Is White Ip204 The Same As Yellow 10 325 E712
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I would like to know what is the difference between ip204 white and yellow 10/325 e712?
Re: Acedaprofessional (# 2)
I agree with you the Endocet does not work as good as the yellow Percocet 10 I have to take 2 at times I will definitely not be getting them next time .
Re: Delana (# 10)
Ip204 worked for me.not all pharmacy carry opiods u have to find a friend who takes opiods to see if she would be nice enough to tell u her pharmacy
Re: NOTSTUPID (# 16)
They actually do prescribe narcotics for migraines. I've suffered from chronic migraines since I was in 1st grade; that's about 48 years now. I've tried every OTC and non-narcotic med out there, and nothing helps. I've been on Fioricet with codeine for about 25 years for migraines, and it's the only thing that works. No, I'm not addicted. I can use them as prescribed which is "as needed." I take about 9-10 capsules a month. My doctor does care, and she also sees that I don't abuse them.
Re: NOTSTUPID (# 16)
Why are you making such a mean comment like that. The reason some of us come in here is because we want to be educated regarding our meds. If I don't take pain meds, I could not fully physically function. Plus, i take muscle relaxers, and Mobic. You must not be a Chronic Pain sufferer. Not everybody who has to take pain meds, are drug heads!
Re: NOTSTUPID (# 16)
It all depends on the Dr. I had vertical sleeve surgery in April then through the months developed a severe hiatal hernia which surgery almost killed me living with chronic pain, I know, but ppl talking about this pill being s***ty ect sounds like they have the problem.
Ip 204 and a333 is nothing like any Percocet I've ever taken. I'm simply wondering what's really in them. There is no oxycodone in them. I took a U/A and it came up clean...
The IP 204 pill is complete garbage. It takes effect after around 45 minutes and wears off in two hours. Something is very poor with its manufacturing. I was taking Watson 932 brand with satisfaction until its sad discontinuation. Ironically, l found an old 932 one in my bathroom cabinet that was lost from years ago. I took it and it wore off the following day. Yes, the manufacturing is solely to blame for the lP 204 dissatisfaction.... Aim for a different brand or change your pharmacy!
kjc7692.....Some CRPS patients have used Soma to help with pain as it is classified as a muscle relaxer. I personally thought it worked as well as a baby aspirin. I read somewhere that it is being banned in the US after the UK banned it so doctors are prescribing alternate muscle relaxers now. For anyone with CRPS, back injury or chronic pain you might try the spinal stimulator implant. They allow a 4 to 6 day trial to see if it works for you before placing a permanent one. I just went through the trial having CRPS TYPE 2 and a crushed foot injury along with scoliosis issues and it worked really well for me.
Can SOMA be used for physical pain? For example, C.R.P.S (complex regional pain syndrome)? My fingers are crossed in hopes that this will work...How much will it take? I have 325mg 4x a day. I was also just told by the doctor, that 16yrs ago I was positive for Lyme Disease...But no one ever mentioned that to me, until now. I have had a hell of a time fighting with doctors who said I suffered from "Invisible Illnesses" which made me feel INSANE and from Chrones Disease, Staph Infections, Neurological Pain & Anxiety, Fear, Panic attacks & 15+ years of treatment for Epilepsy...That was completely misdiagnosed...But the Epilepsy Rx, that I should never have been prescribed + a complexity of other things in my body from the Lyme Disease, made me suffer 1k seizures. PNES (pseudo non-epileptic seizures) is what they were actually called & after so much Traumatic Brain Injuries and 30+ Concussions...I now have to live with 24/7 assistance and Im still denied SSDI...So I must continue to fight. No one here has an easy road and because of all these little kids abusing narcotics & overdosing, it's making it very difficult for the people who live in 24/7 pain it's unfair for the doctors to be punished for writing prescription that the patient actually and physically needs! AND the government needs to recognize that it is a medication classification that needs to be used for the treatment of people who suffer from minute to minute, hour by hour, and up to years and years of everyday pain. Because of pain and not having anything to lesson the severity comma I am alive but I am not living. I can't do anything I don't have any money I have become a burden on myself my family & no hope of finding a person who will stick with me through all of my s***. It's a sad place to be. I can hardly stand up alone and I'm my early thirties, I am afraid of what my forties and fifties will be like, if I get there. Again I apologize to renting any information or an answer to the question above would be Heaven Sent.... I will keep you all in my prayers and hope that you all find relief sometime somewhere someday SOON!!! BEGGING ANYONE FOR HELP!!!
Yes I also had migraines since I was 10 years old, mine was due to a brain tumor. When the tumor was found and taken out, I still had migraines that was in 2010 when brain surgey was done and still I have migraines but not near as severe.
White IP204. I just took this for the first time & it has been about 90mins. I still have no relief & I began feeling sic to my stomach after about 30mins. This is horrible!! It is such a shame to have pain medication that does NOT provide any relief. Truth be told-- my old script for Hydro's worked faster AND better! I'm so disappointed . . . & uncomfortable!!!
if anyone had a hundred milligrams of fentanyl they would be dead do u mean mcg (micro grams per hour)
You're on this site so quit judging my friend..everyone is expressing how they feel and what works best...so unless you are trying to contribute, leave the attitude at the door.
I have the IP 204 pill right now. I preferred the 10/325 as they seen to work best. Manufacturer's name is Mallinckrodt pharm. I am going to my pharmacy to see if they can order from this manufacturer.
Yes your right everyone thinks they no more then the person in pain which they are very stupid if u live in chronic pain like I do anything that helps is God sent.dont judge other people if u don't no what your talking about try living in constant pain.
What area are you in? I was diagnosed with C.R.P.S. which hardly any doctor's understand or know how to treat & at this point claim that there's no cure (sucks). Because of this, it's actually a disease. I was put on oxycodone 30mg & 30mg Oxycontin and presto, body pain gone & it made me wide awake (which was bad for insomniac's). Anyway, not knowing anything about Narcotics, I had no idea how much that was for a 115lb woman. A year+ and he...My Doctor was slapped on the wrist and fired from his position. When the replacement Doctor came in, she did not feel comfortable writing any kind of Narcotics due to the fact that it was my primary care physicians office. So the doctor number 1 kind of messed me up by placing me on so much Oxycodone/Oxycontin that once I found out that I was physically addicted, the weaning off began & that was hell! I'm still in the process of getting off of Oxys and need to know if ANYONE ELSE HAS HAD ISSUES WITH EXTREMELY PAINFUL CHILLS WHILE DETOXING? I have tried Clonidine, Imodium (due to the Poppy seed or an opiate property in there somewhere contained within the medication), I've been on Klonopin for over 15yrs due to a seizure disorder and take at bedtime and now they've put me on a Muscle Relaxer - Which I have ZERO idea how they work or what to expect. I'd like to know, but I'm so suggestive that if I know the side effects, my body will faulsley mimic them or I will just have bad reactions, weird. So PART 2, will this help me with the withdrawal symptoms of Opiate Withdrawal? If not, what will take these insane painful chills away? Sorry for ranting, but I am scared & this thread seemed like it could use a topic change. Looking forward to hearing back from anyone who has some advice on this topic.
Mommyinpain thanks for your reply. Wish I had a Doc who cared. I am coming up with these alternatives myself. I may try the patch if insurance pays, I dont want to be sedated. It is becoming unbearable in my knees. I have put on weight like crazy because my thyroid isnt working and I am practically in a coma no energy at all. I have not seen my Doc who is a new one saw her 4 or 5 times, in 3 months. She is on maternity leave. One month I did not see anyone. The next I saw a.real jerk who was new and was fired b4 I came in this month to the worst yet. She threatened to cut the four lousy percs back to 3 when I told her about worsening of pain, because I had not lost weight? We have never discussed my weight just the thyroid problem they found. Again I left crying, in pain and on the same meds, only she claimed she is doing me a favor letting me have them this time. She only believes in giving 3 and is not going to lose her license she said. The staff said she will probably be gne b4 I come back too because of her attitude. Great but I still have no help. This will just be another month if extreme pain. Is there anything anyone truly recommends that has helped them. I have all 3 compartments in both knees totally degerated and osteoarthritis as well. 5 bulged disk and endplate disease in my spine, basically very degenerated and cannot operate if I wanted to. So much to say but just cannot keep rambling. Diabetic out of control sugar etc..help me friends
They are all the same. They are percocet 10/325. The white IP is,the same as the yellow ones
Imitrex is amazing and a non narcotic!!! It is used for migraine headaches. You must drink plenty of water.
Hi Wannaquithurting, I would definitely try the fentanyl patch. I understand your fear and concern but as long as you take it as prescribed it should help your quality of life and pain level improve. The stories we hear about fentanyl are unfortunately people who are abusing it or using it just to feel high off of. I'd give it a try and take your oxycodone 10's for breakthrough pain. I've read that Opana is much stronger than Oxycodone but that it has a greater sedating effect. If your not receiving enough pain relief from your oxys than give Opana a try but I've heard it's a very powerful, addictive drug and very similar to morphine. Living in pain is horrible as long as you have a doctor who's trying to help you find a med that will give you relief I'd give the ones you haven't tried a shot until you hopefully find one that does. Here's hoping that you, I and everyone with legitimate illness and severe pain find relief!
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