Review: could Oxycodone cause Lupus (Systemic lupus erythematosus)?
Summary: Lupus is found among people who take Oxycodone, especially for people who are female, 40-49 old, also take medication Oxycodone hcl, and have Systemic lupus erythematosus.
We study 25,925 people who have side effects while taking Oxycodone from FDA and social media. Among them, 37 have Lupus. Find out below who they are, when they have Lupus and more.
You are not alone: join a mobile support group for people who take Oxycodone and have Lupus >>>
Oxycodone has active ingredients of oxycodone hydrochloride. It is often used in pain. (latest outcomes from 27,292 Oxycodone users)
Lupus (any of various ulcerous skin diseases) has been reported by people with rheumatoid arthritis, crohn's disease, systemic lupus erythematosus, osteoporosis, multiple sclerosis. (latest reports from 13,108 Lupus patients)
On Feb, 28, 2015: 25,925 people reported to have side effects when taking Oxycodone. Among them, 37 people (0.14%) have Lupus.
Time on Oxycodone when people have Lupus * :
Gender of people who have Lupus when taking Oxycodone * :
Age of people who have Lupus when taking Oxycodone * :
Severity of Lupus when taking Oxycodone ** :
How people recovered from Lupus ** :
Top conditions involved for these people * :
- Systemic lupus erythematosus (10 people, 27.03%)
- Osteoporosis (9 people, 24.32%)
- Thrombocytopenia (7 people, 18.92%)
- Rheumatoid arthritis (7 people, 18.92%)
- Crohn's disease (6 people, 16.22%)
Top co-used drugs for these people * :
- Oxycodone hcl (37 people, 100.00%)
- Methotrexate (18 people, 48.65%)
- Prednisone (15 people, 40.54%)
- Vicodin (14 people, 37.84%)
- Aspirin (13 people, 35.14%)
* 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 Lupus while taking Oxycodone?
You are not alone! Join a mobile support group:
- support group for people who take Oxycodone and have Lupus
- support group for people who take Oxycodone
- support group for people who have Lupus
Drugs in real world that are associated with:
Could your condition cause:
Can you answer these questions (Ask a question):
- What are safe alternatives to oxycontin? since moving to florida., no pharmacy stocks or can order it. suggestions?
I've been on OxyContin for several years with pretty good results managing severe pain. Since moving south I'm finding that pharmacies cannot/will not carry it. Sent ex fr. Local md to mail order--one week later, still waiting.
I'm desperate to find an effective alternative. Ideas?
- Crohns disease and deranged lfts diferential diagnosis
Patient with Crohns disease and deranged LFTs first was on Imuran then withdrawn due to unexplained elevated LFTs.nOW On Ramicid still elevated LFTs (high bilirubin (indirect) and ALT .
- 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 there a support group in the us for people with insulinomas? (1 answer)
SUPPORT GROUP IN UNITED STATES!!!
Hi, the only support group that I've been able to find for people with insulinomas is located in the UK... just wondering if there is one in the US. I had pancreatic surgery to remove my first insulinoma in 2012, we're thinking there's another because I'm still having problems with hypoglycemia... if anyone know anything, PLEASE CONTACT ME!!! :)
I know there can't just be a support group here for FERRETS!!! people are kind of important... I hate this song, but "Don't worry, BE HAPPY" is okay, I guess... I'm trying to force it upon myself. Things will get BETTER!!!
- 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
More questions for: Oxycodone, Lupus
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- 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.
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- Lupus induced by amoxicillin (1 response)
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