^diazepam is metabolised by 1A2, 2C9, 2C19, 3A4 and notably not 2D6. So what exactly is inhibited is not clear from that, but some assumption can be made as gfj is a weak inhibitor of 3A4.
From MIMS Australian pharmaceutical compilation:
From that study one could assume gfj use with benzos (clonazepam/alprazolam) will slightly delay the peak plasma levels but the peak level will be higher and blood levels of the benzo will remain higher for a longer time. So all positive for benzos really unless you just want a whizz bang xanax hit pronto.
From MIMS Australian pharmaceutical compilation:
Examples of some of the more potent CYP3A4 inhibitors
include the antifungals ketoconazole and itraconazole,
the protease inhibitors ritonavir, nelfinavir and indinavir,
and the macrolide antibiotics erythromycin and clarithromycin.
Less potent inhibitors include saquinavir, nefazodone, fluconazole,
grapefruit juice, fluoxetine, fluvoxamine and clotrimazole.
From that study one could assume gfj use with benzos (clonazepam/alprazolam) will slightly delay the peak plasma levels but the peak level will be higher and blood levels of the benzo will remain higher for a longer time. So all positive for benzos really unless you just want a whizz bang xanax hit pronto.
