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Methocarbamol can increase the risk of seizure in epileptic patients, especially with simultaneous use of tricyclic antidepressants,
Forty patients were treated with either Methocarbamol suppositories 100 mg 6 hourly (qds) or acetaminophen/codeine suppositories 1000/20 mg qds.
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Methocarbamol has not been shown to cause histamine release. At therapeutic doses, Methocarbamol has no effect on heart rate,
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Methocarbamol is a centrally acting synthetic opioid analgesic.
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Breast-feeding�Methocarbamol passes into breast milk and may cause unwanted effects in nursing babies.
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Ask your pharmacist if you have questions about which medicines may cause drowsiness.Methocarbamol may cause dizziness; alcohol, hot weather, exercise, or fever may increase this effect.
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The mean absolute bioavailability of a 100 mg oral dose is approximately 75%. The mean peak plasma concentration of racemic Methocarbamol and M1 occurs at two and three hours, respectively, after administration in healthy adults.
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Forty patients were treated with either Methocarbamol suppositories 100 mg 6 hourly (qds) or acetaminophen/codeine suppositories 1000/20 mg qds.
The suitability of Methocarbamol suppositories for inclusion in our hospital formulary,
Taking more than the prescribed amount of this medication could result in seizures or decreased breathing.
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Other medicines�Although certain medicines should not be used together at all,
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which may affect the therapeutic response (see PRECAUTIONS - Drug Interactions). Methocarbamol and its metabolites are excreted primarily in he urine with observed plasma half-lives of 6.3 and 7.4 hours for Methocarbamol and M1, respectively.
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The mean absolute bioavailability of a 100 mg oral dose is approximately 75%. The mean peak plasma concentration of racemic Methocarbamol and M1 occurs at two and three hours, respectively, after administration in healthy adults.
Methocarbamol and M1 elimination half-lives (13 hrs. for Methocarbamol and 19 hrs. for M1).
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Methocarbamol should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.
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Methocarbamol can impair thinking and the physical abilities required for driving or operating machinery. Methocarbamol should be avoided in patients intoxicated with alcohol,
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Intramuscular (i.m.) Methocarbamol increases gastric pH during anaesthesia similar to famotidine.
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since observed maximal placoncentrations after multiple oral doses are higher than expected based on single-dose data.
Methocarbamol has not been shown to cause histamine release. At therapeutic doses, Methocarbamol has no effect on heart rate, left-ventricular function or cardiac index.
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Nonetheless, Methocarbamol nearly doubled the interthreshold range at a concentration near 200 ng/mL.
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Methocarbamol is well absorbed orally with an absolute bioavailability of 75%. Methocarbamol has a volume of distribution of approximately 2.7 L/kg and is only 20% bound to plasma proteins.
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