Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Norio Hobara"'
This chapter summarizes previous experimental data on pharmacological effects of Pyrroloquinoline quinone (PQQ) specifically with respect to acetaldehyde metabolism following ethanol loading to rats and the protective effects of PQQ against hepatotox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6961b29ff850b4bfd898cc1b9c3ba359
https://doi.org/10.1201/9781003067009-18
https://doi.org/10.1201/9781003067009-18
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). 32:27-33
We analyzed the number of inquiries concerning doubts in prescriptions and the nature of the doubts for prescriptions issued at the University of Ryukyus Hospital during the period June—September 2004. Out of the 34,838 prescriptions issued, there
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c18d2305e52fec3fe0e744aed0a40bc6
https://doi.org/10.5649/jjphcs.32.27
https://doi.org/10.5649/jjphcs.32.27
Publikováno v:
Iryo Yakugaku (Japanese Journal of Pharmaceutical Health Care and Sciences). 30:536-542
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e61d0b19ca443dd6c45fcd95b6b1d1c1
https://doi.org/10.5649/jjphcs.30.536
https://doi.org/10.5649/jjphcs.30.536
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