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You are here: Home / Conditions / Fibromyalgia / Cymbalta Side Effects (Sweating, Flushing, and more)

Cymbalta Side Effects (Sweating, Flushing, and more)

Last Updated: November 5, 2010

Welcome! It looks like you might be new here, so I wanted to take a moment to tell you a little about me and my blog. My name is Julie Ryan and I live with Fibromyalgia. I've chosen to live positively, to fight back with diet and lifestyle changes and it's made a huge difference for me. The difference between living all my days in bed, and actually LIVING. I hope you'll keep reading and subscribe to my Newsletter to make sure you don't miss a post. Thanks for visiting!

*BTW, just a heads up that the post below may have affiliate links (some of my posts do).

Welcome back! I'm so glad that you are here again. If you've not already, be sure to subscribe to my Newsletter and I'll update you each time I post (and occasionally I'll send you something special).

Just a heads up that the post below may have affiliate links.

I saw my Rheumatologist today for the first time since some of my latest “symptoms” have developed. I told him about the latest Cymbalta side effects, including excessive sweating and the recent facial flushing. He said that both of those are very common side effects of Cymbalta. I also told him about the recent drowsiness and light-headed feeling I’ve been dealing with the last few weeks. I initially thought this might have been related to my forgetting to take my Cymbalta but it’s continued even after it should have resolved if that was the cause. It’s not consistent or I’d think it was an inner ear issue. In telling him about this issue today he said that also may be related to the Cymbalta.

Cymbalta Side effects

We talked about it and decided to try lowering my dosage of Cymbalta down to 30mg. The theory is that this may still be enough to control the anxiety without the side effects. If it’s not, we’d have to decrease amount anyway before switching me to a new med, so either way this is the direction we’d need to go. We’ll try this for a few weeks and see if it makes a difference. If not, then he’s going to probably put me on Pristique.

I also mentioned to him about the Pineal Cyst and he agreed that it most likely could be the cause of the eye pain and visual issues I’ve been having. He seemed to have a decent grasp on it and also explained that it is easily operable (without being invasive) if it needs to be removed. This made me feel a lot better.

8 Comments Filed Under: Fibromyalgia, Medications Tagged With: cymbalta, depression, eye pain, sweating

About Julie

Spoonie. Fibro Warrior. E-health advocate.

Julie Ryan was diagnosed with fibromyalgia in 2010 and endometriosis in 2012. She's lived with chronic migraine most of her life. In 2019 she was diagnosed with inter-cranial hypertension.

Julie has a degree in Psychology, and works as a freelance writer and marketer. Freelance work allows her to work when she can and not be tied to a desk or a schedule. Julie believes in living an inspired life despite chronic illness.

"I have chronic illness, it doesn't have me."

More about Julie

Blog title inspired by The Spoon Theory, by Christine Miserandino, an excellent explanation of what it's like to live with invisible illness.

Comments

  1. Tom says

    March 4, 2023 at 1:44 pm

    Hello,
    I just found this sight and subscribed. I have Sjogrens, Osteoarthritis and Fibromyalgia. I was taking Citalopram for many years. My Rheumatologist suggested changing to Cymbalta. My PCP prescribed it for me. I reduced the dose of Citalopram for 8 days. I took the first 30 mg dose of Cymbalta this morning. I will titrate up to 30 mg, twice a day in a week. I feel flushed and warm but that’s all as of now. Any experiences, suggestions or advice is welcome..

    Reply
    • Julie says

      May 9, 2023 at 2:12 pm

      Hi Tom, I’ve not been updating regularly for a bit. Been dealing with a new passle of chronic crud this year – including a new diagnosis of Sjogren’s myself (and gastroparesis). Once I can get things more under control I’ll have lots of updates.

      Reply
  2. suzanne bowers says

    October 25, 2020 at 6:38 pm

    I have been off the Cymbalta for two weeks and I am still sweating profusely from my head and upper body. When will this side effect go away?

    Reply
    • Julie says

      October 26, 2020 at 1:27 pm

      I wish I could tell you. It’s been so long now that I don’t recall how long it took for that to go away.

      Reply
    • Kim Thomas says

      November 30, 2020 at 2:51 pm

      I stopped cymbalta 30mg October 29, 2020. It was my daughter’s birthday. I was painting her toenails for a pandemic pedicure! I had one of those red faced sweats pouring out of my head. I had been dealing with this for months in silence. Her reaction was that’s not good for you! I quit cold turkey! Nausea and vomiting the first week. The sweating is still there but doesn’t last as long. I had my first brain zap yesterday November 29 along with a severe red face, sweating, nausea, stomach pain and had to lay down. I’m grateful to all who posted their experience, it’s given me hope and courage to press onward!
      I’d rather have fibromyalgia pain and depression than feeling sick and sweaty!
      About 10 years ago my rheumatologist added cymbalta 60mg. I was yelling cheerfully every morning I’M SO HAPPY! I was a recent widow and was grateful for the respite of grief. I weaned myself off by putting half the cymbalta beads in a clear vegetable capsule. He didn’t like that I did that. My family doctor thought I would benefit from cymbalta last year for fibromyalgia. I explained my previous experience and she said try 20mg. I did until I felt suicidal and ended up in the hospital. They changed meds and I went through withdrawal. When I went home under the care of my own psychiatrist I went back on cymbalta but 30mg.
      The sweating was unbearable! I live in tropical Florida. So I’m a month off cymbalta and stopped Buspar at the same time. I have had enough medicine wheeling! I have a tele-visit on December 8. I’m sure he won’t approve. So I’m going to keep the Xanax and flexiril for now. At some point I will be cutting the dose on them too. I’m 65 and can rest when I need to as I transition into retirement.
      Thank you for shining a light on cymbalta!

      Reply
      • Julie says

        November 30, 2020 at 3:01 pm

        Have you considered CBD oil or even (since you’re in FL) medical marijuana? I’ve gotten so much more help with the sleep issues with CBD oil than anything else. I hope you are able to get through this withdrawal period without too much issue. I also quit cold turkey when I quit (thankfully without any withdrawal symptoms) but I’d not been on nearly as long. It’s been a lot of years now and I am so hesitant any time any doctor tries to give me any prescription med now.

        Reply
        • Kim Thomas says

          November 30, 2020 at 11:34 pm

          Thank goodness for you! I’m using various medical marijuana products as they really help with sleep and anxiety.
          Thank you for being there

          Reply
  3. Kimberly says

    November 5, 2010 at 9:17 pm

    My Dr. wanted me to try Cymbalta and it made me really sick to my stomach. So, I have not taken it since. Sounds like you have a really good Dr. who really listens to you.

    Reply

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About Julie

Spoonie. Fibro Warrior. E-health advocate.

Julie Ryan was diagnosed with fibromyalgia in 2010 and endometriosis in 2012. She's lived with chronic migraine most of her life. In 2019 she was diagnosed with inter-cranial hypertension.

Julie has a degree in Psychology, and works as a freelance writer and marketer. Freelance work allows her to work when she can and not be tied to a desk or a schedule. Julie believes in living an inspired life despite chronic illness.

"I have chronic illness, it doesn't have me."

More about Julie

Blog title inspired by The Spoon Theory, by Christine Miserandino, an excellent explanation of what it's like to live with invisible illness. Read More…

Disclaimer:

I am not a doctor. I do not claim to be a doctor. I do not play a doctor on TV or the internet. I simply share my experiences and what has worked for me. We are all different and before you try any new treatment, exercise, supplement, etc you should talk with your doctor (the real one, not the one on TV).

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