Review: could Morphine cause Systemic lupus erythematosus?
Summary: Systemic lupus erythematosus is found among people who take Morphine, especially for people who are female, 60+ old, also take medication Morphine sulfate, and have Pain.
We study 48,671 people who have side effects while taking Morphine from FDA and social media. Among them, 43 have Systemic lupus erythematosus. Find out below who they are, when they have Systemic lupus erythematosus and more.
You are not alone: join a mobile support group for people who take Morphine and have Systemic lupus erythematosus >>>
Morphine has active ingredients of morphine sulfate. It is often used in pain. (latest outcomes from 49,763 Morphine users)
Systemic lupus erythematosus
Systemic lupus erythematosus (an autoimmune disease, which means the body's immune system mistakenly, attacks healthy tissue) has been reported by people with rheumatoid arthritis, crohn's disease, osteoporosis, multiple sclerosis, high blood pressure. (latest reports from 13,108 Systemic lupus erythematosus patients)
On Feb, 13, 2015: 48,666 people reported to have side effects when taking Morphine. Among them, 43 people (0.09%) have Systemic Lupus Erythematosus.
Time on Morphine when people have Systemic lupus erythematosus * :
Gender of people who have Systemic lupus erythematosus when taking Morphine * :
|Systemic lupus erythematosus||91.11%||8.89% |
Age of people who have Systemic lupus erythematosus when taking Morphine * :
|Systemic lupus erythematosus||0.00%||0.00%||5.88%||5.88%||20.59%||20.59%||14.71%||32.35% |
Severity of Systemic lupus erythematosus when taking Morphine ** :
How people recovered from Systemic lupus erythematosus ** :
Top conditions involved for these people * :
- Pain (6 people, 13.95%)
- Migraine (5 people, 11.63%)
- Rheumatoid arthritis (5 people, 11.63%)
- Systemic lupus erythematosus (4 people, 9.30%)
- Nausea (4 people, 9.30%)
Top co-used drugs for these people * :
- Morphine sulfate (17 people, 39.53%)
- Prednisone (9 people, 20.93%)
- Zofran (8 people, 18.60%)
- Omeprazole (8 people, 18.60%)
- Potassium chloride (8 people, 18.60%)
* 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.
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Drugs in real world that are associated with:
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Can you answer these questions (Ask a question):
- Does morphine cause mouth ulcerations
one month after beginning the drug morphine I developed mouth ulcerations on my mouth palate. My mouth and face has developed soreness and painful pressure.
- 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 .
- Is osteoarthrisis caused by drinking alcohol
Chronic pain in spine, right hip, right hand, swollen joints in both hands, swollen knees.
- Is vomiting all liquids common while taking morphine (1 answer)
I Recently started taking 6mg of Hydro-Morphine per day for pain. Every time i take the drug i vomit up any liquids I drink. i fell just fine without anything in my stomach but as soon as i eat or drink I instantly become nauseated and vomit everything. It is hard not to drink because the drug is making me very thirsty. So i try to drink and my body rejects it over and over again.. this goes on for hours (3-5)because i am sooo thirsty that I can not stop drinking.
- 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!!!
More questions for: Morphine, Systemic lupus erythematosus
You may be interested at these reviews (Write a review):
- Morphine and amenorrhea
For over ten years I have been taking high doses of morphine for chronic pain nerve pain. At one point I was taking 400mg of morphine a day. By splitting up the doses I was able to get it down to 300mg a day. My periods stopped almost immediately, even when i was still taking small doses before I was even raised to 100+ mg a day.
Now I am taking (using) Fentanyl #75 patches plus Fentanyl #12 patches and they work great with no up-n-down from pills wearing off. I have been off morphine and using Fentanyl for almost one year now. I still don't get my period, though. They stopped when I was 43 and I don't miss them at all!! But when I read that there was no link between morphine and Amenorrhea I had to tell my tale...
- Prostatitis and prostate cancer acceleration due to anaesthetics
Caught Chlamydia in 1978. Interestingly, the partnered girl's sister worked in an aviary; and I found out later that Chlamydia originates from handling birdshit and birds are the carriers. Chlamydia was undiagnosed at the time, so it was listed under 'Non-specific urethritis'. Chlamydia wasn't named until about 8 years later. I was given tetracycline and told to stay off alcohol and sex. Yeah, really?
I was 24; highly sexed, and in night clubs and pubs most nights. I laid off the alcohol and after two weeks, I was good. The laying off sex, I understood, because of contamination of others (condoms were little used in 1978 in the singles arena); so I masturbated one night... and that caused me immense in my prostate, and pain and suffering for the rest of my life.
The ejaculation was extremely painful, and chronic prostatitis started. I was on and off medication for two years. I got light-sensitivity, which means in sunlight, I came out in burning rashes. I became allergic to tetracycline.
The message? Consultants are generally poor at communicating what not to do, and why not. Lay off sex he said. All he had to say was no sex, no masturbation; or you may suffer for the rest of your life. That would have done it.
No-one has been able to help me with this chronic prostatitis. In the early years it would come and go, but as the years have gone on, it has become more frequent, and now it is constant.
Four years ago I went in for major foot surgery, and flat-lined. I was in intensive care for 2 days, on a morphine drip for the pain.
When I awoke, I knew immediately I was suffering with my prostate. It was aching badly and I was urinating frequently. The nurses were amazed with how many 'bottles' I filled in such a short time.
For the next few months, I was in agony. I have tried every possible drug going, as well as prostate massage and the indignancy of a urethragram whilst female students were watching.
In November 2011 I went to see another consultant, who suggested a biopsy. I was diagnosed with prostate cancer. After much research, I now know that my diet and lifestyle, coupled with inflammation of the prostate with prostatitis, has caused prostate cancer. Yes, there is a direct relationship between prostatitis and prostate cancer.
I am now beating it, without drugs and without surgery. I have changed my diet to a vegan diet, no sugar, very little alcohol, and a lot of supplementation.
In December 2013, I went in for more foot surgery. I was unaware about the morphine at this time, so didn't consider it being a problem. I talk to the anaesthetist, who wanted me to have an epidural (injection in the spine to numb my lower body). At no point did he talk to me about my prostate history.
In recovery, I sensed a problem as soon as the anaesthetic began to wear off. It was like my prostate and testicles wanted to explode. I knew I was going to have problems. My intuition reminded me of three years ago with the morphine, so I asked the surgeon if he knew of these complications with morphine, but he didn't.
I spoke to the head of the post-operative ward and asked her if she had any experience of post-operative patients who suffered with prostatitis after surgery, and she confirmed she had. So here was a nurse who knew of the problems, but the surgeon and anaesthetist didn't. This is typical in the health service... the lack of sharing.
Not only did I suffer with the chronic prostatitis (and still am 11 month later) I was incontinent. It took 6 months of 4-times daily legal exercises to get back control of my bladder.
For me, morphine has a dire effect on my prostate.
Bear in mind that your prostate is designed to eliminate toxins, so it is flooded with morphine. I will do my best to ensure I check for morphine in any drugs or anaesthetics in future.
My first PSA level was 18, 3 ears ago. I brought it down to 13.5, then 10.4, 10.3, 10.9, 11.3, 14.3 and after the last surgery it spiked at 17.5. As a result, I have gone back to a stricter, greener raw diet to bring it down again.
Oh, and anther tip; you need to get your vitamin D3 blood count above 200n/mols (UK measure) to have any chance of not getting prostate cancer. Mine was 32 when I was diagnosed. Today it is over 200, from supplementation of 10000 ius a day. Minimum in the UK, recommended by scientists, is 75n/mols, and it's too low. OK if you have a great immune system, but not if you want to fight prostate cancer and prostatitis.
Black African males in the Northern US states and in Europe have twice as much risk, due to lack of sunlight. Sunlight on skin promotes vitamin D3, which is essential for the immune system and production of calcium.
Black African males need more sunlight to produce the same amount of vitamin D3 as a caucasian male. Also, any male who is bald and fat has a higher risk, so a Black African, obese bald male, has an extremely high risk of prostate cancer, unless they get their immune system in order.
The main way to fight all this, is on a clean, raw vegetable diet, pure water, no alcohol, sugar, processed or refined food, no meat, no dairy, no vegetable oil, no exceptions, and some breath-taking regular exercise. Just like we did 100 years ago. Go figure! Look at chronic disease studies of 100 years ago. 85% of all disease was from infection. Today 85% is from chronic disease.
Your prostate eliminates toxins, and today, we are overloading it. Remove the toxins (and the stress and anxiety) and things will improve. It's a hard road; but with it is you want to be healthier and live longer.
- Had nms in 2005, will trileptal increase chance of recurrence?
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.
- Androgel for secondary hypogonadism
Severe swelling in legs, ankles and feet after being on my feet for more than one hour. Pain in calves and ankles. Feels like they're being squeezed or compressed. Pain dissipates after laying down for a few hours. Swelling never completely dissipates. Always some swelling in ankles.
- Lupus induced by amoxicillin (1 response)
Was given Amoxicillin for Strep Throat and on day 10 I noticed a rash starting on my torso and began to feel ill, as if I had the flu. Went to emerg and got sent home with Benadryl. Woke up the next morning to the rash getting worse and an overall feeling of fatigue. Went to emerg again and this time had blood taken and the results showed an extreme rise in my white blood cells and by then, I had a fever. I was airlifted to another hospital where they did tests, but really had no idea what was wrong. I discharged myself with a script for corticosteroids and by then my joints began to stiffen, to a point of barely being able to walk and the pain was excruciating! I had to be cared for by my husband and struggled to lift my tea cup, or get out of bed. This lasted for about a month and then gradually began to subside. The doctors never did have answers for any of it. They chalked it up to an allergy to Amoxicillin. One mentioned "Steven Johnson Syndrome".
More reviews for: Morphine, Systemic lupus erythematosus
Comments from related studies:
From this study (4 days ago):
had ptc /ih for 12 years. pyoderma onset dec 3rd 2014. horrible. over 65 blisters, bumps, papules, pustules, nodules all on my face. Had new derm accuse me of doing it deliberately to my face. horrific.
From this study (6 days ago):
coolaero on Feb, 7, 2015:
there wont be side effect other that DEATH
peanuts on Mar, 31, 2010:
my friend is suffering from rhumatory arthertis.and is currenty taking cocaine. oxy cotin,prestine, wellbutrim, predisone 10mg what side effects should she expect ?????
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