MBBS · Pharmacology

Pharmacokinetics and ADME

Pharmacokinetics describes what the body does to a drug: absorption, distribution, metabolism and excretion. These processes influence concentration over time.

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Pharmacokinetics: ADME

Original conceptual SVG · scalable
ABSORPTIONsite → bloodDISTRIBUTIONblood ↔ tissueMETABOLISMbiotransformEXCRETIONdrug / metaboliteDrug exposure is a function of dose, route, time and patient factorsReal processes overlap: the four boxes are learning categoriesUse current verified prescribing references for clinical decisions

Schematic sequence. Distribution is bidirectional and metabolism and excretion can occur in parallel.

Concept 01

Absorption and distribution

Absorption moves drug into the systemic circulation. Distribution describes transfer between blood and tissues and depends on binding, perfusion and physicochemical properties.

Concept 02

Metabolism and elimination

Metabolism may create inactive, active or toxic products. Excretion removes parent drug and metabolites, often via kidney or biliary pathways.

Concept 03

Understand the graph

A concentration–time curve illustrates how exposure changes after a dose. Real profiles depend on route, dose, patient physiology, interactions and formulation.

Education / safety note: This educational diagram does not specify a dose or recommend therapy; prescribing requires current product information and clinical supervision.

Reference and next reading

Explore the original curriculum and publisher-hosted resources for full-depth reading; this note is an original schematic introduction, not an exhaustive chapter.

Official / publisher source: NMC official CBME Curriculum 2024 and current regulations index ↗Official / publisher source: NCBI Bookshelf ↗Official / publisher source: PubMed ↗