Tag Archives: pharma

The Senate Should Grill Trump’s FDA Pick on Antibiotics

Mother Jones

When President Donald Trump tapped Scott Gottlieb to lead the Food and Drug Administration, the pharmaceutical industry breathed a “sigh of relief,” reported Reuters and the Financial Times. That’s because he is “entangled in an unprecedented web of Big Pharma ties,” as the watchdog group Public Citizen put it. If confirmed, he’ll jump to the federal agency that regulates the pharmaceutical industry from the boards of GlaxoSmithKline and several other pharma companies. His work for those industry players netted him “at least” $413,000 between 2013 and 2015, Public Citizen reports. Gottlieb is also a partner at New Enterprise Associates, a venture capital firm that invests in the health care sector.

But Gottlieb, whose Senate confirmation hearing is scheduled for Wednesday, has a scant track record on another aspect of the FDA job: managing the rising crisis of antibiotic resistance. According to the Centers for Disease Control and Prevention, germs that have evolved to resist antibiotics sicken at least 2 million people every year and kill at least 23,000. Last fall, all 193 countries in the United Nations—including the United States—signed a declaration calling antibiotic resistance the “biggest threat to modern medicine.”

The FDA’s most direct contribution to the battle to save antibiotics lies in its regulation of farms. About 70 percent of the antibiotics used in the United States go to livestock operations, and the FDA itself, along with the CDC, the World Health Organization, the UK government, and other public health authorities, warn that overuse of drugs in meat farming is a key generator of antibiotic-resistant pathogens.

Meat operations feed their animals regular low doses of antibiotics for two reasons—to help them gain weight faster, and to avoid infections despite tight, unsanitary conditions. Way back in 1977, the FDA acknowledged that these practices undermine the ability of antibiotics to fight human infections—and then for decades, it neglected to do anything about it, under severe pressure from the meat and pharmaceutical industries (more on that here).

On January 1, 2017, the agency at long last finalized a voluntary set of new rules designed to rein in the meat industry’s addiction to antibiotics. But even if meat companies comply with the new policy, the FDA’s plan leaves a gaping loophole: It asks farmers not to use the drugs as a growth promoter, but blesses the practice of using them to “prevent” disease. As the Pew Charitable Trust notes, the “lines between disease prevention and growth promotion are not always clear”—and for many antibiotics crucial to human medicine, farmers can continue as usual, changing only the language they use to describe their antibiotic reliance.

A recent report from the Government Accountability Office chastised the FDA for leaving the loophole, complaining that the agency failed to crack down on “long-term and open-ended use of medically important antibiotics for disease prevention.” It also found that the FDA doesn’t demand nearly enough usage data from meat companies or pharmaceutical suppliers to assess whether its voluntary program is working.

David Wallinga, who covers antibiotic resistance for the Natural Resources Defense Council, says the Senate Committee on Health, Education, Labor and Pensions, which will hold Gottlieb’s confirmation hearing, should grill him about how the agency will handle farm antibiotic use. A senator should brandish the GAO report and ask how the FDA nominee plans to address its criticisms of the agency’s current antibiotic policy.

Wallinga says that, despite all his ties to Big Pharma, Gottlieb does not seem to be directly involved with companies like Zoetis and Elanco, which specialize in animal drugs. But Gottlieb’s one public statement on antibiotic resistance does not inspire confidence that he fully grasps the issue. In a 2007 post for the conservative American Enterprise Institute, Gottlieb opined that “preventative efforts alone won’t solve our bacterial challenges.” What’s needed, he argued, are incentives for the pharmaceutical industry to develop new antibiotics, which aren’t profitable enough to draw the heavy investment in research and development required for new drugs. That’s true, Wallinga says, but any new antibiotics will quickly succumb to resistance, too, if farm use isn’t reined in.

And this issue is especially relevant for anyone dealing with cancer—that is, everyone. (Gottlieb himself is a cancer survivor, as Wallinga notes. Antibiotic resistance is one of the major threats to chemotherapy patients. A 2015 Lancet study found that at least 26 percent of pathogens causing infections after chemotherapy are resistant to common antibiotics.

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The Senate Should Grill Trump’s FDA Pick on Antibiotics

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America’s 25 Top Restaurant Chains, Ranked by Antibiotic Use

Mother Jones

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Heads up, meat eaters: A new report has rated the antibiotic use in the meat of 25 top fast-food or “fast casual” restaurants, and the results are, well, concerning. The report by Friends of the Earth, the Natural Resources Defense Council, and four other consumer health organizations, examined antibiotic use as well as the restaurants’ transparency about their meat and poultry supply chains. Chipotle and Panera were the only chains to publicly report serving a majority of meat from animals raised without routine antibiotics.

“Chain Reaction,” by Friends of the Earth, Natural Resources Defense Council, et al

The Centers for Disease Control and Prevention calls antibiotic resistance one of the top five health threats facing the nation, killing an estimated 23,000 Americans each year. “When livestock producers administer antibiotics routinely to their flocks and herds, bacteria can develop resistance, thrive, and even spread to our communities, contributing to the larger problem of antibiotic resistance,” the report explains. “The worsening epidemic of resistance means that antibiotics may not work when we need them most: when our kids contract a staph infection (MRSA) or our parents get a life-threatening pneumonia.”

In addition to sending each company a survey, the report authors examined company websites and other publicly available information. They intend for the report to be updated annually as companies change their practices.

Here’s a rundown of what researchers had to say about each restaurant (emphasis added):

Panera and Chipotle are the only chains that publicly affirm that the majority of their meat and poultry offered is produced without routine use of antibiotics.
Chick-fil-A and McDonald’s have established policies limiting antibiotic use in their chicken with implementation timelines.
Dunkin’ Donuts has a policy covering all meats but has no reported timeline for implementation.
While Starbucks has made positive statements supporting what it terms as ‘responsible use of antibiotics to support animal health,’ to our knowledge the company has failed to adopt a clear policy prohibiting routine use of antibiotics in its meat and poultry supply chains or to provide detailed public information on their purchasing practices.
While Subway did not respond to our survey, recent news outlets report that the company’s goal is to ‘eliminate the use of antibiotics in products across the menu’ and that Subway is ‘targeting to transition to chicken raise without antibiotics important to human medicine in 2016.’…It is unclear whether this would entail the end of all routine antibiotic use in its supply chains.
Burger King, Wendy’s, Olive Garden, KFC, Chili’s, Sonic, Denny’s, Domino’s, Starbucks, Papa John’s Pizza, Taco Bell, Pizza Hut, Applebee’s, Jack in the Box, Arby’s, Dairy Queen, IHOP, Outback Steakhouse, and Little Ceasars either have no disclosed policy on antibiotics use in their meat and poultry, or have policies that in our estimation allow for the continued, routine use of antibiotics in the production of all meats they serve.

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America’s 25 Top Restaurant Chains, Ranked by Antibiotic Use

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These Antidepressants May Increase the Risk of Birth Defects

Mother Jones

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Babies born to women who took certain antidepressants during pregnancy may have an elevated risk of birth defects, according to a study published Wednesday in the medical journal BMJ.

Over the past few years, researchers have come to conflicting conclusions about the health impacts of taking common antidepressants called selective serotonin reuptake inhibitors, or SSRIs, early in pregnancy. Some studies have found prenatal exposure to SSRIs to be associated with heart and brain defects, autism, and more, while others have found the risk to be minimal or nonexistent.

The BMJ study, led by researchers at the the Centers for Disease Control and Prevention, shed light on the matter by analyzing federal data of 38,000 births between 1997 and 2009. Researchers interviewed the mothers of children with certain birth defects associated with SSRIs, asking if they took certain antidepressants during the first three months of pregnancy or the month prior to it. Unlike many previous studies, which looked at the effects of SSRIs as a group, the researchers looked at the health impacts of five specific drugs. They found that two drugs were associated with birth defects, while three of the drugs were not. Here are the details:

Sertraline (Zoloft): No increased risk of birth defects. (This was the most common of the five drugs, taken by forty percent of the women on antidepressants.)
Paroxetine (Paxil): Babies were between 2 and 3.5 more likely to be born with heart defects, brain defects, holes between heart chambers, and intestinal deformities.
Fluoxetine (Prozac): Babies were two times more likely to experience heart defects and skull and brain shape abnormalities.
Escitalopram (Lexapro): No increased risk of birth defects.
Citalopram (Celexa): No increased risk of birth defects.

Researchers are quick to note that even in the case of paroxetine and fluexetine, the absolute risk of these defects is still very small. If mothers take paroxetine early in pregnancy, for example, the chance of giving birth to a baby with anencephaly, a brain defect, rise from 2 in 10,000 to 7 in 10,000.

Some doctors worry that studies like this dissuade mothers who truly need mental health treatment from seeking it—particularly since the stress associated with depression in the mother can impact the health of the baby. Elizabeth Fitelson, a Columbia University psychiatrist who treats pregnant women with depression, described this tricky balance to the New York Times earlier this year: “For about 10 percent of my patients, I can readily say that they don’t need medication and should go off it,” she said. “I see a lot of high-risk women. Another 20 percent absolutely have to stay on medication—people who have made a suicide attempt every time they’ve been unmedicated. For the remaining 70 percent, it’s a venture into the unknowable.”

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These Antidepressants May Increase the Risk of Birth Defects

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Sales of ADHD Meds Are Skyrocketing. Here’s Why.

Mother Jones

Attention deficit hyperactive disorder is big business. That’s the conclusion of a new report, published by the market research firm IBISWorld, which showed that ADHD medication sales have grown 8 percent each year since 2010 and will grow another 13 percent this year to $12.9 billion. Furthermore, it projects this growth will continue over the next five years at an annualized rate of 6 percent, and take in $17.5 billion in the year 2020—making it one of the top psychopharmaceutical categories on the market.

This growth does not surprise Richard Scheffler, professor of health economics and public policy at the University of California-Berkeley and coauthor of the book The ADHD Explosion. It is part of a global trend, he says, as ADHD becomes recognized as a disorder around the world, especially in cultures that put a premium on productivity and high academic achievement. Sales outside the United States—especially in Israel, China, and Saudi Arabia—are increasing twice as fast as in the United States, according to an article he penned in the Wall Street Journal with Stephen Hinshaw, professor of psychology and psychiatry at UC-Berkeley and UC-San Francisco.

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Sales of ADHD Meds Are Skyrocketing. Here’s Why.

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New Drugs and Vaccines Can’t Stop This Ebola Outbreak

Mother Jones

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With the death toll in the worst Ebola outbreak in history exceeding 1,000, pharmaceutical companies and health authorities are sprinting to develop new drugs and vaccines. On Monday, drug maker GlaxoSmithKline announced that it would start clinical trials of an Ebola vaccine ahead of schedule. And on Tuesday, the World Health Organization ruled that the use of experimental drugs to treat Ebola patients is ethical so long as the patients give their consent. But for now, there are no proven drugs to treat Ebola, and experts doubt that any new drug or vaccine could beat back the current outbreak in Sierra Leone, Liberia, and Guinea.

“The drugs are not going to stop the outbreak, period,” says Robert Garry, a virology researcher at Tulane University. One problem, he says, is the meager supply of drugs and vaccines. ZMapp, an experimental drug, has already begun human trials. But Mapp Biopharmaceutical, the company developing ZMapp with the help of the US Army, did not expect to start human tests this early, and it has only about a dozen doses. It has already sent two of those doses to Liberia.

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New Drugs and Vaccines Can’t Stop This Ebola Outbreak

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State Attorneys General to FDA: What Were You Thinking When You Approved Powerful New Painkiller?

Mother Jones

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Last month, Mother Jones reported that the Food and Drug Administration had approved a powerful new painkiller called Zohydro over the objections of its advisory board, which voted 11-2 against approving the drug. Now Attorneys General from 28 states (and the US territory of Guam) have asked the FDA to reconsider its approval of Zohydro. In a letter to the agency, the AGs raise many of the same concerns that the advisory panel did, noting that the drug lacks adequate safeguards to prevent it from being abused and could exacerbate America’s epidemic of painkiller deaths. Here’s an excerpt from the AGs letter, which was dated December 10:

State Attorneys General do not want a repeat of the recent past when potent prescription painkilling drugs entered the market without abuse-deterrent qualities and without clear guidance on how they were to be prescribed. This created an environment whereby our nation witnessed a vicious cycle of overzealous pharmaceutical sales, doctors over-prescribing the narcotics, and patients tampering with these drugs, ultimately resulting in a nationwide prescription drug epidemic claiming thousands of lives.

Zohydro, which is made by a company called Zogenix, is five to ten times stronger than Vicodin, making it very similar in potency to OxyContin, a widely abused prescription drug that has contributed to the tens of thousands of painkiller-related deaths in the United States. OxyContin, however, now includes a gel that prevents the drug from being crushed and snorted. Zohydro was approved without that measure. Zogenix has entered into a $750,000 agreement with a Montreal-based company, Altus Formulation Inc, to help make the drug abuse-deterrent, but it’s unclear whether the formula will be ready by the time Zohydro hits the market in a few months.

The Attorneys General don’t think that’s sufficient. “We hope that the FDA either reconsiders its approval of Zohydro ER, or sets a rigorous timeline for Zohydro ER to be reformulated to be abuse-deterrent while working with other federal agencies to impose restrictions on how Zohydro ER can be marketed and prescribed,” they wrote in their letter.

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State Attorneys General to FDA: What Were You Thinking When You Approved Powerful New Painkiller?

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Drug-Company CEO: Top Morning-After Pill May Not Work Over 165 Pounds, Regardless of BMI

Mother Jones

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Since Mother Jones broke the news on Monday that a European drugmaker, HRA Pharma, found that its popular morning-after pill may not work in heavier women, many readers have asked why the company chose to update its product labels with a hard weight limit—instead of a limit on BMI, an obesity measurement that relies on a height-to-weight ratio.

HRA Pharma was prompted to rethink its labels after University of Edinburgh Professor Anna Glasier linked emergency contraceptive failures and an obese body mass index (or BMI) in a 2011 analysis. The new label for the drug, Norlevo—a brand of emergency contraceptive pills which uses levonorgestrel to prevent pregnancy, and is identical to several US drugs, including Plan B—says it is not recommended for women who weigh 165 pounds or more, no matter their height.

Glasier, analyzing data from one study sponsored by the US National Institutes of Health and another sponsored by HRA Pharma, found that the risk of pregnancy in women using levonorgestrel pills increased significantly if a woman had a body mass index of 30 or higher—which the US Centers for Disease Control considers obese.

On Tuesday, HRA Pharma CEO Erin Gainer explained the company’s decision further to Mother Jones. When HRA statisticians reviewed the data Glasier used for her analysis, Gainer says, they confirmed Glasier’s findings about BMI—but they also found that their products’ failure correlated even more strongly with weight, regardless of a woman’s height.

“We were surprised,” Gainer says. “But the findings were really quite striking from a statistical point of view.” She adds that weight is easier for health care providers to discuss with their patients. “People don’t walk down the street knowing what their body mass index is,” she says.

HRA Pharma has not made its analysis public. But based on the media uproar after I first revealed Norlevo’s new guidelines, Gainer says, “We’re thinking now about how best to publish these findings.”

A New York Times article highlights another change HRA Pharma will make to the leaflets included with Norlevo: the new leaflets will say that Norlevo “cannot stop a fertilized egg from attaching to the womb.” This is significant because it contradicts assertions made by abortion opponents in their lawsuits against the Affordable Care Act’s birth control mandate—the so-called “Hobby Lobby” cases that the Supreme Court on Tuesday agreed to hear this spring. The Times’ Pam Belluck explains:

The cases coming before the Supreme Court involve corporations that object on religious grounds to the health care law’s requirement that employers provide insurance coverage for contraception, including emergency contraception. The cases are based on the claim that some types of contraception, including Plan B One-Step, prevent fertilized eggs from implanting in the womb, tantamount to an abortion.

While labels of Plan B One-Step and related pills, which contain the drug levonorgestrel, say they work mostly by blocking the release of eggs before fertilization, they also say the drugs may inhibit fertilized eggs from implanting in the uterus.

Last year, the New York Times reported on new evidence that emergency contraceptive pills do not prevent implantation of a fertilized egg and the FDA now tentatively agrees with their assessment. But HRA Pharma appears to be the first drug company to adjust its labels accordingly—a significant data point against the abortion foes appearing before the Supreme Court.

In her research, Glasier did not determine why the effects of levonorgestrel diminished as BMI or weight increased. She published her research in the international peer-reviewed journal Contraception.

The FDA is investigating whether US emergency contraceptives that use levonorgestrel must change their labels.

Diana Blithe, a contraceptive researcher at the National Institute of Child Health and Human Development and an author of one of the studies Glasier analyzed, told NPR on Tuesday that she supports such a change. “I think it is incumbent upon American manufacturers to put that information on the label now that they’re aware of it,” she said.

But Glasier told CNN that she was still skeptical of warning heavier women not to use Norlevo or similar drugs. “You are probably better to take levonorgestrel emergency contraceptive pills after unprotected sex than just to leave it to chance even if you are obese,” she said.

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Drug-Company CEO: Top Morning-After Pill May Not Work Over 165 Pounds, Regardless of BMI

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Leaked Documents Reveal the Secret Finances of a Pro-Industry Science Group

Mother Jones

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The American Council on Science and Health bills itself as an independent research and advocacy organization devoted to debunking “junk science.” It’s a controversial outfit—a “group of scientists…concerned that many important public policies related to health and the environment did not have a sound scientific basis,” it says—that often does battle with environmentalists and consumer safety advocates, wading into public health debates to defend fracking, to fight New York City’s attempt to ban big sugary sodas, and to dismiss concerns about the potential harms of the chemical bisphenol-A (better known at BPA) and the pesticide atrazine. The group insists that its conclusions are driven purely by science. It acknowledges that it receives some financial support from corporations and industry groups, but ACSH, which reportedly stopped disclosing its corporate donors two decades ago, maintains that these contributions don’t influence its work and agenda.

Yet internal financial documents (read them here) provided to Mother Jones show that ACSH depends heavily on funding from corporations that have a financial stake in the scientific debates it aims to shape. The group also directly solicits donations from these industry sources around specific issues. ACSH’s financial links to corporations involved in hot-button health and safety controversies have been highlighted in the past, but these documents offer a more extensive accounting of ACSH’s reliance on industry money—giving a rare window into the operations of a prominent and frequent defender of industry in the science wars.

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Leaked Documents Reveal the Secret Finances of a Pro-Industry Science Group

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Easy to Get Plan B? Not Always

Mother Jones

Last June, after a protracted political fight and complicated legal battle, the US Food and Drug Administration approved the use of Plan B One-Step emergency contraception for all women of childbearing age without a prescription. The move marked a major victory for reproductive rights activists, and for women and men everywhere who are now supposed to be able to pick up the morning-after pill off of pharmacy and grocery store shelves without being required to show ID or proof of age.

But five months after the FDA’s approval, consumers are still having problems accessing the 72-hour pill. Some of the problems stem from confusion about the law, or from a bureaucracy slow to update the regulations. In other cases, women are deterred by misinformation about the medication; it’s known in pro-life circles, for instance, as an “abortion pill.”

These barriers prompted a group of media outlets to launch “Where is your Plan B?“, a reporting and crowd-sourcing collaboration to determine how easily women can access Plan B One-Step in their communities. (Disclosure: Some of the outlets belong to The Media Consortium, which The Foundation for National Progress, Mother Jones‘ parent organization, co-founded.)

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Easy to Get Plan B? Not Always

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What the Washington Post Didn’t Tell You About the Daily Caller’s Senate Sex Story

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On Monday, the Washington Post published an article that undermined a November report from the conservative Daily Caller alleging that Sen. Robert Menendez (D-N.J.) stiffed two prostitutes who had provided services to him during a trip to the Dominican Republic. Menendez has repeatedly denied the Caller‘s account, and the Post noted that one of the two women said she was paid to make up the claims and had never met the senator. The paper reported:

The woman said a local lawyer had approached her and a fellow escort and asked them to help frame Menendez and a top donor, Salomon Melgen, according to affidavits obtained by the Washington Post. That lawyer has in turn identified a second Dominican lawyer who he said gave the woman a script and paid her to read the claims aloud. The first lawyer said he found out only later that the remarks would be videotaped and used against Menendez, the affidavits say.

In its November story, the Caller reported that the two women were represented by attorney Melanio Figueroa, but provided no details about this lawyer. And the Washington Post report did not mention him by name. Yet Figueroa does have a public profile. He was once an aide to a former president of the Dominican Republic whom Menendez had publicly criticized. This raises an obvious question: Was the Caller drawn into an a politically motivated scheme?

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What the Washington Post Didn’t Tell You About the Daily Caller’s Senate Sex Story

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