Trapped in the Spider Web: How Big Pharma Captured Our Healthcare System

My previous post was dealing with Statin medications, what they did to my muscle weakness and how I am dealing with this today.

 I  initially started with an internet search for:

“Pharma health care cabal” the initial result was a Wikipedia response claiming Big Pharma conspiracy theories, followed by others like the following by Kim Witczack.

I never set out to be an advocate. I wasn’t a doctor, scientist, or policy expert. I was just a regular person who, like so many, blindly trusted that our healthcare system was designed to protect us.

But life has a way of pulling us into the arena when we least expect it.

After the tragic and unexpected loss of my husband Woody to the antidepressant Zoloft that he was prescribed for insomnia, 

I was thrust into a world I never imagined—one where medicine wasn’t solely about healing, but deeply entangled in a system that prioritizes profit over safety, buries harms, and keeps the public in the dark.

For over two decades, I’ve had a front-row seat to how this system truly operates—not the illusion of rigorous oversight we see in medical journals or glossy pharmaceutical ads, but the reality of how industry influence is woven into every stage.

I’ve met with regulators, testified before the FDA and Congress, filed a wrongful death and failure-to-warn lawsuit against Pfizer, and earned a seat on the FDA’s Psychopharmacologic Drugs Advisory Committee as a consumer representative.

I’ve also spoken at, and participated in, global conferences like Selling Sickness, Too Much Medicine, and the Harms in Medicine meeting in Erice, Italy—where some of the world’s leading experts acknowledge what few in mainstream medicine dare to say:

Our healthcare system isn’t about health—it’s about business.

And in this business, harm isn’t an accident. It’s built into the system.

The more I uncovered, the more I realized:

We aren’t just patients. We are customers.

And we are all trapped in Big Pharma’s spider web of influence.

How the Web Works

• Clinical trials are often designed, funded, and controlled by the very companies that stand to profit. They manipulate data to exaggerate benefits and obscure risks, ensuring that negative results are buried, spun, or never published at all.
• Regulatory agencies like the FDA are deeply entangled with the industry they’re supposed to oversee. More than 50% of the FDA’s budget comes from industry-paid user fees, and a revolving door ensures that many key decision-makers come from—and later return to—pharmaceutical companies.
• Medical journals depend on pharmaceutical funding through advertising, reprint sales, and industry-sponsored studies—severely limiting independent scrutiny of drug safety. Many studies are ghostwritten or crafted by paid “key opinion leaders” (KOLs) who serve as pharma’s trusted messengers.
• Doctors receive education through industry-funded programs, learning “best practices” based on treatment guidelines crafted by the very system that profits from overprescription.
• Patient advocacy groups, once independent grassroots organizations, have been co-opted by industry money, ensuring that the loudest voices often serve pharma’s interests rather than patients’ needs. I call them “astroturf” patient groups—they look like real grassroots organizations, but they’re anything but.
• Screenings and guidelines continuously expand the definitions of disease, turning more people into lifelong customers.

This isn’t about one bad actor or isolated corruption—it’s a systemic issue. The entire structure is designed to push more drugs onto the market, medicalize normal human experiences, and only acknowledge harm when it becomes too big to ignore.

It’s a brilliant business model—but a catastrophic public health strategy.

If this sounds like a conspiracy, consider the bold admission made by Henry Gadsden, former CEO of Merck, in a 1976 interview with Fortune Magazine:

“The problem we have had was limiting the potential of drugs to sick people. We could be more like Wrigley’s Gum… it has long been my dream to make drugs for healthy people. To sell to everyone.” – Former Merck CEO Henry Gadsden

Let that sink in.

This wasn’t about curing disease—it was about expanding markets. Gadsden’s vision wasn’t just to treat illness, but to medicalize everyday life—creating a cradle-to-grave model where every person, healthy or sick, became a customer for life. Just like selling a variety of gum—something for everyone. Juicy Fruit, Big Red, Double-mint, Spearmint, and so on.

And that’s exactly what happened.

Today, we live in a system where:

• Everyday emotions—sadness, worry, shyness—are rebranded as medical conditions requiring treatment.
• Preventive medicine often means lifelong prescriptions, not lifestyle changes.
• Drugs are marketed to the “worried well”, turning normal human experiences into diagnoses.

Harms Are Always an Afterthought

Harms from medication are not rare, nor are they unexpected.

But in this system, they are treated as acceptable collateral damage—something to be dealt with only after the damage is done, after lives are lost or forever changed.

I’ve sat in FDA Advisory Committee meetings, reviewing new drug applications, and have seen firsthand how safety concerns are often dismissed in favor of “innovation” or “unmet medical need.”

I’ve heard industry representatives and advisory committee members argue that safety signals can be addressed post-market, meaning after a drug is already in circulation and causing harm or a required REMS (Risk Evaluation and Mitigation Strategies) program upon approval.

But by the time post-market safety issues are acknowledged, it’s often too late.

We’ve seen this play out over and over:

• Opioids—marketed as “non-addictive” and pushed aggressively onto patients, leading to an epidemic of addiction and death.
• SSRIs and antidepressants—long linked to increased risks of suicide and violence, particularly in young people, yet downplayed or dismissed for decades. Other hidden harms include withdrawal syndromes and Post-SSRI Sexual Dysfunction (PSSD), conditions that many patients were never warned about.
• Antipsychotics—widely prescribed for off-label use, leading to severe metabolic and neurological side effects.
• COVID-19 vaccines—an experimental mRNA platform rushed to market, mandated, and imposed on society despite limited long-term safety data and growing concerns over harms. (The narrative has since been debunked to a lab leak.)

The Counterargument: But Don’t We Need Experts?

Of course, some will argue that only experts with MDs and PhDs should be trusted to shape healthcare policy.

But that assumes that the system they operate in is free from bias, conflicts of interest, or financial incentives.

The reality is, many of those with the most letters after their names are also the ones benefiting from pharma funding—whether through consulting fees, research grants, or advisory roles.

Meanwhile, patients and their families—the ones living with the consequences—are too often ignored.

That needs to change.

Asking Better Questions: Reclaiming Our Power

If there’s one thing I’ve learned on this journey, it’s this: no one is coming to save us. The institutions meant to protect us are too entangled in the web to act with true independence.

My late husband, Woody, used to say: “Follow the money.” And when you do, the truth becomes impossible to ignore. Pharmaceutical profits—not patient well-being—drive the system. That’s why the only way to create real change is through awareness, transparency, and fundamentally shifting how we think about medicine and health.

That starts with asking better questions:

• Who funded this research?
• Does this person or institution have financial ties, intellectual bias, or self-interest that could impact their recommendations?
• Who benefits from this treatment?
• What aren’t we being told?
• What are the long-term consequences of this drug or intervention?
• Are there safer, non-drug alternatives being ignored because they aren’t profitable?
• But asking the right questions isn’t enough.

https://www.amazon.com/Selling-Sickness-Pharmaceutical-Companies-Patients-ebook/dp/B001T4YU48/ref=tmm_kin_swatch_0

“Thirty years ago, the head of the drug company Merck made some remarkably candid comments about his distress that his company's market was limited to sick people. Suggesting he would like Merck to be more like the maker of Wrigley's chewing gum, the CEO said it had long been his dream to make drugs for healthy people, to "sell to everyone." That dream now drives the marketing machinery of the most profitable industry on earth. From award-winning Ray Moynihan, -- one of the world's top medical journalists -- Selling Sickness reveals how widening the boundaries of illness and lowering the threshold for treatments is creating millions of new patients and billions in new profits. This in turn is driving up personal drug bills and threatening to bankrupt national health systems all over the world. As more and more ordinary life is "medicalized," the industry moves ever closer to being able to "sell to everyone.”

This is just one book, there are many others as well!

www.kimwitczak.com

Kim Witczak is a leading global drug safety advocate and speaker with over 25 years professional experience in advocacy, advertising and marketing commune-cations. She is currently a very vocal Consumer Representative on the FDA Advisory committee evaluating new drugs coming to market.