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Would you have Neuropathy peripheral when you have Raynaud's phenomenon?

Summary: Neuropathy peripheral is reported only by a few people with Raynaud's phenomenon.

We study 5 people who have Neuropathy peripheral and Raynaud's phenomenon 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 Raynaud's phenomenon and Neuropathy peripheral >>>

 

 

 

 

Raynaud's phenomenon

Raynaud's phenomenon (discoloration of the fingers, toes, and occasionally other areas) can be treated by Nifedipine, Norvasc, Amlodipine Besylate, Procardia Xl, Procardia. (latest reports from 2,928 Raynaud's Phenomenon patients)

Neuropathy peripheral

Neuropathy peripheral (surface nerve damage) has been reported by people with multiple myeloma, osteoporosis, depression, pain, high blood pressure. (latest reports from 27,673 Neuropathy peripheral patients)

On Jan, 4, 2015: 5 people who have raynaud's phenomenon and Neuropathy Peripheral are studied.

Trend of Neuropathy peripheral in raynaud's phenomenon reports

Gender of people who have raynaud's phenomenon and experienced Neuropathy peripheral * :

FemaleMale
Neuropathy peripheral100.00%0.00%

Age of people who have raynaud's phenomenon and experienced Neuropathy peripheral * :

0-12-910-1920-2930-3940-4950-5960+
Neuropathy peripheral0.00%0.00%0.00%0.00%0.00%50.00%0.00%50.00%

Severity of the symptom * :

n/a

Top co-existing conditions for these people * :

  1. Rheumatoid arthritis (3 people, 60.00%)
  2. Somnolence (1 people, 20.00%)
  3. Pain (1 people, 20.00%)
  4. Fibromyalgia (1 people, 20.00%)
  5. Dry mouth (1 people, 20.00%)
  6. Hypothyroidism (1 people, 20.00%)
  7. Neck pain (1 people, 20.00%)
  8. Vitamin supplementation (1 people, 20.00%)
  9. Arthritis (1 people, 20.00%)
  10. Insomnia (1 people, 20.00%)

Most common drugs used by these people * :

  1. Cymbalta (2 people, 40.00%)
  2. Ambien (2 people, 40.00%)
  3. Synthroid (1 people, 20.00%)
  4. Evoxac (1 people, 20.00%)
  5. Metoprolol succinate (1 people, 20.00%)
  6. Nifedipine (1 people, 20.00%)
  7. Prilosec (1 people, 20.00%)
  8. Depo-medrol (1 people, 20.00%)
  9. Simvastatin (1 people, 20.00%)
  10. Albuterol (1 people, 20.00%)

* 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 Raynaud's Phenomenon and Neuropathy Peripheral?

You are not alone! Join a mobile support group:
- support group for people who have Neuropathy Peripheral and Raynaud's phenomenon
- support group for people who have Raynaud's phenomenon
- support group for people who have Neuropathy Peripheral

Could your drug cause:

Other conditions that could cause:

Can you answer these questions (Ask a question):

  • I take klonopin and diltiazem (calcium channel blocker blood pressure medicine) and am concerned about side effects. my accupuncturist recommends the ashwagandha. anyone have any issues with this?
    I take these prescription medications but have been going to an accupuncturist since 2012. I have trouble sleeping at night without my clonazepam and take naps during the day and am having trouble losing weight. She thinks that my adrenal glands may be fatigued and told me to try something called Adrenal Response which contains Sensoril Ashwagandha. When I looked up Ashwaganda it said that it could interact with the Clonazepam or Klonopin and also with High blood pressure medication. I am a little concerned. I mentioned this to her and she said they both are metabolized by the liver and it should be ok to take it, just to take it an hour or more after I take the Clonazepam. Has anyone had any issues with interactions with their prescribed meds while taking Ashwagandha? I don't want to have to monitor my blood pressure because my blood pressure medication works good for me. Any help would be appreciated because I want to try it but I am a little scared too. Thanks, Crystal
  • 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.

More questions for: Raynaud's phenomenon, Neuropathy peripheral

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: Raynaud's phenomenon, Neuropathy peripheral

Comments from related studies:

  • From this study (2 weeks 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.

    Reply

  • From this study (8 months ago):

  • Anxiety and paranoia are controlled. Night sweats numbness in fingertips. Feels like I can't breath yet oxygen levels are fine and lungs are getting air. Sometimes feel like I will pass out. Forget simple things and cant remember a day sometimes. Drop things occasionally. Ana tests and autoimmune blood tests were all negative. Kidney function tests have been a bit off 3 times now. Sometimes my eyes go funny and I can't see straight. Always tired no energy and always in pain

    Reply

    issues all over on Jun, 9, 2014:

    So I too am having some weird things happening to me. I thought maybe it was side effects and that they would go away, however they seem to just be getting worse every day. I'm a 29 year old while female and have been taking this for a little under 6 months. About 2 months ago my finger tips and tips of my toes started feeling numb, 3 weeks ago I started feeling tired, really tired all the time no matter how much rest I was getting, and then started falling asleep while wide awake at work. I'm working on the computer and catch myself when my head drops, but I'm still typing my sentence, can still hear everything, sometimes I'm on hold with an insurance company and today, fell out of my chair. I also have lost too much weight, I feel like I'm always in pain, every thing hurts, and my eyes are doing something weird where they go crossed and I cant see straight. This keeps happening while I'm driving. I also am irratible with my family more often, cant concentrate at all, and I'm very forgetful, and I'm dizzy all the time like I'm not getting enough oxygen when I'm breathing just fine, it makes me feel like I'm going to pass out. My anxiety is under crontrol, but these things are really starting to scare me. I keep getting told I have to wein off the drug and moved to another state and so I don't have a new PCP, and the dr's office I tried to schedule with doesn't have an apt available for over a month.

    Reply

    Deadfingers on May, 25, 2014:

    Wow - I am a 43 yr old woman - your description of symptoms is mine - exactly - I would love to email or talk to hear some of what the doctors you go to are saying - mine all act like I'm a crazy hypochondriac. I have been through so many expensive test all to hear I am within the ranges of normal - but when I read - sometimes dependent on where you fall within normal and what some other level might be that they aren't looking at could spell big trouble - the mind issues, sight, and breathing issues concern me BAD - I feel like I am a time bomb just getting ready to blow - but if I can help the doctors discover what is wrong I might just save my own quality of life. It's not normal - I don't care what they say. My email is lorajamison@me.com if anyone has these symptoms and is dealing with doctors not listening.

    Reply

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