorrhoea": 1, "Dyspnoea": 1, "Dysstasia": 1, "Gait disturbance": 1, "Groin pain": 1, "Heart rate increased": 1, "Hypoaesthesia": 1, "Impaired healing": 1, "Inappropriate schedule of product administration": 1, "Inflammation": 1, "Injection site erythema": 1, "Injection site inflammation": 1, "Injection site rash": 1, "Injection site warmth": 1, "Intermenstrual bleeding": 1, "Loss of personal independence in daily activities": 1, "Menstruation irregular": 1, "Muscular weakness": 1, "Nasal congestion": 1, "Nerve conduction studies abnormal": 1, "Neuropathy peripheral": 1, "Paraesthesia": 1, "Premenstrual syndrome": 1, "Tinnitus": 1, "Tooth fracture": 1, "Walking aid user": 1}, "Adverse Reaction Reports": 18, "Disabilities": 2, "Deaths": 0, "Life Threatening Illnesses": 0, "Company": "MODERNA"}
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{"batchcode": "007CZ1A", "histogram": {"Fatigue": 5, "Pain": 4, "Pain in extremity": 4, "Injection site pain": 3, "Nausea": 3, "Arthralgia": 2, "Chills": 2, "Dizziness": 2, "Headache": 2, "Injection site pruritus": 2, "Injection site swelling": 2, "Mobility decreased": 2, "Pyrexia": 2, "Urticaria": 2, "Abdominal discomfort": 1, "Abdominal distension": 1, "Breast pain": 1, "Breast swelling": 1, "Breast tenderness": 1, "Burning sensation": 1, "Colitis ulcerative": 1, "Cough": 1, "Demyelination": 1, "Diarrhoea": 1, "Dysmenorrhoea": 1, "Dyspnoea": 1, "Dysstasia": 1, "Gait disturbance": 1, "Groin pain": 1, "Heart rate increased": 1, "Hypoaesthesia": 1, "Impaired healing": 1, "Inappropriate schedule of product administration": 1, "Inflammation": 1, "Injection site erythema": 1, "Injection site inflammation": 1, "Injection site rash": 1, "Injection site warmth": 1, "Intermenstrual bleeding": 1, "Loss of personal independence in daily activities": 1, "Menstruation irregular": 1, "Muscular weakness": 1, "Nasal congestion": 1, "Nerve conduction studies abnormal": 1, "Neuropathy peripheral": 1, "Paraesthesia": 1, "Premenstrual syndrome": 1, "Tinnitus": 1, "Tooth fracture": 1, "Walking aid user": 1}, "Deaths": 0, "Adverse Reaction Reports": 18, "Company": "MODERNA", "Life Threatening Illnesses": 0, "Disabilities": 2}
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