So with a lot of new transdermals popping up lately I have a few questions on them. I know absorption and potency will be at a guess vrs injectables. That being said should one assume full potency/absorb and run them mg/mg or ml/ml vrs inject/oral or do they need to be run slightly higher?
Second and especially for the transderm of orals where does liver toxicity come in? I know passing the liver the first time won't be a problem but I'm sure it will still cause some toxicity? Also if it reduces the toxicity of some orals could you stack compounds you normally shouldn't stack in the past?
Lastly is the only downside for transderms assuming a legit product the absorption vs using inject/oral? Or are there other factors I'm not seeing?
Second and especially for the transderm of orals where does liver toxicity come in? I know passing the liver the first time won't be a problem but I'm sure it will still cause some toxicity? Also if it reduces the toxicity of some orals could you stack compounds you normally shouldn't stack in the past?
Lastly is the only downside for transderms assuming a legit product the absorption vs using inject/oral? Or are there other factors I'm not seeing?