Would you have Fibroids (Uterine fibroids) when you have Systemic lupus erythematosus?
Summary: Fibroids is reported only by a few people with Systemic lupus erythematosus.
We study people who have Fibroids (Uterine fibroids) and Systemic lupus erythematosus from FDA and social media. Find out below who they are, other conditions they have and drugs they take.
You are not alone: join a mobile support group for people who have Systemic lupus erythematosus and Fibroids >>>
Systemic lupus erythematosus
Systemic lupus erythematosus (an autoimmune disease, which means the body's immune system mistakenly, attacks healthy tissue) can be treated by Plaquenil, Prednisone, Hydroxychloroquine Sulfate, Cellcept, Methotrexate, Azathioprine. (latest reports from 13,091 Systemic Lupus Erythematosus patients)
Fibroids (non cancerous tumour of muscle layer) has been reported by people with rheumatoid arthritis, multiple sclerosis, breast cancer, birth control, osteoporosis. (latest reports from 1,079 Fibroids patients)
On Dec, 31, 2014: 1 people who has systemic lupus erythematosus and Fibroids is studied.
Gender of people who have systemic lupus erythematosus and experienced Fibroids * :
Age of people who have systemic lupus erythematosus and experienced Fibroids * :
Severity of the symptom * :
Top co-existing conditions for these people * :n/a
Most common drugs used by these people * :
- Synthroid (1 people, 100.00%)
- Lovenox (1 people, 100.00%)
* Approximation only. Some reports may have incomplete information.
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 Systemic Lupus Erythematosus and Fibroids?
You are not alone! Join a mobile support group:
- support group for people who have Fibroids and Systemic lupus erythematosus
- support group for people who have Systemic lupus erythematosus
- support group for people who have Fibroids
Could your drug cause:
Other conditions that could cause:
Can you answer these questions (Ask a question):
- 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!!!
- What causes it? and why is it so painful? (1 answer)
I can lift my arm out in front of me but not out to the side!! The diclofenac doesn't seem to help. Any suggestions? Has anyone been on benlysta?
- Does plaquenil fade lupis discoid lesions? does plaquenil cause you to lose your hair? (1 answer)
I have had lupus discoid for 30+ years and no am experiencing them on my face. I want to know if plaquenil will help me.
- Should i take lamictal if i have sle lupus?
I have SLE Lupus and I was checking the side effect list for Lamictal and it said it could cause Lupus like symptoms. Is this a bad drug for me to take if I already have lupus?
- What is the effect of having prolonged oral sex with my girly who is taking 750 mg mychophenolate, morning and night,and 10 mg prednisone once daily, can this be present in her orgasm fluid (1 answer)
Can the drugs Mychophenolate and or Prednisone be present in a female orgasm, during oral sex, and can they affect their partner
More questions for: Systemic lupus erythematosus, Fibroids
You may be interested at these reviews (Write a review):
- 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".
- Health issues and struggles
I have numerous health issues. Some I've lived with not realizing they were there. Others are caused by meds I've taken in the past or am still using now.
Lupus is the most recent and biggest trouble I have right now. It is caused by the one drug that finally gave me control of my seizures
Some of the worst troubles have been TBI from birth. Epilepsy my entire life. Brain tumor ( surgery to remove it in 1982) Graves Disease. RA and most recently Lupus ( caused by the keppra)
- Transient psychosis in indomethacin
I had taken indomethacin infrequently for years for joint pain but never for more than 2 weeks in a row. One night, when I had been taking it daily for about 2 weeks, I had a bout of psychosis approximately 1/2 hour after ingesting the indomethacin at bedtime. I just waited it out, and in about 5-6 hours the effect wore off and I've been fine since. I had never had a bout of psychosis before that. (I've never taken it again.)
More reviews for: Systemic lupus erythematosus, Fibroids
Comments from related studies:
From this study (6 days ago):
Took steroids for intensely itchy full body rash. Rash did not cease. Last day of prednisone tablets, got nausea sick headache. Second day with black water diaherria, incontinence, can keep no foods in. Will be starting second course prednisone tomorrow. Rash worse than ever.
From this study (1 week ago):
Diagnosed with MCTD when I was 10. Positive ANA, speckled pattern. Developed anti-smith antibodies after first pregnancy. Diagnosed with CREST four-years ago with significant progression recently. Esophogeal dysmotility, hiatal hernia repair, now esophageal stasis and constipation. Had a digital sympathectomy to R hand. Ulceration healed but discoloration same in both hands. Gallbladder removed due to stones. Discoid lupus rash on lower extremities and back, flare with sun exposure. Red inflamed disks on skin of fingers that come and go. Significant telangiectasis, varicose veins with documented valve failure.
From this study (3 weeks ago):
lowerright side pain
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