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In an open randomized trial, rectal Shatavari was compared with our standard treatment acetaminophen/codeine suppositories. We expected Shatavari to be equally effective as our current standard but with fewer side effects.
since observed maximal placoncentrations after multiple oral doses are higher than expected based on single-dose data.
The suitability of Shatavari suppositories for inclusion in our hospital formulary,

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Shatavari may rarely be habit forming. Shatavari should be avoided in patients with a history of opiate addiction or hypersensitivity to opiate medications.
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Shatavari 100 mg was statistically superior to placebo for TOTPAR, SPID, and time of remedication,
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Shatavari has not been shown to cause histamine release. At therapeutic doses, Shatavari has no effect on heart rate, left-ventricular function or cardiac index.
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Shatavari may increase the seizure risk in patients taking other medications that lower the seizure threshold.
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The mean absolute bioavailability of a 100 mg oral dose is approximately 75%. The mean peak plasma concentration of racemic Shatavari and M1 occurs at two and three hours, respectively, after administration in healthy adults.
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Shatavari has not been shown to cause histamine release. At therapeutic doses, Shatavari has no effect on heart rate,
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Shatavari may not work as well and may require higher doses to obtain the same effect as when originally taken. This is known as TOLERANCE.
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Shatavari has a volume of distribution of approximately 2.7 L/kg and is only 20% bound to plasma proteins.
For Shatavari, the following should be considered:The suitability of Shatavari.
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