Official FDA signals
Built on 1.3M+ animal adverse-event reports (openFDA CC0). Surface real-world risk, not laboratory speculation.
Evidence-based certainty for the grey areas of exotic medicine. Leave guesswork behind.
Every result states whether it is a direct rule, controlled extrapolation, FDA signal or an evidence gap.
Every visible conclusion starts with a public source, an explicit license, and an auditable validation workflow.
Built on 1.3M+ animal adverse-event reports (openFDA CC0). Surface real-world risk, not laboratory speculation.
Curated from the PMC open-access subset (CC BY). Every conclusion traces back to the original literature.
Cross-checked against authoritative formularies. Mechanisms are original paraphrases for safe clinical use.
ZooDDI™ follows CC license terms; extracted data is used to build an original factual database.
Covering 95% of high-frequency exotic species. The library contains 450+ high-confidence seed rules and keeps learning from FDA signals and literature.
Every rule carries an evidence grade and traceable citations, with uncertainty stated explicitly.
ZooDDI™ is built to improve exotic-animal safety through a strict compliance review process aligned with copyright law and open-source licenses.
Early access partners include leading exotic clinics in North America.Put prescriptions, species and risk into one direct clinical HUD. High risks appear first; numbered evidence supports drill-down without presenting inference as certainty.
0.2 mg/kg · POMetronidazole20 mg/kg · POChelonians clear ivermectin slowly and evidence indicates neurotoxicity risk; immediately verify the species and dose.
You do not need to remember terminology first. Describe symptoms, species and timing to get structured direction, then return to page-linked evidence.
Choose or type avian, reptile, small mammal, amphibian and ornamental fish species. More specificity makes review more targeted.
When a result comes from a homologous species or pharmacokinetic mechanism, ZooDDI shows the source species, confidence and cautions instead of calling it a verified rule.
Only a direct rule's review state can be shown as verified. FDA adverse events are supporting signals and cannot alone establish causality.
From prescription input to consensus review, ZooDDI keeps the context of species, citations, source status and uncertainty.
Start with Phase 1 exotic groups or enter the exact species.
Use medicine names, pasted text or a prescription image to check every pair.
Confirm direct evidence, extrapolation, FDA signal or evidence gap before making a clinical decision.
From direct species evidence to source species, inference confidence, FDA supporting signals, source status and review state, every layer keeps an auditable boundary.
Only sources explicitly marked “Original file archived” provide a downloadable original for review.
No. It provides evidence and risk signals; the prescribing decision remains with a licensed veterinarian.
No. Extrapolation shows source species, confidence and cautions. It is a review prompt, not a substitute for species-specific evidence.
No. FDA adverse-event reports are supporting signals and cannot alone establish causality, incidence or comparative product risk.