Severe headache with shingles

Posted , 9 users are following.

I was diagnosed with shingles this past Monday. My rash started on my scalp and now has spread to neck and ear. The doctor I saw at the urgent care clinic told me to take Advil for the pain and gave me a rx for antiviral. The pain is much worse than it was on Monday and the rash is spreading, but when I called Dr office to try to get something for the pain they acting like I was being a cry baby and told me to just take Advil for pain. I now have ringing in my ear and a terrible headache that won't go away and the burning pain of the rash just feels like that whole side for my head is on fire. Any advice on what I can do? I'm in the US....

2 likes, 14 replies

14 Replies

  • Posted

    You likely have it in your trigeminal nerve.  It's a VERY painful nerve, and maybe about the worst place you could get it.  I would recommend you phone your regular GP soon and see if you can get in.  If that's not an option try a dermatologist.  There are drugs that can help with this.  One is amitriptyline, which is an old anti-depressant that helps heal your nerves (and this does work).  Also the drugs you see advertised for nerve problems with diabetes can be used.  The sooner you get treatment the better off you may be here.  I would not let this go for several days.

    • Posted

      Actually a dermatologist might be better Tammy.  I ended up having way better luck going that route.
  • Posted

    Tammy,

    Do you have pain localizing in your ear? Do you have a severe ear ache with ringing? A facial droop?

    You need to see another physician as this one is an absolute ignoramus. Herpes Zoster-Shingles causes severe burning lancinating pain and the fact that this doctor doesn't know this means you need to see someone else.

    If it is localizing in your ear, I would encourage you to see an ENT stat. Also, a neurologist is a great specialist to treat the pain of Herpes Zoster-Shingles.

    For the acute stage, Opioids and Neurontin, an anticonvulsant- that helps decrease the burning lancinating pain, work well. Lyrica is also used by certain clinicians.

    Cymbalta, an antidepressant, is another medication they add to the mix.

    You need to find an excellent physician that will actually treat you comprehensively.

    The reason I ask if it is localizing in your ear is the ENT can prescribe Auralgon Ear drops, which helps numb the pain topically inside the ear canal. As you have it on your scalp, you might try Bactine, which contains a numbing agent, as well, four times a day. If you are allergic to Lidocaine or have a seizure disorder, do not use these products.

    Cool compresses help soothe the pain, hot showers will worsen the already excruciating pain.

    You are already fatigued, I am certain, so rest and sleep as much as possible.

    You probably had symptoms such as headache, fever, chills and sweating, aches and pains, fatigue, photophobia, and malaise prior to the rash and pain. It is important to get the acute pain under control so that this does not turn into Post Herpetic Neuralgia PHN.

    I have recurrent Herpes Zoster-Shingles every three to five weeks for the past twenty years and twice in my right eye. I am a Nurse Practitioner in the US.

    May I ask how old you are and if you are in good health?

    Best regards

    Merry Juliana

    • Posted

      Merry.    My husband has had the shingles on the left side of his head, forehead, in his scalp and now that it seemingly has healed he has excruciating headache pain.  His left eye has not gotten the virus in it but he can only open it halfway.  He had hallucinations with the neurontin, lyrica, and Ativan that was prescribed and nothing seems to help his pain.  Spent the past 4 days in the hospital getting off the meds and now only has a lidoderm patch and some cream with lidocaine powder in it.  Do you have any other suggestions as a NPR that we can try to talk to his doctor about?  He has been dealing with this over 5 weeks now and I’m beginning to think he has migraine symptoms with the sensitivity to light.  I gave him my migraine med (imitrex) and it helped a little and cold compresses on his head also help some but nothing else seems to touch his pain.   Any suggestions would be greatly appreciated.
    • Posted

      Susan,

      Did he take the medications one at a time or combined with other medications?

      Was he on Opioids at the same time?

      How old is your husband?

      Does he have any medical problems such as heart disease, liver, or kidney problems?

      Merry Juliana

    • Posted

      He is 78 yrs old.  Shingles started 4/18 and they weren’t diagnosed until 4/23 whrn he was placed on 10 days valacyclovir.   Once the places began to clear up he has such excruciating pain but he began to have new spots breaking out so they put him on an additional 7 days of the antiviral pill but they added Neurontin and Ativan .  He has other meds for pain like tramadol and lortab but it didn’t touch this pain.  Prior to his hospitalization he could hardly walk, couldn’t speak clearly, had no balance and was seeing things! .  He had these shingles 4 days before they were diagnosed and he began receiving treatment.  He has a history in his record of heart attack but has never been told he had one not has he ever received treatment for it.  Doesn’t not have any kidney or liver problems.  He does have asthma and high blood pressure which is under control with hydrolozine 3 times daily.  Everything we have tried doesn’t touch his pain   And I am desperate to try to get him done help and relief.  Anything you can share with me is much appreciated.  After all these drugs am really looking for something natural or houlistic.      
    • Posted

      Susan,

      I was without internet for most of tonight, and was unable to see your message, and reply until now. I will write to you tomorrow when I am more rested.

      Best Regards

      Merry Juliana

    • Posted

      Susan,

      I sent you a private message.

      Merry Juliana

  • Posted

    Tammy, go back to the Doctor, I am not sure how your health system works in the US, but it seems here the UK and in the US they underestimate the level of pain.

    See a specialist, if you can. Hopefully they will find a neurologist for you, who will recomend the best pain relief and see you until things improve.

    This will take time, Shingles is a depressing virus, like flu symptoms. Rest, sleep, give yourself plenty of healing time.

    Your health is very important, go back, take a friend or support person with you. Don't leave the medical practitioners without clear diagnosis, sympathy and follow up treatments and appointments.

    It will get better.

  • Posted

    Mary Juliana has it right. I have used much of her discussions and as a nurse practitioner I know she has had great advice.  It is unfortunate that many doctors haven't had much training on shingle and PHN.  Many patients who were not soon treated or not sufficiently treated end up with PHN.  It is not easy to live with so go see knowledgable doctors and ask questions.  My advice would be to copy and use Mary Julianas discussion even on office visits. OTC's for some meds may be possible.   In Spain I saw  a pharmacist who recognized and who immediately sent me to the ER where I began mediacal treatment.  

    • Posted

      Hi Tammy. I agree with Merry Juliana and Avey. Print all these replies and take them to whichever doctor you see. Merry's info is good so you should follow her advice. It's a horrible illness and takes ages to recover. I still have some tingling/numbness where I had the rash. Best wishes. rolleyes

  • Posted

    Last year I had a reoccurring shingles attack. This time it started on my forehead and temples, moved to my entire head eyes and ears. They affected my hearing and sight. I am a migraine sufferer, but the headache I got from this was more like a spinal headache. I was incapable of doing anything all I could do was lay in bed. We had gone to Colorado for the summer up to our family cabin. I ended up at the ER, the doctor RX for me was antibiotic and hydrocodone for the pain and headache, which just barely took the edge off. Luckily I had my sumatriptin injections to use along with the hydrocodone. Still had the headache but somewhat manageable. I see a neurologist for certain health concerns.
  • Posted

    Is anyone following this? I have shingles in my throat, nose, mouth, eye and scalp (since 11/26/22). I've been to my PCP, and an opthamologist, and was give a Rx for valacyclovir (3 x day for 7 days). it seems to be abating in the eye, but I have debilitating headaches and it seems like it's still spreading with pain in my neck. My valacyclovir Rx runs out in 24 hours. Should I try to have this renewed until my symptoms settle? I am working under the assumption that my headache is a side effect of the valacyclovir. Excruciating!

  • Posted

    I feel for you, Tammy. I had a similar problem. In 2014, when I had severe pain in my neck and upper arm on a Saturday when my family doctor was off, I went to a Walk-In Clinic and the doctor told me to take Advil for pain. A day later, my pain got worse, and rash appeared. Went to see my family doctor, who diagnosed Shingles right away. She prescribed antiviral medication for me but it was well past the first 72 hours and the antiviral drug had no effect. It is very crucial that the antiviral medication be taken within the first 72 hours of Shingles onset, otherwise you will likely get post herpetic neuralgia (PHN) after the Shingles rash went away. In my case, I now have very painful PHN in my upper right arm where Shingles rash was located. I have spent over $2000 trying every kind of treatment, drugs, ointment, Cannabis, herbal cure, etc. possible but nothing worked. I also had bad side effects taking the anti convulsion drugs. I even tried Acupuncture which hurt me even more. Had to ask that acupuncture session be terminated immediately as the pain was just excruciating. Every day, there is severe pain in my upper right arm, some days worse than other days. However, I am very fortunate that when I sleep, I have no PHN pain. It only hurts when I'm awake. I learned online that there are PHN electronic treatment centers in Tokyo, Japan and in the United States. But online comments indicate that the cost of $3000 - $4000 spent travelling there to get such treatment was a waste of money. After the electronic treatments, people still have PHN pain. I hope you are one of the lucky people whose PHN disappears after treatment. Wishing you all the best, Tammy. Take care, and stay well.

Report or request deletion

Thanks for your help!

We want the community to be a useful resource for our users but it is important to remember that the community are not moderated or reviewed by doctors and so you should not rely on opinions or advice given by other users in respect of any healthcare matters. Always speak to your doctor before acting and in cases of emergency seek appropriate medical assistance immediately. Use of the community is subject to our Terms of Use and Privacy Policy and steps will be taken to remove posts identified as being in breach of those terms.