US agencies call for pause in Johnson & Johnson vaccine
bbc.co.uk
bbc.co.uk
Yesterday, Covid19 killed 8,803 people (according to worldometers).
We don't want anyone to die from vaccination, and we don't fully understand what the clotting issue is, so it probably makes sense to pause using J&J as long as the mRNA vaccines (Pfizer, Moderna) have not been implicated (which they haven't). OTOH, if this being in the news causes fewer people to get vaccinated, pausing it may be a mistake that will cause more overall deaths.
Now, your risk of dying either from vaccination or Covid19 depends on various demographic factors not accounted for in my math above. But, nonetheless, the risk of dying from the J&J vaccine is really, really, really tiny.
Like, if I knew there was a 0.00009% chance my car were going to explode every time I got in it and started it, I would not be at all nervous about starting my car everyday for the rest of my life. I'm way more likely, even accounting for my age demographic, to choke to death eating dinner tonight (5,051 deaths from choking in the U.S. in 2015 of which 2,848 were older than 74).
Edit: lifetime risk of car exploding assuming I start it every day for 50 years is about 1.6%. Okay, maybe I wouldn't play that game.
For people under 30, particularly women, the risk of blood clots from AZ is higher, while at the same time the risk from coronavirus infection is lower. When there are alternative vaccines available with no evidence of similar side effects, it makes sense to temporarily stop administering AZ/J&J to those groups to investigate if there are any risk factors we can use to predict and protect those who may be most vulnerable to side effects. (It has been suggested that young women on certain types of birth control are at highest risk of blood clots after AZ.)
That said, as some have pointed out, the risk of blood clots is still thought to be very low, even for women under 30, and anti-vax groups as well as the vaccine hesitant may see this news as a sign that it's not safe for anyone to take any vaccine. However, I don't think we as a society should actively try to conceal news or research about vaccine safety so that people don't worry. In my opinion, people have a right to know, and efforts to conceal concerning information often backfire, producing more public distrust.
I don’t think that’s accurate in this case. The type of vaccine that J&J released had up until months ago only ever been deployed in animals.
IIRC pigs had a problem with corona viruses that we solved”
The J&J is not a heap of dead virus like the common ones we have had forever. But a live harmless (we think) virus dolled up to look like Rona Corona.
No, there have been no previous live viruses that have been genetically modified to look like other viruses (embedding Covid spike proteins) injected in humans before three months ago in any scale.
We have treated animals with exactly this however, including pigs against piggy rona.
I recommend reading the whole post next time, not just stopping at “live virus”.
https://www.cancer.org/cancer/cancer-causes/infectious-agent...
It takes quite a long time to prove the link between a viral infection and a cancer that develops decades later, so it'll be a while before we know for sure.
There are other potential longer term side effects that at least seem to have some emerging data to back them up, which seem more concerning to me.
While this is not cancer, for those poor souls, a lifetime spent struggling to breathe is not much better.
I don't agree with the premise behind this reasoning, but I can see how it'd come about.
I had blood clots in my lungs last week a few days after getting the J&J vaccine. I'm an otherwise totally healthy man in my 30s, no preconditions. The hospital reported it to the vaccine reporting agency, which I assume is reviewing all this information.
I'm not sure if they considered my case when making this decision. My clots were different type than what these women experienced (pulmonary, not cerebral).
Of course vaccinating the public is extremely important right now. If the risks of clotting really are 1 in a million, it makes sense to re-instate it. I also think that's an obvious conclusion and the people working on this are well aware of the public health trade-off.
I suspect they are working with more information than what's in the press release, and its prudent to give them some time to work through it.
What is someone getting a vaccine as such is supposed to look for?
Eventually the pain was severe enough that I went to the ER.
Looking back, the shortness of breath was a key indicator. It wasn't that I was struggling to breathe or anything, but I felt like I couldn't take a big deep breath easily and that's not normal.
The pain would also get worse at night when I tried to lie down to go to sleep. I thought I had pulled a muscle in my back at first, but it was quite painful.
They then put me on pain meds and supplemental oxygen for a few days and watched me. The pain went away after a few days (I assume when the inflammation went down).
They didn’t actually treat the clots themselves. The body apparently does that itself over the course of a few weeks and months. There are invasive surgical ways to try to break them up but they felt I wasn’t bad enough to risk it since I could sit up and breathe on my own.
They checked my heart for tissue damage and thankfully didn’t find any. So now they’re doing a slew of tests to find the cause (genetics? Cancer? So far tests show cancer is unlikely).
Recovery has been good to be honest. I’m not really in pain. I do get out of breathe very easily but they say that’s normal and should go away in a few weeks as the clots dissipate. The lung damage should heal, I think.
The real danger from more clots to the brain or damaging the heart are prevented by the blood thinners, which are apparently highly effective. So I think I got lucky and I’m glad I went to the ER when I did.
But last week (would have been 3 weeks after shot) I awoke in the middle of the night with pretty a bad chest pain like you describe. Felt like it was in middle of my chest and was quite painful. I had to physically sit up in my bed for about 5 minutes hoping it would subside. I got up and got some water and hoped it didn't get worse as I started contemplating what I should do if it does.
I was so tired though I just propped myself up with pillows and slept sitting up against the headboard because laying down seemed to make it come back worse. I eventually fell asleep and when I woke for the day I still felt a small amount of pain still. Went about my day normally and it seemed to go away later in the day.
I would think I am out of the window by now after 4 weeks to which I am in any danger from what I'm reading on news sites? I've been the gym since that episode and have done cardio fine. My wife suggests I take some low-dose aspirin for next few days.
It went away after that night, he was fine for 3 weeks with no pain or issues, was working out fine, etc. and thought nothing of it.
Suddenly one night went from perfectly fine sleeping to suffering a major stroke due to a blood clot in his brain within a 10 minute period, unable to do anything himself to get help as he lost all motor skills.
He said in retrospect he wishes he had followed up with a doctor on the thing he thought was no longer an issue 3 weeks before.
There are genetic tests they can run, as well, such as to see if you might have factor V Leiden.
I would also not dismiss the nagging feeling in the back of your head that something doesn’t feel right. You know your body more than anyone.
But, IDK and I’m super skeptical they’re willing to halt vaccine and take this hit for 6 known cases. My guess is 6 deaths they’re willing to acknowledge and a few more cases that will come out.
But again, I know nothing and I would’ve expected their stock price to take a hit today.
Hope you get better soon.
So I think that's why they're telling people to watch for leg pain. I didn't have any issues with my legs, but it's apparently a common symptom to have pain and swelling there.
If we assume that only 5% of cases are being detected and reported correctly, then the numbers look quite different.
In comparison there have been over 2000 deaths reported (US, all vaccines). But death is not unusual and unless one can find a specific link to vaccination that number alone is not alarming. Sometimes we live with known risk, anaphylactic shocks e.g., because they are unavoidable and benefits outweigh risk. But we do what we can to mitigate such risk.
In summary the current pause is triggered by the particular type of clotting, not just any clotting. But your case should contribute to the overall evaluation of the likely cause and risk.
Make sure to never forget to take your blood thinning medicine. You absolutely must get the blood clots completely dissolved, and the blood thinner medicine is highly effective at getting rid of it, if you take it.
1 death. The other cases are severe blood clotting but still alive by my understanding.
That's literally one-in-6-million chance of death with regards to this blood-clotting issue. A vanishingly smaller chance than the 1-in-40,000 (or 150-in-6-million) a healthy young person has of dying of COVID19.
So 1 death, 5 severe reactions related to blood clotting. Definitely a cause of concern, but lets not overplay the stats here.
This just another "Trolley problem": 150-people (even youngsters) would die from COVID19 vs the 1-person who died from the J&J vaccine.
If we include the general population (instead of focusing on the youngest and healthiest of us): COVID19 mortality rate is 1%ish, or 60,000-people-per-6-million.
You have to multiply the IFR by the odds that the person gets COVID to begin with. In countries where there's no community transmission (Australia) or in countries where it's possible to kill the virus just by vaccinating the at-risk population combined with shut-downs, the multiplier should be pretty small. Even in countries that have handled it badly, it still might be only a 1/3 or 1/2 chance of catching it. So as a young healthy person my chances of dying from COVID are probably less than 1/100000.
I bring this up because I think it misses the actual point. Even if the vaccine had a 1/100000 chance of death or major complications, I would still take it. Because my life is not the only one that matters. Killing the virus is likely (in this country) to require most people who are physically capable (including the young) of taking the vaccine. My taking on a 1/100k risk with the vaccine vs a 1/100k risk without the vaccine is worth it, because for most other adults, the risk is much greater than 1/100k if the population doesn't get vaccinated.
Fortunately, I don't think pausing J&J is necessarily the wrong decision, even given the argument I just made. AFAIK it's the least common of the three vaccines, and so there should not be many "missing" vaccinations that result from the pause. The fact that taking a risk is justified does not mean that pointless risk is justified.
Walk-ins might be affected, though, but I'm not sure what percentage of the total daily vaccinations are walk-ins vs. appointments.
And as a sibling mentions, the general risk of dying from COVID-19 is not 150 in 6M, because the probability of getting (symptomatic) COVID-19 needs to be factored into that figure. I would not be surprised that if that probability drops to under 1 in 6M after accounting for that, though of course the symptomatic infection risk differs based on demographics.
One thing that I am worried about, though, is that this might make people trust all the vaccines less in general. My girlfriend and I had J&J appointments for this Friday; fortunately we were able to get a walk-in Moderna shot today, but the issues with the J&J vaccine did give her a little anxiety even about the Moderna vaccine. I think that (and worse) might be pretty common, and isn't unreasonable.
Would you want the chef at your local takeout to be vaccinated to 66.3% efficiency? or 94%?
Why was this vaccine even approved, instead of just having J&J produce the same vaccine Pfizer and Moderna are making, which would be in the best interest of the world? Is this some utterly idiotic capitalism bullshit that prevents J&J from making a 94% vaccine as well?
Why can't we just take $100B out of the $1T military budget, throw it at Pfizer and Moderna to shut up their patent lawyers, and then hand the formula to J&J to become a 3rd factory for a good 94% mRNA vaccine?
And then hand that formula to the rest of the world including Brazil, India, China, and other recent new COVID hotspots so that the virus doesn't boomerang back to the US in an evolved form?
At least that's what I would do if I was president.
https://www.vox.com/22311625/covid-19-vaccine-efficacy-johns...
A vaccinated person can have no symptoms of covid and still be spreading (This may or may not be true).
Folks are still studying how effective the vaccines are at preventing spread.
Aren't the efficacy numbers from the phase 3 trials based on giving periodic PCR tests to everyone that was participating in the trials? And not just based on people self-reporting symptoms?
It would be very surprising if there were a new kind of asymptomatic carrier that emerged only for people having taken certain vaccines in which they would never test positive on a PCR test but could still spread covid. The odds that this is how the vaccines work seems very small, relative to the number of times this argument that "we don't know yet" is getting repeated.
It just seems strange to me that so many people are hung up on pointing out that this small possibility is still a possibility. It seems more likely that this will drive more people to skip the vaccine, since they're being told they can't even go back to normal once vaccinated, than anything else.
For most trials, no. You have to look at each individual study, but most commonly, they only test after people show specific symptoms.
There's some additional data which indicates Pfizer and Moderna are likely to limit transmission, but from my understanding it's not as ironclad as the symptomatic cases data.
We're not at a stage yet when we can play favorites. It'll be a long time before we have the supply to prefer one over the other (except maybe in the US where there will be enough mRNA vaccines to go around).
https://blogs.sciencemag.org/pipeline/archives/2021/02/02/my...
Such a vaccine would also have two doses and require intense refrigeration which are the primary issues blocking it... additionally many of those jurisdictions might not accept a US vaccine. China, maybe, since they admitted their own vaccines aren't working super well. Russia doesn't have anything wrong with its vaccine but the Kremlin admitted no one is taking it, apparently because they don't believe in covid.
Despite what the press has reported, that's not really what happened. In a conference talk on vaccines, the head of China CDC made a general statement about what to do about "low vaccine efficacy." That's been blown up in the Western media into an "admission" that all Chinese vaccines supposedly have low efficacy.
It doesn't even make sense to talk about the efficacy of "Chinese vaccines." Chinese vaccines run the gamut, from inactivated whole virus to protein subunit to adenovirus vectors. There's even a Chinese partner to Biontech, which is going to manufacture the latter's mRNA vaccine.
That said, I'm smarting a bit (even though I understand why) that the fully vaccinated guidelines cover 2 weeks after J&J, while it's looking likely the mRNA vaccines give you better protection even 2 weeks after the first shot. (You really do want the second... the 6-month Moderna study shows you get about 10x the antibodies from the second one, which means the protection lasts much longer if nothing else.)
The J&J vaccine is marketed as a single-dose vaccine, unlike the others which all require two doses to reach their reported efficacy. Single-dose is a massive advantage which will greatly speed up vaccination progress, especially in developing countries.
And 66% seems pretty good for a single dose.
Exactly. There should be no place for vaccine profiteering, especially now that we have two extremely good vaccines. But in the interest of pharma profits, instead of cooperatively manufacturing the best vaccines, unburdened by patent hurdles, instead we have massive amounts of public funding going to pharma corps so that they can make profits off this medical crisis. Truly shameless.
See "Why you can't compare Covid-19 vaccines":
https://www.youtube.com/watch?v=K3odScka55A
You're welcome.
I bet if I went today he wouldn’t be so dismissive.
Typically they investigate with multiple tools - a CT scan, a D-Dimer blood test, and often an ultrasound to check blood flow in limbs etc.
This is the reason people lost trust in the medical community during COVID.
I understand the need for being cautious and for transparency. Actually, I would like to have even more transparency and actual scientific data and numbers from the news. That would help the public understand better why certain decisions are made.
(Maybe my main problem is just with mainstream press, not much with stopping vaccinations per se. I'd just like to know more and be told by politicians: we are listening to scientists, these are the data, this is how numbers compare to the incidence of other side effects for well known medicines and to the numbers of daily deaths and long term problems caused by COVID, and the decisions are taken because X > Y).
Here is a small problem with this that makes me also consider if I want to take a shot with AZ even if I registered for it months ago waiting for my place:
Before EU started discussing the issue with statistical signifiant number of cases of blood clots in vaccinated population UK Reported 5 cases of blot clots in vaccinated population.
After EU talked second time to suspend vaccination with AZ lo and behold UK discovered that it missed in previous months to report 25 more cases.
Now should I trust any of these agencies that they are telling the truth? I am starting not.
But I had a mild COVID and I am sure after experiencing those symptoms that I really want a vaccine. I am not willing to experience a reinfection.
Also I was able to get another appointment for Moderna vaccine next week. So I just have to spend another 4 weeks or so social distancing. It is better than developing blood clots, imo.
that we know of.
I suspect the lack of understanding about what is happening, and what other knock-on effects there might be is what is behind this.
If a wing falls off of one airplane in a million, we still stop and try to figure out what happened because as far as we know, wings are not supposed to fall off any airplanes, so there's something about the system we need to learn more about.
We don't have the same absolute understanding of mechanisms with vaccines. Therefore, I am not sure we can use this metaphore to suggest that it is the right choice in this terrible time to stop vaccinations, causing slowdowns to happen and scepticism to spread in the population that is bombarded by the press which creates an echo chamber repeating over and over superficial news.
I personally don't expect a vaccine, nor any medicine in general, to be supposed to have absolutely zero incidence of possible negative side effects.
We aren't stopping vaccinations. We are stopping this vaccine. For the moment. To gather more information. Which is precisely the kind of responsible behavior that we need, if we want people to be less skeptical of the vetting process for these vaccines.
>We don't have the same absolute understanding of mechanisms with vaccines.
Wouldn't this support more caution, not less?
>We don't have the same absolute understanding of mechanisms with vaccines.
Having even less knowledge about how vaccines and our immune systems work seems like reason to be even more cautious, not less cautious.
Especially considering the fact that autoimmune disorders have been on the rise for decades, and we don't know why.
Could it be that we are simply diagnosing them better?
Just throwing it out there as a plausible explanation since autoimmune disorders are commonly diagnosed based on a multitude of symptoms none of which definitely indicates an autoimmune disorder independently; similarly, I find it highly likely the rise in cancer diagnosis to be at least partially linked to better diagnostics too.
https://www.cdc.gov/ncbddd/dvt/features/blood-clot-risk.html
> Now, your risk of dying either from vaccination or Covid19 depends on various demographic factors
Your risk of dying, or other health injury, depends on your personal health factors specifically.
Demographic is the statistical data of a population.
1. https://www.cnbc.com/2021/04/13/blood-clots-more-likely-from...
I suspect that what's happening is that these institutions don't think in consequentialist point of view. They are not comfortable with diverting the trolley even if the math checks out.
Unless this is a repeat of AstraZeneca, where many were lamenting the interruption of vaccination and calculating the risk for the entire population of people injected with AZ. Meanwhile, in some countries, the risk of dying from the vaccine for young women was higher than the risk of dying from the virus.
After the concerns about AZ turned out to be justified and AZ being banned for certain age groups you'd think that people would get a clue about unconditional vaccine cheerleading.
Do you have a good source you'd recommend for this? I couldn't find this bit of info from the first few articles I skimmed.
> After the concerns about AZ turned out to be justified and AZ being banned for certain age groups you'd think that people would get a clue about unconditional vaccine cheerleading.
Who is unconditionally cheerleading which vaccines?
Women < 60 years: 10 deaths from covid-19 in total [0]. Four vaccine-related deaths were reported in young, relatively healthy women. Details on three of the vaccine-related deaths have been published [1]. One of the stories had been made public [2].
The astrazeneca vaccine was put on hold, if not, it's not hard to imagine the number of fatalities surpassing the number of covid-19-related deaths, even when ignoring comorbidities
[0] https://www.fhi.no/en/id/infectious-diseases/coronavirus/dai...
[1] https://www.nejm.org/doi/full/10.1056/NEJMoa2104882
[2] https://www.vg.no/nyheter/i/GaOr3l/monica-aafloey-hansen-54-...
Edit, please correct me if I'm wrong, it's very important that we don't spread false information regarding this.
Edit 2: There seems to be four, https://www.globaltimes.cn/page/202103/1219441.shtml
[0] https://www.nrk.no/innlandet/helsearbeider-pa-tynset-dode-ti...
It's much, much worse to kill someone with a vaccine than to allow that person to perhaps die of a virus.
Thankfully, in this case, sanity prevailed.
Don't all vaccines have some extremely low but nonzero probability of killing someone?
> It's intolerable that people die taking a prophylactic.
What do you think about airbags in cars?
The point here is simple. It's worse for someone to die of a vaccine than for someone to die of the coronavirus. How much worse is up for debate, but it's a significant factor and napkin math has to take that into account or it's morally bankrupt.
If there’s (hypothetical overly high numbers here) a 10% chance of dying from a disease or a 1% chance of dying from the vaccine from that disease, I want the vaccine and would like the freedom to do so. But if a new vaccine is coming out and soon after we see a 1% death rate from it, now I’m gonna want to hold off and take my chances with the disease because that 1% may turn out to be as high as or greater than 10% down the track when more is known.
The main complexity here is just like the early days of coronavirus - until things have played out for a while you can’t have confidence about the extent of the harm and that’s true for both the disease (which we now have over a year of information about) and the vaccines (which we have a month or two of in-the-wild info so far).
My comment is more or less ridiculous, but I'd like to understand why an effective vaccine that is dangerous to a few people is different than peanuts, which are dangerous to a few people (many of whom discover this by consuming peanuts).
As someone else pointed out here, you're about as statistically likely to die in a car wreck on your way to get the vaccine than you are to have (not die from) a blood clot from it.
[0] https://www.beckershospitalreview.com/cardiology/blood-clots...
This was what I posted in this post about the European Medicines Agency acknowledging the AstraZeneca vaccine (which I was inoculated with) was linked to something never seen before: https://news.ycombinator.com/item?id=26725232
> "Zero surprises here. Both Norwegian and German research teams identified the /actual specific novel antibody/ that causes this /new previously unclassified syndrome/ that was effectively unheard of before the AstraZeneca COVID-19 vaccine existed. Also, both teams are phenomenally talented for identifying this antibody so quickly. Usually it is on “finding a needle in a haystack” level difficulty. BTW, I am probably going to get downvoted but I am definitely not an antivaxxer and I received the AZ vaccine as innoculation for COVID-19."
In both cases, the situation is clinically similar to Heparin-induced thrombocytopenia (HIT), although there are very distinct differences. It should not be used as a comparison.
This is a good peer-reviewed journal article on diagnosis and management [4]. This is another article describing the syndrome [5].
I should emphasize that the treatment that is used for this specific syndrome is extremely expensive: intravenous immunoglobulin. I personally take the same medication (immunoglobulin) subcutaneously (under-the-skin) twice per week, for 2 rare immune-mediated neurological diseases affecting my peripheral nervous system. I will require this medication for life. When I lived in the USA (I live in Croatia now), my medical insurance was paying $278,000/year for the medication, under contract. I am not talking about how much the medication was being billed for, which was way higher. So, you heard me right, my insurance paid $278,000/year for this type of medication.
[1] Here’s what we know about J&J’s vaccine and rare blood clots: https://www.latimes.com/science/story/2021-04-13/what-we-kno...
[2] ‘It’s a very special picture.’ Why vaccine safety experts put the brakes on AstraZeneca’s COVID-19 vaccine: https://www.sciencemag.org/news/2021/03/it-s-very-special-pi...
[3] Norwegian experts say deadly blood clots were caused by the AstraZeneca covid vaccine: https://sciencenorway.no/covid19/norwegian-experts-say-deadl...
[4] Diagnosis and Management of Vaccine-RelatedThrombosis following AstraZeneca COVID-19Vaccination: Guidance Statement from the GTH: https://zlmsg.ch/wp-content/uploads/2021/04/2021_Diagnosis-a...
[5] A Prothrombotic Thrombocytopenic Disorder Resembling Heparin-Induced Thrombocytopenia Following Coronavirus-19 Vaccination: https://www.researchsquare.com/article/rs-362354/v1
I think we would all be fascinated to hear first hand accounts from someone who's also experienced the abysmal US system.
What does your immunoglobulin cost in Croatia?
I also have a separate issue, Pectus Excavatum, a chest deformity that required me to undertake a fairly difficult surgery called the Nuss Procedure.
I think these two examples do a good job at demonstrating differences between Croatian an US healthcare payment systems. They are very different medical problems.
Diabetes is a chronic illness that requires constant management. I need to inject insulin multiple times a day and require other supplies such as sugar sensors, lancets, needles, and glucose strips. I have a brother who still lives in Croatia and also has Diabetes Type 1. Our treatment plans are almost identical. We take the same medications and need the same supplies.
Managing Diabetes in the US is fairly annoying and expensive. I'm lucky to work in tech which provides me with good pay and insurance but even then my expenses can go up to $200/mo. It is also difficult, sometimes impossible, to get insurance authorization for better insulins that are widely available in Europe. I am on Humalog, or sometimes Novolog, similar insulins but insurance companies only cover a single one, so you have to switch when you change insurances. Newer insulins such as Fiasp, Apidra, or Tresiba, which are newer, quicker to work, and overall "better" are almost impossible to get in the US. I tried multiple times and the insurance never gave me the authorization to use them.
My brother lives in Zagreb, Croatia. He's been a diabetic all of his life. He's using newer insulins such as Fiasp and Tresiba and he doesn't pay anything for them. Literally 0. It's completely covered by the National Insurance. Same goes for all of the supplies like strips and needles, and glucose sensors (which can be pretty expensive in the US). In total he pays $0.00 on diabetes management.
In addition, Diabetes education is terrible in the US. Doctors here will usually tell me that I can eat whatever I want as long as I cover it with enough insulin. This is just awful advice since people are not computers and will never calculate the correct dosage of insulin they need to cover every meal; resulting in bad sugar management and complications that come with it: blindness, limb amputation, and eventually death.
The ONLY way to properly manage diabetes is to be very careful about eating carbs. Not necessarily eliminate them, but come as close to it as possible. This is the way diabetes education works in Croatia. Fix the diet and then use insulin to fix what you can't fix with diet. The result is way better sugar management, and way cheaper treatments. Just the other week I had my checkup here in the US and the doctor told me my blood sugars are "too LOW for a diabetic" (my A1c was 5.9% - still higher than the normal 5.5% for a healthy person). I should change my diet and eat more carbs to raise it up. This is just awful, awful advice and I'm sure it's the result of generally terrible diet in the US.
So overall, healthcare treatment and payment for a chronic illness like Diabetes is just immeasurably better in Croatia. It's not even a contest.
Now, on the other hand.
Pectus Excavatum is a bone deformity. In some cases it's small enough to not present any problems but if it's fairly severe it can cause a lot of cardiovascular issues. Nuss procedure involves implanting multiple steel bars (3 in my case) behind the chest wall in order to force the chest bone out. The bars stay in the body for 3 years and are then removed. Surgery is usually successful and after the bars are removed you are considered "cured". There is nothing more to manage and the rate of complications is very low.
This surgery is complicated. It's most often done on children because it becomes much more difficult to perform it in adults. Video if interested: https://www.youtube.com/watch?v=R8SrRzJqbJ8
As an adult, it's almost impossible to get the surgery performed in Europe. I know there's a center in Italy, and another Netherlands that do perform it, but their rate of success is not great. I've seen a lot of people complain about the results. The place to do it is the United States. Mayo Clinic in Arizona has the absolute world expert on Nuss Procedure and she does surgeries on adult of up to 40ish years of age (I got in at 37, last chance). Her work is absolutely phenomenal and people from all over the world travel to Arizona to do it there. There are also hospitals in Missouri I think and in New Jersey that do it, but I'm less familiar with them.
Now given that there are only a handful of places in the world that perform this surgery on adults, you'd think that the cost of this procedure would be astronomical. In total I paid around $2000 out of pocket. Without insurance it costs around $30k, plus $10k or so for the hospital bed (oh US). Don't get me wrong, it's not cheap, but for something of such difficulty and expertise I expected it to be way more expensive. It's literally impossible to get in most of the world other than the US and it costs less than the price of diabetes supplies for 1 year.
So there you have it. In my opinion the US system is absolutely awful for managing chronic conditions. It's made to exploit you for as much money as possible and even give you bad medical advice that makes sure you're going to need those expensive supplies. On the other hand, the most difficult procedures in the world are sometimes only available in the US, and the price of those is not nearly as high as you'd expect it to be. It's great for acute treatable conditions, and absolutely awful for chronic conditions that require constant management.
Covid kills X. Vaccine Kills Y. Everyone is stupid.
Programmers (and I'm one of them) are very black/white thinkers. Very few people on here had said ANYTHING that the radio said today: The pause give us the opportunity to train nurses and doctors to immediately identify the blood clot and make correct recommendations based on that. Typical anti-clotting protocols make this worse. The pause helps us get this communication out.
It's all identity politics at this point. Anyone has anything bad to say about a vaccine and suddenly the anti-anti-vaxxers pop up. Now that Trump criticized the pause I'm sure there's going to be a wildly popular support for this pause.
If we assume an average of 32km round trip to get to a vaccination site (~10 miles each way). Statistically speaking at least one person has died driving in their car to get the vaccine. The same number as from the vaccine.
I couldn't find good stats on serious injuries per km driven, but I suspect it's an order of magnitude higher than deaths per km. Your risk of dying on your way to get the vaccine is the same as your risk of dying from the vaccine. You are, almost certainly, far more likely to be seriously injured on your way to get the vaccine than you are from the vaccine.
https://en.wikipedia.org/wiki/List_of_countries_by_traffic-r...
https://pbs.twimg.com/media/Ey2oowQWgAApGnK?format=jpg&name=...
As we analyze the data, and see if more data comes in the next two weeks, we'll have a better sense of the risk.
Except for that the government covering up the MMR investigation instead of doing it openly is what caused the anti-vaxx movement in the first place. Compare that with the public rallying around J&J after their Tylenol recall.
I'm certainly not denying Covid19, but I do take all the statistics with a grain of salt. It's important to understand that those people died with, not necessarily of Covid19. Also, why are so many positive tested persons without any signs of illness? I wonder what numbers would result in testing every death for other viruses.
The best, maybe only number we can properly compare is the total death rate. In doing so we see that Covid19 causes additional deaths, but it is far from as severe as the media and politics suggest.
The vaccine is eventually going to be mandated to go back to the office, go places, etc.. That’s a risk that you can’t avoid and will have to take.
I’m all for vaccinations and get them when needed, I’m still not comfortable for vaccines that have not been approved. Right now, they all have emergency approval and not overall approval. According to the cdc, vaccines need at least ten years of data to be considered safe for use. We’re only a little over a year into the development of the vaccine. Not really safe in my eyes.
So the six reported cases in 6.8 million vaccinations seems low. Glad I read about all this because I got the J&J vaccine 12 days ago. No noticeable side effects so far. I exercise a lot and did a 5 mile hike four days ago that resulted in a slightly strained a calf muscle. I have been taking it easy the past few days, meaning sitting and reading a lot more than usual. So after learning about the blood clotting, have started exercising the legs frequently. My optimistic thinking is that even if the vaccine does cause an increased risk of CVST that risk can be eliminated via exercise.
It will be most interesting to learn if those six cases involved people at high risk, if they exercise regularly, etc.
The preliminary theories (backed by the thrombocytopaenia) are that, if there’s a vaccine induced thrombosis with thrombocytopenia, it is probably immune-mediated (similar to HITT - heparin induced thrombocytopenia and thrombosis).
And then there’s some weird thing that makes them form in your venous sinus.
But there were also reports of more typical blood clots (ie DVTs), the first European Medicines Agency advisory (0) said that this was within the level of noise (im now talking AstraZeneca, so apologies for shifting vaccine as generally they should be considered separately until the evidence catches up, although everyone is quickly drawing parallels between them)
(0) https://www.ema.europa.eu/en/news/covid-19-vaccine-astrazene...
Ps apologies for not referencing around HITTs and theories around antibody-mediation for CVT. Basically it’s all pretty noisy anyway at the moment and so my here-say from the medical tea rooms is as good a gossip as any, as long as everyone is aware that no one really has any definitive idea what may be going on yet
Arterial clots with thrombocytopenia is incredibly rare. Additionally the PF4 activity in these patients is very abnormal and appears to be to immune mediated. Lots of science and focus going into the mechanism around this now. The other recent NEJM articles around clots associated with the other adenovirus COVID vaccines are likely a similar phenomena.
Thrombocytopenia has been a known complication of adenovirus vectors that researchers have worked to overcome in recent decades.
These incidents mirror HITT (women are at higher risk for HITT) and seem to be happening in the timeperiod where IgG titers spike post vaccination.
To me this indicates it's not unlikely something with the adenovirus vectored vaccines (J&J, AZ) is causing this issue. And because this thread seems to have gone to hell, I'll add that I support doing subgroup specific risk calculations and allowing vaccinations to proceed where it makes sense.
https://jvi.asm.org/content/81/9/4866 https://ashpublications.org/blood/article/109/7/2832/125650/... https://pubmed.ncbi.nlm.nih.gov/17148587/
[1] https://twitter.com/LJohnsdorf/status/1371721321336475651 (in German)
No, because those 6 cases are something more like "1 per day" rather than "per year". Or maybe "per week". But either way, you need to multiply the "per year" base rate by a large number to get the base rate for "coincidentally happened immediately after a particular event", for some definition of "immediately".
for them it’s more like 1/250k
So the reported cases of are not comparable. They are really, really high.
And while I agree about the relative risk vs covid, again this is not a fair comparison. For many people who are isolating, then a person never leaving the house has a very low risk from covid, both personally and transmitting it. You are not asking people to exchange a very small risk from the vaccine vs a very high risk from covid. You are asking them to exchange a very small but roulette-like risk from the vaccine, versus a presumably equally small if not smaller risk from covid due to their circumstances.
Note, what I am "not" saying is that peoples shouldn't be vaccinated. I'm just saying artificially trivialising the risk further using bad math isn't doing anyone any favours.
CVST with Thrombocytopenia is the name.
If you want something to sit around for a long time, you go for less vascular areas. (Ie insulin for diabetics, subcut abdominal fat)
IM is preferred because of the vascularity which helps in the immune response (ie quick immune response, antigen distributed around the body) as well as any immune reaction confined to the muscle rather than, say the skin. (0) is a quick and dirty on mechanisms of administration.
To your earlier point about ‘into’ a vein, I’d never heard of Dr Campbell before you mentioned him, he seems to have great credentials, but I can’t easily explain why an accidental IV administration of an IM vaccine would cause CVST, my gut is that it’s a bit of a hand wave but who knows.
(0) https://www.forbes.com/sites/quora/2017/11/07/why-arent-vacc...
Time periods seem off (5-14hrs) in mouse models compared to what’s being seen here though, which seems more like an immune reaction rather than a response to the antigen/delivery system
From the CDC [1]: Aspiration before injection of vaccines or toxoids (i.e., pulling back on the syringe plunger after needle insertion but before injection) is not necessary because no large blood vessels are present at the recommended injection sites
[1] https://www.cdc.gov/vaccines/hcp/acip-recs/general-recs/admi...
1: https://www.microbe.tv/twiv/twiv-741/ (towards the end)
That's a bold statement. Sure, no large blood vessels may be present at the recommended injection site on an average human, but it's well known there is more divergence in anatomy than they necessarily teach about in primary school, and vaccines are supposed to go in basically everyone.
Maybe we'll need to do it for AZ. Or maybe subcutaneous?
There are also not a lot of major vessels near common injection sites, for this reason. It's possible and rather common to nick a surface capillary or something, and those can bleed quite a lot, but a vein or artery would be totally different. Swelling, horrible pain, likely a cough.
Source: inject myself with intramuscular estrogen every week.
https://www.sciencedaily.com/releases/2006/10/061031141826.h...
Great, so not only will I have to wait 2-3 months to get vaccinated..
They'll also stick the needle in and pull out a few times just to sure I'm really feeling it!!!
Sorry, but I really hate needles :/
The ideal strategy without hindsight was conventional wisdom: Protect the vulnerable and stiff upper lip for the rest. That would have more than halved casualties.
With the benefit of hindsight, a 3 month shutdown while hospitals got their acts together (combined with protecting the vulnerable) would have roughly quartered the remaining deaths, but at far lower cost than the full shutdown.
This was predicted by some of the old-guard epidemiologists, which is why they were against the shutdown in the first place.
The cancel culture folks lumped them in with MAGA anti-vaxxers (I blame both sides) and got them censored by the big platforms. Here we are, with 100,000’s unnecessarily dead, trillions squandered, and many careers, businesses and educations ruined.
I suspect roughly zero people have learned a lesson from this. Hopefully I’m overly cynical.
Let's not pretend that rational discourse was ever an option, and the media isn't the place for blame.
If true, then social distancing, masks, and lockdowns couldn't have done anything for the rest of us for the past year either.
The argument for "protect the vulnerable" is that these precautions could be more targeted and so, hopefully, more effective.
And he became the darling of the media and even won an Emmy.
https://www.vanityfair.com/news/2021/03/cuomos-nursing-home-...
Where was this "full shutdown" you speak of? Not anywhere in the US. In Wuhan, and some other Asian countries, sure.
Didn't we kind of have the 3 month shutdown-lite you're referring to? Mid-March through about June for most places were at varying levels of shutdown in the US. But recall things started opening up in June of 2020. And cases started rising again into July.
> The US is apparently already at ~50% antibodies, not counting vaccination.
Citation? That seems like about 3X the most optimistic numbers I've heard from credible sources.
Source for 50%: Wall street journal. We were above 33% (based on random sampling, not confirmed cases) a few months ago.
This one from Feb predicted herd immunity a bit too early. They ran one with updated numbers last week, but I can’t find it:
https://www.wsj.com/articles/well-have-herd-immunity-by-apri...
Additionally, you make a few glib statements that don’t really check out - you say give hospitals three weeks to prepare - how? There’s been a lot made of hospitals getting ready, but for the most part, the limiting factor for covid treatment has been how many icu care teams are available. More ventilators don’t help much if there’s nobody to use them. Second, I’m not sure how you protect senior citizens when everyone else, including the people who provide their care, is swimming in a soup of COVID.
Also, we knew by April last year that ventilators were a bad choice: Doctors were jumping to it because of a specific weird symptom (blood oxygen levels impossibly low), but they had to keep turning the ventilators to higher settings to get an effect - to the point it was causing further lung damage. There's a bunch of less damaging ways to get more oxygen into a patient they'd been shifting to: https://www.statnews.com/2020/04/08/doctors-say-ventilators-...
China, Vietnam, Australia and New Zealand used strict lockdowns to eliminate community spread, and then largely opened things up again. People in those countries have been able to live much more normal lives than people elsewhere during the pandemic. With hindsight, that was clearly the correct strategy: eliminate the virus, then reopen and keep a hawk eye out for any new cases.
Another one of those examples has been actively censoring covid information from the start, and thus cannot be trusted.
As for Vietnam, it is an interesting case, and we don't have enough data to rule out cross reactivity or other factors playing a role.
Extrapolating these data points to the entire world with wildly varying sociological, biological, environmental, and countless other factors and saying this is clearly the correct (and implicity achieveable) strategy for all 8 billion people on the earth is at best hypothetical.
Australia and NZ have densely populated cities, and what does being an island have to do with anything? Countries can close their borders. In fact, Australian states closed their borders to one another.
> Another one of those examples has been actively censoring covid information from the start, and thus cannot be trusted.
You don't have to trust the government. Just ask people you know in China what's going on there. Things have been mostly open for a year now, with no sign of the virus (outside of a few localized outbreaks, which have been dealt with through local lockdowns and blanket testing of the population). China is not the black box that many people think it is.
> As for Vietnam, it is an interesting case, and we don't have enough data to rule out cross reactivity or other factors playing a role.
Vietnamese people are not somehow immune to SARS-CoV-2. They're susceptible, just like everyone else.
> Extrapolating these data points to the entire world
This is the wrong way to think about this. These aren't data points generated by some semi-random process. They're countries that effectively implemented a strategy that we know should work, based on the basic principles of epidemiology. The virus is spread between people who are in close proximity to one another. If you drastically reduce contacts between people, the virus has far fewer chances to spread, and the epidemic recedes. If you do that long enough, you get down to a small enough number of cases that you can trace every single one and snuff out the virus completely. After that, you have to have strict measures at the border in order to catch imported cases, and you have to do regular testing in the population to make sure you don't miss the beginnings of any new outbreak.
There's nothing to "extrapolate." The strategy works because of very basic principles of how the virus spreads. The only question is whether each county has the organizational capacity and societal will to carry this strategy out.
Indeed, that's a critical question to the long term success of the strategy.
If the world is unable to put 8 billion people in solitary confinement (nevermind the disastrous effects that would cause) indefinitely until the virus is eliminated (nevermind the fact that we are incapabale of validating if it was actually completely erradicated), the virus is only going to pop back up.
There is no evidence of such a strategy working at scale across the world.
The scientists on the covid team at the WHO have said as much: lockdowns should only be used as a last resort to buy time to scale up health care resources. Should we listen to those scientists?
> the virus is only going to pop back up.
It does indeed pop up every once in a while, because the borders can never be 100% sealed. There have been outbreaks in Beijing, Qingdao, border towns in Heilongjiang and Yunnan, and elsewhere. But the government is understandably on high alert, and these outbreaks were caught early enough to be stopped with local lockdowns, coupled with blanket testing of the population (i.e., testing everyone in a city in a few days).
There was a brief "second wave" in China this winter, in which an outbreak managed to spread to several cities, but it was ended with relatively short lockdowns and mass testing. The number of new infections per day peaked around 100.
The basic lesson here is that you can both have near-zero case counts and let people live their lives almost as normal if you first act decisively to bring cases to zero, by using temporary, strict lockdowns, quarantines and mass testing.
> There is no evidence of such a strategy working at scale across the world.
China is the largest country in the world, so I'd call that "at scale." Vietnam is larger than any EU country. We're not talking about San Marino or Monaco here.
> The scientists on the covid team at the WHO have said as much: lockdowns should only be used as a last resort to buy time to scale up health care resources. Should we listen to those scientists?
A lot of recommendations will be reevaluated after the pandemic is over. Nothing like this has happened in 100 years.
They took shit seriously and everyone prepared the minute news reached them of a possible pandemic. A good friend of mine is from VN and he was shipping PPE back home to his parents around August or October of 2019.
I think most Americans don't realize how common pandemics have been in east Asia. To them, it's like preparing for any other natural disaster. It's like comparing the Michiganders response to a blizzard to that of Texans.
This is why we need more data about cross reactivity playing a role in the relatively favorable health outcomes in Asia and Africa compared to the rest of the world.
Agreed
The problem is the virus, not the government reaction to it. Personally, I tend to think governments under-reacted in most Western countries. I'm not sure how things would have returned to "normal" if the virus was raging out of control. A good precentage of people would see the deaths and still avoid going out to shop or whatever. I'm assuming you mean by "normal" that people would return to some normal pattern of economic activity - and even if 10 or 20% of people changed their behavior that would still impact the economy.
That seems hard to believe, since significantly more people die every year of all causes than could possibly have died of Covid, even if every single person in the world caught it. Most people probably wouldn’t have noticed anything was different.
> even if 10 or 20% of people changed their behavior that would still impact the economy.
Maybe so, but the economy is not the only or even the most important casualty of our Covid response. The importance of human social gatherings, the freedom to leave one’s home and go wherever one pleases, the education of children, and so on cannot be measured in economic terms.
> The problem is the virus, not the government reaction to it.
Places where there were very few or only brief restrictions, like Serbia, Belarus, or Florida, largely avoided the issues I described above with only a small or in some cases unmeasurable increase in all cause mortality for 2020.
Sweden is an interesting example. Comparing Sweden and Finland, for instance, older people essentially cloistered themselves in Sweden because they had no trust that they'd be safe in society, and their spending dropped by a higher amount than old people in Finland, who changed their habits less due to the swift and more stringent government response? My old-person family members in Finland were able to keep shopping, going to church, and having birthday parties with many families due to that response (as opposed to in the US where we limited ourselves to gatherings with max 3 households and did everything masked or outdoors due to several people still working on site).
Perhaps you live in a very different place. You certainly interpret statistics quite differently given your example of Florida.
If, instead, people had behaved responsibly in mass and we had used the time we got from that to establish coherent contact tracing and testing, things would have returned to normal by August as well, only without many the deaths your way would cause.
A lot
I'd argue that the "response" at the Federal level was a massive under-reaction. Months of denial didn't seem to work out so well.
https://www.marketwatch.com/story/deaths-of-despair-during-c...
Besides, in the CDC table, "unintentional injuries" is up by way more than suicides are down. This includes things like car accidents, and is a little suspicious, like suicidal behavior led to a death that wasn't classified as suicide. Also note that the table is "deaths with covid or presumed covid", not "deaths by covid": https://jamanetwork.com/journals/jama/fullarticle/2778234
> Cerebral venous sinus thrombosis is rare, with an estimated 3-4 cases per million annual incidence in adults. While it may occur in all age groups, it is most common in the third decade. 75% are female. [0]
[0] https://en.wikipedia.org/wiki/Cerebral_venous_sinus_thrombos....
Except to the general public this overcautious behavior and resulting media hype raises vaccine suspicions, and will decrease public trust in J&J (and even vaccines in general) as a result. It’s already happening.
https://www.reuters.com/investigates/special-report/johnsona...
1. First assume independence, that CVST is unrelated to vaccination.
2. Take any two weeks, you can calculate the expected cases using population background rate because we assume independence.
3. The number is around 1 using Wikipedia data.
4. The observed case number 6 greatly exceeds the expected number based on independence assumption.
5. We conclude that with high probability that our independence assumption is wrong, i.e. there's correlation with high confidence.
You are not sampling a random, normally distributed event over a fixed interval, you are sampling the spacing between two different events where one of them is systemically linked to how you define the population and the interval.
This is definitely not enough data to conclude a 1 in 30,000 figure. And neither does the cited paper conclude this.
https://www.theguardian.com/world/2021/apr/13/astrazeneca-bl...
All the observed cases occurred shortly after vaccination, so I’m not sure 3 months is the right divisor to use in your comparison.
Otherwise, there isn't a whole lot of difference between "not real" and "real but so rare as not to matter."
There are other options. Give everyone who has got the vaccine some money is one I've heard more than once. Maybe someone else has a different idea.
Also pretty sure risk of death outweighs literally any possible long-tail risk, so still seems sensible for the young to get the vax. Also don't think the long-tail risk of an mRNA vaccine can be worse then COVID's long-tail risk.
Again, we are talking about introducing something that is guaranteed to be in your body anyway if you contract COVID-19. SARS-CoV-2 is viral to the point where, without perpetual lockdowns/mask-wearing/vaccinations, you will get it. So it is still definitely better to get vaccinated, at least with an mRNA vaccine – please stop spreading FUD. Your concerns could be more warranted for vaccines like J&J which use modified viral vectors, but again, exceedingly unlikely that this could be any worse than the virus itself.
Wasn't that the case with J&J also, till they decided to not ignore the clots.
To open up again we need to bring the demand on healthcare services down and we need to do it sustainably, i.e. in a way which prevents another exponential spike. If we can achieve that aim without mass vaccination of healthy young people then great, of course, let's do that. But: if the only way to squash this thing and return everyone to a somewhat normal life turns out to be to keep vaccinating until we get right down to the twenty year olds, shouldn't we do so -- for their sake as much as everyone else's?
How exactly are you so confident about the long-tail risks of contracting COVID-19? Sounds like epistemic arrogance to me.
Continuous mutation of common viruses is the background risk that human beings have evolved over three billion years to withstand as a species. That is different than a completely novel man-made intervention.
In neither case is it possible to know what hidden long-term effects they could have on you. But the virus is known to kill and maim people in the short-term at a much higher rate than the vaccine, which is known to protect you from the virus.
For all we know, mRNA vaccines can alter your gametes. We don't know because this is the first time we ever use them. They aren't like viruses or weakened viruses. They are just a massive injection of genetic material (much of it deformed) that encodes a single foreign protein. No human being has ever had such a thing done to them until very recently. mRNA vaccines are not part of any natural process that modern humans or our ancestors have had to withstand to get to the present day.
I don't know why you have this special concern about the gametes. In any case, if there's a significant bump in miscarriages / infertility from the vaccine, we'll probably know very soon, now that lots of younger people are being vaccinated.
First: does the rate at which the cells are made to artificially produce spike protein follow a different curve than the rate at which SARS-2 would? i.e. could mRNA vaccination cause a much more aggressive "inflammatory cliff", thus the huge percentage of "mild" adverse reactions (mild meaning, you feel like death for a day but end up fine with no detectable long-term issues)? It's possible.
And switching to efficacy, while personally I think resistance to the spike protein alone will be sufficient, because SARS-2 does not have the same ability to mutate/evolve the way Influenza does (for example, I can't imagine SARS-2 evolving away from the spike protein), it's very possible that the diverse epitopes produced by real SARS-2 infection give a much more robust and enduring immunity.
I don't know a single person that has that after flue and cold - and those are with us much longer.
As for viruses mutations etc. do we for sure know that this one is not man made?
> I don't know a single person that has that after flue and cold - and those are with us much longer.
Look into ME/CFS, whose existence is still contested (or rather I should say, whether it's a physical or psychogenic illness is disputed). I know you're just speaking anecdotally but just wanted to mention that post-viral issues (fatigue, memory, etc) absolutely does happen.
> As for viruses mutations etc. do we for sure know that this one is not man made?
At most SARS-2 is the result of extensive gain of function research on https://en.wikipedia.org/wiki/RaTG13. I don't know any credible individual that thinks it's fully artificial / manmade (and to be clear, my definition of "credible" is not the "anyone who agrees with the WHO/CDC and nobody else" definition that the establishment relies on).
Personally I think it's more likely that SARS-2 was GoF'd into existence rather than was a purely natural zoonotic leap, whereas I think the probability that it was fully artificial is almost zero.
If we pick the 25-29 year olds and an estimated infection fatality rate of 0.01% [1] it's still 13.5M x 0.01% = 1,350 deaths. It's not a lot by any means, but it's not 'almost nothing' either.
This is the worst case scenario of cause, sibling comment has already mentioned long Covid, where we don't know prevalence precisely.
I'm aware I've picked the 'worse half' of the 20 year olds, 20-24 will fare better obviously.
[1] https://www.nature.com/articles/s41586-020-2918-0/figures/2
The mRNA in the vaccine lasts a matter hours.
That's not that many. Despite my wife and I getting vaccinated, I'm not completely sure what the correct answer is for our kids.
To put those numbers into perspective, more kids die from the flu in any given year (despite vaccination!). And far more kids die from car related accidents, and cars are a daily fact of life here.
I'm also interested in the other longer term effects of COVID on kids, but there doesn't seem to be a lot of information out there about it.
You talk as if it's a clear cut answer. Given the numbers involved I don't see how it can be.
A college-enrolled 18-24 year old is 3.67x more likely to die of suicide [1][2][3].
A college-enrolled 18-24 year old is 6.08x more likely to die of alcohol [3][4].
A child (0-14 years) is 6.75x more likely to die by motor vehicles [5].
A child (0-14 years) is 3.93x more likely to die of drowning in a pool [6].
All fatalities are compared to present CDC numbers [7].
[1] https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3809451/
[2] https://www.statista.com/statistics/183995/us-college-enroll...
[3] https://nces.ed.gov/programs/digest/d18/tables/dt18_302.60.a...
[4] https://www.niaaa.nih.gov/publications/brochures-and-fact-sh...
[5] https://injuryfacts.nsc.org/motor-vehicle/historical-fatalit...
[6] https://www.cdc.gov/homeandrecreationalsafety/water-safety/w...
[7] https://data.cdc.gov/NCHS/Provisional-COVID-19-Death-Counts-...
BTW the "long tail" of COVID-19 in children is totally unproven and the whole "long haulers" phenomenom is likely (a) a small part normal post-viral fatigue which we see with basically any virus, and (b) mostly psychosomatic/psychogenic illness.
So when faced with the choice of vaccine or virus, it should be a foregone conclusion.
It absolutely could, and that should be self-evident.
> Also pretty sure risk of death outweighs literally any possible long-tail risk, so still seems sensible for the young to get the vax.
This is just not true. The risk of death in children from COVID-19 is so low you literally should not ever worry about it. If you want to compare numbers in an academic sense go ahead, but the fact that actual adults are wasting valuable cognitive and emotional energy worrying about their kids is a great tragedy.
The recorded COVID-19 deaths in children are, by the way, using the absurd definition of a COVID-19 case/death that most of the western world is using; a definition where having PCR-confirmed SARS-2 infection means that ANY death is classified as a COVID death. This is not how this is supposed to work; there is supposed to be a distinction between the virus and the disease, but we define the disease as merely having the virus! It's completely absurd. Indeed I'm writing an article about this concept (pathological vs physiological) right now
https://covid.cdc.gov/covid-data-tracker/#vaccinations
When that reaches +80% the recommendations will ease more but as of now:
https://www.cdc.gov/coronavirus/2019-ncov/vaccines/fully-vac...
Right now across US being fully vaccinated is only 80% effective against infection. When you have 20k vaxed folks meet when the virus is endemic in the pop, some of those vaxed folks will be infected and some will catch it there.
When more folks are vaxed there will be less of the virus circulating and then that calculation then changes. It's all about how prevalent the virus is in the community to begin with assuming no strains appear that dramatically reduce the effectiveness of the vax.
https://www.npr.org/sections/health-shots/2021/04/13/9864114...
You and the other commenters arguing your "side" also seem to completely ignore the phenomenom of natural immunity, which I think very obviously has been fallaciously denied by "experts" precisely because they want to convince everyone in the world to get this vaccine. They're already talking about yearly booster shots because most people's mental models are from Flu which has a much greater space of possible genetic configurations, whereas SARS-2 is relatively constrained in how it can evolve and thus should not need a yearly booster if this weren't just about making absurd amounts of money (which it is).
In any case, you should know that there are people like me - very much in the minority - who refuse to submit to such absurdities and will keep fighting. We will continue to be literally as well as metaphorically discriminated against until your "side" stops brainwashing people into a completely disproportionate response to an endemic respiratory virus.
You can stay inside with a mask on while vaccinated all you want. Be my guest. But please stop advocating for and/or supporting mandates and restrictions on the rest of us who have not caught your specific strain of agoraphobia, germaphobia, OCD and misanthropy.
The annual flu shot is not just for you, it is also to prevent you transmitting what is probably harmless to you but deadly to immuno-compromised like the elderly, they don't have ability to get natural immunity. Pneumonia is significant cause of death amongst senior citizens.
If 600,000 people dying U.S alone in the last year, does not convince you to stay masked and safe and follow some simple instructions for few more months until everyone is vaccinated even if you don't believe in them personally, nothing is going to.
There is no definitive answer whether vaccine will reduce transmission. Those 20,000 people will definitely meet un-vaccinated people in next 10-12 days, and then may pass the disease to them.
Many people cannot get the vaccine, because it is not open yet to them, or have other conditions. So it is selfish for vaccinated people to behave as though the rest of the population does not exist.
There is also the worry that longer the disease lingers anywhere in the world, there can be mutations which are immune to current vaccines, such an mutation could be disastrous as people will loose trust in the vaccine and a second vaccine even when available will have lesser adoption than now . It could become a vicious cycle where there is third mutation, and this then becomes like the flu shots ( but lot more deadlier)
I think we'll get to normality eventually, but it may take longer than anyone has patience for, and that will only push it out further as people give up on social distancing and masking.
I'm hoping that as the vaccination numbers go up, we'll eventually start seeing new cases drop off a cliff as the virus runs out of people to infect. (Though I suspect that we'll have problems for awhile with groups of people who hang out together and for whatever reason don't get vaccinated.)
Another consideration is that if the virus is allowed to continue to spread, there's a real chance that it may mutate into a form that isn't stopped by the vaccine, and then we're right back where we started.
From a public health point of view, I don't see things getting back to ordinary people (and not just the foolhardy) having lunch with coworkers around the same table without masks on unless there isn't any significant amount of community spread going on.
Also it's comparing raw ICU admissions, but there are a number of really nasty adverse reactions that don't throw you in the ICU. The general "second shot syndrome" that something like half of people getting Pfizer/Moderna experience is a great example of that. Yeah it's not bad enough to send them to the ICU, but for many people COVID-19 would be literally asymptomatic or would be minimally symptomatic, whereas the second shot syndrome can be quite brutal.
Why do you believe that? It seems to me that the reputational damage caused by the U of C centre putting out bad slides is going to be stronger than any benefit they might get from being "seen to be a team player" or similar. Skepticism is always good but in this particular case, I do trust that evidence.
> there are a number of really nasty adverse reactions that don't throw you in the ICU
OK, but you can make the same argument for COVID. It seems to me that the slides are at least comparing apples with apples.
If you look at the rates of acute side effects to the vaccines, I forget the exact number but it's at least like 80%. It's insanely high. SARS-2 absolutely does not produce that given the massive proportion of asymptomatic individuals and significant amount of paucisymptomatic individuals
(B) covid-19 might very well become endemic. Like how the common cold is always around. It's not so bad if we're vaccinated. But for those that don't get vaccinated hurd immunity might not cover them.
In practice: I think we just need to be honest about the risk of vaccines. And say that taking it is the patriotic thing to do :)
i guess you can put it like that.
from my understanding the vaccines do reduce the transmissibility of the virus, but they do not lower it to zero [0]. you can still get the virus, but with the vaccine your chances of needing hospitalisation drop to zero [1].
i guess this is why you still need to wear a mask, and still need to socially distance even if you are vaccinated [2].
[0] https://www.lshtm.ac.uk/newsevents/news/2021/covid-19-vaccin...
[1] https://www.astrazeneca.com/media-centre/press-releases/2021...!
[2] https://www.cdc.gov/coronavirus/2019-ncov/vaccines/faq.html
Yeah, but once vaccinated you can start to worry less. And surely we'll see things open up to those who are vaccinated.
The fact that it's possibly still transmissible by vaccinated people is probably the reason why we all need to get vaccinated, and there is no hurd immunity to be gained :/
Everywhere I read about the J&J vaccine, I see something like "the DNA vaccine doesn't alter your DNA". Can somebody please clear this up?
As far as I understand, the mRNA just stays in the cytoplasm of the cell and gets used up by the ribosome to create spike proteins. The adenovirus vector used in the J&J (and other vaccines) injects DNA in the cell's nucleus, which seems at odds with the widely circulated "it doesn't change your DNA" statement.
Do people make this claim because the cell displaying spike proteins is basically always eliminated by CD8 killer T cells?
Btw here's a nice high-level summary by the NYT about how all the vaccines work: https://www.nytimes.com/interactive/2021/health/how-covid-19...
https://www.medpagetoday.com/special-reports/exclusives/9160...
> Adenoviruses -- even as they occur in nature -- just do not have the capacity to alter DNA. Unlike retroviruses such as HIV or lentiviruses, wild-type adenoviruses do not carry the enzymatic machinery necessary for integration into the host cell's DNA. That's exactly what makes them good vaccine platforms for infectious diseases, according to Coughlan.
> And, engineered adenoviruses used in vaccines have been further crippled by deleting chunks of their genome so that they cannot replicate, further increasing their safety.
Some body cells can bounce back after serious trauma, liver cells being a prime example: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2701258/
I'm not a genetic engineer (what a time to be alive, eh?), but I'm pretty sure an adenovirus that did permanently modify cell DNA would be more like CRISPR, including the risks that entails (such as the risk of incorrectly splicing the host genome and potentially creating a precancerous mutation)
But there's a very well known case where DNA delivered via an adenovirus killed a teenager during a genetic engineering study: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC81135/
>> "No one realized that the vector itself might pose a risk"
I'm sure the dosage, type of adenovirus, and modifications to the adenovirus are different. But there are obviously still risks we don't know about.
>> An autopsy and subsequent studies indicated that his death was caused by a fulminant immune reaction (with high serum levels of the cytokines interleukin-6 and interleukin-10) to the adenoviral vector.
>> The data suggested that the high dose of Ad [adenoviral] vector, delivered by infusion directly to the liver, quickly saturated available receptors ... within that organ and then spilled into the circulatory and other organ systems including the bone marrow, thus inducing the systemic immune response.
He was injected with >3 × 10^13 viruses [2]. The typical J&J dose contain: low-dose (5x10^10 viral particles) or high-dose (1x10^11 viral particles) [3].
[1] https://www.uab.edu/ccts/images/steinbrook_Gelsinger_-_Oxfor...
[2] https://www.cell.com/molecular-therapy-family/molecular-ther...
[3] https://www.jwatch.org/na53085/2021/01/26/adenovirus-vectore...
It almost certainly won't have long-term affects, but it may not be trivial to identify if mRNA vaccines have been altering epigenetics.
[1] https://en.wikipedia.org/wiki/RNA-directed_DNA_methylation
I have an aviation, biochem, and skydiving background. My rule is for aviation: "if it hasn't been out five years you're a test jumper."
Humans are way more complex than airplanes. I personally wouldn't take the mRNA vaccine because of this rule. Coupled with being unable to sue or get help from the government I think people IN LOW RISK groups have been way too enthusiastic to sign up.
https://www.cnbc.com/2020/12/16/covid-vaccine-side-effects-c...
Given my risk is very low I'm not too worried about COVID, but I am a little worried (perhaps wrongly) about the risk of finding out about some long-term side effect from these vaccines a few months down the road. I suffer from long-term side effects from another drug I took in the past, and at the time I was told there was no risk of long-term side effects and that it was safe to take. Only recently has the labeling been updated to reflect the discovery that permanent side effects can occur in some cases and for me it's too late, but I learnt my lesson to allow others to be the guinea pig for new drugs wherever possible.
It's really quite alarming how little we know about the body, espically considering the certainty of some "experts" about how extremely low the risk of adverse effects are from newly approved vaccines. I'm aware of a number of drugs which are approved and frequently perscribed which we don't even understand the mechanism of action for -- accutane, for example. Of course in this situation, we do know the mechanism of action, but it would still be wrong to assume we know the full surface area of possible side effects which could occur because our model of the human body is so basic.
I'm happy for someone to explain why I'm wrong on this. I'm obviously not an expert, just an average guy trying to assess the relative risk of two very unlikely events.
About that...
> In December, we asked, “What percentage of people who have been infected by the coronavirus needed to be hospitalized?”
> The correct answer is not precisely known, but it is highly likely to be between 1% and 5% according to the best available estimates, and it is unlikely to be much higher or lower. We discuss the data and logic behind this conclusion in the appendix.
> Less than one in five U.S. adults (18%) give a correct answer of between 1 and 5%. Many adults (35%) say that at least half of infected people need hospitalization.
https://www.brookings.edu/research/how-misinformation-is-dis...
> Many adults (35%) say that at least half of infected people need hospitalization.
This is why so many in low-risk groups have been so enthusiastic - misinformation that has them thinking it really is the Black Death.
Does that not seem a bit ... immoral?
I assume you eschew all other medical advances that are less than 50 years old? Would you eschew remdesivir? Sorry for the questions but thinking such as yours intrigues me and I want to grasp the logic behind it. Why not avoid all new technology for 50 years? Getting vaccinated seems to me like the logical and moral thing to do, but maybe I’m overlooking something.
OP also didn't say 10 years is enough time to know the long-term effects of these vaccines, just that it's traditionally been the minimum amount of time needed for some other drugs.
Love that quote! That's going to be my standard comment from now on when I see a pull request that doesn't include any test cases :-)
Is it possible to do something like tagging the molecules with radioisotopes and following their path?
Here's an example: https://www.nejm.org/doi/full/10.1056/NEJM199001253220403
Pointless FUD to worry about that or even bring it up.
https://newsroom.uw.edu/news/genes-%E2%80%98fossil%E2%80%99-...
> Most of these viral genes come from retroviruses, RNA viruses that insert DNA copies of their own genes into our genomes when they infect cells. HHV-6 is unique because it is the only known human DNA herpesvirus that integrates into the human genome and can be routinely inherited.
I'm a 40 year old man, if I were a woman I wouldn't take J&J or AstraZeneca, but as I'm a man, I think it's worth to take the risk of the side effects of the vaccination.
So what’s the point if you’re a public health admin? Just get the moderna or Pfizer and save yourself and your staff a lot of headache.
The logistical benefits of J&J mean that it’s only logistically beneficial if it can be used for everyone.
We can make a statue for the people that die in the following weeks protecting the rest of us from the J&J vaccine. They’ll be heroes.
Sorry. Really pissed off about this.
Still agree that covid is a way bigger threat than the J&J vaccine though.
Has that percentage of people in any county in the USA actually died from COVID in over a year?
Florida who has been pretty laissez-faire about COVID has 5,980 deaths in Miami-Dade County (their highest amount of deaths in a county). 2.717M population in 2019.
0.22% of their population.
The big enough cities to need many shipments can handle these logistic.
Also, only 1/3 of Astra Zeneca clot victims are male:
https://news.yahoo.com/astra-zeneca-vaccine-blood-clot-risk-...
J&J doses delivered: 7 million.
Reported blood clotting events: 6.
Daily risk of dying of COVID19 in the US: 1 in 330,000.
CDC and FDA: Pause the J&J vaccine.
Draw your own conclusion on how aligned these folks are with your interests.
Hundreds of young and healthy people have died from Covid-19.
The risk is “basically zero” but so is the current known 1 in 7 million risk of dying from this blood clotting.
Even then, let's assume they were. COVID is largely avoidable, if you don't mind being avoiding others. Directly getting a vaccine is not.
It's like saying X% of people riding in cars will be in accidents and die. Yeah, maybe, but that doesn't apply to you if you don't ride in a car in the first place.
25% of those who died under age 21 had no pre-existing condition, according to the CDC analysis. https://www.upi.com/Health_News/2020/09/15/75-of-youths-who-...
I believe the data does support my statement that hundreds of young and healthy people have died from covid. The risk is close to zero, yes, but still greater than the reported risk from this vaccine.
Close to 3000 people ages 25 to 34 have officially died in the USA from covid-19. If the same 75%/25% division the cdc found for under 21 applies to this group, that’s 750 young and healthy people who died so far just in the age 25-34 age group.
> COVID is largely avoidable, if you don't mind being avoiding others
Huge assumption. Many workers need to work in person and are going to be exposed. Many others live in a home with someone who is an essential worker, or doesn’t believe in covid being dangerous or taking precautions.
It really isn’t fair to blame everyone catching covid today and say they could have simply avoided it. Also, getting a vaccine is absolutely avoidable. No one is being forcibly vaccinated right now.
Death is not the only risk factor. Covid-19 carries the risk of serious complications for those who recover, even including those who are infected but asymptomatic.
https://jacksonhealth.org/persistent-pulmonary-problems-in-a...
> Additional studies are required to fully understand the virus, but for now, follow-up testing is essential to understand the long-term effects of the virus.
Isn't it just person (1 person), not people, at this point?
What's this supposed to mean? Is the implication here that the CDC and FDA want to keep people from being vaccinated? WHy?
Otherwise you could delay your updating your side-effects listing because you know FDA will take your druf off-market (and this delay will/could cause harm to people).
In this case, the new side effect kills people. Very rarely, but if you belong to some unlucky group, you're screwed. It is better to figure out which people are endangered. The recommendations and documents have to be good for everybody, not just for the good statistics.
Also: the side effect profile for the moderna and pfizer vaccines in the clinical trials was far WORSE than the jnj vaccine.
Edit: gene-based not gene-therapy
A potential danger of DNA-based vaccines is the integration of plasmid DNA into the cell genome (1). Insertional mutagenesis occurs rarely but can become a realistic danger when the number of events is very large, i.e. as in mass vaccination of a population.
First of all, plasmid != viral vector. That's why the Nature paper you cited had to use electroporation to introduce the payload. As J&J is a viral vector vaccine, I would not be confident in using this paper to make the argument that an adenovirus-based vaccine could modify a host's DNA.
Second, your article does not make the claim you think it does. Specifically, the discussion says:
> Using simple intramuscular injection, the vast majority of plasmid DNA that persists is extrachromosomal, and the frequency of integration, if it occurs at all, is negligible.
> However, even if the residual plasmid in the gel-purified genomic DNA did represent integrated plasmid, one copy... would be at least three orders of magnitude below the frequency of spontaneous gene-inactivating mutations...
That is, the delivered gene does not integrate directly into the genome itself, but rather stays in the cell. To detect whether the gene stays in the host cell, the article compares molecular weight and uses a PCR test. Both methods do not tell us whether the gene inserts itself into the host DNA; one way to detect that would be to sequence the subsequent DNA, which would be monstrously expensive (because the modification incidence is extremely low).
The only way that a gene might integrate itself into the chromosome is if during DNA transcription, an error occurs and the foreign DNA is merged onto the host DNA. But this would be incredibly rare because it would require most base pairs to match up between the host & foreign DNA; otherwise, the cell would attempt to repair itself or induce apoptosis.
And even if the resulting base pairs match up, the resulting DNA might not have any behavioral differences because it's (approximately) the same sequence of characters. (And you would need another transcription error later on that happens to reduce the non-modified strand by approximately the same length. That's also extremely unlikely.)
Fourth, the Pfizer and Moderna vaccines use a mRNA-based vector, which (in my limited knowledge) is very difficult to integrate into the genome. The most plausible mechanism I could imagine would be:
1. (Optional) an enzyme which converts a modified nucleoside mRNA strand into one that mimics the mRNA chemical structure that is compatible with a reverse transcription enzyme [1].
2. A reverse transcriptase to convert the mRNA strand into a (foreign) DNA strand.
3. A restriction enzyme that cleaves the host DNA suitably so that the foreign DNA can be inserted.
4. A matching ligation enzyme which actually inserts the foreign DNA into the the host DNA.
All these above enzymes do not naturally occur in humans, so DNA modification through this mechanism would be incredibly rare.
[1] https://link.springer.com/protocol/10.1007/978-1-4939-6481-9...
Additional dangers of DNA vaccines include production of anti-DNA antibodies and autoimmune reactions(2). I think we should be communicating these dangers to the public so that healthy individuals at no risk can make a proper benefit-risk decision, instead of just saying "vaccines good" and brushing over concerns.
(1) https://coronavirus.medium.com/decoding-johnson-johnsons-cov...
(2) https://link.springer.com/protocol/10.1007/978-1-62703-110-3...
The article you linked estimates the risk of DNA integration is three orders of magnitude times lower than gene deactivation through regular mutations. I think we're safe.
> Additional dangers of DNA vaccines include production of anti-DNA antibodies and autoimmune reactions
Any documented cases in clinical trials?
To date, there is no licensed DNA vaccine for use in humans, which is my whole point we aren't testing for this and instead just using the whole US population as test subjects without informing them of the risk.
There's no plasmids in the Covid vaccines, a virus has been modified to include instructions for the target proteins.
Edit: plasmids are used to encode the virus for production, they aren't part of the delivery mechanism: https://www.addgene.org/viral-vectors/
> and the present coronavirus vaccines have not undergone preclinical testing as normally required by international regulations.
Citation needed.
The risks could be higher, but maybe our data is not yet there.
Just as a side note, the risks (and gains) are different, maybe I really don't want a child accidentally, but I don't consider the coronavirus too dangerous to me (it's just a hypothetical, this hypothetical person could be wrong, but in the end we all operate on incomplete data)
The type of blood clots (low platelet) the J&J causes gets worse with the standard treatment of blood thinners. This was on the CDC call this morning.
In this pandemic, inaction costs lives. The logical and ethical thing to do is evaluate the cost/benefit and choose the path that kills fewer people. You wouldn't say "we should exit the burning house one at a time in case we get hit by a meteor outside, caution here is the logical and ethical thing"; you're making the same kind of logical error, just with a less-absurd difference between the risk of the two options we need to choose between.
I always appreciate an apt analogy.
The rules are not some holy writ handed down from above, they are our way of trying to properly manage risk. When the situation changes, the rules can also change.
I don’t think jerking our knees over an ethics safeguard that led to a pause in administration of a vaccine that soon won’t be widely available anyway is a great habit to get into.
Imposing political pressure on experts and forcing them to approve against their judgment would be a horrible corruption of these regulator institutions.
Maybe the expert regulator think that the bar should be lowered. But then they should come forward. This should not be ordered by politicians or their handlers.
I get the need to make sure medicine is safe and effective, and we absolutely should follow those to a T when it comes to new medicines on the market in non-emergency situations.
However, that's not the case here. vaccines are well studied in general and J&J is one of the more "normally developed" vaccines on the market. After generally ensuring that it's safe (Phase I/II tests), there should have been a damn good reason to pull it even temporarily. The "we are seeing a small increase in blood clots" really doesn't seem like a valid reason to pull a vaccine.
Personally, I lay the blame primarily on anti-vaxxers. They've made us far too cautious around vaccinations. It has screwed up our risk management rules. I've no doubt that this pull back will result in anti-vaxxers publishing BS about the safety of J&J vaccinations to try and scare people away from it.
This has nothing to do with "anti-vaxxers". Vaccines usually take years to develop precisely because we give them to everyone, and rare, long-tail risks matter. This was the case well before the MMR autism scare defined "anti-vax" as it has come to be known today.
In this case, we bypassed that standard development process. It was the right choice, in my opinion, but it's not the right attitude to start claiming that our standard level of risk mitigation for vaccines is excessively cautious because "anti-vaxxers" exist. That's simply reactionary.
If anything, we've tossed out all of our usual standards of evidence in 2020, and did a bunch of stuff willy nilly, with no supporting evidence or rational consideration of trade-offs. We tore off all the safety belts. We don't need lower bars for evidence, we need less reactionary hysteria.
The vaccine trials were limited in their power to detect rare events. The Pfizer trial [1], for example, explicitly said that events rarer than 0.01% are less likely to be detected:
> This trial and its preliminary report have several limitations. With approximately 19,000 participants per group in the subset of participants with a median follow-up time of 2 months after the second dose, the study has more than 83% probability of detecting at least one adverse event, if the true incidence is 0.01%, but it is not large enough to detect less common adverse events reliably. This report includes 2 months of follow-up after the second dose of vaccine for half the trial participants and up to 14 weeks’ maximum follow-up for a smaller subset. Therefore, both the occurrence of adverse events more than 2 to 3.5 months after the second dose and more comprehensive information on the duration of protection remain to be determined. Although the study was designed to follow participants for safety and efficacy for 2 years after the second dose, given the high vaccine efficacy, ethical and practical barriers prevent following placebo recipients for 2 years without offering active immunization, once the vaccine is approved by regulators and recommended by public health authorities. Assessment of long-term safety and efficacy for this vaccine will occur, but it cannot be in the context of maintaining a placebo group for the planned follow-up period of 2 years after the second dose.
Even a 0.001% risk is not small, when you're talking about giving the vaccines to billions of people.
(I don't mean to single out Pfizer here. It's just the one I've read most recently.)
Anti-vax hysteria has been around for longer than MMR and autism.
> rare long-tail risks matter
I agree, but at the same time I also think that it's an overblown problem with vaccinations. We aren't talking about medication that screws around with the metabolism in unusual ways. Vaccines (other than the newer mRNA stuff) are by and large large enough chunks of whatever we are vaccinating against to trigger an immune response when the real thing comes along + preservation/delivery medium.
At the end of the day, the worst case for vaccination is that you might be infected with the disease you are vaccinated against (when live viruses are used).
That's not the case for J&Js vaccine.
So the next question is, if the worst case scenario is you get a disease you were attempting to prevent, then what is the next real biggest threat from a traditionally developed vaccination?
> If anything, we've tossed out all of our usual standards of evidence in 2020, and did a bunch of stuff willy nilly, with no supporting evidence or rational consideration of trade-offs. We tore off all the safety belts. We don't need lower bars for evidence, we need less reactionary hysteria.
I'd argue that pulling a vaccine over a very minor number of reports of increased blood clots is overly reactionary.
Edit: And... reading this it makes it sound like I'm skeptical of mRNA vaxxes. Just to be clear, I'm not and I've gotten the pfizer vaccine myself. I do think they'd have more justifiable scrutiny to make sure they are safe as it's a new technique for mass vaccinations (even though it's been used in immunotherapy for a while now).
The worst case for vaccination isn't that you get the illness. It is that you are one of the unlucky ones that gets some severe reaction and gets killed.
The type of severe reactions you'd expect are allergic reactions. They would show up right away, not as an event 2 weeks later. Given that J&J has already done 6 million dosages it seems pretty safe to say that those allergic reactions are pretty much non-existent.
I see a lot of maybe and mights, yet never any actual evidence or example of the fear around vaccine safety or a cogent explanation of HOW these things could happen. That's because you'd have to explain how proteins from the vaccination are somehow more dangerous than the same proteins present in the diseases.
The linked explanation would have been a reason for a longer and wider phase II/III study. However, now that the cat is out of the bag and we've got millions of people who've been dosed for multiple months, that's the study. Until we start seeing severe negative side effects in the 100s or 1000s of individuals, it doesn't make sense to pull a vaccine.
I think some people would choose the J&J vaccine if it meant getting vaccinated faster. Some people would choose Moderna / Pfizer, later.
It really depends on things like whether or not you can work from home, how depressing it is not interacting with people, or how concerned you are about the risk of long COVID19. That's not something we can answer for anyone centrally.
From a public health perspective, vaccinating people now with Johnson is an obvious win.
I think this is unrealistic for medical application, not only for vaccinations but in general for anything related to side effects of drugs.
First of all, most people don't have the data and in this case part of the risk management is to get more data or consolidate and evaluate existing data more thoroughly. Second, while you might be an exception, the vast majority of people do not have the knowledge and skills to properly assess risks or perform multiattribute cost-benefit analyses. Layman cannot even compare small probabilities correctly and frequently mix up risks that differ from each other by multiple orders of magnitude. Even people with fairly good knowledge of probability theory will have a hard time judging small risks without extensive comparison data and maybe some didactic tools like "micromort" comparisons.
So do public health professionals. The passive death and disability from COVID19 is weighed far less than the active death of side-effects. Providing J&J to everyone in the US would obviously reduce spread and reduce the thousand-or-so deaths we're continuing to see in the US every day by far more than blood clots.
In general, doctors leave medical decision making to patients, is central to medical ethics. This even applies to patients with incomplete capacity.
However, keep in mind we are continuing the vaccinate people are a really high rate, we just are not using the JJ vaccine. No one is stopping all of vaccinations. A brief pause in JJ while they relabel is just a minor hiccup in our overall vaccination plans
And the damn good reason was that there's a bunch of people out there who don't want to take the vaccine for political reasons. And there's a smaller amount of people who don't want to take the vaccine because they're uninteresting in taking a new vaccine. They're looking for reasons to validate their fears.
If you just keep pushing the vaccine even though a bad thing happened to a small number of people, then there will be people who use this as an excuse to avoid all of the vaccines completely.
Take down the vaccine and make a bunch of lab coats spend a hectic two weeks double checking some figures and people will feel listened to and they'll have less arguments to not get the vaccine. The vaccine that you're taking is as safe as it can be. After all when we saw a problem we did something about it.
This is 100% about optics and PR AND that's 100% necessary right now in order to get the job done.
> I lay the blame primarily on anti-vaxxers
Don't even talk about anti-vaxxers right now. The only thing bringing up anti-vaxxers will do is grow that movement. The people who don't want the covid vaccine are not anti-vaxxers. They get the flu vaccine and they get their children vaccines. They're only afraid of the new covid vaccine. They don't like anti-vaxxers any more than you do, BUT if you call them that then some of them are going to decide they might as well join the anti-vaxxer movement.
These are two groups of people who I do not want to join forces. Covid hasn't exactly been a fun time, but I'm really not interested in seeing polio and friends come back.
Have rational debates, quit the name calling, go the extra mile to convince people who don't like your position to do something for the greater good. Otherwise, we're not going to see enough vaccinations to make a difference.
If thousands are dying for lack of a drug or not has, at best, very little impact on the decisions.
The job of the FDA is to enforce regulations, not to save lives.
I'm sorry, but when dealing with healthcare organizations and policy-makers, it's more like the "holy writ" than the idealized system you describe later.
Serious question, how many of those people would have died in the past 12 months if they didn't get COVID? The number is most likely not 500,000, but it also probably isn't 0.
Is it most likely something insignificant like 5,000?
[1] https://www.medrxiv.org/content/10.1101/2021.01.27.21250604v...
This can be answered using “excess mortality” data.
Studies have shown during that time period, about 600,000 more people died than would have been expected compared to deaths in the previous year.
The official covid death count is likely an undercount of deaths caused by covid, because a number of people died from covid related complications and got recorded as pneumonia, Alzheimer’s, or heart disease/attack/stroke related deaths.
https://www.nytimes.com/interactive/2021/01/14/us/covid-19-d...
Also offset by excess deaths over the next few years due to long term effects of a sedentary lifestyle, stress, and all the overcompensating we are likely to see next year with people trying to “make up for lost time”.
I'm not sure how outdoors-y fatalities will be impacted by all of this, but people are definitely not "doing fewer outdoor actives" right now.
That's a theory. Meanwhile, we know that many places are classifying anyone who dies within N days of a positive test (N is typically 30) as a "covid death", regardless of actual cause.
I can guarantee that not all of those people died from Covid-19. Point being: there's likely to be overcount and undercount, for different reasons.
In 2020, approximately 3,358,814 deaths occurred in the United States (Table). The age-adjusted rate was 828.7 deaths per 100,000 population, an increase of 15.9% from 715.2 in 2019.
Assuming the rates stayed the same or roughly so from year to year, it appears that not many of them would have died sans COVID19. Certainly well over 5000. If there is a trend, none of the data I looked at on the CDC site supported this, raw deaths have been rising in the last 5 years but death's per 100,000 have held. So if it's a small increase per 100,000 is "normal" given those trends 16% is still well outside the normal, so it's likely something like 300,000 or there about. I sure someone here could do the math to verify that but I don't feel like it. :)
ref: https://www.cdc.gov/nchs/products/databriefs/db395.htm https://www.cdc.gov/mmwr/volumes/70/wr/mm7014e1.htm
Are those side effects lists just a catch it all sort of exception where they throw anything there just in case? Honest question.
I wish the health agencies were a bit more open about their thought processes. OTOH, the rate of incidence doesn't seem higher than baseline AFAIK, which seems absurd. It also seems absurd that the various health authorities around the world would all make such a big deal of if if there wasn't some elevated risk. So I don't really know what to make of it, but privately, I'm leaning towards the interpretation that the idea is to avoid backlash against the vaccines by being irrationally strict about any potential hazards.
Yes, causation is hard to show with certainty.
However, regulator have to follow rules, and those rules probably err on the side of caution. Similarly to "first, do no harm".
I agree that the matter of public trust is also relevant here. In some countries large part of the population already does not want to get vaccinated. So the vaccinator is naturally motivated to prevent any PR screw-ups even at the cost of slowing down.
Sadly, this is the case. The German regulator's FAQ explicitly called this out; they are not interested in determining the path that saves the most lives, they are simply following the process that checks all of the boxes that the regulations require. In the EU this regulatory pause of AZ has likely killed thousands of people.
> The valid argument would be, those that issue the emergence order for use to should amend the order to acknowledge the issue but not block use immediately.
Or, more generally, in the emergency-order regime, all decisions that can demonstrate a clear 10:1 improvement in expected deaths should be taken, regardless of regulatory red tape.
The FDA and other regulators have over-fitted their process for "minimize likelihood of another Thalidomide, for drugs which have a small chance of saving a life, and a very small chance of causing harm". This is defensible for testing a new statin, where we have existing safe drugs to choose from, and we're looking for incremental improvements. But it's shockingly harmful in an emergency.
One thing that has become very clear is that the FDA and other regulators are structurally incapable of making even rudimentary risk-based tradeoffs in emergency situations, and we need to fix this.
A drug regulator should do its job, which is following established rules for approving and recommending new medicines. Not invent new rules, not push experimental drugs when new problems are being discovered on the go. Advocating for "greater-good" trade-offs and risks is a political effort, the regulator should be immune from political pressures.
I'm glad people there prefer to err on the side of going with established rules and caution.
If what you want is experimental drug being accessible to as many people as possible as soon as possible, you should advocate for the option to bypass the regulator and letting the people decide for themselves.
Do not advocate for corrupting the regulator.
> In the EU this regulatory pause of AZ has likely killed thousands of people.
I don't know how you came to that conclusion, but even if so, how many thousands of people would be eventually harmed or killed if the pause wasn't introduced? We don't know, because we are discovering properties and effects of the vaccines on the go. The data and estimates we have are based on short-term experience with the vaccines. They will change.
In treating people for illness it is a long established rule that "first, do no harm". And vaccine does not even help the patient with any illness - it is rather to help in case the patient would get one in the future. For many people, getting vaccinated has zero to negative benefit.
Nobody is entitled to get a fast-tracked rubber stamp to push vaccines on people. If you want to take experimental drugs, I support your right to do so, however I expect you let other people decide for themselves, including the regulators.
How many people will point to this or feel a bit hesitant about getting J&J vaccine now?
It should be possible to have a mature, good-faith conversation about this, even on a pseudonymous web forum.
That said, this is not a usual situation at all, and I think it's absurd, not least because of lives potentially saved during this pause, but because of the carry on effects with vaccine hesitancy, etc.
- Government breaks standard practice in favor of J&J corporation, allowing sales to continue After These People Died!!1!
- Government pauses J&J vaccine, experts condemn them for extreme caution.
Wrong. In a war you win by outsmarting other people. Maybe that's through democracy, maybe it's by moving faster, maybe it's by having better technology, maybe it's by having more technology.
This is a pandemic. A health crisis caused by a virus. In this situation you win by carefully understanding the nature of the virus and then determining what needs to happen in order to shut it down. Making rash decisions because it's "wartime" doesn't actually stop the virus. We can't blitz a virus. We have to take time to understand the consequences of our actions.
> coddle
Actually, we do have to coddle. If we squash people's concerns about the vaccine, then they just won't get it because they don't feel listened to. On the other hand, if we show people that we're taking their concerns seriously, they're more likely to go and take one of the other vaccines. Because the "unsafe" ones were pulled after all, so the ones left over have to be safe (not true, but it's going to work for a non-trivial number of people).
It also depends on the rate of community spread (and what's spreading) in the communities you're in.
Yes, your risk of dying from COVID varies with age, but not to that extent. Even among children, the death rate for COVID is an order of magnitude over the 0.000015% to 0.000030% chance of death it would have to be for the decision to stop using the J&J vaccine to make sense, based on the numbers we're making that decision based off of. Among the people who are actually being blocked from getting the J&J vaccine (e.g. mostly 20s/30s/40s adults), the decision looks much worse.
From a risk perspective, I wouldn't restrict either vaccine. But since we can easily use Moderna and BiontechPfizer instead for the most at risk groups it doesn't really change things, does it?
It compares the risks of dying from a blood clot after the AZ vaccine (about 1 in a million) to the risks we happily take every single day.
http://whatoneinamillionmeans.com
If you're not willing to take 1 in a million chances, it's gonna be pretty hard for you to get out of bed today
The perceptive gap between zero risk and extremely small risk is enormous. If I’m young and healthy, I can easily avoid the additional 1 micromort risk of taking the vaccine by simply not taking it. Now what?
Let me try one more way I have been thinking about it. I'm also weighing up whether I should get the vaccine and TBH made this site as much for myself as anyone else.
The point of the site is really to show the fallacy of there currently being zero risk in your life. Comparing 'none' to 'additional' isn't really what is happening. You have risks in your life every day, every time you do anything.
On any given day you already have about 1 Micromort's chance of dying from any unnatural causes. So that's 365 a year. So getting that vaccine puts it up to 366.
That's an increase in risk of just under 0.3% for the year, from an already pretty low baseline of likelihood of dying that we enjoy these days.
This way of thinking helps me. I'm hoping it might help some others too.
People's brains don't work that way. It requires a lot of education on probability, and even then the math often conflicts with our instincts.
Of course the real answer is to get more phizer and then stop using second rate shit.
> That's about 10 times less risky than walking down the stairs
and
> That’s the same risk as driving for 5 hours
Which implies that walking down some stairs is equivalently risky to driving for 50 hours. That seems... unlikely.
There are about 150 deaths per 10 billion passenger-miles in the US [1]. That means that a micromort (a 1 in a million chance of death) corresponds to about 66 miles driven, which would probably be about 2 hours of driving.
In 2000, 1,307 people died from falling down stairs[2]. The US population in 2000 was about 280 million, so 1307 / 280e6 / 365 = 1.27e-8, so the average person had about a 12.7 in 1 billion chance of dying by falling down stairs on a given day. It seems reasonable to estimate that on average, each American goes down stairs about once per day (some people never go down stairs, others go down them multiple times per day). As such, I think the estimate for "risk of going down the stairs" should be more like 10 in a billion and less like 10 in a million.
[1] https://en.wikipedia.org/wiki/Transportation_safety_in_the_U...
[2] https://danger.mongabay.com/injury_death.htm -- "Fall on and from stairs and steps"
I took the driving risk as being 250 miles of driving with an average 50mph speed (The risk of dying must be higher at high speed so wanted to take a high average to be fair).
Interestingly, running the numbers for the UK shows that the annualized per-capita risk of dying on stairs in the UK is more than twice as high as it is in the US.
We have approved vaccines with worse side effects before. The difference is that we knew what those side effects were and weighed the risk vs reward and made the call to use it.
You're right that 7 / 7,000,000 are good odds, and most people would likely take them - but it would be unwise to not give people an educated choice between vaccines if there are known risks.
not really. that's not how statistics work. it could grow, it could shrink.
> All six cases were in women aged between 18 and 48, with symptoms appearing six to 13 days after vaccination.
Presumably, some of the 7 million people who have gotten the vaccine did so in the prior 5-12 days. It is reasonable to expect to see more cases over the next 6-13 days from the moment we pause J&J vaccination.
And for anyone that thinks this is just normal incidence of blood clots being blamed on the vaccine - that's what was said about AstraZeneca originally, and if these clots are anything like those it is absolutely not the case. Those are serious clots that are very rare to see period, let alone in young people, and require different treatment than normal clots (they have surprisingly low platelet count).
I suspect US agencies had good reason to want to pause J&J given all of that - the AZ vaccine issues were also disproportionately affecting women interestingly.
I suspect that, as soon as we start looking for blood clotting post-vaccine, then you'll find more cases that may have not been caught otherwise due to their not being severe enough to be noticed.
https://twitter.com/HamidMerchant/status/1381797044495466504
If that is the case we could then target this vaccine to the rest and have it be much safer while giving out the Pfizer-BioNTech or Moderna vaccines to this group.
End result is everyone still getting their vaccine fast but less side effects (and possibly deaths due to worst case side effects). This is why we need more data or the time to study the data in this case most likely
They are not giving people an educated choice, they are taking that choice away until they deem it okay to give it back. Education is knowing that 7/7,000,000 had a blood clot + the other tests that were done leading up to its release. We know that now. We're educated.
We should give people an educated choice. With unknown side effects we are not doing that. Thank you for pointing that out.
Make sure you cover every possible thing, no matter how unlikely.
The CVST incidents give a lower bound on risk. The trial data give a rough upper bound on risk (rough due to the small sample size). Knowledge is being refined here. We can't make educated choices without knowledge.
Hard to give people an educated choice without looking into the issue first. Once they know what is going on it will most likely be back to normal. There was a similar issue in Europe, but that neatly overlapped with a delivery shortage of the affected vaccine.
Don't know if it matters to anyone, but the "FDA has suggested that health care providers pause the use of the vaccine while the side effects are being studied. However, providers are not prohibited from using the vaccine if they feel the benefits to an individual patient outweigh the risks." [1]
1. https://www.npr.org/sections/health-shots/2021/04/13/9867670...
Well, obviously it didn't. Exactly because it is so rare
A clinical study with (I think) 30k people can't detect something that's 1 in a million case
> FDA bureaucrats
You mean doctors. These decisions are done by doctors as they should be. The current (acting) head of FDA is a physician too.
To be clear, we haven't determined that it's actually a side effect. That's why they've stopped, to get a better handle on what actually happened, and what to do about it.
It could be related to the vaccine, it could not be. It could be 1 in a million, it could be 1 in 100k.
It is a two sided equation.
Not sure why the J&J vaccine had to pause for older population where clearly the vaccine has a much better benefit/risk profile though. But at least in my area of the US the vaccination rate for senior citizens is quite high already.
It's not clear that this even has to do with the vaccine. If you gave 7 Million people a glass of water on the same day, I'm sure at least 7 of them would experience some sort of moderate to serious health outcome in the days that followed.
You shouldn't expect side-effects this rare to show up in the trials. The AZ trial was based on ~32k participants (https://www.astrazeneca.com/media-centre/press-releases/2021...). Your probability of observing a 1/1,000,000 occurrence in 32k observations is something like 3%.
It's impossible to uncover (with statistical significance) 1/1,000,000 side effects without giving millions of doses.
The fact that a rare side-effect has (maybe!) shown up should not negatively impact your priors for how safe the vaccine is. If anything, the fact that we're talking about 7 / 7,000,000 cases should reassure you that we're catching extremely rare stuff, which means we would have caught anything more serious too.
A more general way of putting this is that, by doing a trial you don't prove there are _no_ side-effects, you just put an upper bound on how common they can be. This is the best that science can do! Epistemologically speaking, you can never prove the non-existence of something, you can just show that it doesn't occur in the places you've taken measurements, at a frequency that your experiments would detect. (This is the "black swan fallacy", as John Stuart Mill originally formulated it.)
The main benefit of challenge trials is to speed up development as I understand it not to broaden risk estimates.
Right, which is why it was crucial to have such trials a year ago. We could have shipped vaccines 3 months sooner and saved hundreds of thousands of lives.
Unfortunately, no health authority was willing to risk blame for any disabilities or deaths stemming from deliberately exposing consenting people to covid. So we had to use much larger sample sizes and wait longer to know which vaccine candidates were effective.
You know, for all the continual fear mongering about coronavirus last year, the constant reminders of who was most at risk, the hyper importance put on masks and cleanliness, etc it is shocking to see things put this way now.
A quick duck duck go shows that these are the symptoms:
Tiredness or fatigue
Difficulty thinking or concentrating (sometimes referred to as “brain fog”)
Headache
Loss of smell or taste
Dizziness on standing
Fast-beating or pounding heart (also known as heart palpitations)
Chest pain
Difficulty breathing or shortness of breath
Cough
Joint or muscle pain
Depression or anxiety
Fever
Symptoms that get worse after physical or mental activities
Apart from the loss of smell, those are all things that are hard to quantify and could be something you are not aware of until you start looking for them. At which point you might become anexious and really start to notice them.[1] https://www.nature.com/articles/s41586-020-2918-0/figures/2
When not considering any externalities, anti-vaxxers and everyone that comes up with anti-industry and anti-establishment conclusions is rational, but inaccurate only because they dont consider what was not said.
Even with regard to COVID itself, most of the official communication is about avoiding death when the reality is that its not about only avoiding death its about all the additional debilitating effects in the vast “recovered” statistic, so it is rational to decide to ignore that once you do your own math and noticing who is actually dying. But it is not accurate because it doesn't factor in the unsaid aspect.
Its not just the internet, TV and radio also jump on the headline
The entirety of my comment is a cohesive statement and not just about this headline
But I agree J&J will definitely resume in some capacity in the near-ish future.
https://www.bbc.com/news/health-55302595
Quote:
"The MHRA said about four people in a million would normally be expected to develop this particular kind of blood clot - though the fact they are so rare makes the usual rate hard to estimate."
Full disclosure: I took the J&J vaccine last Thursday, and would do so again right now.
And its probable that these incidents are concentrated in a small segment of the population (young & health maybe women). So your denominator is very inflated.
If you can save 20-40 lives by just giving young women Pfizer and using J&J on 50+ year olds (for whom the risk might be literally nothing) then its a no brainer.
Not doing so is killing 20-40 people for no reason.
When that investigation ends, then the J&J vaccine can be opened up for those willing to take the risk, which by that time is better known.
I think we still have to remember that vaccinating everybody is not needed to resume a normal life.
Personally I wouldn't want a vaccine with the problems that AZ and J&J have, but if others are willing then they should have the opportunity.
Even more so because here in Canada we do not have much AZ yet anyways (and no J&J yet), mostly Pfizer and Moderna.
More to the point, they have temporarily paused because the usual treatment for blood clots can make this particular type of blood clot worse. So they are pausing to give the medical community enough lead time to get up to date on treatment protocols.
Vaccines are held to such a high standard. We wouldn't have approved even Aspirin if we applied the same standards.
This is 1:1000000 of a severe event, but affects men as well. HOLD THE LINE - It affects a.... Man!
I'm sure people will be tempted to jump in here and state their case as to why certain long term effects are not possible, and why this is conspiracy theory misinformation. But that's not the point. The reality is that humans regularly fail to understand infrequent or long-term consequences of new innovations, despite the best of intentions and despite the use of the best science available at the time. This has happened repeatedly in the past - see numerous prescription drugs that were recalled, or the use of phthalates in shampoos, or asbestos, or whatever else.
In the case of J&J, consider that this is happening against a backdrop of a continuously changing story about the AstraZeneca vaccine, increasing reports of COVID vaccines affecting menstruation (https://vajenda.substack.com/p/the-covid-19-vaccine-and-mens...), and a rushed emergency use authorization process that bypasses typical methodology for approvals of vaccines. The comparison isn't between the IFR of COVID-19 and the fatality rate associated with this vaccine. It's between the IFR of COVID-19, which is known to be very low, and the unbounded potential of near-term or long-term fatality or other side effects from the vaccine.
I know several people who are not interested in covid vaccines for what as far as I can tell are political reasons (although there are a few concerns about using a new technology before long term studies are performed). Right now they aren't anti-vaxxers. They get vaccines and they get their children vaccinated. It's just the new covid ones that they're hesitant about.
If we just lump them in with anti-vaxxers then they might decide to go make friends with the real anti-vaxxers. And as a big of a problem as covid has been, I'm more concerned about polio making a comeback tour.
[0] that don't target cancer
So where does one draw the line?
What level of shutting something down is justifiable in the name of safety?
Who is allowed to make that subjective decision?
It's a slippery slope.
It's arguable that we should wear masks FOREVER because they reduce death rates for every respiratory disease.
This feeling. Of why are shutting down because of these few lives.
Is exactly how people have felt about shutting down the whole economy over the small-ish fatality rate of Coronvirus.
There's just different levels of risk tolerance.
Who is the more moral person?
So, take pause and examine the situation. Are these people actually anti-vaxxers, ie they oppose all vaccination due to weird paranoia about autism due to a discredited "study". OR are they against this one vaccine because of political affiliation.
I'm really concerned that if we call out the people who are afraid of this one vaccine as anti-vaxxers that we'll only succeed in introducing them to the wider world of being afraid of all vaccines.
Find a different term so that we don't introduce these two groups of people to one another and give them a reason to join forces.
It's not easily attributable to "political affiliation." Trump was touting the vaccines through his whole campaign and is still bragging and taking credit for them. MSNBC did one of those TV segments where they go and interview backwards people from America's hinterland who weren't planning to get vaccinated, and although most were Trump voters, not a single one said they would change their mind if he advocated taking it.
The actual difference between these vaccines and others which is driving skepticism is that we have no observational data about their long-term effects.
US agencies are the ones recommending a halt. US refused to approve AZ, and Europe halted it, in many countries imposing additional restrictions when resumed. Doctors specializing in the field agree these are legitimate concerns.
If people want to argue cost/benefit tradeoffs, or speculate on things we aren't sure about yet that's totally cool, as long as they are upfront about it. And I understand if someone still wants to get J&J and is upset or just generally disagrees with the total/forceful pause.
But I don't understand treating anyone that has a concern about J&J like a brainwashed neanderthal, when literally the actual medical community has reservations about this particular vaccine. As a young woman I would not get J&J right now. Luckily I was able to get Pfizer instead.
Anyway, I agree there is a problem more generally with scientific education that can push "moderately misinformed" people into much deeper rabbit holes instead of working to educate them. I guess my point is just that I think this is a good example of how people have gotten so entrenched in the issue that it has reached a new level. There will be cases when the science is legitimately unclear, but the popular sentiment will all of a suddenly decide "science says X" and then the internet runs with it.
Another example - there was an ~2 week period last March where I had multiple educated/"science supporting" friends talk down to anyone considering a mask. No it was not coming from a hoarding perspective and it had 0 sense of uncertainty about it. These were strongly worded statements about how "masks don't do anything for COVID, the science is pretty clear".
Edit: got the wrong agency, it was FDA, not CDC
It's not only a disservice, it's a biased way of thinking which only serves the one making the statement, given it allows them a way to alleviate their concerns about having received a level of uncertainty from their actions. I get them them because I also got that shot!
It's the same idea though, and should still be called out. It's people who have unqualified medical opinions, and who are then often spreading that opinion to others as if it's useful.
Let the agencies figure it out, pay attention to the latest recommendations from them, and go with that. Anything else is just the blind leading the blind and should be called out.
Iatrogenesis rivals strokes as a cause of death. Most doctors are just slavishly following official doctrines from authorities, and sometimes those authorities get it wrong. We don't even have to look to the Before Covid Times to see examples!
Yes. That's correct. That doesn't change what I said.
Answer me this: why do you think unqualified individuals are better suited to get it right?
Just because there are examples in the past of people who went against the recommendations who ended up being right, doesn't mean you should take everything else into your own hands. Unless, of course, it's literally your job.
It’s a subtle, but IMO important distinction. If people wanna rationalize not getting the shot based on their own misunderstanding of the science, that’s fine. That’s okay.
We don’t need universal understanding here for the vaccine to do it’s thing. Let those who want to get it, get it. And those who don’t, to not get it.
It's not even 3 hours into my day and I've already received 3 texts from family saying something along those lines regarding J&J, even if it gets unpaused. It's a much more prevalent thing to say than you think.
> If people wanna rationalize not getting the shot based on their own misunderstanding of the science, that’s fine. That’s okay.
It's not okay. We need shots in arms. And you're doing your part by enabling those who are misunderstanding the science by making them feel like it's okay to not get the shot.
Most to the point, declining to take painkillers does not adversely impact other people's health.
This is not a good analogy.
eta: ironically, the problem with the opioid crisis was not too much regulation and oversight by "the authorities", but too little; too much freedom for doctors to prescribe stronger painkillers, and for patients to request them.
(Just using masking as an example, if any onlookers strongly believe that masking is efficacious for the stated purpose just imagine I gave a different example, although I don't see how anyone could reach that conclusion about masking specifically based on the research literature out there which is neutral at best)
Or as another example, the CDC loves to try to encourage people to take the flu vaccine, and yet I was shocked to discover that it takes 71 flu shots to prevent a single flu case, 29 flu shots to prevent one ILI (this is a better number than the flu case number since really we care about ILI in general, but even so 29 is an abysmal number), AND that regardless of the mediocre reduction in cases/ILI, it makes essentially no difference in hospitalizations.
Citation on the flu vaccine stuff: https://www.cochrane.org/CD001269/ARI_vaccines-prevent-influ...
--
I didn't realize until this year how much of "public health" involves (a) actively and intentionally lying to the public (for example, if you read about the AIDS crisis you learn about the "noble lies" told about who was vulnerable as well as the not-even-noble lies like when Fauci told people you could get AIDS from close contact with someone with AIDS when the scientific evidence showed that to be false), and (b) is really a giant marketing campaign for various big pharma interests (I say that as someone who is an unashamed free-market capitalist, not that the US is actually a true free market when it comes to the pharma/medical industry)
I'm insisting that the average unqualified individual should not think they have a better chance of being correct over the authorities in question.
There's no other rational option for unqualified individuals than to listen to medical authorities unless you have a medical degree yourself and have read and analyzed the research yourself.
Despite how much smarter and informed humanity is, we still make decisions based on trust. Science can only explain so much and runs out of answers eventually.
Did they? Or was the chance they'd come in contact with Covid at that point very low and those masks would be of much better use at hospitals where the chance of coming into contact with Covid was very high? At least, that was what the experts were saying at the time. I donated my N-95 masks (that I had from California fires) not because we thought they didn't do anything in January 2020, but because the experts said they were of better use in hospitals.
> Science can only explain so much and runs out of answers eventually.
You say this as if there's a better place to find answers. Where is that place?
You're saying a high risk person (high risk meaning they would likely die from covid - immunosuppressed, etc.) wearing an N95 mask and quarantining was a bad choice? I'm not sure how those masks would be better used if the person is at a high risk of dying to covid.
> You say this as if there's a better place to find answers. Where is that place?
Interpreting all the data available to you. Would you have shamed a person for not choosing this man as their surgeon https://en.wikipedia.org/wiki/Christopher_Duntsch after they researched his past operations. There are more factors than just the research that need to be considered.
Critically the problem with your reasoning is the last sentence. No, you do not need to have a medical degree to be right when a doctor is wrong; ask anyone who’s had a medical issue that all doctors agree does not exist.
> appeal to authority
authority -> trust
> disappeal to lack of authority
not authority -> not trust
The contrapositive of the first proposition would be
not trust -> not authority
which is a rather different claim.
There are other sources of information besides the public health agency of your particular country, for example public health agencies in other countries, or directly looking at the stats and research papers. In this case, looking at the stats makes it blatantly obvious that your risk from the J&J vaccine is much, much lower than your risk from getting COVID, so if your choice is "J&J" or "no vaccine for another month or two", you should probably pick J&J.
If you can't be intellectually honest enough to admit that there is a difference between "we've used this platform in theoretical research in small numbers" to "we mass-market and roll out this novel vaccine to billions of humans worldwide", you shouldn't be in the discussion, IMO.
The speed of access for these vaccines is that they started mass production while testing was ongoing, rather than waiting until after testing to start production
TL;DR you can probably s/mRNA/adenovirus vector/g although I will grant that adenovirus vector seems less "experimental" than mRNA does
The mRNA vaccines both seem to be fine, by comparison.
My argument was definitely tailored for the mRNA discussion, although the purpose was more to illustrate the broader principle, but, not knowing a whole lot about adenovirus vector vaccines specifically, is it even the case that adenovirus-vector vaccines have been widely used in the general population?
I couldn't find great info with a cursory search (indeed the top result is the CDC which consistently fails to cite anything they ever claim, ugh), but I wonder if the general argument still applies for these types of vaccines as well.
Anyway, thanks so much for catching and pointing out my error there.
fwiw, new and better better technologies need to get used for the first time, eventually.
No-one disputed that, I'm just pointing out that it is a very valid point for someone to say "I have concerns that we're rushing out an experimental vaccine". You might take issue with the specific wording (I don't) but the general point I hope we can agree on.
You can always argue for making things slower and experiments longer, the problem is, that there is a pandemic going on with 3M deaths in the past year. Actually people seem to think that you can develop vaccines without being rushed, but it doesn't seem to be the case. There are several reasons why other vaccines took years:
- it was a long time ago and scientists had a lot less knowledge, experience and older technology. (Think e.g. the mRNA vaccines, which J&J is not one of, where the first candidate could be completed in something like 2 weeks after the isolation and sequencing of the virus.) - they had to start from 0 for a new virus (because they new less, etc.). Like for the polio, or HIV. In the case of SARS-CoV2, they could build a lot on the experiments from SARS-CoV1. As far as I know, there was a vaccine candidate back in 2003, but by the time it would go into phase-3, the epidemic was over. Also, it seems that research never stopped about the coronavirus vaccines, so there were new results between 2003 and 2020 that the mRNA vaccines built on. - some viruses are easier to develop a vaccine for. (E.g. the HIV is not one of them, because it's very good at evading the immune system) - I've already mentioned this, but if the vaccine candidate doesn't get ready on time because of the above reasons, then you may have to wait for years before you can do a phase3 trial because there will be no people getting infected, so you won't be able to measure the effectiveness. This is what happened with the ebola vaccine in 2014. Now the vaccine is 7 years old, but it doesn't make it any safer, because there weren't people who could be vaccinated. (Well, of course, you could vaccinate them and wait for any long term side effect, just in case, that would show up without being infected, but that doesn't seem like a very important data point.)
But again: why would you want to wait for several years in a situation like this when we do have a pretty clear picture of both the worst case risks of the vaccines and the risks of the disease (which are higher than the worst case risks of the vaccines).
I would disagree that calling it "rushed, experimental, and not necessary for [the original commenter]" is an over-simplifying claim. Indeed I find the "we've done theoretical research with platform X for years" to be the oversimplification. That being said I do agree that there is a difference between an experimental platform and a new platform.
> But again: why would you want to wait for several years in a situation like this when we do have a pretty clear picture of both the worst case risks of the vaccines and the risks of the disease (which are higher than the worst case risks of the vaccines).
Starting with the "higher than the worst case risks of the vaccines" part, FWIW, this is true in general but not for all individuals. For someone like me (20's, active, no major health conditions), the acute side effects of getting a SARS-2 vaccine far outpace the expected level of symptoms from SARS-2 infection itself. (Speaking from a personal risk reduction standpoint only, I don't want to get into the ethics of medical collectivism for the purposes of this discussion). I don't think you would dispute that, but just wanted to mention it because it's because taboo (and indeed you can get actively censored) to say "for my specific health circumstance the vaccine is more dangerous to me".
As for the more general point about understanding the risks of the vaccines and the disease fairly clearly, I would say that we understand the virus far better than the vaccines. Indeed it really saddens me how we've wasted public health dollars on messaging to people that immunity to reinfection is not a thing (when it is most definitely a thing) and to be super spooked about variants despite the fact that SARS-2 is not going to magically mutate away from the spike protein anytime soon (i.e. there's plenty of epitopes for our immune system to work with even for the highly artificial immunity produced by making the body's cells manufacture spike protein exclusively).
I will grant though that we have bounds on how bad short or medium-term adverse reactions could be to the vaccines. Personally I worry less about the (using mRNA as an example here to illustrate a general point) "it's going to turn me into a human GMO" pseudo-argument than I do things like (a) "is the rate at which spike proteins get produced in the body much more of a steep increase followed by a steep dropoff leading to greater potential for acute inflammatory episodes than via naturalistic infection" as well as (b) "could we be over-sentitizing the immune system to react too strongly when it detects spike protein, particularly for those who already had COVID-19 before ever getting the vaccine". If you're not aware, an absurd amount of people who have already gotten COVID-19 and therefore have naturalistic immunity are still getting the vaccine, either because they're "required" to (aka they don't know or want to fight their job's requirements) or more often because they've been brainwashed to think that the variants evade natural immunity which is just a total media-propagated falsehood.
> In the case of SARS-CoV2, they could build a lot on the experiments from SARS-CoV1
Totally agreed and I wish more people knew that the virus causes COVID-19 is called SARS-2 and that it is directly related to SARS-1 (I'm referring to layfolk here). As a separate tangent I wish more people understood that the emergence of SARS-2 means we don't really need to worry about SARS-1 anymore because anyone exposed to SARS-2 will be cross-reactive with SARS-1.
> I've already mentioned this, but if the vaccine candidate doesn't get ready on time because of the above reasons, then you may have to wait for years before you can do a phase3 trial because there will be no people getting infected, so you won't be able to measure the effectiveness.
This is simply not the case for an endemic seasonal respiratory virus. You'll have plenty of cases, especially since we're basically PCR-testing the whole globe (I don't think we should be, to be clear). But I totally agree that the apparent benefit of vaccines declines exponentially as time goes on, particularly with SARS-2 where the fact that it is deadly for the very elderly and harmless for the very young means that yearly recurring mortality is going to essentially vanish after it's propagated through the current world population (as an aside, this fact is one of many reasons why all the hysteria around the virus was absurd from the get-go; amortized over several years the mortality of SARS-2 is entirely unremarkable)
> But again: why would you want to wait for several years in a situation like this when we do have a pretty clear picture of both the worst case risks of the vaccines and the risks of the disease (which are higher than the worst case risks of the vaccines).
Yeah, to conclude I want to bring it back to my earlier point which is that once the virus has propagated through the current world population (more or less), the set of SARS-2-naive individuals will become dominated by the very young, who are not at real risk of COVID-19 and therefore they will develop immunological memory while young when they are incapable of being harmed by SARS-2. This means that recurring yearly mortality will fall off a cliff (albeit, if we keep labelling deaths the way we do we won't see that reflected in the numbers nearly as much as we should). Which is why I think the restrictions and everything else, even if they had worked in places like the US or Europe where they totally failed, were always a bad idea. But the other side of that coin is: yes, insofar as you do think SARS-2 is something worth really freaking out over, we absolutely have to rush the vaccines because if we wait 2 years then there won't be any real COVID-19 deaths left to mitigate.
The batch is not "rushed" more than it's needed: there IS an emergency. It's also not experimental. The experiments have all been done (up to phase 3). It's perfectly normal to only see 1 in a million (or even 1:100 000) side effects after starting the vaccination of the general public. Simply because the phase 3 will never contain millions of people. I've checked, and the 30-40k studies we had with these seem to be indeed large. I.e. safe.
What you think about your immune system is kind of irrelevant for a few reasons, but talking up their immune system seems to be a general self-convincing strategy for a lot of people. First of all, it's not apparent that you have contracted the virus. Unless you have an antibody test showing that you are seropositive, you simply don't know, but the chances aren't very high. What you can be sure about is that you have not contracted "all" variants. If you live in the UK then you had the chance to meet the UK variant (B117, IIRC) and the base variant (D6.... whatever). Very likely not both. And the immunity for the base variant seems to work pretty well for the UK variant, so it doesn't even matter if you met both.
But even if you know you are already immune, the natural immunity doesn't last that long. The vaccines give you higher antibody levels (at least the mRNA ones do, again IIRC) and better immunity especially due to the second dose. (Which you can't really simulate with a second infection within a few weeks.)
And at last: you can't generalize from your own experience. Looking at the numbers, which we do have a lot of, people who haven't met the virus and don't have immunity should by all means get the vaccine. Because the virus is a lot more dangerous (several orders of magnitude more dangerous) than even the J&J or the AZ vaccine. Though the exact risk profile will depend on individual factors, of course, but since you've talked about all vaccines...
That's the definition of "rushed".
Vaccines typically take several years of testing before being approved. These aren't approved according to those standards. Manufacturers are absolved from risks because of this "emergency use" status. Why absolve them if there are no risks? If they truly believed these were safe and of tremendously important benefit, they could stand up and say "we accept responsibility for negative outcomes in accordance with ordinarily approved medication, and waive our rights to emergency use protections". Then everyone would rush to take them as doubts would be broadly eliminated.
(Why are we seeing mRNA vaccines for COVID and not other diseases, if it's not new technology? Because the vaccines for other diseases didn't work.)
You are totally right that there could be some magical protein in the vaccines that causes you to drop dead in two years. There probably isn't though, so what you call "rushed" other people call "saving lives".
If you've seen or lived the effects of starvation firsthand, you'd find it difficult to understand why suddenly everyone is willing to do anything, even destroy their own livelihoods or take rush-developed intravenous shots, to try and save the lives of a significantly smaller number of predominantly elderly people who were about to die of just about anything else anyway, at the expense of those 9 million (or any other of preventable causes of death that kill in higher numbers per year and have been known about for decades, for example: smoking).
Why not spend a year making the manufacturing of cigarettes illegal, have a worldwide crackdown with cigarette company executives hauled to jail for crimes against humanity, make it illegal to depict smoking in any media, censor all images of cigarettes, and launch a 24/7 every news channel, every street corner propaganda campaign, with celebrities publicly blacklisting smokers?
Save significantly more lives in the first year, and keep doing so year after year. Wouldn't need to trash the economy, ruin businesses, or risk plunging anyone into poverty, etc - and no need for anyone to take a rushed, long-term untested shot.
The sad thing about this kind of argument is that it never goes away. Whatever happens. I started an argument more than a year ago with a guy, when we had 3000 deaths. World wide, total. He kept saying that it's less than the number of people who die in car accidents in a day. And he was right. What he didn't get is that without counter-measures it would grow exponentially for quite a long time and to quite a large total.
And it did grow and we continued this argument for months (with 1-2 comments a month) he had to keep raising the stakes. Next it was less than the number of flu deaths per year, next it was less than the number of car accident deaths, this time per year, then the number of HIV deaths, and then he just stopped arguing. I pinged him at 1M last June, never responded. I don't think he changed his mind.
I see your argument as a continuation of that. You just raised the stakes again, but however much the total count will be, you guys will always find something bigger. Implicitly stating that it's only worth taking counter measures against the worst cause of death. (Be it lockdowns or vaccines.) But it doesn't make sense. This is ON TOP of all those. Also, let's not forget that the only way we managed to keep it down to 3M is by imposing pretty strict lockdowns worldwide. Without those it would have been a lot worse. And even with these lockdowns the health care system is waaay overloaded in a lot of places, which means that COVID kills indirectly as well.
Yes, help people who are starving: we can easily do so by donating money. As long as you have the money. But don't make it worse by not vaccinating and letting COVID kill others, kill even those who are very poor (they definitely have worse chances) and kill the economy which obviously means more people starving and less help for those who have already been starving.
The "per year" number for COVID cannot change now, it's been a year. It is what it is.
COVID, in light of other preventable deaths, and especially in terms of life years lost, is not of justifiable greater concern compared to others, and from mortality rates/demographics and seroprevalence, this has been broadly known from not long after the beginning. The dollar cost versus life-years-saved is borderline insanity.
The argument lockdowns saved lives has been thoroughly debunked [0], and even the most cursory common-sense look at any per-capita chart by country and measures employed confirms that at a glance.
If you want to continue killing tens of millions per year so you can save the lives of far fewer, you have no standing. Frankly, that position disgusts me.
[0] https://www.aier.org/article/lockdowns-do-not-control-the-co...
I don't know where you are getting with this. As I said, this is at best an independent problem that can (and should) be handled. In reality it's worsened by the pandemic.
> The "per year" number for COVID cannot change now, it's been a year. It is what it is.
Though I think I didn't say the "per year" number would grow now, you are actually wrong for two reasons:
- while it's been a year, the beginning of that year was pretty mild, less deaths per day than during the summer or these days. So as we move the window, actually the per year number will increase. E.g. if you look at the "total deaths" graph on Worldometer [0], you'll see that it ramped up around the middle of October. It accelerated about 2x (but at least 1.5x).
- we got these "wonderful" results with various restrictions. And you are agruing for no restrictions, but you can't prove that no restrictions wouldn't yield much worse numbers.
> in terms of life years lost, is not of justifiable greater concern compared to others
I've already responded to this: it doesn't have to be a greater concern. It's a preventable concern. As far as I can remember, we were talking about vaccinations.
Also, years of life lost changes as the epidemic goes on and as the virus mutates and seem to get more aggressive (which is an affect of breeding it in a large number of humans). And let's not forget again, that the numbers are affected by how much the health care system is overloaded. Young people will die if they can't get into a hospital because too many people get sick at once.
> The argument lockdowns saved lives has been thoroughly debunked [0],
Yeah, I know. The whole pandemic has been "debunked" quite a few times. The first "debunk" I've read was a year ago, when a guy started lamenting that it would just die because of the network effect. It didn't. I've checked one random article from your link. It looks pretty weak. It just says that no matter what, the epidemic wave just stops after 6 weeks, because that's what it does. It lumps together countries like Sweden and Taiwan, which is crazy in its own right, because Taiwan has 11 deaths/30M people today and Sweden had like 8k/7M back in June (IIRC that's when that article was written). Needless to say, with the 3rd wave in Europe, the 6 week rule is out of the window: our 2nd wave (here in Hungary) was in a decline in mid February, when it started to rise, probably due to the spread of the UK variant. Without any change in the lockdown policy. Our hospitals have been full for about 1.5 months now. We've been world leaders in daily deaths for probably a month or so.
Yeah, so the article after just saying that the lockdowns don't do anything, because all countries seem to behave the same, concludes with "well, we certainly need to explain this..." (they seem to read my mind). And then say nothing about it. But they have included this (just to contradict you): "Certainly, a full complete lockdown reduces the spread of the virus."
People forget, that epidemiology is a well established field of science. It's only new for them. If I'd have to guess why the epidemic could start to decline on its own, I'd say that people just shit in their pants after a while and start to keep more distance. This could probably be seen in the mobile tracking data if anyone cared.
The sad thing about the lockdowns and the restrictions is that they work pretty well. If combined with all the other efforts and if people comply. Because in the end that's what matters: what people do. Not what governments say they should do. If you (or any of those authors) care to look at East Asia, Australia and New Zealand, you'd see that it can indeed be controlled pretty efficiently. Not for free, but for a lot cheaper than what most of the Western world ended up with. What they do is the complete opposite of what we're doing and what you re suggesting. Instead of ignoring, they react very quickly and vigorously. Closing entire counties if they found a few infected (that's e.g. what I've heard from a guy living in Thailand - they have 70 dead for 70M). And this allows them to have less restrictions overall. Because math. You can stop it when it's just a very low number or you can fuck around and stop it when you have a lot of dead people, when your hospitals are full. Of course, if you can stop it by testing, contact tracing, light restrictions (no mass gatherings), masks, etc., all the better.
Another piece of interesting (but not unexpected) information is that the economic effects indeed correlate with the number of deaths. [1]
> If you want to continue killing tens of millions per year so you can save the lives of far fewer, you have no standing. Frankly, that position disgusts me.
I don't kill anyone, but you definitely look angry and seem to handle this on an emotional level. Which I get, a lot of people do this but it doesn't help with having a logical argument.
[0] https://www.worldometers.info/coronavirus/ [1] https://ourworldindata.org/grapher/q2-gdp-growth-vs-confirme...
I've linked to 30+ studies supporting mine, none of which you've mentioned or shown studies that counter them (I'd expect at least 10's of counter studies if you have any kind of a point, hundreds if it has merit deserving of such servitude).
Your examples of lockdowns "working" are East Asia, Australia and New Zealand. Firstly, most of East Asia actually did comparatively little versus the West, especially early on - when they were at the epicentre - and is hampered in implementing lockdowns by a significantly higher population density, and in general, in the case of Japan, a significantly older population, placing them at an immediate disadvantage at that outset.
Your other examples of Australia and New Zealand are poor. If anything is prone to be an outlier, and worthy of less consideration versus other countries, it's these two. Especially New Zealand. It's one of the most isolated countries on the planet, has a tiny population and little through traffic. Compare numbers against any other pandemic (eg, Swine Flu 2009), and you'll see it's always going to do well just fine regardless of what measures may or may not be employed.
Considering the well-established link between the sun and the proliferation of these kinds of viruses (ie, a "flu season"), which happens for a variety of reasons (not least is Vit D production), nullifies those countries as useful controls, particularly against Europe and North America.
Finally, we have the figure of 9 million people who starve, and 8 million people who smoke, both of which are preventable, and both of which could be solved which much less effort, less expense and less social cost, and these are just two - but you still wish to persist in saving the lives of considerably fewer, the bulk of whom were already near death anyway.
None of your arguments make logical sense, and you are unable to back them up with science.
Further, you haven't bothered to even attempt to refute my core logical arguments or the bulk of science I've presented to back them up.
I'm not learning anything from this conversation, but thank you for your engagement. Go well.
The so called long-term effects have been mostly non-existent with any vaccine. First of all, the very expression "long-term effects" is vague. Do we mean effects that only materialize over the long term (i.e. a long time after being administered) or effects that last for a long time? The latter can be known (well, with a worst case estimation) even with short testing.
And as far as I am aware, there is very little evidence of the former happening with former vaccines. I.e. the vaccine inducing some systemic change in your body that remains undetectable for years.
> If they truly believed these were safe and of tremendously important benefit, they could stand > up and say "we accept responsibility for negative outcomes in accordance with > ordinarily approved medication, and waive our rights to emergency use protections".
First of all who? You seem to mingle several groups into one here. It's not the pharma companies who believe that that these are very important, but the society. (Well, at least the ones who don't live in denial.) The importance stems from the seriousness of the epidemic.
And safety is not a binary/boolean attribute. Safety can be measured and the accuracy of the measurement has a confidence (i.e. a probability that it's within the estimated limits). Now the claim is that this measured safety is way above the safety of contracting COVID. And this is the very reason we know that it's beneficial. For the society. It's pretty clear that pharma companies don't make nearly as much profit as much it is beneficial for the individual countries. Just try to add up the cost of the lockdowns e.g. for a year and then devide it by the number of doses and see how much they should cost if calculated like that. You know what, let me do the math for you: a year of lockdown has been estimated to cost 251bn GBP for the UK[1]. The UK has 66M population. Let's calculate with 266M doses. That would give you 19GBP/dose (~26USD) for the vaccines per dose. Per year. But they won't vaccinate everyone, 80% would already be an over estimation (which would increase the value of price/dose to 32.5GBP and we're not just talking about money we're also talking about lost lives and a lot of frustration, which would further increase the value of these shots.
Comprared to that, the AstraZeneca costs about 2USD, IIRC, the EU pays about 16EUR (14GBP) for the Pfizer/Biontech one.
So it's not that the tremendous value gets all snatched up by the pharma companies. Also, they do have a responsibility. In the US they have been waived, but not in the EU. And guess what: a lot of people keeps saying the same things over here. (Including* that they don't take responsibility.)
The reason the US waived these companies is exactly because the vaccines are so important and valuable for the sate (i.e. for the people). A quick rollout was more important for them, than for the pharma companies. As a side note: some politicians over here (EU) think that the US did it the right way by not wasting time on negotiating hard with the pharma companies and that the EU is behind exactly because of that and that we should have waived them as well. (I'm not sure I buy into it.) But the EU non-waiver is an assurance for everyone else, including the US citizens. Yes, you may not get a million $ check if you happen to be unlucky, but it still shows that the companies indeed do have the confidence in their product you were talking about.
[1] https://www.theguardian.com/business/2021/mar/22/a-year-of-c...
Do you still really need to get the vaccine in that case?
The CDC says yes, but their reasoning is purely based on FUD: "experts do not yet know how long you are protected from getting sick again".
According to the available data, there has been only 71 confirmed cases of reinfection out of over 137,000,000 cases.[1]
Meanwhile, states in the US are reporting hundreds of "breakthrough cases" of fully vaccinated people.
So, the data we have indicates naturally gained immunity is stronger than vaccinated immunity.
It's funny how many people treat nuanced, data driven discussion like this as heresy to be shamed and censored.
[1]https://bnonews.com/index.php/2020/08/covid-19-reinfection-t...
> I expect I've had all variants
No evidence of this.
> and apparently my immune system is on top of it
No evidence of this.
> in which case there's nothing to pass on
Even if the above were true, we don't know how long you'd have immunity.
> and the people in my area clearly don't care if I did.
They would if they caught it and had severe symptoms.
I mean, you can question anything, but that has about zero value. Answers with evidence backing them have value.
I'll also point out some anecdata. I know someone in their late 20s that got COVID. They have felt miserable every day in the 9 months since having it. Others have relayed similar stories. Public health authorities are worried about severe consequences like death, but death isn't the only possible outcome. You could just feel like shit for the rest of your life.
To me, this is a nasty disease that I do not want to contract. I probably won't die if I get it, but there is more to life than merely not being dead. As a result, I got the vaccine as soon as I could.
No, it's not. That's a misunderstanding of how the vaccine development process works and what takes time.
What takes time in the normal course of development is testing the vaccine, yes. Specifically, determining how effective it is. The reason that takes so long is that in general there are very, very few cases of most of the diseases vaccines are developed to prevent -- and you can't just go giving people Ebola to check how many of them catch it.
It's fearmongering, plain and simple.
There's mountains of data for your perusal online explaining how and why it got done fast -- here's one example. [1]
[1] https://www.immunology.org/coronavirus/connect-coronavirus-p...
Similarly, while wider population testing for safety and efficacy would likely correlate with long term safety, it’s not a total substitute.
I think it could be completely rational for young, healthy, low BMI people to delay vaccination till they’re more comfortable with any potential long term issues.
Those folks aren't being immunized to protect themselves but those around them. This is a team effort and everyone's gotta pitch in.
I got my J&J a week ago. No side-effects here.
How many injections do you personally need to feel comfortable? Seven million people is way more than any clinical trial for any drug you've ever taken, and I guarantee you any of them is more likely to kill you.
Every single year 150 people die from taking Tylenol in the US in the normal course of treatment -- and 500 die of acute liver failure due to acetaminophen overdose. 25,000 hospital admissions. 50,000 ER visits. If we pretend that 350,000,000 people take Tylenol each year, that makes Tylenol 50% more likely to kill you than this vaccine.
It's simply not ok. They are anti-vaxxers.
We should be honest about the (low) risks and benefits of vaccination without turning it into a political campaign of shame and bullying, and trust people to make the right choice for them and the public.
Perhaps you also think the US government is anti-vaxxer, as it runs a publicly funded National Vaccine Injury Compensation Program - https://hrsa.gov/vaccine-compensation/index.html
The government's response is to pacify anti-vaxxers.
I’m 25 and I’m relatively healthy. The risk that the disease kills me is significantly less than 1 in 100; it’s hard to find numbers but one chart had the hospitalization rate for me at 1%, and the death rate 0.01% (edit: though the death rate only covered age and didn’t divide by other factors such as obesity). The “chance” the vaccine kills you is currently zero as there have been no recorded deaths that have been linked to a COVID vaccine. The blood clotting risk has been cited as 1 in a million, but we’re working with limited data. This is the problem with making such extrapolations.
I write all of this as I’m on day 2 of dealing with the side effects of J&J.
The reason everyone has to get it is so that the average goes down to 0, for everyone.
7 million trials is not limited data. It's dramatically, and I do mean dramatically more data than basically any other clinical trial for any other drug you've ever heard of. By probably 2 orders of magnitude. It's simply not limited data.
The average phase 3 trial has 300-3000 participants [1]. Not seven million.
Also a week in after J&J.
[1] https://en.wikipedia.org/wiki/Phases_of_clinical_research
It's 6 in 1000 if you listen to the CDC; personally I think the real number is closer to 3 in 1000. That's not too far off from what you said but I prefer being more explicit rather than using such a fuzzy resolution.
And just to be explicit, that's the general IFR, the IFR for, say, people in their 20's, or even people in their 40's, is a fraction of that.
---
Anyway, your point about risk management is somewhat true, but it is much more true if you apply that logic to the general public's fear of SARS-2 in the first place. I can't find it in my notes but surveys that have asked people what their chance of dying is if they catch the virus, are off by MULTIPLE orders of magnitude. And young people rank their individual risk of death higher than old people do (both estimate too high, even the old people), presumably due to them being more "plugged in" to "the system" so to speak.
Personally speaking, since I'm in my 20's, almost everyone I know who has gotten the vaccine has done so because they believe outright falsehoods about the virus that have been propagated not just by the media but by our so-called health experts themselves.
For example, I have multiple friends who had PCR-confirmed COVID-19, recovered months ago, and still got the vaccine. In the times I've probed at them to see why, they muttered some vague things about "the variants" and essentially said that the variants bypass naturalistic immunity which is just completely false.
I know for a fact that my likelihood of an acute adverse reaction (the all-too-common "feeling like death for a day" reaction) is far higher than the likelihood of comparable symptoms from SARS-2 infection. So I'm not getting the vaccine, and I'm not embarrassed to say so. For many people, the risks of the virus are less than risks of the vaccine; however, much less people than you would think. We don't have good enough data yet but I'd bet it crosses over somewhere in the 40's or 50's age range.
There's a huge difference between being an "anti-vaxxer" in the true sense of the word - i.e. you think all vaccines are inherently bad, period - and being someone who takes the same attitude towards vaccines that we do towards drugs: no drug is inherently safe; rather drugs that are proven to be safe are safe. By extension, no vaccine is inherently safe; vaccines that are proven to be safe are safe.
The latter statement is my personal view of it, and unfortunately such a statement can get you banned from social media platforms if you get unlucky.
This binary way of dividing the world into "anti-vaxxer" vs not, "AIDS denialist" vs not, etc is not just oversimplified but is intentionally done to suppress dissent. I refuse to participate in such a culture and I humbly implore you to do so as well.
Imagine if the FDA says "no big deal, low chance of it happening, keep going", then a week from now "oh seem like the rate has doubled, still low, keep going", then a week later "ok, if you have any risk of blood clots don't take the J&J vaccine". That scream "we didn't think this would happen".
You've just eroded trust in the system and the next time some weird side effects comes up you won't have to pause, people will just refuse to take it.
Again, the point is, when we observe adverse effect in the out-of-trial phase, it has hard to pin-point cause and effect. It is not a guarantee that the 7 million necessarily represent a random sample so proceeding with caution is warranted. We know, for example, vaccines have been distributed by age, and chances are, the 7 million is bias towards the older demographic.
> Every single year 150 people die from taking Tylenol in the US in the normal course of treatment -- and 500 die of acute liver failure due to acetaminophen overdose. 25,000 hospital admissions. 50,000 ER visits. If we pretend that 350,000,000 people take Tylenol each year, that makes Tylenol 50% more likely to kill you than this vaccine.
Again, the point isn't that {insert_your_favourite_drug} is 10x more likely to kill you - the point is, when we do not understand why something is happening, it is better to pause and detect whether there is a more fundamental issue. For example, suppose that every single injection that caused an adverse reaction was produced at the same facility and as part of the same batch - we would definitely be better off in investigating the root cause than to leave it be. Until we fully understand what mechanism is causing this adverse effect and how to best counteract it, in my opinion, a pause is warranted.
My point is that yes, an investigation should be carried out, but stopping the trial obviously - trivially - does more harm than good due to the extenuating circumstances of the global pandemic.
By stopping they can at least find out if it's 5000 out of 7 million (and more deaths).
The CDC and FDA both agree that use of the J&J vaccine should be paused so they can further study this previously unknown side effect.
Maybe someone here could help you get in touch with them since you clearly know something they don't?
Do we have any data on the total number of women 18-38 who received this vaccine? It may actually be fairly low given we may have selection bias to give these vaccines to an older population.
The outcome may simply be to recommend that members in this demographic avoid this particular vaccine until further analysis is done.
Though rates of increasing the risk of blood clots for different birth controls vary, the ones that do range from 2-6x. The FDA estimates that in US out of every 10 thousand women using combination oral contraceptives or birth control pills 3 to 9 will develop blood clots each year while for comparison the same rate for women who are not pregnant and do not take COCs is 1 to 5 which is interesting considering the age range of the six cases.
https://www.fda.gov/drugs/drug-safety-and-availability/fda-d...
That said research is beginning to understand the mechanism of these rare blood clots in connection to adenovirus vector meds and since it is so rare it's hard to get a precise number but other studies predict an excess increase of severe blood clots in the range of 1 in every 500 thousand to million patients.
https://www.sciencedirect.com/science/article/pii/S000649712...
This will almost certainly now be a problem with the J&J vaccine in the US. More people will get sick and die because of this.
https://www.politico.eu/article/trust-oxford-astrazeneca-cor...
This is misinformation (and I call it that because it is being widely repeated in major new sources). It's an improper generalization from what was observed in a very small sample of confirmed Covid cases in the vaccine trials.
https://www.forbes.com/sites/brucelee/2021/04/11/3-breakthro...
>So far, more than 74 million people have gotten fully vaccinated in the United States. It's unclear how many have later gotten infected with the coronavirus anyway. But Michigan, Washington and other states have reported hundreds of cases. Most people have gotten only mildly ill, but some have gotten very sick. Some have even died.
Curious about your answer.
2) It's still very possible to have a Very Bad Time with covid if you're not obese.
Then why are people still asked to wear masks in stores even if they are vaccinated? I've heard from the media non-stop that even if you have the vaccination you need to wear a mask - it doesn't make sense.
a) it's not entirely whether vaccinated people can still be carriers. I think it's now /mostly/ clear that they don't.
b) people are fscking awful. If you let vaccinated people not wear masks, you're going to have a bunch of philosophical zombies lying about their vaccination status to avoid wearing masks in public spaces. So, everybody wears masks until this thing is over and then some.
I haven't seen enough numbers for J and J, but you have to untangle the various risk factors before you can say anything about what you should do as an individual.
I know this pandemic is fustrating as hell, but if you call people who use science and numbers to see problems with the current vaccines anti-vaxers then you will be taken as seriously as you deserve.
Please cite a source here. Survival rate usually means IFR not CFR, and even the CDC's own number (the CDC is going to be incentivized to overstate risk) puts it at around a 99.4% general survival rate. Other estimates put it closer to 99.7% or even higher.
1 per million adverse effects is nothing. If that would be a solid fact, there would be no reason to pause vaccinations. The pause happens very early so that experts have time to check the data and methodology and verify that it's all that there is.
When a new drug is given for emergency evaluation or a new side effect is discovered he works 14 hours per day 7 days a week with a team going through a massive amount of data and documentation to verify and check everything.
The media and most commentators don't understand why decisions can take weeks. Why you don't have the scheduled emergency approval meeting just now. They fail to understand that fact-finding is not happening in the meeting just by people giving their expert opinions. Experts work around the clock without taking any time off to figure out what is happening. But lazy bureaucratic regulators, right?
The reported data simply doesn't explain stopping use of this vaccine. It seems like either:
1) They are overreacting based on sparse data, which will cast doubt on the validity of their actions.
2) There is information being withheld that implicates, though perhaps without certainty, that the vaccine is the specific cause of these issues.
Either way, the net result will be more distrust & greater reluctance to get vaccinated. There has to be a better way to handle this problem.
As such 1 is no longer correct, if we didn't have a compare these numbers are high but within expected chance. However these numbers are looking like within the range of the compare even more than normal.
It would help if details were released about the physical condition of the 6 people impacted by this. If all of them were otherwise perfectly healthy people with no risk factors for this sort of issue, then yes-- that's a bit of a smoking gun.
But where things stand right now I just don't know what to make of the issues, which is just so damn frustrating because I know it gives ample reason to anyone inclines to doubt the experts or avoid vaccination a reason to do so.
The BBC is usually pretty good about sticking to relevant information (at least compared to US media), so I was a bit disappointed to see this blurb - especially since it's only the fourth sentence in the article. What does it add? It has nothing to do with the subject (ie the safety of the J&J vaccine) and isn't even particularly useful data in almost any other context aside from half-baked political jabs between nations.
"Until that process is complete, we are recommending a pause in the use of this vaccine out of an abundance of caution. This is important, in part, to ensure that the health care provider community is aware of the potential for these adverse events and can plan for proper recognition and management due to the unique treatment required with this type of blood clot.", from https://www.cdc.gov/media/releases/2021/s0413-JJ-vaccine.htm...
The thing I'm trying to understand is whether Johnson & Johnson and AstraZeneca are meaningfully different. All the media just assumes they are (until proven equivalent), but is the genetic code publicly known so we can compare? The Pfizer and Moderna ones are extremely similar. Now, I imagine the adenovirus ones have an order of magnitude more genetic material, but is the code publicly know to compare?
As far as I can tell, they both should have been approved ages ago, if only to depress prices and get more redundancy.
Reaching beyond the parent’s words, both AstraZeneca and J&J have now had issues with blood clots. If it’s a similar formulation then perhaps you’ve found something and Adenovirus vaccines with a different formulation are unaffected. If they’re very different then perhaps other variations of Adenovirus vaccines need more attention.
> whether Johnson & Johnson and AstraZeneca are meaningfully different
Grammatically, that asks about the difference between J&J & AZ. Your response instead compared them collectively to the mRNA vaccines, rather than comparing them to each other. Thus the response saying "[t]hat’s not the difference the parent is asking about."
> 6 cases out of 7 million people. What a disaster. This is going to get people killed. And it's going to create more vaccine hesitancy. These people don't understand cost-benefit analysis. They keep making mistakes by orders of magnitude.
I am seeing this argument from people of all political views this morning, but I am most surprised to see it from the political left. Why isn't the same data-driven approach used when we're talking about policing, or gun violence, or traffic deaths? In all these cases, the frequency of negative outcomes (policing deaths of unarmed black people, homicides committed with guns, traffic fatalities per mile traveled) is very low and when weighed with the positive outcomes, it is clear that people are acting irrationally when they try to defund police, or ban firearms, or restrict driving. And yet, the data is never brought up so directly in those conversations by either everyday people or news media.
The J&J vaccine issue is frankly less alarming to me than this open hypocrisy or disconnect in our societal discourse.
"...since the ACE2 receptor belongs to the renin-angiotensin system (it regulates blood pressure), the virus cannot but affect the blood vessels. Apparently, it is capable of causing local inflammation of the walls of blood vessels and capillaries. This results in an increased release of VWF into the blood, which, in turn, provokes clotting." [0]
[0] https://www.news-medical.net/news/20200706/COVID-19-complica...
The best thing to get people to understand risk is to actually follow the process in the EUA. Pause, evaluate the outcomes, change the labels and dosing. Which this does.
At the same time, the FDA/CDC need to start taking other countries data into account. At this point, there is no excuse not to be using a UK style "first dose first" strategy, especially if mRNA is all we have for a while.
I guess you’re suggesting culling a small fraction of the population might encourage better behavior at the voting booth? We already have plenty of historical evidence suggesting that’s not true.
GP was saying that the US health agencies haven't looked very good in the past few years, and on Covid, they really have fumbled the comms execution. Before Covid, these issues existed in the agencies, but that was highlighted by the emergency + executive branch that was either incapable or unwilling to make it a priority. That's when it's even more important for our processes, led by our major agencies, to be crisp.
None of this past year was unpredictable. If these health agencies are so affected by the whims of politics, it reveals a systemic flaw.
That's not anti-vax denialism, those are the actual numbers. A one in a million risk isn't a good deal for the individual when case rates and IFR are low.
This would be a good deal if you were in Michigan, or if you were over 65.
On the other hand this extra cautiousness shows how robust the safety of the system is: even minor glitches get caught and examined which practically pretty much rules out that there are side effects of orders of magnitudes more likely that we don't realize. And that may indeed worth it overall. Though in practice it would still make more sense if they continued until it reached a higher threshold (if it is ever to reach it).
Unfortunately, while this should be seen as very reassuring WRT the safety and the level of trust we can have in the vaccines, fear is irrational and for some people it proves that the vaccines are not safe.
E.g. here in Hungary, we have the EMA licensed vaccines (same as the FDA licensed ones) and also a Chinese (Sinopharm) and a Russian (Sputnik-V), with a permission from the Hungarian authorities. Now when the blood clotting issue emerged with AstraZeneca, some started to say "see, that's how much the EMA license is worth. BUT the Sputnik-V is good because you never heard about such issues with it". Which is, needless to say, completely upside down. (Not suggesting that the Sputnik does have the same problem, though I wouldn't be surprised, since it's the same technology as the AZ and the J&J. Also, I wouldn't be surprised if all vaccines had the same issue as the virus itself causes clotting.)
I know personally a long hauler who has blood clotting issues and low platelets. They fall into the demographic of concern with the JJ and AZ vaccine. Anecdotally we have lost both a close relative and a young and healthy friend to Covid blood clotting related issues.
Again, I’m not weighing in on the FDA’s job. But just saying: as someone who’s anecdotally been hyper-aware of the blood related aspects of Covid, this thread has picked up my ears and I’m really interested in finding out what the linkage here is.
https://www.theguardian.com/world/2021/apr/13/astrazeneca-bl...
https://www.vice.com/en/article/z3xbk9/johnson-and-johnson-c...
Whether it's an airplane crash or a blood clot caused by a vaccine, human minds simply can't 'feel' that a phenomenon is rare when it is repeated over and over again in their newsfeed.
The paper details several cases (and index case in more detail) as well as a plausible mechanism behind the thrombotic events. Even better, there are some therapeutic possibilities as well arising from the heparin induced analogue condition.
"Over 189 million doses of COVID-19 vaccines were administered in the United States from December 14, 2020, through April 12, 2021. During this time, VAERS received 3,005 reports of death (0.00158%) among people who received a COVID-19 vaccine."
https://www.cdc.gov/coronavirus/2019-ncov/vaccines/safety/ad...
No matter what they come back with, the JnJ vaccine is done. We might as well start shipping them out to other countries that desperately need them, especially if we supposedly have enough mrna vaccines coming for everyone.
[0] one can hope
Is it surprising that the vaccines cause clotting too? Isn't this sort of obvious?
https://en.wikipedia.org/wiki/Heparin-induced_thrombocytopen...
That’s not an explanation, of course, I don’t know the reason. But it places this in a larger category.
https://covid19-sciencetable.ca/sciencebrief/vaccine-induced...
There is a well established link between oestrogen and increased blood coagulability. Whilst it is possible females are more affected by the vaccine I suspect one factor is that their baseline coagulation risk increases their likelihood of thrombus due “reaction induced coagulability” compared to males.
> Cerebral venous sinus thrombosis is rare, with an estimated 3-4 cases per million annual incidence in adults. While it may occur in all age groups, it is most common in the third decade. 75% are female. [0]
[0] https://en.wikipedia.org/wiki/Cerebral_venous_sinus_thrombos....
Deciding whom to give these vaccines to is a complicated decision for each country to make and depends on:
a) The incidence rate for each demographic of CSVT-type clotting from the vaccine[s].
b) The expected distribution of clinical outcomes from those events, making reasonable assumptions about likelihood of early detection and outcomes with treatment for heparin induced thrombosis.
Those two give you the clinical cost.
Then you compare those with the clinical benefit from:
1) The relative likelihood of infection for a person, given their demographics, personal exposure profile etc.
2) The absolute likelihood of infection in the country / region in question based on assumptions about the future of the pandemic
3) The expected distribution of clinical outcomes from infection given the person's characteristics
(2) is important because you're comparing a one-time risk of side-effects with a time-related risk of infection.
Clearly, the same person in Manaus or Adelaide is not really making the same trade-off even if in the abstract, the side-effects and IFR are the same.
You also need the counterfactual: If you decide not to give an ad vectored vaccine, you are not deciding never to vaccinate, you are deciding that this person will get a different vaccine, probably later. How much later depends on the location. If you're in the US, you've got Moderna and Pfizer/Biontech coming out of your ears so it might only delay any individual vaccination by a few weeks. If you're a healthy 25 year old who can work from home, the risk trade-off of having to wait an extra 6 days is very different than that same person if they have to wait another 6 months.
As a result, different countries, looking at the same data will rationally make different decisions. The US has lots of mRNA vaccines so will choose one thing, the EU has been badly hit by the failure of Sanofi/GSK to deliver a working vaccine (and by AstraZeneca scaling problems) but has quite a lot Pfizer production capacity, the UK has used up its Pfizer stocks and will now only use it for second shots. CureVac and Novavax may be able to supply some doses at some point but aren't in the picture yet. Several European countries are negotiating to get Sputnik but that is also ad vectored so may have the same problem. That changes the risk calculation because it changes the time that people will remain unvaccinated in the counterfactual where ad vectored vaccines are not used for their age group.
All of this is before the complicated public health element of keeping messages for the public simple and the issues caused by changing that message frequently.
I don't know to what degree countries that had set relatively high minimum ages for the use of AZ had been counting on J&J for younger people. In many cases, AZ deliveries were sufficiently slow due to yield problems that it was "free" from a scheduling point of view to restrict it to only the oldest since the expectation was that they would only receive enough for those anyway and could use other vaccines for younger groups. If J&J was a big part of that, then they now have to update that calculation because the counterfactual to using AZ for those people is no longer "do them with J&J next week". That may be hard to communicate to people who had been told that a particular vaccine was not safe in their age group previously but may now be asked to take it anyway.
I'm glad that I don't have to make these decisions. They are not easy ones.
People are absolute garbage at thinking about scale.
If they follow your line of thinking and it's all fine... no-one's going to be writing articles praising them.
If they follow your line of thinking and more people die form blood clots... people will write articles attacking them. Questions will be asked, and careers may be harmed. Etc.
It kills less than that in the demographic in question, not to mention that is only of those who contract the virus.
> People are absolute garbage at thinking about scale.
I don’t think it is that, I think it is that for better or worse humans tend to view wrongs through inaction as less atrocious than wrongs through action. Additionally - they already have better alternatives and plenty of supply in the US (Moderna and Pfizer vaccines) so they are opting to just use those at the moment.
Second, there’s evidence that even if people don’t die, there can be long term neurological effects [2].
Third, even if we accept your number, 1 in 200 would still be 1.5 million Americans dead, not even considering the rest of the world. I am personally not comfortable doing nothing to stop that number.
I agree that being super worried about a 1 in a million blood clot might be short sighted, especially since the death rate from catching the virus is 2 in 100.
People with asymptomatic infections (which are the majority of them) do not have any reason to get tested, so they do not count as "cases".
As I said, that still implies that if everyone in the United States got it, 1.5 million of them would die (320,000,000 * .005). That's a lot of people.
If a government did nothing to prevent a terrorist attack that killed 1.5 million people, most people would (rightly) be pretty upset.
EDIT: Also, forgot to mention, it's totally disingenuous to only look at "deaths". We do not fully know the long term health effects, but as I stated there's potential neurological effects, potential risks of type 1 diabetes, and people permanently losing smell.
You have 100M infected in US as the estimate. A 2% death rate is 2M deaths from COVID alone. I've not seen anything like that as credible death rates - it's at least half if not a quarter of this rate - more like 0.5% or less. Do the same thing in countries with 70% infected rates - if fatality was really 2%+ death counts would be insane.
You really start to understand how people start to doubt the crap COVID "experts" put out when basic math shows it is garbage.
Johns Hopkins University. I don't feel like that's typically considered a bad source. Maybe it's a bit high or they're looking at different data sets.
But again, and I cannot overstate this enough, even if I accept the 0.5% number, that's still a lot of deaths, about 1.5 million if everyone in the US gets it.
According to the NYTimes [1], there's been about half a million deaths from COVID. If your provided number of 100M infected people is correct, then that would be consistent with 1.5M dying if everyone gets infected (US population ~= 3 * 100M, 3 * 500,000 = 1.5M).
[1] https://www.nytimes.com/interactive/2020/us/coronavirus-us-c...
Not really. 1 in 200 is fewer than how many die a year anyway of all causes.
Surprisingly, even the elderly and sick people often do not understand the risks.
We want if there are safer options. Not all vaccines are equal. Important question is why we unable to scale up production of mRNA vaccines?
Where are you getting the idea that we can't?
Hundreds of millions of doses of the Pfizer and Moderna vaccines have already been made. Pfizer expects to make 2 billion doses this year.
https://www.novartis.com/news/media-releases/novartis-signs-...
> Novartis announced today that it has signed an initial agreement to leverage its manufacturing capacity and capabilities in order to address the COVID-19 pandemic by supporting the production of the Pfizer-BioNTech COVID-19 Vaccine. The agreement will see Novartis utilizing its aseptic manufacturing facilities at its site in Stein, Switzerland.
https://www.merck.com/stories/why-were-excited-to-partner-on...
> On March 2, we announced a partnership with Johnson & Johnson to expand manufacturing capacity and supply of its COVID-19 vaccine. Under the Biomedical Advanced Research and Development Authority (BARDA) agreement, our company is adapting and making available some of our existing manufacturing sites to accelerate manufacturing efforts for the vaccine and enable more timely delivery and administration.
https://investors.modernatx.com/news-releases/news-release-d...
> Under the terms of the agreement, the companies plan to establish manufacturing suites at Lonza’s facilities in the United States and Switzerland for the manufacture of mRNA-1273 at both sites. Technology transfer is expected to begin in June 2020, and the companies intend to manufacture the first batches of mRNA-1273 at Lonza U.S. in July 2020.
https://www.astrazeneca.com/media-centre/press-releases/2021...
> AstraZeneca and IDT Biologika also intend to strengthen Europe’s vaccine manufacturing capability with a joint investment to build large additional drug substance capacity for the future. Details of the agreement are to be finalised. Both companies plan to invest in capacity expansion at IDT Biologika’s production site in Dessau, Germany to build up to five 2,000-litre bioreactors capable of making tens of millions of doses per month of AstraZeneca’s COVID-19 vaccine. The new assets are estimated to be operational by the end of 2022.
1. https://theconversation.com/how-patent-laws-get-in-the-way-o...
2. https://www.thedailybeast.com/heres-why-it-will-be-hard-to-r...
I think of all the comments about how "MBAs" and "marketing people" just don't get software development. And then I look at software development people who seem to think they clearly get medical research and regulation.
whatoneinamillionmeans.com
If you're not willing to take 1 in a million chances, it's gonna be pretty hard for you to get out of bed today.
This vaccine seems to have about the same rate, which makes sense as I think it uses the same technology.
This was the first one your website presented and I have no idea what it means.
Maybe tonight I can work out do an IP address lookup and personalise it for your locality ;)
Similar distance/time as DC to NYC.
(It's true though by the way, go enjoy the sun while you still can...)
TBH I've made this site for myself as much as anyone - I'm just under 40 so the risk/benefit is tight for me personally, but I want to do my bit for everyone else and stop the spread so I'll take any vaccine they'll give me.
Good luck with you flying dreams and say safe!
Where is the math that suggests that pausing the J&J vaccine is prudent? Inputs being risk of getting covid, risk of getting a blood clot, risk of injury/death from covid, risk of a new covid variant appearing, etc.
Without that transparency we’re all just guessing.
You’re probably right, but if we keep trying to front-run people’s reactions to events over and over again, I’m not sure we’re going to get great results in the long run. I get the impression that anticipating how people will respond to news is engendering more extreme responses to future events.
Does pausing to investigate such an incredibly rare occurrence increase the public's trust in vaccines (because they see the government is being extra careful with safety data) or decrease it (because skeptics will use this as evidence that there are problems with the vaccines)? I feel like it's mostly the latter, but I dunno.
Not to mention all the COVID cases that might have been prevented while the rollout is paused to investigate a potential side effect that's less than one in a million.
Right, but the clots happened about 2 weeks after the vaccine, so that what portion of those ~7 million were administered over two weeks ago? Clots happened to a similar demographic, so what portion of those ~7 million were to women in the right age group? What about clots that cause damage that’s not immediately obvious (and thus not spotted).
I hesitate to dismiss the risk outright, but I do think that we should hold the CDC/FDA to the standard of “methodical.”
According to that graphic, if you are in a time of medium COVID infection rates (60 per 100k per day), the risk from COVID outweighs the vaccine risks in that age group. If you in a time of low rates (20 per 100k per day) the vaccine risks outweigh the COVID risks.
The vaccine risk goes down as patient age goes up, and the COVID risk goes up as age goes up.
The J&J risks will probably follow a similar pattern and it also appears that the J&J clots require unusual treatment. That suggests a pause to at least figure out where the risk curves cross and to make sure that doctors and hospitals are prepared to recognize and treat the J&J clots.
[1] https://arstechnica.com/science/2021/04/us-cdc-fda-call-for-...
At least they have alternatives. Meanwhile, in Europe ...
This reminds me about all those governments that allow people to buy and sell cigarettes, but ban the sale of raw milk.
Can we just name this "Raw Milk Syndrome"?
Cigarettes and raw milk are, regrettably, a specious comparison. In the USA, the rules concerning both are handled by different governing bodies. For the longest time, cigarettes had been explicitly excluded from the FDA's jurisdiction, according to a law passed by Congress, and confirmed by a Supreme Court decision. And rules concerning raw milk vary from state to state, but are generally also set by legislatures. In both cases, what you see there is political interests come into conflict with, and perhaps override, the more level-headed, science-driven, technocratic approach that the FDA is theoretically expected to take.
The disease left to its own accord has the potential to kill millions (someone please correct me on this). Why would we pause a vaccine because 6 people in 7 million got blood clots? Why would we do that and risk fueling anti-vaccine viewpoints?
I'm baffled, but perhaps I'm a fool.
In the US, the other vaccines are starting to become really readily available.
Maybe other parts of the country are different.
That the vaccination rate is supply-limited is manifest in the fact that less than a third of the U.S. population has been vaccinated at all.
Yes, there are places where there are vaccine surpluses, but this is not because the supply isn't the limiting factor. It's because in some rural areas there are large numbers of vaccine denialists who are choosing to forego the vaccine altogether. That leaves some localized surpluses. But overall supply is still the limiting factor, and it will continue to be until everyone who wants a vaccine can get one without having to wait.
> there are large numbers of vaccine denialists who are choosing to forego the vaccine altogether. That leaves some localized surpluses.
The people that do not want the vaccine are a part of why. There are different reasons for this, with some just wanting others to get a chance first. But noone is going to force people to take it.
Its also really unfair to characterize this as "rural areas" with "large numbers of vaccine denialists". We have urban areas with vaccines available and rural areas with full appointment books.
Really? Where?
Be careful to click through to the actual pharmacies, though. It is often out of date with actual availability being lower than indicated. Our state has also been running mobile events that have generally not been fully booked.
I'm in no hurry personally, but I'm not seeing where it would be difficult to get for me.
My experience with VF was the exact opposite: it was showing lots of availability where in fact there was none.
But the burden of proof is still on you: what urban areas in the U.S. has good vaccine availability? By which I mean: anyone who wants one can get one same-or-next day.
That's exactly what I said, actually. Though it wasn't none, just low. Be sure to check back after a day or so. Availability swings pretty quickly.
It is starting to become really easy to get this vaccine in the US now with just Pfizer and Moderna.
What we do know is that the alternative to not being vaccinated is much worse.
It's between "continued rapid vaccination with all three approved US vaccines" and "somewhat delayed vaccination with one of the three approved US vaccines". That's not remotely a million-person delta, though the number is surely much higher than the 1/1M case rate on these blood clots.
Honestly the worst effect isn't with the vaccinations per se, it's the potential that this may delay vaccine acceptance rates among people sitting on the edge, due simply to fear.
The communication that public gets is outrageously bad.
(I'd be good if someone with more knowledge could comment)
I would still get this vaccine (or the AZ one) if offered because I consider it my duty to be part of the herd immunity. But not everyone will do that, and the moment you have people in privileged position refusing one of the vaccines, you start (1) exacerbating inequalities (2) fueling conspiracy theories, mistrust, and vaccine hesitancy.
If you assume that the world is perfectly rational, then you are right, but it is a running joke on HN to point out how economists used to make that same mistake and derive silly conclusions.
It is my actual choice to have the vaccine and go from 0 chance of vaccine-related blood clots to some non-zero value. Whereas catching covid feels more like I'm in control of not catching it by not leaving the flat, and even if I did catch it, chances are it'd not affect me that much.
I know this is not totally logical, but it is difficult to get past emotionally. Imagine if I did get blood clots from the vaccine - I'd go from safe in my flat and healthy, to dead, and for what? To protect me from a virus that has an even lower chance of causing long-term problems, and from which I can protect myself by being careful.
Because J&J isn’t the only vaccine in the inventory, and the others don’t have that problem (or, IIRC, the same level of other adverse reactions), and because:
> Why would we do that and risk fueling anti-vaccine viewpoints?
What risks fueling anti-vaccine viewpoints is ignoring adverse impacts which are known and plowing forward, especially giveb that people often don’t have a choice of which vaccine they are administered.
Your point about other vaccines being available is totally valid and sound, but... what is our standard here, then? For absolute-zero people to die of any vaccine we produce? What if it was 1 person who got a blood clot? It probably sounds like I'm being pedantic, but I'm serious in that I want to know why people find it reasonable to pull an otherwise effective vaccine because of this. It just doesn't seem worth it to tell everyone that the vaccine is dangerous enough that it had to be pulled entirely.
Ignoring adverse impacts definitely fuels anti-vaccine sentiment, but so does giving people concrete evidence that the vaccine can possibly kill people, possibly leading them to be resistant to getting any COVID vaccine at all until they're forced to get it. I mean, if I were at all skeptical of getting a COVID vaccine, and I was told the J&J vaccine was so dangerous they had to pause it, why would I get any of the more experimental vaccines knowing that they also have the potential to kill me but we don't even know yet because they're experimental?
I don't think people on HN realize the full magnitude to which the public can be timid and irrational. It just doesn't seem worth it to me for us to possibly fuck up the rollout of vaccinations when we are facing a possible 4th wave of COVID and more virulent variants.
Let's compare some numbers here.
The number of known blood clot cases with the J&J vaccine seems to be 6 in 7 million. That's a ~0.00000085% chance of getting a blood clot caused by the vaccine, give or take a zero since I suck at math and calculators refuse to not use scientific notation. According to the CDC, around 100,000 people die of blood clots in the United States every year, and the US population is 308,401,808, meaning that Americans have a ~0.0003% chance of dying of a blood clot in their lifetime. The only concerning factor as far as I can tell is that the people who got the blood clots were women under 50.
I mean, fine, if that's a risk profile we are averse to, then so be it. I don't really understand that.
The standard is not to distribute a vaccine with a known side effect that standard treatment protocols will catastrophically fail for without pausing to get information about it to healthcare poviders needed to implement protocols to identify and properly treat it.
That’s explicitly what the pause is for per the article.
> The number of known blood clot cases with the J&J vaccine seems to be 6 in 7 million.
It’s not, because the effect is seen 6-13 days after vaccination, and much of the 7 million (per the article, 6.45 million is the most recent cumulative figure I can find elsewhere but its two days old, if both are accurate that's over 0.5 million doses in the last two days...) J&J doses that have been delivered are within 13 (and even 6) days. And the clots have all been in women 18-48, who aren't the only people getting the vaccine, so, unless that’s a fluke (and the numbers are small enough that that’s merely unlikely but not implausible) the prevalence in that demographic is even higher.
> During Johnson & Johnson's clinical trial, there were reports of other types of blood clots, too. Some are relatively common, such as deep vein thrombosis, so it wasn't surprising that among roughly 20,000 participants who received the vaccine, some would experience those clots.
> What made FDA scientists take note, however, is that in the trial, about the same number of people received a placebo -- a shot of saline that does nothing -- as received the vaccine. However, when comparing the two groups, more study participants developed clots after receiving the vaccine than the placebo.
> Calling it a "slight numerical imbalance," the FDA noted that there were 15 events in 14 participants who received the vaccine, compared to 10 events in 10 participants who received the placebo.
I think the 6 in 7 million people are the serious and unusual blood clots, but would not include the +50% increase in blood clots of any type noted above. However I appreciate that you did include the extra data about 100,000 people dying per blood clots per year.
I also like to pay attention to the numbers for this stuff. I was scheduled for a J&J shot today, which was cancelled. It wasn't my first vaccine choice. I'll be trying to get an appointment for one of the other vaccines, I guess.
[0] https://www.cnn.com/2021/04/13/health/johnson-vaccine-blood-...
COVID risk goes up with age. In the other COVID vaccine with a clotting issue (the AZ vaccine) clotting risk goes down with age. If that turns out to also be the case with J&J, then for a lot of people in the US (up to 20% or so) at the current levels of COVID the vaccine has a good chance of being more of a danger to them than COVID.
A short pause to determine if they should add a minimum age (possibly a variable minimum age that depends on the overall COVID rates) for J&J is prudent.
“I think this is a very low risk issue, even if causally linked to the vaccine: 6 cases with about 7 million doses (lower than the risk of clots with oral contraceptives) is not something to panic about,” Dr. Amesh Adalja, an infectious disease expert at the Johns Hopkins Center for Health Security in Baltimore, said in an email.
something is weird here. i’m not saying this is due to mass hysteria generated by people that don’t want the vaccine but this does sure look like a case where we don’t understand relative risk.
i may be ignorant and not understand all the factors but I don’t see the data that allows me to understand if suspending this vaccine is a good thing or nkt.
Meanwhile, hormonal birth control causes clots in 1/1,000 women. No one blinks an eye.
The vaccine hesitancy this engenders is likely gonna kill more than that one person.
https://twitter.com/NateSilver538/status/1381936112311148548
> Public health bureaucrats have some weird habits in how they reason under uncertainty and how they communicate to the public. It might help if they sought out experts from economics, sociology, psychology, etc., instead of telling everyone to stay in the their lane.
There is enough anti-vaccine & Covid rhetoric that we should all cool it a little bit and let the experts do their jobs.
> That said I trust that the government agencies know what they are doing here.
If 2020 didn't finally shatter that trust, is there anything that can? FDA was already obviously a regulatory capture vehicle for pharma. And CDC got nearly everything wrong in the ebola outbreak of 2014. Then, both of them blundered their way through this pandemic.
For example, we know from the email leaks that FDA felt it was under pressure from Trump to approve vaccines[0], and then never disclosed this fact to the public. That doesn't seem like dispassionate science and expertise to me.
By contrast, many of the medical journals, preprint houses, and academic institutions have looked like far more stable sources of knowledge.
It seems to me that the internet age asks us to replace our state institutions of expertise with something more thoughtful and genuinely connected to science.
I’m the opposite. Covid caused my trust in them to plummet. Perhaps made with the best of intentions, but all the noble lies have eroded my trust.
Same framework that's lead to all of the poor policy decisions over the past year.
It's not enough to say you're being cautious. You have to explain why you think it is better to be cautious about administering the vaccine with its attendant risks or to pay the QALYs incurred by the delay when people who would have received this vaccine don't.
This is a low probability event, and the appropriate mitigation may be to do nothing; but there may be some common factor for these patients that might indicate use of a different vaccine or maybe informing people of symptoms of blood clots and what to do if they see symptoms.
The real risk here is eroding confidence in government health sources in general, and vaccines in specific. There were certainly unknown risks before, but now there is a known risk which deserves some study.
What erodes confidence is the complete absence of cost/benefit discussions about virtually any decision that has been made. Including this one.
If this turns out to be about what it looks like now, unpause and go forward. If it turns out to be much more significant, all the better for having stopped; maybe restrict this vaccine to populations at higher risk of COVID or lower risk of blood clots (if that risk can be determined). Both mRNA vaccines and modified adenovirus vaccines are new types of vaccines not used before on a wide scale; pausing to get clarity on a major negative side effect is warranted.
A credible decision would give your estimates of harm/benefit for delaying vaccinating people. You seem all too willing to ignore the people who will become sick or die because of delaying the vaccine. You are only looking at potential harm from not delaying the vaccine. Unfortunately, you have a lot of company.
Leading to more people delaying their vaccination. Supply is currently at a level that all doses available are administered, but to the extent lost confidence results in longer delay for high risk patients, that has a cost. When supply exceeds demand, lost confidence will have a cost for those low risk people who delay, as well as the general population which loses out on wider immunity. Delaying the vaccine now certainly also has some cost of the same type, but it's bounded. Another case of a vaccine campaign ignoring warning signs and proceeding without pausing to consider appropriate response to issues as they arise will affect this campaign as well as future campaigns.
Suggesting that effects on the order of the ones seen here is a good reason to delay the vaccine should make people doubt the ability of our public health authorities to make reasonable tradeoffs.
[1] Michigan's Democratic Gov. Gretchen Whitmer declared her state a "COVID hotspot" as cases continue to rise and has asked the federal government to increase vaccines in response. https://abcnews.go.com/Politics/cdc-director-michigan-vaccin...
It seems to me that the delay imposed by a pause in use of the J&J vaccine to make sure healthcare providers are informed of and have appropriately updated diagnostic and treatment protocols is minor, its basically pulling forward by a few days the effects of the 80% week-over-week drop in J&J vaccine supply that was just in the news.
ETA: I see you made ninja edits to your comment....
Edit 2: So now you replied that you only added a word or two and then deleted you comment while I were replying. Your comment was only half as long when I replied (all the Twitter stuff wasn't there for example).
> A joint statement from the FDA and CDC clarified that the blood clotting was cerebral venous sinus thrombosis (CVST).
I don’t believe birth control is associated with CVST at a rate of 1/1000. It feels very misleading to use it as a point of comparison.
* Hormonal birth control - years of research. Years of evidence and practice. Knowing what to do when this and that happens. Recommendations for women with known conditions not to take this and that hormonal birth control.
* Novel vaccination - barely month of research. Weeks of evidence and practice. We don't have best practices yet.
I'm fine with anyone to make a decision on them own to take these vaccinations. As someone with a not-so-uncommon mutation causing thrombosis easily, I'm happy I hesitated and haven't received either J&J or AstraZeneca.
That is completely untrue. This vaccine has been through several clinical trials for months. We know that there are no side effects that are common enough to be of real concern. The reason we are only seeing this one now is that it is so rare.
How did they establish that there are no long term side effects?
That's not to say that it's completely out of the question that there will be long-long-term side effects. But if anything is going to cause long-term issues, my money is on the virus, not any vaccine.
Past performance...
Vaccines are not the stock market. No one doubts gravity because "past performance is not indicative of future results".
How many genetically engineered adenovirus vaccines have there been before?
The vaccines that are your prior are typically attenuated or inactivated virus.
Majorly different category, we are in untreaded space (I'm still planning on getting one)
I don't think we know long-term how this may impact the immune system: does bypassing certain systems/mechanisms cause other problems with future immune response?
It took how long for us to realize as common sense that use of antibiotics allows superbugs to more likely evolve?
Fair enough, but the comment I responded to said: "We know that there are no side effects that are common enough to be of real concern."
Given this statement is not qualified for timescale, I want to know what the basis for it is.
How does the person who made it know there are no side effects on the order of six months or a year that are common enough to be a concern?
Look I am all happy chappy with the vaccine, I will inject that sweet MRNA Pfizer or Moderna vaccines as soon as someone lets me at it, but I still think we need to avoid what Fauci does, which is knowingly lie in order to get people to do what we want them to do.
There is blood clotting risk from AZ? Great, tell me what the risk is and I can deal with it, but lie to me and we are done talking.
There is a good chance for long term effects from covid. Completely the opposite for the vaccine.
Maybe you are responding to the wrong person? I never made any claims regarding what long term effects to anticipate. I asked how the person I responded to know there are no serious side effects on time scales longer than we have tested things on.
> There is a good chance for long term effects from covid. Completely the opposite for the vaccine.
Yes. I know.
From what I can gather, there’s not terribly much info on what’s known about what’s going into people’s bodies, and what info does exist has arisen from a thick soup of trade secrets and conflicts-of-interest.
With vaccines we know from decades of experience that severe side effects tend to occur very shortly (days or maybe weeks) after the injection. So this is why vaccine trials observe participants for weeks or months, not years, before concluding that the vaccine is safe. Of course this doesn't guarantee that the Covid vaccine don't happen to be an exception. But if that was the approach we took then we would never be able to approve anything, and never get the benefits we know for sure it brings.
But you can? e.g. "We know that there are no side effects that are common enough to be of real concern."?
What deficiency do I have that prevents me from knowing anything for sure that you don't have?
I personally don't see any good reason to think that the risk for long term side effects from the vaccine is higher for the vaccine than for COVID itself.
You can however guess, and make good guesses (I'm planning on getting the vaccine). But it does no one any good to fail to outline unknowns that are steelmanned by "we can't possibly know".
This is a common, but confusing, use of "you" in American English.
Keep in mind that we also don't know the long-term effects of COVID-19. It's possible that people who were infected with mild cases drop dead 1 year and 6 months after the infection. The disease hasn't been around that long, so we simply don't know.
Also, to all those saying "clinical trials have succeeded", I strongly suggest them to read said published trial results and look at _measured_ sample sizes used in the results, not total inoculation numbers.
Applying the precautionary principle, particularly if you are not at risk, is a perfectly reasonable position, IMHO.
No, we can't know that. Some affects don't show up for a long time. One example is women.
Women's bodies are complex because they go through so many changes. These changes affect how they respond to medical treatments. In other words:
- Just because pre-menopause women respond well doesn't mean post-menopause women will.
- Just because pre- or post-menopause women respond well doesn't mean women who are going through menopause respond well.
- Just because non-pregnant women respond well to the vaccine for a month doesn't mean that pregnant women will respond well.
- Just because 6-month pregnant women respond well doesn't mean 3-month pregnant women will respond well.
- Any issues with the vaccine during pregnancy may not show up until after the child is born.
- Women's hormones are fluctuating wildly at the beginning and after pregnancy. These are also times that need a lot of representation in the study.
In fact, the amount of change women's bodies undergo affects medical treatment so much that many clinical trials deliberately under-represent women to simplify the study, and then use the results of the trial to recommend prescriptions for women.
[0] https://www.cnn.com/2021/04/13/health/johnson-vaccine-blood-...
The "you woudn't care about women dying" narrative completely derails the essential discussion (aka when do we determine vaccine to be save) by selectively picking facts from a completely unrelated health area to turn it into an activist subject.
It reminds me on the magnet-troll-logic memes, only this one trying to come up with the completely insane narrative: "If you are concerned of a few more people dying because of a vaccine, you hate women."
Sometimes the answer is easy.
> Hormonal birth control - years of research
This is kneejerk status quo bias.
> I'm fine with anyone to make a decision on them own to take these vaccinations.
Great, but the FDA is not. That's the issue here.
> This is kneejerk status quo bias.
mind expanding why years of research is a 'bias'?
This is a highly unusual situation insofar as phase III monitoring is far from complete and there is no 'phase IV' (confirmatory) trial data at all yet. In the normal course of research, this is how we'd catch rare but consistent adverse effects.
So, if we had complete trials on a normal timeframe, then obviously there's a different calculus to apply.
But given what we know at this moment, these six incidents might actually be far more normal than the crude use of six as numerator and seven million as a denominator.
A pause to assess the data and allow any lag to resolve seems prudent.
And, while this will be very difficult to quantify until much later, if then, I surmise that this will only create temporary vaccine hesitancy and only outside the high-risk tier, which is perfectly rational.
For people in the low-risk tier, there's nothing wrong with waiting until the conclusion of the RCT monitoring in the first place, even if adverse events weren't the basis of that decision.
I don't think the drug safety system is set up to effectively evaluate the cost/benefit of the pause itself in a pandemic scenario.
How does one do that math ethically? There are risks if you do and risks if you don't. The FDA is the wrong group to make that call, because they're only concerned with the first kind of risk.
In Canada we reserved the Astra Zenica vaccine for people over 55 because of the blood clot issue. I think that's probably the right call.
“Don’t wear masks.” “No, no: wear masks.” “COVID kills over 10%.” “COVID kills less than 0.1%.” Once we realized the difference in makeup between the over-10% and sub-0.1% populations, we still couldn’t bring ourselves to make data-backed differentiations for many, many months (and still today have many small businesses closed or restricted based on what they do rather than the risk profile of their owners and employees).
These are difficult decisions to be sure, but when being seen as on the “safe side” confers benefits without a commensurate charge for the risk of the “safe” action, you get a society which moves in the direction of perceived safety (and where perceived safety may be strongly sub-optimal).
yes, security theater abounds. it's a multidimensional optimization problem with no absolutely safe side in the long run, only relatively, but often initially unintuitively, safer non-linearly intertwined sets of actions. it's hypocritical to discount the tiny risk of vaccines while dramatizing the tiny (but larger) risk of death by covid. further, it's myopic to look at the risks of covid in isolation (which is what all the frenzy around it has been doing for over a year) rather than in relation to all the similar risks in our lives and couching our responses now within our existing responses to those other ongoing risks.
I don't disagree. But I will observe that many people in the low(er) risk tier are going to be traveling, eating out, having parties, etc. sooner rather than later--vaccine or not. In my very Blue state people are very obviously relaxing a whole lot more. So the question isn't whether things open up or not. It's whether people are vaccinated when they do. (Which doesn't mean all vaccines are equally safe.)
J&J is also widely used in the US for people who might have issues with scheduling a second shot, for example people who are homeless, or are home-bound.
Even today Physicians still think the body is Art, or a combination of Art and Science.
And the only reason we don't have a science based alternative to the Physician cartel is that they spent literally $400,000,000 on lobbying/bribery in the last 30 years.
Edit- for further reading look up "evidence based medicine debate"
Anecdotally, my pediatrician has an inverted "trust pyramid" in some of their examination rooms. At the bottom—least trust—is "expert opinion."
> Even today Physicians still think the body is Art, or a combination of Art and Science.
I'm not sure why you would think these two things are opposed?
Science most broadly speaking means knowledge, and the scientific method is a means (but certainly not the only means) of acquiring knowledge. But what you do with it is art/craft. Separating the two seems unnecessarily dualistic.
This actually happened.
We 'spend' about one micromort of risk per day of being alive. Or you can spend one walking for 6 hours, or driving 250 miles (or 6 miles on a motorbike)
I just made a website to show all the other stuff we do all the time without worrying with the same (extremely low) level of risk
In the UK there's been 19 people die after ~20 million vaccinations.
Of course some more may show up in coming days from prior vaccinations.
[0] https://www.cnn.com/2021/04/13/health/johnson-vaccine-blood-...
Edit: I looked into it more and I can get IPv6 and IPv4 DNS servers to serve me both A and AAAA records. The site is now down, however :)
Yeah I banked too much on Cloudflare... I've ramped up its dyno a bit now too. Hopefully that'll keep it up!
It's ridiculous.
Or as per someone that actually knows statistics: https://twitter.com/NateSilver538/status/1381925025964515330
Build a dam, which if it broke would kill hundreds-of-thousands, or let millions die for lack of water? Oh, we'll just over-engineer it, now we can't afford to buy food to keep the people alive long enough to need the dam; or the lead engineering firm embezzles the money and installs dodgy iron.
We can't wait around for long term studies, whatever point we decide to start vaccines - where they can still be effective for the current population - it's always possible we should have waited a bit longer.
Deaths by Covid are still much more likely than deaths by the vaccine.
Hospitalizations as well, except for the 20-29 cohort https://twitter.com/VikiLovesFACS/status/1379833789334089734
I mean there's still stuff between "fully healthy" or "deadly dead".
Nonetheless, just because version 1/2 COVID vaccines are good enough for you does not others should just jump on board when other options exist that can vastly reduce risk of infectionand/or death.
In short, blowing the death problem our of proportion unless the options are only nothing vs vaccine.
Masks are supposed to protect others from you. Wearing a mask is not meant to help a person who may be at risk decrease his/her own risk of infection.
In any event, now that spring weather is here in the northern hemisphere and the vaccination campaign has given people hope, social-distancing rules are being flaunted in many countries and at-risk populations may find it hard to properly distance when they leave their homes for e.g. basic shopping. So, since the "other options" don’t always work, keeping up the vaccination campaign is very important to reducing infections.
For those willing to receive vaccination right now under informed consent, I'm all for it. I agree people are over the pandemic and making the situation worse. I disagree with many commenters here that are shaming and/or implying that people like myself are anti-vax vs simply being willing to wait for much more evidence before jumping on board with incredibly widespread usage of an incredibly not well understood treatment.
I'm in a low risk bracket. My country saw an uptick in people canceling vaccination appointments. 40% of 60+ people here are now 'unsure' of taking the vaccine.
I've done nothing but work and follow the rules since this whole thing began. Young people without partners, or young people in general, that are active, have a social life did a complete 180* in their "allowed lifestyles".
I've paid with money, time, a year of my otherwise busy life, for people in risky age brackets, at _little_ benefit to myself. *
But I'm so done, don't tell me you're asking people like me to be stuck in our anti-social and unhealthy living arrangements, while there's a solution that's _safer_ than going to a covid shower?
People like me are done paying, I'm not going to wait around another year, you take the vaccine or you take covid for all I care.
A legitimate reason for the pause is to assess whether the people impacted have anything else in common. There are alternative vaccines that can be used if a commonality is identified.
As far as hesitancy, the idiot media already does a story for every vaccinated person that gets sick, this isn't going to tip huge swaths of people in either direction.
www.medscape.com/viewarticle/949108
Per https://vaccinetracker.ecdc.europa.eu/public/extensions/COVI..., that's 30M AZ doses. You're still talking about one in a million chance of death here.
> And if you compare that to CFR from COVID for person <50 years old without diabetes and hypertension
Add a few more exclusions and no one dies of COVID, sure.
10 in a million chance of death from covid in the 5-9 age group (the lowest risk group)
This is the perfect example of anti-vacc logic. They pick the latter because they heighten the risk of the former in their mind, while ignoring or downplaying the risk of the latter. Looking at the actual numbers, it makes no sense for anyone at any age to take their chances with covid over the vaccine.
The specific issue being observed is "cerebral venous sinus thrombosis (CVST)" in combination with "low levels of blood platelets (thrombocytopenia)" per the Joint CDC and FDA statement (1).
Low blood platelets means anti-clotting treatments can pose a substantial bleeding increase, making this already dangerous condition difficult to treat.
(1) https://www.fda.gov/news-events/press-announcements/joint-cd...
This assumes that we have enough safe vaccines, which we wildly don't.
6 cases in 7 million over 3 months with mostly women being affected is exactly what we'd expect to see.
[0] https://en.wikipedia.org/wiki/Cerebral_venous_sinus_thrombos....
> Birth control pills can also cause thrombosis. So why is there all the fuss about the COVID-19 Vaccine AstraZeneca? > It is true that for birth control pills thromboses, even with fatal outcome, are known as a very rare side effect. They are listed in the Summary of Product Characteristics (SmPC). The birth control pill is available only on prescription. Every woman must be informed of this risk by the prescribing physician. For the COVID-19 Vaccine AstraZeneca, there is currently a suspected very rare side effect of sinus vein thrombosis with accompanying platelet deficiency, sometimes fatal. It is not listed in the SmPC.
https://www.pei.de/EN/service/faq/coronavirus/faq-coronaviru...
Agreed that if everyone is rational/good at math the optimal outcome is proceed with dosing, but sadly that is not the world we live in and the “broken trust” scenario might be more damaging.
Who cares how many clots birth controls produce? What matters is the outcome compared to the thing birth controls prevent - pregnancy.
Do you get more blood clots from being pregnant or from being on the pill? It's order of magnitudes more from being pregnant, therefore if you're sexually active it's safer to be on the pill compared to not.
How is this the top post? People have no knowledge of basic Bayesian statistics.
Same with the vaccine.
> Do you get more blood clots from being pregnant or from being on the pill?
Again, same with the vaccine. COVID itself causes clots, in a very substantial percentage of hospitalized patients.
"The benefits of this medical intervention are worthwhile, despite the risks, given the alternative" is precisely the point being made.
No, because there are other vaccines that don't give you blood clots at all. Your entire point is moot. Pausing temporarily to investigate is hardly controversial. The comparison with birth control is nonsensical.
A vaccination for COVID is not the same as getting birth control. Even if it was, why would you get J&J if you could get Pfizer that doesn't have the same issue?
If all vaccinations had the same blood clotting issue then perhaps you and the original poster would have a point. Given a huge disparity between them with regards to blood clotting taking a moment to investigate this is simply prudent. Making nonsensical comparisons to birth control, well, is not.
Seeing US agencies halting J&J while continuing the other vaccines could even be reassuring. It shows that US agencies really are pretty cautious, and are willing to halt vaccines that show signs of problems.
>> In China you disappear if you publicly say bad things about CCP.
> Yeah, I know what you mean, I called somebody motherfucker and got banned on HN. Freedom of speech is nowhere these days.
The vaccine was given to people, under threat of exclusion from society, without knowledge of the side effects. Not comparable.
[0] https://www.cnn.com/2021/04/13/health/johnson-vaccine-blood-...
It doesn't matter that globally it could cause more deaths. It's not the job of the FDA or CDC to act as your parent and decide for you what risk is and isn't acceptable.
Informed consent is a cornerstone of medical policy.
What will happen is they will modify the consent form to let people know about the risk, and let them decide for themselves.
Its not “a pause on vaccines” it’s a pause on one vaccine. And its not 1 in 1 million, because many of the 6.45 million doses administered of J&J are still, or even not yet, within the 1-2 week window after administration where this complication has been observed. And the pause is to get information to healthcare providers and permit them to establish appropriate protocols for handling the clots, not for open ended study. And it coincides with the timing of a short-term supply drop (-80% from prior week) in J&J vaccines that was going to force a sharp drop in the rate of adninistration at some point in the very near future anyway.
So this should actually give you more confidence in vaccine safety, because if there are problem, you will be informed.
I'm not sure how to get through that... from what I understand it takes alot of effort and time per person.
Why wouldn't you pause J&J? It's just a drop in the bucket in total vaccinations anyway and the other two don't have this issue.
Earlier attempts to use adenovirus vectors for gene therapy had issues due to, wait for it, thrombocytopenia.
The the one and only COVID vaccine that uses more or less tried and true technology and looked excellent in trials is Novavax. (AIUI Novavax’s adjuvant is newish, fancy, and not necessarily that easy to scale, and it may well be responsible for the excellent performance.)
The US CDC website[1] currently says the 7-day death rate per 100k people is 1.4. Without the J&J vaccine, that's almost 100 additional people dying per week - and just in the US.
[1] https://covid.cdc.gov/covid-data-tracker/#cases_deathsper100...
Pausing briefly to investigate this seems prudent. If we had the same prudence with COVID overall we wouldn't be in this situation to begin with.
It's really not complicated. Count up the bodies in Column A, count up the bodies in Column B, then pick one.
Given there are some organizations that are forcing you to get a vaccination. 1 in a million chance of dying from something you were forced to do is different than 1 in a million chance of a pseudo-random event. Makes no sense to continue with J&J given the other two don't have this issue at the moment.
Of course, the utilitarian approach is to simply continue vaccinating with J&J since surely more people are helped than harmed. I'm sure they'll reverse this decision soon enough.
Fixed that for you.
If the article was saying J&J was permanently discontinued perhaps I'd agree with you.
There are also jobs. I don't disagree with the forced vaccinations, but it is what it is.
It is very encouraging that this appears to be a science led decision.
Unsure why I've been downvoted, but if you've worked in FAANG level tech and with scientific staff of the CDC/FDA, you would not think that the caliber of people on either side was much different. There are a very, very large number of Moderna and Pfizer/Biontech doses going out at this point. The bigger risk is 501Y.V2 and company evolving to escape the vaccine, and that is not going to be fixed by a week long pause in J&J/Jannsen to identify the source and treatment for the errant platelet response.
COVID is the single worst thing to happen to civil discussion in my lifetime. The virus is obviously a risk. So are the vaccines. Acting any other way is just downright disingenuous.
At the end of the day, any person with a working brain is free to calculate those risks on their own. No persuading, name-calling, or outright rudeness is needed. (Yes, the top 5 comments I'm talking about you)
In times like this, I'm reminded of most historical calamities...in which a small minority stood on one side, another small minority on the other, but the vast majority simply stood in the middle and thought "Please let this end"
Please upvote this if you're just an average person waiting in the middle.
Oh, your society believes, at a deep ethical and philosophical level, in individual freedoms, personal responsibility, and general laissez-faire attitude regarding behaviors that do no harm to others? Okay. Here's an invisible threat that is on average low-probability fatal but with wide error bars and a step-function if enough people decide to ignore it. If enough people take collective actions that are uncomfortable, inconvenient, and in some cases heavily disruptive (possibly resulting in loss of individuals' livelihoods), the odds of dying from it are minimized for everyone (but nonzero). If not enough people do these things, the odds spike up (hard to say by how much). In terms of personal responsibility, you don't know if you're spreading the disease and if someone catches it and dies, we only have probabilities to estimate responsibility regarding who it came from.
Oh, and a handful of the mitigations might also have nonzero risk of harm or death, with some noteworthy error bars on the estimates.
... and all this on top of a population that barely understands what probability is in general, let alone error bars. Most citizens are, in fact, not nearly educated enough to calculate those risks. But they sure want to think they are, because we put personal responsibility for one's health on the person.
It's like the crisis was hand-tuned to be everything Americans hate.
I was in a zoom call with a large number of people I consider educated. They were talking about the California propositions and they didn't want to talk about what they said or to argue for or against, they just wanted to know who supports and opposes which one and if they were on the right team.