BriterSide
10-30-2003, 02:09 PM
I am starting to get concerned about the levels of pain medication I am on and not getting any relief. I have an appt tomorrow a.m. with my pain dr. and need to ask to have my dose increased. I have had a 4 level fusion with rods and screws 2 years ago and since been in a lot of pain. After having several different types of nerve blocks I have gotten no relief. I am on Oxycontin 60 mg 2 x's day and percocet 1-4 x's day and do not get relief. Does this seem like a high dose? I am not sure. I know I must be developing a tolerence but how much more can they increase my meds before its dangerously high? I appreciate any input. I am new to the boards but have learned so much from the few times I have read.
Thank you!!
Thank you!!
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susieq03
10-30-2003, 02:29 PM
Hello, Read your post and just wanted to tell you that I have been on Oxy for about a year and my dose is 3-4 40's 3x a day(360mg. a day) and am taking ms contin ir for any breakthru pain. I feel as if I am on a very high dose, but have been at this dose for quite awhile and it seems to really help with my chronic pain. Good luck and may God Bless you,SusieQ
BriterSide
10-30-2003, 02:45 PM
Susie - Thanks for your reply. I thought oxycontin was a 12 hour med. I really feel it only last me 6-7 hours if that and tnen it only takes a little edge off the pain. I have a great PM doc and everytime he sees my films of all the hardware they put in my lumbar spine, he literally gets excited and calls all the med students in too look at them. He says that what makes a dr.s day when they can see something that profound. I hope to get my does increased and maybe ask to take it 3 x's daily. I work full time in an office and sitting in this chair is no picnic. Is oxy IR stronger than percocet? Take Care
RubySlippers
10-30-2003, 02:59 PM
Briter,
Although I'm not taking as high a dose of oxy as you - 20mg 3x day - I wanted to let you know that it does NOT last the whole 12 hours...for me it usually lasts about 6 hours. I take one at 5 am, one at around 11-12 depending on pain level, then the last one around 5 pm.
I also take vicodin 5/500 1 1/2 in between for b/t pain. The pain never goes away.
I too sit in a chair all day and you're right...it's no picnic. Today I'm feeling exta bad :( It's one of those really bad pain days.
My pain is in my stomach and I use a heating pad almost all day...seems to help a bit.
Anyway, just wanted to reasure you that oxy's do not last 12 hours.
Have as pain free a day as possible :)
Angela
Although I'm not taking as high a dose of oxy as you - 20mg 3x day - I wanted to let you know that it does NOT last the whole 12 hours...for me it usually lasts about 6 hours. I take one at 5 am, one at around 11-12 depending on pain level, then the last one around 5 pm.
I also take vicodin 5/500 1 1/2 in between for b/t pain. The pain never goes away.
I too sit in a chair all day and you're right...it's no picnic. Today I'm feeling exta bad :( It's one of those really bad pain days.
My pain is in my stomach and I use a heating pad almost all day...seems to help a bit.
Anyway, just wanted to reasure you that oxy's do not last 12 hours.
Have as pain free a day as possible :)
Angela
RubySlippers
10-30-2003, 04:01 PM
Briter...
I got to thinking...I also wanted to say that I have only been on oxy for about 4 months. I started at 10 mg 2x day and quickly needed the increased dose.
I've seen many posts on this board of people who need a much higher dosage due to tolerance, pain issues, etc.
I guess I just wanted to let you know why my dosage is low, and that you probably need a much higher dosage to control your pain.
Angela
I got to thinking...I also wanted to say that I have only been on oxy for about 4 months. I started at 10 mg 2x day and quickly needed the increased dose.
I've seen many posts on this board of people who need a much higher dosage due to tolerance, pain issues, etc.
I guess I just wanted to let you know why my dosage is low, and that you probably need a much higher dosage to control your pain.
Angela
Shoreline
10-30-2003, 04:09 PM
Hi Briter side, The only dose that is too high is one that impairs or hinders your ability to function rather than increases.
Your dose may appear high to an opiate naive person that has always gotten relief from 1 Vicodin. But we are a different population where there is no such thing as a ceiling dose unless a dangerous preservative is used in the pure LA opiate.
For instance, Avinza, the 24 hour new LA morphine product has Fulmaric acid as a preservative so the dose is limited to 1600mgs of morphine per day. Not that you couldn't take a couple hundred mgs of MSIR on top of the Avinza.
You are nowhere near that amount.
I don't know of any LA opiate that has a ceiling as far as pure opiate aside from Demerol. It can build up a metabolite that cause seizures.
Most people do stabilize eventually or at least stabilize to the point that only slight adjustment need to be made. I'm on a much higher dosage of methadone but have been very stable for almost 4 years now. I can switch to an equienalgesic dose of morphine and switch right back to the same dose of methadone. Sometimes rotating opiates can help slow tolerance, particularly rotating BT meds.
When one starts to become ineffective I switch to another for a few months and then can switch back and get better relief this way. We all have a med that works best but sometimes need to switch to avoid cross tolerance, I don't believe in that particular theory. That if your tolerant to a particular dose of Oxy you wouldn't recieve better relief from an equianalgesic dose of say morphine.
If your not getting relief you reach a point where it really you really can't focus on number of mgs, so what if it takes 200mgs or 800mgs a day. If you function better and can handle the side effects than the dose is appropriate.
Limiting your dose to prevent tolerance will just make the next working dose that much higher. Say a 40 mg increase after 2 years would help but your doc makes you wait an extra 6 months, by then you may need an extra 100mgs to bring your level of pain under control.
There is no chart that says a 2 level fusion should take X and a 4 level Y and a 6 level Z to relieve the pain.
I'm fused from L1-S1 and have just broken another screw on this set of hardware. Fusion's tend to cause a domino effect of deterioration. I bet your doc didn't tell you that. The tend to put a heap of stress above and below.
I know exactly what your going through. I started with 3 levels and 2 surgeries later I was up to 6. L1-S1 IT can't go lower and I won't go any higher so we live the best we can with the help of meds, that is if they help and don't just sedate you. Don't get hung up on mgs if it improves function.
You also have to realize that meds have their limits. No amount will enable me to tolerate being on my feet the way I could before the last failed fusion after I broke that set of hardware.
I went from bed ridden to managing the house, cooking and cleaning and shopping. Only because I can take 12 hours to do 2 hours worth of work and I have the ability to manage a high level of pain and some freedom with BT meds. Often I'll take 90mgs of MSIR just to bring brfeakthrough pain back down to a level I can catch my breath.
My wife can't even tell when I have taken BT meds nor ayone that knows me. You do become tolerant to side effects or any euphoria but the anelgesic effects last much longer.
Acknowledge your limits but the number of mgs doesn't reflect anything, especially level of function. Those numbers are different for everyone.
I agree twice a day dosing of OxyC is a terrible way to live, UP and down, up and down. You may do better at 40mgs TID and sustain a steadier serum level with less highs and lows.
Welcome and good luck. IF your doc is at his level of comfort and has nothing else to offer it's time to change docs if you believe increasing your meds will increase your level of function and your doc isn't willing to try. I'm sure you understand the difference between dependence and addiction. You are already dependent so what does it matter if your dose is 40mgs TID or 100mgs TID. IF you think more surgery can't hurt, believe me it can. Unimaginable can become very imaginable.
If you increase and only create more side effects than you decrease back down or change to a different med.JMO
Do you have a lot of leg pain or nerve pain or just that crushing back pain above and below the fusion? Different types of pain respond to different types of meds.OxyIR is just Oxycodone without apap. Roxicodone comes in 15mg and 30 mgs. MSIR comes in 15 and 30 mg too.
Often a differnt BT med from your Base med will hit a broader range of opiate receptors and provide better anelgesia. If your taking OxyC as your base med why not try MSIR, morphine sulfate for BT pain.
Someone else that's been Pedicle screwed,
I know what you mean about Xrays. I have broken screw tips embedded in L5 and L2 from my last set of hardware that snapped and couldn't be backed out. A fresh broken screw head that just floats and horizontal cross bars on every level they could get 2 screws in to prevent twisting, along with the verticle harrington rods and 9 remaining good screws.
When the fusions fail , the harware eventually fails too because it's not meant to bear the weight indefinitely.I call it Jacob's ladder.I expected more out of titanium. Shore
[This message has been edited by Shoreline (edited 10-30-2003).]
Your dose may appear high to an opiate naive person that has always gotten relief from 1 Vicodin. But we are a different population where there is no such thing as a ceiling dose unless a dangerous preservative is used in the pure LA opiate.
For instance, Avinza, the 24 hour new LA morphine product has Fulmaric acid as a preservative so the dose is limited to 1600mgs of morphine per day. Not that you couldn't take a couple hundred mgs of MSIR on top of the Avinza.
You are nowhere near that amount.
I don't know of any LA opiate that has a ceiling as far as pure opiate aside from Demerol. It can build up a metabolite that cause seizures.
Most people do stabilize eventually or at least stabilize to the point that only slight adjustment need to be made. I'm on a much higher dosage of methadone but have been very stable for almost 4 years now. I can switch to an equienalgesic dose of morphine and switch right back to the same dose of methadone. Sometimes rotating opiates can help slow tolerance, particularly rotating BT meds.
When one starts to become ineffective I switch to another for a few months and then can switch back and get better relief this way. We all have a med that works best but sometimes need to switch to avoid cross tolerance, I don't believe in that particular theory. That if your tolerant to a particular dose of Oxy you wouldn't recieve better relief from an equianalgesic dose of say morphine.
If your not getting relief you reach a point where it really you really can't focus on number of mgs, so what if it takes 200mgs or 800mgs a day. If you function better and can handle the side effects than the dose is appropriate.
Limiting your dose to prevent tolerance will just make the next working dose that much higher. Say a 40 mg increase after 2 years would help but your doc makes you wait an extra 6 months, by then you may need an extra 100mgs to bring your level of pain under control.
There is no chart that says a 2 level fusion should take X and a 4 level Y and a 6 level Z to relieve the pain.
I'm fused from L1-S1 and have just broken another screw on this set of hardware. Fusion's tend to cause a domino effect of deterioration. I bet your doc didn't tell you that. The tend to put a heap of stress above and below.
I know exactly what your going through. I started with 3 levels and 2 surgeries later I was up to 6. L1-S1 IT can't go lower and I won't go any higher so we live the best we can with the help of meds, that is if they help and don't just sedate you. Don't get hung up on mgs if it improves function.
You also have to realize that meds have their limits. No amount will enable me to tolerate being on my feet the way I could before the last failed fusion after I broke that set of hardware.
I went from bed ridden to managing the house, cooking and cleaning and shopping. Only because I can take 12 hours to do 2 hours worth of work and I have the ability to manage a high level of pain and some freedom with BT meds. Often I'll take 90mgs of MSIR just to bring brfeakthrough pain back down to a level I can catch my breath.
My wife can't even tell when I have taken BT meds nor ayone that knows me. You do become tolerant to side effects or any euphoria but the anelgesic effects last much longer.
Acknowledge your limits but the number of mgs doesn't reflect anything, especially level of function. Those numbers are different for everyone.
I agree twice a day dosing of OxyC is a terrible way to live, UP and down, up and down. You may do better at 40mgs TID and sustain a steadier serum level with less highs and lows.
Welcome and good luck. IF your doc is at his level of comfort and has nothing else to offer it's time to change docs if you believe increasing your meds will increase your level of function and your doc isn't willing to try. I'm sure you understand the difference between dependence and addiction. You are already dependent so what does it matter if your dose is 40mgs TID or 100mgs TID. IF you think more surgery can't hurt, believe me it can. Unimaginable can become very imaginable.
If you increase and only create more side effects than you decrease back down or change to a different med.JMO
Do you have a lot of leg pain or nerve pain or just that crushing back pain above and below the fusion? Different types of pain respond to different types of meds.OxyIR is just Oxycodone without apap. Roxicodone comes in 15mg and 30 mgs. MSIR comes in 15 and 30 mg too.
Often a differnt BT med from your Base med will hit a broader range of opiate receptors and provide better anelgesia. If your taking OxyC as your base med why not try MSIR, morphine sulfate for BT pain.
Someone else that's been Pedicle screwed,
I know what you mean about Xrays. I have broken screw tips embedded in L5 and L2 from my last set of hardware that snapped and couldn't be backed out. A fresh broken screw head that just floats and horizontal cross bars on every level they could get 2 screws in to prevent twisting, along with the verticle harrington rods and 9 remaining good screws.
When the fusions fail , the harware eventually fails too because it's not meant to bear the weight indefinitely.I call it Jacob's ladder.I expected more out of titanium. Shore
[This message has been edited by Shoreline (edited 10-30-2003).]
BriterSide
10-30-2003, 04:12 PM
Angela - Thanks...I have been on oxy since my 3rd surgery, 2 yrs ago and also started out at a very low dose. If I can remember I think it was 10 mgs 2x's a day. I don't want to take too much and I am sure my dr. would not prescribe an overdose. I wanted to get a feel for what other people were on. I am in constant pain and it used to help alot, but lately it's like taking pills for nothing. Hope your stomach is better. I also have crohns and had surgery on that last summer for the 3rd time. So I know how awful stomach pain can be. Those gel heating pads are great, just don't over do it, that makes it worse. Today is bad for me also, I am counting the minutes til I can get in my car, drive home, run to my big bed and lay flat. How pathetic is that! On such a beautiful day! Oh well, maybe tomorrow will be better for all.
Thanks again!
Thanks again!
BriterSide
10-30-2003, 04:33 PM
Shore - that was quite a detailed response. I appreciate you sharing your knowledge. I don't want to sound like and idiot, because I have been on meds a long time, but never asked to have them increased, the have always automatically increased them after the blocks did nothing. "Crushing Back Pain" thats exactly what I have, and also nerve pain. I can touch several parts of my back and get shocks down about 8-10 inches where I pressed. The PM dr. says its from having all the nerves cut so many times and from all the scar tissue. It's very disturbing. I also get a shock in my foot when I am walking and also down my leg. Weird Hugh! Maybe they did turn me into the Bionic Woman! hahah. Anyways, I appreciate your input and my Dr. is great and will try to make me comfortable. I know a 20 mg.2x's a day increase is what I need becuase sometimes when its unbearable I do take an extra but have to be careful I don't run out. So wish my luck tomorrow. I also am getting the results of my MRI which will show if there are further disc tears above the fusion site. No more surgery for me.
Briter
Briter
chriztene
10-31-2003, 09:29 AM
Shoreline,
I am printing out your post and saving it for future reference. Thank you for the time regarding the dose amounts of opiates ~ it's really appreciated.
I didn't realize changing your bt med from your base time release medication would have greater analgesic benefits. I will ask my doctor about this as I take the same bt med as my base med.
Also, it was interesting to read other posters time release medication lasting around 6-7 hours. I, too, have experienced my time released med lasting about 7 hours.
I am curious regarding the manufacturer's prescribing information stating they last for 12 hours? This seems to me, a 5 hour difference is more than a little discrepancy.
I am interested in your views in regard to the above?
Warmest Regards,
~C
I am printing out your post and saving it for future reference. Thank you for the time regarding the dose amounts of opiates ~ it's really appreciated.
I didn't realize changing your bt med from your base time release medication would have greater analgesic benefits. I will ask my doctor about this as I take the same bt med as my base med.
Also, it was interesting to read other posters time release medication lasting around 6-7 hours. I, too, have experienced my time released med lasting about 7 hours.
I am curious regarding the manufacturer's prescribing information stating they last for 12 hours? This seems to me, a 5 hour difference is more than a little discrepancy.
I am interested in your views in regard to the above?
Warmest Regards,
~C
BriterSide
10-31-2003, 01:46 PM
Hello eveyone and Happy Halloween! My Dr. visit went well I think. My MRI results were not great. I have spinal stenosis and also herniated disc above where I had the 4 level fusion at L3-L2, which is not good. He did increase my Oxycontin from 60 to 80 mgs. 2 x's a day and also prescribed Topamax. Has anyone had results with this? The phamisist said it's an anti seizure med but used for different things. The doc was hesitant to prescibe because I am thin but he started me at a low dose only at night to maybe help me sleep. He also wants to ry another round of blocks of facet joints. The sun is shinning and warm in NY today and the sun usualy helps a little. I appreciate all your insight Shore. You seem to have your share of pain issues also and I wish you the best (everyone). Have a great day and try to look on the briteside. The one thing that keeps my spirits up is thinking my condition could be worse.
BriteSide!!
BriteSide!!
callie3
10-31-2003, 05:40 PM
Briterside,
I am currently on Topamax 25mg 2x a day for nerve pain. It has helped in the month I have been on it but the side effects are enough to make you think you are going crazy until you adjust to it. Start slow(25 mg doses and give your body a chance to adjust. Expect dizziness,extreme thirst(soda's will taste so nasty)loss of appetite,loss of memory(I forgot how to do a job I have been doing for 4 years)(I really had to concentrate for about 2 weeks until I got used to the 50 mg a day). You literally "forget" things you have always known. Your fingers,toes, and lips may tingle(this goes away),you slur your speech,you speak and the wrong word will come out(this goes away too) but most of these side affects took about 2 weeks to actually abate. A nickname for Topamax is "Dopamax" or "Stupidmax" because for about 2 weeks and everytime they increase your dose you have to go thru the side affects again and you really appear stupid!!!. I thought I was going crazy!!!Another s/e not mentioned on the pamphlet is hair loss!! If you begin taking Topamax, go to Walmart or Target and get Biotin(3000 mcg a day) b12, and selenium and Nioxx shampoo is said to help. I also found a board at EZ boards called Topamax Talks devoted to uses of this drug(a member here recommended it and many of the healthboards members are members there also)Topamax is used for migraines,nerve pain, bipolar and seizures so there are many different reactions both pro and con to this drug. Good luck and do lots of research. Like I said, I have noticed a BIG difference in my nerve pain but the side affects those fisrt 2 weeks almost did me in!!!!
I am currently on Topamax 25mg 2x a day for nerve pain. It has helped in the month I have been on it but the side effects are enough to make you think you are going crazy until you adjust to it. Start slow(25 mg doses and give your body a chance to adjust. Expect dizziness,extreme thirst(soda's will taste so nasty)loss of appetite,loss of memory(I forgot how to do a job I have been doing for 4 years)(I really had to concentrate for about 2 weeks until I got used to the 50 mg a day). You literally "forget" things you have always known. Your fingers,toes, and lips may tingle(this goes away),you slur your speech,you speak and the wrong word will come out(this goes away too) but most of these side affects took about 2 weeks to actually abate. A nickname for Topamax is "Dopamax" or "Stupidmax" because for about 2 weeks and everytime they increase your dose you have to go thru the side affects again and you really appear stupid!!!. I thought I was going crazy!!!Another s/e not mentioned on the pamphlet is hair loss!! If you begin taking Topamax, go to Walmart or Target and get Biotin(3000 mcg a day) b12, and selenium and Nioxx shampoo is said to help. I also found a board at EZ boards called Topamax Talks devoted to uses of this drug(a member here recommended it and many of the healthboards members are members there also)Topamax is used for migraines,nerve pain, bipolar and seizures so there are many different reactions both pro and con to this drug. Good luck and do lots of research. Like I said, I have noticed a BIG difference in my nerve pain but the side affects those fisrt 2 weeks almost did me in!!!!
igy76
10-31-2003, 08:02 PM
Hi BRITERSIDE,
If you may benefit from it, I also wanted to quickly throw in my knowledge of Topamax. I was taking it recently for nerve pain. I cannot agree with Callie enough (in fact, I think she was one of the people who really helped me when I was on it :) that you must titrate your dosage slowly. Although sorry to say even then, you most likely will be at risk for the side effects. Callie covered most of them, but one very important one I also wanted to make you aware of is the depression. Please don't let me scare you or anything, you may not even experience it (believe it or not, for all the s/e this drug has, some lucky people don't get ANY of them!), but from what I'm learning most people do. It took me awhile to realize the validity in this, and thankfully I had a friend explain it very simply (because it also sort of ties in with the slowed thinking): Topamax slows your cognitive abilities, which means the neurons in your brain are firing slower, which in turn means the serotonin is being produced at a much slower rate (serotonin is the chemical in your brain that's basically responsible for you being happy, up, etc), which biochemically will cause depression. It's just something I want you to be aware of, because although for me it was gradual because I was already sort of depressed before I took it, it hits some people like a brick wall, out of nowhere. I also experienced a massive amount of apathy, and for a few days was annoyned that anyone was simply talking to me. So, I started at 50mg/day, then every week added 50mg so that by the end of 1 month was on 200mg/day. But it didn't seem to be helping my nerve pain a lot (and weighing against all the s/e I was experiencing) my doc thankfully took me off it.
But again - PLEASE DON'T LET ME SCARE YOU, THAT IS NOT MY INTENT. A good amount of people find Topamax a lifesaver for their pain, and can easily cope with whatever side effects they experience. And thanks to a few particular people on here, I made it through the rough spots without jamming a pencil in my ear (um... just kidding... mostly ;) So good luck and I hope you feel better! :)
If you may benefit from it, I also wanted to quickly throw in my knowledge of Topamax. I was taking it recently for nerve pain. I cannot agree with Callie enough (in fact, I think she was one of the people who really helped me when I was on it :) that you must titrate your dosage slowly. Although sorry to say even then, you most likely will be at risk for the side effects. Callie covered most of them, but one very important one I also wanted to make you aware of is the depression. Please don't let me scare you or anything, you may not even experience it (believe it or not, for all the s/e this drug has, some lucky people don't get ANY of them!), but from what I'm learning most people do. It took me awhile to realize the validity in this, and thankfully I had a friend explain it very simply (because it also sort of ties in with the slowed thinking): Topamax slows your cognitive abilities, which means the neurons in your brain are firing slower, which in turn means the serotonin is being produced at a much slower rate (serotonin is the chemical in your brain that's basically responsible for you being happy, up, etc), which biochemically will cause depression. It's just something I want you to be aware of, because although for me it was gradual because I was already sort of depressed before I took it, it hits some people like a brick wall, out of nowhere. I also experienced a massive amount of apathy, and for a few days was annoyned that anyone was simply talking to me. So, I started at 50mg/day, then every week added 50mg so that by the end of 1 month was on 200mg/day. But it didn't seem to be helping my nerve pain a lot (and weighing against all the s/e I was experiencing) my doc thankfully took me off it.
But again - PLEASE DON'T LET ME SCARE YOU, THAT IS NOT MY INTENT. A good amount of people find Topamax a lifesaver for their pain, and can easily cope with whatever side effects they experience. And thanks to a few particular people on here, I made it through the rough spots without jamming a pencil in my ear (um... just kidding... mostly ;) So good luck and I hope you feel better! :)
igy76
10-31-2003, 08:18 PM
CALLIE-
I'm trying to find that Topamax Talks board you were talking about through Google, but to no avail. I'd REALLY like to find it, I have a friend that it might really help. If you wouldn't mind, can you at least give me a hint on how to find it? Like how you did? Thanks!
[This message has been edited by igy76 (edited 10-31-2003).]
I'm trying to find that Topamax Talks board you were talking about through Google, but to no avail. I'd REALLY like to find it, I have a friend that it might really help. If you wouldn't mind, can you at least give me a hint on how to find it? Like how you did? Thanks!
[This message has been edited by igy76 (edited 10-31-2003).]
Shoreline
10-31-2003, 10:12 PM
Hey Christine, As far as Oxycontin lasting 12 hours, no way no how. Purdue compares taking a 10mg OxyContin as maintaining serum levels similar to taking one percocet every 6 hours. Anyone that's had surgery knows percs don't last 6 hours.
The way the time release mechanism works with Oxy is that it releases about half it's contents at the like 1hour and 15 minutes and the second half at about the 6th hour.
If your pain spikes beyond the ability of the second release to bring it back in check it will certainly have the appearance it doesn't last 12 hours. This doesn't mean taking additional meds during the twelve hours of that first oxy won't have a combined effect with what remains in your system. I would feel overlap after 8 hours from meds but on it's own the last 4 hours are miserable without BT meds or more frequent dosing.
Maintaining specific blood levels for 12 hours doesn't necessarily equate to how long the analgesic action will last. Letting pain spike and trying to bring it back down after it''s out of control has no medical benefit. The design is definitely flawed and you have to wonder about the raw data they created to sell this to the FDA as a 12 hour med.
For example, Methadone has a 30 hour half life, Giving you the impression you will get prolonged relief, however when dosed for acute pain the recomended interval is Q4, it's given every 4 hours.
If serum levels are the end all answer to how long a medication provides anelgesia then even the most acute pain would benefit from a med that still has half it's serum level at 30 hours. There are suggested guides for effective anelgesic serum levels of methadone that show more frequent dosing is neccesaary to keep acute pain in check that show 4 hour dosing is appropriate for acute pain.
As far as I know Purdue has done no such study to coralate serum levels to pain relief.However Purdue has stuck to their guns on this 12 hour dosing. Manufacturer reps have called on or notified every PM doc and pharmacist that OXyC should not be prescribed more frequently than Q12. They won't allow it for their patient assictance program. THere are ways around this and ways to convert your BID dosing into TID dosing which would provide smoother more effective serum levels.
I've tried taking larger doses hoping it would last longer, I've seen dozens of docs do the same thing and acheive absolutely no benefit. A higher doses
of OxyC at twice a day dosing does not solve the duration problem.
You are better to adjust yourself to what works as long as you don't go beyond the prescribed daily dose.In the long run your daily dose will be minimized if your doc works with you providing the right size pills he can still order it BID and have you take it TID. 60mgs BID can easily be changed to take two 40's in the am and one in the PM. The doc tells you to take 40 TID but writes the scripts in a way that won't deviate from the manufacturer's recommendation.
I've seen docs think that because Oxy only is available now in an 80mg pills that is the most they can prescribe. 80mgs twice a day. This is just ridiculous but some docs are so afraid to deviate from the manufacturers recommendation their patients suffer.
Purdue tested Oxy Up to 320 mgs per day. There is no ceiling once a patient becomes safely accomadated to the med. Meth is trickier because of the half life but there truly is no ceiling or toxic build up that damages organs. More people die each year from taking too much APAP or OTC NSAIDS like motrin and aleve.
17,00 people each year die from OTC meds just trying to find relief. A few hundred deaths from Oxyc over 3 years is hardly a large number for the #1 prescribed pain med. I'm not sure they can still make that claim but morphine is safer than Tylenol by a long shot.
I consider my pain acute and long lasting, I don't buy the whole chronic pain is that different from acute pain other than the psychological effects CP has.My pain rsponds the same way acute pain rsspnds to opiates. Acute pain is a breeze when you know you will feel better in 3-4 days. You don't have near the issues in dealing with acute pain other than the idea acute requires more frequent dosing.
I feel meth wear off in 4-5 hours and require redosing, but after 4 doses in my system I guess I reach the combined serum level of repeated dosing and have no problem coasting through the night longer than I do in the day. I have BT meds for extra night pain.
My dose has been stable for years and rotating BT meds and hitting a broader range of receptors can't possible do anything but help manage pain.
I know folks that have only been able to climb out of the bed by combining 3 long acting opiates, Meth, Kadian and 4 100ugh Duragesic patches. That's what it takes to manage his pain. I know what he's dealing with and know his wife and have no doubt his goal is to simply live his life and function to the best of his ability thanks to a knowledgeable doc that understands the benefits of combining opiates.
His doc is a CP patient herself which certainly gives her a different perspective. PM docs believe they don't have to have experienced severe pain to treat it but it has to give them a perspective only a CP patient has. Mgs don't matter. ;)
As far as Toppamax, Finding the right med to treat burning nerve pain is just as tough as finding the right opiate. There are plenty of choices. using anti seizure meds for nerve pain is very effective for some people. It is an off label use for anti seizure meds but the way it was described to me it was like the med would remove every other letter out of each word in a sentance. Doing this disrupts the pain signal. I know people that had shingles that swear antiseizure meds saved their life. They do tend to be mind numbing in the beginning or once you reach your limit. Fortunately surgery relieved my burning nerve pain. I have numbness from the waste down but numb is better than on fire.
I understand completely not wanting to even get into the cycle of nerve blocks every 6 months for minimal help. So what, it's not worth getting your nerve branches skewered every 6 months and during each test. Being fused 6 levels they did 12 test blocks at once on me and that was enough lighting my legs up for a lifetime.
I wouldn't do the blocks as long as relief can be obtained through less invasive methods. They have their place but you can't slam every square peg into a round whole. They do cause scarring and I already have enough to bend a large gage needle. serriously. PT for scar management is a must and PT for myofacial release is worth it's wait in gold if you have the right therapist.
My bro had surgery 3 months ago and is stiff as a board and this was just a lami/iscectomy. No fusion so PT couldn't possibly hurt him , and the doc doesn't believe in PT. He thinks it can all be done at home, and this is the chief of Neurosurgery at Duke. The scar management alone is worth it.
Every doc has their own ideas, and that's all they are. No more valid than someone that has the ability to research their own problem and be proactive in their care.He should have his PCP order the PT since his surgeon is so ignorant about the benefits. I guess he thinks he's the cure all. Don't let a doc do this to you and condemn you to pain for the rest of your life.
Take care, Shore
[This message has been edited by Shoreline (edited 10-31-2003).]
The way the time release mechanism works with Oxy is that it releases about half it's contents at the like 1hour and 15 minutes and the second half at about the 6th hour.
If your pain spikes beyond the ability of the second release to bring it back in check it will certainly have the appearance it doesn't last 12 hours. This doesn't mean taking additional meds during the twelve hours of that first oxy won't have a combined effect with what remains in your system. I would feel overlap after 8 hours from meds but on it's own the last 4 hours are miserable without BT meds or more frequent dosing.
Maintaining specific blood levels for 12 hours doesn't necessarily equate to how long the analgesic action will last. Letting pain spike and trying to bring it back down after it''s out of control has no medical benefit. The design is definitely flawed and you have to wonder about the raw data they created to sell this to the FDA as a 12 hour med.
For example, Methadone has a 30 hour half life, Giving you the impression you will get prolonged relief, however when dosed for acute pain the recomended interval is Q4, it's given every 4 hours.
If serum levels are the end all answer to how long a medication provides anelgesia then even the most acute pain would benefit from a med that still has half it's serum level at 30 hours. There are suggested guides for effective anelgesic serum levels of methadone that show more frequent dosing is neccesaary to keep acute pain in check that show 4 hour dosing is appropriate for acute pain.
As far as I know Purdue has done no such study to coralate serum levels to pain relief.However Purdue has stuck to their guns on this 12 hour dosing. Manufacturer reps have called on or notified every PM doc and pharmacist that OXyC should not be prescribed more frequently than Q12. They won't allow it for their patient assictance program. THere are ways around this and ways to convert your BID dosing into TID dosing which would provide smoother more effective serum levels.
I've tried taking larger doses hoping it would last longer, I've seen dozens of docs do the same thing and acheive absolutely no benefit. A higher doses
of OxyC at twice a day dosing does not solve the duration problem.
You are better to adjust yourself to what works as long as you don't go beyond the prescribed daily dose.In the long run your daily dose will be minimized if your doc works with you providing the right size pills he can still order it BID and have you take it TID. 60mgs BID can easily be changed to take two 40's in the am and one in the PM. The doc tells you to take 40 TID but writes the scripts in a way that won't deviate from the manufacturer's recommendation.
I've seen docs think that because Oxy only is available now in an 80mg pills that is the most they can prescribe. 80mgs twice a day. This is just ridiculous but some docs are so afraid to deviate from the manufacturers recommendation their patients suffer.
Purdue tested Oxy Up to 320 mgs per day. There is no ceiling once a patient becomes safely accomadated to the med. Meth is trickier because of the half life but there truly is no ceiling or toxic build up that damages organs. More people die each year from taking too much APAP or OTC NSAIDS like motrin and aleve.
17,00 people each year die from OTC meds just trying to find relief. A few hundred deaths from Oxyc over 3 years is hardly a large number for the #1 prescribed pain med. I'm not sure they can still make that claim but morphine is safer than Tylenol by a long shot.
I consider my pain acute and long lasting, I don't buy the whole chronic pain is that different from acute pain other than the psychological effects CP has.My pain rsponds the same way acute pain rsspnds to opiates. Acute pain is a breeze when you know you will feel better in 3-4 days. You don't have near the issues in dealing with acute pain other than the idea acute requires more frequent dosing.
I feel meth wear off in 4-5 hours and require redosing, but after 4 doses in my system I guess I reach the combined serum level of repeated dosing and have no problem coasting through the night longer than I do in the day. I have BT meds for extra night pain.
My dose has been stable for years and rotating BT meds and hitting a broader range of receptors can't possible do anything but help manage pain.
I know folks that have only been able to climb out of the bed by combining 3 long acting opiates, Meth, Kadian and 4 100ugh Duragesic patches. That's what it takes to manage his pain. I know what he's dealing with and know his wife and have no doubt his goal is to simply live his life and function to the best of his ability thanks to a knowledgeable doc that understands the benefits of combining opiates.
His doc is a CP patient herself which certainly gives her a different perspective. PM docs believe they don't have to have experienced severe pain to treat it but it has to give them a perspective only a CP patient has. Mgs don't matter. ;)
As far as Toppamax, Finding the right med to treat burning nerve pain is just as tough as finding the right opiate. There are plenty of choices. using anti seizure meds for nerve pain is very effective for some people. It is an off label use for anti seizure meds but the way it was described to me it was like the med would remove every other letter out of each word in a sentance. Doing this disrupts the pain signal. I know people that had shingles that swear antiseizure meds saved their life. They do tend to be mind numbing in the beginning or once you reach your limit. Fortunately surgery relieved my burning nerve pain. I have numbness from the waste down but numb is better than on fire.
I understand completely not wanting to even get into the cycle of nerve blocks every 6 months for minimal help. So what, it's not worth getting your nerve branches skewered every 6 months and during each test. Being fused 6 levels they did 12 test blocks at once on me and that was enough lighting my legs up for a lifetime.
I wouldn't do the blocks as long as relief can be obtained through less invasive methods. They have their place but you can't slam every square peg into a round whole. They do cause scarring and I already have enough to bend a large gage needle. serriously. PT for scar management is a must and PT for myofacial release is worth it's wait in gold if you have the right therapist.
My bro had surgery 3 months ago and is stiff as a board and this was just a lami/iscectomy. No fusion so PT couldn't possibly hurt him , and the doc doesn't believe in PT. He thinks it can all be done at home, and this is the chief of Neurosurgery at Duke. The scar management alone is worth it.
Every doc has their own ideas, and that's all they are. No more valid than someone that has the ability to research their own problem and be proactive in their care.He should have his PCP order the PT since his surgeon is so ignorant about the benefits. I guess he thinks he's the cure all. Don't let a doc do this to you and condemn you to pain for the rest of your life.
Take care, Shore
[This message has been edited by Shoreline (edited 10-31-2003).]
callie3
10-31-2003, 10:21 PM
igy76,
You are so right about the depression in some people. I also got the "weepies" at times. LOL. At Google type in EZ Boards, then when it asks for your interest or topic put in topamax and it will give you Topamax Talk. You have to join EZ boards then you can apply for the community(both free) I heard about them from members at Healthboards(SeattleShea from the Backpain board told me about it) Its a great site and the people there know everything about Topamax. Some have been on it for years. They offer lots of support whether you are on it for nerve pain,migraines,bipolar or epilepsy. Topamax is a very strange drug and unfortunaatly lots of Doctors are starting to prescribe it but they really do not know the s/e's. My DR told me when I mentioned it to him that I wanted to try it that he knew nothing about it and wrote my prescription for "1 or 2 a day" so everything I have learned I have learned here and at Topamax Talk from people who have actually taken it and can tell me both good and bad what to expect. My biggest surprise was the hair loss. If I had not read it from another poster I would not have known to expect it.
You are so right about the depression in some people. I also got the "weepies" at times. LOL. At Google type in EZ Boards, then when it asks for your interest or topic put in topamax and it will give you Topamax Talk. You have to join EZ boards then you can apply for the community(both free) I heard about them from members at Healthboards(SeattleShea from the Backpain board told me about it) Its a great site and the people there know everything about Topamax. Some have been on it for years. They offer lots of support whether you are on it for nerve pain,migraines,bipolar or epilepsy. Topamax is a very strange drug and unfortunaatly lots of Doctors are starting to prescribe it but they really do not know the s/e's. My DR told me when I mentioned it to him that I wanted to try it that he knew nothing about it and wrote my prescription for "1 or 2 a day" so everything I have learned I have learned here and at Topamax Talk from people who have actually taken it and can tell me both good and bad what to expect. My biggest surprise was the hair loss. If I had not read it from another poster I would not have known to expect it.
Mo7609
11-03-2003, 10:37 AM
Hi Brite,
Boy do I know partly what you are going through. I too have spinal stenosis alond with bulging discs and everthing else. I am do for my first Facet joint injections in a few weeks as soo as the insurance co appproves it. I have had all the different kids of injection so far and none have helped. Did you find that this type of injection helped you? My Dr said that if this doesn'twork that I would most likely have a spinal fusion. Scary thought! I too take Oxycontin at 40 mg 2x a day and as everyone else says I do notice that they do not last for 12 hours. 8 is usually as long as it goes for me but my Dr won't change it just yet. So what is your opinion on ll of this. I say that you said that you have also had a fusion so was wondering what your results were regarding that and the injections. Hope you are having a good day and the meds are working for you now. Thanks for your time. :) Mo
Boy do I know partly what you are going through. I too have spinal stenosis alond with bulging discs and everthing else. I am do for my first Facet joint injections in a few weeks as soo as the insurance co appproves it. I have had all the different kids of injection so far and none have helped. Did you find that this type of injection helped you? My Dr said that if this doesn'twork that I would most likely have a spinal fusion. Scary thought! I too take Oxycontin at 40 mg 2x a day and as everyone else says I do notice that they do not last for 12 hours. 8 is usually as long as it goes for me but my Dr won't change it just yet. So what is your opinion on ll of this. I say that you said that you have also had a fusion so was wondering what your results were regarding that and the injections. Hope you are having a good day and the meds are working for you now. Thanks for your time. :) Mo
chriztene
11-04-2003, 09:14 AM
Thank you shoreline for taking the time to explain the dosing information. It's validating to know other cp sufferers also find the 12 hour dose not adequate, too.
Warmest Regards,
~C
Warmest Regards,
~C
kmail
11-06-2003, 02:06 AM
My husband started with Vicodin about 6-7 years ago. He was then prescribed Oxycontin after I did research and ASKED for it for him. Thanks God he's got a Dr. who isn't afraid to treat pain! Otherwise they would have kept him on Vicodin.
His dosage has steadily increased - I don't even remember where it started - probably 20mg / 2x per day. He is now up to 80 mg in AM, 40 mg at noon, and 80 mg at bedtime (which he usually takes even well before 6pm). And he still takes vicodin for bt pain.
NO, they do not last 8 hrs.
Also, as far as tolerance, I think he's built up quite a tolerance. But everyone is different.
And, I think it's true - the pain never goes away completely (you just might sleep through it and not notice it - or be preoccupied with whatever your doing).
Best of luck to you for a less painful day.
His dosage has steadily increased - I don't even remember where it started - probably 20mg / 2x per day. He is now up to 80 mg in AM, 40 mg at noon, and 80 mg at bedtime (which he usually takes even well before 6pm). And he still takes vicodin for bt pain.
NO, they do not last 8 hrs.
Also, as far as tolerance, I think he's built up quite a tolerance. But everyone is different.
And, I think it's true - the pain never goes away completely (you just might sleep through it and not notice it - or be preoccupied with whatever your doing).
Best of luck to you for a less painful day.

