Lidocaine and shingles

Common Questions and Answers about Lidocaine and shingles

lidoderm

- use scissors to shape the patch to fit the troublesome areas - you can only wear a patch for 12 hours (once per day) - first use the patch only at night to help sleep - by week three I switched over to wearing the patch during the day I hope this helps and sorry I caught this post so late. my prayers are with you and hope things are better now. the pain is indescribable. bless your heart.
Treatment options include antidepressants, anticonvulsants and topical agents such as lidocaine patches or capsaicin lotion. Opioid analgesics may also help. If it persists, talk to your doctor about this for proper management. Take care and regards.
I get a herpes out break when I stress real bad well I had an out break when I was on treatment for Hep C and it was a shingles outbreak and it hurt real bad and it was in my face but it dont break out to bad. But recently I had a herpies outbreak on my lower back where I usuall get it when I stress a lot.
My 89 yr old grandmother was diagnosed with "the worst cast of shingles I have ever seen" by her gp last year. While the original outbreak has healed she is still have frequent pain and itching in the same location (scalp, face and eye lid). Other than pain meds are there any other treatments that she could benefit from at this point? She lives in Washington state, are there any specialists there that she should consider going to? Thank you.
High readings can be a sign of pain. I've had shingles and took care of my father in law who still has his shingles. They ARE very painful. They can attack the nerves, as they did with my father in law, and I know from his experience that there is pain medication available for these symptoms. This is my two cents. Call the doctor is my vote.
I went to my doctor 2 days later and found out I had shingles and it was too late to treat it. It spread down my shoulder to my arm and hand. It was so bad and so painful I felt my bones were burning. It is a year and a half later now and I am paralized, my left arm and hand and am on narcotics and neurontin for damaged nerves, yet i suffer with pain everyday. My ulner nerve was killed and the other 2 main nerves are barely alive.
Lidocaine (INN) ( /ˈlaɪdɵkeɪn/), Xylocaine, or lignocaine (former BAN) ( /ˈlɪɡnɵkeɪn/) is a common local anesthetic and antiarrhythmic drug. Lidocaine is used topically to relieve itching, burning and pain from skin inflammations, injected as a dental anesthetic or as a local anesthetic for minor surgery.
There are also some prescription options such as topical Lidocaine which can numb the area temporarily and topical acyclovir which might help hasten resolution slightly. Oral Acyclovir or other antiviral medications can help too. Good luck!
The doctor prescribed Prednisone, Valtrex, and Lidocaine they all help but none are stopping the evening pain making it very hard to sleep.
It will be best that you consult a neurologist and treatment options could be anticonvulsants such as gabapentin, antideprassants and topical lidocaine lotion. Now a day, few recent treatments could be rhizotomy (cutting the affected nerve to relieve pain) and TENS (a electrical pulse therapy). Hope this helps.
The neuro gave me lidocaine patches to help with the shingles pain and I'm taking Valtrex and using a cream for the rash. I'm managing is pretty well. Thanks for your messages.
I could not figure out for the life of me why my back felt this way. Then i went on line and read more about Shingles and the after effects. I finally after all these years know what i have. Out of all the 20+ doctors i have seen over the years, you think one of them would have told me what i have, NO. I have been in pain all these years for nothing. Accupunture, Chiropractor, physical theropy, sports doctors, back specialist, 2 familiy doctors, etc...
But of course, I knew better because the internet told me so. She dismissed my request to test for Shingles (swab) and tested me for Herpes and HIV (blood test). The results would take about a week. By now I was broke. My insurance is laughable and I had spent all I could at this point in trying to treat my hemorrhoid problem (script is $40 for about a weeks worth) and copays for office visits trying to get this diagnosed and treated.
I had shingles in June this year and am getting a bit worried due to the fact I have still got pain in my back which does not want to go away,how long will or can this continue for its particularly painful when I rest on the back of a chair or in bed propped up on a pillow
I didn't know what it was, couldn't see the rash very well, it being on my back and all, and I was already quite used to odd and severe pain. My conclusion was Poison Ivy, I'd been out running and resting against trees previously, so it seemed logical. I treated it with calamine lotion for the better part of a month, but it just got worse and worse, to the point I couldn't put on my upper undergarments or shirt without bursting into tears.
My Mom, 82 years old, recently got over shingles. However, she still has the residual pain. The shingles outbreak was on her back, right side, around shoulder. Her doctor gave her hydroco (which she doesn't like because it made her dizzy) and subsequently Neruotin which gave her really bad diarrhea. He had discussed the possiblity of a cortisone shot and she finally said, yes because the pain was so bad. He referred her to a pain clinic.
I don't know if your doctor would approve but there is a patch called a Lidoderm patch that was created by a doctor for his wife who was suffering from shingles. It is not a narcotic, just a lidocaine patch. It works really well for pain in a specific area, they can even be cut and placed on various spots. I have one on my shoulder right now and it is helping with the pain.
doctors prescribed lidocaine patch which I wore for a week or so. I stopped and experienced a persistent numbness on left side running from just under my arm pit down to just below last rib. The numbness is felt slightly in from middle of chest to my side about 6-8 inches. 8 months later I still have it. Doctors ignore me.
My 80 year mother has myathenia gravis and got shingles 11/2 years ago. She is in constant pain and has not left the house in all that time except for a couple Doc. appointments. She can not wears a shirt because even that is too painful. Fears all medications for the shingles because she is afraid it might affect the medications she is on for the MG. Her last Doctors appointment they told her she may have shingles for the rest of her life.
What should I do, I have had shingles for bout 9yrs now and they come every once in a blue moon, for the past month 1/2 I got them 3 times im on my 3rd one right now and it's on my knee and I have this pain that hurts and sometimes uncomfortable to bend knee or even relax, what should I do
raging UT infection and Shingles! I emailed my doctor about this on Friday and he said he will see me immediately which looks like Monday4/29. The shingles pain starting in friday night and I'd hoped the large quantity of antivirals would kill it off. It only gets worse and tonight the nerve pain and rash on my back and under arm is spreading....absolutely unbearable pain.
) This seems to be the best combination of drugs we've tried (demerol, lyrica and various others were not as helpful) but she is still in a lot of pain each day, primarily where she had the shingles, across the chest, and down the right side of the back. She just started going in for epiderals once a week and has had three so far which she feels may or may not provide any relief. She takes sublingual B-12 and lysine as well as prescribed by a nurse in her assistant living community.
Drugs like tramadol, lidocaine, venlafaxine, naproxen can be used to treat the allodynia. Other topical agents are capsaicin and aspercreme, which can relieve the symptoms. Hope this helps. Take care.
The symptoms include burning sensation, numbness, itching and sensitiveity to touch of the area that was effected with shingles. The treatment options include lidocaine skin patches, tricyclic antidepressants, anticonvulsants and opioid painkillers. Please discuss these options with your dermatologist. It is very difficult to precisely confirm a diagnosis without examination and investigations and the answer is based on the medical information provided.
Sometimes it is a little worse and sometimes it is a little better, but for the most part is is a constant 3 - 4 I have also tried accupuncture, Infra-red treatments, pain management w/ nerve block injections in my eyebrow and forehead areas.
Allodynia (and often hyperalgesia) can be secondary to migraines (often complex or silent migraines), RSD/CRPD, polyneuropathy (sensory), autonomic neuropathy (which is why it may be a symptom in a small subset of POTS patients and dysautonomia patients), and other pain syndromes like fibro and myofascial pain syndrome. There is also such a thing as primary allodynia.
I am a worrier and axoius person been like that since early childhood and this anxoiusness is probably a contributing factor, but regardless of the cause, the physical suffering is still very real. 1999 I got shingles and the nerve pain never went away , the docs didn’t really listen to me so after one year I caved in and started self medicating on buprenorphine 1-2 mg a day.
First I developed a rash, then little red round shape blisters would develope and pretty soon my back, legs, and chest was filled with the shingles. My doctor admitted me to the hospital gave me Acyclovir I.V., creams EMLA (lidocaine, benzocaine) and morphine & neurontin for the pain, and Atarax and Ativan for the itching, sedation, and nausea. At the time I was 1 year post bone marrow transplant, I had leukemia. Also at the time my white blood cell count was 0.5-1.
The difference this time and the dead giveaway is the pain in the hip and back. Shingles effects the nerves in your back and hips and sometimes you will have a breakout of a rash and sometimes you will not. This time I had very few blisters. Other times I have had a million blisters but I have never had this kind of pain before. The Dr. stated that Shingles usually appears after a person becomes older, I am now 50 Y.O. At any rate I was prescribed Acyclovir. I hope it works!
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