switched from 0.25mg to 15mg and the muscle cramps got better, not worse
Genuinely asking, not being difficult. Everyone in c/tapering repeats that pharmacology is important. I believe it, but I have never seen anyone show why, and when I search I get 4 threads of people agreeing with each other. Is there a paper? Is there a measurement? Or is this one of those things that is true because…
The receptor literature is interesting but rodent models do not scale linearly to human dosing.
Removed a chain here. The rule is one line long and it is not negotiable.
do not extrapolate rodent data to human dosing without saying so
Removed a chain here.
Yes, exactly this, and it is the bit that took me 9 weeks to accept.
central appetite signalling is real but people overweight it
receptor distribution matters, GLP-1 is not everywhere
do not extrapolate rodent data to human dosing without saying so