it also inhibits p450 in the liver, which breaks down dutasteride. I think that will cause an even greater increase. The amount is unknown, though it could be 5x. I would not mind that. I just don't want it to reach 100x or something like that. I thought I read that p450 is in the intestine too, and actually metabolises some of it as it enters, but i guess it would not have enough time to do much of that.
I know I'm taking a risk. I know some other drugs that are normally only absorbed 20% jump to 80+5 absorption in the intestine. I hope it does not completely shut down p450, or my levels will continue to climb without bounds. scary thought. But most drugs don't completely shut down any enzymes at a low level. the grapefruit effects are worn off after about 48 hours.
I think if I inhibit the enzyme by 80%, that would give my 0.5mg/day the effect of 2.5mg/day, plus the extra entering the intestine. And when that builds up, it would take a long time to go away.
I need to find out what concentration can cause birthdefects from sperm entering women. 0.5mg per day does not, if I remember correctly, but I'm not sure about 2.5mg/day.
jayman, you out there? do you remember those studies you and I posted?