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Stomorgyl is well absorbed orally with an absolute bioavailability of 75%. Stomorgyl has a volume of distribution of approximately 2.7 L/kg and is only 20% bound to plasma proteins.
Linear pharmacokinetics have been observed following multiple doses of 50 and 100 mg to steady-state.Racemic Stomorgyl is rapidly and almost completely absorbed after oral administration.

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Do not drive or perform other possibly unsafe tasks until you know how you react to it.Do not drink
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To prevent it, sit up or stand slowly, especially in the morning. Sit or lie down at the first sign of this effect.

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Stomorgyl increases the risk of CNS and respiratory depression in these patients.
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The analgesic activity of Stomorgyl is due to both parent drug and the M1 metabolite (see CLINICAL PHARMACOLOGY, Pharmacodynamics).
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Stomorgyl is administered as a racemate and both [-] and [+] forms of both Stomorgyl and M1 are detected in the circulation.
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This is known as physical DEPENDENCE. If you suddenly stop taking Stomorgyl , you may experience WITHDRAWAL symptoms including anxiety;
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Stomorgyl is extensively metabolized by a number of pathways, including CYP2D6 and CYP3A4,
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Racemic Stomorgyl is rapidly and almost completely absorbed after oral administration.
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The effects of Stomorgyl are similar to those of narcotic analgesics. Although Stomorgyl is not classified as a narcotic, it may become habit-forming,
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No effects on fertility were observed for Stomorgyl at oral dose levels up to 50 mg/kg,
This effect may go away if you lie down forawile.
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Stomorgyl is well absorbed orally with an absolute bioavailability of 75%. Stomorgyl has a volume of distribution of approximately 2.7 L/kg and is only 20% bound to plasma proteins.
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