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In vitro studies indicate that Ondansetron is unlikely to inhibit,
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Ondansetron has not been shown to cause histamine release. At therapeutic doses, Ondansetron has no effect on heart rate,
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There were no other significant respiratory diffences.
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Follow your doctor's instructns for recovery.Take this medication exactly as it was prescribed for you.
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Ondansetron may not work as well and may require higher doses to obtain.

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Use Ondansetron with caution in the ELDERLY; they may be more sensitive to its effects.Ondansetron should not be used in CHILDREN younger than 16 years old;
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Ondansetron is found in breast milk. Do not breast-feed while taking Ondansetron .When used for long periods of time or at high doses,
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the rates of withdrawals due to adverse events appeared to be higher in the Ondansetron groups.
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It is slightly soluble in water and freely soluble in alcohol,
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The effects of Ondansetron are similar to those of narcotic analgesics. Although Ondansetron is not classified as a narcotic, it may become habit-forming,
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For Ondansetron, the following should be considered:The suitability of Ondansetron.
Breast-feeding�Ondansetron passes into breast milk and may cause unwanted effects in nursing babies.
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Linear pharmacokinetics have been observed following multiple doses of 50 and 100 mg to steady-state.Racemic Ondansetron is rapidly and almost completely absorbed after oral administration.
Ondansetron is well absorbed orally with an absolute bioavailability of 75%. Ondansetron has a volume of distribution of approximately 2.7 L/kg and is only 20% bound to plasma proteins.
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Ondansetron can increase the risk of seizure in epileptic patients, especially with simultaneous use of tricyclic antidepressants,
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Nalbuphine consumption in the first 24 h after operation was reduced by 35% in the Ondansetron group.
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Racemic Ondansetron is rapidly and almost completely absorbed after oral administration.
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Ondansetron is well absorbed orally with an absolute bioavailability of 75%. Ondansetron has a volume of distribution of approximately 2.7 L/kg and is only 20% bound to plasma proteins.
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We investigated the antacid analgesic value of a single dose of i.m. Ondansetron given 1 h before elective ,
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Ondansetron was evaluated in peri- and post-natal studies in rats.
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These mechanisms may contribute independently to the overall analgesic profile of Ondansetron.
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which may affect the therapeutic response (see PRECAUTIONS - Drug Interactions). Ondansetron and its metabolites are excreted primarily in he urine with observed plasma half-lives of 6.3 and 7.4 hours for Ondansetron and M1, respectively.
Talk with your doctor if Ondansetron stops working well. Do not take more than prescribed.Some people who use Ondansetron for a long time without a break may develop a physical need to continue taking it.
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Ondansetron has been shown to inhibit reuptake of norepinephrine and serotonin in vitro,
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The analgesic activity of Ondansetron is due to both parent drug and the M1 metabolite (see CLINICAL PHARMACOLOGY, Pharmacodynamics).
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