Institute for Safe Medication PracticesQuarterWatchMonitoring FDA MedWatch ReportsJanuary 28, 2015
Executive SummaryThe U.S. Food and Drug Administration’s Adverse Event Reporting System [FAERS] — based on MedWatch reports – is the government’s primary safety surveillance system designed to identify harms from therapeutic drugs. For the last six years these vital data have formed the core of ISMP’s QuarterWatch™ drug safety reports. In this issue we decided to look closely at the system itself. Our conclusion: it seems clear that this drug safety monitoring system is in need of modernization. It suffers from a flood of low quality reports from drug manufacturers and has not yet been updated for the changing environment in which drugs are marketed to health professionals and consumers. We discuss key problems below and offer some recommendations as an organization that relies heavily on data collected through FAERS. This issue of QuarterWatch includes two recently released calendar quarters of FAERS data, from 2013 Q4, and 2014 Q1. To provide a broader perspective, the main analysis focuses on the 12 months ending with 2014 Q1, and includes all adverse event reports received by the FDA in that one-year period. Previous issues of QuarterWatch have focused on a subset of these case reports, those with a serious outcome and reported by patients in the United States…
One of the important dimensions of the risk/benefit equation is TIME. If you are rendered totally miserable by a case of poison ivy, I can radically [and safely] improve your lot with a short, but generous tapering course of corticosteroids – the powerful suppressor of inflammation. But I’ve got to be sure you don’t have a condition like a Herpes eye infection that can be exacerbated by even a short course. The same with an asthma attack that doesn’t respond to bronchodilators. You might say time is on your side, because the diseases themselves are time-limited. But if you show up with a generalized case of Rheumatoid Arthritis, the corticosteroids are a double edged sword. The disease is going to be around for a while – long enough for the prodigious down side of chronic steroid treatment to raise its ugliest of heads. So the job is to look for a long term treatment from Day 1, and only use steroids up front, if at all. The same thing is true of anti-anxiety drugs or narcotic analgesics. Benzodiazepines are the cat’s meow for a crisis state with unmanageable anxiety, but danger, danger for the patient with a lifelong anxiety disorder because of tolerance and addiction ["if one is good, two is better"]. The same goes for narcotics. Just right for a heart attack or a kidney stone, but danger, danger, danger for some chronic back and other pain problems. Once you know they work, it’s harder and harder not to take them, and then you enter the nightmare of addiction.
And even if our short term Clinical Trials are conducted and analyzed thoroughly and honestly, they tell us little about long term use. That’s a real problem for psychoactive drugs [all of them]. It’s also a problem for many treatments of medical conditions that stick around for a long time [or forever]. So we need to know about the long term toxicity, and our Clinical Trials can’t tell us – emphasis on can’t. So we need a long term monitoring system to give us the information we need, and we just don’t have it. The current FDA MedWatch Report System just doesn’t seem to be it. Good for them that they noticed.
Besides a reporting system that works, identification of adverse effects is often a problem in and of itself, particularly in a poly-medicated world. You can’t report a side effect to a drug if you don”t know it’s a side effect. I was once called to see a patient in the hospital to be worked up for a neuromuscular problem with periodic extreme weakness. A morning muscle biopsy hae been aborted in the face of him having a panic attack. He was a fit male lying in the bed with a wet towel on his forehead in an obvious terror state – very hard to interview. He reported episodes of extreme weakness, mostly at work, worsening over several months. He worked in in a factory that made electrical cables, the big kind that are strung from tower to tower across the landscape. He ran the last machine in the process that wrapped the twisted cable onto huge spools for storage and transport. It was all done in a big un-airconditioned warehouse that was like an oven in the Georgia summers. The punchline was, "Doc. I feel like if I could just sweat, I’d be all right!" Flash back to a routine physical the winter before when he had mild hypertension and was started on medications. After trying several different drugs he couldn’t tolerate, he saw a specialist and was put on a new drug, Inderal, brand new at the time. It’s a Norepinephrine Beta-Blocker that incidentally turns off the sweating process. So he was right. And his panic disorder? As a boy, he had witnessed the slow demise of a favored uncle from Lou Gehig’s Disease, which is what he privately thought he had. His Blood Pressure? "White Coat Syndrome." It was normal when taken by his wife at home. Once we knew what was wrong, the cure was simple. Another example close at hand is the frequent misinterpretation of antidepressant withdrawal symptoms as a recrudescence of the original depression or the emergence of an anxiety syndrome, and the problem medication is restarted. Unfortunately, that maneuver works and perpetuates the cause. So side effects, adverse events, are difficult to spot.
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