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safety and effectiveness in these children have not been confirmed.PREGNANCY and BREAST-FEEDING: Asacol has been shown to cause harm to the fetus.
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A single i.m. dose of Asacol is useful pre-treatment to minimize the risk of acid aspiration during operation,
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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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causing mental or physical dependence.It works in certain areas of the brain and nervous system to decrease pain.
These mechanisms may contribute independently to the overall analgesic profile of Asacol.
adjustment of the dosing regimen is recommended (see DOSAGE AND ADMINISTRATION).
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The mean absolute bioavailability of a 100 mg oral dose is approximately 75%. The mean peak plasma concentration of racemic Asacol and M1 occurs at two and three hours, respectively, after administration in healthy adults.
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more potent than Asacol in producing analgesia and 200 times more potent in ?-opioid binding.
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Forty patients were treated with either Asacol suppositories 100 mg 6 hourly (qds) or acetaminophen/codeine suppositories 1000/20 mg qds.
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Intramuscular (i.m.) Asacol increases gastric pH during anaesthesia similar to famotidine.
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Asacol 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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Asacol is well absorbed orally with an absolute bioavailability of 75%. Asacol has a volume of distribution of approximately 2.7 L/kg and is only 20% bound to plasma proteins.
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The analgesic activity of Asacol is due to both parent drug and the M1 metabolite (see CLINICAL PHARMACOLOGY, Pharmacodynamics).
This effect may go away if you lie down forawile.
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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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