Review: could Oxycodone cause Rheumatoid arthritis?
Summary: Rheumatoid arthritis is found among people who take Oxycodone, especially for people who are female, 50-59 old, have been taking the drug for < 1 month, also take medication Oxycodone hcl, and have Rheumatoid arthritis.
We study 25,916 people who have side effects while taking Oxycodone from FDA and social media. Among them, 122 have Rheumatoid arthritis. Find out below who they are, when they have Rheumatoid arthritis and more.
You are not alone: join a mobile support group for people who take Oxycodone and have Rheumatoid arthritis >>>
Oxycodone has active ingredients of oxycodone hydrochloride. It is often used in pain. (latest outcomes from 27,274 Oxycodone users)
Rheumatoid arthritis (a chronic progressive disease causing inflammation in the joints) has been reported by people with osteoporosis, high blood pressure, pain, high blood cholesterol, osteopenia. (latest reports from 218,584 Rheumatoid arthritis patients)
On Dec, 30, 2014: 25,916 people reported to have side effects when taking Oxycodone. Among them, 129 people (0.50%) have Rheumatoid Arthritis.
Time on Oxycodone when people have Rheumatoid arthritis * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years |
|Rheumatoid arthritis||50.00%||0.00%||0.00%||0.00%||0.00%||25.00%||25.00% |
Gender of people who have Rheumatoid arthritis when taking Oxycodone * :
|Rheumatoid arthritis||73.76%||26.24% |
Age of people who have Rheumatoid arthritis when taking Oxycodone * :
|Rheumatoid arthritis||0.00%||0.00%||0.00%||0.00%||7.02%||25.44%||36.84%||30.70% |
Severity of Rheumatoid arthritis when taking Oxycodone ** :
|least||moderate||severe||most severe |
|Rheumatoid arthritis||0.00%||100.00%||0.00%||0.00% |
How people recovered from Rheumatoid arthritis ** :
Top conditions involved for these people * :
- Rheumatoid arthritis (85 people, 65.89%)
- Pain (32 people, 24.81%)
- Depression (15 people, 11.63%)
- Prophylaxis (10 people, 7.75%)
- Anxiety (9 people, 6.98%)
Top co-used drugs for these people * :
- Oxycodone hcl (129 people, 100.00%)
- Methotrexate (60 people, 46.51%)
- Prednisone (55 people, 42.64%)
- Humira (53 people, 41.09%)
- Folic acid (36 people, 27.91%)
* 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 Rheumatoid Arthritis while taking Oxycodone?
You are not alone! Join a mobile support group:
- support group for people who take Oxycodone and have Rheumatoid Arthritis
- support group for people who take Oxycodone
- support group for people who have Rheumatoid Arthritis
Drugs in real world that are associated with:
Could your condition cause:
Can you answer these questions (Ask a question):
- What does unmasking mean; and does it mean that i always had hight cholesterol and triglycerides, or did actemra increase them?
I have failed many RA meds, and now receive actemera x's 10 months I have never had high cholesterol or triglycerides and did not get my cholesterol checked except for the baseline 2/2014 and 12/2014 I was 198 TChol and now am 245; my tri up 85 points. my MD said that now that my inflammation is normal it shows my true cholestorol. I don't understand.
- 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.
- Is it safe to take zocalo if you are taking humora and methotrexate
Is it safe to take all three of these together? I need to know if there is any adverse side effects of taking these drugs at the same time?
- Among those having had a previous tia or stroke; what percentage had another such incident while take uloric?
Have written more details just a few minutes ago. Wasn't sure I made my question clear.
- How many/what percentage of older males who have had a stroke, have another while taking uloric?
Concerned as my Rheumatologist wants me to start using Uloric40 mg and while I see that their is a relatively small incidence of stroke occurring (unless you are part of the "small" group); I have been unable to locate statistics for those previous stroke patients that are now using or have used Uloric, and had another stroke.
More questions for: Oxycodone, Rheumatoid arthritis
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In 2005 I had NMS, which was not detected by my drs for 4 months. I'd been on Lexapro & Seroquel for 2 yrs, but was weaned from Lexapro & placed on Lamictal 3/05. Began getting low-grade fevers, which I was told were not caused by the Lamictal. I quit taking it anyway, fevers (along with uncontrollable shivering) continued & got higher. By 5/05 my temps were reaching 105 deg F. Husband said I became combative, refused to go to hospital. Early June/05 he came home to find me wrapped in blankets, with a temp over 105 F. He tried to place me in a tub of cold water, said I was rigid & screamed when he tried to move me. I was in the tub, speaking "in tongues" (his description, I have no memory of this). He called 911, took me to hospital. I woke, no idea where I was or why. After a lumbar puncture & 2 days in ICU I went home. The fevers continued...2 weeks later he came home to find me wrapped in sheets, towels, blankets, with the heat on full (it was in the 90's outside) he called ambulance again. I awoke to find myself under an ice blanket with nurses pushing large vials of dantrolene into both arms, several liters. Another LP, a stint in ICU...this time they told me it was NMS. The dr who dxd me said he was surprised I was alive, & not a vegetable, as my temp had peaked at 109 deg F. I suffered brain damage; short-term memory loss, brain can't control my body temp, my blood pressure went up. An arteriogram showed completely healthy heart & arteries, no plaque at all. I lost all body fat as well as some muscle mass. The fevers continued even after stopping the Seroquel. I visited my PCP for a checkup in 9/05, temp was normal. I started shuddering, my temp went up a full degree every 5 minutes. PCP admitted me to ER, my heart rate was over 272 B/M; they stopped my heart 3 times to "reset" it, which didn't work. I spent 3 days in hospital. Several months later my P doc tried me on Lamictal alone; I got Stevens-Johnson syndrome. I stopped the drug as soon as the signs appeared. I've been untreated, except for Neurontin & Primidone, until my manic episodes became unlivable. 3 weeks ago I went 8 days with no sleep, became psychotic. My P doc gave me Trileptal, which has evened my moods, but I've been getting low-grade fevers (highest was 103.6). Would having had NMS in the past make me more prone to falling to it again with the Trileptal? It's the only new med I've taken in over a year.
- 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. ..
- Sulfasalazine and the never ending menstrual cycle
I started this drug and never had menstrual problems begore. Within 3 months, I started my period and it never stopped even with stopping the drug for 3 mon ths. I ended up going my gyne and he prescribed megace. I had been bleeding for a total of 6 months. Made an appt with my rhuemy and explained this situation. His words were "it hasn't been listed in the literature as a side effect". Keep taking it. I started it again. Same situation and same treatment. Never took it again and changed rheumy.
- 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.
More reviews for: Oxycodone, Rheumatoid arthritis
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Symptoms started in 2008 shooting pain in right leg from lumbar area down to foot.
Was diagnosed with 3 herniated discs. Pinching of sciatica nerve from disc herniation. Went to Physiotherapy for 4 months. Corrected 90% but left with right foot 2 middle toes nerve damage. 2010 all over body pain started. Could not sit or stand for long periods of time. Bouts of sciatica started again. Went for a 3rd MRI. Sent to neurosurgeon. Could not do anything. Sent to neurologist. Diagnosed with fibromyalgia. Taking oxyneo for pain, pregabalin & cymbalta for nerve pain. I'm able to live with the pain but I can't handle the side effects. I have started treatment with a naturopathic doctor to see if I can go off some of the pills like the pregabalin that is causing weight gain, extreme sweating and mood swings.
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