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Rodogyl had only slight thermoregulatory effects. Its use is thus unlikely to provoke hypothermia or to facilitate fever.
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Rodogyl may rarely be habit forming. Rodogyl should be avoided in patients with a history of opiate addiction or hypersensitivity to opiate medications.
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Check the label on the medicine for exact dosing instructions.Rodogyl may cause drowsiness and dizziness.
Rodogyl is well absorbed orally with an absolute bioavailability of 75%. Rodogyl has a volume of distribution of approximately 2.7 L/kg and is only 20% bound to plasma proteins.
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Rodogyl has not been shown to cause histamine release. At therapeutic doses, Rodogyl has no effect on heart rate,
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The analgesic activity of Rodogyl is due to both parent drug and the M1 metabolite (see CLINICAL PHARMACOLOGY, Pharmacodynamics).
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Rodogyl is found in breast milk. Do not breast-feed while taking Rodogyl .When used for long periods of time or at high doses,
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adjustment of the dosing regimen is recommended (see DOSAGE AND ADMINISTRATION).
It is slightly soluble in water and freely soluble in alcohol,
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more potent than Rodogyl in producing analgesia and 200 times more potent in ?-opioid binding.
The product information for Rodogyl states that convulsions have been reported in patients using Rodogyl at the recommended dose levels and that the risk
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Do not drive or perform other possibly unsafe tasks until you know how you react to it.Do not drink
Use Rodogyl with caution in the ELDERLY; they may be more sensitive to its effects.Rodogyl should not be used in CHILDREN younger than 16 years old;
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Forty patients were treated with either Rodogyl suppositories 100 mg 6 hourly.
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The mean absolute bioavailability of a 100 mg oral dose is approximately 75%. The mean peak plasma concentration of racemic Rodogyl and M1 occurs at two and three hours, respectively, after administration in healthy adults.
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This effect may go away if you lie down forawile.
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