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Linear pharmacokinetics have been observed following multiple doses of 50 and 100 mg to steady-state.Racemic Atacand is rapidly and almost completely absorbed after oral administration.
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IMPLICATIONS: The authors evaluated the effects of the analgesic Atacand on the three major
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Atacand 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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Atacand increases the risk of CNS and respiratory depression in these patients.
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The analgesic activity of Atacand is due to both parent drug and the M1 metabolite (see CLINICAL PHARMACOLOGY, Pharmacodynamics).
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adjustment of the dosing regimen is recommended (see DOSAGE AND ADMINISTRATION).
Atacand is used to relieve moderate to moderately severe pain.
Other medicines�Although certain medicines should not be used together at all,
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The product information for Atacand states that convulsions have been reported in patients using Atacand at the recommended dose levels and that the risk
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tests indicates that Atacand does not pose a genotoxic risk to humans.
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Do not stop using this medication suddenly without first talking to your doctor.
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Taking more than the prescribed amount of this medication could result in seizures or decreased breathing.
Atacand has a volume of distribution of approximately 2.7 L/kg and is only 20% bound to plasma proteins.
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Forty patients were treated with either Atacand suppositories 100 mg 6 hourly (qds) or acetaminophen/codeine suppositories 1000/20 mg qds.
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Atacand was not mutagenic in the following assays:
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Atacand is found in breast milk. Do not breast-feed while taking Atacand .When used for long periods of time or at high doses,
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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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Forty patients were treated with either Atacand suppositories 100 mg 6 hourly (qds) or acetaminophen/codeine suppositories 1000/20 mg qds.
The mean absolute bioavailability of a 100 mg oral dose is approximately 75%. The mean peak plasma concentration of racemic Atacand and M1 occurs at two and three hours, respectively, after administration in healthy adults.
Atacand is well absorbed orally with an absolute bioavailability of 75%. Atacand has a volume of distribution of approximately 2.7 L/kg and is only 20% bound to plasma proteins.
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