Every fortnight, every third week, seasonally: an unstudied practice
What the exposure arithmetic says about a fortnightly schedule, and where the arithmetic stops being informative.
TheCompound Journal
Reporting on incretins, compounding & the peptide supply chain
Page 13 of 14 of this archive, newest first.
What the exposure arithmetic says about a fortnightly schedule, and where the arithmetic stops being informative.
The evidence on stopping is better than the evidence on almost anything else in this field, because somebody deliberately randomised it.
A single drug producing both constipation and diarrhoea looks contradictory until the motility data is read properly.
Cost is the modal reason for discontinuation in every dataset we have seen, and it is absent from the clinical literature.
This is the single interaction with ordinary medical care that patients most need to disclose, and it is the one most often not asked about.
The ceiling varies severalfold between people, and nothing measurable at baseline predicts where it sits.
Why the reason for stopping changes what happens afterwards.
The convention — resume lower, re-escalate — is not caution. It follows directly from the elimination half-life.
The convention — resume lower, re-escalate — is not caution. It follows directly from the elimination half-life.
A survey of the maintenance evidence, which is shorter than the survey of the withdrawal evidence.
The features that should prompt urgent assessment, stated once and plainly.
The ceiling in this class is anatomical: the same receptor populations that suppress appetite provoke nausea, and they saturate together.
A survey of the maintenance evidence, which is shorter than the survey of the withdrawal evidence.
The dose-response curve in this class flattens near its top. That has direct consequences for whether the final rung is worth climbing.
What the published pharmacokinetics permit, what the labels state, and where the two diverge.
We give background rates alongside trial rates, because an event occurring during treatment is not thereby caused by it.
Almost nothing in the standard management repertoire has been tested in a randomised trial in this specific population. We say what is extrapolated and from where.
What the regulatory dossiers actually contain on dose selection is remarkably thin, and worth knowing before treating the ladder as settled science.
The ceiling in this class is anatomical: the same receptor populations that suppress appetite provoke nausea, and they saturate together.
A supply interruption is a discontinuation with no notice, no taper and no plan. That is a distinct clinical situation.