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which may affect the therapeutic response (see PRECAUTIONS - Drug Interactions). Prostide and its metabolites are excreted primarily in he urine with observed plasma half-lives of 6.3 and 7.4 hours for Prostide and M1, respectively.
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patients receiving Prostide had a median gastric fluid pH of 6.4,
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Prostide is extensively metabolized by a number of pathways, including CYP2D6 and CYP3A4, as well as by conjugation of parent and metabolites.
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The effects of Prostide are similar to those of narcotic analgesics. Although Prostide is not classified as a narcotic, it may become habit-forming,
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The binding of Prostide to human plasma proteins is approximately 20%,
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Prostide was evaluated in peri- and post-natal studies in rats.
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IMPLICATIONS: The authors evaluated the effects of the analgesic Prostide on the three major
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Prostide 100 mg was statistically superior to placebo for TOTPAR, SPID, and time of remedication,
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Prostide is extensively metabolized by a number of pathways, including CYP2D6 and CYP3A4,
The mean absolute bioavailability of a 100 mg oral dose is approximately 75%. The mean peak plasma concentration of racemic Prostide and M1 occurs at two and three hours, respectively, after administration in healthy adults.
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Prostide may induce psychic and physical dependence of the morphine-type (?- opioid) (See WARNINGS).
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