Skip to content
Side effects of meds for fibromyalgia
avatar
deartam posted:
I have been taking a prescription for Lyrica approx 6 mos now. I kept losing my balance, gained 30 lbs and retained water... oh and bp increased. I have a new doctor who was willing to keep prescribing Lyrica for me but suggested Savella might be easier for me to tolerate. 8 days ago I began the transition from Lyrica to Savella as prescribed. I am miserable with constant cold sweats, dripping sweats. I called my physician who said to wait a few more days & come in if not better. Has anyone experienced this extreme sweating when changing meds? Fatigue has also increased. Is this normal, will this balance out?
Reply
 
avatar
booch007 responded:
First I am so sorry that this is going on.

I am on savella and can only take the little blue pill (12.5mg) Be careful of the savella side effects. IT is totally different to any other SNRI (seratonin/norepinephrine reuptake inhibitor)

It increases norepinephrine 3 times that of seratonin. So you get palpatations, increased BP, sweats. Norepinephrine is your adrenaline (fight or flight) chemical.....it is as the story goes...when people are so scared they can lift a car on a crushed child...it is this chemiacl that does it. YOU also feel little pain......It works so well for me, but only at the 12.5 to 25mg dose once a day.

Any higher then that I am in side effect city! Not tolerable. Just remember that you don't need to take 50mg twice a day...it should be taken slowly to raise up and tailored to you.

Talk to that doctor. When I suggested the 12.5mg tablet the neuroligist she decided this is what she is ALWAYS GOING TO DO.

No more dose pak to start people...titrate up slow. She had someone in the ER with arrythmias and so on.

I love this med I hope it helps you like it did me. The window of trial and error for this disease can be painful and filled with side effects. Just try and be knowledgable and learn what you are taking there is a simple site called (drugs.com) that you can research on, not complicated. Also here on WebMD they help with meds.

Talk with the doc...small steps. I never took Lyrica though I have been asked many times , even my vascular surgeon wants me on it...NOT happeneing. I couldn't tolerate Neurontin so I am not crossing to Lyrica.

We are all different and you have to figure you out. Sad but true.

I wish you all the luck in the world. Hope you are almost off the lyrica and watch the piounds fall away....the sweating is always going to be, but less with less a dose on the savella.

Hugs from me, Nancy B
 
avatar
foreversore responded:
I too take Savella and have noticed that I tend to overheat and sweat a little more. Luckily that is the only Savella side effect I have and it is still at a tolerable level. I DO take 50 mg twice a day but I was brought up to it slowly. My doc gave me 3 of those dose paks and I was to take 12.5 mg for 10 days then 12.5 twice a day for 10 days and so on and so forth. I THINK the Savella may be helping me but its sometimes hard to tell because of the other pain related conditions I have that Savella doesn't help. I can say that I have less brain fog days with the Savella. My rheumy first told me Savella may help with the fatigue but I didn't notice any difference. I do have sleep apnea and use a CPAP and he wants me to ask my GP about Provigil because I take 2 one to two hour naps a day and then sleep anywhere between 4 to 12 hours when I finally fall asleep at night. I also take 1800 IU of Vit D a day and 2000 mcg of B12 a day. I am thinking of getting a B complex and not just the B12 and I want to try the magnesium maleate I have heard about. At this point I am willing to try just about anything to have a bit more pep during the day but still get restful sleep at night.

I wish I had more info to give you other than my personal experiences but hopefully there will be some tiny tidbit that helps.
 
avatar
deartam replied to booch007's response:
Hi Nancy B - I am nearing the end of my 2nd week (2 more days) of decreasing Lyrica and very slowly increasing Savella. The sweats or, body heat (nicer term) have decreased slightly. I notice that they seem to last approx 2 hrs now after I take my meds (2x per day). At night, they come and go... reminds me of hot flashes of long ago. I'm 65 now, well almost... God willing and the creek don't rise, I will be on 11/30! I remember when I first started Lyrica, the body heat was terrible then but it balanced out after approximately 3 months. I am hoping that maybe this will balance out with the Savella. I won't hold my breath though! LOL.... I am glad to know that others experience the same thing. Also, glad to know about the warning signs too.

I am so grateful for your response, your experiences and suggestions! They are excellent. I will definitely talk these things over with my doctor. He is expecting me to have questions and probable dose adjustments as we work through this.

I am sleeping a bit less during the day (only 1 nap/2hrs instead of 2 or 3) and finding energy when I wake up that I did not have b4, so something good is going on! I am glad to know the information on the neurotransmitters, esp Norepenephrine! I am going to research further in drugs.com

Night sleep is disrupted, but I manage to fall back asleep after reading a page or 2 of a novel. My restless legs are calmed, I take 7.5 mg of Meloxicam which helps that and also the aching in my legs. I have had my veins examined throughly by a secialist and they are great. .

Again, I thank you for caring enough to respond and you have helped to ease my anxiety. I was so excited to get the email from this site telling me I had a response!
Hugs back to you!
Tamara
 
avatar
forgetful88 responded:
The medications for FM, gave me worse symptoms than I already had.

For me the switch off from some relief to other symptoms were not worth it. That was all of them..

I just live on advil & Ibuprofen 800. My mind is so much clearier than it was on the medication.

It has been about 3yrs since I threw all the junk out of my medicine cabinet. Mentally could not be happier, still have FM flares & bad days, but deal with them the best I can.
 
avatar
deartam replied to foreversore's response:
Thank you so much for your kind response! I appreciate it very much. Sometimes I feel so alone with the FM as I do not know anyone who has it. And, of course you are probably well-aware that friends and family have their own ideas about FM and those of us who suffer through it, in my case their opinions are not encouraging nor are they helpful... in fact, they can be down-right disturbing. I no long try to defend myself about the symptoms I have. It is like going to a hardware store to buy a loaf of bread.

I take B-complex (a very powerful one) and B-12. They help. I have been told, by my doctor and pharmacist; and read that B-12 is more effective if all of the B vitamins are taken with it. I also take Calcium, Magnesium, Zinc and Malic Acid. For years, those supplements helped me tremendously. Now, as I age (will be 65 on 11/30) I am finding they are not enough. The pain was unmanageable.

I also have multiple other chronic pain problems (arthritis in spine, neck, hands, feet; bursitis in shoulder & elbow; and several degenerated discs.... too many to fuse). So, breaking down the causes of each type of pain has been a long ordeal, but well worth the effort.

I am finding that my energy level is already increasing a wee bit! I made my bed for the first time in many months, this morning! AND.... I did not feel like I needed to drop back into it. The exhaustion was overwhelming, there was nothing I could do but give into it and sleep. I slept as much as you! I still need a nap, but no longer 2 or 3 naps per day. I am very happy about that!

The sweating is a wee bit less, but still awful, especially since I am icey cold the whole time! I called my doctor and was told to wait a few more days and see what happens.

This is such a mysterious condition. It seems no two of us are alike. I often wonder if this is a new thing, or if past generations had it and just never named it.

Anyway, I thank you again for your response to my questions and your encouragement. I appreciated that so very much!
Hugs, Tamara
 
avatar
deartam replied to forgetful88's response:
Hi forgetfull88,
I am so glad you find relief w/advil & Ibuprofen800. That is awesome! FM is so different with each of us. I wish it was so simple for the rest of us because adjusting to the side effectss of FM meds is challenging. I am very grateful for the meds and am finding that very slowly, the side effects are subsiding, with the recent switch to Savella. Lyrica was not working out as I mentioned in my original post. It relieved the FM pain, but the side effects that I experienced were to harsh.

I wish you continued success in this battle with FM pain!
I also with you a wonderful Thanksgiving holiday!
 
avatar
unhappybeoch replied to forgetful88's response:
forgetful88, I did the same as you. but there are side effects to those pills also. after a few years advil and Ibuprofen I ended up with a stomach ulcur. Read the box, it tells you about the chance of getting them. The ulcur I have blocks proteins from going to my brain. So now I just added another problem to the list beside FM. So please be carefull on taking them on a long term bases.
 
avatar
forgetful88 replied to unhappybeoch's response:
Oh I know. My gyno preaches to me about the advil & Ibuprofen.

I do only take it during flares, & switch with Alleve off and on.
 
avatar
tiredpain responded:
I have had problems taking Lyrica. Acouple of yrs ago I had mild swelling in my lower legs and feet so I titrated myself off of med and swelling went away. I stayed off of it for several months and then due to pain I tried lyrica again and had no trouble for a while. About 3 months ago my feet and lower legs began to swell until they were huge! It was scary how big they got and no one even mentioned to me it could be the Lyrica. They thought it could be a vascular problem. I tried a couple of their solutions including lasixand compression stockings. Nothing happened. I remembered a family member who had problems with swelling with lyrica so I titrated myself off and within 48 hrs the swelling was gone. But for the next month I was off and on sick to my stomach and the nurse thought it might have been related to coming off the lyrica but wasn't sure. Now we have to find something to replace the lyrica which really helpedmy pain.
 
avatar
rickie3grandsons responded:
I was also on Lyrica and experienced swelling and having blk outs on thoughts, not remembering things..losing balance as well it was HORRIBLE ,my dr weaned me off in a couple mths I was taking 12 pills a day the highest perscrpition...it was very hard coming off the drug with alot of side effects.a friend of mine and my specialist asked me to mention to my family dr about medical marijuana...it took a long process to get the lience to obtain it legally and I only take it when I need it I make brownie' s and cookie's.... do not drive when Im taking it and really it has been a god send.....the weather is very hard on my fibro I have DDDD. ,REFLEX ASP. IBS,SCOLIOSIS,AND IAM NOT OVER WEIGHT NOW I was over weight on the Lyica I wish you well and try to get on something differant ....if you can try what I have good luck and gentle hugs!!!!
 
avatar
deartam replied to tiredpain's response:
Tiredpain, Thank you for your response! Wow, that is exactly what I experienced: extreme swelling of feet, legs and hands too. Fortunately my primary care physician knew about the side effects of Lyrica, even though he was not my prescribing physician.

I have "fired" the other doctor and sticking with the doctor who knows the most about FM !!! The switch to Savella has been the most terrible experience ever. Not because of the Savella, but because of withdrawals from Lyrica. Even though I am titrating slowly; I was drenched in sweat on Wed, I felt light-headed, not dizzy... kind of like I was fading away.... I had errands and appointments. As I drove past my dr's office I suddenly decided to turn in & ask if they would ck my bp. Normally, my bp is on the low side. It was SKY-HIGH and I was soaked in perspiration. He immediately did and ekg, which thank God, was fine. He sent me for a stress test & it is fine. Today, Saturday, I am better. I stayed in bed all day Friday and read. Some sweating still happening, but not like it was Wed & again on Thanksgiving Thursday!

The good news is, this is my last week on Lyrica! I advise everyone to be very, very careful with FM meds and discuss possible side effects in detail with physicians b4 starting. They do relieve the unbearable pain. I am hoping Savella will not have the severe side effects as Lyrica. Swelling is down, nearly vanished, balance is good although I do have to watch if I make a quick stop & turn as I'm walking!

I wish all of you success with your FM treatments. This condition, illness, whatever it is.... is HORRIBLE. Get help!
 
avatar
deartam replied to rickie3grandsons's response:
Hi rickie3grandsons! Oh my goodness, I forgot about the thought-losses with Lyrica! Yes, I experienced those too. Fortunately they are improving as I near the end of titrating off of Lyrica and onto Savella! I have also lost 2 whole pounds (even after eating so well on Thanksgiving Day!).

Interesting about the medical marijuana. I did not know that is an optional pain reliever for FM. I am so happy for you that you have found relief! It is good to have that information for those of us who cannot tolerate the side effects of Lyrica or Savella. I will keep the information in mind. I once tried Cymbalta, a couple of years ago. It did nothing for me.

Happy 4 U and gentle hugs back!
 
avatar
deartam replied to deartam's response:
LOL.... I re-read this and am laughing at my stmt "I forgot about the thought-losses with Lyrica!" Guess they are still going on. It is Sunday and I am feeling much better than I have the past 4 days.

I discovered that excessive sweating is called "hyperhidrosis" and the loss of fluids and electrolytes needs to be addressed w/my doctor on Monday. I made a big pot of vegetable soup, filled with "Potassium" veggies (sweet potatoes, potatoes, beet greens several others for flavor. I felt good after eating it. It couldn't hurt!

I also read in a google search that hyperhidrosis can cause rhinitis (sinus swelling), which I have and also blocked breathing. Interesting how one thing can lead to another. I now have a small notebook to show my physician.

Gentle hugs to each of you!


Helpful Tips

Living Well with Fibromyalgia
Greetings! I have learned patience and a positive attitude is key to my pain management. I developed Fibromyalgia after a hysterectomy in ... More
Was this Helpful?
193 of 210 found this helpful

Related News

There was an error with this newsfeed

Related Drug Reviews

  • Drug Name User Reviews

Report Problems With Your Medications to the FDA

FDAYou are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.