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Following a single dose of 500 mg, the apparent terminal elimination half-life of azithromycin is 68 hours. [8] Biliary excretion of azithromycin, predominantly unchanged, is a major route of elimination. [50] Over the course of a week, about 6% of the administered dose appears as an unchanged drug in urine. [8]
Chemical structure of the prototypical Z-drug zolpidem. Nonbenzodiazepines (/ ˌ n ɒ n ˌ b ɛ n z oʊ d aɪ ˈ æ z ɪ p iː n,-ˈ eɪ-/ [1] [2]), sometimes referred to colloquially as Z-drugs (as many of their names begin with the letter "z"), are a class of psychoactive, depressant, sedative, hypnotic, anxiolytic drugs that are benzodiazepine-like in uses, such as for treating insomnia [3 ...
The term dosage form may also sometimes refer only to the pharmaceutical formulation of a drug product's constituent substances, without considering its final configuration as a consumable product (e.g., capsule, patch, etc.). Due to the somewhat ambiguous nature and overlap of these terms within the pharmaceutical industry, caution is ...
Zopiclone is known colloquially as a "Z-drug". Other Z-drugs include zaleplon and zolpidem and were initially thought to be less addictive than benzodiazepines. However, this appraisal has shifted somewhat in the last few years as cases of addiction and habituation have been presented.
More severe side effects include memory problems and hallucinations. [7] While flumazenil, a GABA A –receptor antagonist, can reverse zolpidem's effects, usually supportive care is all that is recommended in overdose. [20] Zolpidem is a nonbenzodiazepine, or Z-drug, which acts as a sedative and hypnotic.
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Many drugs have more than one name and, therefore, the same drug may be listed more than once. Brand names and generic names are differentiated by capitalizing brand names. See also the list of the top 100 bestselling branded drugs, ranked by sales. Abbreviations are used in the list as follows: INN = International Nonproprietary Name
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