Scroll down to read the hi-lighted section. Normally every patient receives a VAERS ID in the database. In this case 726 deaths were reported and received a single VAERS ID.
The CDC gives itself 4 to 6 weeks to review each adverse event report it receives prior to deciding whether or not to publish it to VAERS. 'Company representative' is likely pharma agent. The pharma companies receive reports of adverse events directly from consumers.
