{"url_path":"/fda/adverse-events/26940259","section_key":"summary","section_title":"FAERS report 26940259: Bradycardia, Product administration issue, Wrong patient received product","topic":"fda","document":{"doc_type":"adverse-event","doc_date":"2026-06-30","source_url":"https://api.fda.gov/drug/event.json?search=safetyreportid:%2226940259%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"LAMICTAL"},"word_count":94,"has_tables":false,"body_markdown":null}