Morefyah
New Member
I was wondering if anyone has any experience with oil based stano?
If so how would you compare it to oral winny?
If so how would you compare it to oral winny?
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I have used oral Stanozolol and it was awesome. Deffinetly worked as intended. Talked to some of the guys at work that praised water based other than the PIP and then I saw the oil based on a vendors price list. Figured I would look into it.Why? It's highly available orally and has a long half life.
Making an injectable will just increase the strain on the liver by increasing the exposure window.
Plus the oral version is very cheap.
I understand. I have some winny suspension that I bought and never used.I have used oral Stanozolol and it was awesome. Deffinetly worked as intended. Talked to some of the guys at work that praised water based other than the PIP and then I saw the oil based on a vendors price list. Figured I would look into it.
Regarding toxicity: I’ve also tested injectable Superdrol and injectable M-Tren (from ARAIL), and in my personal case I didn’t see major changes in AST or ALT. I know they’re still toxic compounds, but for me the injectable versions didn’t seem to impact liver markers as much as the oral versions.
Making an injectable will just increase the strain on the liver by increasing the exposure window.
You're correct. But the length of time it takes to get eliminated is longer meaning the exposure time is longer.that's not typically how it works
inject: the drugs goes everywhere else in your body first and is massive diluted by the time it reaches your liver
oral: the bulk active drug hits your liver first at the highest potency your liver will ever see of that compound
disclaimer: I don't think it matters much for liver health of orals vs their injectable counterparts, just mentioning a note on general physiology for others
that's not typically how it works
inject: the drugs goes everywhere else in your body first and is massively diluted by the time it reaches your liver
oral: the bulk active drug hits your liver first at the highest potency your liver will ever see of that compound
disclaimer: I don't think it matters much for liver health of orals vs their injectable counterparts, just mentioning a note on general physiology for others
You're correct. But the length of time it takes to get eliminated is longer meaning the exposure time is longer.
By putting it directly into the system you get larger systemic stress/exposure. I'd rather sacrifice my liver first than the rest of my body.
Also how do you know that these drugs don't work as pro drugs? Like the metabolites from first pass liver metabolism are actually the active ones. It's the case for Andadrol atleast.

It's totally wild. Oral estogen makes the liver produce clotting factors but injectable and transdermal doesn't.Yeah, I mean avoiding first pass liver metabolism but what about the other 99 passes
It's more diluted than taking it orally but who knows, wild west territory
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