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    the rates of withdrawals due to adverse events appeared to be higher in the Pravachol groups.
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    The analgesic activity of Pravachol is due to both parent drug and the M1 metabolite (see CLINICAL PHARMACOLOGY, Pharmacodynamics).
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    The effects of Pravachol are similar to those of narcotic analgesics. Although Pravachol is not classified as a narcotic, it may become habit-forming,
    Taking Pravachol together with medicines that are used during surgery or dental,
    In general, both enantiomers of Pravachol 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.
    Ask your pharmacist if you have questions about which medicines may cause drowsiness.Pravachol may cause dizziness; alcohol, hot weather, exercise, or fever may increase this effect.
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    Pravachol can impair thinking and the physical abilities required for driving or operating machinery. Pravachol should be avoided in patients intoxicated with alcohol,
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    These mechanisms may contribute independently to the overall analgesic profile of Pravachol.
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    Pravachol can impair thinking and the physical abilities required for driving or operating machinery. Pravachol should be avoided in patients intoxicated with alcohol,
    To prevent it, sit up or stand slowly, especially in the morning. Sit or lie down at the first sign of this effect.
    Pravachol has not been shown to cause histamine release.
    Pravachol was not mutagenic in the following assays: Ames Salmonella microsomal activation test,
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    which may affect the therapeutic response (see PRECAUTIONS - Drug Interactions). Pravachol and its metabolites are excreted primarily in he urine with observed plasma half-lives of 6.3 and 7.4 hours for Pravachol and M1, respectively.
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    which may affect the therapeutic response (see PRECAUTIONS - Drug Interactions). Pravachol and its metabolites are excreted primarily in he urine with observed plasma half-lives of 6.3 and 7.4 hours for Pravachol and M1, respectively.
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    Pravachol was evaluated in peri- and post-natal studies in rats.
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    A single i.m. dose of Pravachol is useful pre-treatment to minimize the risk of acid aspiration during operation,
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