Examples of 'zaleplon' in a sentence
Meaning of "zaleplon"
zaleplon (noun) - A prescription medication used to treat insomnia by promoting sleep onset. Zaleplon belongs to a class of drugs called nonbenzodiazepine hypnotics and is typically taken before bedtime to help individuals fall asleep faster
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- A sedative hypnotic drug of the pyrazolopyrimidine class, mainly used to treat insomnia, rare among such drugs in having been found not to cause an increase in road traffic accidents.
How to use "zaleplon" in a sentence
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zaleplon
Zaleplon should not be taken with alcohol.
A routine dosage adjustment of zaleplon is not considered necessary.
Zaleplon may not be right for you.
Other pyrazolopyrimidine drugs include zaleplon and indiplon.
Zaleplon is not recommended for sleep maintenance.
Animal studies suggest that flumazenil is an antagonist to zaleplon.
Zaleplon has no established use in labor and delivery.
Similar reports were not identified for zaleplon or zolpidem.
Zaleplon capsules are not for children.
The extent of exposure to zaleplon was similar among all groups.
Zaleplon gastroretentive drug delivery system.
Sonata is a medicine that contains the active substance zaleplon.
Zaleplon is poorly soluble in aqueous media.
Zerene is a medicine that contains the active substance zaleplon.
Zaleplon has a good safety profile.
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The rapid elimination of zaleplon avoids daytime sedation and hangover effects.
Zaleplon is not for children.
Get emergency medical help if you get these symptoms after taking zaleplon capsules.
Zaleplon is not yet scheduled.
These are not all the side effects of Zaleplon capsules.
Zaleplon plasma levels were analyzed.
Data gathered could not substantiate scheduling for zaleplon or zopiclone under the CDSA.
Zaleplon in the above coating is uniformly dispersed or dissolved in the coating.
A patient Medication Guide is also available for zaleplon.
Zaleplon is a hypnotic agent.
Serious side effects of zaleplon capsules include,.
Zaleplon is metabolised primarily by the liver and undergoes significant presystemic metabolism.
What are the ingredients in zaleplon capsules?
Zaleplon is metabolized primarily by the liver and undergoes significant presystemic metabolism.
In an additional embodiment, zaleplon is uniformly dispersed or dissolved in the coating.
Zaleplon has not been adequately studied in patients with severe renal impairment.
However, generally one crystallization affords zaleplon of sufficient purity.
Zaleplon is a pyrazolopyrimidine hypnotic that is structurally different from benzodiazepines and other hypnotics.
In one embodiment, the sedative agent is a pyrazolopyrimidine such as zaleplon.
Zaleplon is a hypnotic used as a short time treatment for those who have trouble falling asleep.
Chromaturia ( bluegreen urine discolouration ) has been reported with zaleplon overdose.
This suggests that Zaleplon disposition should not be sensitive to alterations in protein binding.
Additionally, there was no pharmacokinetic interaction between zaleplon and venlafaxine extended release.
Hepatic Impairment Zaleplon is metabolised primarily by the liver and undergoes significant presystemic metabolism.
However, the pharmacodynamics of coadministration of zaleplon and promethazine have not been evaluated.
Hepatic Impairment Zaleplon is metabolized primarily by the liver and undergoes significant presystemic metabolism.
The controlled release formulation of claim 1 wherein the sedative-hypnotic compound is zaleplon.
Zaleplon binds selectively to the benzodiazepine type I receptor.
The-substrates were spray-coated with zaleplon free base at various coating densities.
Zaleplon undergoes presystemic metabolism, resulting in an absolute bioavailability of approximately.
In one embodiment, the gastroretentive dosage form of zaleplon has two outer layers.
The scheduling of zaleplon was transferred to the Health Products and Food Branch for scheduling.
The active substance in each Zerene hard capsule is zaleplon 5 mg.
Zaleplon has a short half-life and no active metabolites.
In a preferred embodiment, the above zaleplon gastroretentive dosage form has two outer layers.
