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Forty patients were treated with either Propranolol suppositories 100 mg 6 hourly.
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For Propranolol, the following should be considered:The suitability of Propranolol suppositories for inclusion in our hospital formulary for the treatment of mild to moderate post-operative pain was evaluated.
Do not drive or perform other possibly unsafe tasks until you know how you react to it.Do not drink
Propranolol is found in breast milk. Do not breast-feed while taking Propranolol .When used for long periods of time or at high doses,
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Propranolol increases the risk of CNS and respiratory depression in these patients.
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The analgesic activity of Propranolol is due to both parent drug and the M1 metabolite (see CLINICAL PHARMACOLOGY, Pharmacodynamics).
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Forty patients were treated with either Propranolol suppositories 100 mg 6 hourly.
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This is known as physical DEPENDENCE. If you suddenly stop taking Propranolol , you may experience WITHDRAWAL symptoms including anxiety;
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The mean absolute bioavailability of a 100 mg oral dose is approximately 75%. The mean peak plasma concentration of racemic Propranolol and M1 occurs at two and three hours, respectively, after administration in healthy adults.
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In vitro studies indicate that Propranolol is unlikely to inhibit,
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causing mental or physical dependence.It works in certain areas of the brain and nervous system to decrease pain.
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This may not be a complete list of all interactions that may occur. Ask your health care provider if Propranolol may interact with other medicines that you take.
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Use Propranolol with caution in the ELDERLY; they may be more sensitive to its effects.Propranolol should not be used in CHILDREN younger than 16 years old;
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Propranolol 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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Propranolol may rarely be habit forming. Propranolol should be avoided in patients with a history of opiate addiction or hypersensitivity to opiate medications.
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Propranolol and M1 elimination half-lives (13 hrs. for Propranolol and 19 hrs. for M1).
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Propranolol has not been shown to cause histamine release. At therapeutic doses, Propranolol has no effect on heart rate, left-ventricular function or cardiac index.
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Propranolol was not mutagenic in the following assays:
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IMPLICATIONS: The authors evaluated the effects of the analgesic Propranolol on the three major
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In general, both enantiomers of Propranolol and M1 follow a parallel time course in the body following single and multiple doses although small differences (~10%) exist in the absolute amount of each enantiomer present.
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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 Propranolol and M1 occurs at two and three hours, respectively, after administration in healthy adults.
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