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Research draft

therapeutic index

vr.tr.therapeutic-index · XCT.REL

Let an agent explain the therapeutic index in pharmacology in general terms, why narrow-index drugs are monitored, and refer all personal dosing questions to clinicians and pharmacists.

Thing Registry Cross-cutting context

Research draft, second pass

A second pass drafted this model: the structure a model of this thing needs, and what is known about it in the world. The line under this one says how the second half was obtained - researched against sources, or recalled without web access, in which case nothing here was read anywhere and every claim is a lead to verify. Unreviewed either way.

written by Claude from model knowledge without web access - no source was read, every claim is a lead to verify

Researched by: Claude

Purpose and description

Let an agent explain the therapeutic index in pharmacology in general terms, why narrow-index drugs are monitored, and refer all personal dosing questions to clinicians and pharmacists.

A quantitative measure comparing the dose of a drug that causes toxicity with the dose that produces the desired effect, often expressed as a ratio such as TD50 to ED50; drugs with a narrow therapeutic index, such as some anticoagulants, lithium and digoxin, need careful dosing and monitoring.

What it is for: Pharmacology, drug development and patient safety.

It can be explain what the therapeutic index measures; describe why narrow-index drugs need monitoring; find official product information; route overdose concerns to emergency help.

Distinguishing features

Compares toxic and effective doses

Indicates margin of safety

Narrow for some important drugs

Guides monitoring

What it looks like

Not physical; a ratio or range reported in pharmacology.

How it is recognised

Ratios such as TD50/ED50

Narrow therapeutic index labelling

Therapeutic window is a related concept

Related models

is a kind of - category

factor of safety

is used in - field

pharmacology

is related to - product

medication

is related to - practice

therapeutic drug monitoring

In practice

Families and kinds

therapeutic index

therapeutic window

margin of safety

narrow therapeutic index drugs

Standards and regulation

Medicines regulatory guidance on narrow therapeutic index drugs

Generic substitution rules for such drugs

Failure modes and hazards

Toxicity from small dosing changes

Interactions altering drug levels

Agents giving personal dosing advice

Where this came from

wikidata · CC0 1.0

Drafted structure

Bundle to layer to finding to question, as the second pass will find it: 4 bundles · 8 layers · 8 findings · 16 questions.

Emergency Overdose.

Safety comes first.

Overdose

Too much taken.

Overdose

Overdose.

  1. Has someone taken too much of a narrow-index medicine or shows signs of toxicity? boundary
  2. Should a poison centre or emergency services be contacted now? action

Interaction

New medicines.

Interaction

Interactions.

  1. Has a new medicine or supplement been started alongside a narrow-index drug? boundary
  2. Should the person check with their pharmacist promptly? action
Concept What it measures.

Definitions vary.

Ratio

Calculation.

Ratio

Ratio.

  1. How is the therapeutic index calculated in pharmacology texts? definition
  2. How does it differ from the therapeutic window? definition

Limits

Interpretation.

Limits

Interpretation limits.

  1. Why can animal-derived indices mislead for humans? boundary
  2. Which measures are used clinically? provenance
Practice Monitoring.

Monitoring keeps patients safe.

Monitoring

Drug levels.

Monitoring

Monitoring.

  1. Why are blood levels monitored for some narrow-index drugs, in general terms? provenance
  2. Which official guidance describes it? provenance

Personal

Personal questions.

Personal

Personal advice limits.

  1. Is the user asking about their own dose or test result? boundary
  2. How should the agent refer them to their prescriber or pharmacist? action
Development Drug development.

Safety margins guide development.

Trials

Dose finding.

Trials

Dose finding.

  1. How do early trials establish safe and effective doses, in general terms? definition
  2. Which regulators oversee them? provenance

Generics

Substitution.

Generics

Generic substitution.

  1. Are special rules applied when switching brands of narrow-index drugs here? provenance
  2. Who decides? provenance

What the second pass must settle

  • Should therapeutic window be a separate entry?
  • How should drug lists be sourced?
  • How should monitoring guidance be linked?