Why You Shouldn’t Trust Anyone Who Claims 80 Percent of America’s Drugs Come From China

While reading about the COVID-19 outbreak, you’ve probably encountered this particularly shocking statistic at one time or another: 80 percent of America’s pharmaceutical drug supply comes from China.

It’s a statistic that has made the rounds in right-wing publications for a while—offered as proof that China-heavy global supply chains are putting Americans at risk—but it has also popped up in mainstream outlets, including in pieces published in Politico and The Atlantic. Wherever it is deployed, the stat carries an unstated implication: What if China decides to cut us off in the middle of a pandemic? Could America face a dramatic shortage of key pharmaceutical drugs at the moment when we are most in need? And that distorted claim that says America has been too reliant on China has been seized by politicians like Sen. Josh Hawley (R–Mo.) as evidence that globalization has undermined America’s pandemic response.

In fact, because the Food and Drug Administration (FDA) does not track the volume of drug imports from any foreign countries, it is impossible to say with any certainty how much of America’s pharmaceuticals come from China. Or from anywhere else.

But that has not stopped politicians and media outlets from recycling this shocking statistic. That statistic is based on an inaccurate presentation of a single government report that says no such thing—and, in fact, suggests the opposite. At very best, it omits crucial context. At worst, it simply misleads. One expert who has repeated this stat in numerous publications and in congressional testimony refuses to share her source for that shocking bit of information.

The figure, in other words, is both misleading and mistaken. And the politicians and pundits who have seized on it have done so in order to make it seem as if they know with great certainty a supposed fact that no one actually knows.

II.

Tracing this “80 percent of American drugs come from China” claim back to its source reveals a game of “whisper down the lane,” in which a rather innocuous piece of data about the global manufacturing base for pharmaceutical drugs has been inaccurately summarized and stripped of important context.

In December, when the U.S. and China signed the “phase one” trade deal—and when the coronavirus outbreak was still very much in the background—Politico published a story (with some reporting from the South China Morning Post) framed around the idea that “U.S. policymakers” were worried that China could “weaponize” its drug exports to gain leverage in a trade dispute.

The piece was designed to scare. “The U.S. relies on imported medicines from China in a big way,” authors Doug Palmer and Finbarr Bermingham wrote right at the top. “Antibiotics, over-the-counter pain meds and the stuff that stops itching and swelling—a lot of it is imported from China.”

How much is a lot? “In all, 80 percent of the U.S. supply of antibiotics are made in China,” they wrote, linking back to a press release from Sen. Chuck Grassley (R–Iowa).

But that’s not what the press release says.

Grassley’s statement was publicizing a letter Grassley sent on August 9 to the Department of Health and Human Services (HHS) and the FDA, asking them to conduct more inspections of foreign drug manufacturing facilities to make sure they meet American standards.

“Unbeknownst to many consumers…80 percent of Active Pharmaceutical Ingredients are produced abroad, the majority in China and India,” Grassley wrote.

There’s the first bit of context collapse: the authors of the Politico piece merged Grassley’s “80 percent…are produced abroad” into “80 percent…are made in China.”

All of this also raises another question: Where is Grassley getting that information? His letter sources that claim to a 2016 Government Accountability Office report which itself cited FDA data on pharmaceutical manufacturers around the world. And that report makes it clear that the U.S. has a diverse supply chain for drugs that goes well beyond India and China.

“Nearly 40 percent of finished drugs and approximately 80 percent of active pharmaceutical ingredients (API) are manufactured in registered establishments in more than 150 countries,” is how the GAO summed up America’s pharmaceutical supply chain.

In two jumps, we’ve gone from “80 percent of American drugs are manufactured in more than 150 countries around the world” to “80 percent of drugs come from two countries” to “80 percent of drugs come from China.”

Now, a further complication. The FDA only tracks drug manufacturing facilities—not the supply chains of specific drugs.

That “lack of structural transparency and available supply chain data about drugs,” researchers at the University of Minnesota researchers wrote last month, is one of the reasons why making accurate assessments about potential drug shortages is difficult. Indeed, it was this same bit of missing information that Grassley was encouraging the FDA to address back in August.

It does seem like a reasonable thing to ask of the FDA. But for now, the lack of actual evidence means that no one can say with any certainty what percentage of America’s drugs come from which foreign countries.

The FDA’s most recent report on drug supply chains, published in October, makes clear that the agency does “not currently know whether API manufacturing facilities are actually producing the drug, or in what volume,” and therefore it is impossible to determine “what portion of U.S. drug consumption is dependent on APIs from China or India.”

That’s because many drug manufacturers make their products in various places around the world for reasons that range from the cost of labor to the availability of raw materials to access to consumer markets.

What the FDA does track, again, is manufacturing facilities that export drugs to America. In that October report, when the agency took its most recent statistical snapshot of the United States’ pharmaceutical supply chains, here’s what it found:

Source: FDA; Safeguarding Pharmaceutical Supply Chains in a Global Economy, October 2019

There are nearly 2,000 manufacturing facilities around the world that provide pharmaceutical drugs to the United States. Of those, 230 are in China. There are 510 in the United States and 1,048 in the rest of the world. Even though the number of manufacturers in the United States is at a historical low, the supply chain is clearly quite diverse.

At the same time, the FDA took a narrower look at the supply chains for the 370 drugs listed on the World Health Organization’s (WHO) list of “essential medicines,” which includes “anesthetic, antibacterial, antidepressant, antiviral, cardiovascular, anti-diabetic, and gastrointestinal agents.” The results were similar: 21 percent of production facilities are in the United States, with 15 percent of them in China, and 64 percent located somewhere else in the world.

There are only three drugs on the WHO essential medicines list whose active ingredients are sourced entirely in China, the FDA found. They are capreomycin and streptomycin, which are used to treat tuberculosis, and sulfadiazine, which is used to treat trachoma, among other things.

Here’s another way to look at the question. According to the United Nations’ COMTRADE database of world trade flows, the United States imported more than $115 billion of finished pharmaceutical products in 2018, the most recent year for which complete data is available. Only $1.5 billion of that total came from China.

Nevertheless, Grassley’s letter and the underlying FDA data have been misinterpreted to give the impression that the U.S. is singularly dependent on China when the data actually show quite the opposite.

When Reason contacted the authors of the Politico piece, Palmer said he wasn’t sure why they’d linked to Grassley’s release.

“I don’t recall why we linked to that letter since it talk[ed] about API production rather than finished pharmaceuticals,” he wrote in an email. “It looks like a mistake. But it does express concern in Congress about U.S. dependence on China in the pharmaceutical sector.”

Unfortunately, that misinformation has fully entered the mainstream through other channels too. In a piece published in The Atlantic earlier this month, Uri Friedman notes that “about 80 percent of the active pharmaceutical ingredients in American drugs come from China and India,” and sources that information to a report from the Council on Foreign Relations.

And what does that report say? “It is believed that about 80 percent of the basic components used in U.S. drugs, known as active pharmaceutical ingredients (APIs), come from China and India, though the exact dependence remains unknown since no reliable API registry exists.”

Follow the link: It goes back to that same Grassley press release from August. Again, the article is inferring a conclusion that is not supported by the underlying data—and The Atlantic left out crucial context about lack of reliable information that was included in the Council on Foreign Relations’ report.

III.

Naturally, China hawks are seizing the misinformation, and the larger coronavirus crisis, to push for the confrontation they’ve wanted all along.

In that same Atlantic article, Peter Navarro, President Donald Trump’s top trade adviser, says the coronavirus outbreak should be a “‘wake-up call’ about American vulnerabilities in a globalized world.” Commerce Secretary Wilbur Ross, who along with Navarro has been the driver of Trump’s crusade to raise tariffs and reduce U.S. trade with the rest of the world, has said the coronavirus outbreak might be a good thing because it will “help to accelerate the return of jobs to North America.”

In Congress, Sen. Josh Hawley (R–Mo.) has, unsurprisingly, taken the lead. “It is becoming clear to me that both oversight hearings and additional legislation are necessary to determine the extent of our reliance on Chinese production and protect our medical product supply chain,” Hawley wrote in a letter to the FDA in February. He called America’s supposed dependence on Chinese-made drugs “inexcusable” and appears to be laying the groundwork for some sort of pharmaceutical-industrial policy.

And at the center of that idea is a woman named Rosemary Gibson.

Gibson is a senior fellow at the Hastings Center, a nonpartisan bioethics research center, and the author of China RX, a 2018 book detailing “the risks of America’s dependence on China for medicine.” In recent months, she’s become the darling of right-wing media and politicians who see the coronavirus outbreak as an opportunity to ramp up a U.S.-China cold war. “All Our Drugs To Treat The Coronavirus Depend on Chinese Suppliers” noted a headline in The American Conservative on February 17 in which she argued that “we depend on China for 80 percent of the core components” that go into U.S. drugs. She had used the same “80 percent” stat in a December 13 article too, both times without attribution. In the December Politico piece highlighting how policy makers were worried about China “weaponizing” drug exports, Gibson was the first expert quoted. “Medicines can be used as a weapon of war against the United States,” she warned.

On March 12, when Gibson was called to testify before the Senate Committee on Small Business and Entrepreneurship, she argued that “The United States faces an existential threat posed by China’s control over the global supply of the ingredients in thousands of essential generic medicines.” Those generics account for 90 percent of the drugs used in hospitals and sold in drug stores she said.

That sounds bad. But how many of America’s generic drugs come from China? That would be 9 percent, Gibson said in the same testimony.

A bigger concern would seem to be India, which manufacturers 25 percent of America’s generic drugs, according to Gibson. India imports a large amount of the ingredients in those drugs from China, which helps to demonstrate why it’s so difficult to put a number on exactly how much of America’s drug supply comes from China. Global supply chains care little for national borders.

Still trying to get to the bottom of the “80 percent” claim, I called Gibson last month to discuss her research and recent congressional testimony.

I came away from the conversation with the sense that Gibson is motivated by a sincere belief that Americans’ health is put at risk by shoddily-made drugs often manufactured overseas and that the FDA is not doing enough to prevent problems—or to collect the necessary data to identify where those problems might be. After the past few weeks have put a spotlight on the agency’s bureaucratic malfeasance and myopia, it is easy to be sympathetic to such arguments.

Gibson says the FDA’s data about drug manufacturing facilities is “misleading” because the agency fails to track actual supply lines from where the first chemical compounds are produced to where active ingredients are assembled to where the final products are shipped. This is pretty much the only thing everyone can agree on: that the FDA’s data is severely lacking context. That context might show the true complexity of pharmaceutical supply chains that wrap around the world, or the China-dependency that has nationalists worried.

But when it came to the question of how she knows that America is thoroughly dependent on China, Gibson was less transparent. I asked about the statistics she’d used in her pieces for The American Conservative and in her congressional testimony. Where, I asked, did she find this data that not even the FDA is tracking?

“I asked very fine people with 150 years [of] experience in making drugs,” she said. “I went around the table. First person said, ’90 percent, conservatively.’ Next person said, ’90 percent.’ Next person said, ’90 percent.'”

I’m sorry, I interjected, but if you can just clarify for me: Who were you speaking too? Where was this?

“These are people I know who actually make generic drugs or their components,” she said. “They know the best place, or the only place, where you can get” the necessary components.

So if I wanted to confirm that information on-the-record, how would I find it? “No, you can’t find that,” Gibson said. “No. I haven’t seen that.”

We went around a few more times: Who is telling you this? Is there another on-the-record source—a study, a paper, anything—that says this? But the answer was always the same: No.

Eventually, it became clear that the data weren’t the most important thing.

“Let’s put it at 90 percent of the chemical and other ingredients needed to make components—needed to make our generic drugs—are sourced from China,” Gibson said. “And if you want to…say it’s 75 [percent], that’s fine.”

But, hold on, doesn’t that distinction matter? Is the answer just that we don’t know?

“Well, what we do know is it’s enormous. Huge,” she said. “This is what they said: ’90 percent, 90 percent, 90 percent.'”

Who said?

“These are very seasoned people who have worked in manufacturing. It’s like the best chefs. You’re asking the best chefs ‘I need cinnamon or I need turmeric or mace or nutmeg. Where does it come from?'” she said. “They know that, but it’s not going to be written down in a book.”

(Cinnamon is exported by lots of countries all around the world —places as diverse as Madagascar, the Netherlands, and Vietnam. And those numbers are indeed written down.)

To be fair to Gibson, it is frustrating that the FDA does not track this information. But that’s no reason to substitute speculation for fact. And it is certainly possible that Gibson has sources providing this data point to her. But her unwillingness to identify those sources should be enough to make observers question the conclusions she is drawing from them. At the very least, you might expect Congress to want to hear this information firsthand from one of her sources.

And if the information is coming from industry insiders, as she suggests, and if they are as worried as Gibson says they are, one is left to wonder why they don’t do the prudent thing and shift their supply chains. No one is forcing them to manufacture in China.

But soon, someone might be forcing them to manufacture here. Whether the sourcing is sincere or not, there’s little doubt that Gibson’s research has become a tool for China hawks like Hawley, who blasted out excerpts from her March 12 testimony in a press release announcing his introduction of the Medical Supply Chain Security Act. Hawley says the bill would give greater authority to the FDA to get information from drug manufacturers about where they source ingredients, including raw materials, “and any other details the FDA deems relevant to assess the security of the U.S. medical product supply chain.”

That basic idea was incorporated into the Coronavirus Aid, Relief, and Economic Security Act (CARES Act), the massive $2.3 trillion stimulus bill passed by Congress and signed by Trump last month. Under section 3010 of the law, HHS is directed to asses “the dependence of the United States…on critical drugs and devices that are sourced or manufactured outside of the United States.” Regardless of what the fact-finding mission might uncover, in another part of the bill Congress has already directed the department to include in its report “strategies to…encourage domestic manufacturing.”

It’s a telling bit of legislative text. In one fell swoop, Congress admitted that the federal government is ignorant about the extent to which drug supply lines are dependent on China—so much for that 80 percent figure that’s been repeated so much—and simultaneously announced its plans to change how those supply chains work.

What might those changes look like? In her testimony on March 12, Gibson outlined a few ideas. She wants the federal government to be intimately involved in process of manufacturing pharmaceuticals, covering capital costs for drug companies to build out manufacturing facilities “for domestic production of essential generic drugs and their core components” and controlling drug pricing to ensure that companies were making only “a fair rate of return” off the federal investment.

“Any federal investment in assuring essential generic drugs should be considered a national security asset that cannot be sold to companies whose governments are strategic competitors to the United States,” says Gibson. “This investment will help reinvigorate the U.S. generic manufacturing base and the capacity for the United States to eventually achieve a minimum level of self-sufficiency in the making of essential medicines vital to the nation’s health security.”

Tim Morrison, a senior fellow at the nationalist Hudson Institute and former member of the Trump White House’s National Security Council, told lawmakers at the same March 12 hearing that the federal government must intervene to prop-up domestic pharmaceutical suppliers. “The term ‘industrial policy’ is considered by some economic theorists and purists to be dirty words,” Morrison said. “I ask you to think about all of the tools of economic statecraft you can use to support American producers in strategic industries.”

Whatever comes next, it is likely to be a bipartisan process. In an op-ed for The Washington Post last year, Reps. Anna Eshoo (D–Calif.) and Adam Schiff (D–Calif.) cited the “80 percent” stat without proper context and linked to Gibson’s research to argue that “China has a virtual monopoly on the ingredients required to manufacture critical medicines.”

IV.

Bad facts make bad laws. Add into the mix a crisis and already high anti-China fervor within some segments of American politics. Whether due to context collapse—confusing all drug imports with drug imports from China, as some publications have done—or a panic-driven response to an unprecedented public health crisis, it appears that Congress has already decided to pursue a policy response based on theorized potential drug shortages that have yet to materialize.

“Instead of trying to get the FDA to figure out if its 75 [percent] or 90 percent, the reality is we gotta have the capability to make some of this here because countries will shut their doors,” Gibson told me.

Will they? India cut export capacity by about 10 percent in response to the pandemic, but so far they are (thankfully) the exception rather than the rule. Initial fears that China would cut off exports of medical equipment in order to hoard supplies for their own battle with the coronavirus have proven to be unfounded.

To the degree that drug shortages are likely to happen, experts say they will be the result of spiking worldwide demand—not countries cutting off trade.

“The pandemic itself may lead to increased demand for normal uses of certain drugs, such as acetaminophen to treat fever, and the crisis may also prompt hoarding,” researchers from the University of Minnesota warned in a study released last week. “In addition, drug production may be slowed or stopped in countries hit hard by the virus.”

Most drug companies are positioned to survive short-term supply shocks, J.P. Duffy, an attorney who specializes in the pharmaceutical trade, told European Pharmaceutical Review, a trade publication. That’s because most have a stockpile intended to last for six months to a year.

Like the University of Minnesota researchers, Duffy believes logistical problems are likely to be the cause of shortages—not political or manufacturing issues.

That’s why diverse supply chains are important, so that parts of the world unaffected by a major catastrophe can supply goods to areas more hard hit. The coronavirus outbreak may give some companies good reason to seek more diverse supply chains in the future. But it should not be seen as an argument for forcing pharmaceutical companies to make their products exclusively in the United States. Indeed, the question that policymakers should be asking isn’t “where do these drugs come from” but “can we be sure we’ll get them when they are needed.” Leave the specifics to the private sector.

Even at the height of the COVID-19 outbreak in China, when many factories were shut down across the country, the Food and Drug Administration reported that America was facing a shortage of exactly one drug. After checking with the producers of more than 180 imported drugs to assess the state of their supply chains in the midst of the outbreak, FDA Commissioner Stephen Hahn released a statement saying that “none of these firms have reported any shortage to date. Also, these drugs are considered non-critical drugs.”

Meanwhile, the global supply chain for pharmaceutical drugs appear to be more diverse than the “80 percent from China” statistic suggests. There are only three drugs on the WHO’s “essential medicines” list for that the United States sources solely from China, according to FDA data. Chinese drug makers—while growing in recent years—account for only 13 percent of the global manufacturing base that supplies pharmaceuticals to America.

To be sure, there is plenty of space for American policy makers to criticize China’s handling of the COVID-19 outbreak. China’s leaders failed to communicate the seriousness of the disease at an early stage, and even now appear to be covering up the extent of the destruction the coronavirus has caused. There are documented cases of Chinese-made drugs failing to meet FDA standards that may call for greater scrutiny being applied to certain producers. The coronavirus pandemic may give some pharmaceutical companies a good reason to reconsider their supply chains.

But the fear that China would deliberately withhold drugs and other crucial equipment does not appear to be based on information that’s any more solid than the claim that 80 percent of America’s pharmaceuticals rely on Chinese suppliers.

There remains a big difference between fearmongering about China cutting off Americans from life-saving drugs and the reality of a pandemic that is stressing supply chains everywhere. The former serves as a call for political action. The latter, for simply letting markets work.

Whatever policies are crafted after the pandemic, they should be written with that context in mind—and with an awareness of the global reality of modern medicine. America’s supposed dependence on China has been overstated, but it does remain absolutely true that the United States imports most of the drugs that Americans consume. That, too, is an argument for keeping global supply chains open. It’s a reason for maintaining good diplomatic relations with other countries—not a reason to pursue autarky and continue an unnecessary trade war over fears that may not materialize.

“The world’s COVID-19 patients and medical experts need their policymakers to allow vital supplies and equipment to flow unimpeded from one country to another, wherever needed, as the crisis continues to evolve,” writes Chad Bown, senior fellow at the Peterson Institute for International Economics, a trade-focused think tank. “Global cooperation is the only way countries can minimize the devastation COVID-19 is leaving in its path.”

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Why the Government Is No Good at Fighting Coronavirus

One of the defining features of the coronavirus pandemic has been the failure of government, especially at the federal level, to act in a wise, timely, or effective fashion. When cases of coronavirus started showing up in Washington state in January, researchers turned to the Centers for Disease Control and Prevention (CDC) for approval to test nasal swabs but were rebuffed by bureaucrats there and at the Food and Drug Administration (FDA). Officials told local doctors to stop running unauthorized tests, then waited until February 29 to let biotech companies and non-government research labs develop and deploy new tests for the virus. The two main agencies charged with protecting the nation’s public health screwed up from the very beginning.

In a devastating new story, the AP reports that “the Trump administration squandered nearly two months that could have been used to bolster the federal stockpile of critically needed medical supplies and equipment.” As China and then Italy wrestled with the spread of coronavirus, the president publicly minimized dangers and privately kept various agencies under his control from increasing supplies of equipment from N-95 masks to ventilators. “State and local officials report receiving broken ventilators and decade-old dry-rotted masks,” says the AP, which quotes presidential son-in-law and adviser Jared Kushner’s statement on Thursday that “the federal stockpile” is “not supposed to be state stockpiles that they then use.”

Bad as this is, it’s important to underscore that the calamitous federal response is not simply the fault of Donald Trump and the people around him. As The Washington Post‘s Dan Balz, no supporter of the president, reported over the weekend,

The problems go far broader and deeper than what a president does. Lack of planning and preparation contribute, but so too does bureaucratic inertia as well as fear among career officials of taking risks. Turnover in personnel robs government of historical knowledge and expertise. The process of policymaking-on-the-fly is less robust than it once was. Politics, too, gets in the way.

Balz has interviewed many federal, state, and local officials involved in the responses to the 9/11 attacks, Hurricane Katrina and other natural disasters, and the Ebola and SARS outbreaks. One common thread was that agencies, especially at the federal level, are excessively rule-bound and slow to innovate on the ground, despite the reality that virtually every major event presents unique circumstances that call for deviations from standard-operating procedures.

Andrew Card was President George W. Bush’s chief of staff, and as result was involved in the responses to both 9/11 and Hurricane Katrina. (The federal response to the latter is widely considered to be one of the most incompetent emergency responses in federal history.) Before that, he had coordinated President George H.W. Bush’s response to Hurricane Andrew in 1992.

“I found that FEMA [Federal Emergency Management Agency] is a great organization, but they were all afraid to do things that weren’t, quote, by the book,” Card said. “FEMA was always being challenged…second-guessed after a disaster.”

Card learned through that experience and later as White House chief of staff to President George W. Bush during 9/11 and Katrina the obstacles that the combination of fear and bureaucratic inertia can impose when immediate and innovative action is required.

“Each bureaucracy has its own momentum,” he said. “The challenge in dealing with a disaster is addressing the momentum or the inabilities. If something’s not moving, it takes a lot of effort to get them to move.”

That helps explain why CDC and FDA officials simply denied the Washington state doctors’ requests for testing approval.

If the track record of the government so far is dispiriting, there’s even more cause for concern going forward. Yesterday the U.S. Surgeon General, Jerome Adams, said that the coming week will bring record surges in the number of coronavirus cases and deaths. But despite the fact that we’ve known about the disease since the first reported cases surfaced in China late last year, the nation’s top doctor instinctively reached for metaphors about surprise attacks, telling Chris Wallace on Fox News Sunday:

This is going to be the hardest and the saddest week of most Americans’ lives, quite frankly….This is going to be our Pearl Harbor moment, our 9/11 moment.

If our leaders are still acting as if the coronavirus pandemic is a sneak attack, it’s no wonder the federal response has been such a disaster.

It’s comforting to know that officials are waiving stupid and counterproductive regulations, and it’s heartening to see all the workarounds the private sector is doing to comfort people and save lives. But it’s an outrage that we’re not simply fighting a pandemic, but fighting the government that is supposed to protect us from just such a thing.

Related: Economist Alex Tabarrok says “the FDA and CDC’s coronavirus is a failure of ‘historic proportions'”:

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Why the Government Is No Good at Fighting Coronavirus

One of the defining features of the coronavirus pandemic has been the failure of government, especially at the federal level, to act in a wise, timely, or effective fashion. When cases of coronavirus started showing up in Washington state in January, researchers turned to the Centers for Disease Control and Prevention (CDC) for approval to test nasal swabs but were rebuffed by bureaucrats there and at the Food and Drug Administration (FDA). Officials told local doctors to stop running unauthorized tests, then waited until February 29 to let biotech companies and non-government research labs develop and deploy new tests for the virus. The two main agencies charged with protecting the nation’s public health screwed up from the very beginning.

In a devastating new story, the AP reports that “the Trump administration squandered nearly two months that could have been used to bolster the federal stockpile of critically needed medical supplies and equipment.” As China and then Italy wrestled with the spread of coronavirus, the president publicly minimized dangers and privately kept various agencies under his control from increasing supplies of equipment from N-95 masks to ventilators. “State and local officials report receiving broken ventilators and decade-old dry-rotted masks,” says the AP, which quotes presidential son-in-law and adviser Jared Kushner’s statement on Thursday that “the federal stockpile” is “not supposed to be state stockpiles that they then use.”

Bad as this is, it’s important to underscore that the calamitous federal response is not simply the fault of Donald Trump and the people around him. As The Washington Post‘s Dan Balz, no supporter of the president, reported over the weekend,

The problems go far broader and deeper than what a president does. Lack of planning and preparation contribute, but so too does bureaucratic inertia as well as fear among career officials of taking risks. Turnover in personnel robs government of historical knowledge and expertise. The process of policymaking-on-the-fly is less robust than it once was. Politics, too, gets in the way.

Balz has interviewed many federal, state, and local officials involved in the responses to the 9/11 attacks, Hurricane Katrina and other natural disasters, and the Ebola and SARS outbreaks. One common thread was that agencies, especially at the federal level, are excessively rule-bound and slow to innovate on the ground, despite the reality that virtually every major event presents unique circumstances that call for deviations from standard-operating procedures.

Andrew Card was President George W. Bush’s chief of staff, and as result was involved in the responses to both 9/11 and Hurricane Katrina. (The federal response to the latter is widely considered to be one of the most incompetent emergency responses in federal history.) Before that, he had coordinated President George H.W. Bush’s response to Hurricane Andrew in 1992.

“I found that FEMA [Federal Emergency Management Agency] is a great organization, but they were all afraid to do things that weren’t, quote, by the book,” Card said. “FEMA was always being challenged…second-guessed after a disaster.”

Card learned through that experience and later as White House chief of staff to President George W. Bush during 9/11 and Katrina the obstacles that the combination of fear and bureaucratic inertia can impose when immediate and innovative action is required.

“Each bureaucracy has its own momentum,” he said. “The challenge in dealing with a disaster is addressing the momentum or the inabilities. If something’s not moving, it takes a lot of effort to get them to move.”

That helps explain why CDC and FDA officials simply denied the Washington state doctors’ requests for testing approval.

If the track record of the government so far is dispiriting, there’s even more cause for concern going forward. Yesterday the U.S. Surgeon General, Jerome Adams, said that the coming week will bring record surges in the number of coronavirus cases and deaths. But despite the fact that we’ve known about the disease since the first reported cases surfaced in China late last year, the nation’s top doctor instinctively reached for metaphors about surprise attacks, telling Chris Wallace on Fox News Sunday:

This is going to be the hardest and the saddest week of most Americans’ lives, quite frankly….This is going to be our Pearl Harbor moment, our 9/11 moment.

If our leaders are still acting as if the coronavirus pandemic is a sneak attack, it’s no wonder the federal response has been such a disaster.

It’s comforting to know that officials are waiving stupid and counterproductive regulations, and it’s heartening to see all the workarounds the private sector is doing to comfort people and save lives. But it’s an outrage that we’re not simply fighting a pandemic, but fighting the government that is supposed to protect us from just such a thing.

Related: Economist Alex Tabarrok says “the FDA and CDC’s coronavirus is a failure of ‘historic proportions'”:

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White House Recommends Against Grocery and Pharmacy Trips While Trump Says Go Ahead and Try Hydroxychloroquine

Stay really, really at home now? On Saturday, White House coronavirus response coordinator Deborah Birx said of the next two weeks: “This is the moment to not be going to the grocery store, not going to the pharmacy, but doing everything you can to keep your family and your friends safe.”

Yikes. Keeping safe now means avoiding shopping for even food, toiletries, and medicine? No wonder President Donald Trump has been hoping so hard for hydroxychloroquine to work against COVID-19.

But Trump advisor and infectious disease expert Anthony Fauci isn’t so sure about the anti-malarial drug as a cure for the new coronavirus. In a meeting Saturday, “Fauci pushed back against [economic adviser Peter] Navarro, saying that there was only anecdotal evidence” for it, reports Jonathan Swan at Axios. More:

Eventually, [Jared] Kushner turned to Navarro and said, “Peter, take yes for an answer,” because most everyone agreed, by that time, it was important to surge the supply of the drug to hot zones.

The principals agreed that the administration’s public stance should be that the decision to use the drug is between doctors and patients.

Trump ended up announcing at his press conference that he had 29 million doses of hydroxychloroquine in the Strategic National Stockpile.

One thing driving this may be a desire not to drop the ball again on COVID-19 prep, as the administration has already done with tests, masks, and ventilators. Not that Trump will admit his team has faltered in the slightest. He’s spent the past week bragging about how big his backup of medical supplies is, while simultaneously declaring this Strategic National Stockpile mostly off-limits to American states.

The president now regularly describes the supply of ventilators and masks in terms of negotiations he allegedly made well and states didn’t, making this into a competition where there should be cooperation to save lives.

Last weekafter Trump advisor and son-in-law Jared Kushner called it “our” stockpile at press conference (“our” meaning the federal government, Trump clarified) and Trump scoffed at states like New York for lacking suppliesthe language on the Strategic National Stockpile’s website was changed:

But while Trump has been bashing state leaders for not stocking up pre-pandemic, the federal government waited until mid-March to bolster its supplies, according to a new report from the Associated Press. AP’s review of federal purchases “shows federal agencies largely waited until mid-March to begin placing bulk orders of N95 respirator masks, mechanical ventilators and other equipment needed by front-line health care workers.”

By the time these agencies were starting to place orders, “hospitals in several states were treating thousands of infected patients without adequate equipment and were pleading for shipments from the Strategic National Stockpile,” AP reports. The stockpile is “now nearly drained.”

If hydroxychloroquine may be useful, it’s not unreasonable for Trump to want to get an early jump on that. (“If it does work, it would be a shame we did not do it early,” as Trump said on Saturday.) And Trump’s underlying rhetoric about people and hospitals having the right to decide for themselves about experimental cures is also sound. (“It’s their choice. And it’s their doctor’s choice,” Trump said Saturday.) It has a lot in common with more general arguments for “right to try” lawsbut with a critical difference, too.

Right-to-try advocates generally argue that when specific people are dying from diseases that can’t be cured by treatments the Food and Drug Administration has approved, they should be able to try experimental drugs, generally ones that have proved promising in clinical trials or are already approved in other countries. They don’t generally push for masses of patients to try barely tested and potentially risky cures for communicable diseases on a whim or a hunch.

So far, the case for hydroxychloroquine amounts to little more than a handful of studies with no control patients and a report from Chinese doctors posted to a non-peer-reviewed website. The Chinese doctors said that in a small sample of patients with mild to moderate cases of COVID-19, hydroxychloroquine seemed to help fevers and pneumonia dissipate faster and may have helped stop cases from turning more severe. It was not tested on severe or asymptomatic cases.

Another recent study found “no evidence” of hydroxycholorquine helping patients with severe COVID-19 infections.

All that said, it’s certainly preferable that doctors can try treating patients with hydroxychloroquine without federal bureaucrats saying they must wait until we’ve done years of trials.

“With no proven treatment for the coronavirus, many hospitals have simply been giving hydroxychloroquine to patients, reasoning that it might help and probably will not hurt, because it is relatively safe,” notes The New York Times.

But some doctors note that while hydroxychloroquine may be relatively safe, it’s far from harmless. “There are side effects to hydroxychloroquine,” Brown University emergency physician Megan L. Ranney told the Times. “It causes psychiatric symptoms, cardiac problems and a host of other bad side effects.”


FREE MARKETS

Against pantry policing. Shaming people for their pandemic-time purchases has become a new national pastime. At Arc Digital, Phoebe Maltz Bovy takes a calm look at how people are responding to the fact that “slowly yet suddenly, everything changed”:

Human activity has been divided into the essential and the inessential, with breathing falling into the former category (as long as there are ventilators available, at least) and just about everything else, the latter. Office jobs, clothes-shopping, bar-going, sex (or just in-person conversation) with anyone you don’t happen to live with—all of these everyday pursuits have been put on hold, their eventual return uncertain.

Falling somewhere ambiguous between necessity and frivolity, however, is food. On the one hand, we’ve all got to eat. On the other, the discourse about eating in the era of coronavirus has a way of suggesting food is a luxury, a pseudo-requirement the more noble among us would somehow transcend. As though if you believe yourself and your family entitled to food, now and in the foreseeable future, then you’re exhibiting a level of unacceptable entitlement….

A figure has emerged of the Bad Grocery-Shopper, the proverbial Karen who buys more than is correct (even though, and I cannot emphasize this enough, no one knows or can know what “correct” would mean), and who is definitely, definitely buying toilet paper in excess. Indifferent to the fate of her local businesses (or, perhaps, newly unemployed herself?), she isn’t even sending a few bucks here and there to her preferred bars and cafés. The problem isn’t coronavirus; it is—it’s soothing to think, apparently—middle-aged, middle-class women buying groceries for their families.

Read the whole thing here.


FREE MINDS

Businesses are beginning to sue over mandatory shutdown orders. From The New York Times:

Some of those suing their state governments seek redress for specific, local grievances, as with the [Blueberry Hill Public Golf Course and Lounge lawsuit] or in a similar suit in Pennsylvania being pursued by a company that says it is the country’s oldest manufacturer of orchestra-quality bells and chimes. Those lawsuits and one in Arizona are rooted in the Fifth Amendment, which requires due process and guarantees compensation for property seized by the government.

Other constitutional amendments have been invoked in several lawsuits in recent weeks attempting to force open gun stores, or to argue that measures to curb the virus should not outweigh rights like freedom of assembly and religion.

“Those may be serious, but they may also be part of an attempt to make an argument in the press about overreach,” said Tom Burke, a political-science professor at Wellesley College who studies the politics of litigation.

History dating back to the time of 15th-century plagues shows that lawsuits typically plummet during pandemics, Mr. Burke said, for the obvious reason that courts are closed. But legal experts anticipate a tidal wave of court activity afterward—especially in fields like insurance and debt collection—because of the economic dislocation caused by the pandemic.

More here.


QUICK HITS

  • A tiger at the Bronx Zoo has COVID-19.
  • People in Kentucky who violate self-isolation orders are being forced to wear ankle monitors.
  • Supreme Court update: “Following postponement of arguments scheduled for the last two weeks of March, the court on Friday announced that it would delay another round of oral arguments—its last for the term—scheduled for the second half of April,” reports NPR.
  • COVID-19 deaths in the area around New Orleans are drastically outpacing those in New York City. The former has 37.93 per 100,000 people, and the latter 18.86 per 100,000 people, per Johns Hopkins University figures and a Wall Street Journal analysis. Louisiana Gov. John Bel Edwards attributed the high death rate to the state having “more than our fair share of people who have the comorbidities that make them especially vulnerable.”
  • States across the South could see similar situations to Louisiana, argues Margaret Renkl, who lives in Nashville.
  • America has now seen nearly 10,000 deaths from COVID-19.
  • We’re all guinea pigs in a pandemic:

  • “One of the many things revealed by the political response to the coronavirus pandemic,” writes Nick Gillespie, is “that there are very few meaningful differences between the Republicans and Democrats.”
  • Corona suspending production.

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Germany Announces “Limitless” Aid Program For Small Business: SBA Are You Listening?

Germany Announces “Limitless” Aid Program For Small Business: SBA Are You Listening?

To anyone who fell asleep some time in early February and woke up today, it will come as a shock that Germany – which until very recently was perceived as the fiscally stingiest nation in Europe, if not the world – is fast emerging as the most generous provider of government stimulus, and this morning we got confirmation of that when Angela Merkel’s government announced a new “limitless” aid program for small- and medium-sized companies (note: not a bailout of Germany’s mega corporations) as part of an effort to support Europe’s largest economy in the coronavirus pandemic.

Merkel’s government will provide guarantees of as much as 100%, German Finance Minister Olaf Scholz announced at a joint press conference with Economy Minister Peter Altmaier Monday, Bloomberg reports, adding that loans of up to 800,000 euros ($862,000) that will pay out very quickly will be available.

The existing program only provides for an 80% to 90% loan guarantee and banks have been reluctant to take on new risk as the economy falters. Private lenders have thus pressed the government to expand the existing program by guaranteeing 100% of the loans, which it now appears to be doing.

So… SBA are you listening? In light of the very strict limits on a similar program in the US where funding is limited to 2.5x the average monthly payroll of small and medium businesses, assuming it is disbursed which as we just reported it isn’t with BofA reporting just 100 loans have been actually funded, it is certainly time for the Trump administration, which unlike Germany has the benefit of the world’s reserve currency, to consider a similar “unlimited” program especially with the US economy rapidly sliding into depression.

The program for loan guarantees is the latest in a range of measures introduced by the German government, which said the economy might contract even more this year than the 5% drop caused by the global financial crisis in 2008 and 2009.

Of course, the question is whether companies will use the money to actually pay down debt/fund employment, or simply use it for stock buybacks. Indeed, so habituated is the market to stock repurchases that the news sent the DAX to session highs, some 5% higher.


Tyler Durden

Mon, 04/06/2020 – 09:55

via ZeroHedge News https://ift.tt/2XkzS8a Tyler Durden

“Nobody’s Traveling For Next Two Months” – Airlines Dumping Chemicals In Fuel Tanks To Prevent Algae

“Nobody’s Traveling For Next Two Months” – Airlines Dumping Chemicals In Fuel Tanks To Prevent Algae

The unprecedented collapse of airline traffic across the world has left many carriers on the brink of bankruptcy. Parking lots of commercial jets are scattered across the globe as carriers reduce flights amid travel restrictions due to the COVID-19 pandemic

Carriers are under severe financial pain, learning how to survive with much of their fleets grounded, reported The Wall Street Journal. In the US, airlines have applied for $25 billion in government funds. The problem is that the bailout might not be able to float the industry for the next several months as consumers will stay away from flying for the time being. 

“Nobody’s traveling in the next 30 or 60 days,” said Vasu Raja, American Airlines Group Inc.’s senior vice president for network strategy. “But nobody is really making any plans to go travel in the next 90 to 150 days, either.”

President Trump recently said that his administration is looking into grounding some domestic air travel between cities that are COVID-19 hotspots. Internationally, airlines have been reducing flights for the summer season. 

In Frankfurt, Deutsche Lufthansa AG Chief Executive Carsten Spohr said there is a “pause” in the airline industry, and any restart could be gradual.  

“I think it’s a stop, reverse the tape, and then restart at a slower speed,” Spohr said. “There will be no reset to normal.”

Spohr has spoken with government officials where his carriers are based, indicating that his airlines, which also includes Austrian Airlines, Brussels Airlines, and Swiss International Air Lines, have reduced its capacity by 94%. He said 700 of its 763 aircraft are grounded. 

Spohr said with 700 planes parked for an extended period, there’s a risk that algae will grow in the fuel tanks. He’s been searching for supplies of a chemical that can be put into the fuel tanks that would prevent algae from developing. 

As for smaller airlines, one European carrier has kept its planes flying to avoid creditors from seizing the aircraft, a source told The Journal. 

“We’re getting many inquiries from airlines about protecting their assets, including protecting from repossession,” said Regina Lee, a managing director at consulting firm Alix Partners.

József Váradi, CEO of Budapest-based Wizz Air Holdings PLC, said operations are being wound down, and salaries have been cut in half. 

Váradi has found a new business in these challenging times, one where flying “repatriation missions for governments” has been in high demand for the last several months. He also said his business has transformed into a cargo carrier, shuttling medical supplies from country to country. 

“Over the last 10 days we became a cargo airline and an intercontinental airline flying between Los Angeles and Beijing, China,” Váradi said. “I don’t think I would have ever thought that.”

It has become evident that many large carriers have grounded a majority of their fleets as travel restrictions persist across the world. Airlines in the US have applied for government bailouts that will bridge them for several months. Other carriers are trying to adapt to survive. 

But as Raja said, consumer demand for flights could be two months out, and even then, people have not made plans to travel for the next five months, which could lead to a bankruptcy wave in the airline industry or at least further consolidation. 

Mark Cuban told Fox News over the weekend that the pandemic will usher in a massive transformative period called “America 2.0,” where “everything” will fundamentally change about this country. One significant change will be consumer choices, and no American is going to step into an airplane anytime soon.

What could save the airline industry is the ushering of “immunity certificates” to people who have developed resistance to COVID-19. This would allow people who have developed antibodies to the virus to travel freely. 


Tyler Durden

Mon, 04/06/2020 – 09:45

via ZeroHedge News https://ift.tt/2JFcsTc Tyler Durden

“This Is The End Of Western Capitalism As We Knew It…”

“This Is The End Of Western Capitalism As We Knew It…”

Authored by Garfield Reynolds via Bloomberg,

The sheer speed of the coronavirus crisis means investors are way behind the curve in assessing its long-term impact on economies, companies and stock market valuations.

The global business environment is being transformed – we are all socialists now.

This is about more than just the failure of earnings estimates to keep up with the virus impact – investors need to disregard projections that an end to the crisis will restore the pre-outbreak status quo.

Decades of pushing government out of business are being reversed in mere weeks, with policy makers telling companies where, how and if they should operate – whether they can pay dividends, buy back stock or fire employees.

In other words, governments are almost fully taking over free markets, with the profit principle dethroned as the key business driver.

This changes the rules of the game for investors.

Look at crude oil for example, where U.S. companies that were on the way to going bust amid last year’s supply and demand shocks could end up surviving as Washington intervenes to prop up all businesses.

Once governments start deciding wholesale which firms live or die, how do you roll that back?

The same goes for the massive ramp up in what has been derided at times as the “nanny state.” Welfare and increased spending on health care will likely become a larger part of most economies.

The massive public borrowing to fund this – and the surge in stimulus programs – will take years to go away. The world is going to be awash with debt that will limit governments’ room for maneuver on things like infrastructure spending and tax cuts.

Companies are also busy taking on more debt, and that will constrain them going forward – funneling profits to paying it back or rebuilding cash reserves rather than dividends, buybacks or, heaven forbid, expansion.

The recognition of the role lower-paid workers are playing in keeping supply chains, supermarkets, delivery systems etc. running will likely fuel a renewed call for increases to minimum wages, further pressuring margins.

And calls to keep production closer to “home” will lead to an overhaul of supply chains that won’t come without cost.

Companies will likely emerge from this downturn with a permanent hit to their long-term potential margins – one that is not yet reflected in analyst valuations.

Any investor who assumes that the business models of December 2019 will work just fine in December 2020 faces a very rude awakening.


Tyler Durden

Mon, 04/06/2020 – 09:30

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Millions Of Applicants But “Only 100 Loans Disbursed” In Latest Small Business Bailout Shock

Millions Of Applicants But “Only 100 Loans Disbursed” In Latest Small Business Bailout Shock

On Friday, we reported that millions of small business owners around the country were stunned to learn that they weren’t eligible for loans via the government’s “Paycheck Protection Program”, or would at least face more roadblocks, and more critical delays, as landlords demand rent and vendors demand payment.

Last week, Treasury Secretary Steven Mnuchin and SBA Secretary Jovita Carranza scrambled to publicly assure investors that rumors of a “power struggle” between the Treasury and SBA were false, and that the big banks were finally beginning to process loan applications. He even enthusiastically tweeted out aggregate totals for approved loans. But amazingly, as more businesses owners went about applying for loans only to learn they weren’t eligible or would need to try again at a different bank, finally, BofA’s BriMo had to appear on CNBC to explain that businesses should apply for their stimulus loans via lenders with which they have “preexisting relationships”.

But as the administration and the big banks scramble to save the American economy from a far more brutal collapse (which is what would happen if half of the small businesses in the country close), even more roadblocks are popping up on Monday.

In a phoned-in interview on CNBC, Wilfred Frost urgently reported that Bank of America has received 177,000 applications for some $32.6 billion in emergency liquidity, but so far, only 100 of these loans have been disbursed.

The bank hopes to get most of the stack processed by mid-week, but it’s unclear what they’re basing these hopes on. Also, in case you dear reader still harbored any doubts about just how devastating this has been for small businesses, which typically don’t have the ‘fortress’ balance sheets that corporations do, nor the access to cheap capital, that $32.6BN figure represents 10% of the total Congressional allocation from the $2.2 trillion stimulus package for all the banks.

BofA described the demand as “fierce” – something that shouldn’t be a surprise to anyone, but is apparently a surprise for the bankers down in Charlotte.

About a week ago, we explained the infrastructure-related difficulties that government agencies and the big banks would face in doling out the money, one reason why it might take longer than Americans would ideally like, posing an existential threat to potentially hundreds of thousands of businesses.

Importantly, BofA was the first major lender to set up and launch its portal for the program.

And BofA isn’t the only big bank having trouble: CNBC reported last night that Wells Fargo will only be able to do $10 billion of the PPP loans due to the Fed asset cap that the central bank imposed on WFC back in January 2018. Because of this, Wells will focus on companies with fewer than 50 employees, as well as nonprofits. The bank also said it would donate “all fees related to program to nonprofits focused on small businesses,” Frost reported.

How did regulators and Congress not anticipate this, and ask the Fed to suspend the asset cap that has prevented the bank from growing its assets, essentially stopping it from growing? Imagine being a small business or other business whose ‘regular bank’ is Wells Fargo, only to learn that they can’t give you a loan because the Fed won’t allow it?

Howard Schultz said on CNBC Monday morning that small businesses are facing a period of “carnage and fear.” We doubt this will help offer any peace of mind.

That certainly doesn’t inspire confidence in banks’ ability to ‘execute’ here. They’ve already demanded their extra 50bp in ‘tribute’. Does the administration need to dangle another ‘incentive’ in their faces?


Tyler Durden

Mon, 04/06/2020 – 09:18

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White House Recommends Against Grocery and Pharmacy Trips While Trump Says Go Ahead and Try Hydroxychloroquine

Stay really, really at home now? On Saturday, White House coronavirus response coordinator Deborah Birx said of the next two weeks: “This is the moment to not be going to the grocery store, not going to the pharmacy, but doing everything you can to keep your family and your friends safe.”

Yikes. Keeping safe now means avoiding shopping for even food, toiletries, and medicine No wonder President Donald Trump has been hoping so hard for hydroxychloroquine to work against COVID-19.

But Trump advisor and infectious disease expert Anthony Fauci isn’t so sure about the anti-malarial drug as a cure for the new coronavirus. In a meeting Saturday, “Fauci pushed back against [economic adviser Peter] Navarro, saying that there was only anecdotal evidence” for it, reports Jonathan Swan at Axios. More:

Eventually, [Jared] Kushner turned to Navarro and said, “Peter, take yes for an answer,” because most everyone agreed, by that time, it was important to surge the supply of the drug to hot zones.

The principals agreed that the administration’s public stance should be that the decision to use the drug is between doctors and patients.

Trump ended up announcing at his press conference that he had 29 million doses of hydroxychloroquine in the Strategic National Stockpile.

One thing driving this may be a desire not to drop the ball again on COVID-19 prep, as the administration has already done with tests, masks, and ventilators. Not that Trump will admit his team has faltered in the slightest. He’s spent the past week bragging about how big his backup of medical supplies is, while simultaneously declaring this Strategic National Stockpile mostly off-limits to American states.

The president now regularly describes the supply of ventilators and masks in terms of negotiations he allegedly made well and states didn’t, making this into a competition where they should be cooperation to save lives.

Last weekafter Trump advisor and son-in-law Jared Kushner called it “our” stockpile at press conference (“our” meaning the federal government, Trump clarified) and Trump scoffed at states like New York for lacking suppliesthe language on the Strategic National Stockpile’s website was changed:

But while Trump has been bashing state leaders for not stocking up pre-pandemic, the federal government waited until mid-March to bolster its supplies, according to a new report from the Associated Press. AP’s review of federal purchases “shows federal agencies largely waited until mid-March to begin placing bulk orders of N95 respirator masks, mechanical ventilators and other equipment needed by front-line health care workers.”

By the time these agencies were starting to place orders, “hospitals in several states were treating thousands of infected patients without adequate equipment and were pleading for shipments from the Strategic National Stockpile,” AP reports. The stockpile is “now nearly drained.”

If hydroxychloroquine may be useful, it’s not unreasonable for Trump to want to get an early jump on that. (“If it does work, it would be a shame we did not do it early,” as Trump said on Saturday.) And Trump’s underlying rhetoric about people and hospitals having the right to decide for themselves about experimental cures is also sound. It has a lot in common with more general arguments for “right to try” lawsbut with a critical difference, too.

Right-to-try advocates generally argue that when specific people are dying from diseases that can’t be cured by treatments the Food and Drug Administration has approved, they should be able to try experimental drugs, generally ones that have proved promising in clinical trials or are already approved in other countries. They don’t generally push for masses of patients to try barely tested and potentially risky cures for communicable diseases on a whim or a hunch.

So far, the case for hydroxychloroquine amounts to little more than a handful of studies with no control patients and a report from Chinese doctors posted to a non-peer-reviewed website. The Chinese doctors said that in a small sample of patients with mild to moderate cases of COVID-19, hydroxychloroquine seemed to help fevers and pneumonia dissipate faster and may have helped stop cases from turning more severe. It was not tested on severe or asymptomatic cases.

Another recent study found “no evidence” of hydroxycholorquine helping patients with severe COVID-19 infections.

All that said, it’s certainly preferable that doctors can try treating patients with hydroxychloroquine without federal bureaucrats saying they must wait until we’ve done years of trials.

“With no proven treatment for the coronavirus, many hospitals have simply been giving hydroxychloroquine to patients, reasoning that it might help and probably will not hurt, because it is relatively safe,” notes The New York Times.

But some doctors note that while hydroxychloroquine may be relatively safe, it’s far from harmless. “There are side effects to hydroxychloroquine,” Brown University emergency physician Megan L. Ranney told the Times. “It causes psychiatric symptoms, cardiac problems and a host of other bad side effects.”


FREE MARKETS

Against pantry policing. Shaming people for their pandemic-time purchases has become a new national pastime. At Arc Digital, Phoebe Maltz Bovy takes a calm look at how people are responding to the fact that “slowly yet suddenly, everything changed”:

Human activity has been divided into the essential and the inessential, with breathing falling into the former category (as long as there are ventilators available, at least) and just about everything else, the latter. Office jobs, clothes-shopping, bar-going, sex (or just in-person conversation) with anyone you don’t happen to live with—all of these everyday pursuits have been put on hold, their eventual return uncertain.

Falling somewhere ambiguous between necessity and frivolity, however, is food. On the one hand, we’ve all got to eat. On the other, the discourse about eating in the era of coronavirus has a way of suggesting food is a luxury, a pseudo-requirement the more noble among us would somehow transcend. As though if you believe yourself and your family entitled to food, now and in the foreseeable future, then you’re exhibiting a level of unacceptable entitlement….

A figure has emerged of the Bad Grocery-Shopper, the proverbial Karen who buys more than is correct (even though, and I cannot emphasize this enough, no one knows or can know what “correct” would mean), and who is definitely, definitely buying toilet paper in excess. Indifferent to the fate of her local businesses (or, perhaps, newly unemployed herself?), she isn’t even sending a few bucks here and there to her preferred bars and cafés. The problem isn’t coronavirus; it is—it’s soothing to think, apparently—middle-aged, middle-class women buying groceries for their families.

Read the whole thing here.


FREE MINDS

Businesses are beginning to sue over mandatory shutdown orders. From The New York Times:

Some of those suing their state governments seek redress for specific, local grievances, as with the [Blueberry Hill Public Golf Course and Lounge lawsuit] or in a similar suit in Pennsylvania being pursued by a company that says it is the country’s oldest manufacturer of orchestra-quality bells and chimes. Those lawsuits and one in Arizona are rooted in the Fifth Amendment, which requires due process and guarantees compensation for property seized by the government.

Other constitutional amendments have been invoked in several lawsuits in recent weeks attempting to force open gun stores, or to argue that measures to curb the virus should not outweigh rights like freedom of assembly and religion.

“Those may be serious, but they may also be part of an attempt to make an argument in the press about overreach,” said Tom Burke, a political-science professor at Wellesley College who studies the politics of litigation.

History dating back to the time of 15th-century plagues shows that lawsuits typically plummet during pandemics, Mr. Burke said, for the obvious reason that courts are closed. But legal experts anticipate a tidal wave of court activity afterward—especially in fields like insurance and debt collection—because of the economic dislocation caused by the pandemic.

More here.


QUICK HITS

  • A tiger at the Bronx Zoo has COVID-19.
  • People in Kentucky who violate self-isolation orders are being forced to wear ankle monitors.
  • Supreme Court update: “Following postponement of arguments scheduled for the last two weeks of March, the court on Friday announced that it would delay another round of oral arguments—its last for the term—scheduled for the second half of April,” reports NPR.
  • COVID-19 deaths in the area around New Orleans are drastically outpacing those in New York City. The former has 37.93 per 100,000 people, and the latter 18.86 per 100,000 people, per Johns Hopkins University figures and a Wall Street Journal analysis. Louisiana Gov. John Bel Edwards attributed the high death rate to the state having “more than our fair share of people who have the comorbidities that make them especially vulnerable.”
  • States across the South could see similar situations to Louisiana, argues Margaret Renkl, who lives in Nashville.
  • America has now seen nearly 10,000 deaths from COVID-19.
  • We’re all guinea pigs in a pandemic:

  • “One of the many things revealed by the political response to the coronavirus pandemic,” writes Nick Gillespie, is “that there are very few meaningful differences between the Republicans and Democrats.”
  • Corona suspending production.

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Here Comes Round Two: China Just Report The Most New Covid Cases In A Month

Here Comes Round Two: China Just Report The Most New Covid Cases In A Month

Last week we reported that even as the world’s attention had shifted to the new global coronavirus outbreak epicenters of New York, Italy, Spain and other western nations, China – which rushed to restart its economy at any cost as the alternative was too dire to even consider – had put a major county on lockdown after a new cluster of coronavirus infection had emerged. To wit, last Wednesday we learned that in post on its social media account, Jia county – which has a population of about 600,000 – said that no one can travel out of Jia county without proper authorization after one person tested positive.

This new cluster emerged just days after China once again revised its virus reporting methodology to also include asymptomatic carriers of the disease, which naturally begged the question why China wasn’t reported his subset of infections previously.

We got the answer overnight when Mainland China reported 39 new coronavirus cases as of Sunday, up from 30 a day earlier, and the number of asymptomatic cases also surged, as Beijing continued to struggle to extinguish the outbreak despite drastic containment efforts.

China’s National Health Commission said in a statement on Monday that 78 new asymptomatic cases had been identified as of the end of the day on Sunday, compared with 47 the day before.

Of the new cases showing symptoms, 38 were people who had entered China from abroad, compared with 25 a day earlier, although how China keeps track of this on an instantaneous basis is unclear. Also it’s odd to blame “imports” as China also closed off its borders to foreigners, though according to Beijing most imported cases involve Chinese nationals returning from overseas.

Separately, one new locally transmitted infection was reported, in the southern province of Guangdong, down from five a day earlier in the same province. The new locally transmitted case, in the city of Shenzhen, was a person who had travelled from Hubei province, Guangdong provincial authorities said.

As Reuters reports overnight, imported cases and asymptomatic patients, who have the virus and can give it to others but show no symptoms, have become China’s chief concern in recent weeks after draconian containment measures succeeded in slashing the infection rate.

This means that whether asymptomatic or not, imported or domestic, Hubei-based or not, on April 5, China reported the most new Coronavirus cases in a month as slowly the disease appears to be reestablishing itself in the world’s most populous nation.

As a result, the Guangdong health commission raised the risk level for a total of four districts in the cities of Guangzhou, Shenzhen and Jieyang from low to medium late on Sunday.

In its panicked scramble to reboot the economy, China has been reporting that daily infections have fallen dramatically from the peak of the epidemic in February, when hundreds were reported daily, but new infections continue to appear daily. Despite a miraculous rebound in China’s latest PMIs, the truth is that China’s economy has been very slow to recover and by some metrics – as shown below – appears to already be double dipping.

Mainland China has now reported a total of 81,708 cases, with 3,331 deaths. The real number is likely orders of magnitude higher, and what’s worse, a rebound in cases likely means that round two of the pandemic may just be starting.


Tyler Durden

Mon, 04/06/2020 – 09:00

via ZeroHedge News https://ift.tt/3e15Pbx Tyler Durden