Construct · 1 fields · 1 citations
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In pharmacokinetics, the first pass is the metabolism a drug undergoes, chiefly in the gut wall and liver, after oral absorption but before it reaches the systemic circulation, which can sharply reduce how much active drug becomes available. Pond and Tozer's 1984 review set out the basic concepts and clinical consequences of first-pass elimination. The referent is the fraction of an oral dose removed on its initial transit through eliminating organs, and it is unrelated to a compiler's opening scan beyond the shared image of a first traversal.[1]
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