updating VAERS data
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{"batchcode": "006F21A", "histogram": {"Expired product administered": 2, "Pain in extremity": 2, "Pruritus": 2, "Anxiety": 1, "Chills": 1, "Condition aggravated": 1, "Dizziness": 1, "Erythema": 1, "Extra dose administered": 1, "Flushing": 1, "Hyperhidrosis": 1, "Inappropriate schedule of product administration": 1, "Injection site reaction": 1, "Mobility decreased": 1, "Musculoskeletal stiffness": 1, "No adverse event": 1, "Pallor": 1, "Palpitations": 1, "Presyncope": 1, "Product storage error": 1, "Rheumatoid arthritis": 1, "Skin irritation": 1, "Tachypnoea": 1}, "Life Threatening Illnesses": 0, "Company": "MODERNA", "Adverse Reaction Reports": 7, "Disabilities": 0, "Deaths": 0}
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{"batchcode": "006F21A", "histogram": {"Expired product administered": 2, "Pain in extremity": 2, "Pruritus": 2, "Anxiety": 1, "Chills": 1, "Condition aggravated": 1, "Dizziness": 1, "Erythema": 1, "Extra dose administered": 1, "Flushing": 1, "Hyperhidrosis": 1, "Inappropriate schedule of product administration": 1, "Injection site reaction": 1, "Mobility decreased": 1, "Musculoskeletal stiffness": 1, "No adverse event": 1, "Pallor": 1, "Palpitations": 1, "Presyncope": 1, "Product storage error": 1, "Rheumatoid arthritis": 1, "Skin irritation": 1, "Tachypnoea": 1}, "Life Threatening Illnesses": 0, "Disabilities": 0, "Company": "MODERNA", "Adverse Reaction Reports": 7, "Deaths": 0}
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