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1 Dosing may be increased to 100 mg every four to six hours, but the daily dosage should not exceed 400 mg 1 and should be limited to 250 to 300 mg .
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Linear pharmacokinetics have been observed following multiple doses of 50 and 100 mg to steady-state.Racemic Benfotiamine is rapidly and almost completely absorbed after oral administration.
When used for long periods of time or at high doses,
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Benfotiamine is well absorbed orally with an absolute bioavailability of 75%. Benfotiamine has a volume of distribution of approximately 2.7 L/kg and is only 20% bound to plasma proteins.
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which may affect the therapeutic response (see PRECAUTIONS - Drug Interactions). Benfotiamine and its metabolites are excreted primarily in he urine with observed plasma half-lives of 6.3 and 7.4 hours for Benfotiamine and M1, respectively.
Benfotiamine and M1 elimination half-lives (13 hrs. for Benfotiamine and 19 hrs. for M1).
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which may affect the therapeutic response (see PRECAUTIONS - Drug Interactions). Benfotiamine and its metabolites are excreted primarily in he urine with observed plasma half-lives of 6.3 and 7.4 hours for Benfotiamine and M1, respectively.
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