I'm assuming that disclaimer is just to cover their rear end? Also, I was told .25 mg of the AI is needed every other day. The liquidex oral injector is in ML anyone have an easy number for me to go by?
Thank you
I'm assuming that disclaimer is just to cover their rear end? Also, I was told .25 mg of the AI is needed every other day. The liquidex oral injector is in ML anyone have an easy number for me to go by?
Thank you
They're research chemicals, for your Lab Rats. Get it?
Liquidex is not injectable, it's oral. What is an oral injectable?
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"It's human nature in a 'more is better' society full of a younger generation that expects instant gratification, then complain when they don't get it. The problem will get far worse before it gets better". ~ kelkel
hahahahaso is .25 ml correct for our purposes?
.25 ml =.25mg
Thanks captain!
is arimidex (liquidex) not a schedule III drug? Is that how they are able to sell legit stuff?
You need to understand the drug discovery process. Any drug or bio similar (liquidex in this case) needs to apply for an IND and complete at least two phases of testing in humans to be granted an NDA for use in humans.Originally Posted by porter321
Drugs NOT approved for human use by the FDA, EU, or any other regulatory body must bare the disclosure, "not approved for human consumption".
and so why can't they just do this same thing for the rest of the anabolic steroids? say "not for human consumption?"
In many countries, steroids are illegal. SERMs and AIs are not and are used for therapeutic value and off label use (in our cases). Any company is free to develop and manufacturer but efficacy and safety claims for bioequivalent or biosimilar drugs (Ar-r would fit the latter category) can NOT be made until an NDA is issued by the FDA (or appropriate regulatory agency). Penalties for doing so prior to regulatory approval carry significant penalties under FDA regulations, Federal Claims statutes, as well as incarceration.Originally Posted by porter321
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