Cerner’s drug safety solutions and services enable coding of drug and adverse event terminology into preferred terms so safety data can be standardized to enable aggregation and analysis.

We also provide the ability for drug safety experts to analyze and explore Freedom of Information (FOI) data released from the FDA’s Adverse Event Reporting System (AERS) safety databases.

Our solutions allow you to:

• Code verbatim terms for medications and adverse events into standard terms
• Provide secure interchange of drug safety information between sponsor partners and regulators
• Explore the AERS drug safety database for identification of potential safety signals

Key Benefits

• Automated coding with workflow engine, intelligent searching and high-performance auto-encoding
• Multiple dictionaries and versions
• Analysis of post-marketing drug safety data submitted to the FDA by clinicians and patients