Long-term Effects of Opioid Pain Relievers

As someone who suffers from chronic pain, I was wondering what are the long term effects of my pain medication? At this point in time Lyrica is not available to me and SSRIs, like Cymbalta, have horrible side-effects with me. So, my doctor in all his wisdom prescribes me Vicodin to control my pain. So, what are the long-term effects of it’s usage?

During my research I found very little on the long term effects. Most of what I found dealt with addiction to opioids and opioid-mix drugs. Currently, very few people become addicted to drugs like Vicodin and Percocet, though they do become physically dependent– which is not the same as addicted (explained further below). Some of what I found also dealt with the effects of overdose on opiods mixed with acetaminophen, such as liver and kidney damage that could ultimately lead to death (which is the case with any drug that contains acetaminophen).

Here are some of the facts regarding addiction and physical dependency to opioid/opioid-mix drugs from WebMD:

Addiction Myths1 :
Addiction: Hospice patients worry about becoming addicted to opioids. With hospice, however, it is rarely an issue. People with chronic pain also worry about addiction, but it turns out that for most adults, if they do not already have a substance (alcohol or drug) abuse problem, addiction is not much of an issue even when opioids are used on a long-term basis.

  • A study was done in which 12,000 nonaddicted people who needed opioids were followed up to see if they had become addicted. Four out of 12,000 showed addictive behavior (less than one tenth of 1%).
  • Generally, the only people who develop addictive behavior after being given opioids had an addiction problem before the opioids were given for pain. Most people take opioids until the pain goes away. Then they stop taking them because they do not want to feel dizzy or drowsy. Once the pain goes away, the toxic side effects of dizziness and drowsiness come back.
  • Anyone who takes any medication just to “get high” is already showing addictive behavior and needs to stop taking addictive substances, including opioids, other addictive drugs, and alcohol, immediately.
  • Some people with actual painful illnesses are addicted to mind-altering substances. They get prescriptions because of their actual illnesses. Here’s how the patient or the family can tell the difference between someone who needs opioids for pain and someone who is abusing opioids. Normally, the dose of opioids is arrived at by the patient telling the doctor how they are doing with the pain and by participating in their activities of daily living. A chronic pain patient who is not addicted to medication will tell the doctor the truth about his or her ability to function and do what needs to be done in daily life.
  • Addicts will lie about performing activities of daily living. The addict will claim that the pain is so severe that they need a higher dose until they get to a dose that causes them to be asleep most of the time. Then, they will tell the doctor that they are doing fine and are able to do all the activities that they need to do.
  • Selling the medicine to others is a federal crime that could get the seller a very long jail sentence and could lead to government seizure of your car or your house.
  • Family members must let the doctor know what is actually happening in this sort of situation. When an addicted person actually has a painful syndrome, the doctor, with the help of the family, may have to decide what the dose of medication should be, without reference to the dose the pain patient thinks would be best. Sometimes, in severely addicted people, the opioids should not be used at all. Some addicted people can be treated with opioids if necessary as long as they cooperate carefully with the treatment plan.

The physical dependency of my Vicodin is well documented, but I’m glad to know that the kind of addiction exhibited in such shows as “House” is so rare. Still, I worry about the damage my body will have due to long-term use. The WebMD article tells me that opiod/acetaminophen and opioid/NSAID (ibuprophen, naproxen) aren’t recommended for long-term use by chronic pain sufferers simply because over time they can damage the liver, kidneys and stomach (NSAIDs). However, an article from the Mayo Clinic states2:

No evidence indicates that long-term use of single-agent opioid analgesic preparations results in end-organ failure, as may be seen with other analgesics (eg, NSAIDs), or with certain combination opioid analgesics

And the WebMD states:

Strong opioid medications are slightly different in this regard, and this is fortunate for people who suffer from severe pain. With strong opioids, the dose depends on the amount of pain. These medications should not mixed with acetaminophen or other non-opioid drugs when used to treat chronic pain. People with intense pain can take very high doses of opioids without getting side effects. Some people with intense pain get such high doses that the same dose would be fatal if taken by someone who was not suffering from pain. In the pain patient, that same high dose can control the pain and still allow the person to be wide awake enough to do his or her activities of daily living.

  • Long-acting opioid: The best way to treat chronic, severe pain is by keeping it under control all the time. Your doctor can do this by using a long-acting opioid to keep the pain under control and a short-acting opioid to deal with those few times during the day when the pain breaks through. So, if you are on morphine, you would get a slow-release tablet that would keep your pain under control most of the time, and a short-acting tablet or liquid for those times when your pain breaks through.
  • Bad opioids: Some opioids are not recommended for chronic pain.
    • Demerol (meperidine), which is used often for acute pain after surgery, is a poor drug for chronic pain. It is not absorbed well when taken by mouth, and it causes dysphoria (feeling truly lousy) and seizures if used for more than a few days.
    • Talwin (pentazocine) is also bad for chronic pain. It has a ceiling effect. There is a maximum dose after which raising the dose gives no further pain relief. It also causes withdrawal symptoms when given to someone who is also taking another opioid.
    • The opioid/acetaminophen or opioid/NSAID combination drugs are fine for short-term use, but acetaminophen is poisonous to the kidneys and liver when used for a long time or in high doses. Many NSAIDs are toxic to the kidneys and stomach when taken for a long time or in high doses.

Doctor’s Argoff and Silverstein, writing the article located on the Mayo Clinic Proceedings, clearly states that “single agent” opioids show no long-term effect leading to organ failure, but combined with acetaminophen or NSAIDs can have dire results as shown by WebMD. So, am I to take from this that I should find another way to manage my chronic pain? I’m thinking that over the long haul I will be forced to go back to Amitriptyline and possibly try Lyrica– after I talk to my doc about this new drug.

Yesterday, while I was doing my research for this post, the FDA was busy approving a new, long-acting opioid for moderate to severe chronic pain.

The US Food and Drug Administration (FDA) has approved morphine sulfate/naltrexone hydrochloride (Embeda), an extended-release oral opioid analgesic for the management of moderate to severe pain when a continuous, around-the-clock opioid analgesic is needed for an extended period of time. This Schedule II agent is the first FDA-approved long-acting opioid that is designed to reduce drug liking and euphoria when tampered with by crushing or chewing.

Does this drug count as a “single agent opioid” and will it be safer to use than Vicodin (mixed with acetamenophin) or Percocet (mixed with NSAIDs)? Can this be something that will have fewer adverse long-term effects for chronic pain sufferers? As I’m not a doctor, I can’t really answer those questions– but they will be posed by me to my own doctor. It’s something I’m genuinely interested in. I have chronic noncancer pain and want relief from that without having to wonder if I know anyone close who would be willing to donate part of their liver later on in my life3. This is something that I’ve been thinking about for quite some time and I believe it’s time to review my options and sit down with my doctors again.

A note on physical dependency:
Physical dependency is different than addiction in that addiction causes people to seek the drugs anyway that they can get them, including lying to their doctors about their pain and daily activities. Physical dependency cause the withdrawal symptoms when people stop taking the drugs as well as heightened tolerance over time. That means that people suffering from chronic pain are likely to take more of the medication to get relief– which is what can lead to the most damage. This is why it’s so important to talk to your doctor honestly about the need to increase your dose of medications if and/or when that happens.

One more note: One of the side-effects of Vicodin is intense itching all over. I’ve recently discovered this in my research (having developed this recently and wondering what is going on). It’s normal and you should make sure to tell your doctor if you experience. I was under the impression that this was an effect of long-term use of the medication, but I’m wrong. It’s normal and can occur in people that have just started taking it.

Sphere: Related Content

  1. WebMD: Chronic Pain Guide: http://www.webmd.com/pain-management/guide/narcotic-pain-medications []
  2. Contemporary Clinical Opioid Use: Opportunities and Challenges * W. L. Lanier and E. D. Kharasch
    Mayo Clin Proc. July 1, 2009 84(7):572-575 []
  3. That statement is only half tongue-in-cheek, by the way. []
Posted in Featured, Living with Pain, health&wellness | Comments closed

Sometimes It’s Just Not Possible

I was browsing a support forum when someone asked about apidexin. I was thinking of chiming in with everyone else that the best way to lose the weight is to exercise and monitor what kind of foods go into your belly. Then I remembered that I hate those kinds of spiels. I always have. “Well, if you only…”. So easy for someone on the outside of their body to say that. And, of course, the cliché of “Everyone is unique” popped into my mind to replace my original thought. Who am I to advise someone to stop trying different methods of weight loss? How do I know what they’ve tried and which have failed?

It really hits home for me this week because I’ve been fighting a terrible flare. Today I couldn’t even pull Mags in her wagon from the back yard to the front walk. I was exhausted just from that little bit of walking. I actually had to disappoint my child because I couldn’t continue any further. It was physically impossible for me to do so. So, there went my plan for moderate exercise today. My body refused to cooperate and I was left languishing on the couch the rest of the day. My husband cooked dinner for us and he’s nothing if not the king chef of out-of-the-box cooking. I only ate a little, but what went into me was full of calories, fat and sodium. I couldn’t do the cooking. I couldn’t even stand up for longer than 3 minutes. I had no choice but to eat what the dear man put on my plate.

Who am I to tell someone else to get up and move when I can’t do the same? What if that person is in the same, or similar, position as I have been for the past few days? My words would be cruel and cause too much pain. Yes, it’s better to get up and get around, but it’s not always feasible. Sometimes a person is not physically able to do that.

And if that person is physically disabled because of obesity, for instance, then more power to them for choosing diet pills and/or surgery. After they’ve lost a significant amount of weight, then exercise will be more realistic because it will be less of a real, physical struggle. I can empathize with someone whose knees won’t permit them to walk around the block—whether from a chronic disease or their weight (wherever it originated from). I can feel the exhaustion, humiliation and frustration of someone who can’t walk just one more step. I’ve been there. It would be completely unfair of me to assume that I’m the only one who struggles to find the physical strength to do even the most mundane exercise.

I am jealous, though, of those that will someday lose a great amount of weight and suddenly have more energy and strength than they’ve had in however long. They will lose the pounds, their hearts will (quite literally) rejoice and they’ll have a renewed lease on life and it doesn’t matter if that started with pills (I hope they’re healthy pills), surgery or whatever. If weight and the issues related directly to that weight are the only problems they have in that regard, then I am terribly jealous. I’ve got about 15 pounds to lose. Not much, in the scheme of things. And when I lose that I will still have the FMS and CFS1 and will still fight bouts of severe depression. Shoot, when I’m finally healed from my accident, I will still have all of this. And when I’m at a healthy weight I will still have days like today, stuck on the couch wanting to be in the kitchen but unable to do so. It would be, I think, petty and a little selfish of me to mention that in the particular forum of which I’m speaking. And maybe it’s a little petty and selfish here. But I wish the only thing I needed to do to be healthier was lose the weight. If that was the case I wouldn’t hesitate to try whichever miracle pills I could find. You can believe that.

By the way, I’ve lost 5 pounds since I’ve begun my newest journey. Of course, I over extended myself the first week and am now paying the price, but it’s still something. If I can recover from this flare before I regain that 5 pounds and then lose a few more before the next flare it’ll be a job well-done for me.

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  1. Chronic Fatigue Syndrome []
Posted in Living with Pain, health&wellness | Comments closed

Next Time I Won’t Miss It

I mentioned on my other blog that I was out researching Price Pfister faucets when I missed a golden opportunity. Now, I didn’t want to go into details over there because I didn’t feel it was the proper venue for telling such a tale. This is my personal blog where I chronicle my trials and tribulations with my family, illness and career goals (and possibly my accomplishments, which have to date been few and far between). So, I’ll expand a little here.

On Tuesday I had the opportunity to participate in a conference call with Sharon Gless and Bruce Campbell, two stars from USA Network’s "Burn Notice". I don’t get paid by USA Network for anything I write about regarding them. I do my little bit of work with a marketing company that works with them because I am honored to have been chosen to do so (someone from the company ran across the work I was previously doing on Bella Online and contacted me via them). I have the opportunity to pre-screen shows as well as interview people working on those shows. Again, I am grateful for the opportunity to work with them. Especially because “Burn Notice” is one of my favorite shows. At any rate, I was unable to participate in the call, but they were kind enough to give me a transcript of the question/answer session. I was so incredibly disappointed that I missed that chance and am kicking myself for it.

You see, Grump doesn’t take my ambitions and goals seriously. And so neither does any of his family. His mother will gladly keep Mags for him while he’s at a VFW meeting, but will find 1000 reason to deny me when I want someone to watch her while I’m doing my work. Because I don’t get paid to write about “Burn Notice” or any of the other programs (“The Cleaner” and “The Andromeda Strain” are two others about which I’ve written) they don’t see it as “serious”. They believe that I’m just wasting my time.

Now, my mother-in-law works in realty. She’s quite good at it and has a good clientele. She makes good money. But she does things to increase her exposure and improve her “brand” that actually cost her money and for which she doesn’t immediately see a return. She’s done this for years and so has become quite successful. I’ve tried to explain to her that I, too, would like to one day become successful in my chosen field and that one of the ways to do this is through exposure and “working” for pretty much nothing. I explained that some of the work I do via my blogs do pay me, though I’m not getting rich, but that work helps pay the bills that will eventually allow me to receive more money in the long run. I explained that this is important to me and for my future goals. Grump poo-poos my time online and sees no reason why I would need a babysitter while I’m at home—even though I would be on the phone and need that time to be uninterrupted. Neither of them are capable, I think, of seeing the long-term benefits. And that’s very frustrating to me.

The good news is that Mags will start school in a couple of weeks. That will give me plenty of time during the day to do the work I want to do and see where that takes me. I’m also in school so that I can earn a degree and possibly have a career in something completely unrelated. So I’ll have that too. While I’m waiting for all of this to come to fruition (and struggling with my disease on top of it all!) I also have a brick-and-mortar job that helps pay the bills. I’m not lazing around watching soaps all day and being unproductive. I’ve got goals and need to be able to work on reaching those goals—at the same time I’m meeting my responsibilities as a mother and wife. I believe that I’m due a little leeway and understanding here.

I understand that this post seems to be more whining than anything. It’s not. I’m frustrated. I was so proud to be contacted by that marketing firm because of the writing I am capable of doing (though you wouldn’t know it to read me the last few months, would you) and I really want to participate in their campaigns—regardless of the lack of monetary payment. I did something that was recognized as good and capable and asked to participate in something. That made my head swell to gigantic proportions. It’s upsetting to me that my spouse and family fail to recognize how this is important to me. And so I vent. Hopefully I won’t need to do that much longer and will be able to post my accomplishments more (as I have more time to concentrate on my writing). I’m looking forward to that. My initial plan was to take classes during the day—while Mags is in school, but that’s changed.

I’ve decided that I’ll be taking two nights of classes and working during the day. My brick-and-mortar job only requires a few hours a week at a time (for which I make pretty decent money in this area: $1,200 a month) and I’ll be able to that primarily on weekends. I’ll find the time for all of that and still be able to mother Mags in the evening and weekend afternoons. I’ve wasted plenty of life not doing what I want to do and doing for other people what they expected of me. I don’t think that it’s so bad that I do for myself with this free time I’ll finally have. Grump won’t even know that I’m not going crazy trying to find 5 full minutes to type up a post. Then maybe we’ll both be happier.

I wish, though, that I could have participated in that conference call. Next time, if I’m offered the opportunity, I’ll be the first one to call in. For sure I won’t miss that again. If only for myself so I can say I did it. That’s really important to me at this point.

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Posted in family, meta, sinful pleasures, writing gigs | Comments closed
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