Absolute vs Relative Risk
In my last commentary, one of several key things I am recommending that RFKjr fix in the FDA, is how they portray effectiveness (of drugs.
Vaccines, etc.) to the public. Currently, the effectiveness that is almost exclusively shown is relative risk. I am advocating that absolute risk be shown. I cited two important examples where others have (so far unsuccessfully) made a case for the same thing:
Example 1: This position is stated in an important FDA advisory publication. A key conclusion (see page 60) is that the public is: “unduly influenced when risk information is presented using a relative risk approach; this can result in suboptimal decisions. Thus, an absolute risk format should be used.”
Example 2: The CONSORT 2010 Statement —Updated Guidelines for Reporting Parallel Group Randomized Trials states: “… presentation of both absolute and relative effect sizes is recommended…”
Since statistics is over most people’s heads, several readers asked me to explain the difference. OK, here goes…
I’ll use COVID-19 vaccines as a telling example. I put together three tables (below) based on two studies: here and here. (If you’d like further elaboration, here is an MD’s good discussion about those two studies.)
The first table shows the relative effectiveness of several popular COVID-19 vaccines:
Now most people would say that these are good numbers — and the ones above 90% are VERY good. That’s exactly what the FDA and the pharmaceutical companies want us to think… Now let’s fill out the next column: absolute risk…
Whoa! The absolute numbers are radically different — and MUCH less! What does this mean in the real world? A third variable might be the easiest to understand: how many people need to be treated (injected) to prevent ONE case of COVID-19?
This is called NNT (Number Needed to Treat = 1/ARR). Here is a study that delves into the merit of using NNT. The table below shows what NNT is for the same COVID-19 injections:
NOTE: The exact numbers here may be slightly different due to several variables, and are not important. What is significant is to see the extraordinary differences between Relative and Absolute Risk Reductions.
NNT Observation —
Let’s look at a real-world example… If citizens realized that roughly one hundred people had to be injected before ONE case of COVID-19 was prevented, would very many people have said:
“I’m willing to risk the known potentially serious side-effects of these injections, plus accept the fact that zero long-term studies have been completed, in the hopes that I’ll hit the jackpot and be the lucky one in 100± people who is prevented from getting COVID-19”?
The answer to that is why the FDA (and pharmaceutical companies) emphasize the Relative effectiveness number.
An Even Better Analysis —
Some very smart people said let’s take the NNT data one step further — and add the treatment cost to it! In other words, if two treatments have the same NNT, but one costs 10 times the other, shouldn’t we factor that in? Look at this fabulous COVID-19 table:
Compare two COVID-19 early oral treatment competitors: Ivermectin and Paxlovid. To get the same end result (save one life from COVID-19) we can spend $26 for Ivermectin or $206,705 for Paxlovid… Note also that cost and impacts of side-effects are not taken into account here.
The side-effects for taking Ivermectin are very low, while the potential side-effects for Paxlovid are relatively high. In other words, the cost difference between Ivermectin and Paxlovid is likely MUCH more that what is shown in this table!
Takeaway —
My recommendation to RFKjr is that (as a minimum) BOTH Relative and Absolute numbers should be prominently displayed, as well as NNT. This is not some academic matter, as it has GREAT bearing on assuring that Americans are able to make an informed consent when they agree to an injection or to take a drug. Without the facts, we are severely handicapped in being a critical thinker.
PS — Here is an excellent two minute video that explains the difference between Absolute and Relative Risk reduction…
PPS — Just like here, there are more detailed explanations for each of the other 15± recommendations I made for RFKjr re the FDA and its EUA and Approval processes. Also just like here, the other recommendations make good medical and scientific sense.
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Doesn’t risk depend on the individual? Isn’t that why there are side effects that may, or may not occur, sometimes causing death?
How does one account for that in the real world?
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Seriously
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The pharmaceutical industry Relies on this inability to know ‘absolute risk’…because we are all individuals, and that risk changes due to genetics, environment, diet, individual immune systems, for each and every human injected. So they make up numbers, propaganda to get pop to comply…and then have plausible deniability in the court of law because there’s no ABSOLUTE PROOF that their drugs have caused any individual illness, death. It called ‘smoke and mirrors’ and its been used by all snake oil salesmen for millenia. Consider that the swine vx was pulled after 50 people died in 2009…and look what’s happening now. All moral obligation on the part of pharmaceutical & medical establishment has eroded to non-existance in the name of capitalism gone rogue
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