Tag Archives: weight-loss

NICE and Wegovy – so much that cannot be seen

[Part two of a review on the National Institute for Health and Care Excellence (NICE). Which approved Wegovy (semaglutide) for use in preventing CV disease].

Stripping it down to basics, the key messages from the NICE report were:

You may have noticed three little black boxes. Yes, redacted, redacted, and … yes, well, redacted once more. We minions are not allowed to know the [newly negotiated] cost of Wegovy for the NHS. Nor the number of QALYs (Quality Adjusted Life Years) it provides. Nor the number of added life years. And very little else either.

[A QALY represents one, additional, year of perfect health. Or two years of additional health at 50% perfect health etc. NICE dodges and dives to ensure no-one really knows the exact figure. But normally, they will recommend a healthcare intervention that cost less than (approx.) £30K. per QALY. Range £25 – 35K (~$30 – 40K). These figures were plucked from thin air in the first place, in case you are wondering].

The only important thing we are allowed to know it seems, is that the cost per additional QALY is £14,702. This is within the range that NICE consider acceptable for approval. The lower the better. I find this to be an incredibly precise figure. Are they sure it was £14,702 and not, perhaps, £14,703?

You know what I think. I think it is impossible to be this precise. In fact, I don’t think… I know. When I see a figure like this, my antennae start to twitch. ‘Dr Watson, things are not what they may seem. The game is afoot’

The first problem to confront here is that NICE won’t let anyone see the data they are using to calculate a QALY. Which does make it rather tricky to check their homework.

[—] x [—] ÷ [—]/ [—] = £14,702 per QALY

Is this correct? Well, it could be. If you would allow me to see what [—] or [—] or [—] or [—] might be. [My redacted equation used for illustrative purposed only]

Yes, I did look up the cost of Wegovy on the BNF (British National Formulary) website. Which usually has all has information you need on medications, formulations, indications….and cost.  However, it is made clear in the NICE document that a completely different price was used their calculation. What price?

The closest I could get to a possible answer was on page eighteen, where they talk about a maintenance dose of Wegovy at £175.80 per pack. In this case, a pack consists of four pre-filled pens. A one-month supply.

My immediate problem is that this formulation does not appear to exist in the British National Formulary BNF, and it does not appear to represent anything like the negotiated price either? I am unsure where this maintenance dose, and cost, comes from. But this was stated in the NICE document:

List price and average course of treatment – maintenance: ‘2.4 mg presentation: £175.80 per pack. Each pack contains 1 pre-filled pen of 4 x 0.75 ml doses. Each dose contains 2.4 mg of semaglutide.’

Which is considerably cheaper than the BNF listed price of £73.25 a week. But I am not entirely sure why £175.80 was even mentioned. If it is not the figure being used to calculate cost per QALY.

In their defence, if this can be considered a defence, NICE states that Novo-Nordisk have done a deal with the NHS to provide Wegovy at a discount. And, as you can see on pages 425/6 of the report, this price has been decreed to be utterly confidential. On pain of death? 1

It is important to ensure that the current net price remains confidential in all documentation until such a time that price confidentiality is formally removed.’

Formally removed …. by whom, exactly? Hmmmm …. This is commercially sensitive data dontcha know. I imagine the very gates of hell would be opened if a pharmaceutical company allowed the lumpen proletariat to know how much they were being charged. Cry havoc and let loose the dogs of war.

And yet, what is that noise, in the distance? I think I hear pitiful cries and wailing, as tens of billions of dollars in profit slips between their bony fingers. The CEO’s bonus drops from fifty million to twenty-five million. My heart bleeds for them. Or maybe not.

Looking at this from a different direction we, the people, do actually pay for the drugs out of our taxes. Would the world of pharmaceutical marketing really implode if we were ever to learn how much they were charging us.

Moving on. If you do try to find out about the clinical outcomes, such as causes of death, you cannot see them either. See table 17. Which I mentioned in the last blog.

I really would like to know what is in these black boxes. Including the information on what, for example, is an ‘undetermined’ cause of death. And who decides if it can be considered undetermined, or not?

As a GP I would never be allowed to write ‘undetermined cause’ on a death certificate. Had I done so, the coroner would have given me a right earful. ‘Cause of death, um let me think … sorry. Beats me. I’ll let you decide.’ Bong! How many of these mysterious undetermined causes of death were there? No idea.

Although, the report does confirm that in SELECT, the one trial they used to create their report, they did say the following.

‘..in SELECT, deaths of undetermined cause were presumed to be CV deaths.’

Say what … You may wish to read that statement again and wonder at how this approach can possibly be justified. And if you do find some way of justifying it, please let me know.

Currently, I see it purely and simply as a way of inflating cardiovascular death figures, in order to reach statistical significance for CV deaths. I wouldn’t, of course, dream of using the word fraud …. but you know. Not sure what other word best fits. Suggestions welcome.

Why the data are hidden

I can understand why a pharmaceutical company would work hard to ensure their competitors don’t know about any financial deal they struck with the NHS. Perish the thought there might be some competition allowed.  A bit of market forces at work.

Company B:  ‘Novo Nordisk are selling drug x, for Y. We’ll sell ours for less.’

NICE:           ‘How very dare you. There will be no grubby competition in our world. It might save the taxpayers money.’ [As would getting rid of NICE – just a little daydream of mine]

But keeping clinical outcomes a secret? That’s a different level. How can it be justified? One possible answer although, once again, I feel this represents a feeble excuse rather than any sort of justification, is as follows. If you have the time and inclination, you could reverse calculate the cost per QALY figure from the information in the report. Then you would know the discounted price.

And a long and thankless task that would be. Although I am sure company B would throw the necessary time and resources to throw at it. Pharma companies employ entire departments to do this sort of stuff. But you are not going to get very far if you can’t see the data they used. As NICE confirmed, on page something or other:

The use of the list price in the EAG report, when paired with the results reported in the CS allows back calculation of the confidential discount used in the CS.

And so, we must, just, trust … NICE? Why bother to produce a report at all, if it going to be as pointless and uninformative as this. They might as well have just stamped ‘Top Secret’ on it. ‘Contents not to be made public for thirty years, by order of HM Govt.

In case you think page 74 was the only one with redactions. Below is figure 13. Page 88. [There are hundreds of redactions all over the place, but showing black box after black box may not be terribly interesting].

And if you want to know about Serious Adverse events (SAEs). Here you go. Page 109.

The company wrote the damned report anyway.

And, just in case you think NICE did the grunt work on this. Think again. The main report was put together by Novo Nordisk all by their clever little selves. It was called the Company Submission (CS).

It is not until you reach page 191 of the NICE report that you get anything that is actually written by NICE. Sadly, it is rather disappointing. Eighteen pages of guff which are all about process, and nothing to do with anything of interest, or importance.

Then some more guff about various stakeholders and conflicts of interest, blah, blah.

So, what did NICE actually do? You could say they simply reached for a great big rubber stamp, with the word ‘approved’ written on it. Bosh! Job done. £4.5Bn down the drain? Maybe, maybe not. I am leaning towards … certainly.

As far as I can see, they made a few ineffectual noises about a few issues, then scuttled off into the night. The cost per QALY in the NICE report remained exactly as calculated by Novo Nordisk. Not a penny more, not a penny less.

Below is one of the questions asked by NICE, and includes the answer – if that is what it can be called – from Novo Nordisk. You may, or may not, enjoy this. To do so, you will probably have to read it several times to work out what the bleeding hell they are saying.

C3. Priority question. Please clarify whether the deaths described as “CV death” and “undetermined cause of death” in CS, Table 17 are all cardiovascular deaths (as in the SELECT clinical trial report, Tables 11-14).

In the SELECT CSR, a distinction is made between “CV death” (including both “cardiovascular death” and “death of undetermined causes”) and “cardiovascular death” (written out fully). The former is also the definition for confirmatory endpoints. The CS used the abbreviation “CV” for “cardiovascular” throughout, therefore the distinction between “CV death” and “cardiovascular death”, e.g. in Tables 15 and 17 of the CS, was not as clear as in the SELECT CSR. Analyses of CV death in the economic evaluation are also aligned to the CSR definition of “EAC*-confirmed CV death”. Please note that further details on Deaths of undetermined cause are provided in Section 11.2.3 of the SELECT CSR.

*An EAC, by the way, is an endpoint adjudication committee (perhaps more on this ridiculousness later) and a CSR is a Clinical Study Report.

You may wonder why I find clinical trial reports unintentionally hilarious. In a grim sort of, banging my head against the desk, sort of a way.

Somehow or another, CV …which is shorthand for ‘cardiovascular’ (in every paper I have ever read in this area) does not mean the same as cardiovascular when the word is written out in full. Thus, a CV death and cardiovascular death are not remotely the same thing. ‘Oh, no, not at all. How silly of you to think they might be.’

‘Contrariwise,’ continued Tweedledee, “if it was so, it might be; and if it were so, it would be; but as it isn’t, it ain’t. That’s logic.”

You know, people actually write this stuff down on paper and don’t shrivel up into a little desiccated ball of burning shame. They also manage the mental gymnastics that allow them to decide that an undetermined cause of death is the same thing as a CV death. Or would that be a cardiovascular death. Or is an undetermined CV death a completely different thing altogether. Who, bloody, knows.

Why is a raven like a writing desk?

Their main protection against any criticism is that no-one, other than a masochistic madman will ever, ever … ever read the entire NICE report. Certainly not any journalist – or doctor. Or any fully functioning human being – with a life.

Even if they do, it is highly unlikely they will have any idea what it is they just read. Four hundred and sixty-six pages of [please insert insult of choice here]. I blame no-one for avoiding this report like the plague. Life is too short.

If anyone did read the report, they may inadvertently stumble across lines like this

‘The company included non-statistically significant results in the economic model.’

To be found on page 337 – of 466. If you can be bothered reading that far.

At which point I pretty much gave up. A man can only be expected to review so much of this before losing his ever-weakening grip on reality. Yes, gentle reader, they included non-significant results in their economic model. They might as well have added in hopes, dreams and aspirations and stuck on a little a meme for Hello Kitty at the side. And breathe.

As a compete coincidence, the choir I am in decided to rehearse The Boxer the other night. It contains these classic lines:

I have squandered my resistance
For a pocketful of mumbles
Such are promises
All lies and jest
Still a man hears what he wants to hear
And disregards the rest

It seemed to strike a chord for some reason. Although, to be frank, I wasn’t sure what a ‘mumble’ was. Google AI explains the line pretty well – I think.

This is a metaphor for empty, vague, and meaningless talk. “Mumbles” refers to words spoken so unclearly they are hard to understand. The narrator gave up his life’s energy, only to be paid in meaningless, deceitful words.

I need to stop here before I wander into territory that would definitely be considered libellous. If I haven’t already done so.

I will content myself with Drummond Rennie’s famous quote on clinical papers.

“There are scarcely any bars to eventual publication. There seems to be no study too fragmented, no hypothesis too trivial, no literature citation too biased or too egotistical, no design too warped, no methodology too bungled, no presentation of results too inaccurate, too obscure, and too contradictory, no analysis too self-serving, no argument too circular, no conclusions too trifling or too unjustified, and no grammar and syntax too offensive for a paper to end up in print.”

Next. What is an EAC and why…oh why.

1: committee-papers

WEGOVY THE WONDER DRUG

Lose weight, reduce the risk of CV disease – unless you are taking Wegovy?

[A tale of mystery and intrigue unfolds].

A lot of people have asked me about the weight loss drugs known as glucagon-like peptide-1 receptor agonists (GLP-1 agonists) e.g. Wegovy (semaglutide), or Mounjaro (tirzepatide). What do I think of them, are they any good? Should we be worried about adverse effects? Is it a good idea to take them?

Up to now I have rather stood on the sidelines, watching as these drugs have taken over the world. Various friends and colleagues have shrunk before my very eyes. Money has most certainly been made – in eye-watering amounts.

My general view, before having reviewed at the research in any great detail, is that GLP-1 agonists are certainly effective for weight loss. They also have benefits for the ‘metabolic syndrome.’ Sometimes called pre-diabetes, or insulin resistance, or … it has had many names. Reaven’s syndrome, syndrome X. It will probably have a few more in the future.

Metabolic syndrome is, essentially, a derangement of the metabolism which results in a whole set of abnormalities. The most mentioned ones include:

  • Raised insulin levels
  • Raised blood glucose levels
  • Raised blood pressure
  • High VLDL (triglycerides)
  • Low HDL (a.k.a. ‘good’ cholesterol – hollow laugh)
  • Central/abdominal obesity
  • Fatty liver (non-alcoholic fatty liver disease – it now has a different name).

They are all bad news. Each one is associated with an increased risk of cardiovascular disease … to a greater or lesser degree. If a drug can improve metabolic syndrome, you would certainly expect to see a reduction in strokes, heart attacks and other cardiovascular related disorders.

How significant a reduction? I have no idea. But if people want to lose weight, for whatever reason, and various other factors improve at the same time, then what’s not to like? Apart from problems with the gall bladder and also, it seems, the pancreas.

In reality, the main ‘what’s not to like’, is the cost. In the UK Wegovy, at whatever dose, costs £73.25 per injection, per week. The other GLP-1 agonists cost much the same 1.

Cost per person, per year = £3,809. Prescribe that for a million people and we are looking at £3,809,000,000.00p per year (£3.8Bn). Which represents two per cent of the entire NHS budget. And this would pay for ninety thousand nurses per year – for example.

On top of this, there is a dispensing fee of £1.46 – per month. Which would end up costing the NHS another seventy-five million a year. [A mere one thousand six hundred nurses]. I am not sure if I should continue to use nurses as a method of currency.

Senior NHS manager:         ‘That’s going to cost me five and a half nurses, are you mad…’

Nurse:                              ‘I am not just a number…

There is a reason for my one million figure. It was not plucked from thin air. Which is that the new NICE recommendations mean an extra 1.2 million people are now eligible for Wegovy on the NHS – rather than buying it themselves. Potential cost £4.5Bn/year.

Recent NICE guidance (National Institute for Health and Care Excellence) 2

I must say that my relative disinterest in Wegovy (semaglutide) changed when NICE recommended that it should now be offered to: ‘People who have had a heart attack, stroke, or serious circulation problem in their legs, and who also carry excess weight.’ Excess weight defined as a BMI above twenty-seven. This recommendation came about because:

‘Evidence from a clinical trial shows the injection reduces the risk of a heart attack, stroke, or cardiovascular death. Importantly, this benefit was seen early in the clinical trial, before significant weight loss occurred, suggesting the drug works directly on the heart and blood vessels, not just through weight loss.’

Suggesting … a word that does a lot of heavy lifting in this, and many other clinical trials. ‘Suggesting’ is both vague, and yet strangely powerful. Hinting at great mysterious powers, without the need for any evidence, or even a mode of action. Or, it seems, any further research on the matter.

In this case, it also shoves a significant problem under the carpet. How can Wegovy show benefit on cardiovascular disease … before weight loss occurs? It is widely believed that weight loss itself causes the improvement in metabolic syndrome. Followed by improvement in CV disease. But …

Below is a graph from, ‘a clinical trial’. The one NICE use to make its recommendation. It was called SELECT by the way.3 The graph demonstrates weight loss on placebo, and also weight loss on Wegovy, and the relationship with major adverse cardiovascular events (MACE). CV disease to you and me.

There are four lines. Those who lost more than 5% of their weight, and those who lost less than 5% of their weight – for both placebo and Wegovy. I found it extremely puzzling, and I do like a puzzle.

What this graph shows is two things.

  • On placebo, the more weight you lose the greater your risk of CV disease – top two dotted lines
  • On Wegovy, the degree of weight loss was not associated with CV disease, at all – bottom two lines, that look stuck together.

Now that is interesting. Well, it interested me. To quote Isaac Asimov, the most exciting phrase in science is not “Eureka!” but “That’s funny …” Unexpected findings are the most exciting scientific discoveries of all.

I did write to one of the authors of paper about this, and other issues. The response to the specific question on MACE, and weight loss on placebo was:

‘The relationship between weight loss magnitude and CV benefit is indeed quite complicated, with adiposity changes likely only mediating a minority of CV benefit.’

Quite complicated? The researchers did not start off this study thinking that obesity would have zero effect on CV disease – or that you might even be looking at a reverse effect. As the paper itself states in the introduction, which sort of covers the rationale for the study.:

‘Overweight and obesity are independently associated with an increased risk of cardiovascular events…

And:

‘… the concept of treating obesity to reduce the risk of cardiovascular complications has been hampered by the lack of evidence from trials indicating that lifestyle or pharmacologic interventions for overweight or obesity improve cardiovascular outcomes.’

In other words, they set out to discover if reducing ‘obesity’ would improve cardiovascular outcomes – in isolation. In effect, this was what they were trying to prove. You could argue they managed to prove the exact opposite.

The problem they were faced with

At this point everyone involved with this trial had just run into a tricky problem. I am certain they wanted to say, something like … “Wegovy reduced weight by around fifteen per cent – on average. And this reduction in weight led to the expected reduction in the risk of cardiovascular disease.” Nice and simple, and reinforcing what everyone thought they already knew.

But the evidence, at first sight, and probably at second sight, contradicted their argument … terms and conditions apply. With Wegovy, weight loss and risk were unrelated. By which I mean that greater weight loss had no effect on CV outcomes. However, with placebo, greater weight loss increased CV risk. The plot thickens.

Now, I have known for many years that a BMI of around twenty-seven is associated with the lowest mortality rate – in the majority of studies. I wrote about it this in my book Doctoring Data, which caused a few people to explode in disbelief, and anger. How very dare I use facts to contradict things they know to be correct.

Just to check this hadn’t changed recently I asked Google AI and got this answer:

‘Recent studies suggest that in modern cohorts (2003–2013), a Body Mass Index (BMI) of 27.0 is associated with the lowest all-cause mortality risk, shifting upward from the previously accepted optimal range of 23–24. This range, often classified as “overweight” (25–29.9), showed the lowest mortality rate, suggesting a shift in what is considered the healthiest weight.’

Despite this, a BMI of 27 is still defined as overweight, and thus unhealthy. I think this will never change. At least not in my lifetime. To quote Google AI again.

While some data points to 27 as optimal, conventional guidelines from the World Health Organization and other groups still technically recommend a “healthy” BMI range of 18.5–24.9.

Some data? They actually mean, the overwhelming majority of data. ‘Don’t confuse me with facts – my mind it already made up.’ I also like the use of the phrase technically recommend…. Which means what? Ah, I do love a weasel word or two, used to muddy the waters. You either recommend something, or you don’t. Or to be a little more assertive, you shut up.

So, could this study have simply proved that if you lower the BMI below twenty-seven, the mortality rate goes up?  As per the data on obesity. That is, of course, a possible answer. However, it was not an answer that anyone wished to contemplate.

New sales pitch for Wegovy: ‘Please don’t try to lower your BMI below 27, or you are more likely to die.’

I can’t see that going down a storm with the Novo Nordisk board of directors. Half your market gone, overnight.

In truth, after looking at this graph for about two seconds, I knew exactly and precisely what was going to happen. The form of words that would be used, and why. Not because I am a super-genius. Simply because I have seen an almost identical anomaly before. And the tactics brought to bear in order to dismiss it.

Reverse/inverse causality.

I do love causality. And I especially love it when you turn causality upside down and inside out, then stomp it to death. It happened many years ago with LDL cholesterol. To quote Google AI again – because it is very good at summarizing stuff like this, and saves me the effort of thinking what to write:

‘Reverse causality regarding LDL cholesterol occurs when an underlying disease (like cancer, infection, or malnutrition) lowers a patient’s LDL-C levels, creating a false appearance that low LDL causes the illness, rather than the disease, causing low LDL. While high LDL-C is a validated risk factor for cardiovascular disease, very low LDL-C levels in some epidemiological studies correlate with higher all-cause mortality, often attributed to this hidden disease process rather than a causal effect of low cholesterol.’

It’s a seductive argument and widely believed. In simplest form it goes like this. The reason why people (over about 65) with low LDL are more likely to die is because they have an underlying ‘hidden’ disease which both lowers the LDL and also kills them.

Huzzah, the low LDL is not a problem – how could it possibly be, when we absolutely know high LDL is dangerous and must be lowered to the greatest degree possible. Phew. Hidden diseases are, of course, remarkably convenient for this argument. After all, you can hardly be expected to demonstrate a disease that is hidden, can you? It is ‘The cat who wasn’t there.’

When I say that this explanation is widely believed, I mean it is universally believed. And with the greatest fervour by those whose interests it best serves so to do. A few of us looked at this issue a few years back in our paper: Lack of an association or an inverse association between low-density-lipoprotein cholesterol and mortality in the elderly: a systematic review.4

Our findings:

‘A common argument to explain why low lipid values are associated with an increased mortality is inverse causation, meaning that serious diseases cause low cholesterol. However, this is not a likely explanation, because in five of the studies in (table 1) terminal disease and mortality during the first years of observation were excluded. In spite of that, three of them showed that the highest mortality was seen among those with the lowest initial LDL-C with statistical significance.’

People believe what they want I suppose. The reverse causality argument is essentially a defense created to discount an extremely significant contradiction to the LDL hypothesis. Lift that carpet and sweep … problem gone. ‘Lump, under the carpet … I think you are seriously mistaken young man.’

Thus, it came as no surprise to me to find that that the exact same argument was going to be used to explain away the data from the SELECT trial. The explanation I received from one of the authors was that:

‘The highest MACE [major cardiovascular adverse events] rate in the placebo patients losing the most weight likely relates to underlying comorbidities associated with weight loss.’ 

Yup, it’s the old reverse causality argument again. Care to say what these underlying comorbidities might be? Did you look for them, did you find them … Ah, no. Despite my scepticism, the reverse causality argument could still be true, maybe, perhaps – benefit of doubt given.

However, as the SELECT trial was randomized you would expect to see the same number of people with ‘underlying co-morbidities’ driving their ‘increased co-morbidity related weight loss’ in the Wegovy arm. But you didn’t, Here, weight loss and CV risk were locked together.

What is going on? This quote from the GP Magazine Pulse nicely summarizes the next immunizing tactic.

‘Presenting the evidence to NICE, pharmaceutical company Novo Nordisk said the cardiovascular benefit was seen early in the clinical trial, before significant weight loss occurred. 5’

The press releases made the general statement(s) that:

‘Evidence suggested the reduction in cardiovascular risk was observed before significant weight loss occurred, indicating that semaglutide may act directly on the heart and blood vessels.’

Aha, Wegovyis protecting against CV risk via a direct effect on blood vessels. So, we can entirely ignore the entire weight loss argument? Phew, move on. Throw in a few words such as likely, and may and suggests, and even suggesting and … problem solved.

I suppose this direct effect could exist. However, I think we should always be suspicious of made up, ad-hoc, hypotheses created for the sole purpose of sweeping aside findings you don’t like. Findings which just contradicted your rationale for doing the trial in the first place. And could seriously question the entire premise behind weight reduction, at the same time.

Final anomaly – for now

In truth, I don’t mind unexpected findings in clinical trials. In fact, I welcome them. They open channels for new thinking. However, I do not like to see anomalies brushed aside and forgotten about. In the graph below, you can see a major problem for the ‘underlying diseases’ argument. Also, the ‘Wegovy provided direct protection’ argument.

DEATH FROM CARDIOVASCULAR DISEASES

[over 48 months]

Grey line placebo, orange line Wegovy

Everyone in this trial had established CV disease, in some cases it was quite severe. In addition, the majority of those who died in this trial, died from a CV disease. You could argue [and I would], that any ‘hidden’ underlying disease would likely be cardiovascular in origin. Which would lead to an increased death rate from CV disease.

Now it is true that, at end of the trial, there were more CV deaths in the placebo arm. However, as you may have noticed, there is a strange phenomenon which lasts from about two years to three and a half years. Here, the mortality graphs converge before separating again.

If someone has an underlying disease that both lowers their weight and causes them to die …It seems highly unlikely that you would have to wait three and a half years for this effect to show up.

Furthermore, if Wegovy ‘may act directly on the heart and blood vessels,’ then why did benefits on cardiovascular death disappear for eighteen months, before reappearing again.

So what?

Yes, I have raised a number of issues here. Why?

First, I think this trial produced some fascinating results. None of which have been explored in the popular press, or the medical press. Or in the NICE report. Or, in fact, anywhere – that I have seen. The message has remained simple, and unchanging. Wegovy reduces weight and reduces the risk of cardiovascular death. Good job, message ends.

But the sky darkens with black swans, and there are anomalies flying all over the place. The arguments used to sweep them aside do not stack up. Primarily, reverse causality, and direct effects on heart and blood vessels.

So what… does it really matter. Wegovy does exactly what it says on the tin. It reduces weight, it reduces CV risk. [Although that risk reduction does disappear for a considerable amount of time, before reappearing which … well, you know]. That may be all we need to be told. It is certainly all you are ever going to be told. Don’t muddy the waters with the actual findings.

However, when I see anomalies, and hastily created ad-hoc hypothesis that exist only to explain things away, it does stimulate me to look deeper, and deeper. Because, to me, these represent warning signs that all is not well in the state of Denmark.

Are other important issues also being shoved under the carpet. What issues, and why? I will have a look at them next. In so far as this is possible. I say this because almost all the important data in the NICE report have been redacted and thus rather difficult to critique.

Here, from page 74.

No, you can’t scrape off the little black stickers to see what lies underneath. Commercially sensitive data, dontcha know. Why should we, the public, who fund NICE and who will pay for every single NHS prescription written for Wegovy, be allowed to see such things as … what it actually does. Our poor little brains would probably explode, or something.

1: https://bnf.nice.org.uk/drugs/semaglutide/medicinal-forms/

2: https://www.nice.org.uk/guidance/TA1152

3: https://www.nejm.org/doi/full/10.1056/NEJMoa2307563 It

4: https://bmjopen.bmj.com/content/6/6/e010401

5: https://www.pulsetoday.co.uk/news/clinical-areas/cardiovascular/nice-recommends-semaglutide-injections-to-prevent-heart-attack-and-stroke/