Learning Objectives
1. Summarize a systematic approach to the identification, investigation, and assessment of medication events including methods for managing a successful institutional event reporting program.
2. Explain the relationship between adverse drug events (ADEs), adverse drug reactions (ADRs), and medication errors.
3. Contrast examples of skill-based, rule-based, and knowledge-based errors.
4. Evaluate algorithms and tools available to assist in system-based investigations, assessment, and outcome classification of medication events.
5. Explain major steps and components of a root cause analysis (RCA) process.
Identify regulatory expectations for event management to protect patients, improve systems, and prevent harm.
6. Compare alternative methodologies available for conducting cause analyses.
- Provider:American Society of Health-System Pharmacists
- Activity Link: https://elearning.ashp.org/
- Start Date: 2022-08-24 05:00:00
- End Date: 2022-08-24 05:00:00
- Credit Details: AMA PRA Category 1 Credit™️: 2.0 hours
- Commercial Support: No
- Activity Type: Enduring Material
- CME Finder Type: Online Learning
- Fee to Participate: Yes
- Measured Outcome: Learner Competence, Learner Knowledge
- Provider Ship: Jointly Provided
- Registration: Open to all