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since observed maximal placoncentrations after multiple oral doses are higher than expected based on single-dose data.
Cephalexin may not work as well and may require higher doses to obtain the same effect as when originally taken. This is known as TOLERANCE.
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In vitro studies indicate that Cephalexin is unlikely to inhibit,
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Cephalexin is well absorbed orally with an absolute bioavailability of 75%. Cephalexin has a volume of distribution of approximately 2.7 L/kg and is only 20% bound to plasma proteins.
tests indicates that Cephalexin does not pose a genotoxic risk to humans.

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which may affect the therapeutic response (see PRECAUTIONS - Drug Interactions). Cephalexin and its metabolites are excreted primarily in he urine with observed plasma half-lives of 6.3 and 7.4 hours for Cephalexin and M1, respectively.
Cephalexin has not been shown to cause histamine release.
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