Drug and chemical toxicity assessment via adverse outcome pathways (AOPs), real-world FAERS adverse event signals, FDA labels, and toxicogenomic associations. Triangulates molecular initiating event to cellular outcome to organ-level toxicity to clinical adverse event. Use for hepatotoxicity/cardiotoxicity/nephrotoxicity prediction and toxicology reports.
Standardmäßig ist der Prompt ausgewählt, der zuerst die Quelle prüft. Sie können zu einem direkten Befehl wechseln oder eine lokale Kopie herunterladen.
Quelldateien prüfen
Lesen Sie SKILL.md und alle von SkillsMP angezeigten Begleitdateien, bevor Sie sich für eine Installation entscheiden.
Mit Codex oder Claude installieren Kopieren Sie diesen Prompt, fügen Sie ihn in Codex, Claude oder einen anderen Assistant ein und lassen Sie die Skill-Seite prüfen und installieren.
Ein direkter Befehl überspringt den Prüf-Prompt. Prüfen Sie die Quelle, bevor Sie ihn ausführen.
Drug and chemical toxicity assessment via adverse outcome pathways (AOPs), real-world FAERS adverse event signals, FDA labels, and toxicogenomic associations. Triangulates molecular initiating event to cellular outcome to organ-level toxicity to clinical adverse event. Use for hepatotoxicity/cardiotoxicity/nephrotoxicity prediction and toxicology reports.
disable-model-invocation
true
Toxicology Assessment via Adverse Outcome Pathways & Signal Detection
Systematic toxicology analysis that links molecular initiating events (MIEs) through adverse outcome
pathways (AOPs) to apical adverse outcomes, then triangulates with real-world FAERS signals, FDA
label data, and toxicogenomic associations.
Domain Reasoning
Toxicity has many mechanisms, and the first interpretive question is temporal: is this acute toxicity (immediate effect from a high dose) or chronic toxicity (cumulative damage from long-term low-dose exposure)? Acute and chronic toxicity operate through different mechanisms — acute hepatotoxicity may reflect direct mitochondrial damage, while chronic hepatotoxicity may involve fibrosis from repeated low-level inflammation. They also have different regulatory frameworks: acute toxicity is captured by LD50 and emergency protocols, while chronic toxicity requires long-term carcinogenicity and repeat-dose studies.
LOOK UP DON'T GUESS
Adverse outcome pathways for a chemical: query AOPWiki_list_aops and AOPWiki_get_aop; do not describe mechanisms from memory.
FAERS adverse event signals: retrieve from FAERS_count_reactions_by_drug_event and FAERS_calculate_disproportionality; never estimate PRR values.
FDA label warnings: call DailyMed_parse_adverse_reactions and related tools; do not state boxed warnings from memory.
CTD chemical-gene and chemical-disease associations: query CTD_get_chemical_gene_interactions and CTD_get_chemical_diseases; do not infer gene targets without database evidence.
COMPUTE, DON'T DESCRIBE
When analysis requires computation (statistics, data processing, scoring, enrichment), write and run Python code via Bash. Don't describe what you would do — execute it and report actual results. Use ToolUniverse tools to retrieve data, then Python (pandas, scipy, statsmodels, matplotlib) to analyze it.
When to Use This Skill
Triggers:
"What are the toxicity mechanisms for [drug/chemical]?"
"Find adverse outcome pathways for [chemical]"
"What AOPs are relevant to [target/organ/effect]?"
"FAERS signal analysis for [drug]"
"Toxicogenomic profile for [chemical]"
"What is the mechanism of hepatotoxicity / cardiotoxicity / neurotoxicity for [drug]?"
Use Cases:
AOP Tracing: Map chemical MIE through key events to apical outcome using AOPWiki
Real-World Signal Detection: Quantify FAERS adverse event signals with PRR/ROR
Label Safety Mining: Extract FDA boxed warnings, contraindications, nonclinical toxicology
Toxicogenomics: Chemical-gene-disease associations from CTD