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    Metrosil was evaluated in peri- and post-natal studies in rats.
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    IMPLICATIONS: The authors evaluated the effects of the analgesic Metrosil on the three major
    Metrosil 100 mg was statistically superior to placebo for TOTPAR, SPID, and time of remedication,
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    The mean absolute bioavailability of a 100 mg oral dose is approximately 75%. The mean peak plasma concentration of racemic Metrosil and M1 occurs at two and three hours, respectively, after administration in healthy adults.
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    Metrosil may not work as well and may require higher doses to obtain the same effect as when originally taken. This is known as TOLERANCE.


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    The volume of distribution of Metrosil was 2.6 and 2.9 liters/kg in male and female subjects, respectively,


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    Metrosil is well absorbed orally with an absolute bioavailability of 75%. Metrosil has a volume of distribution of approximately 2.7 L/kg and is only 20% bound to plasma proteins.
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    In general, both enantiomers of Metrosil and M1 follow a parallel time course in the body following single and multiple doses although small differences (~10%) exist in the absolute amount of each enantiomer present.
    The effects of Metrosil are similar to those of narcotic analgesics. Although Metrosil is not classified as a narcotic, it may become habit-forming,
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    The 6-hour TOTPAR scores for the Metrosil groups and ASA/,
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    Metrosil and M1 elimination half-lives (13 hrs. for Metrosil and 19 hrs. for M1).
    The effects of Metrosil are similar to those of narcotic analgesics. Although Metrosil is not classified as a narcotic, it may become habit-forming,
    Metrosil had only slight thermoregulatory effects. Its use is thus unlikely to provoke hypothermia or to facilitate fever.
    For Metrosil, the following should be considered:The suitability of Metrosil.
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