The arithmetic of a step: what doubling a dose actually asks of you
We work the arithmetic out in full, because it is arithmetic and it is short.
TheCompound Journal
Reporting on incretins, compounding & the peptide supply chain
Page 5 of 18 of this archive, newest first.
We work the arithmetic out in full, because it is arithmetic and it is short.
What the trials measured, which in the case of micronutrients is very little.
A flag is a probability statement about a population. It is not a statement about the person holding the printout.
The published ladder exists because a protocol needed a single number. Practice has never followed it exactly, and the regulatory file never assumed it would.
A substantial proportion of the abnormal results generated during rapid weight loss are consequences of the weight loss rather than findings about the person.
Why the reason for stopping changes what happens afterwards.
Two withdrawal-design trials tell us what happens when treatment stops. Neither tells us what the lowest effective maintenance dose is.
The assay is not the problem. The interpretation of a lagging integral as a current measurement is the problem.
The dose-response curve in this class flattens near its top. That has direct consequences for whether the final rung is worth climbing.
The instrument determines the answer more than the drug does, and the trade quotes the answer without naming the instrument.
A plausible mechanism, a measurable change, and no outcome data. This is what an open question looks like.
What was pre-specified, what was exploratory, and what was calculated afterwards by people who did not run the trial.
What the labels permit, what clinicians do, and the size of the gap between them.
Mass and function are different endpoints and training affects them differently. Most coverage treats them as one.
A supply interruption is a discontinuation with no notice, no taper and no plan. That is a distinct clinical situation.
An accumulation model, drawn from published parameters, with its assumptions stated.
Reduced intake is a plausible mechanism for deficiency. Reduced absorption is not, and the two are conflated in most of the advice.
The class is described as though every molecule in it did the same thing. At the receptor, they demonstrably do not.
A substudy powered to describe a mean is not a substudy powered to detect a clinically meaningful individual change.
The evidence on stopping is better than the evidence on almost anything else in this field, because somebody deliberately randomised it.