Interaction study between remoxipride and biperiden.

Abstract:

:Twelve healthy male volunteers took part in a double-blind randomised cross-over study composed of three treatment sessions: remoxipride 100 mg; remoxipride 100 mg plus biperiden 4 mg; and biperiden 4 mg. Plasma and urine concentrations of remoxipride and biperiden, plasma prolactin levels, salivary flow and adverse events were recorded to assess pharmacodynamic interactions. Remoxipride and biperiden had no effect on each other's plasma concentrations. Biperiden did not affect the urinary recovery or renal clearance of remoxipride. Prolactin levels were unaffected by biperiden but increased following remoxipride administration. Differences in prolactin Cmax and tmax following remoxipride versus concomitant (remoxipride + biperiden) treatment were not statistically significant. However, a slight but statistically significant (P = 0.04) increase in prolactin AUC was observed after concomitant treatment. No significant differences could be observed between the recorded salivary flow in all the treatment sessions. Single doses of remoxipride and biperiden showed no pharmacokinetic or pharmacodynamic interaction.

journal_title

Psychopharmacology

authors

Yisak W,Farde L,von Bahr C,Nilsson LB,Fredriksson G,Ogenstad S

doi

10.1007/BF02257403

subject

Has Abstract

pub_date

1993-01-01 00:00:00

pages

27-32

issue

1

eissn

0033-3158

issn

1432-2072

journal_volume

111

pub_type

临床试验,杂志文章,随机对照试验
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    更新日期:1986-01-01 00:00:00

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    pub_type: 杂志文章

    doi:10.1007/BF02245944

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    更新日期:1995-04-01 00:00:00

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    pub_type: 杂志文章

    doi:10.1007/BF00432374

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    更新日期:1980-01-01 00:00:00

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    pub_type: 杂志文章

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    pub_type: 临床试验,杂志文章

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    更新日期:1988-01-01 00:00:00

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    更新日期:1998-01-01 00:00:00

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    更新日期:1986-01-01 00:00:00

  • Chronic treatment with a selective inhibitor of casein kinase I delta/epsilon yields cumulative phase delays in circadian rhythms.

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    pub_type: 杂志文章

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    pub_type: 杂志文章

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    更新日期:1979-01-31 00:00:00

  • Effects of T-type calcium channel blockers on cocaine-induced hyperlocomotion and thalamocortical GABAergic abnormalities in mice.

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