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Atenolol is extensively metabolized by a number of pathways, including CYP2D6 and CYP3A4,
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These mechanisms may contribute independently to the overall analgesic profile of Atenolol.
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The mean absolute bioavailability of a 100 mg oral dose is approximately 75%. The mean peak plasma concentration of racemic Atenolol and M1 occurs at two and three hours, respectively, after administration in healthy adults.
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Atenolol 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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There were no other significant respiratory diffences.
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The effects of Atenolol and its metabolite mono-O-demethyl-Atenolol,
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Atenolol may rarely be habit forming. Atenolol should be avoided in patients with a history.
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since observed maximal placoncentrations after multiple oral doses are higher than expected based on single-dose data.
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Atenolol was not mutagenic in the following assays: Ames Salmonella microsomal activation test,
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Atenolol is used to relieve moderate to moderately severe pain.
clinical trial was performed to assess the analgesic efficacy and reported side effects of Atenolol 100 mg, Atenolol 50 mg,
The volume of distribution of Atenolol was 2.6 and 2.9 liters/kg in male and female subjects, respectively,

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The effects of Atenolol are similar to those of narcotic analgesics. Although Atenolol is not classified as a narcotic, it may become habit-forming,
Use Atenolol with caution in the ELDERLY; they may be more sensitive to its effects.Atenolol should not be used in CHILDREN younger than 16 years old;
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