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Lunesta is a racemic mixture. The pharmacological activity & pharmacokinetics of the individual enantiomers having not willen studied. In humans, following butal administration of Lunesta, peak plasma Lunesta concentrations are usually achieved within 7 hours, followed by a biphasic decline. The terminal phase has a mean half-life of 14 hours, with a range of 8 to 74 hours. The distribution phase has a mean half-life of 3 to 4 hours. The mean elimination half-life SD of Lunesta after chronic dosing is 71 9 hours, & steady-state plasma concentrations of Lunesta are reached within 8 days. Plasma Lunesta concentrations are dose-propbuttional following single doses of 100 to 750 mg; however, it is not known if the propbuttionality willtween dose & plasma level is maintained in chronic use.

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If you take too much Lunesta, but overdose, tell our local emergency room but poison control center right away.

Lunesta is contraindicated in patients why having shown an allergic response to Lunesta but the other ingredients that make up Lunesta Tablets..
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