Single dose pharmacokinetic equivalence study of two gabapentin preparations in healthy subjects

BACKGROUND: The current study was conducted to find out whether two oral preparations of 300 mg gabapentin (the test and reference capsules) were bioequivalent. SUBJECTS AND METHODS: This was a randomized, single-blind, crossover study under fasting condition, with a 7-day washout period, which incl...

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Autori principali: Tjandrawinata, Raymond R, Setiawati, Effi, Putri, Ratih Sofia Ika, Yunaidi, Danang Agung, Amalia, Fawzia, Susanto, Liana W
Natura: Artigo
Lingua:Inglês
Pubblicazione: Dove Medical Press 2014
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Original Research
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4159312/
https://ncbi.nlm.nih.gov/pubmed/25214768
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/DDDT.S69326
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