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Would you have Uterine prolapse when you have Neuropathy peripheral?





Summary: there is no Uterine prolapse reported by people with Neuropathy peripheral yet.

We study people who have Uterine prolapse and Neuropathy peripheral 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 Neuropathy peripheral and Uterine prolapse >>>

Neuropathy peripheral

Neuropathy peripheral (surface nerve damage) can be treated by Gabapentin, Lyrica, Neurontin, Cymbalta, Amitriptyline Hydrochloride, Nortriptyline Hydrochloride. (latest reports from Neuropathy Peripheral 27,652 patients)

Uterine prolapse

Uterine prolapse has been reported by people with osteoporosis, multiple sclerosis, rheumatoid arthritis, breast cancer, osteopenia.(latest reports from Uterine prolapse 749 patients)

On Dec, 22, 2014: No report is found.

Do you have Neuropathy Peripheral and Uterine Prolapse?

You are not alone! Join a mobile support group:
- support group for people who have Neuropathy peripheral
- support group for people who have Uterine Prolapse

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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 does emphysemic change in the lungs mean (1 answer)
    Doctor told me I have emphysema changes in my lungs.could this be causing my nausea every day all day?
  • Can gabapentin cause bladder distension? there is no urinary symptom .
    Existing illness are Chronic renal failure (after hydro uretero nephrosis due to BPH) and peripheral neuropathy (vit B6 deficiency ) after ATT are the major problems along with BP .At present , the problem is that creatinine gas risen from 1,1 to 1.5 in 6 months .Since 6 months , I am taking medicines for neuropathy so I doubt some side effect of these medicines as Ultrasound has shown bladder distension but I do not feel any urinary problem at present. I also have kidney stones but seeing the ultrasound report , doctor said it is not hindering with urine passage . I feel some tightness , fullness and protruded lower abdomen part. I am aged 72 from India and am vegetarian.I also take some drugs for controlling blood pressure . I have elevated Blood urea at present (52) . I was given medicine to relax prostrate muscles for last 20 days but I did not feel any improvement in my bladder size. I had had my prostrate operated 2 years back.
  • Will aoolprinol increase my creatine level
    Foot pain, stage 2 kidney disease and recent laminectomy. Weakness of legs and foot pain inhibit ability to exercise via walking and bicycling. Stage 2 kidney disease caused me to switch from allopurinol to Lyrica. Do not tolerate side effects very well of Lyrica dosage of 75 mg, twice a day. Lyrica has not improved my foot condition. Please advise.
  • Is the a correlation with mycobacterium and myasthena gravis? (2 answers)
    I was exposed to a leper colony for about five months while in Vietnam. Many of the lepers died with open wounds and I actually wore some of their beads and trinkets around my neck. I slept on their beds and drank from their water source. Out of the clear blue almost 40 years later with no indication at all I came down with Myasthenia Gravis. Thyroid plays no role in my disease, so that has been rules out.

    Does the Mycobacterium in Leprosy have any possible correlation with me getting Myasthenia Gravis?

    Thank you.

More questions for: Neuropathy peripheral, Uterine prolapse

You may be interested at these reviews (Write a review):

  • Idiopathic insomnolence (1 response)
    So...

    In 1997 I was diagnosed with Narcolepsy with an intolerance to Dexamp(hetamine) tablets.

    After 3 years of nose operations, and sleep tests to remove other potential issues (lung problems or apnoea) I have finally been re-diagnosed (2013) with idiopathic insomnolence.

    Modaphinil caused a reaction of insane nausea, pains behind the eyes, dizzy spells, with no real change in blood pressure.

    Dexamphetamine was erratic (on recent retrial) with extremes causing dizzy spells and slow progressive drop in BP over 3 weeks from average 125/75 to 105/60. Occasionally it would wake my body up but my brain would be slow to follow, and the conflict would take me to the cleaners for the next two days.

    I was diagnosed with IgAN in 2004, and have progressive idiopathic neuropathy in my feet since 2011.

    The sleep specialist wants me to try Klacid (clarithromycin) as it has reportedly caused insomnia on a regular basis. I've not yet agreed.

    That's me in a nutshell.

    To many idiopathics and drug rejections.

    Somebody has not got their finger on the pulse, but no idea who yet.

    Jus thought I'd throw this out there in case anyone else is having difficulties aswell.

    Cheers !
  • Avelox with prednisone and nabumetome = disaster
    I was prescribed that combination of drugs in January 2013 when I went to my family doctor with a bad chest congestion and painful knees. After starting on the drugs, I got a severely painful neck and thumb and noticed some tingling in my left foot. I took the whole course of the avelox and prednisone, though I discontinued the nabumetome. I kept getting weaker and weaker till I could hardly walk. I ended up in the emergency room and was first diagnosed with Rhabdomyolysis but rushed to a bigger hospital for further diagnosis and treatment. I was close to needing blood, my kidneys were shutting down and I could barely walk. I was so weak! My right hand and left foot went "to sleep" and still haven't woken up. ( as of October 2013)

    After many, many tests, they came up with a tentative diagnosis of vasculitis and myositis.

    Then I had a kidney biopsy which confirmed the vasculitis and I was immediately treated with chemotherapy -- cytoxin for 6 months.

    IAlthough I do feel much better, I am still suffering and taking drugs for the vasculitis and I am told that I may go into remission, but it could flare up again anytime. I am convinced that it was the drug combination that caused all this. I had been feeling great and had a daily walking routine of walking 2 to 5 miles per day, and no other complaints.

    The nephrologist did say that while it might be that the vasculitis was drug induced, it didn't matter because I have it and he's treating it and would be doing it this way no matter how I got it.

    When I told my family doctor that I thought it was the drug combination that caused my problems, he seemed surprised and really no discussion. I told them to put it in my medical records to NEVER give me a flouroquinolone drug again.

    Yesterday when I went for a blood test and urinalysis ( which I was doing biweekly, but now every 6 weeks), it showed that I have a UTI and guess what the family doctor called in a prescription for? Cipro!!!! And he knows I'm still on prednisone and have only 30% kidney function!!!!!!

    While I am not a litigious person, this really makes me so upset!!! I don't have the money to try to sue, but if telling my story will help keep unsuspecting people from the horrible damage this has caused, I feel obligrdmtomspeak up. I have had a terrible year. And I'm still not okay. And the drugs 'm taking make me susceptible to other problems. I'm still all puffed up from the prednisone. A couple of weeks ago I decided to try going for walks again, hopefully to lose some of this weight and build up my strength. It is so hard for me and my left foot hurts so bad. My legs feel so heavy it is a real struggle to walk a mile. But at least I can. When I was at my sickest, could barely walk to the bathroom and I could not get up from the toilet without using my arms to pull myself up. I couldn't go up the two steps to get into my house without help. I couldn't go upstairs to my bedroom for months.

More reviews for: Neuropathy peripheral, Uterine prolapse

Comments from related studies:

  • From this study (1 week ago):

  • I just developed the neuropathy about 3 weeks ago and have been prescribed gabapentin. I have it only in my right foot, but I have tingling and numbness in my fingers also.

    Reply

  • From this study (11 months ago):

  • I am also on IVIG for the CIDP neuropathy. I do not know if these drugs can cause neuropathy but I need to find out. I have been on IVIG for 15 years now. Currently, gamagard 50 g in 10% solution. I know that these drugs can cause the very thing they are supposed to treat.

    Reply

  • From this study (12 months ago):

  • which med causes clotting

    Reply

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