CILE consolidates fragmented drug safety data across the FDA, Beers Criteria, and pharmacogenomic resources — normalized via RxNorm and returned as machine-readable HL7 FHIR output.
Launch Engine View GitHub RepositoryDeterministic catch for the high-risk scenarios for Geriatric (Beers Criteria), Pediatric, Pregnancy, and Renal populations.
CILE utilizes regex patterns to detect pharmacogenomic (PGx) markers to flag gene-drug interaction risks, including HLA-alleles, Retinoid Receptors, and Teratogenic vectors to flag medications that might have genetic risks.
Two-tier Drug-Drug Interaction checker using localized database and Global NLM RxNav API that translate into structured outputs, generating both professional PDF Reports and HL7 FHIR-interoperable files.