Review: could Oxycodone cause Pancreatitis?
Summary: Pancreatitis is found among people who take Oxycodone, especially for people who are female, 60+ old, have been taking the drug for < 1 month, also take medication Oxycodone hcl, and have Pain.
We study 25,916 people who have side effects while taking Oxycodone from FDA and social media. Among them, 163 have Pancreatitis. Find out below who they are, when they have Pancreatitis and more.
You are not alone: join a mobile support group for people who take Oxycodone and have Pancreatitis >>>
Oxycodone has active ingredients of oxycodone hydrochloride. It is often used in pain. (latest outcomes from 27,274 Oxycodone users)
Pancreatitis (inflammation of pancreas) has been reported by people with type 2 diabetes, depression, diabetes, high blood pressure, bipolar disorder. (latest reports from 31,816 Pancreatitis patients)
On Jan, 13, 2015: 25,916 people reported to have side effects when taking Oxycodone. Among them, 163 people (0.63%) have Pancreatitis.
Time on Oxycodone when people have Pancreatitis * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years |
Gender of people who have Pancreatitis when taking Oxycodone * :
Age of people who have Pancreatitis when taking Oxycodone * :
Severity of Pancreatitis when taking Oxycodone ** :
|least||moderate||severe||most severe |
How people recovered from Pancreatitis ** :
|while on the drug||after off the drug||not yet |
Top conditions involved for these people * :
- Pain (38 people, 23.31%)
- Depression (14 people, 8.59%)
- Contraception (12 people, 7.36%)
- Anxiety (11 people, 6.75%)
- Insomnia (11 people, 6.75%)
Top co-used drugs for these people * :
- Oxycodone hcl (163 people, 100.00%)
- Aspirin (31 people, 19.02%)
- Promethazine (29 people, 17.79%)
- Lisinopril (27 people, 16.56%)
- Omeprazole (26 people, 15.95%)
* Approximation only. Some reports may have incomplete information.
** Reports from social media are used.
How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.
Do you have Pancreatitis while taking Oxycodone?
You are not alone! Join a mobile support group:
- support group for people who take Oxycodone and have Pancreatitis
- support group for people who take Oxycodone
- support group for people who have Pancreatitis
Drugs in real world that are associated with:
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Can you answer these questions (Ask a question):
- I amwondering if i have myathesia gravis (1 answer)
I am thinking that after a long bout of going nowhere with Drs. That I might have Myathesia Gravis. My Grandmother had it and I am thinking that my brother had it when he was born.He failed to thrive at first as he was unable to suck very well. He did make it though with a forced feeding of milk and bananas. He was sickly all his life though and recently died of cancer. I noticed that my eye is drooping on the left side. I have periods of extream fatigue, my left arm is tingly and I can't seem to feed myself without changing to my right hand. I have spinal stenosis and severe pain in my hip area but my right big toe seems to be tingly from time to time. I also have a swallow problem that causes me to choke or throw up the food or drink. Pills stay part way down a lot. My G.I. guy wants to strech my esophegus. I tend to eat soft foods and stay away from steak or anything chewy. I have congestive heart failure, sudden cardiac death, syncope all of which I greatfully managed to survive. I have fibromyalgia, and some nodules on my chest wall ( i forget what that is called) I have had 5 or 6 bouts with Costochrondritus which was way worse than actually having my heart stop. Costo hurts like a beech! I am frequently short of breath, exercize intolerant and have trouble holding my water.I have good dsys and bad days. Also my left hand and the base of my scalp goes all numb and tingly sometimes. There is also a terrible electric shock type feeling in my mid back area that makes me completely stop in my tracks and feel like I have been hit with a 350 lb pro football player. I have been hypokalimic after taking water pills (Ferosimide) i have taken prendisone for the Chosto and feel better immediatly, but I have mental reactions to too much Prendisone. I am very allergic to NSAID'S and pennicillian. Anyone got any ideas that the Drs have maybe not thought of... I would sure like to get better and go dance but the last time I danced I lasted 3 minutes before I had to fall into a chair.
- Do you have issues snoring from testosterone
I was in an IED explosion in Afghanistan, had a TRAUMATIC BRAIN INJURY, 2005.JULY 28THlevels were extremely low. my V.A. doctor put me on testesterone 2011 BREAST CANCER, AUG 11TH 2012 HIT AND RUN ON MY MOTORCYCLE. DUE TO all the pain meds chemo, etcetera. MY testosterone. At first it was the best thing that had happened to me since I woke up in the hospital now I snore like a drunk Marined. and the culprit is the testosterone. I need to save my marriage and do something aboot this. any ideas what I can do
- Can you get chills with multiple myeloma?
Do multiple myeloma patients have the chills without fever? My husband was diagnosed 2 months ago and has had 2 months of chemo 2x weekly for 3 weeks. He has Velacade and a steroid Decadron. He has also had 3 rounds of cytoxan. Why is he getting chills?
- I wanna know how fentanyl and oxycontin taken together like me works for patients?
I have been taking these meds. For the last 10months due to a auto accident that's happened in 1995!! And have bee in chronic Pain ever since, had to resign from my good paying job!! I could no longer work due to the constant pain...it took my Dr. And I over 3 yrs. To come up with this regimen to even get out of bed to be mobile!! I need to take care of all my adopted animal's, my two adopted children and my elderly mother!!! It I did not have these medications
ations I would be bed ridden!!
- I need to come of oxycontin and need a different pain med one that doesn't give you severe constipation or cause bone loss as i have severe ostio porosis and ostio arthritis
I also have Ostio porosis and don't know what to take for it it also is cronic like my arthritis I real want a pain med that is non adictive and doesn't cause bone loss a big ask but I don't know what to do as doctors don't seem to care
More questions for: Oxycodone, Pancreatitis
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I got Chronic Pancreatitis from taking Rebetol brand capsels of Rivavirain and Interferon. Had the VA used a diferent brand of Rivavirain besides Rebetol I'd most likley would have never gotten the Pancreatitis...
- Mensis cycle and oxycontin
I have severe back injuries. When I lived in another state, I was put on oxycontin and immediately my menstrual cycle (period] stopped for 1 year. When I moved to another state, I stopped taking this drug and my period returned normal. I eventually had to go back on this drug, (oxycontin) and since this time, 2 years now, I again have not had a period since beginning. If you are on this drug and are worried about your period stopping, fear not, it is a normal side effect. Hope this helps. ..
- Which issue has caused my periodontitis, my fibromyalgia or spinal stenosis? (2 responses)
At the age of 38 yrs old, I was diagnosed with Fibromyalgia and Spinal Stenosis. Obviously I had both of the disease for some years, and was struggling with the pain and symptoms for some time before I finally got checked, went through years being told they didn't find anything, told I had Herniated disks in My back only. Now with all the findings, there are 7 Herniated disks from My neck to My lower back.
Also since 2010, I was diagnosed with Periodontitis and have been losing all of My teeth in the top of My mouth.
I am 44 yrs old now, have been on disability for the last 4 years. I am down to 6 teeth in the top of My mouth, since having 1 removed just last week. They are telling Me that 3 more need to come out, and I am trying not to sink into total depression, especially since these are now My front teeth. I have a appointment today for a Denture Exam.
I started researching today to see if this Periodontitis is related to either My Spinal Stenosis or My Fibromyalgia. Especially since I once again looked up the definition for Periodontitis. Which States;
**Periodontal Disease and Bone Health. Periodontitis is a chronic infection that affects the gums and the bones that support the teeth. Bacteria and the body's own immune system break down the bone and connective tissue that hold teeth in place.
Of course with My disease of Spinal Stenosis and the bone loss as well as the nerve narrowing, I thought the breaking down of the bone in the gums might have a connection. Research didnt find any linking.
Now with Fibromyalgia, research showed 6 out of 17 thousand that they found. LOL Wow.. Well I guess I am "Number 7". Lucky Me! But it does make more sense now that looking at the definition. It is a Chronic infection (which Fibromyalia does create these) that effects the gums and bones. Bacteria and The Body's own Immune System break down the bone and connective tissue that hold the teeth. Which with Fibromyalgia, our Immune System is always all kinds of "Crazy"!
Oh course you can not have any of these diseases, or any other health issues and wind up with Periodontitis. It happens. But I know from lots of reading, researching and living with Fibromyalgia, that it is "Very Possible"!
I would sure like to know what others with these 2 diseases are experiencing.
Have a Blessed Day.
- Who cares about the patient? (1 response)
I can't believe I'm still alive but quality of life is greatly diminished and no one cares. Not one doctor cares about how this one dr. prescribed all these drugs over a period of 5 years and I lost everything. I flat-lined sept 18, 2005 and was told by dr there in er that I would live 1-5 years and I had just lost my job as letter-carrier of over 17 years and my daughter was killed in dec of 2000, which I will always feel great responsibility because I knew I should have called her, it would have saved her life as she was killed in the firdale village apt fire and she didn't live there, she lived with me she was only 20 years old. So this crappy dr steven a creelman of seattle just kept throwing pills at me, telling me there was nothing wrong with any of the pills just me. I feared dr's and still do, I know they are just people and most people are good and caring but a lot are not. The Celebrex started after I was hit by a truck on the job in march of 2000. I will admit it relieved some pain but I had side affects immediately, within days to weeks. I was told by the crappy dr to shut up and take them as he originally told me they were not anti-inflamatorys but a new drug that did not upset stomach but they did. I felt trapped because it was an L&I and I didn't want to lose my job and so healthy and strong figured w/PT and rest I could overcome the accident pain which was lower back and neck well I couldn't sleep from pain and stomach but I couldn't tell crappy dr it would do no good. My daughter was killed Christmas night and that's a very hard one. I went back to work because my job was most of my life and I had friends at work. I continued to have more problems from Celebrex and I thought my stomach was on fire, it was blood clots that broke lose and I had to have an operation on my small instestine and what was worse is creelman, the crappy dr, when he told me it was an emergency umbililical hernia I told him I was going to get papers from owcp DOL as I would be off work at least 6 weeks. He said NO!!!!!!!!!! He closed the door and told me no, no I won't say it's from Celebrex when He really did know it was. I had an endoscopy 6 months later and that specialist said no more Celebrex. After that operation I just never felt good again I was swelling up my legs etc and fatique all kinds of not feeling good things and I was pissed at the crappy dr who by the said to me that no other dr would diagnose any different or believe me. So, it was in July of 04 and I was so sick I just went in there andhe was on vaction so another dr ran a bunch of blood tests for hiv which I told her was impossible and lupus and a few other things but no one there looked at any of the drugs except the pain medication which ironically was one of the only ones that didn't contribute to dvt & PE. when creelman got back I was still so sick I had left work and said I would be back in 2 weeks after I had some PT and rest. I couldn't sleep. That's when he prescribed REMERON. It was for sleep which it did help but I gained 50 lbs and within a couple months acquired tonsillitis, bhroinchitis, pneumonia, Phlebitis and a dvt which instead of referring me to a specialist he just presibed me an anti-inflammatory and another anti-depressant plus all the drugs He gave tons of samples which were never in noted in my files. I think he should have to pay me MONEY!! I have none since I have no job and I feel so terrible I wish I could just have my job back. And my Daughter but my health has been a Hematologist and injectable blood thinners. I hate the state of wash medical care about doctors but not the patients and I have no money to sue and it has been my experience not to mention crappy doctor SO WHO DO THE PATIENTS THAT ARE BADLY AFFECTED BY CRAPPY DCTORS GO TO? Oh I also couldn't be in the class-action suit because I didn't flat-line from heart attack. REALLY?
- I got acute psychosis from 60mg oxycontin
I hate the new oxys with glue! Thanks to big brother! I got off 25 mg of methadone after 2 years and took oxys for two days then took subutex and was fine. then a few days later I took oxys for ten days straight and when I got off I was in psychosis for 3 weeks and ended up in three mental hospitals for four months they wouldn't let me out and my kid got taken away! I literally thought it was the end of the world and that god was coming back and I thought the fbi and local police were after me!! I hate oxycontin!!
More reviews for: Oxycodone, Pancreatitis
Comments from related studies:
From this study (3 years ago):
Paul Minard on Jun, 18, 2012:
Scottish descent Male, 55; quit cold turkey from oxycontin (50mg 2X day for arthritis hips & lower spine) for what I thought was a constipation-related cramp. A week later, after withdrawal, another one happened & I called the ambulance, the pain was so bad. Emergency at first thought the same thing but the doctor in the morning said it was pancreatitis, caused by the oxycontin, as I had also quit drinking nearly two years before. I.v. liquids for a day with ALL drugs stopped; clear liquid diet the next. My numbers went down, the liver numbers climbed for a bit, but probably because I was being allowed 3 percocets a day. They stayed steady long enough to try a boiled turkey sandwich, which I did without pain & I was allowed to go home...
I've been on the Glycemic Index diet for 5 months & lost close to 60 lbs. I still smoke, about 10 cigarettes a day. I had been planning to quit when I hit my good BMI, but fate loves to change the rules of the game on ya...Slowly getting back on the diet which is already low fat & trying to be careful.I don't have to worry about losing time from the diet - I dropped five pounds in three days at the hospital... Taking a Sennokot stool softener & 3-4 litres of water against the Percocet. And keeping my fingers crossed...
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