matt21irby21
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Basically just wanting to know how harsh transdermals are on your liver compared to the oral version. like dermatren vs oral tren. I've done quite a bit of googling but no one seems to talk about it.
transdermals avoid the first pass of the liver. However the compound used will have a substantial impact.Basically just wanting to know how harsh transdermals are on your liver compared to the oral version. like dermatren vs oral tren. I've done quite a bit of googling but no one seems to talk about it.
very very true. The first bypass may help but they're in no means completely side free. I have had ast and alt levels 3-4x the above normal range. After that scare I have been very cautious of the compounds I used. tbh have stayed away from Ph's other than 1-Andro for a while now.It's more specific to the particular drug, not the delivery method.
what were you running? Do you have evidence that it was the carrier and not the compound or is this just your own conclusion?they still put stress on the liver. And it is probably some of the transdermal carriers that do more of the harm the the PH's themselves.... I just got done running a cycle with transdermals and despite using Tudca @ 500mg a day and also running Damage Control too, my Alt/Ast enzymes were quite elevated. I did pre and post bloodwork. Pre bloodwork they were within normal range, post Alt was 3 times the limit and Ast was about 50% over limit. Though Bilirubin was within range in the pre and post.
Not sure how the carrier would be hepatotoxic Vujade. Would bet money it was instead the steroid you were using.they still put stress on the liver. And it is probably some of the transdermal carriers that do more of the harm the the PH's themselves.... I just got done running a cycle with transdermals and despite using Tudca @ 500mg a day and also running Damage Control too, my Alt/Ast enzymes were quite elevated. I did pre and post bloodwork. Pre bloodwork they were within normal range, post Alt was 3 times the limit and Ast was about 50% over limit. Though Bilirubin was within range in the pre and post.
No I don't have evidence of such. I just made an educated guess about this because of the fact that some transdermal carrierswhat were you running? Do you have evidence that it was the carrier and not the compound or is this just your own conclusion?
Your probably correct, like I said in my reply above, it was more of an educated guess more then anything.Not sure how the carrier would be hepatotoxic Vujade. Would bet money it was instead the steroid you were using.
Three times the normal range upper limit is worthy of concern although it's nice to see your Bilirubin levels were maintained.
Given the fact you were also using decent ancillary support (provided it was legit) with liver protective attributes makes this theory more logical.
In addition to this, you may innately just be a poor metabolizer of hepatotoxic compounds. Some of us just aren't as lucky in this department.
Perhaps consider double (or tripling when warranted) your dose of the TUDCA next time as an added layer of protection.
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