Review: could Methadone hydrochloride cause Skin rash (Rashes)?
Summary: Skin rash is found among people who take Methadone hydrochloride, especially for people who are male, 40-49 old, have been taking the drug for < 1 month, also take medication Zometa, and have Pain.
We study 2,080 people who have side effects while taking Methadone hydrochloride from FDA and social media. Among them, 53 have Skin rash. Find out below who they are, when they have Skin rash and more.
You are not alone: join a mobile support group for people who take Methadone hydrochloride and have Skin rash >>>
Methadone hydrochloride has active ingredients of methadone hydrochloride. It is often used in pain. (latest outcomes from 2,842 Methadone hydrochloride users)
Skin rash (redness) has been reported by people with rheumatoid arthritis, high blood pressure, high blood cholesterol, osteoporosis, depression. (latest reports from 146,454 Skin rash patients)
On Jan, 26, 2015: 2,080 people reported to have side effects when taking Methadone hydrochloride. Among them, 52 people (2.50%) have Skin Rash.
Time on Methadone hydrochloride when people have Skin rash * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years |
|Skin rash||25.00%||25.00%||12.50%||0.00%||25.00%||12.50%||0.00% |
Age of people who have Skin rash when taking Methadone hydrochloride * :
|Skin rash||0.00%||0.00%||0.00%||4.08%||18.37%||40.82%||14.29%||22.45% |
Severity of Skin rash when taking Methadone hydrochloride ** :
|least||moderate||severe||most severe |
|Skin rash||0.00%||66.67%||33.33%||0.00% |
How people recovered from Skin rash ** :
|while on the drug||after off the drug||not yet |
|Skin rash||0.00%||0.00%||100.00% |
Top conditions involved for these people * :
- Pain (11 people, 21.15%)
- Anxiety (7 people, 13.46%)
- Metastases to bone (7 people, 13.46%)
- Osteoporosis (5 people, 9.62%)
- Crohn's disease (4 people, 7.69%)
Top co-used drugs for these people * :
- Zometa (20 people, 38.46%)
- Aredia (16 people, 30.77%)
- Prednisone (15 people, 28.85%)
- Celebrex (14 people, 26.92%)
- Clonazepam (13 people, 25.00%)
* 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 Skin Rash while taking Methadone Hydrochloride?
You are not alone! Join a mobile support group:
- support group for people who take Methadone hydrochloride and have Skin Rash
- support group for people who take Methadone hydrochloride
- support group for people who have Skin Rash
Drugs in real world that are associated with:
Could your condition cause:
Can you answer these questions (Ask a question):
- 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?
- Can long-term methadone use cause or increase the risk of colon cancer?
I had a two-level spinal fusion at L4-S1 in 2000 after being injuried at work in Sept. 24, 1997. I lost everything after...the unjury, ability to do my job, my wife and family (couldn't take the strain) my home, my sense of self and purpose, direction and belonging...credit rating and ability to pay my bills.
After a long period of waiting to settle my workmens' comp. case, I returned home, from the Bat Area back to Arizona to take of my mother with a yet un dianosed case of moderate dementia.
Then, in 2011 I had a 2nd surgery to relieve spinal stenosis btwn. L2-L4, just above the fusion site.
I've been taking methadone since early 2004, a little over ten years, now. I've had high blood pressure since my injury.
Now, I waiting to be scheduled for a colonoscopy, with my father having had polyps and the way I've been feeling..drained, tired all the time, and stomach pains ( in addition to my chronic low back pain), I...
find myself wondering if there is any relationtionship between the methadone and other meds and cancer?
- 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?
- Does ginger treats skin rashes?
i have skin rashes and i treated it with ginger is it right to treat to treat skin rashes with ginger?
More questions for: Methadone hydrochloride, Skin rash
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- 3 strong drugs together against neuropathic pain
Neuropathic pain debuted when I was 24, now I'm 50. Received diagnosed with Ehler-Danlos syndrome (EDS), joint hypermobility type, when I was 35 years old. So it can take some time to get a diagnose. And as EDS-patient I do not belong to any clinic. Orthopedics says that EDS is not orthopedic, rheumatology says that EDS is not an autoimmune disease, GPs say that EDS is too difficult, and so on. Sooner or later we all end up at Psychiatry, even if we are not depressed.
The first kind of pain I got when I was 24 came from low back, but I experienced as pelvic pain and leg pain. It was clearly a neuropathic pain, but it took years to find out. Later it was treated by a pain clinic with cortisone around the genitofemoral nerves (both sides). Since this treatment didn't result in lasting freedom from pain, the pain clinic started to give me RF (radio frequency) treatment. This made the pain disappeared after one year, and I was 80% free from it between 2002 and 2014, 12 years. The pain doctors said pain could return after 10 years.
The other kind of neuropathic pain started 2003 with intense stomach pain. During 6 months I could hardly eat nothing due to nausea and vomiting. After this 6 months, stomach pain changed to almost unbearable pain in upper back.
What happened 2003, and what all the doctors missed, was that the right lowest ribs slid up over the sternum. This rib dislocation is till there today, but now with a lot of cartilage formed around the rib where it is stuck in the lower end of the sternum. The dislocation is clearly visible on X-ray. This has greatly affected the thoracic spine. I have a scoliosis which I had not before 2003. And I still have severe pain in the thoracic spine.
It was initially treated with morphine daily, and later with Durogesic (fentanyl), but this didn't help much. 2005 I was hospitalized because I had too much pain to take care of myself and my hygiene. After some months the doctors started to give me clonazepam because the muscles along the spine was in a chronic seizures. Clonazepam helped, but I could still have a lot of pain in two vertebrae in the thoracic spine. It felt as if someone drilled into the vertebrae without anesthesia. After a few months, doctors also prescribed me methadone. Then the pain disappeared almost completely. Since 2006, I have eaten clonazepam and methadone every day, and I need to sleep in an armchair to not get more pain because of moving during sleep.
There are side effects. After 1,5 years with clonazepam and methadone I started to have panic attacks. Or rather one long panic attack which didn't stop before I got treatment with amitryptilin and pregabalin (Lyrica). These 2 medicines stopped the panic disorder completely after some hours, and the panic was then gone. Then I got side effects of these 2 medicines, amitryptilin & Lyrica, too. I gained a lot of weight (from 83 to 148 kg) and got much water (edema) in both my legs under the knees and in both feet. The feet could swallow to the double size. 2012 I stopped with amitryptilin and started to loose weight again (in Aug 2014 below 80 kg) and get less water in my legs. Today I eat as little medicines I can, but I have to take methadone, clonazepam and Lyrica every day, twice. If I try to take away one of these 3 medicines, I got pain problems at once. Lyrica is the most painful one to take away. In Sept-Dec 2013 I lowered Lyrica from 300 mg daily, to 150, then to 75 and finally 0 mg. The pain I had was extremely difficult to handle. It didn't help to take more methadone or anything else. I have checked on Internet and found that many people got pain from quitting with Lyrica. Most people start eating it again. So did I. But 2006 and 2007 it was enough to treat the pain with methadone and clonazepam, I got the Lyrica against anxiety not pain. But today I take Lyrica against pain.
Beside weight gain and leg edema, clonazepam and Lyrica significantly affect the sexual desire. And Lyrica alone makes it almost impossible to ejaculate. All four drugs together (clonazepam, methadone, amitryptiline and Lyrica), make one forget all about sex life. You don't even miss it. When I stopped with amitryptiline and lowered Lyrica (still taking clonazepam and methadone), I could suddenly easily get erections again, feel desire, but not getting orgasms. This is quite difficult to deal with.
The pain pattern is greatly affected, by pain and by the medicines. So is the mood. I get something which feels like heavy depression, especially if I take the medicines late that day. I should take a medicine like methadone 3 times a day, because the effects of the tablet lasts around 8 hours. But I take them every 12 hours, to have a low consumption in case doctors prescribe them too late (which happens, and then it's good to have a spouse going to the pharmacy buying them for you, because you have too much pain to go yourself).
Since methadone is also used for treating heroine addicts, medical staff treat you with disrespect when they see that it says "methadone" in your health record. I need to show a certificate that says that I deal with chronic neuropathic pain, that I never have had problems with drug addiction, to get normal respect.
I wanted to share this because I think I am alone in the world with these medicines in combination against neuropathic pain caused by hypermobile joints, joint dislocation and muscle spasms. After trying almost everything else, including surgery cutting nerves, methadone, clonazepam and Lyrica seems to be the only way to kill my pain. But it's a life where you always is questioned, because of the use of methadone. I can guarantee that everybody in the world should accept these medicines if they had experienced the unbearable pain I had in upper back before they started to give me clonazepam and methadone.
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Comments from related studies:
From this study (2 years ago):
started a year ago with small itchy bumps on back, then moved to blister, pestilules, all over bottom part of both legs, itching, burning for days and days, then turning in to scabs, then clearing, then just left over rashy spots, then a week later break out again. Now some around face, and all in back of neckline around hair, in hair, a itching sensation almost all over my body.
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