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Posts Tagged ‘Drug ads’

Anemia drugs hasten death in some cancer patients

Posted by medconsumers on July 13, 2009

For seven years Johnson & Johnson ran deceptive ads on prime time TV and in magazines with this recurring theme: A cancer patient cannot continue working because of debilitating fatigue due to chemotherapy. The ads told people in similar circumstances to ask their doctors about Procrit, which always quickly put an end to the fatigue. There is no published evidence to support the cure-for-fatigue claim, according to a 2007 press briefing at the FDA. Eventually, the agency required warning labels for Procrit, Aranesp, and Epogen —- all drugs widely prescribed to treat anemia in cancer patients. Warning label refers to the black box warning that appears in the 20 or so pages of information that comes with the drug (sometimes). The warnings for Procrit, Aranesp, and Epogen now list a higher incidence of potentially fatal blood clots, heart damage and increased tumor growth.

Now they can add “decreased survival” to the list. This week, the Cochrane Collaboration, the independent, international organization that evaluates research, published a meta-analysis of the information generated by the care of nearly 14,000 cancer patients entitled, “Anti-anemia drugs shorten survival for some cancer patients.” This meta-analysis is co-authored by Maryann Napoli, Center for Medical Consumers. For background on how their drugs came on the market and how financial incentives encouraged oncologists to overprescribe them, see her testimony on this topic before the FDA’s Oncologic Drug Advisory Committee in 2007 and one year later in 2008.

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The Marketing of Osteoporosis

Posted by medconsumers on May 19, 2009

How a risk factor (bone loss) became a disease (osteoporosis) by Maryann Napoli. American Journal of Nursing. For PDF version, go to “article tools” at top right.

Posted in Drug ads, Drugs, Scans and X-rays, Screening, Women's Health, osteoporosis | Tagged: , , , , , | Comments Off

Our Daily Meds: A book review

Posted by medconsumers on August 29, 2008

Yes, we knew that the pharmaceutical industry has been creating new diseases for at least four decades (recall how menopause became a hormone-deficiency disease curable by taking estrogen for the rest of your life). But the author of Our Daily Meds, a new book by journalist Melody Petersen, shows that one drug company, Pharmacia, was not shy about acknowledging it publicly.

Overactive bladder was created by Pharmacia in the mid-1990s in order to sell its new drug Detrol. (See TV ads with this obnoxious voice-over: “Gotta go, gotta go, gotta go right now.”) Petersen, then a business reporter for The New York Times, describes how she covered the 2003 Pharmaceutical Marketing Global Summit in Philadelphia, where Neil Wolfe, Pharmacia’s vice president, outlined the steps taken to make Detrol into the $3 billion a-year-product it is today. The first slide of his presentation: “Positioning Detrol (Creating a Disease).”

Detrol was initially intended as a treatment for urinary incontinence, but the market for this condition was too small, and a cheap alternative drug was already available. Besides, doctors weren’t keen on prescribing drugs for what was seen as a normal part of aging. Pharmacia’s first step in overcoming these obstacles was to hire doctors judged to be knowledgeable opinion leaders (KOLs) as “consultants,” fly them to medical meetings, including two symposia in London, where they were expected to come to a consensus about the definition and treatment of this new disease called overactive bladder. While being expensively wined and dined, the doctors heard from other doctors hired by Pharmacia about the disabling consequences of having to go to the bathroom more than eight times in a 24-hour period. If any KOLs objected to such an absurd notion, no such comments made it into the dozens of articles that Pharmacia paid to have written for medical and lay publications about the benefits of Detrol, writes Peterson. “And another disease was born.”
After a new disease is identified, the next step is creating buzz in the media. Of course, there’s no story unless the disease is perceived as extremely prevalent. No problem, the necessary statistics are generated by Pharmacia-financed surveys and passed on by a credulous media, including publications that should know better. (Consumer Reports lists Detrol as one of its “Best Medicines for Less 2008” along with this statistic: “overactive bladder affects some 15 to 20 million people in the U.S.”)

The standard formula for disease creation is complete once the drug maker saturates the airways, print media and medical journals with ads for Detrol. (Pfizer took over this role when it bought Pharmacia in 2002.)

Fast forward to the fall-out now that Detrol has been on the market for nearly a decade. New adverse effects have come to light—hallucinations and memory impairment, severe enough to be mistaken for Alzheimer’s disease. Oh, and there’s that question hardly anyone seems to ask (and not addressed in this book): How good is Detrol at reducing the number of trips to the toilet? The 12-week trial that won FDA approval showed that people taking Detrol LA (long-acting) had one less “episode” a week than those taking a placebo. Detrol costs $4 to $6 a day, depending upon where it is purchased.

The story of Detrol is but one of many jaw-dropping nuggets of information from Our Daily Meds. Here are a few more:

-Prescription medicine is one of the leading causes of death in the U.S., estimated to kill 270 people a day.
-Americans spent $197 billion on prescription drugs in 2003—up from $12 billion in 1980.

-It can take a hundred years before all the risks of a medicine are known, said FDA’s Janet Woodcock, in a 2005 presentation to a panel of experts reviewing the safety of the nation’s drugs.

-Once, the most successful pharmaceutical companies were those with the brightest scientists searching for cures. Now the most profitable and powerful drugmakers are those with the most creative and aggressive marketers.

-The pharmaceutical industry spent more on lobbying between 1998 and 2004 than any other industry. It has won new laws that have allowed the companies to profit from medical discoveries made by taxpayer-funded scientists. And when these new measures boosted the drug companies’ profits, other laws gave them tax credits so lucrative that as a group they pay far lower taxes on average than other major industries.

-The public is told that high profits are needed due to the high cost of innovation, but in fact the true cost of developing a new medicine is actually a closely guarded secret. What’s more, the industry hasn’t come up with many innovative drugs in the last 20 or so years.

-“Copycat drugs” are the money-makers. It’s much easier to cash in on a competitor’s blockbuster with a “new” drug that is virtually the same, simply by making doctors and consumers think it is better or has fewer annoying side effects.

The most troubling aspect of the industry’s marketing practices is the extent to which they have corrupted medical research. Over the course of the last 25 years, drug companies have been using clinical trials and medical journals to market their products. This trend was described as “the marketing approach to research” by Richard Daly, senior VP , Takeda Pharmaceuticals, at a 2002 breakfast meeting in Manhattan of executives from the largest pharmaceutical companies and advertising companies that work with them. The marketers aren’t working with test tubes and injecting patients, Petersen explained, “Instead they are standing besides the scientists, telling them what studies to do, what research questions to ask, what data to gather.”

Withholding data about serious adverse reactions from drug trials has become so common that there’s a medical term for it—“selective reporting” of trial results, also known as cherry-picking only the results the drug company wants made public. No one knows how many pharmaceutical studies have been kept secret after they showed a drug does not work or caused harms, writes Petersen, but several reviews have found that at least 50% of pharmaceutical trials were never published. Thus, a complete picture of a drug’s harms is unknown.

Prescribing physicians can no longer trust the information published in medical journals. And the doctor-patient relationship itself has become severely compromised by drug marketing. It is nearly impossible for most people to know whether their doctors are prescribing on the basis of the best available scientific evidence or the best available marketing scheme.

Petersen put it this way: “The pharmaceutical companies have become so wealthy and powerful that the whole medical system has become unbalanced. Inside hospitals and medical offices, corporate marketers are now calling the shots. They decide how patients will be treated and the doctors follow along. How else can you describe a system where doctors now prescribe a pill called Detrol for a disease called overactive bladder.”


Reviewed by Maryann Napoli, Center for Medical Consumers© August 2008

Posted in Book Reviews, Drug ads, Drugs, Women's Health | Tagged: , | Comments Off

Women-in-Towels Evista Ad Critiqued

Posted by medconsumers on July 1, 2008

The women in Eli Lilly’s new ad campaign are attractive, healthy-looking and wearing nothing but towels. “Cut two risks with Evista. The only agent indicated to treat osteoporosis and reduce the risk for invasive breast cancer.”

That two-for-one claim for Evista makes it different from other drugs taken by symptom-free people. Studies showed that the harm related to each disease drops a percentage point or two in those who took Evista, compared to those who did not. The drug is better than a placebo (or it would not get FDA approval), but not much better. This is a recurring theme in Center for Medical Consumers articles because it’s a recurring theme in many drug trials. And often the small risk of a serious adverse reaction to the drug equals that small chance of benefit.

Evista (generic name: raloxifene) has been on the market since 1997 as an osteoporosis drug. It produces a 2%-3% increase in bone density; reduces the rate of vertebral (spinal) fractures; but does not prevent the most serious type of fracture (hip). Vertebral fractures can cause pain and a dowager’s hump in advanced age, but many are symptomless. The studies did not last long enough for Lilly to make claims regarding prevention of a dowager’s hump or loss of height.
Breast Cancer “Risk Reduction”

Last year Lilly received FDA approval to promote Evista as a drug that can “reduce the risk of invasive breast cancer.” This careful wording from the Evista ads is important. Lilly cannot claim its drug prevents breast cancer because the disease can take anywhere from 8 to 17 years to develop. There were, in fact, fewer breast cancers diagnosed in the women taking Evista, compared to those taking placebos. But the trials didn’t last long enough to determine whether the drug prevents breast cancer or simply delays its onset. In Evista trials that lasted up to eight years—breast cancer was diagnosed in 2.5% of the women taking a placebo and 1% of the women taking Evista.

The other claim for Evista is based on the fact that the women in the studies already had osteoporosis (bone loss). One way bone drug companies can inflate the benefit of their product is to count symptomless vertebral fractures that can be detected only on x-ray. (In other words, the women are unaware of them.) At the start of the Evista trial about half the women had painful vertebral fractures and the other half had “fractures diagnosed radiographically.” After four years, things looked better for Lilly when results for all women were combined, but less impressive when women with painful fractures were singled out. In the latter group, only about 1% fewer Evista-treated women had new painful vertebral fractures than the women taking placebos.

Thus far serious adverse reactions to Evista include deep vein thrombosis, pulmonary embolism, retinol vein thrombosis and an increased risk of fatal stroke. (See boxed warning of the FDA-approved label). Separately, each is classified as rare, which, according to FDA standards, describes any drug reaction that occurs in less than 2% of study participants. Collectively, though, these potentially fatal adverse reactions could reach 1-2% which comes close to the percentage of women who benefited from Evista in the FDA-required clinical trials.

And lastly, the visual message conveyed by the women-in-towels ad is misleading. Most of the women look to be in their fifties. At the start of the Evista trials, however, most participants were over age 65 years, a time of life when vertebral fractures are far more likely to occur.

Maryann Napoli, Center for Medical Consumers ©
July 2008

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Anemia Drugs For Cancer Patients

Posted by medconsumers on March 13, 2008

Testimony Submitted to FDA Oncologic Drugs Advisory Committee Meeting
March 13, 2008

Maryann Napoli, Associate Director, Center for Medical Consumers

As a consumer advocate who attended the May ODAC meeting, I came away wondering why these drugs remain on the market. They cause some patients to die sooner. They have many other risks that are severe and well documented, and any quality-of-life benefit has yet to be proven. The FDA approved the first ESA because it reduced the percentage of patients transfused. But the agency has since acknowledged that the infectious disease risks of a blood transfusion are far lower now than they were in 1993.

No doubt there are many cancer patients who see these drugs as an instant cure for chemotherapy-induced fatigue or as the means of allowing chemotherapy to continue. The former indication was fostered by Johnson & Johnson’s fraudulent ad campaign for Procrit, which continued for seven years in the mainstream TV and print media. I urge ODAC to discuss the misconceptions imparted by these ads and to consider recommending that the FDA require J&J to run a corrective ad campaign.

The ability of a cancer patient to make a truly informed decision with the help of her oncologist is seriously compromised by J&J’s and Amgen’s reprehensible practice of offering rebates—that is, kickbacks—to oncologists. Patients are always encouraged to discuss their treatment decisions with their doctors. Yet it’s hard for patients to believe oncologists’ recommendations are unbiased when they are “reaping millions” from the prescription of anemia drugs, as The N.Y. Times reported last May. (1) Companies that give kickbacks and other financial incentives intended to manipulate oncologists into using the most expensive drugs are poisoning the doctor/patient relationship.

Where can people turn for unbiased information? It should be the FDA, but it’s not clear to me that black box warnings are the way to go. The changes in the product labeling in 2004 did not change clinical practice. (2) And what do we know about the effects of black box warnings on the ones who need them the most—the cancer patients? The cancer patient should be given scientifically accurate, written information about ESA well before she needs it. The time to weigh the risks and benefits is not when she’s awaiting her next chemo treatment and just learned that her hemoglobin is too low for the next round.

Patients cannot make truly informed decisions unless they are given quantitative information to help them decide whether ESA is appropriate. They need to know, for example, the chances of…1) needing a transfusion; 2) suffering harm by foregoing a transfusion, 3) experiencing a serious adverse effect from the transfusion itself, and 4) having a severe adverse effect from the ESA. Patients need to know the magnitude of each of these four risks. Telling them that ESA will reduce their risk of having a blood transfusion is simply too vague. It gives them no way to compare this purported benefit with the other risks of taking ESA. If the FDA will not remove these drugs from the market, it must find the best ways to get clearly written, accurate quantitative ESA information to cancer patients.

(1) Berenson A, Pollack A. “Doctors Reap Millions for Anemia Drugs.” N.Y. Times, May 9, 2007

(2) Blau AC. “Erythropoietin in Cancer: Presumption of Innocence?” Stem Cells 2007; 25;2094-2097; originally published online Apr 26, 2007.

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Honesty in Drug Advertising: Some rare examples

Posted by medconsumers on May 1, 2007

“In patients with multiple risk factors for heart disease, LIPITOR REDUCES RISK OF HEART ATTACK BY 36%* If you have risk factors such as family history, high blood pressure, age, low HDL (‘good’ cholesterol) or smoking.”

The noteworthy part of this New York Times ad is the asterisk and this explanation of the 36% statistic: “That means in a large clinical study, 3% of patients taking a sugar pill or placebo had a heart attack compared to 2% of patients taking Lipitor.”

Take a moment to appreciate the significance of this rare finding of candor in one of those ubiquitous Lipitor ads featuring Dr. Robert Jarvik, “inventor of the Jarvik Artificial Heart and Lipitor user.” Most drug ads would rather proclaim a “36% reduction” and leave it at that, but this version shows exactly what it means. Take Lipitor for years and your risk of having a heart attack drops 1%. Granted, the explanation is in much smaller type than the 36%, but at least it’s there.

Another Jarvik/Lipitor Times ad proclaims: “In patients with type 2 diabetes, LIPITOR REDUCES RISK OF STROKE BY 48%* If you also have at least one other risk factor for heart disease…” The explanation: “That means in a large clinical study, 2.8% of patients taking a sugar pill or placebo had a stroke compared to 1.5% of patients taking Lipitor.”

It’s rare to see ads with drug benefits expressed in what statisticians call absolute risk terms, which are more understandable to the public as well as doctors. Tom Abrams, director of the FDA Division of Drug Marketing, Advertising and Communications, explained in a telephone interview that the FDA encourages drug companies that provide quantitative information (e.g., 36% reduced risk of heart attack) in their ads to show what it means. In other words, the ad must answer the question: 36% of what?

Whether quantitative information goes into an ad is up to the drug companies, but once it does, the FDA wants them to put in the explanation, Abrams said, though only the most egregious non-compliers get a warning letter. Why no explanation of the quantitative information in all TV versions of these ads? “This is a quicker media and companies believe that people can’t process the information?” he said.

Well, honesty in some print ads is better than nothing. The next thing to look for is the quantification of the drug’s severe adverse effects…in absolute risk terms.

Maryann Napoli, Center for Medical Consumers ©
May 2007

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Those Ubiquitous Gardasil Ads

Posted by medconsumers on March 1, 2007

The first thing you notice about the Gardasil TV ads, featuring teen-age girls engaged in various athletic activities, is that there is no mention of the fact that the Gardasil vaccine is for the prevention of a sexually transmitted disease.

The voiceover says, “Every year thousands of women die of cervical cancer. I want to be one less woman who will battle cancer.” The first sentence is entirely true (3,700 in the U.S.); the second is merely a wish.

One version of these ads, which features mothers and daughters, was found to be cleverly manipulative by a New York Times reporter, Claire Dederer. The ad shows cool, self-reliant girls involved in cool, self-reliant physical activities with the repeat message: I want to be one less woman who will battle cancer.

“The mothers appear about halfway through [the ad] and they’ve got the bad news,” writes Dederer. “In loving tones they break it to their daughters: ‘Gardasil may not fully protect everyone,’ they say. Tenderly they list the side effects.This is an ingenious ploy: the cool girls want to be ‘one less’; the moms are the ones putting on the brakes. Having mothers voice the downside of Gardasil reinforces the message that if you get this vaccination, you’re the rebellious, independent thinker: ‘forget the side effects. Forget Mom. I’m getting vaccinated.’”

Maryann Napoli, Center for Medical Consumers© March 2007

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Dueling Osteoporosis Drug Ads

Posted by medconsumers on February 1, 2006

The goal of osteoporosis drug therapy is not to stop bone loss or improve bone density. Rather it is to reduce the chance of having a serious fracture. Over the years, osteoporosis researchers have found that improving bone density does not always lead to fracture reduction. The drug class called bisphosphonates has dominated the osteoporosis drug market ever since Fosamax became available in 1994. Actonel, another bisphosphonate soon followed. Boniva is the latest drug in this class.

How good are these drugs at reducing the rate of hip fracture, the most serious consequence of osteoporosis? Not very. The first clinical trial proving Fosamax’s benefit showed that at three years, 1% of the drug-treated women had had a hip fracture, compared with 2% of the women on the placebo. Significantly, the elderly women in this trial all had evidence of a previous fracture; whereas many younger women are inappropriately put on long-term Fosamax purely because a bone-mineral density test showed bone loss.

As Fosamax nears the end of its patent life, its competitors, Actonel and Boniva, are promoted in ads that emphasize the fact that they do not have to be taken daily. For example, the TV and print ads for Boniva feature its once-a-month dose convenience, but the ads for once-a-week Actonel also mention its proven fracture-prevention. These two different promotional approaches merit scrutiny.

What did the clinical trials prove?

In a three-year trial, Boniva was no better than a placebo in reducing non-spinal fractures (hence the Boniva ads’ focus on once-a-month dosing). As for Actonel, its advertised claims are correct but misleading: “Actonel is clinically proven to help protect many bones where a woman is most vulnerable to fractures caused by osteoporosis: The spine and a combination [emphasis added] of wrist, hip, collarbone, upper arm, leg and pelvis.”

Clustering the non-spinal fractures together clearly makes the clinical trial results look more impressive. 11% rate of the women on a placebo had a non-spinal fracture, compared to 7% for the women on Actonel.  However, where it concerns hip fracture, the same trials showed Actonel to be much less impressive. The rate of hip fracture of the women on Actonel was identical (2%) to that of the women on the placebo. (These findings appear in Actonel’s “label,” known as the packet insert which provides prescribing information for doctors.)

Who were the study participants?

In both the Boniva and the Actonel clinical trials, the participants were postmenopausal women with documented osteoporosis—that is, spinal fractures shown on x-ray—but only some had symptoms. In many cases, women are unaware of their spinal fractures.

Cautions

The bisphosphonates, particularly Fosamax and Actonel, are usually prescribed for five years or more. In her excellent Web site, Susan Ott, MD, one of the country’s leading osteoporosis researchers, explains why five years is enough. “The bisphosphonates get deposited in the bone and will accumulate for years. It is possible that many years of continuous medicine would make bone more brittle or impair the ability to repair damage. Bisphosphonates do reduce fractures and improve measurements of bone strength for the first five years in both animal studies and in women who have osteoporosis. After five years, the fracture rates are as high in the women who keep taking alendronate [Fosamax] as in the women who quit.” (http://courses.washington.edu/bonephys)

Alternatives:

Reduce the chances of falling by eliminating scatter rugs from the home and by avoiding certain prescription drugs like tranquilizers and barbiturates. Regular exercise will also reduce the risk of fracture.  Daily supplements of 1000 mg calcium and 800 IU vitamin D3 decrease the likelihood of a first hip fracture, according to an analysis of relevant clinical trials published last year in the Journal of the American Medical Association. This is a lower amount of calcium and a higher amount of vitamin D than the longstanding recommendations.

For updates on this topic, read our more recent articles: Prevent falls with vitamin D3, “The Marketing of Osteoporosis—How a risk factor became a disease,” (April 2009 issue of the American Journal of Nursing), “Fosamax-induced osteonecrosis of the jaw—more common than previously thought,” and “Osteoporosis drug: New adverse effects.”

Maryann Napoli, Center for Medical Consumers ©

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Painkiller’s Ads Hype New Combo of Old Drugs

Posted by medconsumers on February 1, 2006

Combunox:

Combunox is advertised by Forest Pharmaceuticals as though it were a new drug. Actually, it is a combination of two old drugs: the semi-synthetic opioid prescription drug, oxycodone, plus the popular over-the-counter anti-inflammatory painkiller, ibuprofen. The combination supposedly provides an extra punch. But The Medical Letter (1/2/06), a physician publication without drug advertising, assessed the studies supporting the use of this fixed combination drug and concluded that people with acute pain might be better off taking ibuprofen alone.

At a dose of 400 mg (the amount in Combunox), ibuprofen is doing the lion’s share of the painkilling. “A 400-mg dose of ibuprofen is generally superior to 1000 mg dose of acetaminophen (brand name: Tylenol) and is comparable to acetaminophen/codeine combinations,” according to The Medical Letter. “The analgesic effect of ibuprofen does not increase with doses greater than 400 mg; the anti-inflammatory effect does and so does the drug’s gastrointestinal toxicity.”

Who were the study participants?

In one clinical trial, Combunox was better than a placebo in women with moderate to severe pain 14 to 48 hours after abdominal or pelvic surgery, and in another trial that involved people who have had dental surgery.

What’s New About Combunox?

Not much. Oxycodone was introduced over 50 years ago and reintroduced in the ensuing years under numerous brand names (including OxyContin and Percolone) and in combination with over-the-counter painkillers, such as aspirin/oxycodone (Percodan) and acetaminophen/oxycodone (Percocet). Combunox represents the first time oxycodone has been combined with ibuprofen.

Cautions

Combunox is approved for the short-term (seven days) treatment for moderate to severe acute pain because prolonged use can lead to dependence. The warning is based on longstanding concerns about oxycodone. As with all opioids, abuse is a strong possibility. Under its most popular brand name OxyContin, oxycodone has received considerable media attention because of continuing reports of abuse. One risk of taking a fixed combination, according to The Medical Letter is this: Dependence upon oxycodone may cause people to increase the dose, which in turn could lead to overdosage of ibuprofen.

Alternatives

A week’s supply of Combunox costs $10.08 to $40.32, says The Medical Letter, whereas, the same amounts of generic ibuprofen and oxycodone would cost $4.80 to $19.20. The Medical Letter findings suggest that 400 mg of ibuprofen alone might be the safest choice.

Maryann Napoli, Center for Medical Consumers ©
February 2006

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Advertising Drugs To The Public: A Bad Idea

Posted by medconsumers on May 1, 2004

Center for Medical Consumers to the FDA: Rein in Those Deceptive Ads

The FDA is currently rethinking its guidelines for corporations that advertise their prescription drugs and medical devices to consumers. Don’t think that the regulatory agency has your best interests at heart. For one thing, the FDA cannot screen the ads for accuracy before they are unleashed upon the public, nor does it have the staff to track all the print and broadcast ads after the fact. The new guidelines currently under consideration by the FDA are just as wimpy as the old ones. The FDA can only provide guidance to the drug and device industries thereby living up to its reputation as a toothless tiger.

In a perfect world, one where the FDA actually served the public’s interest, these ads would be abolished altogether. That’s never going to happen. Here’s the Center for Medical Consumers’ pie-in-the-sky recommendations that the FDA is unlikely to follow:

  • Make those entrepreneurial radiologists hawking whole-body scans and heart scans reveal the risks in their ads. They should be made to identify the radiation doses involved, as well as the high likelihood that scans will lead to unnecessary biopsies and detection of a type of cancer that would have remained dormant. As things stand now, a company can advertise any outrageous claim about, say, its digital mammography or scans with impunity as long as the brand name of the equipment is not revealed in the ad.
  • Include the rate of effectiveness in all ads. Only about 10% of all drug ads currently address this important issue; the rest give the impression that everyone benefits from the product. To get FDA approval, a drug must prove to be better than nothing (i.e., a placebo). Let the public know how much better.
  • Stop telling us that drug advertising is a good form of consumer education. Ads are designed to sell a product, not to provide balanced information. That’s why you see so many ads devoted to new, i.e., expensive, “me-too” drugs (think: Celebrex and Vioxx, Prilosec and Nexium, Lipitor and Zocor). That’s why you see little in the way of education— just a few promising words in the headlines like power and strength.
  • Abolish all “disease awareness” ads. They masquerade as public service announcements because no drug is named. This type of ad is all about selling fear of a disease, the need for testing, and drumming up customers for lifelong drug therapy. Merck, maker of the osteoporosis drug, Fosamax, provides a classic example: “Osteoporosis—could you be at risk…. ask your doctor whether a bone density test is right for you.”
  • Don’t allow companies to advertise diagnostic or screening tests to the public without proof that the new technologies are better than the old. Ads touting the expensive Pap screening technology called ThinPrep are a case in point. Such promotional activities have raised the cost of Pap testing without improving the accuracy of finding cervical cancer. To gain FDA approval, the maker of ThinPrep (and any other screening technology) has to prove only that it could find cancer, not that it is any better at finding cancer than the standard Pap test.
  • Be straight with the public about the limits of FDA testing requirements. Each ad should have a disclaimer, such as: To be approved by the FDA, a drug has only to be proven safe and more effective than a placebo, not better than older drugs prescribed for the same condition. The drug trials required for FDA approval typically last eight to 12 weeks.
  • Require the drug companies to list a few of the most common and most serious side effects in the body of the ad. Print ads are currently mandated to include the misnamed “brief summary” in tiny type on the reverse side of the ad. Anyone who reads the entire brief summary—and not many people do—will appreciate the concept of befuddling the public with too much information.
  • Speed up the process for pulling a misleading ad. The FDA usually waits for someone to complain about a misleading ad. Then the agency takes too long to remove it, according to a report from the U.S. General Accounting Office. What’s more, there is no penalty. Corrective ads are rare, though deception is not. We were cheered to see the recent corrective ad for Pravachol, the cholesterol-lowering drug. Its maker, Bristol-Myers Squibb, had to run full-page ads in such publications as The New York Times and Parade, stating that Pravachol “has not been proven to help prevent stroke in people without heart disease. Pravachol is proven to help prevent stroke only in people with coronary heart disease.” [Note: Though most ad complaints come from a competing drug maker, according to an FDA spokesman, the Bristol-Myers Squibb lie was found by FDA staff.]

Our suggestions to the FDA were made last month in a letter written in response to the agency’s request for comments on its guidance to industry. We do not have high hopes that they will be taken seriously given the current political climate. (Political contributions from the drug industry totaled $29 million in 2002.) The FDA’s hands are tied by a Congress unwilling to release the necessary funds or rein in the pharmaceutical industry. Meanwhile, drug costs continue to rise, much of it because advertising promotes the most expensive new drugs, not necessarily the safest or best drugs.

Maryann Napoli, Center for Medical Consumers(c)

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