Janine Jackson interviewed Public Citizen’s Peter Maybarduk about Covid-19 vaccines and treatments for the September 11, 2020 episode of CounterSpin. This is a lightly edited transcript.
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Janine Jackson: Donald Trump says the US won’t participate in the Vaccines Global Access Facility, or COVAX, whose stated aim is to speed vaccine development, secure doses for all countries and distribute them to the most high-risk segment of each population. Global cooperation in the face of a global pandemic might make sense to some but, a White House spokesperson told the press, the US “will not be constrained by multilateral organizations influenced by the corrupt World Health Organization and China.” But when it comes to possible vaccines and treatments for coronavirus, Trump’s jingoistic sociopathy is not the only obstacle between science and public health. Peter Maybarduk is director of Public Citizen’s Global Access to Medicines Program. He joins us now by phone. Welcome back to CounterSpin, Peter Maybarduk.
Peter Maybarduk: Good to be with you.
JJ: Starting with vaccine development, how meaningful are Trump’s isolationist protestations? We know sometimes he mouths off, but it doesn’t translate to much. But could this impede Americans’ access to a vaccine?
PM: It impedes the world‘s access to a vaccine, and it’s massively consequential in that sense, and it could extend the pandemic, so that’s obviously bad for people living in the United States. This is a time when US leadership is absolutely critical in order to help the world make vaccines, get enough vaccines for the world’s people, and not see a delay of many years in access in low- and middle-income countries, for example. And, of course, the Trump administration, as you said, is hurling that to the wind, and the consequences will be a global vaccine apartheid. The consequences will be many millions of people around the world, in the most vulnerable communities, not having safe and effective vaccines when they need them, and communities that are already hard-hit or already suffering from poverty or political instability, those situations getting worse and the consequences amassing for years.
So the lack of cooperation here, it also accelerates the race, right? Trump is adding to the tension in the sense that it’s every country for themselves. And to have high-income countries buying up limited doses of vaccines and not looking at the cooperative solutions, not only to distribute equitably the vaccine doses that we will have to end the pandemic faster and take care of the most vulnerable people and make sure healthcare workers have vaccines, but also neglecting solutions that might help the world manufacture more vaccine doses more quickly through cooperation, public production, technology transfer. Instead, it’s every country from themselves, and also each corporation entrusted to act in its individual profit interest. And we’re just handing out grants to the corporations and hoping that that solves the pandemic, which is no way to proceed.
JJ: Yeah, some news media have pointed to Trump’s claims that a vaccine could be ready by Election Day as a troubling indication that the process could be “polluted by politics,” but the same outlets see nothing at all worrisome about describing AstraZeneca, for example, as being a “frontrunner in the race” for a Covid-19 vaccine. That a desperately needed medicine should be the “spoils” given to the lucky victor of an each-against-all competition is just, you know, that’s how you do healthcare for US news media, it seems; that’s nature’s way.
PM: A race is a bad metaphor, of course; it’s just all people against the virus. So it’s unfortunate.
JJ: Yeah, well, as we move from possible vaccines to treatments for Covid, we remember that America First-ism isn’t the only problematic thing, isn’t the only villain of the piece. When we last spoke to you in May, you were talking about remdesivir, a drug that had shown promise against Covid, and the CEO of Gilead, which makes remdesivir, was saying that he was “humbled” to be making it, and he was talking about collaborative efforts. What’s the update there?

Peter Maybarduk: “If we can’t deal with the problem of pharmaceutical monopolies, if we can’t deal with the problem of politics influencing health criteria, before there is a safe and effective vaccine, then we can see that we’re in for a world of hurt.”
PM: Remdesivir is the first experimental treatment approved to treat Covid. Of course, we now know that steroids that have been on the market for a long time are also proving useful. But remdesivir has a big market, and there are hospitals and states that want it to shorten hospital stays. It’s not yet proven to save lives, but it can reduce the length of hospital stays by some days, which is important in reducing hospital burden and keeping our health facilities running as efficiently as possible.
But cities and states are experiencing shortages of remdesivir: 38 hospitals in 32 cities in 12 states have reported shortages of the drug, because Gilead is not making enough to meet demand. Gilead has a monopoly on the drug because of the government-granted patents and exclusivities. So despite the fact that there are sources of generic supply, including a company called Beximco and others that could be getting into the market, they’re precluded from getting into the US market because of monopoly.
So monopoly is leading to a shortage of the drug, but also Trump’s Health and Human Services Administration has failed to allocate the drug rationally. We ran an analysis with all the states’ remdesivir data and HHS remdesivir allocation data, built our own database, and found that states that had a bit larger pandemics and more hospitalizations were nevertheless receiving less remdesivir.
What we know actually is that states that reported directly to the White House, governors that said to the White House, “We need more remdesivir,” got more remdesivir. And so politics played a role and, unfortunately, HHS’s own stated criteria of allocating this drug according to hospital burden was not followed, because of that insider track. Now, this is all concerning for us, both because of what it means for this particular drug, but if we can’t get our act together, if we can’t deal with the problem of pharmaceutical monopolies, if we can’t deal with the problem of politics influencing health criteria before there is a safe and effective vaccine, then we can see that we’re in for a world of hurt. Things could get worse.
JJ: Let me ask you, can we ask how a drug developed with public money can actually be in shortage to begin with, or is that too communist? I mean, didn’t millions of dollars of—as the media like to say—“taxpayer dollars” go into developing remdesivir?
PM: That’s right, at least $70 million. The federal government was a partner in the development of remdesivir from early days. Remdesivir was first developed as part of a suite of candidate treatments for hepatitis C; Gilead made about $200 billion globally off its hepatitis C drugs. It was later tested against Ebola in cooperation with federal scientists and now, finally, NIH is running clinical trials to move remdesivir forward today.
But, yeah, there’s production shortages. And it’s not necessarily outrageous on its face that Gilead wasn’t making enough to meet initial demand. It’s a pandemic; everybody is sort of trying to get up to scale. But it is very unfortunate that the public is constrained from producing more because only Gilead is allowed to produce it.
JJ: Right. I worry, I guess, about the presentation of the vaccine as a kind of holy grail, as though it will magically put all of this behind us; or as a way forward, you know? That we’ll just kind of: pandemic, vaccine, pandemic, vaccine. Obviously, as you’re saying, as lots of folks are saying, this is not going to be our last public health crisis, so we have to be looking at the processes, we have to be looking at the systems that are in place. I’ve seen a lot of breathless stories on the clinical hold on the AstraZeneca study because one participant got ill, lots and lots of coverage: What does that mean, what does that not mean? I guess I wish some of that airspace would be given to these questions that you’re bringing up, about what is our whole process for distributing life saving medicine, and what’s in the way of that?
PM: Yeah. And as you say, first there’ll be the issue of making sure a vaccine is safe and effective. And it’s very important that we get all the Phase 3 clinical trial data in. Having a misfire, an unsafe vaccine, would be a catastrophe. So as much as we’re in a hurry to get safe and effective vaccines to the world, first we’ve got to prove they’re safe.
But once there is a safe, effective vaccine on the market, it may still be the case that the first vaccine is not the best one; it may only prevent Covid or transmission for a limited period of time, it may require multiple doses. Some of the vaccines in development require cold chain storage that will be hard to deliver to remote areas. So there can be multiple candidates; it may take time to get the right candidates out there. And we just have to be doing everything we can, both to manage the pandemic meanwhile, and also deliver great volumes later on. But as you say, we can’t just sit around and wait for a silver bullet. We have to be taking the testing measures now and recognizing this is going to be a challenging process that’s going to be with us for a while and not everyone’s going to get it at the same time. The consequences of that could be very bad, but they can be mitigated.
JJ: Let me just ask you, finally, in terms of things that media could be putting their lens on: We’re not all scientists, we can’t all interpret data, necessarily. But we are all political actors who have some role in demanding transparency from our government, in calling for access, for information. I just wonder if you could turn reporters’ attention to something, what would you have them be paying attention to as we go forward?
PM: Technology transfer, or the concept of a people’s vaccine, that a vaccine can be a public good. While only you or I can take any single given dose of the vaccine, all of humanity can benefit from the technology underlying that vaccine and we can teach the world to make it. I’m not naive about that, there are massive technical challenges to producing new vaccines well. But right now we’re simply being deferential to the exclusivities, the confidential information, the patents, the monopoly control of these vaccines by individual companies who are all benefiting from public funding anyway, rather than saying, “What’s the best technology that we as a people have? And how can we get to scale as quickly as possible as one world?” If we don’t do that, the rationing is going to be very severe.
And I think there is underreporting on the possibility that we could expand production capacity beyond current plans, and the consequences of not doing so are going to be…. It’s going to be one of the great humanitarian catastrophes of our time. And we’re going to be responsible for reporting out to the next generation how we let so many vulnerable people around the world suffer because we weren’t imaginative about this moment, because we didn’t grab the power of the US government or global production capacity and say, “We can rise to meet the scientific and technical challenge.” We’re simply being too deferential to some of the moneyed interests that are at stake, and it’s an especially dangerous time for that way of thinking.
JJ: We’ve been speaking with Peter Maybarduk, director of the Global Access to Medicines Program at Public Citizen. You can find their work, including the new study on the mishandled distribution of remdesivir, online at citizen.org. Peter Maybarduk, thank you so much for joining us this week on CounterSpin.
PM: Thanks for your reporting.





Is anyone working on a vaccine for heedless greed
And how much would they charge for it?
Janinie, I don’t know about “breathless stories”, but I would settle for the truth and not the spin which often accompanies too much of the reporting on all things SARS-CoV-2. The participant didn’t just become ill. The woman in the UK developed symptoms consistent with transverse myelitis ™ an inflammation of the spinal chord resulting in weakness of the limbs, problems emptying the bladder and paralysis. People with tm can become severely disabled and there is currently no effective cure. It’s the second time this trial has been paused for a similar case of tm which was latter attributed to participant developing multiple sclerosis. The so-called “independent” panel that evaluates these adverse events are made up of doctors, a biostatistician and a member representative of the sponsoring company running the trial. Too much is left to these so called independent panels to make subjective judgments on a vaccine reaction.
Concerns over associations between TM and vaccines are well known. A review of published case studies in 2009 documented 37 cases of transverse myelitis associated with vaccines.
Janine you asked:,,,,,,things that media could be putting their lens on…”. Janine the media can demand all the raw data associated with these vaccine trials. The Astra Zenca trial is using another reactive vaccine for its placebo to determine safety. Do you, Peter Maybarduk or anyone see the inherent problem? And if(?) this trial is like Modernas, the efficacy of the vaccine will be followed for two years, but adverse events will be only captured for 1 month and serious adverse events for six months. Do you see the red flag? The FDA under its current guidelines may not consider serious reactions include these life altering conditions: alopecia, autoimmune disease, lupus erythematosus, vasculitis, Bell’s Palsy, hypotonia, migraine, myelitis, neuropathy, seizures, mental disorders, rhinitis, and vertigo.
Do you or anyone truly believe that the drug companies developing vaccines are going to change their fraud, greed, zebra stripes because it’s a vaccine? Something’s are always rotten in Denmark and anything with PHARMA especially vaccines should be assumed to be rotten first and verified, verified verified before they can be trusted. Placing any trust in the FDA, or CDC is the wolf guarding the hen house.
In 1954 when Jonas Salk developed the 1st polio vaccine, the 1st human guinea pig to get an injection of it was Salk himself. He did not patent it, & did not make any money from it other than his pay as a university scientist. The making of vaccines today has become an unregulated high profit zero liability business.
Vaccine companies have no liability for injuries caused by vaccines & there is no US Government testing of vaccines
The link below connects to a video with Robert F. Kennedy Jr. discussing how the CDC, where Dr. Fauci works, has been captured by the vaccine companies that the CDC is supposed to regulate. Not discussed here is that over 30 yrs. ago Congress passed a law which exempts vaccine companies from being sued for defective vaccines. When the law was passed it also stated that the US Government would do safety studies on vaccines & release the reports to the public every 2 yrs. Over 30 yrs. went by & the government never released a vaccine safety report. RFK Jr. requested to see the vaccine safety reports, & the government refused to release them. RFK Jr. sued the US Government to force the release of the vaccine safety reports. RFK Jr. won the lawsuit. However, the US Government, said they couldn’t release the vaccine safety tests because, in violation of the law, they had never done a safety study of a vaccine.
https://m.facebook.com/watch/?v=607386286749107&_rdr
Face Masks
The article below came from the US Government CDC website in May of this year. It was based on a number of research studies done from 1946 to 2018. The conclusion was that surgical masks, cleaning hands with hand sanitizers, & cleaning of surfaces, i.e. countertops, tables, etc. had no significant effect on the transmission of influenza. The article did not address Covid 19 directly, but both influenza & Covid 19 are thought to be spread by droplets expelled by talking, coughing, sneezing, etc. Such droplets usually measure about 700 to 1000 nm. Human corona virus particles are generally spherical, 120-160 nm in diameter. Flu viruses are usually about 80-120 nm in diameter.
Since both flu & Covid 19 are thought to be spread by droplets significantly bigger than either virus, one might expect that a mask would not be any more effective in blocking the spread of Covid 19 than it is for blocking the spread of the flu virus.
https://wwwnc.cdc.gov/eid/article/26/5/19-0994_article
Government of Denmark says it has no evidence that masks slow the spread of Covid 19:
https://www.globalresearch.ca/europe-top-health-officials-say-masks-arent-helpful-beating-covid-19/5720652
Back in March, 12 experts in immunology stated that shutting down the economy would very likely kill more people than it would save, but I doubt that what these experts had to say was put on mainstream news:
https://www.globalresearch.ca/12-experts-questioning-coronavirus-panic/5707532
Here is an analysis by a Stanford doctor indicating that we have killed more people in the US with the lockdown than we saved from Covid 19:
https://m.youtube.com/watch?v=kZqGSnVt8c8
Newsweek article by Yale School of Public Health Professor Harvey Risch stating that large clinical trials have shown that Hydroxychloroquine is safe & effective for treating Covid 19 if treatment is started early:
https://www.newsweek.com/key-defeating-covid-19-already-exists-we-need-start-using-it-opinion-1519535
The credentials of Professor Risch can be read at this website of the Yale School of Public Health:
https://medicine.yale.edu/profile/harvey_risch/
Here is a video of Dr. John Ioanidas of Stanford University discussing Covid 19. Part of what he says is that it is now known that the case fatality rate for Covid 19 is about the same as the rate for ordinary seasonal flu.
https://m.youtube.com/watch?v=T-saAuXaPok
Information about Dr. Ioanidas:
https://med.stanford.edu/profiles/john-ioannidis
Here is some more information on the gross errors that have been made in estimating the case fatality rate & other statistics about Covid 19:
https://www.globalresearch.ca/what-should-define-a-covid-19-death-the-unreliability-of-covid-19-data-dr-ioannidis/5719380
The above commentators have added much that should be part of the official discussion.
One more treatment that has been successfully done is raising people’s vitamin F level to keep them out of ICU and discharge them as healthy back into the community.
Dr. Tom Frieden deserves credit for the interest in vitamin D and healthy living as an approach to this and all other respiratory viruses. He made it a public issue in March, 2020. As head of the CDC for 7 years of the Obama administration, his observation gave direction to many in the medical community.
The timidity of FAIR in dealing with a sustainable way forward is disappointing.
In a time of a disintegrating climate, an approach that employs industrial medicine is non-viable.
My career was in industrial medicine, i.e., conventional American medicine. It is still valuable but as much as possible we need to teach people how they can take care of their own health. Vitamin D at or slightly above 50 ng/ml, the sunshine vitamin, whole food eating, exercise, BMI less than 30, exercise, sleep at night, no alcohol or smoking.
I drink and I smoke quite heavily. I guess I just wait for the Russian vaccine to pass the final tests. I bet it will be way cheaper and safer (yet to be seen, but they don’t do it for cash but for national pride) than anything coming from the USA.
Why people still use to read news papers when in this technological globe all is presented on web?
Hi there,
Firstly, A bunch of thanks for sharing such valuable information with us.
Actually, I was doing some research about peter Maybarduk views on vaccine development & distribution plan & update. And I get landed over your article & it was too informative.
Thank you
Source: https://myeveschoice.com/