Skill UI

Provides programmatic access to DrugBank drug and target data, covering downloads, queries, interaction networks, targets/pathways, and chemical similarity analyses for pharmacology research and safety reviews.

Provides Python access to openFDA endpoints for drugs, devices, foods, veterinary products, and substances, enabling regulatory analysis, safety monitoring, recalls tracking, and pharmacovigilance research.

Provides GraphQL queries to the Open Targets Platform for target-disease associations, tractability, safety, drugs, and multi-omics evidence to guide therapeutic target identification, safety assessment, and repurposing research workflows.

This library provides comprehensive patterns for building robust Clinical Decision Support Systems (CDSS) integrated into Electronic Medical Records (EMR). It ensures patient safety by implementing critical checks such as drug interaction screening, weight/age/renal-adjusted dose validation, and standardized clinical scoring (e.g., NEWS2). The engine uses pure functions, guaranteeing high testability and reliability for critical medical insights.

A comprehensive guide detailing architectural patterns for developing robust Electronic Medical Record (EMR) and Electronic Health Record (EHR) systems. Covers critical areas like patient safety protocols, structured clinical workflows, drug interaction checking, audit trail implementation, and WCAG accessibility standards. Essential for building highly reliable and compliant healthcare IT solutions.

This library provides comprehensive patterns for building robust Clinical Decision Support Systems (CDSS) integrated into Electronic Medical Records (EMR). It ensures patient safety by implementing critical checks such as drug interaction screening, weight/age/renal-adjusted dose validation, and standardized clinical scoring (e.g., NEWS2). The engine uses pure functions, guaranteeing high testability and reliability for critical medical insights.

A comprehensive guide detailing architectural patterns for developing robust Electronic Medical Record (EMR) and Electronic Health Record (EHR) systems. Covers critical areas like patient safety protocols, structured clinical workflows, drug interaction checking, audit trail implementation, and WCAG accessibility standards. Essential for building highly reliable and compliant healthcare IT solutions.

This skill computes disproportionality metrics (PRR, ROR, EBGM, IC) using FAERS/OpenFDA drug-event data. It analyzes spontaneous reports to statistically screen for potential drug-reaction associations (Signal of Disproportionate Reporting, SDR). By constructing a 2x2 contingency table, it helps pharmacovigilance professionals identify over-reported adverse events, providing a statistical hypothesis for drug safety assessment.

This skill connects extracted drug entities with authoritative regulatory facts from the public OpenFDA API. It retrieves Structured Product Labeling (SPL) data, NDC package codes, approved indications, boxed warnings, and current recall/enforcement status. It is essential for enriching drug profiles, providing regulatory context, and supporting unexpectedness checks. Note: This skill provides information, not clinical decision support.

This skill structures free-text adverse event narratives into the mandatory ICH E2B(R3) format. It populates critical fields required for regulatory submissions (like FAERS/EudraVigilance), including suspect drugs, reactions (mapped via MedDRA), seriousness criteria, and reaction outcomes. Use it when generating Individual Case Safety Reports (ICSRs) from clinical narratives.