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Forty patients were treated with either Spanor suppositories 100 mg 6 hourly (qds) or acetaminophen/codeine suppositories 1000/20 mg qds.
The mean absolute bioavailability of a 100 mg oral dose is approximately 75%. The mean peak plasma concentration of racemic Spanor and M1 occurs at two and three hours, respectively, after administration in healthy adults.

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tests indicates that Spanor does not pose a genotoxic risk to humans.
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more potent than Spanor in producing analgesia and 200 times more potent in ?-opioid binding.
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Although Spanor is known to exhibit a local anaesthetic effect, how Spanor exerts this effect is not understood fully.
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The effects of Spanor are similar to those of narcotic analgesics. Although Spanor is not classified as a narcotic, it may become habit-forming,
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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If you suddenly stop taking Spanor , you may experience WITHDRAWAL symptoms including anxiety;
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Spanor has not been shown to cause histamine release.
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Spanor and M1 elimination half-lives (13 hrs. for Spanor and 19 hrs. for M1).
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No effects on fertility were observed for Spanor at oral dose levels up to 50 mg/kg,
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Spanor is administered as a racemate and both [-] and [+] forms of both Spanor and M1 are detected in the circulation.
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But she was with child, and it ended up that this child was Spanor's.
alcohol or use medicines that may cause drowsiness (eg, sleep aids, muscle relaxers) while you are using Spanor ; it may add to their effects.
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