Send a Tweet
Most Popular Choices
Share on Facebook 2 Share on Twitter 2 Share on LinkedIn Share on Reddit Tell A Friend Printer Friendly Page Save As Favorite View Favorites
OpEdNews Op Eds

Picked Out a Coffin Yet? Take Ibuprofen and Die

By       Message Mike Whitney       (Page 1 of 2 pages)     Permalink    (# of views)   4 comments

Related Topic(s): ; ; ; ; ; ; ; , Add Tags
Add to My Group(s)

Supported 3   Must Read 2   News 2  
View Ratings | Rate It

opednews.com Headlined to H2 7/25/15

Author 33
Become a Fan
  (47 fans)
- Advertisement -

Reprinted from Counterpunch

From twitter.com/Chimp999/status/623164262559649793/photo/1: Prescription and non-prescription drugs
Prescription and non-prescription drugs
(Image by Twitter User Chimp999)
  Permission   Details   DMCA

"Today we know that the risk of heart attack and stroke may occur early in treatment, even in the first weeks ... 'There is no period of use shown to be without risk,' says Judy Racoosin, M.D., M.P.H., deputy director of FDA's Division of Anesthesia, Analgesia, and Addiction Products." -- FDA website

- Advertisement -

In case you missed it: The FDA has just issued a warning on various prescription and non-prescription drugs that Americans ingest by the boatload. As it happens, these seemingly benign pain relievers can kill you even if you scrupulously follow the recommended dosage. But don't take my word for it. Here's a blurb from the FDA website:

"FDA is strengthening an existing warning in prescription drug labels and over-the-counter (OTC) Drug Facts labels to indicate that nonsteroidal anti-inflammatory drugs (NSAIDs) can increase the chance of a heart attack or stroke, either of which can lead to death. Those serious side effects can occur as early as the first few weeks of using an NSAID, and the risk might rise the longer people take NSAIDs." (FDA Strengthens Warning of Heart Attack and Stroke Risk for Non-Steroidal Anti-Inflammatory Drugs, FDA website)

Notice how the FDA refers to "death" as "a serious side effect." How's that for an understatement? Here's more from the FDA warning:

- Advertisement -

"The OTC drugs in this group are used for the temporary relief of pain and fever. The prescription drugs in this group are used to treat several kinds of arthritis and other painful conditions. Because many prescription and OTC medicines contain NSAIDs, consumers should avoid taking multiple remedies with the same active ingredient." The New York Times includes "Motrin IB, Aleve and Celebrex" in this group of "widely used painkillers."

Why isn't this headline news? People take tons of these chemicals everyday thinking they've been thoroughly tested and are totally safe. Now we find out that's not the case. Now we discover that you can get a heart attack or stroke "as early as the first few weeks of using" them. Doesn't that come as a bit of a shock to you, dear reader? Doesn't that make you suspect that the FDA is not telling the whole truth here, but is simply covering up for a profit-obsessed industry that doesn't give a rip about its customers health?

Take a look at some of these articles I dredged up on Google News on the topic:

"Doctors issue Ibuprofen toxicity warning." Daily Telegraph. "Warning: Runners May Be At Risk From Ibuprofen Use." Australian Marathon Review. "Ibuprofen 'trebles the risk of a stroke' doctors warn," Daily Mail Online. "Ibuprofen Side Effects Land Thousands in the Hospital," Side-Effects. com. "The FDA's Dilemma About Ibuprofen And Cardiovascular Risk," Forbes. "Ibuprofen Blunts Aspirin's Cardioprotection. FDA Issues Warning," lexi.com. "Aspirin, Ibuprofen Warnings Advised -- Health: Consumers need to be told the painkillers can cause internal bleeding and kidney damage, a panel tells the FDA," LA Times.

And how reliable is FDA in determining the toxicity of these medications anyway? Wasn't the so-called "watchdog" agency implicated in pay-to-play flap just a couple years ago? Some readers might recall another incident when the FDA was caught in a "spying program on its own scientists, lawmakers, reporters and academics" to "discourage whistleblowing." According to Truthout's Martha Rosenberg: "top FDA managers "committed the most outrageous misconduct by ordering, coercing and intimidating FDA physicians and scientists to recommend approval, and then retaliating when the physicians and scientists refused to go along." Review procedures at the agency (which approves stents, breast implants, MRIs, and other devices and machinery) were so faulty that unsafe devices -- including those that emit excessive radiation -- were approved, charged the scientists, provoking an OSC investigation " For reporting the safety risks, the scientists became targets of the now-disclosed spy program and some lost their jobs. ..."

(According to FDA drug reviewer Ronald Kavanagh) "While I was at FDA, drug reviewers were clearly told not to question drug companies and that our job was to approve drugs. We were prevented, except in rare instances, from presenting findings at advisory committees. In 2007, formal policies were instituted so that speaking in any way that could reflect poorly on the agency could result in termination. If we asked questions that could delay or prevent a drug's approval -- which of course was our job as drug reviewers -- management would reprimand us, reassign us, hold secret meetings about us, and worse. Obviously in such an environment, people will self-censor." (Former FDA Reviewer Speaks Out About Intimidation, Retaliation and Marginalizing of Safety, Martha Rosenberg, Truthout)

- Advertisement -

Nice, eh? And this is the agency that's supposed to protect the public from risky drugs?

Right. Does the name "Vioxx" ring a bell? If not, here's a little refresher from an article by Fred Gardener in Counterpunch titled "Merck Pays a Pittance for Mass Deaths":

"'Merck has agreed to pay $950 million and has pleaded guilty to a criminal charge over the marketing and sales of the painkiller Vioxx,' the New York Times reported Nov. 23 ...

"The FDA had initially approved Vioxx (after a hasty 'priority review') in May, 1999 to treat osteoarthritis, acute pain, and menstrual cramps. By September 30, 2004, when Merck announced its 'voluntary recall,' some 25 million Americans had been prescribed the widely hyped drug. Evidence that using Vioxx doubled a patient's risk of suffering a heart attack or stroke --based on a review of 1.4 million patients' records -- was about to be published in Lancet by David Graham, MD, an FDA investigator. The FDA director's office, devoted valet of Big PhRMA, had contacted the Lancet in a futile effort to stop publication of their own scientist's findings.

"Graham's data indicate that 140,000 Americans suffered Vioxx-induced heart attacks and strokes; 55,000 died, and many more were permanently disabled. The Merck executives' real crime was conspiracy to commit murder ... An early clinical trial had alerted them to the fact that Vioxx caused coronary damage. Their response was to exclude from future trials anyone with a history of heart trouble!

Next Page  1  |  2

 

- Advertisement -

Supported 3   Must Read 2   News 2  
View Ratings | Rate It

opednews.com

Mike is a freelance writer living in Washington state.

Share on Google Plus Submit to Twitter Add this Page to Facebook! Share on LinkedIn Pin It! Add this Page to Fark! Submit to Reddit Submit to Stumble Upon Share Author on Social Media   Go To Commenting

The views expressed herein are the sole responsibility of the author and do not necessarily reflect those of this website or its editors.

Writers Guidelines

Contact AuthorContact Author Contact EditorContact Editor Author PageView Authors' Articles

Most Popular Articles by this Author:     (View All Most Popular Articles by this Author)

Class Warfare Scoreboard -- Guess Who's Winning?

Newt's Victory: Was it a "Surge" of popularity or faulty voting machines?

Is Fukushima's Doomsday Machine About to Blow?

Troublemaking Washington: Pushing Ukraine to the Brink

Dominique Strauss-Kahn was trying to torpedo the dollar

The Broken Chessboard: Brzezinski Gives Up on Empire