Adverse Events Dashboard
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Problem Statement:
Millions of patients experience adverse events due to medical care, drug usage, procedures, or healthcare settings. These events can result from errors, substandard care, known side effects, or unexpected complications.
Stakeholders Involved:
- Healthcare Providers (Physicians, Nurses, Pharmacists)
- Patients and Caregivers
- Healthcare Administrators and Quality Improvement Teams
- Regulatory Agencies (e.g., FDA, EMA)
- Pharmaceutical Companies, Medical Device Manufacturers
- Legal and Insurance Professionals
Solution:
The Adverse Events Dashboard by OmniData™ is a comprehensive tool designed to track and analyze incidents that result in harm to patients during medical care. These adverse events can include medical errors, complications of treatment, healthcare-associated infections, falls, medication errors, and other adverse outcomes. The dashboard provides detailed documentation and insights into these events, regardless of whether the harm was intended or not.
- Provides a Power BI business dashboard for analyzing adverse events by event type, gender, age, facility, race, etc.
- Offers a comprehensive data model, Azure CICD pipeline, and real-time dashboards.
- Supports business processes to improve adverse event occurrences.
Benefits of Adverse Event Reports:
- Improve patient safety
- Enhance quality of care delivery
- Support regulatory compliance
- Aid in risk management
- Provide legal protection
- Ensure product safety
Attributes Captured in Adverse Event Reports:
- Patient Information (demographics, medical history, medication history)
- Event Details (date, time, description, location)
- Product Information (name, dosage, manufacturer, lot number)
- Healthcare Provider Information (name, specialty, role)
- Clinical Assessment (diagnosis, lab results, clinical findings)
- Severity and Outcome (severity, outcome, interventions)
- Causality Assessment (expectedness, suspected cause, contributing factors)
- Concomitant Medications (other medications, potential interactions)
- Follow-Up Information (actions taken, follow-up visits, resolution status)
- Reporting Source (source, method of reporting)
- Contextual Information (concurrent illnesses, environmental factors)
- Regulatory Information (reporting requirements, regulatory actions)