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which may affect the therapeutic response (see PRECAUTIONS - Drug Interactions). Rhodogil and its metabolites are excreted primarily in he urine with observed plasma half-lives of 6.3 and 7.4 hours for Rhodogil and M1, respectively.
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Taking more than the prescribed amount of this medication could result in seizures or decreased breathing.
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Linear pharmacokinetics have been observed following multiple doses of 50 and 100 mg to steady-state.Racemic Rhodogil is rapidly and almost completely absorbed after oral administration.
Rhodogil may rarely be habit forming. Rhodogil should be avoided in patients with a history.
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Some people who use Rhodogil for a long time without a break may develop a physical need to continue taking it.
Breast-feeding�Rhodogil passes into breast milk and may cause unwanted effects in nursing babies.
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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The volume of distribution of Rhodogil was 2.6 and 2.9 liters/kg in male and female subjects, respectively,

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In vitro studies indicate that Rhodogil is unlikely to inhibit,
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The analgesic activity of Rhodogil is due to both parent drug and the M1 metabolite (see CLINICAL PHARMACOLOGY, Pharmacodynamics).
The analgesic activity of Rhodogil is due to both parent drug and the M1 metabolite (see CLINICAL PHARMACOLOGY, Pharmacodynamics).
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