Delayed emptying explains some of this, and not all of it
A single drug producing both constipation and diarrhoea looks contradictory until the motility data is read properly.
TheCompound Journal
Reporting on incretins, compounding & the peptide supply chain
Page 3 of 5 of this archive, newest first.
A single drug producing both constipation and diarrhoea looks contradictory until the motility data is read properly.
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.
Constipation is the most tractable of the effects and the most consistently under-managed.
What scintigraphy and breath-test studies established about emptying rate, and what they did not.
The ceiling varies severalfold between people, and nothing measurable at baseline predicts where it sits.
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 discontinuation figures are a floor, not an estimate: trial populations are supported in ways ordinary patients are not.
Pancreatitis is rare, was adjudicated in the outcome programmes, and did not show the imbalance early case reports suggested.
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.
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.
We set out the questions that distinguish a symptom to manage from a dose to change.
Dietary measures are widely recommended, plausible on mechanism, and supported mainly by observational data and clinical experience.
We give background rates alongside trial rates, because an event occurring during treatment is not thereby caused by it.
The clinical effect profile is almost fully predictable from where the receptor is expressed, which is unusual and useful.
Roughly four to seven per cent of trial participants discontinued for adverse events, mostly gastrointestinal, mostly during escalation. That is the empirical size of the…
What scintigraphy and breath-test studies established about emptying rate, and what they did not.
Roughly four to seven per cent of trial participants discontinued for adverse events, mostly gastrointestinal, mostly during escalation. That is the empirical size of the…
We separate what is supported, what is reasonable, and what is folklore, and we do not pretend the boundaries are crisp.
Dietary measures are widely recommended, plausible on mechanism, and supported mainly by observational data and clinical experience.
Roughly four to seven per cent of trial participants discontinued for adverse events, mostly gastrointestinal, mostly during escalation. That is the empirical size of the…