Would you have Neuropathy (Peripheral neuropathy) when you have Myasthenia gravis?
Summary: there is no Neuropathy reported by people with Myasthenia gravis yet.
We study people who have Neuropathy (Peripheral neuropathy) and Myasthenia gravis 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 Myasthenia gravis and Neuropathy >>>
Myasthenia gravis (a chronic condition that causes muscles to tire and weaken easily) can be treated by Mestinon, Prednisone, Cellcept, Pyridostigmine Bromide, Azathioprine, Imuran. (latest reports from 2,872 Myasthenia Gravis patients)
Neuropathy (damage to nerves) has been reported by people with multiple myeloma, high blood cholesterol, diabetes, high blood pressure, pain. (latest reports from 5,843 Neuropathy patients)
On Jan, 29, 2015: No report is found.
Do you have Myasthenia Gravis and Neuropathy?
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- support group for people who have Neuropathy
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Can you answer these questions (Ask a question):
- I have myasthenia gravis. is it safe to take zetia?
Fearful of exacerbating the Myasthenia. Problems noted in a study that lists Myasthenia as a complication. Fearful it may make it worse.
- Can herpes simplex 1 cause vasculitis which would in turn cause peripheral neuropath
I developed tingling and numbness in my feet (and soreness)over the past 2 years. I've had various tests: back mri, b-12, uric acid, ultrasound for pad,etc. Haven't been diagnosed yet. I thought it could result from the herpes simplex 1 flare-ups (3 or 4 per year) and that in turn could have vasculitis of the small vessels. What do you think?
- Does anyone else have peripheral neuropathy? anyone have pn with lichen sclerosus? i have pain in hands, feet and face. (1 answer)
Pain much worse at end of day and when I overdo. Sleep difficult - but essential! Feel so much better if I get 6+ hours. At the moment, very distressed by swollen lips (mostly inside mouth) and tissue surrounding eyes. I'm sure I have some arthritis in my fingers and toes. I also have had lichen sclerosus on my skin for nearly 20 years. Have had the PN for 15 years or so. I'm afraid that the medications can actually make the condition worse. If anyone has any suggestions, I'm all ears!
- Can an im phenergan injection cause neuropathy, where the injection was given?
I was given a phenergan injection in PACU. Once I was discharged and home, I felt numbness in my leg where the injection was given. I called my MD and was told the numbness was from the position my leg was in during surgery. It has now been 5 months and my upper thigh has neuropathy. Can Phenergan do this?
- Has abilify affected your ability to make good decisions?
My husband and I are 73. We had a paid off home and money in the bank until the past 3 years. We have made some terrible decisions and now we are practically penniless. We couldn't understand why we had made such bad decisions and let someone talk us into losing our money. We have also been on Abilify about the same amoount of time and I noticed that the commercials say a side affect can be lack of judgement or something to that effect. Has anyone else had this happen?
More questions for: Myasthenia gravis, Neuropathy
You may be interested at these reviews (Write a review):
- Lisinopril caused peripheral neuropathy
I began taking 10mg of Lisinopril recently and within a month began having moderate peripheral neuropathy. The neuropathy was shooting or stabbing sharp pains in hands and feet, burning calves, pins and needles in and around the eyes and ears, and burning eyes. This was so pronounced that I requested the doctor to switch me to Losartan immediately. The peripheral neuropathy quickly subsided and is gone ! My doctor had never heard of the Lisinopril causing this but now she knows. So people - you need to be your own advocate when you know something isn't right.
- Adderall xr 30 mg and peripheral neuropathy
I have been taking adderall xr 30 mg for the past five years, with some breaks. I started showing symptoms of peripheral neuropathy the second year. This year (my 5th year on adderall) has been the worst and most difficult for my peripheral neuropathy. I also suffer from major depressive disorder and HSV, and I have heard that both of them may be related to peripheral neuropathy.
- Lyrica varied widely
I was prescribed Lyrica for treatment of chronic pain. It was ineffective, but it knocked out the symptoms of interstitial. However, it also caused rapid weight gain (I went from 110 to 130 lbs. in just a few weeks) and my ankles started to swell. The pain doctor advised me to discontinue the drug, but the urologist suggested lowering the dose. I did, and the swelling went down. I weighed myself daily and watched what I ate, and my weight returned to normal within a month. Subsequently, I continued taking the lower dose and had no further problems. Then I developed severe spinal stenosis, and my dosage of Lyrica was increased to six 75 capsules daily, in addition to 480 mg of morphine sulphate. I tolerated the Lyrica well. After surgery, however, my ankles began to swell again, and although I didn't have a problem with weight gain, I developed a bright red rash from ankles to knees. I dropped the dosage of Lyrica to 50 mg twice daily, and had no further side effects. The rash simply disappeared, with no damage to the skin. Following the surgery, I was able to titrate off morphine completely. I continue to take Lyrica twice daily. It doesn't seem to affect pain (I still ache a bit, as I have degenerative changes in all joints) but it does dampen peripheral neuropathy, which I experience both in my toes and balls of my feet. It also dampens the neuropathy in my forehead, where I had four surgeries to remove a malignant melanoma. I have had no side effects other than those mentioned, and find it interesting the I could tolerate a high dosage of Lyrica prior to surgery, but after surgery could not, and that adverse side effects varied not only with the dosage but with my own physical condition. I don't find it to be highly effective in treating neuropathy, but it does still the tingling enough to let me sleep and take my mind off the condition.
- I need advise, badly ckd!! (1 response)
The orthostatic BP started in mid April, I was only dizzy upon wakening then it would subside. I have never been a big breakfast eater so I started doing that. We were in Disney later in April and I was extremely fatigued, to the point of not wanting to walk, Disney would be the first time I passed out when getting dizzy. I of course said I had gotten too warm and was exhausted from work the previous week. The dizziness continued in the mornings & I passed out several more times. On May 1st, I passed out while putting my make-up on and hit my eye on the faucet and head on the tile floor, despite that I went to work thinking it would subside, it didn't. I went to the ER directly after work. They ran a B-met on me and my GFR was 11 and creatinine 3.95. They admitted me to a larger hospital for evaluation. While in there, they pumped me with fluids continuously, saying I had severe dehydration. My kidney function improved, my creatinine levels went back down to 1.34. After 5 days I was discharged and told to see a cardiologist and endo. The endo doc cancelled my appointment on the basis it was not his area. I had had a cortisol and ACTH testing which I guess was normal. I saw the cardiologist, who said it wasn't cardio. I had had an echocardiogram in the hospital and EKG monitoring. Cardio sent me to neurology, the PNRN did a basic neurological exam and drew blood for disease markers such as Lupus, sjorgens, hepatitis, ect. All disease markers came back negative, but my GFR was at 11 again and creatinine was 4.25, BUN 50 along with an elevated ACE level. They called me and said I sarcoidosis. I really don't have any of the primary S/S of this autoimmune disease. I don't know where to go from here, they are referring me to another neurologist at a bigger hospital. I can't live my normal life, can't walk on my feet due extreme pain and I pass out at least 2x a week, which is not good for my old body. My BP upon laying and sitting runs like 117/72, upon standing it drops to like 70/50-50/30. I am on 0.1 mg of florinef, I tried increasing it but then my legs swelled up for a gain of 23#. I talked to Mayo Clinic today and all there specialists are booked out thru December. I have to be able to work, I can't stay home any longer than September 8th! Please advise me!
- Review: could lyrica cause intracranial pressure increased?
One dose (75mg) caused severe head pain (increased intracranial pressure) and nausea.
More reviews for: Myasthenia gravis, Neuropathy
Comments from related studies:
From this study (1 month ago):
Neuropathy accurs after two weeks on drug. Twitching keeps me from a good nights sleep. Also causes pain in my arms
From this study (2 months ago):
developed numbness and tingling in hands 3-4 months ago. nerve tests are normal.
From this study (2 months ago):
I just stopped taking lomotil, day two of four day wean. Very saddened to think this med is causing. Only thing so far that stopped my wattery diahrrea. I have sever IBS-D. I am very hyper sensitive, have been on meds since October 27, 2014.
Only thing they could rule out it was only thing new. Sad face.
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