A good person on here asked me to post a question as I and so many others seem to be having terrible side effects from the new OP formulation that Purdue Pharma put out to make tamper proof so that abusers couldn't cut them open anymore.
I started the new OP on 9/6 feeling as good as I ever can with RSD in chronic pain with this being the only long acting opiate that not only ever helped my pain but also that I wasn't severely allergic to.
A few days before Tuesday, 9/14 I felt constipated attributing it to the new OP formula. On 9/14 I began vomiting knowing it was the medication/constipation problem. I stopped vomiting but the next day woke up feeling flu like symptoms with a fever of 100.9 and what is medically called; malaise which means a general feeling of being ill also with my stomach still out of sorts.
It is now day 17 on this new OP formula and I'm not as bad as I was on 9/14 through 9/18 but I'm still daily feeling ill, having a low grade fever, and my stomach just isn't right and I feel it gets worse after the usual time that it always took for the old formulation of OC to kick in; about 1 1/2 hours.
I feel I could have the same pain relief personally if I could take the amount I'm prescribed but my stomach won't allow it along with not being able to take the Percocet for breakthrough pain; usually 3 to 4 a day but with the stomach problems, I've only been able to take one most days; maybe a 2nd.
I called my pharmacist who has had other complaints of very similar symptoms that I reported. He didn't say how many but it didn't sound good.
I've had the same pharmacist for over 11yrs and he knows me well and does talk to me.
I have thought that maybe we are having withdrawals from the old formulation and it could take time for our bodies to adjust to the new OP formulation as the compounds have changed.
I am trying to not just psych myself out due to these side effects knowing that the compound change could be the problem and give it time to see if my stomach can handle this and start feeling better in general.
My doctor knows that ALL other long acting opiates that I have been prescribed have given me serious allergic reactions so I must have an extremely sensitive system. Last year I was even put on Opana and I couldn't breathe after taking only the 1st pill.
I would have already gone off of this entirely if there were other options for me but feel I have to give it a try.
I would like anyone who is taking this new OP kind and was on the old OC formulation to post here on this question and keep up to date with any side effects or symptoms they may be having as we just need to try to help each other here.
Maybe we can figure this out together. I was only able to take the dose I'm supposed to for the 1st 8 days so I also don't know if this is going to relieve my own chronic pain the way the OC did along with my breakthrough meds.
I see my doctor soon and will have to tell her what is going on after I figured out this was not a flu bug or virus but this new OP itself.
I was extremely upset as I tried to do an online search today only to find the drug abusers trying to figure out how to cut it open to abuse it more.
The people I've met here are usually genuine and together we can help each other.
I also promise to keep you up to date on my own issues and hopefully we can start feeling better soon.
Oxycontin side effects on new OP?
- Posted:
- 23 Sep 2010 by RSDHurtzme
- Topics:
- oxycontin, pain, side effect
Added 30 Oct 2010:
Please read: If you have called Purdue Pharma and they are sending you a form to fill out over the side effects of the new OP Oxycontin, please get the lot # from your pharmacy if it's not on your prescription bottle (which usually it isn't) or they won't be able to process your claim. I just received my form after calling them before September 20th and without the lot # they refuse to make it apart of the ongoing investigation.
Call your pharmacist as soon as possible if you are going to be part of Purdue's investigation so they can help us all.
Added 29 Nov 2010:
After taking the generic Ethex version of Oxycontin made in the same way as the old formula, I've found that in only 2mos none are now available for my prescription due this week. My pharmacist said that there is NO form of generic Oxycontin available now and only had some left overs in the 80mg dose only when I'm on the 40mg dose.
I took my script for November in and was only able to get 88 of the 90 pills prescribed to me. Due to my pharmacist's fear due to severe allergic reactions to ALL other long acting opiates, my pharmacist said he feels there is NO long acting formulation of any pain medicine that I could tolerate and could only recommend the 10mgs of Oxy IR in a generic version. That is breakthrough dosage for me as I'm on 10/325 of generic Percocet for that up to 6 times a day PRN.
I have refused any increases when the original Oxycontin was out for at least 8yrs and offered to me at least 7 times due to my own fear of any medication along with the age I was injured and my age now; 43 knowing this pain is for life as I see it now.
I would give ANYTHING to not have to need a medication like this. I have put a call to my doctor in and hope to get an answer by today or early tomorrow as she mentioned a medication that starts with an "N" and I've researched everything online I can even asking my pharmacist about other meds.
I fear now that if I have to go on another med that if I'm not allergic to it, I will go through euphoria again after not having this problem for around 5 or 6yrs.
At this point, I PRAY that the new Oxycontin OP is taken off the market completely as it's their 1.5 BILLION dollar a year baby that they've held a patent on for way too long and only because of their power of keeping this patent are we left with NO generic.
IF one is made eventually, it will probably be formulated like the OP.
I see a HUGE lawsuit against Purdue for doing what they have to the people I've read about on this site/post along with how many others not on this site who must have gotten ill due to this reformulation also.
I am a responsible pain patient who has never abused my medications as are so many of you here and why do we have to pay for abusers and junkies? So far there are NO widespread news reports about so many getting sick from OP version and we need a voice; our own and together we are strong.
I can hope for us that we can pull together to get a major network to do a story about what Purdue has done to us.
Added 19 Dec 2010:
UPDATE: My doctor finally got me off of any form of Oxycontin and now taking Kadian; it's working so much better than the OC ever did.
I began taking this in early December after going without any long acting opiate for a while and ending up in a wheelchair vs on a cane.
Even though I've always been honest telling any of my doctors that I am allergic to Morphine, I explained to my Int Med Doctor that the way I found this out was at least 6yrs or more before RSD/Chronic pain during an outpatient surgical procedure and only had IV Morphine and never took a synthetic Morphine pill since becoming "opiate tolerant".
She was brave enough to give me Kadian; a Morphine pill like MS Contin but better, and I was brave enough to begin to take it finding the best pain control I've ever had in my 11 1/2yrs in chronic pain.
This all worked out for the absolute best and now able to take less medication a day bc of it.
I hope others too are finding an even better medication for chronic/severe pain.
Added 23 Dec 2010:
Before being put on Kadian, she was afraid of my allergic reactions to some of these meds and only gave me Oxy IR 30mg 6 a day. That is closer to Percocet than a strong long acting pain med. That is how I ended up on a walker before seeing her again and realizing I had to have a long acting med, she gave me Kadian capsules 100mgs which equals about 80mg of OC.
60mgs equals 30 to 40mgs of OC.
I hope this helps as I know way too many who are/have suffered from this change.
Responses (37)
Hi mrspage 82: A quick comment from Sacosams..:For what it's worth dept: As long as Big-Pharma, backed by F.D.A. grants, can continue to manufacture drugs? like this for $1.00... fool a gullible public into believing that someone there actually CARES whether you or I, live or die... [I'm a poet & don't know it.& feet show it , they're Longfellows. And we ,the gullible public continue to accept thier word as gospel, and buy that crap at $5 to $10 a copy, it will not only last ,but continue to fluorish.! ! "Uh oh!
"Ok , ok, I'm sufficiently recovered , but I gotta' get off the floor. See I read this add for a NEW DRUG (L.o.L.) & I got to chuckeling, over the name,
Sacasam, every word so poetic was so true and you made me laugh while I'm in a lot of pain; loved it and thank you.
I agree w/ you about the Big Pharma business; ads they run in the US but not allowed to in other countries pushing their next big fix or cure for someone is getting to be like the old "snake oil" salesman but they have our full attn on TV. You are sitting there trying not to focus on your pain, disease and "some guy comes on TV telling me more and more about some useless information, trying to drive my imagination; I can't get no... no, no, no; Satisfaction"; The Rolling Stones say; still so true even today.
23 Sep 2010
Unfortunately, a good medication like OC, needed to be changed in order to prevent people from abusing it and accidentally over dosing. We now know people are still dying from the new version (OP) because it doesn't seem to work fast enough. The ones who end up suffering the most are the responsible users, like you, and I can only hope the adverse side effects will subside with time. Thank you for keeping us posted on how this medication has affected you.
My best wishes,
Chris
23 Sep 2010
After posting this last night, I woke up today feeling even worse. I haven't even taken my pain medication yet taking my last dose around 1AM last night; less than 12 hours ago.
My stomach is still feeling like it's churning but today I woke up to also feel like I have congestion in my head, ears, and a little bit in my throat (but no sore throat). I haven't been outdoors so I can't say it's allergies that I do normally suffer from this time of year but never with a low grade fever.
It's been 18 days today; 9/23 since I started taking the new OP version of Oxycontin. I still can't take my required and needed dose of this or my Percocet due to my stomach problems.
Hi R, It sounds like you either have the flu, or you are going through withdrawal! Call that doc today.
Hope you feel better,
sweetlemon
I am so fortunate to have no allergies to anything and have just a shattered mid spine. I can't imagine what you are going through! I sure wish you feel better soon. Hopefully your doc will be able to help you out with this dilemma. We'll keep cheering you on and keep us posted!
23 Sep 2010
i know exactly how you feel. i had takin oxycontin 4 a long time and the new OP formula didn't help my cronic pain much at all. i took it 4 less than a month and told my dr. he agreed that others had said things also. so i just gave him the rest of my months suppy and im trying fentanyl. but this is my 1st week on it and its not doing gd either. plus im having detox from the oxys. i sure hope i will be done soon its not fun. take care folks god bless
try the opana if you can get them three times a day because the overlap will make you feel good for atleast twelve hours out of the day
24 Sep 2010
I feel for you RSDHurtzme, I think a lot of us here are trapped in a tragic system. Personally, I believe that as long as law enforcement is involved in our medical care, we're all in BIG trouble. I'm old enough to know that the process of receiving medical care didn't used to be this way. People used to go to their family doctor who would write prescriptions based entirely on their physical symptoms and/or test results. You only saw a specialist when you had a very serious medical issue. Now, everyone has to see a specialist, and the doctors and hospitals are scared of writing certain prescriptions regardless of their patients medical issues. I had a doctor at a hospital tell me she wanted to write me a particular prescription, but she was scared because of the doctors who would be reviewing the prescriptions she had written. She didn't want to get in trouble.
24 Sep 2010
I saw my doctor today and since I made the appt yesterday and she is very caring, she had spoken to my pharmacist and looked online. She believes that this medication is not working as strongly due to not only what is on the inside but also saying they changed the coating on the outside too. My pharmacist said he had some generic Oxycontin left but it too will be either reformulated or discontinued in some strengths by early December at the latest. My doctor feels I need to try to get used to this due to my severe allergic reactions to any other long acting opiate ever tried on me as I'm allergic to anything with Morphine in it which covers most of them and my pharmacist agreed with that saying he felt there was nothing else that could be changed.
Thank you RSDhurtzme for updating us. You may be a guinea pig for now, but you are a sweet guinea pig!
26 Sep 2010
I was taking the oc version and have also been switched to the new op. Last months supply was 1/2 the oc and 1/2 the op so I didn't really notice anything too much. I just got this months supply and it is all the new op ones. (this was Friday 9/24) I have been very busy lately, doing a lot. My daughter got hurt in a soccer game on Thurs. night so Friday was taking her to the dr., so I sat quite a bit since the dr. is a hour away and sitting for long periods make my hips hurt more. Friday night I had to clean a house which aggravated (sp?) my lower back. Then Sat. we went grocery shopping (again sitting in the car for a hour there and hour back) and walking a lot shopping. ANYHOW... the result is I am in A LOT more pain. I realize I have done a lot more in the past few days but it doesn't seem like I am getting any relief what so ever from the pain med. The only thing helping is I have just a few instant release oxy pills.
Hi there Yaya! It's been a while. You certainly did do a lot of activities so it may be hard to tell. When you have a few "normal" or less active days, please let us know if the medication isn't working as well. And no one here cares about spelling. Take care and please post more often!
Chris
26 Sep 2010
Id say try using Roxicodone 30mg for now because they are still the original formula and stay on those until Perdue has time to decide whether to change them or not. It will get you by until then. I know you will have to take more pills during the day but if it makes you pain go away without making you sick, then Id certainly be willing to go that route if it was me. Maybe they will end up changing the oxycontins again and then you can switch back. But at least for the time being you can be ok. Keep us updated with whatever you decide to do. The more information we all get from a direct source such as yourself, the more we can all help each other. Take care and good luck.
Roxicodone would be a good alternative, Ocean. And right on about getting DIRECT information. I've made many misstatements about this new OP already.
Take care.
roxicodone is not made by purdue and as of now there are no plans for a change in the roxis at all...
27 Sep 2010
Hello RSDHurtzme,
I am very much in the same boat as you are. I have been taking oxycontin cr 20mg 3x a day for over two years now with about 4 10mg of norco for break through pain. My pain WAS under really good control up untill freaking purdu pharm recentley changed there formula of oxycontin the this new one that has OP on it and not OC. It was changed to stop people from abusing it but its sounding like the new formula is creating more probs than good.
Last mouth was my first month on it and about a week after I started on the new OP's I quickly started going through withdraw systems. Total flu like systoms and the worst diarea I have ever had. It is so bad I just had to stop taking it al together. All I have now is my norco untill I can see my pain doc.
27 Sep 2010
Call your local Walgreens. My pharmacist does carry the so called ,"old ones", the OC's. But they aren't old. Purdue is still making them and distributing them through Ethex. My Walgreens only has the 10mg and 40mg right now.
The coating on the OP's could to so strong that maybe some of you can't digest the pill at all. It might be passing straight through your system.
doesnt matter the distributor . by mid-december the "oc's " will not be made any longer. weather it's brand name or generic . just saying don't plan on walgreens or any other that still has "oc" ,having it too much longer
Ethex closed down due to other generics they made that were harming patients but not due to generic Oxycontin. Soon if not now, nobody will be able to get ANY form of a generic Oxycontin so we have NO choice but to have our doctors/pharmacist switch all of us to a new medication.
My heart now hurts as much as my body over this as I've read about all of you who are also suffering. For December my doctor has no choice but to put me on a different med. If I didn't have the severe allergic reactions I do, I wouldn't be so worried. This is causing fear that I've not had since I got sick on the OP to begin with to know there is NO other option now.
30 Sep 2010
I too have RSD and am on the oxycontin 80 mg along with oxycodone for breakthrough and dilauded. Being a lab rat most of the time with new drugs and procedures that may or may not work, trial and error. I have felt similar side effects to the new formula, the only problem is that they added another med at the same time as i got the new formula of oxycontin so i haven't yet sorted out which one is responsible for the worst side effects. I too looked up info on the new formula and ran across only people who were upset that they couldn't get high anymore, trying to find a way to get around the new formula.
I'm sorry to hear that you also have RSD as I know how painful it is. You are right that if there was ever anything to cure it or put it into remission, that is something I would try in a heartbeat. I've had it for over 11yrs now; 11 1/2yrs in December.
I don't know what other med they put you at the same time as the new OP Oxycontin; I could be able to help you sort it out possibly and if not others on here I'm sure would be helpful.
I hate even having to take these meds to begin with and have been smart enough to fear my own medications ever since I was put on them; way before Oxycontin was touted as something so dangerous that others abused.
I thank everyone who has told me that the old formula will still be made and that I can get it as when I see my doctor on Monday, we have already discussed this option if I didn't get to feeling better.
Unfortunately even calling Purdue will not change their choice, and as sick as it makes me and as frustrating this whole situation is - there are so many kids out there getting addicted and dying on these meds. Its so sad - i cant stand the meds, hate that i have to take them everyday. I am 24, was diagnosed when i was 16, so 8 years already. I have to deal with when someone finds out about my disease from a close friend or family hearing from people how "lucky" i am that i get these drugs and get katamine infusions, this infuriates me, not only do i loathe the meds, no matter how few side effects they are still taking a toll on your body, your kidneys and liver, and will always have some side affects, even if minimal. And they don't understand what its like to live in so much pain everyday.
I certainly wouldnt think thats weird. I know people with allergies to peanuts & seafood.. I am not. But, have allergies to band aids and i cant touch my mouse to my computer without having a reaction.Everyone is different. If the new ones are working for you-Im glad.I dont want anyone to suffer the way some of us are.I had finally got to a point where I could function in life-Now I am back to square 1.
there are a handfull of generic versions that were not rushed on the market, have you tried any of those? There are also fentanyl patches that are pretty interchangable with oxycontin have you tried that?
18 Oct 2010
I received my first prescription of 30 mg OP on October 4th. On Oct. 5th I was admitted to the hospital with severe gastric distress. I have stomach issues anyway and did not relate my hospital admission to the new OP till I was released from the hospital 4 days later and started doing some online research on the new oxycontin formula.
I am NOT getting the same pain relief with the new formula. I take 30 mg. every 8 hours and am only getting pain relief for about 3 hours out of every 8. It takes the pills apx. 2 hours to work, then I am knocked out sleeping for 2 to 3 hours. I then awaken in severe pain. That is a total of 5 hours from when I first take the pill. This leaves me in pain for 5 more hours- 3 more hours till I can take the next pill, 2 hours for it to work then back to sleep for 2 to 3 hours.
It took me several days to get sick to my stomach on the new OP however I tried to stay on it to see if my body could get used to it knowing I have problems with allergies to any other long acting opiate ever prescribed to me sending me to the ER more times than I can count.
I too noticed it took about 2 1/2 hours to even feel any of the medication and also would get very sick to my stomach after taking it. I also lost any abilities I had to function on the OP version.
The pain relief was at least 50% less than the old ones.
The old kind never caused me nausea or drowsiness but looking back I was sleeping a lot more when I was taking it.
I was switched to the generic 40mgs that have not been changed and after only one day, I felt so much better even though I believe the generics aren't as effective but they are more so than the new OP.
At least I'm not sick anymore.
We are being punished for what the abusers/junkies do.
I emailed my pain Doctor yesterday & he worked me in today for an appt. I gave him what was left of my op prescription and he wrote me a script for Immediate release 15 mg oxycodone 6 times a day till we can figure out what to do. I am already feeling much better, no more stomach distress, no more fever & chills. I believe I was going through withdrawal due to the OP's not disolving properly and so does he. I emailed him several links to sites where people had written in complaining about the new OP formula. He apologized for what I had been through and told me to research a drug called Exalgo. It is an extended release (new on the market) that has a hydromorphone base and works very similar to oxycontin. Of course my medicare part D will not cover it so I am on a search for a different Part D that will cover it.
20 Oct 2010
I have been taking 30mg of the OC's qid (4 times a day) for almost 2 years with minimal side effects. The only side effect that I do get is the decreased bowel motility, leading to the occasional bout of constipation. I have been able to easily manage this side effect by increasing my daily intake of water and fiber. I also DO NOT have a history of allergies, or sensitivities to medications. Two weeks ago my pain management doctor switched me to the OP 40mg tid (3 times a day), and gave me OC 15mg,bid (two a day) for break through pain. Ever since I started taking the OP's I have had daily bouts of nausea that occasionally lead to me vomiting. I also find that they give me headaches on a daily basis, and that they make me a little drowsy (I never experienced drowsiness from the OC's). To top it off the pain relief that I get, or I should say don't get, from the OP's is significantly less then what I got from the lower dosage OC 30's.
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i hate that u are on meds. like this because of the abusers, that they have had to change meds like this for people like us who need them! IT"S shameful,@?
Inmanmike, I couldn't' t agree with you more, because of the Dr. shoppers, the abusers etc. It can and does impact all of the folks who truly need the help of medications that can give them some relief and hope for some normalcy in their lives. I too pray this person can discuss with their physician about getting some pain meds that are effective and no longer needs to suffer as a result of the switching this Oxycontin from OC to OP.
My prayers go out to all who need to suffer this indignity. God Bless
midwestma/Gwendolene
Hello everyone, I too have been on oxycontin for over 2 years and what a complete difference in my life. I was back to doing the normal things I did with my family and even work. I fractured my spine 95 and have herniated discs, bulging discs, degenerative disc disease and just last year my doctor says it is also Fibromyalgia from all the trauma. The pain was just everywhere. I had a spinal fusion in 96 leaving me with 4 screws 2 bolts and a piece of my hip to hold my spine together. I have tried all types of steroid injections, therapy, vicoden, percocet, patches and they really made me feel terribly awful. Finally, my doctor found something that really worked for me. I did not even have to take the break though meds. I am now very scared as I am experiencing what I am reading, not all the symptoms but some and they are very bothersome especially the headaches and increased pain, stiffness and cold like symptoms. Addicts make it impossible to have SEVERE PAIN or any pain at all.
Expand this post...
If they cannot figure out a way to abuse the new substance then they will move on to the next drug so I can't understand why punish us who take the medication as DIRECTED and NEEDED to live our lives normally. This is just awful and I cannot believe that we have to experience this as if we don’t have enough to deal with.
Please FDA or whoever is responsible; give us our life back!
i to started the new formula i dont think its as good as the old it doesnt work like the old and my stomach can tolerate but not this i have vometed never did i do that before and now have a very hurtful ras and i mean it hurts so why cant something when works they leave it alone cause of drug users where we are being punished now another trip to drs and see whats up i know i hurt worse than i did before help
My name is Carolyn from Milwaukee, WI and I too have been taking original OC's(oxycontin) for pain control for years due to multiple failed spine fusion surgeries resulting in chronic pain disorder. I started taking the new reformulation in September. I thought in the begining the sickness was because of the change but that is no longer the case; now it is two months later and I am still staying sick. Last August I underwent Gastric Bypass surgery for weight loss to relieve some of the pressure off my spine and I will always have to take vitamin supplements to keep therapeutic levels.
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Since taking the new reformulation all I do is throw-up not only the pain meds but my supplements as well. My body stays weak all the time and I have started have much more spinal pain, problems with leg spasm's, headaches, and constant throwing-up after taking this new form. This is not good or healthy for my new stomach or my severe spinal pain. It is not fair for the FDA or Drug Companies to injure or insult everyone because some choose to be stupid. When I talked to my pharmacist about my symtoms he informed me that this is occuring with qute a few of his patients and this formulation needs to be recalled because its's hurting more than helping.
I was doing fine until this abrupt change instead of trying to weed out the abusers by doing weekly lab testing for therapeutic levels. They punished everyone, even-though the original helped alot of people who suffers with daily pain like myself. This was the only thing that helped due to my allergies to most meds and now I just stay sick all the time. I even went to my doctor this month and we lowered the milligrams to see if that would help and still no change, the pain is worse, and i'm still sick.
I guess they donot care about the sick as long as they cater to a section of society that chooses to categorize everyone as being guilty of illegal behavior. I take this as an insult to my character as well as my health, because I have never abused drugs or alcohol in my life mainly due to my dislike for either. Until I became sick from a serious injury resulting from a work related injury, I never took anything more than a regular Tylenol or Alleve.
Things have changed in my life because of my injuries. I'm not ashamed to say I need the medication to help me with pain control daily in my life. It helps me be more mobile and independant because it removes the pain element that keeps me miserable and unable to participate in everyday joys because I hurt all the time. I have never complained about any treatment prescribed by my doctors' until now for we have always had a good relationship and their concern about my medical needs
. Please! I ask everyone involved not to develope a one quick fix for everyone and everything. You are hurting the ones you are supposed to help, I mean this is why we pay high prescription drug cost, and high health insurance premiums to receive the best possible care. We are not supposed to suffer because you cannot police the corrupted entities in society. People doing bad things will find a way no matter what, so what are you going to do next, remove or replace all medicine that have addicted behavior? After all, that is an individual choice to abuse or not.
Thank you
Contacted my Pharmacist about the new OP. Told him it was not working on my pain. He informed me that he has had over fifty customers complain about the same problem. Talked to Purdue, they are aware of the problem but don't seem to care. They are more intrested in dealing with the criminals that abuse their medication then they are about helping the legitimate people dealing with severe chronic pain. It is not their place to control criminals. That is for Law Enforcement.
I too started having what I thought were flu like symptoms including hot flashes, much fatigue, along with stomach aches/pain, when I started the OP version. I thought I had a virus of some sort.
* I had thought I had a new compression fracture because of new/worse back pain, so had an MRI done. No new fracture. Just more pain. ( It took me about 3 weeks more before I connected the problems I was having with the new formula.)
* 2 months later and I still have severe pain flares that lasts all day until I take enough break-through meds to cover what I'm not getting from the same dosage of the new OP version.
* It almost seems like it's working less well than it was at first.
* The pain coverage is inconsistent.
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*The OP stop covering pain abruptly. So I can easily go into another flare if I don't pay enough attention to pain levels through-out the day. A conversation on the phone distracts me enough that I can be in a flare when I'm done talking a half hour later. And you know what they say about
"chasing the pain". Not a good thing to do, so now I have made the mistake of taking an extra break-through med at the first sign of a flare, when sometimes it turns out I did not need it and am over-medicated.
This is so sad. Like so many others it took years to find a combination of medications that helped the pain but where I could still function well.
I am highly medication sensitive so options are extremely limited.
I have no idea what dosage I would need to go up to, to get the same relief, even if I could afford it!
Some people say they find them in the toilet. I haven't yet, but something is keeping my body from absorbing the medicine in the manner they were intended for.
My doctor is against Opana, the only pain medicine I have not tried yet, and I can not function on the other pain medicines.
I too think it is a good idea to let the FDA know about problems, but remember they won't go back to the old formula, they will simply take this off the market.
Those abusers you make me so angry!
For what it's worth, my mom and pop pharmacy who works with Hospice and so deals a lot with chronic pain patients, told me that people are saying they have less stomach nausea with these. Hm... hard for me to believe.
Can we talk the truth here? Probably not, because at least 98% of Americans are drug users and yet quickly and absolutely deny their drug use. Instead Americans all sing the following insane little ditty, "My drug's better than your drug. My drug's better than yours! My drug's better because I say so! My drug's better than yours." Or the ever popular "Oh my drug is not a drug." Yes that's the truly insane attitude Americans have concerning their drug use. If you have a problem understanding that at least 98% of Americans are drug users, kids included, well then I have a little wake up call for you. All drugs, are drugs, are drugs, are drugs, and drugs are U.S. Still not getting it? Well go have a Coke, or a cup of coffee, or a soda pop, an aspirin or Tylenol, or how about an alcoholic drink or cigarette to help you THINK! Alcohol and cigarettes the two most deadly drugs are legal.
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Or how about "Yep my drug's better than yours because Uncle Sam says so? Well a snappy sieg heil to you and Uncle Sam, and please pick up your brain at the government hat check stand. And what does legal versus illegal mean? It means nothing as to availability as all drugs are available everywhere. So what does legal really mean? It means Government v gang or Black opps. distribution and control (See Iran Contra, Air America etc.). So ponder me this, why are the two most deadly drugs legal but the Government gives distribution rights for controlled substances to gangs and Black opps.? Or how about this, a woman can rip a living child from her womb under the principle of control over her own body but the government gets to control my blood chemistry? PLEASE EXPLAIN! Do you really want the Government controlling your reproductive organs and blood chemistry?
Jon Marsh, I completely agree with your post here. I know after 11 1/2yrs as a chronic pain sufferer/survivor that ALL drugs be it legal or not are bad for us esp in the long run. We are all so different in our pain as well so what works for one may be the worst option for another.
I don't believe pain meds are the only answer to chronic pain however after going off of the original Oxy last year for over 3mos last year and recently having to have med changes due to no generic version of the OC and going without a stronger opiate for a while, I have realized the quality of life taking these dangerous meds give to me and many others.
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Even though I did withdrawal just like an addict last year doesn't mean I am one; if anything I realize that the disease that causes my spreading nerve pain disease is far worse than I knew and fully believe that once on something that helps usually no more than 60/70% if that, there is NO reason to keep upping the dose as there is NO pain med that takes all of the pain away. As responsible Chronic Pain patients we must take meds as prescribed not taking more or continually upping doses.
There is a plant that is so natural that I feel is the best for pain and the safest. It was why I was able to stay on the same dose of the original OC for over 9yrs refusing increases offered by doctors many times over as I also refused to take all of them daily.
I did however recently realize after being switched to a dose of Kadian that is more than what I took on the Oxycontin that I stayed way under medicated for a few years due to my fear of prescription meds and knowing the long term consequences. Now I'm down to ONE pill a day with little breakthrough meds like before.
I now feel thankful that Purdue messed this med up as I am getting better pain relief than I ever have after being allergic to most long acting opiates.
I HATE taking medications but if I had Diabetes, Cancer, Heart Disease, HBP etc, I would be taking other dangerous meds; just different ones.
I realize the meds will harm my body more than the disease itself but finding out that "some" quality of life is given if I do take them is by far priceless even if it cuts a few years off of my life span as I'd rather have enough life to help others, help myself and family, go to church having about 10 to 15 hours a week with pain relief vs NO time at all and going from a cane to a wheelchair than to be trapped in a body that doesn't work without the meds at all and end up bedridden.
This comes down to a choice we have to make and I also know there are those that feel if they could only take ONE more pill or more than that, they would feel no pain at all which is so not true.
I choose quality over quantity as I have no children but do want to have some type of life even though it's nowhere near the life I had back 1999 & prior to.
Thank you for your comment
I have been on Oxycontin for several years. I also have allergic reactions to many painkillers or they just don't work. I really didn't think about it when they said they were coming out with a new formula, as my pharmacist and Dr. assured me there was no difference. since then I've noticed that not only do i have to take more, but i am also nauseous most of the time and constipated. I never had any of these problems with the OCs. With the OCs my pain level stayed at about a 5 on the 1-10 the Drs use. now with the OPs I'm at at least an 8, even with the increase in meds.My Dr. said that next month she would try the oxy instant release. but after reading your blog i dont know what to do. any advice? susanlocal324
To susanlocal, My doctor gave me the Oxy IR which is basically the same as taking 3 Percocet but a bit stronger but they are NOT long acting and my doctor did the same; put me on Oxy IR 30mgs 6 a day and my pain got worse than on the sickening OP.
She then got brave enough to put me on Kadian; a synthetic Morphine pill and I've had better relief as I stayed on the original OC dose of 40mgs for over 9yrs and was under medicated if anything.
Most likely you will also need a long acting pain med. The only choices left are; MS Contin, Kadian, Opana ER. I got sick on Opana feeling nausea and couldn't breathe after taking only one pill. Now on Kadian, I feel better than I have in a long time and I ended up on a walker while on Oxy IR WITH Percocets also.
I'm back on my cane now and doing better. We are all different in our pain and what med works for each of us. I hope your doctor is as patient and understanding as my own.
For anyone having problems due to side-effects, lack of pain relief, etc., with Oxycontin Op please read my reply to the very first post in this thread. (I don't think I can re-post it here.)
I'm just one person trying to make a difference in what happens with our pain medication options. Oxycontin was a very good option until they reformulated it. But there are things we can do. Plus another pharmaceutical manufacturer has submitted an application for approval of a new tamper proof time release oxycontin. The FDA has six months to approve it. But perhaps if the FDA (and not just Purdue who doesn't care) knows exactly how many people are having problems with Oxycontin OP they will approve this new formulation sooner. Especially since the FDA rushed to approve Oxycontin OP due to pressure from parents who's children abused the old formula.
ou all have just helped me so much. It wasn't until just recently I thought about see if others might be having issues with the new oc formula. Now that I think back, since I've been on new formula I've been sick, feeling weaker and weaker with stomach issues and I can't seem to think right I've noticed over the last couple of weeks. My pain level is so much worse, and i am angry at pain management dr. that would not try another medication. Pump? No way, my insurance doesn't cover it, the stupid drugs are bad enough. I'm scared about work next week, I feel amost catatonic todaty, and mean. I'm scaring myself, and I don't feel like doing anytthing. I now feel like I'm not alone, but I don't knwo what to do either. Depression has come on in a new form I've never experienced, and I was thinking today about how much longer I can live like this.
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I'm not living, I'm just a drag on everyone, my daughter is getting married and I can't feel one bit of joy. Oh my gosh, what are we going to do. I thought maybe my lower body pain had settled down a bit, and if I could get a Dr. that does what there are supposed to do that might find why my left arm/hand are in such pain and weakness since surgery 2 years ago, just maybe I could wean off medication. Well, nope, I tried going to a craft fair with my sweet mom, and was in agony after only 1/2 hour, same with another weekend, and I feel so bad, she is the most wonderful person, that likes to get out and do things. Now i know why, the medication isn't working. I don't know what is wrong with my thinking, I do not feel right, and this stuff is causing major constipation that I never had before. So much so, i put in earlier post, I was in ER thinking I had a blockage due to weakness, no laxative working, and feeling so irate. I will call that Purdue and complain too, and will get lot number, thank you for telling us this!!!
I have been on oxycontin and since the switch I am now taking 3 times the oxycontin 80 twice a day and am lifeless hopeless severe bowel compacting and I feeel worse than ever and for 3 years I have hardly gotten out of bed... I need new opiate but am afaid to try them... morphine dont help me and I need something
the saddest part about people who really need the medication will end up addicted as well ive seen it happen all to often its sad that you get hurt and hte rest of your life you are reliant on something everyday. and the addicts who keep making it harder for the painsufferers to get normal "untamperable" meds just continue to find ways to tamper with the meds anyways its a never ending circle. guess thats god testing our intelligence. i wish you all happiness and less pain hope it all works out.i know people who have overcome these fears i hope yall can too. takecare!.