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ForumsPublic SquareCommunity poll: What medication are you currently on? — March 2026

Community poll: What medication are you currently on? — March 2026

PharmD_Rodriguez Tue, Sep 2, 2025 at 2:58 PM 10 replies 1,256 viewsPage 1 of 2
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PharmD_Rodriguez
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Sep 2, 2025 at 2:58 PM#1

Collecting this in one place because it comes up every few weeks and the answer is always assembled from scratch. It is about the trial evidence, and it is deliberately narrow — everything I am not confident about is marked as such.

What is actually established

The gap between trial results and real-world results is consistent and it is not fraud. Trial participants get titration by protocol, scheduled contact, free drug and dietetic support; removing that infrastructure costs a few percentage points every time it has been measured. When your own curve sits below the published mean, that is the likeliest explanation before anything about you or your material.

The condition it depends on

Subgroup analyses deserve particular suspicion. With enough subgroups something is significant by chance, and pre-registered subgroups are a different animal from ones found afterwards.

The practical version

A quick sanity check on any figure quoted here: is it mean or median, is it intention-to-treat or completers, and what was the comparator. Three questions, and they resolve most disagreements in these threads.

What I am not sure about

What I actually want to know is how to read a result like this without either dismissing it or over-reading it, since the summaries all read like press releases. I have searched first, so if this is covered somewhere point me at it and I will read it.

— PharmD_Rodriguez · corrections welcome and will be edited into this post with credit
21 16paul_denver, TinaHashiRN, robert_kc and 18 others
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PharmacoVig_BOS
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Sep 2, 2025 at 3:32 PM#2
PharmD_Rodriguez said:
The gap between trial results and real-world results is consistent and it is not fraud.

That is correct as far as it goes, and here is where it stops going. Read four things before the headline number. The population, because trial populations are selected and supported in ways that real cohorts are not. The comparator, because "better than placebo" and "better than the current standard" are different claims and get reported identically. The primary endpoint as pre-registered, because a secondary endpoint promoted after the fact is a hypothesis rather than a finding. And the completion rate, because a large effect in the half of participants who finished is a different result from a large effect in everybody enrolled.

Last edited: Sep 2, 2025 at 6:32 PM
20 15Dr.GutHealth, amsterdam_pete, LondonLisa and 17 others
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Dr.RaviCardio
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Sep 2, 2025 at 4:06 PM#3
PharmD_Rodriguez said:
The gap between trial results and real-world results is consistent and it is not fraud.

I read this differently from PharmD_Rodriguez, on substance rather than tone. I would add the less popular caveat: these trial populations under-represented several groups, older adults and the highest BMI categories among them. The results probably generalise, and "probably" should be stated as an assumption rather than dropped.

19 14mark_tokyo, hans_munich, jason_sac26 and 16 others
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pat_auckland
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Sep 2, 2025 at 4:40 PM#4

Taking the question as asked, rather than the general version of it. Relative and absolute effects need reading together. A 20% relative reduction on a high baseline risk is a large absolute benefit; the same relative figure on a low baseline risk is a small one, and press summaries almost always quote the relative number because it is bigger.

Last edited: Sep 2, 2025 at 8:40 PM
18 13MeganSA_TX, LarryQC_SD, wanda_boise and 15 others
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pete_RVA
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Sep 2, 2025 at 7:49 PM#5
PharmacoVig_BOS said:
Read four things before the headline number.

Can confirm. Same sequence, different timescale.

Last edited: Sep 3, 2025 at 12:49 AM
17 12Dr.LeslieOBGYN, MikeNYC_runner and 14 others
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