Review: could Oxycodone cause Rash generalised (Rashes)?
Summary: Rash generalised 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, 1,134 have Rash generalised. Find out below who they are, when they have Rash generalised and more.
You are not alone: join a mobile support group for people who take Oxycodone and have Rash generalised >>>
Oxycodone has active ingredients of oxycodone hydrochloride. It is often used in pain. (latest outcomes from 27,274 Oxycodone users)
Rash generalised (rash on most of body parts) has been reported by people with rheumatoid arthritis, high blood pressure, high blood cholesterol, osteoporosis, depression. (latest reports from 146,455 Rash generalised patients)
On Jan, 10, 2015: 25,916 people reported to have side effects when taking Oxycodone. Among them, 1,134 people (4.38%) have Rash Generalised.
Time on Oxycodone when people have Rash generalised * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years |
|Rash generalised||69.57%||14.49%||4.35%||2.90%||5.80%||2.90%||0.00% |
Gender of people who have Rash generalised when taking Oxycodone * :
|Rash generalised||55.83%||44.17% |
Age of people who have Rash generalised when taking Oxycodone * :
|Rash generalised||0.00%||0.00%||0.18%||1.23%||5.79%||21.49%||27.11%||44.21% |
Severity of Rash generalised when taking Oxycodone ** :
|least||moderate||severe||most severe |
|Rash generalised||0.00%||71.43%||14.29%||14.29% |
How people recovered from Rash generalised ** :
|while on the drug||after off the drug||not yet |
|Rash generalised||0.00%||0.00%||100.00% |
Top conditions involved for these people * :
- Pain (260 people, 22.93%)
- Multiple myeloma (185 people, 16.31%)
- Metastases to bone (134 people, 11.82%)
- Breast cancer (109 people, 9.61%)
- Diabetes mellitus (96 people, 8.47%)
Top co-used drugs for these people * :
- Oxycodone hcl (1,134 people, 100.00%)
- Zometa (398 people, 35.10%)
- Oxycontin (391 people, 34.48%)
- Aspirin (295 people, 26.01%)
- Aredia (264 people, 23.28%)
* 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 Rash Generalised while taking Oxycodone?
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- support group for people who take Oxycodone and have Rash Generalised
- support group for people who take Oxycodone
- support group for people who have Rash Generalised
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- 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.
- What drug helped most to get rid of rash?
Antihistamines did not help my itchy rash from this drug. What else can I use or get from my doctor?
- 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
- How long does redness last after picato?
After 3 and a half weeks, I still have a huge red splotch on my face where I applied picato gel according to directions from my dermatologist. I'm very worried that it will be permanent. I had a huge water filled blister the morning after my first application of the gel. I used it two more times as directed. After a week, some of the redness was going away but I've seen no more improvement in the past two weeks. I'm still scaley, rough and red.
Has anyone else experience this? I went by the doctors office the first morning and was told it was as expected. I've called back and been told not to worry. I see the dr in two more weeks, but for now, I'm quite upset that permanent damage has been done. I was not warned at all that this could happen. The photos in the medication packaging led me to believe that in 3 weeks, all redness would be gone. Info needed for sure. Please let me know. Thanks
- I used coartem and developed redish all over my body. can coartem cause rashes
i developed rashes which is itching me after using coartem for three days. also having sensation in my mouth and blister at the angle of my lips. could it be a side effect from coartem?
More questions for: Oxycodone, Rash generalised
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- Lamotrigine severe rash
I started taking 100mg of Teva-Lamotrigine Nov 22 once daily. I got a refill on Dec 5 that was Mylan-Lamotrigine. Two days later I woke up with an odd hot feeling rash all over my body and severe fatigue. I went back to bed 1/2 hour later after taking my regular Wellbutrin and the Lamotrigine. I woke up late morning. It got progressively worse during the day and I had a headache,fever and chills. I took the anti-histimine Aerius later that day which didn't help. The next day I went to a walk in clinic and they said it wasn't the Lamotrigine and thought it was a virus and did a throat swab. The fever and chills went away after a few days but I still have the rash. Finally after a week I saw a doctor that agreed it was the drug and I am now on the second week of Prednisone steroid treatment and prescription Reactin which is helping slowly. I have reported it to the Mylan drug company.
- Rash from eating kale
I ate kale for the first time on Monday. I only had a small bowl of fresh mixed green salad, so it wasn't entirely Kale. By Tuesday, I had a small rash on my left hip. I ignored it at first. Thursday evening, I decided to eat a large kale salad with other veggies and salmon, all of which I have eaten regularly aside from kale. Friday morning, my entire body was covered in the same rash that appeared Tuesday. I went to the ER. The doc said it was some type of allergic reaction. The ONLY thing I did/consumed different was the kale. I can't find much about it's reactions, though.
- Mensis cycle and oxycontin
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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.
- 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?
More reviews for: Oxycodone, Rash generalised
Comments from related studies:
From this study (5 months ago):
Dry, red, bumpy rash. Mostly on face, neck and upper body.
SpaceMan on Sep, 1, 2014:
Male 43 White, also with scaly bumpy red rash started in shins, completely surrounded lower legs in two years time, started after I turned 40 and using Oxycodone 120 mg per day for four years. Now into 7th year, interfering with ambulation, massive foot and ankle swelling, developed idiopathic pulmonary hypertension over last 12 months with tricuspid valve failure.
From this study (1 year ago):
the rash coincides with when i started taking the viagra. is there another ED drug that works as well without causing a rash on my chest and back?
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