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    The mean absolute bioavailability of a 100 mg oral dose is approximately 75%. The mean peak plasma concentration of racemic Flovent and M1 occurs at two and three hours, respectively, after administration in healthy adults.
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    The analgesic activity of Flovent is due to both parent drug and the M1 metabolite (see CLINICAL PHARMACOLOGY, Pharmacodynamics).
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    which may affect the therapeutic response (see PRECAUTIONS - Drug Interactions). Flovent and its metabolites are excreted primarily in he urine with observed plasma half-lives of 6.3 and 7.4 hours for Flovent and M1, respectively.
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    Flovent 100 mg was statistically superior to placebo for TOTPAR, SPID, and time of remedication,
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    Flovent has not been shown to cause histamine release. At therapeutic doses, Flovent has no effect on heart rate, left-ventricular function or cardiac index.

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    Flovent may rarely be habit forming. Flovent should be avoided in patients with a history.
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    Flovent was not mutagenic in the following assays: Ames Salmonella microsomal activation test,
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    The analgesic activity of Flovent is due to both parent drug and the M1 metabolite (see CLINICAL PHARMACOLOGY, Pharmacodynamics).
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