The interventions with trial support, and the much longer list without
The intervention with the clearest evidence is the one nobody frames as an intervention: adjusting the dose.
TheCompound Journal
Reporting on incretins, compounding & the peptide supply chain
Page 5 of 6 of this archive, newest first.
The intervention with the clearest evidence is the one nobody frames as an intervention: adjusting the dose.
An effect is dose-limiting when it prevents adequate intake, prevents normal activity, or produces a risk of its own. Discomfort alone is not the test.
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.
The receptor populations that produce satiety and the ones that produce nausea overlap substantially. That is why the ceiling of this drug class is where it is, and it is…
Pancreatitis is rare, was adjudicated in the outcome programmes, and did not show the imbalance early case reports suggested.
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.
Pancreatitis is rare, was adjudicated in the outcome programmes, and did not show the imbalance early case reports suggested.
Almost every figure in circulation about tolerability comes from six publications. This is what they say.
We give background rates alongside trial rates, because an event occurring during treatment is not thereby caused by it.
We give background rates alongside trial rates, because an event occurring during treatment is not thereby caused by it.
The evidence is real, modest, and mostly retrospective. The guidance is correspondingly cautious and has been revised toward individualisation.
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 receptor populations that produce satiety and the ones that produce nausea overlap substantially. That is why the ceiling of this drug class is where it is, and it is…
A small number of serious gastrointestinal events occur in people taking these drugs. Distinguishing them from the expected effect profile is the most consequential…
Trial adverse-event tables count episodes reported to a study nurse. They are the best data we have and they systematically under-record the mundane.
We set out the questions that distinguish a symptom to manage from a dose to change.
Trial adverse-event tables count episodes reported to a study nurse. They are the best data we have and they systematically under-record the mundane.
A single drug producing both constipation and diarrhoea looks contradictory until the motility data is read properly.
A drug that delays gastric emptying complicates the assumption behind every fasting instruction in perioperative medicine. The professional bodies have moved twice on this…
Trial adverse-event tables count episodes reported to a study nurse. They are the best data we have and they systematically under-record the mundane.