I’ve been blogging about the dangers of NSAID drugs like Motrin and Aleve for many years. Why? These are by far the most dangerous drugs you can buy over the counter. Now the FDA has finally acted on what’s been clear in the medical literature for years by placing additional warnings on these pills, but is it too little too late?
Patients look like I’ve just told them aliens have landed in DC when I inform them that the drug their orthopedic surgeon or family doctor told them to take is very dangerous. While a few have some sense that some of these drugs can cause a bleeding stomach ulcer, they have no idea that NSAID drugs triple to quadruple their risk of dying from a sudden death heart attack. They also don’t know that not only do NSAID drugs increase the risk of stroke, but that they also increase the likelihood that they’ll die from a stroke if they have one.
First, the FDA warning is based on meetings that reviewed additional data and scientific publications in February of 2014. Why it took the FDA 17 months to go from decision to public warning is anybody’s guess. Be that as it may, the new labeling for drugs like Motrin, Ibuprofen, Advil, Aleve, Celebrex, Mobic, Meloxican, Voltaren, and others will be:
“Heart attack or stroke risk can increase as early as the first weeks of NSAID use, and the risk may increase with longer NSAID use. The risk appears to be greater at higher doses.
Based on our review and the advisory committees’ recommendations, the prescription NSAID labels will be revised to reflect the following information:
So how is it possible that America’s little middle aged helper pill is so dangerous and so few people know about it? Also, if we’ve known about these risks and dangers of NAIDS drugs since 2005 (actually much earlier, but that’s when the FDA finally acted), why has it taken so long to step up the warnings? Some would argue that it’s taken awhile for new data to convincingly show that these drugs are even more dangerous than we knew in 2005, but to me and many other physicians the data has been really clear since about 2010/2011. In fact, another huge organization, the American Heart Association, began a public awareness campaign about NSAID dangers in 2013. The reason why is something that’s been discussed by many journalists and academics, “Regulatory Capture“. In agencies like the FDA, the regulated begin dictating to the regulator how they should be regulated. In this case, the Pharma companies making big bucks off NSAID sales have hired many university docs to sit on or convince FDA panels that there was a pressing need for these drugs despite the risks.
The upshot? These are dangerous drugs and it’s good to see FDA finally stepping up the warnings. However, I think it’s too little too late. Educating the public about the dangers of these drugs to avoid unnecessary deaths would take a multi-million dollar, public education campaign, something big pharma would never allow.
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About the Author
Christopher J. Centeno, M.D. is an international expert and specialist in regenerative medicine and the clinical use of mesenchymal stem cells in orthopedics. He is board certified in physical medicine as well as rehabilitation and in pain management through The American Board of Physical Medicine and Rehabilitation.…