I'm saying when the first dose reaches peak bioavailability and peak side effects in 3 days, and the second reaches peak bioavailability almost immediately, you now have a potential peak of bioavailability higher than that reached by taking the same amount once week, when albumin blood concentrations are strong enough to quickly bind more of the drug at once.
This isn't like steroids you retards. Testosterone becomes bioavailable as the ester is broken off. You divide the dose to SLOW the rate of bioavailability in order to MINIMIZE PEAKS to minimize side effects like aromatization.
That's not how GLPs work. There is no ester to slow release. IT MUST BIND TO ALBUMIN, to slow its release over time. Three days after the first dose albumin concentration will be lower than it is at 7, leaving more of the hormone immediately available, CAUSING a spike, ironically, right at the time the first dose is peaking in bioavailability.
I used GLPs before you ever read a story about anyone in Hollywood using it, and I've seen countless people "top up" midweek thinking it wasn't strong enough, only to end up suffering sides worse than the cumulative dose would suggest. This is a case where for the purposes of peak level side effects, .50mg+.50mg in the same week didn't equal sides similar to 1mg once a week, but more like the effects you'd see going from .50mg to 2mg on a once a week schedule.
But just keep applying your "common sense" to this topic. Splitting the dose must reduce side effects, because that's how testosterone works right?