{"database": "openregs", "table": "documents", "rows": [["FDA-2018-N-4131-0001", "FDA", "FDA-2018-N-4131", "Agency Information Collection Activities; Proposed Collection; Comment Request; Food and Drug Administration Adverse Event Reports;\nElectronic Submissions", "Notice", "60 Day Proposed Information Collection", "2018-11-30T05:00:00Z", 2018, 11, "2018-11-30T05:00:00Z", "2019-01-30T04:59:59Z", "2019-01-30T02:09:21Z", "2018-26031", 0, 0, "0900006483915990"]], "columns": ["id", "agency_id", "docket_id", "title", "document_type", "subtype", "posted_date", "posted_year", "posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2018-N-4131-0001"], "units": {}, "query_ms": 36.854784935712814, "source": "Federal Register API & Regulations.gov API", "source_url": "https://www.federalregister.gov/developers/api/v1", "license": "Public Domain (U.S. Government data)", "license_url": "https://www.regulations.gov/faq"}