Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Hiromasa Kameya"'
Publikováno v:
Journal of Pharmacy and Pharmacology. 59:383-386
Drug interaction between rizatriptan benzoate, an anti-migraine agent, and sodium valproate (VPA-Na), an anticonvulsant, was studied in rats. When rizatriptan benzoate was administered orally immediately after VPA-Na oral administration, the pharmaco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b2aeee0a21a734eedd7a2dfb5e78b19
https://doi.org/10.1211/jpp.59.3.0007
https://doi.org/10.1211/jpp.59.3.0007
Publikováno v:
Iryo Yakugaku (Japanese Journal of Pharmaceutical Health Care and Sciences). 33:496-501
The drug interactions between tandospirone citrate,a non-benzodiazepine antianxiety drug,and oxazolam,a minor benzodiazepine tranquilizer and antianxiety agent,and valpronic acid (VPA),an anti-convulsant,were studied in rats.When tandospirone citrate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79f013a44de0b57864af22e594d1414e
https://doi.org/10.5649/jjphcs.33.496
https://doi.org/10.5649/jjphcs.33.496
Publikováno v:
Iryo Yakugaku (Japanese Journal of Pharmaceutical Health Care and Sciences). 29:491-494
The effect of timing on the administration of spherical charcoal (Kremezin) on the pharmacokinetics of valproic acid (VPA) in the coadministration of sodium valproate and Kremezin was examined in rats.Kremezin, when administered either immediately or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::abaec561cb52256b9b553c91886011b2
https://doi.org/10.5649/jjphcs.29.491
https://doi.org/10.5649/jjphcs.29.491
Publikováno v:
Biogenic Amines. 17:409-420
Drug interaction between meropenem (MEPM), a carbapenem of antibiotic agent, and sodium valproate (VPA), an anticonvulsant, was studied in rats and human volunteers. When sodium VPA and MEPM were administered simultaneously, the plasma VPA level was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::380aa340c1fadf8560b0ae52dfb338de
https://doi.org/10.1163/15693910260698357
https://doi.org/10.1163/15693910260698357
Publikováno v:
Biogenic Amines. 17:401-407
Effects of salicylate on the pharmacokinetics of valproic acid (VPA) after oral administration (p.o.) of sodium valproate were investigated in rats. When salicylic acid was administered orally after sodium valproate p.o., the plasma VPA concentration
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02414c0e17dfdaa02c53a8e18452190f
https://doi.org/10.1163/15693910260698348
https://doi.org/10.1163/15693910260698348
Publikováno v:
Journal of Pharmacy and Pharmacology. 54:821-825
The effect of two kinds of 1,4-dihydropyridine calcium-channel blockers, nicardipine hydrochloride and nifedipine, on the disposition of carvedilol, was studied in rats. Blood samples were assayed for carvedilol levels using solid-phase extraction an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c2358d62ece04a69a5952009f00c268
https://doi.org/10.1211/0022357021778998
https://doi.org/10.1211/0022357021778998
Publikováno v:
Japanese Journal of Hospital Pharmacy. 25:155-161
We investigated the effects of metoclopramide and propantheline bromide on the bioavailability of carvedilol in rats. To determine the concentration-time profile of plasma carvedilol, the blood samples were obtained from the tail vein after the simul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b34df5348f957a99e37ce0d519265416
https://doi.org/10.5649/jjphcs1975.25.155
https://doi.org/10.5649/jjphcs1975.25.155
Publikováno v:
Japanese Journal of Hospital Pharmacy. 25:319-322
The drug interaction between sodium valproate (VPA), an anticonvulsant, and faropenem sodium (FRPM), a new penem antibiotic drug, was studied in rats. No significant change was observed in the plasma VPA concentration when compared with the control a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56fcdf7a605f38ce2fa9d738c084007f
https://doi.org/10.5649/jjphcs1975.25.319
https://doi.org/10.5649/jjphcs1975.25.319
Publikováno v:
Japanese Journal of Hospital Pharmacy. 25:1-7
The purpose of the present study was to evaluate the pharmacokinetic interaction in rats between carvedilol and three kinds of dihydropyridine calcium-channel blockers, including nicaldipine hydrochloride, nifedipine and felodipine by high-performanc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::391da58adcd193be5a3900a22f36a77f
https://doi.org/10.5649/jjphcs1975.25.1
https://doi.org/10.5649/jjphcs1975.25.1
Publikováno v:
Japanese Journal of Hospital Pharmacy. 25:8-14
The pharmacokinetic interaction between carvedilol, a nonselective β-blocking agent and amlodipine besilate, a dihydropyridine calcium-channel blocker were investigated in rats. To determine the concentration-time profile of plasma carvedilol, blood
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30503bf7438a22ec9559dac70259cc12
https://doi.org/10.5649/jjphcs1975.25.8
https://doi.org/10.5649/jjphcs1975.25.8