Big Pharma: Creating what ails you (Part 1) - Baltimore Post-ExaminerBaltimore Post-Examiner

Big Pharma: Creating what ails you (Part 1)

*Author’s Note: I wrote this for a Sociology class at WSU, but found the issues are still relevant. Furthermore, all of the complaints, regulations and legalities regarding marijuana, tobacco and perhaps even e-cigarette use are hypocritical considering our history of prescribing much more potent substances.

Medicating For Profit

Currently, the U.S. “uses over … forty percent of all the drugs produced in the world each year, according to the World Health Organization” (Murray, 2009, p.9). Since 2009, that percentage has gone up, which isn’t surprising if you consider that we are one of only two developed countries who allow direct to consumer marketing of pharmaceutical drugs, the other being New Zealand. From blood pressure medication to antidepressants, the average American stands a good chance of watchingcommercials for prescription drugs on a daily basis.

There is no doubt that we live in a culture that endorses the idea of supposed “need.” You “need” to be, have and produce many things, according to our many explicit and implied cultural messages. From toothpaste to tanning, we are constantly being told that we need something.

Naturally, when it comes to matters of health, people are all too eager to get what they need. But what if that’s an issue of dispute? The industrial nature of such a marketing and business alliance — all in the name of medicine — of today’s lobbyists, politicians, psychiatrists and pharmaceutical companies (Big Pharma) presents a major health concern for the average United States citizen.

The History of Pharmaceuticals

In some ways, the use of drugs for medicinal purposes has been even less regulated than it is now. Pharmaceutical drugs used to be sold just like anything else on store shelves (Mosher, 2007). These drugs included some that are now illegal, such as cocaine and heroin (Cohen&Inaba, 2011). In 1970, not only were many of these items off the shelf, but the United States passed the Controlled Substances Act, mostly in response to the prevalent drug use of the 1960s.

According to the Seventh Edition of “Uppers, Downers, All Arounders,” the main obligations of the Drug Enforcement Administration were: “to classify all psychoactive drugs, to control their manufacture and sale, to limit imports and exports, [and] to define criminal penalties” (Cohen &Inaba, 2011, 1.38). To this day, the classifications of psychoactive substances are widely disputed.

An extremely relevant example of this can be found in our recent decision to legalize Marijuana use in Washington and Colorado. Technically, marijuana is classified as a Schedule 1 drug, associated with a high potential for abuse and defined as having no medical value, and yet people have been using it for medicinal purposes to cope with pain for years in several states.

It is perhaps due to such an irrational coexistence of contradicting facts that a leading college textbook can confidently state: “The U.S. government’s views of drug and alcohol use and abuse have varied widely over the centuries, but most policy decisions made in the past 50 years were due to the prevailing political climate rather than scientific and sociological research. The budget for the U.S> “War on Drugs” has gone from $3.7 million in 1971 to $15.1 billion in 2011” (Cohen &Inaba, 2011, 1.39).

Now, although we’ve made “hard” drugs theoretically more difficult to access, pharmaceutical companies have found ways around safety and labeling regulations, as well as increasing sales at an alarming rate due to excessive advertising. Let’s begin with dissecting their marketing strategy.

In 1937 over 100 people died after ingesting what was then called an “elixir” — sulfanilamide. As a result Congress passed the Federal Food, Drug and Cosmetic Act of 1938 the prohibited false advertising and proof that the food, drug or cosmetic were safe for use. As it turns out sulfanilamide is the main ingredient of antifreeze. (Wikipedia)

In 1937 over 100 people died after ingesting what was then called an “elixir” — sulfanilamide. As a result Congress passed the Federal Food, Drug and Cosmetic Act of 1938 the prohibited false advertising and proof that the food, drug or cosmetic were safe for use. As it turns out sulfanilamide is the main ingredient of antifreeze.
(Wikipedia)

Medical Marketing

Before 1997, advertising these drugs was illegal (Murray, 2009, p.213). Since 1997,we have been advertising prescription drugs with very little to no FDA regulation in place to put a barrier between consumers and drug companies. Like any other marketing ploy, the strategy continues to be employed only if it appears to be working—and it does.

Two years after the U.S. began advertising pharmaceutical drugs, Americans were being exposed to nine ads for prescription drugs per day, on average (Mosher, 2007). By 2009, drug companies were spending “more than $57.5 billion per year marketing to physicians” (Murray, 2009), much less consumers.

Not surprisingly, the public’s acceptance of pharmaceutical drugs had more to do with well-trained salesmen than medical science, beginning with “detail men” who were trained with sale literature and in-house company newsletters after World War II (Greene, 2004).

More recently, two Canadian researchers found that drug companies now spend at least twice the money on marketing as they do on the research and development of their drugs (Gagnon &Lexchin, as cited in Murray, 2009).

Unfortunately, the common practice of DTC (direct to consumer) marketing is one of the biggest culprits for what we now refer to as “Big Pharma,” afive hundred billion dollar industry (Moynihan &Cassels, 2005)that has leaked into the facets of medical education and general medical practice.

Pharmaceuticals Going Mainstream

Merck, a leading international pharmaceutical company, provides a perfect illustration of how all these principles come into play, how they affect consumers, and what actions (if any) are taken against drug companies. Henry Gadsden, the head of Merck over three decades ago, was once quoted as saying he wanted Merck’s brand to be sold to everyone, even the healthy (Murray, 2009, p.15) Essentially, we must ask ourselves whether there is there a need or they are manufacturing one.

Peter Whitehouse, a former consultant for pharmaceutical and biotechnological industries, asserted that large pharmaceutical companies were indeed doing just that. In“Why I No Longer Consult for Drug Companies,” he writes of giving up his careerbecause [the pharmaceutical companies] were “[creating] diseases for drugs” (Whitehouse, 2008). Kristin Barker of Social Science & Medicine holds a similar opinion.

Barker argues that there is a “cultural logic whereby the existence (and marketing) of an officially approved prescription medication for a condition lends support to the biomedical existence of the condition itself,” which she calls “pharmaceutical determinism.”

She cites the example of fibromyalgia, an illness that physicians cannot even agree exists. Not only do patients diagnosed with this disease face skepticism with their symptoms, but they may be taking a drug that was formulated with no purpose other than to relieve symptoms and make profits, rather than actually treat a viable, authentic syndrome. The drug Barker references is Lyrica, an FDA approved prescription medication.

According to her article,“Listening to Lyrica: Contested Illnesses and Pharmaceutical Determinism,” Barker sees evidence that “pharmaceutical companies…[play a large role]in promoting and legitimating contested diagnoses and validating those who are so diagnosed.” (Barker, 2011) In other words, a patient’s diagnosis could have more to do with the greed of pharmaceutical companies than a scientific analysis of their symptoms.

This opinion is echoed by Dr. Marcia Angell, who acknowledges that though drug companies used to make drugs for treatment purposes, the culture has changed drastically. “Now it is often just the opposite. They promote diseases to fit their drugs” (as quoted in Murray, 2009, p.101).

By all accounts, it appears as though there is not so much a rising surge in ailments and mental cases since the early 1900s but a greater number of drugs needing to be sold. To illustrate how this principle works, take into consideration that the ratio of surgeons in an area actually increases the number of surgeries performed (Murray, 2009).

Dr. Michael Murray writes, “One research study found that an area with 4.5 surgeons per 10,000 …experienced 940 operations … whereas an area with 2.5 surgeons per 10,000 experienced 590 operations per 10,000. Basically, when the concentration of surgeons doubles, so does the rate of surgeries” (Murray, 2009, p.14).

This profit-seeking or “pharmaceutical determinism” extends to the decisions made by pharmaceutical companies in regards to patents. In an article released by the Economic Development Quarterly in 2004, they reported a connection between patent activity within the U.S. pharmaceutical industry and economic conditions of a geographic location, finding that “local business conditions play an important role in the innovation and financial performance of U.S. pharmaceutical companies” (MacPherson &Boasson, 2004).

If pharmaceutical companies were truly rooted in fulfilling the needs of a specific population, it stands to reason that economic factors would not have such a notable impact.

Part 2 of this post.


About the author

Megan Wallin

Megan Wallin is a young writer with a background in the social sciences and an interest in seeking the extraordinary in the mundane. A Seattle native, she finds complaining about the constant drizzle and overabundance of Starbucks coffee therapeutic. With varied work experiences as a residential counselor, preprimary educator, musician, writing tutor and college newspaper reporter/editor, Megan is thrilled to offer a unique perspective through writing, research and open dialogue. Contact the author.
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