Troches of Anavar? Anyone used Troches before?

[Stocks_and_Steroids]

I was wondering how is the liver toxicity compared to pills? Is less of the chemical wasted using Troches VS pills? Overall effectiveness?

 

[Zyglamail]

Liver toxicy really applies to the liver first pass which is reserved for oral applications. Transdermal bypass the liver first pass so arent as toxic.

 

[d_rson]

Doesn't make sense. Var is metabolized mostly in the kidneys, and is highly bioavailable, so seems a waste to me.

 

[Stocks_and_Steroids]

Doesn't make sense. Var is metabolized mostly in the kidneys, and is highly bioavailable, so seems a waste to me.

I wish you could expand on that in laymens terms. And anyone else that could chime in too.

 

[ArmaniAK47]

I didn't know oral (via gumline, troche) anavar was made..

 

[d_rson]

Most oral AAS are metabolized in the liver, and the 17aa structure that makes them highly bioavailable causes stress on the liver as the liver tries to break the substance down. However, var is metabolized mostly in the kidneys and beause of this causes very little stress on the liver. Now, many UG pharms that produce var sometimes cut their var with other compounds, or fake their var entirely. Because of this, UG var can cause liver stress because of the other compounds it is cut with.

Now sublingual applications are designed to allow the substance to get to the blood stream directly - either to bypass the liver's first pass breakdown, or for other bioavailability reasons. However, since var doesn't hit the liver much, it's kinda a waste.

 

[Stocks_and_Steroids]

Most oral AAS are metabolized in the liver, and the 17aa structure that makes them highly bioavailable causes stress on the liver as the liver tries to break the substance down. However, var is metabolized mostly in the kidneys and beause of this causes very little stress on the liver. Now, many UG pharms that produce var sometimes cut their var with other compounds, or fake their var entirely. Because of this, UG var can cause liver stress because of the other compounds it is cut with.

Now sublingual applications are designed to allow the substance to get to the blood stream directly - either to bypass the liver's first pass breakdown, or for other bioavailability reasons. However, since var doesn't hit the liver much, it's kinda a waste.

So as I understand you liver toxicity is the same in Troche and pills. Which is almost none.
It seems you are saying they are both troche and pills are equally effective in strength. Assuming both are pharma grade?