io.github.rootsbymenda/pharma-regulatory

Retrieve FDA FAERS post-market adverse event reports and safety signals for a drug or active ingredient. Input: drug brand name or generic active ingredient (e.g. 'ibuprofen', 'metformin'). Returns: total FAERS report counts, serious outcome counts, death report counts, top 10 adverse reactions by frequency, most common patient age groups, and drug ranking. Source: FDA Adverse Event Reporting System (FAERS) — 2,000 top-reported drugs with aggregated safety signals. For pharmacovigilance and post-market drug safety assessment. Do not use for interaction mechanisms (use check_drug_interactions), regulatory approvals (use check_drug), or supplement/nutrition questions.

Retrieve pharmaceutical regulatory reference data for a drug, medicine, or active ingredient across multiple authoritative datasets. Input: drug brand name, generic active ingredient, or CAS number (e.g. 'metformin', 'ibuprofen', '50-78-2'). Returns: DrugBank compound data (ID, groups, targets, SMILES, DDI count), WHO Essential Medicines listing (ATC code, formulations, indications, dosage, contraindications, pregnancy safety), Australian TGA ARTG records (ARTG ID, sponsor, category, schedule, dosage form, route, indications), and FDA NDI notifications (NDI number, FDA response, intended use). Sources: DrugBank (4,947 compounds), WHO EML, Australian TGA ARTG (23,259 medicines), FDA NDI (1,330 notifications). For pharmaceutical regulatory compliance and drug safety reference. Do not use for drug-drug interactions (use check_drug_interactions), adverse events (use check_adverse_events), or cosmetic/food/cannabis substances.