Interventional Improvement in Hospital Based Intensive Monitoring of Adverse Event

In India Intensive Event Monitoring (IEM) programme has been used for the adverse event monitoring where the pharmacovigilance officer used to collect the adverse event from the various department of the hospital. The system has many lacunas for reporting the adverse event as fear of personal and organizational liability, labor-intensive, complex, and time-consuming reporting processes, minimal feedback provided to reporters, no incentives, rewards, or motivation to report. There is no study till date which focused on the improving the IEM of the ADRs. The present study was planned to rule out the underreporting causes in the intensive event monitoring and interventional improvement in the same.