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- Jun 6, 2002
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I've heard different opinions of some saying to take orals with meals and others say that 17aa orals are best absorbed on an empty stomach. What is the best way to take them for the most absorbtion?
i don't think there is a problem with absorbtion. why do you think there is a problem?
if there is a study showing one method(empty stomach vs. with food) better than the other i'm not familiar with it, i really don't think it matters. i think the absorbtion is excellent either way with the 17a oral steroids. i personally if i have the time like to try and get it sublingually as to avoid the liver processing. i'm not sure why you say that orals some get pissed out, i haven't heard that. truth is, the orals are some of the most potent steroids for strength and size your body will ever know.
Yeah but they aren't absorbed as much as an IM injection going through the liver. Empty stomach with grapefruit juice is supposed to be the best. I know orals are strong.
You're probably right on the 17aa & grapefruit juice thing, but I tried that with some UG Viagra & got a splitting headache that lasted 3 days, so DON'T do that with Viagra unless you really like pain...
I've heard different opinions of some saying to take orals with meals and others say that 17aa orals are best absorbed on an empty stomach. What is the best way to take them for the most absorbtion?
Yeah I remember seeing it posted to take ph's with a fatty meal and 17aa tabs on an empty stomach, so I was a little confused as to what the best way may be with my winstrol tabs. So you guys think with a fatty meal is the best way to go? Maybe a peaunut butter sandwich for breakfast first thing in the morning? So grapefruit juice doesn't matter then? Sorry, I'm a little confused with so many different viewpoints.the whole point of the methylation is to make them more absorbable, which is why the handful of non-17aa orals (like some of the prohormones) are supposed to be taken with fats to aid their absorption
Flavonoids from grapefruit juice have been reported to affect hepatic metabolism by influencing Cytochrome P450 enzyme system, or CYP3A4. Many medications are metabolized in the liver by the cytochrome P450 enzyme complex or CYP3A4, including calcium channel blockers, HMG-CoA reductase inhibitors, anxiolytics, and some neuropsychiatrics. Adverse reactions have been reported by this drug-food interaction.