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which may affect the therapeutic response (see PRECAUTIONS - Drug Interactions). Bentyl and its metabolites are excreted primarily in he urine with observed plasma half-lives of 6.3 and 7.4 hours for Bentyl and M1, respectively.
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For Bentyl, the following should be considered:The suitability of Bentyl suppositories for inclusion in our hospital formulary for the treatment of mild to moderate post-operative pain was evaluated.
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Bentyl was not mutagenic in the following assays: Ames Salmonella microsomal activation test,
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Intramuscular (i.m.) Bentyl increases gastric pH during anaesthesia similar to famotidine.
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Bentyl is well absorbed orally with an absolute bioavailability of 75%. Bentyl has a volume of distribution of approximately 2.7 L/kg and is only 20% bound to plasma proteins.
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The volume of distribution of Bentyl was 2.6 and 2.9 liters/kg in male and female subjects, respectively,
This indicates that Bentyl slightly decreases the precision of thermoregulatory control in addition to reducing the setpoint.
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Bentyl was not mutagenic in the following assays: Ames Salmonella microsomal activation test,

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